JPS63195438A - Wet-type friction material - Google Patents
Wet-type friction materialInfo
- Publication number
- JPS63195438A JPS63195438A JP2682287A JP2682287A JPS63195438A JP S63195438 A JPS63195438 A JP S63195438A JP 2682287 A JP2682287 A JP 2682287A JP 2682287 A JP2682287 A JP 2682287A JP S63195438 A JPS63195438 A JP S63195438A
- Authority
- JP
- Japan
- Prior art keywords
- friction
- hollow glass
- friction material
- porous hollow
- inorganic additive
- 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
Links
- 239000002783 friction material Substances 0.000 title claims abstract description 26
- 239000011521 glass Substances 0.000 claims abstract description 20
- 239000000654 additive Substances 0.000 claims abstract description 18
- 230000000996 additive effect Effects 0.000 claims abstract description 15
- 239000000463 material Substances 0.000 claims abstract description 14
- 239000011347 resin Substances 0.000 claims abstract description 10
- 229920005989 resin Polymers 0.000 claims abstract description 10
- 239000002245 particle Substances 0.000 claims abstract description 4
- 239000003607 modifier Substances 0.000 claims description 9
- 239000011148 porous material Substances 0.000 claims description 7
- 238000000465 moulding Methods 0.000 claims description 4
- 230000014759 maintenance of location Effects 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract description 3
- 238000001816 cooling Methods 0.000 abstract description 2
- 230000035699 permeability Effects 0.000 abstract description 2
- 238000005299 abrasion Methods 0.000 abstract 1
- 230000001050 lubricating effect Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 238000010521 absorption reaction Methods 0.000 description 6
- 239000005909 Kieselgur Substances 0.000 description 5
- 239000002585 base Substances 0.000 description 4
- 244000226021 Anacardium occidentale Species 0.000 description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 3
- 235000020226 cashew nut Nutrition 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- -1 synthetic pulp Polymers 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000004760 aramid Substances 0.000 description 2
- 229920003235 aromatic polyamide Polymers 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- INJRKJPEYSAMPD-UHFFFAOYSA-N aluminum;silicic acid;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O INJRKJPEYSAMPD-UHFFFAOYSA-N 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 239000010443 kyanite Substances 0.000 description 1
- 229910052850 kyanite Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Braking Arrangements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、耐熱性、耐久性の向上した湿式摩擦材に関す
る。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a wet friction material with improved heat resistance and durability.
[従来の技術]
従来油中で使用する湿式摩擦材は、繊維、摩擦調整剤、
無機添加剤にフェノール樹脂を添加混合して成形してラ
イニング材とし、それをリング状に加工し、同じくリン
グ状に加工された金属板の両面に接着していた。[Prior art] Wet friction materials conventionally used in oil include fibers, friction modifiers,
A lining material was formed by adding and mixing a phenol resin to an inorganic additive, which was then processed into a ring shape and adhered to both sides of a metal plate that was also formed into a ring shape.
例えば特開昭58−7793’7号公報では繊維として
ガラス繊維を全摩擦材量100重量部に対し30〜60
重量部使用する摩擦材の開示がある。For example, in Japanese Patent Application Laid-Open No. 58-7793'7, glass fibers are used in an amount of 30 to 60 parts by weight per 100 parts by weight of the total friction material.
There is a disclosure of the friction material used in parts by weight.
また特開昭59−81340号公報にはパルプ繊維をベ
ースにして、これに摩擦総重量部に対して5〜70重量
部のバルーン状シリカを添加した摩擦材が開示されてい
る。Further, Japanese Patent Application Laid-open No. 59-81340 discloses a friction material based on pulp fibers, to which balloon-shaped silica is added in an amount of 5 to 70 parts by weight based on the total friction weight.
[発明が解決しようとする問題点]
上記の湿式摩擦材は無機添加剤または摩擦調整剤と呼ば
れる添加物のケイソウ土が主体として用いられている。[Problems to be Solved by the Invention] The above-mentioned wet friction material mainly uses diatomaceous earth, which is an additive called an inorganic additive or a friction modifier.
このケイソウ土は天然に産出されるものでありその粒径
は、O1数ミクロンから数百ミクロンと範囲が広い。こ
のため成形時の樹脂との混合が不完全となりやすくまた
抄紙時の定着率が一定しなかった。また上記ケイソウ土
は多孔質のものではあるが、その気孔のうち有効な気孔
径が全気孔中の40%程度しかない。従って湿式摩擦材
の油中での油の保持性、吸収性、なじみ性に限界があり
、耐熱性、耐久性に問題があった。This diatomaceous earth is naturally produced, and its particle size ranges widely from several microns to several hundred microns. For this reason, mixing with the resin during molding tends to be incomplete, and the fixing rate during paper making is inconsistent. Furthermore, although the diatomaceous earth is porous, the effective diameter of its pores is only about 40% of the total pores. Therefore, there are limits to the oil retention, absorption, and conformability of wet friction materials in oil, and there are problems with heat resistance and durability.
本発明は無機添加剤等の油の浸透性を向上させることに
より上記の問題点を解消した湿式摩擦材を提供すること
を目的とする。An object of the present invention is to provide a wet friction material that solves the above problems by improving the permeability of oil such as inorganic additives.
[問題点を解決するための手段]
本発明は基材と摩Wt調整剤と無機質添加剤と樹脂とか
らなる混合材料を成形して得られる湿式摩擦材において
、該無機質添加剤の少なくとも一部は多孔質中空ガラス
であることを特徴とする。[Means for Solving the Problems] The present invention provides a wet friction material obtained by molding a mixed material consisting of a base material, a friction Wt modifier, an inorganic additive, and a resin, in which at least a portion of the inorganic additive is is characterized by being a porous hollow glass.
本発明の湿式摩擦材の基材は、有ms!維および無機繊
維のいずれも用いることができる。有機繊維としては、
リンクパルプ、木材パルプ、合成パルプ、ポリエステル
系繊維、アクリル繊維、ポリアミド系繊維、ポリビニル
アルコール変性繊維、ポリ塩化ビニル繊維、ポリプロピ
レンtlH1炭素U&維などを1種または複数種類混合
して用いることができる。≠だ無機繊維としては、チタ
ン酸カリウム繊維、ガラス繊維、カオリン繊維、シリカ
繊維、ボーキサイト繊維、カヤナイト繊維、ホウ゛素繊
維、マグネシア繊維、ロックウール繊維、金a繊維など
を1種または複数種類用いることができる。なお軽量化
には有機繊維を主体とするのが効果的である。The base material of the wet friction material of the present invention is ms! Both fibers and inorganic fibers can be used. As an organic fiber,
Link pulp, wood pulp, synthetic pulp, polyester fibers, acrylic fibers, polyamide fibers, polyvinyl alcohol-modified fibers, polyvinyl chloride fibers, polypropylene tlH1 carbon U & fibers, etc. can be used alone or in combination. As the inorganic fiber, one or more types of potassium titanate fiber, glass fiber, kaolin fiber, silica fiber, bauxite fiber, kyanite fiber, boron fiber, magnesia fiber, rock wool fiber, gold a fiber, etc. are used. be able to. Note that it is effective to use organic fiber as the main material for weight reduction.
摩擦調整剤はIIJ擦係擦合数上し安定化するためのも
ので、例えばアルミニウム粉、銅粉、鉄粉などの金属粉
、ゴム粉、カシューダスト、グラファイト粉などである
。The friction modifier is used to increase and stabilize the number of IIJ frictions, and includes, for example, metal powder such as aluminum powder, copper powder, and iron powder, rubber powder, cashew dust, and graphite powder.
本発明の最大の特徴は、無機添加剤として多孔質中空ガ
ラスを用いることである。この多孔質中空ガラスは粒径
が10〜1100t1を有し、0゜1〜5μmの気孔径
を有するものが好ましい。気孔径が0.1μmより小さ
いと油の吸収特性が悪く5μmを越えると油の保持性が
悪(なり好ましくない。さらに粒子径が10〜100μ
mの範囲に分布していることが油とのなじみ性、保持性
、吸収性などに好結果を与える。The greatest feature of the present invention is the use of porous hollow glass as an inorganic additive. This porous hollow glass preferably has a particle size of 10 to 1100 t1 and a pore size of 0.1 to 5 μm. If the pore size is smaller than 0.1 μm, oil absorption properties are poor, and if it exceeds 5 μm, oil retention is poor (and undesirable).
Distribution in the range of m gives good results in terms of compatibility with oil, retention, absorption, etc.
この多孔質中空ガラスは例えば中空ガラスをアルカリ処
理することで容易に得られる。この多孔質中空ガラスの
量が20重量%未満であると油のなじみ、吸収性が悪化
し60重量%を越えると定着率が落ちるので好ましくな
い。This porous hollow glass can be easily obtained, for example, by treating hollow glass with an alkali. If the amount of this porous hollow glass is less than 20% by weight, oil absorption and oil absorption will deteriorate, and if it exceeds 60% by weight, the fixing rate will decrease, which is not preferable.
無機添加剤は上記の多孔質中空ガラス以外に従来から使
用されているシリカ、タルク、酸化マグネシウム、カオ
リン、硫酸バリウム、リン酸カリウム、炭酸カルシウム
、ケイツク土などを添加して用いることもできる。In addition to the porous hollow glass described above, conventionally used inorganic additives such as silica, talc, magnesium oxide, kaolin, barium sulfate, potassium phosphate, calcium carbonate, and siliceous earth can also be used.
樹脂は添加物を結合するもので従来と同様フェノール樹
脂、エポキシ樹脂、メラミン樹脂、尿素樹脂などが用い
られる。The resin binds additives, and as in the past, phenol resin, epoxy resin, melamine resin, urea resin, etc. are used.
本発明の摩擦材を製造するには、水中に基材の繊維、摩
擦調整剤、無機質添加剤とからなる混合物を抄紙し、こ
の抄紙体に樹脂を含浸させて硬化するか、または基材、
摩tlA調整剤、無機添加剤、樹脂とからなる混合物を
成形型内にて加熱加圧成形することにより容易に製造す
ることができる。To produce the friction material of the present invention, a mixture of base fibers, a friction modifier, and an inorganic additive is made into paper in water, and the paper product is impregnated with a resin and cured, or the base material,
It can be easily manufactured by heating and press-molding a mixture consisting of a tlA modifier, an inorganic additive, and a resin in a mold.
[発明の作用および効果]
本発明の湿式摩擦材は、無機添加剤の少なくと゛も一部
に多孔質中空ガラスを使用することにより、油の保持性
、吸収性、なじみ性が向上しこれにより摩擦材の油によ
る冷却効果潤滑効果が高まるものと推定される。これに
より耐久性、耐熱性が向上し、摩擦係数の長期安定化、
摩耗量低下により寿命を長くすることが可能となった。[Operations and Effects of the Invention] The wet friction material of the present invention improves oil retention, absorption, and conformability by using porous hollow glass as at least a part of the inorganic additive. It is estimated that the cooling and lubrication effects of the oil in the material will increase. This improves durability and heat resistance, stabilizes the friction coefficient over the long term, and
It has become possible to extend the lifespan by reducing the amount of wear.
[実施例] 以下実施例により具体的に説明する。[Example] This will be explained in detail below using examples.
(実施例1)
有am維A (セルo−スli!Ift>2011%と
有機4!雑B(芳香族ポリアミド繊維)30重量%と、
摩擦調整剤(カシューダスト)10重量%、多孔質中空
ガラス(日本板ガラス社製のC−10グレード中空ガラ
スを多孔処理(アルカリ処理)して気孔径0.2〜1μ
mの多孔質中空ガラスとした)40重量%の混合物を水
中で撹拌混合して均一の懸濁液とした後抄紙した。得ら
れた抄紙体にフェノール樹脂を含浸し加熱成形して実施
例1の摩擦材を得た。(Example 1) Am fiber A (cell o-li! Ift>2011% and organic 4! miscellaneous B (aromatic polyamide fiber) 30% by weight,
Friction modifier (cashew dust) 10% by weight, porous hollow glass (C-10 grade hollow glass manufactured by Nippon Sheet Glass Co., Ltd., treated with pores (alkali treatment) to have a pore size of 0.2 to 1μ
A 40 wt. The obtained paper body was impregnated with a phenol resin and hot-molded to obtain the friction material of Example 1.
(実施例2)
有機繊維A(セルロース繊維)13.3重量%、有様繊
維B(芳香族ポリアミド繊維>20重量%、摩擦調整剤
(カシューダスト)6.7重量%、実施例1と同じ多孔
質中空ガラス60m1%の混合物から実施例1と同様の
方法で摩擦材を作製し実施例2の湿式I!!擦材とした
。(Example 2) Organic fiber A (cellulose fiber) 13.3% by weight, structured fiber B (aromatic polyamide fiber >20% by weight, friction modifier (cashew dust) 6.7% by weight, same as Example 1 A friction material was prepared in the same manner as in Example 1 from a mixture of 60 ml of porous hollow glass and used as a wet type I!! friction material in Example 2.
(比較例)
実施例1にあい多孔質中空ガラスの代りにケイソウ土を
用いた他は同様にして摩擦材を作製し比較例の湿式I!
J擦材とした。(Comparative Example) A friction material was prepared in the same manner as in Example 1 except that diatomaceous earth was used instead of the porous hollow glass, and a wet type I! comparison example was prepared.
It was made of J rubbing material.
(評価)
実施例1、実施例2、比較例の各製品についてSAE#
2試験機により摩擦試験を行った。条件以下の通りであ
る。ライニング内径108mm、外径127m11、芯
金厚1ffiIl11摩擦材片側厚さ0.5mm、相手
材プレート厚さ1,811111.油デクスロン■、継
合回転数500Orpm、イナーシャ2゜□kg−cn
+−5ec ライニング枚数5枚、クラッチ押付荷1
300kg、油温100℃、継合サイクル30secで
ある。試験結果を第1図に示す。実施例1、実施例2は
比較例と比べその摩擦係数μ、安定性が良好である。ま
た実施例1、実施例2は上記試験を6000回まで行っ
たが比較例は4000回で試験を中断した。(Evaluation) SAE# for each product of Example 1, Example 2, and Comparative Example
A friction test was conducted using 2 testing machines. The conditions are as follows. Lining inner diameter 108mm, outer diameter 127mm11, core metal thickness 1ffil11, friction material one side thickness 0.5mm, mating plate thickness 1,811111. Oil Dexron■, joint rotation speed 500Orpm, inertia 2゜□kg-cn
+-5ec Number of linings: 5, clutch pressing load: 1
The weight was 300 kg, the oil temperature was 100°C, and the joining cycle was 30 seconds. The test results are shown in Figure 1. Examples 1 and 2 have better friction coefficient μ and stability than the comparative example. Further, in Examples 1 and 2, the above test was conducted up to 6,000 times, but in the comparative example, the test was interrupted after 4,000 times.
この時の試験品の状況を観察した所、実施例1は黒変が
中〜大のものの存在が認められた。実施例2の多孔質中
空ガラスが60重問%の時は黒変が小であるのに対し比
較例では炭化剥離が認められていた。以上の結果、実施
例量は比較例のものに比べて耐熱性が向上している。When the condition of the test product at this time was observed, it was found that Example 1 had medium to large black discoloration. In the case of the porous hollow glass of Example 2 with a concentration of 60%, blackening was small, whereas in the comparative example, carbonization peeling was observed. As a result of the above, the heat resistance of the examples was improved compared to that of the comparative examples.
この時の摩耗量を比較したのが第2図である。Fig. 2 shows a comparison of the amount of wear at this time.
比較例(従来品)が4000回でQ、4mff1である
のに対し実施例1では6000回で0.1311111
%実施例2では6000回で0.111IIlと摩耗量
が少なくなっており耐久性が向上している。Comparative example (conventional product) has a Q of 4mff1 after 4000 times, while Example 1 has a Q of 0.1311111 after 6000 times.
% In Example 2, the amount of wear was reduced to 0.111 IIl after 6000 cycles, and the durability was improved.
以上の結果多孔質中空ガラスを添加したものは、従来の
ケイソウ土のものに比べて耐熱性、耐久性の向上した湿
式摩擦材である。As a result of the above, the material to which porous hollow glass is added is a wet friction material with improved heat resistance and durability compared to conventional diatomaceous earth.
第1図はSAE#2試験機による動的摩擦係数を測定し
た結果を示すグラフであり、第2図は試験後の摩耗量を
示すグラフである。
特許出願人 トヨタ自動車株式会社代理人
弁理士 大川 宏
同 弁理士 丸山明夫
第1図
に’@’すAグル
第2図
ZFIG. 1 is a graph showing the results of measuring the dynamic friction coefficient using an SAE #2 tester, and FIG. 2 is a graph showing the amount of wear after the test. Patent applicant: Toyota Motor Corporation Agent
Patent Attorney Hirotoshi Okawa Patent Attorney Akio Maruyama Figure 1 '@' A Group Figure 2 Z
Claims (3)
る混合材料を成形して得られる湿式摩擦材において該無
機質添加剤の少なくとも一部は多孔質中空ガラスである
ことを特徴とする湿式摩擦材。(1) A wet friction material obtained by molding a mixed material consisting of a base material, a friction modifier, an inorganic additive, and a resin, characterized in that at least a portion of the inorganic additive is porous hollow glass. Wet friction material.
の全体を100重量%としたとき20〜60重量%であ
る特許請求の範囲第1項記載の湿式摩擦材。(2) The wet friction material according to claim 1, wherein the proportion of the porous hollow glass is 20 to 60% by weight when the entire other components excluding the resin component are 100% by weight.
.1〜5μmの気孔径を有する特許請求の範囲第1項記
載の湿式摩擦材。(3) Porous hollow glass has a particle size of 10 to 100 μm and 0
.. The wet friction material according to claim 1, having a pore diameter of 1 to 5 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2682287A JPS63195438A (en) | 1987-02-06 | 1987-02-06 | Wet-type friction material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2682287A JPS63195438A (en) | 1987-02-06 | 1987-02-06 | Wet-type friction material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63195438A true JPS63195438A (en) | 1988-08-12 |
Family
ID=12203969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2682287A Pending JPS63195438A (en) | 1987-02-06 | 1987-02-06 | Wet-type friction material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63195438A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7326741B2 (en) | 2003-07-18 | 2008-02-05 | Akebono Brake Industry Co., Ltd. | Friction material |
WO2009049584A1 (en) * | 2007-10-16 | 2009-04-23 | Luk Lamellen Und Kupplungsbau Beteiligungs Kg | Friction lining |
-
1987
- 1987-02-06 JP JP2682287A patent/JPS63195438A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7326741B2 (en) | 2003-07-18 | 2008-02-05 | Akebono Brake Industry Co., Ltd. | Friction material |
WO2009049584A1 (en) * | 2007-10-16 | 2009-04-23 | Luk Lamellen Und Kupplungsbau Beteiligungs Kg | Friction lining |
US8047350B2 (en) | 2007-10-16 | 2011-11-01 | Schaeffler Technologies Gmbh & Co. Kg | Friction lining |
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