JPH0526049B2 - - Google Patents
Info
- Publication number
- JPH0526049B2 JPH0526049B2 JP63096580A JP9658088A JPH0526049B2 JP H0526049 B2 JPH0526049 B2 JP H0526049B2 JP 63096580 A JP63096580 A JP 63096580A JP 9658088 A JP9658088 A JP 9658088A JP H0526049 B2 JPH0526049 B2 JP H0526049B2
- Authority
- JP
- Japan
- Prior art keywords
- friction
- friction material
- weight
- oil
- formaldehyde resin
- 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
- 239000002783 friction material Substances 0.000 claims description 30
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 15
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical class O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 15
- 238000001035 drying Methods 0.000 claims description 14
- 239000000835 fiber Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 235000019256 formaldehyde Nutrition 0.000 claims description 7
- 239000003607 modifier Substances 0.000 claims description 7
- 150000002989 phenols Chemical class 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- ZYUVGYBAPZYKSA-UHFFFAOYSA-N 5-(3-hydroxybutan-2-yl)-4-methylbenzene-1,3-diol Chemical class CC(O)C(C)C1=CC(O)=CC(O)=C1C ZYUVGYBAPZYKSA-UHFFFAOYSA-N 0.000 claims 1
- 239000003921 oil Substances 0.000 description 13
- 235000019198 oils Nutrition 0.000 description 13
- 230000005540 biological transmission Effects 0.000 description 11
- 239000000463 material Substances 0.000 description 8
- 230000003068 static effect Effects 0.000 description 8
- 239000002383 tung oil Substances 0.000 description 7
- 239000002585 base Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 244000226021 Anacardium occidentale Species 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 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
- 235000020226 cashew nut Nutrition 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 229920006282 Phenolic fiber Polymers 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 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
- 238000007598 dipping method Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical class O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- -1 linter pulp Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
Landscapes
- Braking Arrangements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は油中で使用される摩擦材、特に低摩擦
特性化されたオートマチツク・トランスミツシヨ
ン・フルード(以下ATFという)に適した摩擦
材に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention is a friction material suitable for use in oil, especially automatic transmission fluid (hereinafter referred to as ATF) with low friction characteristics. It is related to materials.
[従来の技術]
内燃機関を原動機とする自動車などでは、原動
機と変速機との間にクラツチを設ける。このクラ
ツチは発進時や変速時などに必要なすべりを与え
ると共に、歯車変速機の変速後の切換えに動力の
断続を行う必要がある。これらの機能をはたすた
め、摩擦クラツチが広く採用されている。[Prior Art] In automobiles that use an internal combustion engine as the prime mover, a clutch is provided between the prime mover and the transmission. This clutch provides the necessary slip when starting or changing gears, and is also required to intermittent power when changing gears after shifting the gear transmission. Friction clutches are widely used to perform these functions.
摩擦クラツチには、乾燥状態で使用される乾式
摩擦板と、油中に浸して使用される湿式摩擦板と
にわけられる。 Friction clutches can be divided into dry friction plates, which are used in a dry state, and wet friction plates, which are immersed in oil.
湿式摩擦板に用いられる摩擦材は古くは焼結合
金であつたが、最近は熱硬化性樹脂を含浸、硬化
させた紙質基材の摩擦材が主流である。この種の
摩擦材は有機繊維、無機繊維の繊維基材、および
無機充填材と摩擦調整剤とを湿式抄造し、フエノ
ール樹脂などの熱硬化性樹脂を含浸させ、乾燥、
圧縮成形したものである。(例えば特開昭57−
85876号、特開昭59−175639号)
[発明が解決しようとする問題点]
自動車等に装着されている自動変速機の構成要
素を円滑に作動させるためにATFは、動力伝達、
変速制御、潤滑作用および摩擦材の潤滑と適正な
摩擦特性を維持させる役割をはたしている。最近
の車輌は、エンジンの高出力化、4輪駆動車(以
下4WDという)等の駆動方式の多様化や省燃費
対策のためのロツクアツプクラツチの装着などの
設計条件が拡大し、ATFに対する要求特性も同
様に拡大されている。 Friction materials used in wet friction plates used to be sintered alloys, but recently paper-based friction materials impregnated with thermosetting resin and hardened have become mainstream. This type of friction material is produced by wet-forming a fiber base material of organic fibers and inorganic fibers, an inorganic filler, and a friction modifier, impregnating it with a thermosetting resin such as phenolic resin, drying,
It is compression molded. (For example, JP-A-57-
(No. 85876, Japanese Unexamined Patent Publication No. 59-175639) [Problems to be solved by the invention] In order to smoothly operate the components of automatic transmissions installed in automobiles, etc., ATF is a power transmission,
It plays a role in speed change control, lubrication, and lubrication of friction materials to maintain appropriate friction characteristics. Recently, design conditions for modern vehicles have expanded, such as higher engine output, diversification of drive systems such as four-wheel drive vehicles (hereinafter referred to as 4WD), and the installation of lock-up clutches for fuel efficiency measures, and the demands on ATF have increased. The properties have been expanded as well.
自動変速機における変速フイーリングの向上の
ためや、湿式摩擦材を用いた4WD用自動変速機
の開発につれて、ATFの低摩擦特性化(以下低
μ化という)が要求されてきている。 In order to improve the shift feel of automatic transmissions, and with the development of 4WD automatic transmissions using wet friction materials, there is a growing demand for ATF to have low friction characteristics (hereinafter referred to as low μ).
ATFが低μ化されると、変速時のフイーリン
グは向上するが、静摩擦係数が低下するため、従
来の自動変速機では、静トルク容量不足となり、
摩擦材にすべりが生じ焼損の原因となるという問
題点がある。 When the ATF is lowered, the feeling during shifting improves, but the static friction coefficient decreases, resulting in a lack of static torque capacity in conventional automatic transmissions.
There is a problem in that the friction material slips, causing burnout.
これらの対策として、摩擦板の枚数を増加させ
たり、またはクラツチ制御油圧を高める方法が考
えられるが、自動変速機自体が大きくなり、他の
解決方法が望まれている。 Possible countermeasures to these problems include increasing the number of friction plates or increasing the clutch control oil pressure, but as the automatic transmission itself becomes larger, other solutions are desired.
[問題点を解決するための手段]
本発明の目的は、上記の問題点を解決し、変速
フイーリングに優れ、かつ始動時のトルク伝達容
量の大きな湿式摩擦材を提供するものである。[Means for Solving the Problems] An object of the present invention is to solve the above problems and provide a wet friction material that has excellent shift feeling and a large torque transmission capacity at the time of starting.
すなわち本発明の湿式摩擦材は、繊維成分、熱
硬化性樹脂および摩擦調整剤からなる湿式摩擦材
において、前記熱硬化性樹脂がフエノール類、ホ
ルムアルデヒド類および乾性油を反応させて得ら
れる変性フエノールホルムアルデヒド樹脂であ
り、かつ前記変性フエノールホルムアルデヒド樹
脂に対して乾性油の変性量が15〜55重量%である
ことを特徴とする。 That is, the wet friction material of the present invention is a wet friction material comprising a fiber component, a thermosetting resin, and a friction modifier, in which the thermosetting resin is made of modified phenol formaldehyde obtained by reacting phenols, formaldehydes, and drying oil. The resin is characterized in that the amount of modification of the drying oil is 15 to 55% by weight based on the modified phenol formaldehyde resin.
本発明の湿式摩擦材の骨格部分を構成する繊維
成分は、木材パルブ、リンターパルプ、芳香族ポ
リアミド繊維、ノボロイド繊維などの有機繊維や
ガラス繊維、チタン酸カリウム繊維、シリカ繊
維、ロツクウール繊維などの無機繊維であり、こ
れらの単独または2種以上を混合して使用され
る。繊維成分の適正な配合量は、全摩擦材中の40
〜75重量%である。 The fiber components constituting the skeleton of the wet friction material of the present invention include organic fibers such as wood pulp, linter pulp, aromatic polyamide fibers, and novoloid fibers, and inorganic fibers such as glass fibers, potassium titanate fibers, silica fibers, and rock wool fibers. These fibers are used alone or in combination of two or more. The appropriate blending amount of fiber components is 40% of the total friction material.
~75% by weight.
本発明の変性フエノールホルムアルデヒド樹脂
に使用するフエノール類としてはフエノール、ク
レゾール、キシレートなどがあり、ホルムアルデ
ヒド類としてはホルマリン、パラホルムアルデヒ
ド、ヘキサメチレンテトラミンなどである。ホル
ムアルデヒド類/フエノール類モル比は1.1〜2.5
が適している。変性剤としての乾性油としては、
アマニ油、桐油、ヒマシ油、トール油などのよう
な脂肪酸中に不飽和二重結合を2個以上有する脂
肪油が用いられ、その乾性油の変性量は変性フエ
ノールホルムアルデヒド樹脂に対して15〜55重量
%が有効であり、好ましくは20〜50重量%であ
る。乾性油の変性量が15重量%未満では静摩擦係
数を増大させる効果が少なく、55重量%を越える
と摩擦材の耐熱性が低下する。 Phenols used in the modified phenol-formaldehyde resin of the present invention include phenol, cresol, xylate, etc., and formaldehydes include formalin, paraformaldehyde, hexamethylenetetramine, etc. Formaldehyde/phenols molar ratio is 1.1 to 2.5
is suitable. As a drying oil as a modifier,
Fatty oils having two or more unsaturated double bonds in their fatty acids, such as linseed oil, tung oil, castor oil, and tall oil, are used, and the amount of modification of the drying oil is 15 to 55% relative to the modified phenol formaldehyde resin. % by weight is useful, preferably from 20 to 50% by weight. If the amount of modification of the drying oil is less than 15% by weight, the effect of increasing the coefficient of static friction will be small, and if it exceeds 55% by weight, the heat resistance of the friction material will decrease.
本発明の変性フエノールホルムアルデヒド樹脂
は、フエノール類、ホルムアルデヒド類および乾
性油をアルカリ性触媒、たとえばアルカリ金属又
はアルカリ土類金属の水酸化物、またはアンモニ
アあるいはアミン類の存在下で縮合反応させ減圧
脱水した後、メタノール等の溶剤を加えることに
より液状樹脂として得られる。 The modified phenol formaldehyde resin of the present invention is produced by condensing phenols, formaldehydes, and drying oil in the presence of an alkaline catalyst, such as an alkali metal or alkaline earth metal hydroxide, or ammonia or amines, followed by dehydration under reduced pressure. , obtained as a liquid resin by adding a solvent such as methanol.
乾性油は、フエノール類、ホルムアルデヒド類
と同時に反応させてもよく、あるいは乾性油とフ
エノールとをあらかじめ反応させ、そののちホル
ムアルデヒドを加え縮合反応をさせてもよい。 The drying oil may be reacted simultaneously with phenols and formaldehyde, or the drying oil and phenol may be reacted in advance, and then formaldehyde may be added to cause a condensation reaction.
本発明で用いる摩擦調整剤としては、例えばア
ルミニウム粉、ゴム粉末、カシユーダスト、グラ
フアイト粉末であり、その他に硫酸バリウム、炭
酸カリウム、酸化酸、珪藻土などの無機充填材を
使用することもできる。 Examples of the friction modifier used in the present invention include aluminum powder, rubber powder, cashew dust, and graphite powder, and inorganic fillers such as barium sulfate, potassium carbonate, oxidized acid, and diatomaceous earth can also be used.
本発明の湿式摩擦材を製造するには、繊維成
分、摩擦調整剤、必要に応じて無機充填材や定着
剤を水中に分散させたのち、抄造機で抄紙し、乾
燥後所定の型に打抜く。つぎに打抜かれた基材に
変性フエノールホルムアルデヒド樹脂を含浸さ
せ、乾燥後加熱加圧成形して湿式摩擦材が得られ
る。 To manufacture the wet friction material of the present invention, fiber components, a friction modifier, and if necessary, an inorganic filler and a fixing agent are dispersed in water, and then paper is made using a paper machine, and after drying, it is stamped into a predetermined mold. Pull it out. Next, the punched base material is impregnated with a modified phenol formaldehyde resin, dried, and then heated and press-molded to obtain a wet friction material.
[発明の作用および効果]
本発明の湿式摩擦材は、繊維基材、摩擦調整剤
および15〜55重量部の乾性油で変性されたフエノ
ールホルムアルデヒド樹脂からなることにより、
柔軟性が増し、摩擦する相手材とのなじみが向上
する。よつて当り面の増加がみられその結果静摩
擦係数が増大する。[Operations and Effects of the Invention] The wet friction material of the present invention comprises a fiber base material, a friction modifier, and a phenol formaldehyde resin modified with 15 to 55 parts by weight of drying oil.
Increases flexibility and improves compatibility with mating materials. As a result, the contact surface increases, resulting in an increase in the coefficient of static friction.
本発明の湿式摩擦材を、低μ化されたATF中
で用いることにより、低μ化されたATFの作用
で変速シヨツクに大きな影響を与える最終動摩擦
係数を小さくし、変速フイーリングを向上する。
さらに摩擦材の静摩擦係数の増大で始動時のトル
ク伝達容量が大きくなり、摩擦材のすべりを防止
する。 By using the wet friction material of the present invention in a low-μ ATF, the final dynamic friction coefficient, which has a large effect on the shift shock, is reduced by the action of the low-μ ATF, and the shift feeling is improved.
Furthermore, the increase in the coefficient of static friction of the friction material increases the torque transmission capacity at the time of starting, which prevents the friction material from slipping.
上記のように本発明の湿式摩擦材は低μ化
ATFとの組合せにより変速フイーリングに優れ、
かつ焼損の原因となる摩擦材のすべりがなく、耐
久性に優れた摩擦材である。 As mentioned above, the wet friction material of the present invention has a low μ
In combination with ATF, the shift feeling is excellent.
It is also a highly durable friction material that does not slip, which can cause burnout.
[実施例]
以下本発明の実施例を示すが、本発明はこれに
限定されるものではない。[Example] Examples of the present invention will be shown below, but the present invention is not limited thereto.
実施例 1
リンターバルブ45重量%、ガラス繊維5重量
%、アラミド繊維10重量%を水中にて口水度480
〜520mlになる様に叩解したのち、カシユーダス
ト30重量%、珪藻土10重量%を順次仕込み、分散
させ、硫酸バンドにより定着させたのち、丸網式
抄造機により所定の坪量、厚さに抄紙する。この
抄紙した基材を所定のリンクに打抜き、30重量%
の桐油で変性した変性フエノールホルムアルデヒ
ド樹脂[比重=0.983、粘度(at25℃)=0.4ポイ
ズ、ゲルタイム(at165℃)=98秒]を上記抄紙し
た基材100重量部に対して28重量部をデイツピン
グ方法により含浸し、乾燥後、170℃×2分間加
熱加圧成形と同時に金属板からなるデイスクプレ
ートに接着して湿式摩擦材を得る。Example 1 45% by weight of linter valve, 5% by weight of glass fiber, and 10% by weight of aramid fiber were submerged in water at a mouth water level of 480.
After beating to a volume of ~520 ml, 30% by weight of cashew dust and 10% by weight of diatomaceous earth are sequentially charged, dispersed, and fixed with sulfuric acid bands. After that, paper is made to the specified basis weight and thickness using a circular mesh paper making machine. . This paper-made base material is punched into specified links and 30% by weight
Dipping method: 28 parts by weight of modified phenol formaldehyde resin modified with tung oil [specific gravity = 0.983, viscosity (at 25°C) = 0.4 poise, gel time (at 165°C) = 98 seconds] for 100 parts by weight of the above paper-made base material. After drying, the material is heated and pressed at 170°C for 2 minutes and simultaneously adhered to a disk plate made of a metal plate to obtain a wet friction material.
実施例 2
30重量%の桐油で変性した変性フエノールホル
ムアルデヒド樹脂に代えて40重量%の桐油で変性
した変性フエノールホルムアルデヒド樹脂[比重
=0.978、粘度(at25℃)=1.1ポイズ、ゲルタイム
(at165℃)=86秒]を用いた以外は実施例1と同
様にして湿式摩擦材を得た。Example 2 Modified phenol formaldehyde resin modified with 40 wt% tung oil instead of modified phenol formaldehyde resin modified with 30 wt% tung oil [specific gravity = 0.978, viscosity (at 25°C) = 1.1 poise, gel time (at 165°C) = A wet friction material was obtained in the same manner as in Example 1 except that 86 seconds] was used.
実施例 3
30重量%の桐油で変性した変性フエノールホル
ムアルデヒド樹脂に代えて50重量%の桐油で変性
した変性フエノールホルムアルデヒド樹脂[比重
=0.972、粘度(at25℃)=1.1ポイズ、ゲルタイム
(at165℃)=99秒]を用いた以外は実施例1と同
様にして湿式摩擦材を得た。Example 3 Modified phenol formaldehyde resin modified with 50 wt% tung oil instead of modified phenol formaldehyde resin modified with 30 wt% tung oil [specific gravity = 0.972, viscosity (at 25°C) = 1.1 poise, gel time (at 165°C) = A wet friction material was obtained in the same manner as in Example 1 except that 99 seconds] was used.
比較例
30重量%の桐油で変性した変性フエノールホル
ムアルデヒド樹脂に代えて、未変性のフエノール
ホルムアルデヒド樹脂[比重=1.072、粘度
(at25℃)=0.4ポイズ、ゲルタイム(at165℃)=
55秒]を用いた以外は実施例1と同様にして湿式
摩擦材を得た。Comparative Example Instead of the modified phenol formaldehyde resin modified with 30% by weight of tung oil, unmodified phenol formaldehyde resin [specific gravity = 1.072, viscosity (at 25°C) = 0.4 poise, gel time (at 165°C) =
A wet friction material was obtained in the same manner as in Example 1, except that 55 seconds] was used.
つぎに、実施例1〜3、比較例で得られた湿式
摩擦材をSAENo.2テスターにより2000サイクル
の摩擦試験を実施した。 Next, the wet friction materials obtained in Examples 1 to 3 and Comparative Example were subjected to a 2000 cycle friction test using a SAENo.2 tester.
試験条件は、イナーシヤ;2.5Kgcm sec2、回
転数;3600rpm、負荷;332Kgである。 The test conditions were inertia: 2.5Kgcm sec 2 , rotation speed: 3600rpm, and load: 332Kg.
ATF;トヨタオートフルードタイプT 油
温;120℃、 SAENo.2テスターで得られた係合
サイクル回数と静摩擦係数の関係を第1図に、最
終動摩擦係数との関係を第2図に表わした。 ATF: Toyota Auto Fluid Type T Oil temperature: 120°C The relationship between the number of engagement cycles and the static friction coefficient obtained with the SAENo.2 tester is shown in Figure 1, and the relationship with the final dynamic friction coefficient is shown in Figure 2.
第1図および第2図に示されるように、本発明
による実施例1〜3の摩擦材は、比較例と同等の
最終動摩擦係数(0.155〜0.165)を保持しつつ、
静摩擦係数を比較例に比べ0.010〜0.023増加させ
ていることがわかる。 As shown in FIG. 1 and FIG. 2, the friction materials of Examples 1 to 3 according to the present invention maintain the same final dynamic friction coefficient (0.155 to 0.165) as the comparative example.
It can be seen that the static friction coefficient is increased by 0.010 to 0.023 compared to the comparative example.
第1図、第2図は実施例1〜3および比較例の
摩擦材の試験結果を表し、第1図は係合サイクル
回数と静摩擦係数を表すグラフである。第2図は
係合サイクル回数と最終動摩擦係数を表す。
1 and 2 show the test results of the friction materials of Examples 1 to 3 and Comparative Example, and FIG. 1 is a graph showing the number of engagement cycles and the coefficient of static friction. FIG. 2 shows the number of engagement cycles and the final dynamic friction coefficient.
Claims (1)
らなる湿式摩擦材において、該熱硬化性樹脂がフ
エノール類、ホルムアルデヒド類および乾性油を
反応させて得られる変性フエノールホルムアルデ
ヒド樹脂であり、かつ該変性フエノールホルムア
ルデヒド樹脂に対して乾性油の変性量が15〜55重
量%であることを特徴とする湿式摩擦材。1. In a wet friction material comprising a fiber component, a thermosetting resin, and a friction modifier, the thermosetting resin is a modified phenol-formaldehyde resin obtained by reacting phenols, formaldehydes, and drying oil, and the modified phenol A wet friction material characterized in that the modified amount of drying oil is 15 to 55% by weight based on formaldehyde resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9658088A JPH01269734A (en) | 1988-04-19 | 1988-04-19 | Wet friction material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9658088A JPH01269734A (en) | 1988-04-19 | 1988-04-19 | Wet friction material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01269734A JPH01269734A (en) | 1989-10-27 |
JPH0526049B2 true JPH0526049B2 (en) | 1993-04-14 |
Family
ID=14168898
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9658088A Granted JPH01269734A (en) | 1988-04-19 | 1988-04-19 | Wet friction material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01269734A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5624403B2 (en) * | 2010-08-26 | 2014-11-12 | 昭和電工株式会社 | Wet friction material |
US10260584B2 (en) * | 2017-03-16 | 2019-04-16 | Schaeffler Technologies AG & Co. KG | Wet friction material having increased pressure cycle life |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3307969A (en) * | 1963-02-21 | 1967-03-07 | Johns Manville | Friction material |
JPS5075692A (en) * | 1973-11-06 | 1975-06-20 | ||
JPS57108180A (en) * | 1980-12-25 | 1982-07-06 | Teijin Ltd | Friction material |
JPS58217577A (en) * | 1982-06-11 | 1983-12-17 | Dainippon Ink & Chem Inc | Friction material |
JPS5977139A (en) * | 1982-10-25 | 1984-05-02 | Dainippon Ink & Chem Inc | Friction material |
JPS6152433A (en) * | 1984-07-31 | 1986-03-15 | Aisin Chem Co Ltd | Friction material for car |
JPS61192711A (en) * | 1985-02-22 | 1986-08-27 | Shin Etsu Chem Co Ltd | Binder for friction material |
-
1988
- 1988-04-19 JP JP9658088A patent/JPH01269734A/en active Granted
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3307969A (en) * | 1963-02-21 | 1967-03-07 | Johns Manville | Friction material |
JPS5075692A (en) * | 1973-11-06 | 1975-06-20 | ||
JPS57108180A (en) * | 1980-12-25 | 1982-07-06 | Teijin Ltd | Friction material |
JPS58217577A (en) * | 1982-06-11 | 1983-12-17 | Dainippon Ink & Chem Inc | Friction material |
JPS5977139A (en) * | 1982-10-25 | 1984-05-02 | Dainippon Ink & Chem Inc | Friction material |
JPS6152433A (en) * | 1984-07-31 | 1986-03-15 | Aisin Chem Co Ltd | Friction material for car |
JPS61192711A (en) * | 1985-02-22 | 1986-08-27 | Shin Etsu Chem Co Ltd | Binder for friction material |
Also Published As
Publication number | Publication date |
---|---|
JPH01269734A (en) | 1989-10-27 |
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