JPH0467051B2 - - Google Patents
Info
- Publication number
- JPH0467051B2 JPH0467051B2 JP10930486A JP10930486A JPH0467051B2 JP H0467051 B2 JPH0467051 B2 JP H0467051B2 JP 10930486 A JP10930486 A JP 10930486A JP 10930486 A JP10930486 A JP 10930486A JP H0467051 B2 JPH0467051 B2 JP H0467051B2
- Authority
- JP
- Japan
- Prior art keywords
- friction
- fibers
- pores
- base material
- wet
- 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
Links
- 239000011148 porous material Substances 0.000 claims description 35
- 239000002783 friction material Substances 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 20
- 239000000835 fiber Substances 0.000 claims description 17
- 229920005989 resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 239000011256 inorganic filler Substances 0.000 claims description 5
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 5
- 239000003607 modifier Substances 0.000 claims description 5
- 239000012784 inorganic fiber Substances 0.000 claims description 4
- 230000000052 comparative effect Effects 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- 238000005259 measurement Methods 0.000 description 6
- 239000010425 asbestos Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229910052895 riebeckite Inorganic materials 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 244000226021 Anacardium occidentale Species 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000004640 Melamine resin Substances 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
- 235000020226 cashew nut Nutrition 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920006282 Phenolic fiber Polymers 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 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
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000006163 transport media Substances 0.000 description 1
Landscapes
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Braking Arrangements (AREA)
Description
〔産業上の利用分野〕
本発明は、クラツチの摩擦材、特に油液中で使
用するに適した湿式摩擦材に関するものである。
〔従来の技術〕
例えば自動車、建設機械、農業機械、モーター
ボートなどで原動機からの駆動を変速機に伝達す
るクラツチは、常時は充分に動力を伝達する一
方、発進時などは適度な滑りを与えると共に変速
機の変速歯車の切り替え時には動力を遮断する機
能が要求される。かかる機能を満たすクラツチと
して摩擦式のクラツチが広く採用されている。そ
して摩擦式のクラツチには乾燥状態で使用される
乾式クラツチと油液中で使用される湿式クラツチ
とがある。後者の湿式クラツチは遊星歯車式の自
動変速機内の構成要素として多板クラツチの形で
多く使用されているものである。
摩擦式のクラツチでは摩擦熱が発生するため、
前述の機能が安定して果されるには、摩擦部分か
ら熱が効率良く放出されなければならない。湿式
クラツチでは油が熱の運搬媒体として重要な役割
を負つている。摩擦面で発生した熱は、油が媒体
となつて系全体に拡散放出される。従つて摩擦材
自身の油保有量並びに油の出入りが少ないと過熱
し、摩擦材の熱劣化及び油の酸化、分解が起り、
摩擦材としての機能が低下してしまう。
湿式摩擦材は、セルロースなどの有機質繊維、
アスベストなどの無機質繊維、無機質充填剤およ
びカシユーダストなどの摩擦調整剤とを湿式抄造
した紙質基材に、フエノール樹脂やメラミン樹脂
などの熱硬化性樹脂を含浸させたものである。こ
の紙質基材の気孔部分に油が保持され循環するも
のと考えられる。
従来の摩擦材は、例えば特開昭60−23774号公
報に開示されている。
〔発明が解決しようとする問題点〕
従来の湿式摩擦材では、素材原料の種類、組成
比率に重きが置かれて研究されており、気孔部分
(油が保持される部分)についての研究が必ずし
も充分になされていなかつた。各種繊維の繊維
径、無機質充填剤、摩擦調整剤の粒径について格
別な配慮がなされていないため、抄紙された紙質
基材の組織が凝集する一方で、一つずつの気孔は
大きくなる傾向があつた。紙質基材の組織が凝集
していると、それに熱硬化性樹脂を含浸させた摩
擦材は、凝集した部分では油を循環、保持しない
ため、冷却が充分になされず、耐熱性が弱いもの
になつてしまう。
また、かつては摩擦材の素材原料として優れて
いるとされ、頻繁に使われていたアスベストが健
康に有害であるということが解り、使用が困難に
なつているため、素材原料の選択巾が狭まつてい
る。そのため充分な性能を持ちながら健康面で害
のない摩擦材は得られていない。
本発明はこれらの点に鑑みなされたもので、耐
熱性、摩擦性能に優れ、有害物質を含まない摩擦
材を安価に提供しようとするものである。
〔問題点を解決するための手段〕
本発明者らは、気孔部分に油が保持され循環す
ることによつて湿式摩擦材の性能が左右されるこ
とに着目し、その研究を続けた結果、本発明を完
成するに至つた。すなわち本発明の湿式摩擦材
は、少なくとも基材の骨格部分を構成する繊維と
フイブリド繊維と無機質繊維と無機質充填剤と摩
擦調整剤とを湿式抄造した紙質基材に、熱硬化性
樹脂を含浸してあり、気孔率が40〜75%で、かつ
5μm以下の気孔による気孔量が70%以上を占る
ものである。
基材の骨格部分を構成する繊維は、例えばパル
プ、芳香族ポリアミド繊維、カイノール繊維(ノ
ボロイド繊維)が使用できる。太さが5〜30μ
m、好ましくは15μm以下が良い。適正な配合比
は、紙質基材中の5〜30重量%である。
フイブリツド繊維は、例えばセルロース繊維、
アラミツドパルプなどを0.2〜2μmの太さに微小
化した繊維で、湿式抄造によりフイブリル化する
性質を有しているものである。特にセルロース繊
維を原料とするMFC(微小繊維状セルロース)は
フイブリル化しやすい。適正な配合比は、紙質基
材中の10〜50重量%である。
無機質繊維は、例えばガラス繊維、チタン酸カ
リウム繊維、ロツクウール、セラミツク繊維、金
属繊維が使用可能であるが、アスベストは前記の
ように健康面から考え不適当である。繊維径は
0.1〜10μm、好ましくは5μm以下が良い。適正な
配合比は、紙質基材中の10〜50重量%である。
無機質充填剤は、例えば珪藻土、アルミナ粉、
硫酸バリウム、炭酸カルシウム、シリカである。
粒径が0.5〜10μm、望ましくは3μm以下が好まし
い。適正な配合比は、紙質基材中の5〜50重量%
である。
摩擦調整剤は、例えばグラフアイト、カシユー
ダストなどである。粒径は10〜50μmのものが好
ましい。適正な配合比は、紙質基材中の0〜30重
量%である。
上記の各原料を混合して水に分散させ、例えば
丸網式抄造機や長網式抄造機などにより所望の抄
き上げ量(坪量、g/m2)及び厚さに抄紙し、紙
の気孔率が60〜90%の紙質基材を得る。この紙質
基材100重量比に対し、熱硬化性樹脂、例えばフ
エノール樹脂、メラミン系樹脂、エポキシ樹脂な
ど20〜40重量比を含浸させ熱硬化させる。これを
所定の形状に裁断してから芯金に接着する。この
時、完成品で気孔率が40〜75%、好ましくは50〜
65%になるように、紙は圧縮成形される。上記に
より限定した各原料を使用すると、紙質基材の段
階では気孔径が若干大きいが、熱硬化性樹脂が含
浸され圧縮成形されることにより、完成品では
5μm以下の気孔による気孔量が70%以上を占て
いる摩擦材になる。
〔作用〕
本発明の湿式摩擦材は、第1図の気孔分布グラ
フに示すように、従来の湿式摩擦材より径の小さ
い気孔が多くなつている。上記の各原料の働き、
特にフイブリツド繊維の働きにより気孔が微小に
なり分散する。気孔率が40%以下では少ないため
油の保持、循環が不充分であり、気孔率が75%で
は摩擦材そのものゝ機械強度が不充分である。そ
れに対し本発明の摩擦材は、気孔率が40〜75%
で、しかも5μm以下の気孔による気孔量が70%
以上を占る。したがつて気孔部分に油が保持され
循環するので、冷却性が向上し、耐熱性、摩擦性
能に優れている。またアスベストのような有害物
質を含まなくても充分な耐熱性、摩擦性能を得る
ことができる。
〔実施例〕
以下、本発明の実施例を詳細に説明する。
下記の第1表(配合表)に示す各原料を坪量
し、混合して水に分散させ、丸網式抄造機により
所定の坪量、厚さに抄紙し、紙質基材を得る。こ
の紙質基材にフエノール樹脂を配合表に記載の重
量比をスプレイ法により吹付けて含浸させ、加熱
硬化させる。上記により湿式摩擦材が製造され
る。なお符号1〜5(実施例)は本発明を適用し
た湿式摩擦材の例、6〜8(比較例)は本発明を
適用外の例である。
[Industrial Field of Application] The present invention relates to a friction material for a clutch, particularly a wet friction material suitable for use in an oil solution. [Conventional technology] For example, in automobiles, construction machinery, agricultural machinery, motorboats, etc., clutches that transmit drive from the prime mover to transmissions transmit sufficient power at all times, but when starting, they provide appropriate slippage and A function is required to cut off the power when changing gears of a transmission. Friction type clutches are widely used as clutches that satisfy this function. Friction type clutches include dry type clutches that are used in dry conditions and wet type clutches that are used in oily liquid. The latter wet clutch is often used in the form of a multi-disc clutch as a component in planetary gear type automatic transmissions. Friction type clutches generate frictional heat, so
In order for the above-mentioned functions to be stably performed, heat must be efficiently released from the frictional parts. In wet clutches, oil plays an important role as a heat transport medium. The heat generated on the friction surface is diffused and released throughout the system using oil as a medium. Therefore, if the amount of oil held in the friction material itself and the amount of oil flowing in and out are small, it will overheat, causing thermal deterioration of the friction material and oxidation and decomposition of the oil.
Its function as a friction material deteriorates. Wet friction materials are organic fibers such as cellulose,
A paper base material made by wet papermaking of inorganic fibers such as asbestos, inorganic fillers, and friction modifiers such as cashew dust is impregnated with a thermosetting resin such as phenol resin or melamine resin. It is thought that oil is retained and circulated in the pores of this paper base material. A conventional friction material is disclosed in, for example, Japanese Patent Laid-Open No. 60-23774. [Problems to be solved by the invention] In conventional wet friction materials, research has focused on the type and composition ratio of raw materials, and research on pores (areas where oil is retained) has not necessarily been conducted. It wasn't done enough. Because no particular consideration is given to the fiber diameters of various fibers, inorganic fillers, and particle sizes of friction modifiers, the structure of the paper base material from which paper is made tends to aggregate, while the individual pores tend to become larger. It was hot. If the structure of the paper base material is aggregated, friction materials impregnated with thermosetting resin will not circulate or retain oil in the aggregated areas, resulting in insufficient cooling and poor heat resistance. I get used to it. In addition, asbestos, which was once thought to be an excellent raw material for friction materials and was frequently used, has been found to be harmful to health, making it difficult to use, and the range of raw materials to choose from has narrowed. It is worshiped. Therefore, a friction material that has sufficient performance and is not harmful to health has not been obtained. The present invention has been made in view of these points, and it is an object of the present invention to provide a friction material that is excellent in heat resistance and friction performance and does not contain harmful substances at a low cost. [Means for solving the problem] The present inventors focused on the fact that the performance of wet friction materials is influenced by the retention and circulation of oil in the pores, and as a result of continuing research, The present invention has now been completed. In other words, the wet friction material of the present invention is made by impregnating a paper base material with a thermosetting resin into a paper base material made by wet papermaking of fibers, fibrid fibers, inorganic fibers, an inorganic filler, and a friction modifier that constitute at least the skeleton of the base material. with a porosity of 40 to 75%, and
The amount of pores is 70% or more due to pores of 5 μm or less. The fibers constituting the skeleton of the base material may be, for example, pulp, aromatic polyamide fibers, or kynol fibers (novoloid fibers). Thickness is 5~30μ
m, preferably 15 μm or less. The appropriate blending ratio is 5 to 30% by weight in the paper base material. Fibrillated fibers include, for example, cellulose fibers,
It is a fiber made by micronizing aramid pulp or the like to a thickness of 0.2 to 2 μm, and has the property of being fibrillated by wet papermaking. In particular, MFC (microfibrous cellulose), which is made from cellulose fibers, is easily fibrillated. The appropriate blending ratio is 10 to 50% by weight in the paper base material. Examples of inorganic fibers that can be used include glass fibers, potassium titanate fibers, rock wool, ceramic fibers, and metal fibers, but asbestos is unsuitable from the health standpoint as described above. The fiber diameter is
The thickness is preferably 0.1 to 10 μm, preferably 5 μm or less. The appropriate blending ratio is 10 to 50% by weight in the paper base material. Examples of inorganic fillers include diatomaceous earth, alumina powder,
These are barium sulfate, calcium carbonate, and silica.
The particle size is preferably 0.5 to 10 μm, preferably 3 μm or less. The appropriate blending ratio is 5 to 50% by weight in the paper base material.
It is. Examples of friction modifiers include graphite and cashew dust. The particle size is preferably 10 to 50 μm. A suitable blending ratio is 0 to 30% by weight in the paper base material. The above raw materials are mixed and dispersed in water, and paper is made into the desired paper weight (basis weight, g/m 2 ) and thickness using, for example, a circular wire paper making machine or a fourdrinier paper making machine. A paper base material with a porosity of 60 to 90% is obtained. A thermosetting resin such as a phenolic resin, a melamine resin, an epoxy resin, etc. is impregnated in a weight ratio of 20 to 40% with respect to 100% of this paper base material, and the paper material is thermally cured. This is cut into a predetermined shape and then glued to the core metal. At this time, the finished product has a porosity of 40-75%, preferably 50-75%.
The paper is compression molded so that it is 65%. When each raw material limited above is used, the pore size is slightly large at the paper base stage, but the finished product is impregnated with thermosetting resin and compression molded.
This is a friction material in which more than 70% of the pores are pores of 5 μm or less. [Function] As shown in the pore distribution graph of FIG. 1, the wet friction material of the present invention has more pores with smaller diameters than the conventional wet friction material. The function of each of the above raw materials,
In particular, the pores become minute and dispersed due to the action of fibrid fibers. If the porosity is less than 40%, oil retention and circulation will be insufficient, and if the porosity is 75%, the mechanical strength of the friction material itself will be insufficient. In contrast, the friction material of the present invention has a porosity of 40 to 75%.
Moreover, the amount of pores is 70% due to pores of 5 μm or less.
Predict the above. Therefore, oil is retained and circulated in the pores, improving cooling performance and providing excellent heat resistance and friction performance. Furthermore, sufficient heat resistance and friction performance can be obtained even without containing harmful substances such as asbestos. [Examples] Examples of the present invention will be described in detail below. Each raw material shown in Table 1 (formulation table) below is weighed, mixed and dispersed in water, and paper is made to a predetermined basis weight and thickness using a circular mesh paper making machine to obtain a paper base material. This paper base material is impregnated with a phenolic resin by spraying in the weight ratio shown in the formulation table, and then heated and cured. A wet friction material is manufactured by the above process. Note that numerals 1 to 5 (examples) are examples of wet friction materials to which the present invention is applied, and 6 to 8 (comparative examples) are examples to which the present invention is not applied.
【表】
各例の湿式摩擦材についてポロシメータ(気孔
率測定計 島津製作所(株)製)により気孔率および
気孔径の分布を測定する。気孔径の分布は、試料
(摩擦材)に圧力をかけて粘性流体を充填させ測
定する。加圧の始めは大きい気孔が充填されてゆ
くが、圧力が上るに従つて細かい気孔が充填され
てゆくから、圧力と充填量の関係が測定できる。
すなわち充填量は、圧力の変化に応じ径が大きい
気孔から充填されてゆくから、圧力と充填量の関
係を微分すると、気孔径とその気孔径における気
孔量が求まる。
その結果が第2図に示してある。曲線〜は
実施例1〜5の摩擦材の気孔径分布を示し、〜
は比較例6〜8の摩擦材の気孔径分布を示す。
実施例1〜5の摩擦材は、気孔径の分布中心が3
〜4μm程度であり、比較例6〜8の摩擦材(気
孔径の分布中心が10μm程度)に比べて、径の小
さい気孔が多くなつている。実施例1〜3は5μ
m以下の気孔が90%であり、実施例4,5は同じ
く5μm以下の気孔が80%である。また比較例6,
7は5μm以下の気孔が30%であり、比較例8は
同じく5μm以下の気孔が25%である。なお各例
とも気孔率はすべて55〜60%である。
また各例の湿式摩擦材について摩擦係数(μd)
および耐熱性を測定する。試験片は上記各例の湿
式摩擦材を所定の大きさに裁断し、金属のセンタ
プレートを挾んで貼り付けたものを使用する。
摩擦係数の測定は、SAE#2摩擦試験機によ
り慣性回転している摩擦材に荷重をかけ、そのト
ルクから摩擦係数を算出する。
測定条件
摩擦面数:4、イナーシヤ:2.5Kg・cm・
sec2、
回転数:3600rpm、荷重:7.2Kg/cm2、
油液中、油温度:120℃、
各例の摩擦係数の測定の結果は、第3図に示し
てある。同図に示す摩擦係数(μd)は100〜2000
サイクルのときの値で、このサイクルの間摩擦係
数は略安定している。実施例1〜5の摩擦材と比
較例7〜8の摩擦材ものとは略同等の摩擦係数を
示している。
耐熱性の測定は、摩擦係数の測定と同じく
SAE#2摩擦試験機により測定する。
測定条件
摩擦面数:6、イナーシヤ:2.0Kg・cm・
sec2、
回転数:3000〜5200rpm、
荷重:制動時間が1Secになるように調整、
油液:流量1.0c.c./cm2・mmシヤフト吹出し
(qs=10〜30cal/cm2)、
油温度:120℃
耐熱性の測定結果は下記第2表に示してある。
耐熱性の判定は、摩擦係数(μd)が初期安定時
より1割落ちるときまでを、または剥離が発生す
るときまでを良好とする。[Table] The porosity and pore diameter distribution of each wet friction material were measured using a porosimeter (porosity measuring meter manufactured by Shimadzu Corporation). The pore size distribution is measured by applying pressure to a sample (friction material) and filling it with viscous fluid. At the beginning of pressurization, large pores are filled, but as the pressure increases, smaller pores are filled, so the relationship between pressure and filling amount can be measured.
That is, since the filling amount is filled starting with the pores having a larger diameter as the pressure changes, by differentiating the relationship between the pressure and the filling amount, the pore diameter and the pore amount at that pore diameter can be determined. The results are shown in FIG. The curve ~ shows the pore size distribution of the friction materials of Examples 1 to 5, ~
shows the pore size distribution of the friction materials of Comparative Examples 6 to 8.
The friction materials of Examples 1 to 5 had a pore diameter distribution center of 3
~4 μm, and there are more pores with smaller diameters than in the friction materials of Comparative Examples 6 to 8 (the center of pore diameter distribution is about 10 μm). Examples 1 to 3 are 5μ
90% of the pores are 5 μm or less, and in Examples 4 and 5, 80% of the pores are 5 μm or less. Also, Comparative Example 6,
Sample No. 7 has 30% of pores of 5 μm or less, and Comparative Example 8 also has 25% of pores of 5 μm or less. In addition, the porosity of each example is 55 to 60%. Also, the friction coefficient (μd) for each wet friction material
and measure heat resistance. The test piece used was one in which the wet friction material of each of the above examples was cut into a predetermined size, and a metal center plate was sandwiched and pasted. To measure the friction coefficient, a load is applied to the friction material rotating inertia using an SAE #2 friction tester, and the friction coefficient is calculated from the torque. Measurement conditions Number of friction surfaces: 4, inertia: 2.5Kg・cm・
sec 2 , rotation speed: 3600 rpm, load: 7.2 Kg/cm 2 , in oil, oil temperature: 120°C. The results of measuring the friction coefficient for each example are shown in Figure 3. The friction coefficient (μd) shown in the same figure is 100 to 2000.
The friction coefficient is approximately stable during this cycle. The friction materials of Examples 1 to 5 and the friction materials of Comparative Examples 7 to 8 have approximately the same coefficient of friction. Measurement of heat resistance is the same as measurement of friction coefficient.
Measured using SAE #2 friction tester. Measurement conditions Number of friction surfaces: 6, inertia: 2.0Kg・cm・
sec 2 , rotation speed: 3000 to 5200 rpm, load: adjusted so that the braking time is 1 sec, oil fluid: flow rate 1.0 cc/cm 2 mm shaft blowout (q s = 10 to 30 cal/cm 2 ), oil temperature: The measurement results of 120°C heat resistance are shown in Table 2 below.
Heat resistance is evaluated as good until the coefficient of friction (μd) drops by 10% from the initial stable state or when peeling occurs.
以上説明したように本発明の湿式摩擦材は、冷
却性が向上し、耐熱性、摩擦性能に優れている。
従来の使用部位に使用しても、摩擦係数レベルを
変えることなく、熱耐久性が向上する。またアス
ベストのような有害物質を含まなくても充分な耐
熱性、摩擦性能を得ることができ安全である。
As explained above, the wet friction material of the present invention has improved cooling properties, and is excellent in heat resistance and friction performance.
Even when used in conventional areas, thermal durability is improved without changing the friction coefficient level. Furthermore, it is safe because it can provide sufficient heat resistance and friction performance even without containing harmful substances such as asbestos.
第1図・第2図は気孔率分布を説明する図、第
3図は摩擦係数の測定の結果を示す図である。
1〜5…本発明の実施例、6〜8…比較例。
FIG. 1 and FIG. 2 are diagrams explaining the porosity distribution, and FIG. 3 is a diagram showing the results of measurement of the friction coefficient. 1-5...Examples of the present invention, 6-8...Comparative examples.
Claims (1)
フイブリド繊維と無機質繊維と無機質充填剤と摩
擦調整剤とを湿式抄造した紙質基材に、熱硬化性
樹脂を含浸してあり、気孔率が40〜75%で、かつ
気孔径5μm以下の気孔の量が全気孔量の70%以
上を占ることを特徴とする湿式摩擦材。1 A paper base material made by wet papermaking of fibers, fibrid fibers, inorganic fibers, an inorganic filler, and a friction modifier that constitute at least the skeleton of the base material is impregnated with a thermosetting resin, and has a porosity of 40 to 40. A wet friction material characterized in that the amount of pores with a pore diameter of 5 μm or less accounts for 70% or more of the total pore amount.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10930486A JPS62266238A (en) | 1986-05-12 | 1986-05-12 | wet friction material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10930486A JPS62266238A (en) | 1986-05-12 | 1986-05-12 | wet friction material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62266238A JPS62266238A (en) | 1987-11-19 |
| JPH0467051B2 true JPH0467051B2 (en) | 1992-10-27 |
Family
ID=14506798
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10930486A Granted JPS62266238A (en) | 1986-05-12 | 1986-05-12 | wet friction material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62266238A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3219151B2 (en) * | 1989-04-08 | 2001-10-15 | 日清紡績株式会社 | Heat resistant dry friction material |
| JP2004138121A (en) | 2002-10-16 | 2004-05-13 | Nsk Warner Kk | Wet friction material |
-
1986
- 1986-05-12 JP JP10930486A patent/JPS62266238A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62266238A (en) | 1987-11-19 |
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