JP2008143937A - Non-asbestos-based friction material - Google Patents

Non-asbestos-based friction material Download PDF

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JP2008143937A
JP2008143937A JP2006329455A JP2006329455A JP2008143937A JP 2008143937 A JP2008143937 A JP 2008143937A JP 2006329455 A JP2006329455 A JP 2006329455A JP 2006329455 A JP2006329455 A JP 2006329455A JP 2008143937 A JP2008143937 A JP 2008143937A
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friction
friction material
metal oxide
clay mineral
asbestos
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JP5500760B2 (en
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Katsuhiro Kikuchi
克浩 菊地
Motonori Kuroe
元紀 黒江
Hiroshi Idei
浩 出井
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Akebono Brake Industry Co Ltd
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Akebono Brake Industry Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To obtain a friction material for a brake, which has an environmental loading lower than that of a friction material using an antimony compound, an excellent high-temperature abrasion resistance, a low aggresiveness to a mating material and retains a high coefficient of friction. <P>SOLUTION: The non-asbestos-based friction material contains no antimony compound as the compounding material of a friction material and comprises 1-20 mass% of a composite material obtained by inserting metal oxide particles into the interlayers of a layered clay mineral. The weight ratio of the metal oxide/layered clay mineral of the composite material is 0.1-2.0, the layered clay mineral is synthetic fluorine mica and the metal oxide is preferably a titania particle and an alumina particle. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、アンチモン化合物を使用しないノンアスベスト系摩擦材に関するものであり、特に産業機械、鉄道車両、荷物車両、乗用車などに用いられるロータ攻撃性を抑え、かつフェード特性が向上した摩擦材に関するものであり、とりわけアンチモン化合物を使用しなくても高温耐摩耗性を確保することができ、しかも高い摩擦係数を保持しつつ、相手材攻撃性を低く抑えた摩擦材に関するものであり、より具体的には前記の用途に使用されるブレーキパッド、ブレーキライニング、クラッチフェーシングに関するものである。   The present invention relates to a non-asbestos friction material that does not use an antimony compound, and more particularly to a friction material that suppresses rotor aggression and has improved fade characteristics used in industrial machinery, railway vehicles, luggage vehicles, passenger cars, and the like. In particular, it relates to a friction material that can ensure high-temperature wear resistance without using an antimony compound, and that keeps a high coefficient of friction while keeping the other material's aggressiveness low. Relates to brake pads, brake linings, and clutch facings used in the aforementioned applications.

ディスクブレーキやドラムブレーキなどのブレーキ、或いはクラッチなどに使用される摩擦材は、摩擦作用を与え、かつその摩擦性能を調整する摩擦調整材、補強作用をする繊維基材、これらの成分を一体化する結合材などの材料からなっている。そのうちの繊維基材には、金属繊維、無機繊維、有機繊維などの種類があり、それぞれの特徴があり、1種類ではすべての要求を満足することができないので、通常2種類以上のものが組み合わされて使用されている。   Friction materials used in brakes such as disc brakes and drum brakes, or clutches, etc., provide a frictional effect and adjust the friction performance, a fiber base material that reinforces, and these components are integrated. It is made of materials such as binding material. There are various types of fiber base materials, such as metal fibers, inorganic fibers, and organic fibers. Each type has its own characteristics, and since one type cannot satisfy all requirements, usually two or more types are combined. Has been used.

一方、摩擦材の摩擦特性を調整する材料としては摩擦調整材及び固体潤滑材があるが、これらにも無機系と有機系とがあり、それぞれの特徴があり、1種類ではすべての要求を満足することができないので、通常2種類以上のものが組み含わせて使用されている。そして、摩擦調整材としては、例えばアルミナやシリカ、マグネシア、ジルコニア等の無機摩擦調整材、合成ゴムやカシュー樹脂等の有機摩擦調整材を、固体潤滑材としては、例えば黒鉛や二硫化モリブデン等を挙げることができる。   On the other hand, there are friction modifiers and solid lubricants as materials that adjust the friction characteristics of friction materials, but these also have inorganic and organic types, each with their own characteristics. One type satisfies all requirements. In general, two or more types are used in combination. Examples of friction modifiers include inorganic friction modifiers such as alumina, silica, magnesia, and zirconia; organic friction modifiers such as synthetic rubber and cashew resin; and solid lubricants such as graphite and molybdenum disulfide. Can be mentioned.

また、充填材として、硫酸バリウム、炭酸カルシウム、金属粉、バーミキュライト、マイカなどが用いられている。
そして、これらの成分を配含してなる摩擦材の相手攻撃性を抑え、耐フェード性、耐摩耗性を改善したノンアスベスト系摩擦材として種々の配合の摩擦材が提案されている。
As the filler, barium sulfate, calcium carbonate, metal powder, vermiculite, mica, and the like are used.
In addition, friction materials of various blends have been proposed as non-asbestos-based friction materials that suppress the attack of the friction material containing these components and improve the fade resistance and wear resistance.

特許文献1は、自動車などに用いられるブレーキノイズの低減したブレーキ用摩擦材、特にオートマチック車の発進時における低周波異音が発生しないブレーキ用摩擦材として、補強繊維、摩擦調整材、潤滑材及び結合材よりなる摩擦材において、摩擦調整材成分の一部としてゼオライト2〜5質量%、酸化アンチモン0.8〜2質量%及びフッ素系ポリマー0.2〜1質量%を含有するブレーキ用摩擦材を開示している。
特開2001−181607号公報
Patent Document 1 discloses a brake friction material with reduced brake noise used for automobiles and the like, in particular, as a brake friction material that does not generate low-frequency noise when starting an automatic vehicle, a reinforcing fiber, a friction adjusting material, a lubricant, and Friction material comprising a binder, brake friction material containing 2-5% by mass of zeolite, 0.8-2% by mass of antimony oxide and 0.2-1% by mass of fluoropolymer as part of the friction modifier component Is disclosed.
JP 2001-181607 A

しかしながら、特開2001−181607号公報に開示されたブレーキ用摩擦材には、酸化アンチモン配合量が2質量%を超えると耐フェード性が低下するという欠点があった。
しかも、アンチモン化合物は環境保護の観点から制定されたPRTR法(特定化学物質の環境への排出量の把握等及び管理の改善の促進の関する法律)の指定物質であることから、アンチモンを含まない高温で潤滑性を有し、摩擦特性を調整できる材料が求められるようになった。
However, the brake friction material disclosed in Japanese Patent Application Laid-Open No. 2001-181607 has a drawback in that fade resistance decreases when the antimony oxide content exceeds 2 mass%.
In addition, antimony compounds do not contain antimony because they are designated substances in the PRTR Law (Act on Understanding the Release of Specific Chemical Substances into the Environment and Promoting Improvements in Management) established from the viewpoint of environmental protection. Materials that have lubricity at high temperatures and can adjust friction characteristics have been demanded.

本発明は、このような従来の事情よりなされたものであり、アンチモン化合物を用いた摩擦材よりも環境負荷が小さく、高温の耐摩耗性が優れ、相手攻撃性が低く、高い摩擦係数を保持できるブレーキ用摩擦材を提供することを目的とする。   The present invention has been made under such conventional circumstances, and has a lower environmental load than a friction material using an antimony compound, excellent high-temperature wear resistance, low opponent attack, and maintains a high coefficient of friction. An object of the present invention is to provide a friction material for a brake.

本発明者等は、上記の目的を達成するために鋭意研究を続け、合成雲母のような層状粘土鉱物の層間に金属酸化物粒子を挿入してなる複合材を、摩擦材の原材料に摩擦調整材の一部として適量配合することにより、アンチモン化合物を使用しなくても高温での耐摩耗性を確保でき、高い摩擦係数を保持しつつ、相手材攻撃性を低く抑えることができることに着目して、本発明に到達した。   The inventors of the present invention have continued intensive research to achieve the above-mentioned object, and friction adjustment is performed on the raw material of the friction material using a composite material in which metal oxide particles are inserted between layers of layered clay mineral such as synthetic mica. Paying attention to the fact that by blending an appropriate amount as part of the material, wear resistance at high temperatures can be ensured without using an antimony compound, while maintaining a high coefficient of friction and keeping the other material aggressive. The present invention has been reached.

すなわち、本発明は、下記の手段により、上記の課題を解決した。
(1)摩擦材の配合材料として、アンチモン化合物を含有せず、層状粘土鉱物の層間に金属酸化物粒子を挿入してなる複合材を1〜20質量%含有することを特徴とするノンアスベスト系摩擦材。
(2)前記複合材の金属酸化物/層状粘土鉱物の質量比率が0.1〜2.0であることを特徴とする前記(1)記載のノンアスベスト系摩擦材。
(3)前記複合材の層状粘土鉱物が合成フッ素雲母であることを特徴とする前記(1)又は(2)記載のノンアスベスト系摩擦材。
(4)前記複合材の金属酸化物粒子がチタニア粒子であることを特徴とする前記(1)〜(3)のいずれか1項に記載のノンアスベスト系摩擦材。
(5)前記複合材の金属酸化物粒子がアルミナ粒子であることを特徴とする前記(1)〜(3)のいずれか1項に記載のノンアスベスト系摩擦材。
That is, the present invention has solved the above problems by the following means.
(1) A non-asbestos system containing 1 to 20% by mass of a composite material containing no antimony compound and having metal oxide particles inserted between layers of a layered clay mineral as a blending material of a friction material Friction material.
(2) The non-asbestos friction material according to (1) above, wherein the composite material has a metal oxide / layered clay mineral mass ratio of 0.1 to 2.0.
(3) The non-asbestos friction material according to (1) or (2) above, wherein the layered clay mineral of the composite material is synthetic fluorine mica.
(4) The non-asbestos friction material according to any one of (1) to (3), wherein the metal oxide particles of the composite material are titania particles.
(5) The non-asbestos friction material according to any one of (1) to (3), wherein the metal oxide particles of the composite material are alumina particles.

本発明によれば、補強用繊維基材、摩擦調整材、これらの成分を一体化する結合材などの材料からなるノンアスベスト系摩擦材において、摩擦調整材の一部として層状粘土鉱物の層間に金属酸化物粒子を挿入してなる複合材を使用することにより、環境保護の観点から問題となるアンチモン化合物を使用することなしに、300℃以上の高温摺動時の摩耗量を低減でき、摩擦材の300℃以上の高温摺動時における摩擦係数を高くし、同時に相手材の摩耗を抑えることができる。   According to the present invention, in a non-asbestos-based friction material made of a reinforcing fiber base material, a friction adjusting material, a binding material that integrates these components, etc., as a part of the friction adjusting material, between the layers of the layered clay mineral By using a composite material in which metal oxide particles are inserted, the amount of wear when sliding at a high temperature of 300 ° C. or higher can be reduced without using an antimony compound that is problematic from the viewpoint of environmental protection, and friction can be reduced. The coefficient of friction when the material slides at a high temperature of 300 ° C. or higher can be increased, and at the same time, wear of the counterpart material can be suppressed.

以下、本発明の実施の形態を説明する。
本発明のノンアスベスト系摩擦材においては、摩擦材の原材料を摩擦調整材の一部として、層状粘土鉱物の層間に金属酸化物粒子を挿入してなる複合材を1〜20質量%配合することにより、ノンアスベスト系の摩擦材の300℃以上の高温摺動時での摩擦、摩耗性能をアンチモン化合物を使用した摩擦材と同様にすることを特徴とするものである。
Embodiments of the present invention will be described below.
In the non-asbestos-based friction material of the present invention, 1 to 20% by mass of a composite material in which metal oxide particles are inserted between layers of a layered clay mineral, with the friction material as a part of the friction modifier. Thus, the friction and wear performance when the non-asbestos friction material slides at a high temperature of 300 ° C. or higher is made the same as that of the friction material using the antimony compound.

配合量が1質量%未満では、余りに少量過ぎて高温での充分な摩擦、摩耗性能を発揮することができない。一方、20質量%を超えると、それ以上の摩擦、摩耗性能の向上が発揮できなくなり、不経済的になる。それゆえ、適切な含有量としては、1〜20質量%になる。   If the blending amount is less than 1% by mass, the amount is too small and sufficient friction and wear performance at high temperatures cannot be exhibited. On the other hand, if it exceeds 20% by mass, further improvement in friction and wear performance cannot be achieved, which is uneconomical. Therefore, the appropriate content is 1 to 20% by mass.

本発明において、層状粘土鉱物としては、例えばカオリナイト、スメクタイト、バーミキュライト等のイオン交換能を持つ天然粘土鉱物や人工合成粘土が用いられる。スメクタイトにはモンモリロナイト、サポナイト、ハイデライト、ノントロナイト等が例示される。中でも天然の層状粘土鉱物に比べて品質のバラツキが小さい合成フッ素雲母が、本発明に使用するのに好適なものであり、ナトリウム四ケイ素フッ素雲母(NaM2.5Si10)が例示される。 In the present invention, as the layered clay mineral, for example, a natural clay mineral having an ion exchange ability such as kaolinite, smectite, vermiculite, or artificial synthetic clay is used. Examples of smectites include montmorillonite, saponite, hydelite, and nontronite. Among them, a synthetic fluorine mica having a small quality variation compared to a natural layered clay mineral is suitable for use in the present invention, and sodium tetrasilicon fluorine mica (NaM 2.5 Si 4 O 10 F 2 ) is used. Illustrated.

また、本発明において、金属酸化物の金属の種類としては、アルミニウムやチタンのように、陽イオン化し得る性質を有するものが好ましい。
そして、複合材の金属酸化物/層状粘土鉱物の重量比は、0.1〜2.0であることが好ましい。
In the present invention, the metal type of the metal oxide is preferably a metal having a property capable of being cationized, such as aluminum or titanium.
The weight ratio of the composite metal oxide / layered clay mineral is preferably 0.1 to 2.0.

本発明の摩擦材を製造するには、繊維基材、摩擦調整材、潤滑材、充填材、結合材からなる摩擦材用諸原料を配合し、その配合物を通常の製法に従って予備成形し、熱成形することにより製造することができる。上記において、繊維基材としては、例えば芳香族ポリアミド繊維、耐炎化アクリル繊維等の有機繊維や銅繊維、スチール繊維等の金属繊維、チタン酸カリウム繊維やAl−SiO系セラミック繊維等の無機繊維が挙げられる。無機充填材としては、例えば銅やアルミニウム、亜鉛等の金属粒子、バーミキュライトやマイカ等の鱗片状無機物、硫酸バリウムや炭酸カルシウム等が挙げられる。 In order to produce the friction material of the present invention, various materials for friction material consisting of a fiber base material, a friction modifier, a lubricant, a filler, and a binder are blended, and the blend is preformed according to a normal manufacturing method, It can be manufactured by thermoforming. In the above, examples of the fiber substrate include organic fibers such as aromatic polyamide fibers and flame-resistant acrylic fibers, copper fibers, metal fibers such as steel fibers, potassium titanate fibers, Al 2 O 3 —SiO 2 ceramic fibers, and the like. Inorganic fiber. Examples of the inorganic filler include metal particles such as copper, aluminum and zinc, scaly inorganic materials such as vermiculite and mica, barium sulfate and calcium carbonate.

結合材としては、例えばフェノール樹脂(ストレートフェノール樹脂、ゴム等による各種変性フェノール樹脂を含む)、メラミン樹脂、エポキシ樹脂、ポリイミド樹脂等の熱硬化性樹脂を挙げることができる。また、摩擦調整材としては、例えばアルミナやシリカ、マグネシア、ジルコニア、酸化クロム等の金属酸化物、合成ゴムやカシュー樹脂等の有機摩擦調整材を、固体潤滑材としては、例えば黒鉛や二酸化モリブデン等を挙げることができる。摩擦材の組成としては、種々の組成割合を採ることができる。すなわち、これらは、製品に要求される摩擦特性、例えば、摩擦係数、耐摩耗性、振動特性、鳴き特性等に応じて、単独でまたは2種以上を組み合わせて配合すればよい。   Examples of the binder include thermosetting resins such as phenol resins (including various modified phenol resins such as straight phenol resins and rubbers), melamine resins, epoxy resins, and polyimide resins. Examples of the friction modifier include metal oxides such as alumina, silica, magnesia, zirconia, and chromium oxide; organic friction modifiers such as synthetic rubber and cashew resin; and solid lubricants such as graphite and molybdenum dioxide. Can be mentioned. As the composition of the friction material, various composition ratios can be adopted. That is, these may be blended singly or in combination of two or more according to the friction characteristics required for the product, for example, friction coefficient, wear resistance, vibration characteristics, squeal characteristics, and the like.

以下、実施例により本発明を具体的に説明する。ただし、本発明はこれらの実施例のみに限定されるものではない。   Hereinafter, the present invention will be described specifically by way of examples. However, the present invention is not limited to only these examples.

実施例1及び比較例1〜3
<チタニア粒子挿入複合材>
(複合材試料の製造)
2リットルの蒸留水に合成フッ素雲母を20g投入し、室温で24時間攪拌した。一方で、酢酸80%水溶液500ミリリットルにテトライソプロポキシシランを56g投入し、50℃で1時間混合した後、室温まで冷却して合成フッ素雲母分散水溶液に投入した。室温で2時間混合した後、遠心分離にて試料を取り出し、2リットルの蒸留水で水洗、遠心分離をpH5以上になるまで繰り返した。試料を室温で減圧し、72時間乾燥させた後、500℃で2時間加熱処理を行い、粉砕処理を経てチタニア粒子を合成フッ素雲母の層間に挿入した複合材料を得た。
上記の手順に従って、合成フッ素雲母の層間にチタニア粒子を40%挿入した複合材(試料A)が得られた。
(摩擦材試料の調製)
下記第1表に示す配合で摩擦材を試作した。また、複合材試料の代わりに硫化アンチモン、又は雲母を配合した比較材1、比較材2を作製し、別に試料、硫化アンチモン、又は雲母を配合しないものを比較材3として作製した。
Example 1 and Comparative Examples 1-3
<Titania particle insertion composite>
(Manufacture of composite materials)
20 g of synthetic fluorine mica was added to 2 liters of distilled water and stirred at room temperature for 24 hours. On the other hand, 56 g of tetraisopropoxysilane was added to 500 ml of an 80% aqueous solution of acetic acid, mixed at 50 ° C. for 1 hour, cooled to room temperature, and added to a synthetic fluoromica-dispersed aqueous solution. After mixing at room temperature for 2 hours, the sample was removed by centrifugation, washed with 2 liters of distilled water, and centrifuged until the pH reached 5 or more. The sample was depressurized at room temperature and dried for 72 hours, followed by heat treatment at 500 ° C. for 2 hours, and a pulverization process was performed to obtain a composite material in which titania particles were inserted between synthetic fluorine mica layers.
According to the above procedure, a composite material (sample A) in which 40% of titania particles were inserted between the layers of synthetic fluorine mica was obtained.
(Preparation of friction material sample)
A friction material was made with the formulation shown in Table 1 below. Moreover, the comparative material 1 and the comparative material 2 which mix | blended antimony sulfide or mica instead of the composite material sample were produced, and the thing which does not mix | blend a sample, antimony sulfide, or mica was produced as the comparative material 3.

Figure 2008143937
Figure 2008143937

(摩擦試験)
試作した摩擦材を用いて下記第2表に示す条件で摩擦試験を行った。
(試験結果)
実施例1及び比較例1〜3の試験結果を下記第3表に示す。
実施例1の400℃摩耗試験における摩耗量は、アンチモン化合物を使用した比較例1と同等であることから本発明の効果が確認された。
(Friction test)
A friction test was conducted using the prototype friction material under the conditions shown in Table 2 below.
(Test results)
The test results of Example 1 and Comparative Examples 1 to 3 are shown in Table 3 below.
Since the wear amount in the 400 ° C. wear test of Example 1 is equivalent to that of Comparative Example 1 using an antimony compound, the effect of the present invention was confirmed.

Figure 2008143937
Figure 2008143937

Figure 2008143937
Figure 2008143937

実施例2及び比較例4
<アルミナ粒子挿入複合材>
(複合材試料の製造)
塩化アルミニウムの水和物24gを蒸留水500ミリリットルに溶解し、撹拌した。その溶液に水酸化ナトリウム10gを蒸留水2500gに溶解した水溶液を50ミリリットル/minで滴下した。滴下後に95℃で還流を48時間行い、合成フッ素雲母を20g加えて室温で3時間撹拌した。遠心分離機で水洗いを行い。80℃で2時間乾燥処理を行った。
さらに400℃の加熱炉で2時間加熱処理を行い、粉砕処理を経てアルミナ粒子を雲母の層間に挿入した複合材(試料B)を得た。
(摩擦材試料の調製)
上記のように合成した複合材を用いて第4表に示す配合にてテストピースを成形し、摩擦特性の評価を次に行った。これとともに、複合材(試料B)を配合しない摩擦材を作製し、これを比較例4とした。
Example 2 and Comparative Example 4
<Alumina particle insertion composite>
(Manufacture of composite materials)
24 g of aluminum chloride hydrate was dissolved in 500 ml of distilled water and stirred. An aqueous solution prepared by dissolving 10 g of sodium hydroxide in 2500 g of distilled water was added dropwise to the solution at 50 ml / min. After the dropwise addition, the mixture was refluxed at 95 ° C. for 48 hours. Wash with water in a centrifuge. A drying treatment was performed at 80 ° C. for 2 hours.
Further, a heat treatment was carried out in a heating furnace at 400 ° C. for 2 hours, and a composite material (sample B) in which alumina particles were inserted between mica layers through pulverization was obtained.
(Preparation of friction material sample)
Using the composite material synthesized as described above, a test piece was molded according to the formulation shown in Table 4, and the friction characteristics were then evaluated. At the same time, a friction material not containing the composite material (sample B) was produced, and this was designated as Comparative Example 4.

Figure 2008143937
Figure 2008143937

(摩耗試験)
第4表の配合で成形したテストピースの摩耗試験を行なった。
摩耗試験は制動初速度50km/h、制動回数200回、制動ブレーキ温度100℃、及び400℃の条件で、摩擦材の摩耗量(mm)とディスクロータの摩耗量(g)を測定した。
(試験結果)
結果を下記第5表に示す。
(Abrasion test)
A wear test was performed on test pieces molded with the formulations shown in Table 4.
In the wear test, the friction material wear amount (mm) and the disk rotor wear amount (g) were measured under the conditions of an initial braking speed of 50 km / h, a braking frequency of 200 times, and a braking brake temperature of 100 ° C. and 400 ° C.
(Test results)
The results are shown in Table 5 below.

Figure 2008143937
Figure 2008143937

第5表に示した摩耗試験結果から明らかな如く、実施例2の摩擦材は比較例4の摩擦材に比較して、400℃での摩擦係数が高く、しかもロータ摩耗量が少ないことから、本発明の層状粘土鉱物の層間に金属酸化物粒子を挿入してなる複合材を、摩擦調整材の一部に使用することの優れた効果が確認された。   As is apparent from the results of the wear test shown in Table 5, the friction material of Example 2 has a higher coefficient of friction at 400 ° C. and a smaller amount of rotor wear than the friction material of Comparative Example 4. The excellent effect of using a composite material obtained by inserting metal oxide particles between layers of the layered clay mineral of the present invention as a part of the friction modifier was confirmed.

本発明のノンアスベスト系摩擦材は、合成雲母のような層状粘土鉱物の層間に金属酸化物粒子を挿入してなる複合材を、摩擦材の原材料に摩擦調整材の一部として適量配合することにより、アンチモン化合物を使用しなくても高温での耐摩耗性を確保でき、高い摩擦係数を保持しつつ、相手材攻撃性を低く抑えることができるので、特に産業機械、鉄道車両、荷物車両、乗用車などの摩擦材、より具体的には前記の用途に使用されるブレーキパッド、ブレーキライニング、クラッチフェーシングに特に有用なものである。   In the non-asbestos friction material of the present invention, an appropriate amount of a composite material in which metal oxide particles are inserted between layers of a layered clay mineral such as synthetic mica is mixed as a part of the friction modifier in the raw material of the friction material. By this, it is possible to ensure wear resistance at high temperatures without using an antimony compound, and while maintaining a high coefficient of friction, it is possible to keep the opponent material attack low, especially industrial machinery, railway vehicles, luggage vehicles, It is particularly useful for friction materials such as passenger cars, more specifically, brake pads, brake linings, and clutch facings used in the above-described applications.

Claims (5)

摩擦材の配合材料として、アンチモン化合物を含有せず、層状粘土鉱物の層間に金属酸化物粒子を挿入してなる複合材を1〜20質量%含有することを特徴とするノンアスベスト系摩擦材。   A non-asbestos-based friction material containing 1 to 20% by mass of a composite material that does not contain an antimony compound and is formed by inserting metal oxide particles between layers of a layered clay mineral as a blending material of the friction material. 前記複合材の金属酸化物/層状粘土鉱物の質量比率が0.1〜2.0であることを特徴とする請求項1記載のノンアスベスト系摩擦材。   2. The non-asbestos friction material according to claim 1, wherein the composite material has a metal oxide / layered clay mineral mass ratio of 0.1 to 2.0. 前記複合材の層状粘土鉱物が合成フッ素雲母であることを特徴とする請求項1又は請求項2記載のノンアスベスト系摩擦材。   3. The non-asbestos friction material according to claim 1, wherein the layered clay mineral of the composite material is synthetic fluorine mica. 前記複合材の金属酸化物粒子がチタニア粒子であることを特徴とする請求項1〜3のいずれか1項に記載のノンアスベスト系摩擦材。   The non-asbestos friction material according to any one of claims 1 to 3, wherein the metal oxide particles of the composite material are titania particles. 前記複合材の金属酸化物粒子がアルミナ粒子であることを特徴とする請求項1〜3のいずれか1項に記載のノンアスベスト系摩擦材。   The non-asbestos friction material according to any one of claims 1 to 3, wherein the metal oxide particles of the composite material are alumina particles.
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JP2009263577A (en) * 2008-04-28 2009-11-12 Akebono Brake Ind Co Ltd Friction modifier, method of producing friction modifier, and friction material
JP2009275063A (en) * 2008-05-12 2009-11-26 Akebono Brake Ind Co Ltd Frictional material
JP2010059396A (en) * 2008-08-08 2010-03-18 Akebono Brake Ind Co Ltd Solid lubricant and method of manufacturing the same

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JPH04114084A (en) * 1990-09-01 1992-04-15 Sumitomo Electric Ind Ltd Friction material for disc brake
JPH04198388A (en) * 1990-11-28 1992-07-17 Akebono Brake Res & Dev Center Ltd Non-asbestos friction material
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JPH09508420A (en) * 1994-01-21 1997-08-26 フェロド リミテッド Friction material for use in Al alloy rotor
JPH11246211A (en) * 1998-03-06 1999-09-14 Toichiro Izawa Alumina crosslinked fluorine mica, its production and its sintered compact

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JPH03239784A (en) * 1990-02-19 1991-10-25 Hitachi Chem Co Ltd Friction material composition and manufacture of friction material therefrom
JPH04114084A (en) * 1990-09-01 1992-04-15 Sumitomo Electric Ind Ltd Friction material for disc brake
JPH04198388A (en) * 1990-11-28 1992-07-17 Akebono Brake Res & Dev Center Ltd Non-asbestos friction material
JPH09508420A (en) * 1994-01-21 1997-08-26 フェロド リミテッド Friction material for use in Al alloy rotor
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JPH11246211A (en) * 1998-03-06 1999-09-14 Toichiro Izawa Alumina crosslinked fluorine mica, its production and its sintered compact

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009263577A (en) * 2008-04-28 2009-11-12 Akebono Brake Ind Co Ltd Friction modifier, method of producing friction modifier, and friction material
JP2009275063A (en) * 2008-05-12 2009-11-26 Akebono Brake Ind Co Ltd Frictional material
JP2010059396A (en) * 2008-08-08 2010-03-18 Akebono Brake Ind Co Ltd Solid lubricant and method of manufacturing the same

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