JPS63152735A - Wet type friction material and its manufacture - Google Patents
Wet type friction material and its manufactureInfo
- Publication number
- JPS63152735A JPS63152735A JP30056786A JP30056786A JPS63152735A JP S63152735 A JPS63152735 A JP S63152735A JP 30056786 A JP30056786 A JP 30056786A JP 30056786 A JP30056786 A JP 30056786A JP S63152735 A JPS63152735 A JP S63152735A
- Authority
- JP
- Japan
- Prior art keywords
- friction
- layer
- surface side
- paper
- base material
- 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.)
- Granted
Links
- 239000002783 friction material Substances 0.000 title claims abstract description 48
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000000835 fiber Substances 0.000 claims abstract description 24
- 239000000463 material Substances 0.000 claims abstract description 20
- 239000006185 dispersion Substances 0.000 claims abstract description 8
- 229920005989 resin Polymers 0.000 claims abstract description 8
- 239000011347 resin Substances 0.000 claims abstract description 8
- 239000003365 glass fiber Substances 0.000 claims abstract description 6
- 239000010410 layer Substances 0.000 claims abstract 11
- 239000002344 surface layer Substances 0.000 claims abstract 2
- 239000011148 porous material Substances 0.000 claims description 55
- 239000003607 modifier Substances 0.000 claims description 7
- 239000011256 inorganic filler Substances 0.000 claims description 6
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 4
- 239000000945 filler Substances 0.000 abstract description 3
- 239000012530 fluid Substances 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 238000009826 distribution Methods 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 9
- 239000002994 raw material Substances 0.000 description 6
- 238000010586 diagram Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000010425 asbestos Substances 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
- 239000000428 dust Substances 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920006282 Phenolic fiber Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 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
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002996 emotional effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000002609 medium Substances 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
- 229920001568 phenolic resin Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000006163 transport media Substances 0.000 description 1
Landscapes
- Braking Arrangements (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、クラッチの摩擦材、特に油液中で使用するに
適した湿式ItI!擦材とその製造方法に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention provides a friction material for a clutch, particularly a wet type ItI! suitable for use in an oil solution. This article relates to rubbing materials and methods of manufacturing them.
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ッチは、
常時は充分に動力を伝達する一方1発進時などは適度な
滑りを4えると共に変速機の変速歯車の切り巷え時には
動力を遮断する機能が要求される。か−る機能を満たす
クラッチとしてL!9!擦式のクラッチが広く採用され
ている。そして摩擦式のクラッチには乾燥状態で使用さ
れる乾式クラッチと油液中で使用される湿式クラッチと
がある。後者の湿式クラッチは遊星歯車式の自動変速機
内の411成要素として多板クラッチの形で多く使用さ
れているものである。For example, the clutch that transmits the drive from the prime mover to the transmission in automobiles, construction machinery, agricultural machinery, motor boats, etc.
While sufficient power is transmitted at all times, a function is required to provide adequate slippage during a first start, and to cut off power when the gears of the transmission shift. L as a clutch that fulfills these functions! 9! Friction type clutches are widely used. Friction type clutches include dry clutches that are used in dry conditions and wet clutches that are used in oil. The latter wet type clutch is often used in the form of a multi-disc clutch as a 411 component in a planetary gear type automatic transmission.
摩擦式のクラ−2チでは摩擦熱が発生するため、前述の
機部が安定して果されるには、摩!部分から熱が効率良
く放出されなければならない、湿式クラッチでは油が熱
の運搬媒体として重要な役割を負っている。摩擦面で発
生した熱は、油が媒体となって系全体に拡散放出される
。従って摩擦材自身の油の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a悌が低下してしまう。Friction-type clutches generate frictional heat, so friction is required for the above-mentioned machine parts to function stably. In wet clutches, where heat must be efficiently released from parts, 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, resulting in a decrease in its agility as a friction material.
湿式摩擦材は、有機質繊維、無機質繊維、無機質粉末充
填剤およびカシュ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、フェ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。Wet friction materials are made by impregnating thermosetting resins such as phenolic resins and melamine resins onto paper base materials that are wet-printed with organic fibers, inorganic fibers, inorganic powder fillers, and friction modifiers such as cashew dust. be. It is thought that oil is retained and circulated in the pores of this paper base material.
従来の摩擦材は、例えば特開昭80−23774号公報
に開示されている。A conventional friction material is disclosed in, for example, Japanese Patent Laid-Open No. 80-23774.
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
かった。そのため、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った0
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
のになってしまう。In conventional wet friction materials, research has focused on the types and composition ratios of raw materials, and the pores (the areas where oil is retained) have not necessarily been sufficiently studied. Therefore, while the structure of the paper base material from which paper was made aggregated, the individual pores tended to become larger.
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. turn into.
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、使用が困難になっているため、素材
原料の選択[口が狭まっている。そのため充゛分な性能
を持ちながらIP康面で害のない摩擦材は得られていな
い。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. It's getting narrower. Therefore, a friction material that has sufficient performance but is not harmful in terms of IP stability has not been obtained.
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。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.
本発明者らは、気孔部分に油が保持され循環することに
よっ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った。すな
わち本発明の湿式摩擦材lは、第1図(断面図)に示す
ように、摩擦面側の層2と固定面側の層3との二層を有
している。摩擦面側の層2は骨格部分を構成する繊維成
分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、その紙質基材の気孔
率が50〜65%で気孔径5ミクロンm以下の気孔が全
気孔中の80%以上を占めている。The present inventors have focused on the fact that the performance of a wet friction material is influenced by the retention and circulation of oil in the pores, and as a result of continued research, they have completed the present invention. That is, the wet friction material 1 of the present invention has two layers, a layer 2 on the friction surface side and a layer 3 on the fixed surface side, as shown in FIG. 1 (cross-sectional view). Layer 2 on the friction surface side is made of a paper base material made by wet paper-making of a fiber component constituting a skeleton, an inorganic filler, and a friction modifier, and impregnated with a thermosetting resin, and the paper base material has a porosity of 50. ~65%, and pores with a pore diameter of 5 microns or less account for 80% or more of all pores.
固定面側の層3は気孔率が40〜70%で気孔径5ミク
ロンm以上の気孔が全気孔中の60%以上を占めている
。The layer 3 on the fixed surface side has a porosity of 40 to 70%, and pores with a pore diameter of 5 microns or more account for 60% or more of the total pores.
摩擦面側の層2は、繊m成分の少なくとも一部として例
えばフィブリッド繊維10〜50重量%を含み、無機質
充填剤の粒径が5ミクロンm以下、摩擦調整剤の粒径が
50ミクロンm以下が好ましい、また固定面側の層3は
繊維成分に、例えばガラス繊維またはパルプ、若しくは
その両方を含んでいる。The layer 2 on the friction surface side contains, for example, 10 to 50% by weight of fibrid fibers as at least part of the fiber m component, the particle size of the inorganic filler is 5 microns or less, and the particle size of the friction modifier is 50 microns or less. is preferable, and the layer 3 on the fixed surface side contains a fiber component, for example glass fiber or pulp, or both.
フィブリッド繊維は、例えばセルロース繊維、芳香族ポ
リアミド繊維などを0.2〜2ミクロンmの太さに微小
化した繊維で、湿式抄造によりフィブリル化する性質を
有しているものである。摩擦面側の層2には繊維成分と
して、上記のフィブリッド繊維以外に、例えばノボロイ
ドmta、ガラス繊維、ロックウール、セラミック繊維
、金属繊維を一部に混入してもよい。Fibrid fibers are fibers made of, for example, cellulose fibers, aromatic polyamide fibers, etc., which have been miniaturized to a thickness of 0.2 to 2 microns, and have the property of being fibrillated by wet paper forming. In addition to the above-mentioned fibrid fibers, for example, novoloid mta, glass fibers, rock wool, ceramic fibers, and metal fibers may be partially mixed into the layer 2 on the friction surface side as fiber components.
無機質充填剤は、例えば珪藻上、アルミナ粉。Examples of inorganic fillers include diatom and alumina powder.
硫酸バリウム、炭酸カルシウム、シリカである。These are barium sulfate, calcium carbonate, and silica.
摩擦調整剤は1例えばグラファイト、カシューダストで
ある。Friction modifiers include, for example, graphite and cashew dust.
上記本発明の湿式摩擦材lを製造する方法は、例えば第
2図に示すように、少なくとも一部にフイブリッド繊維
を含む繊維成分と無機質充填剤と摩擦調整剤を混合した
水溶分散液5を抄紙網6上に流して抄紙し、その抄紙を
した未乾燥の紙匹7上にガラス繊維または(および)パ
ルプを含む水溶分散液8を流して抄紙した二層の紙質成
分10を基材にすることを特徴としている。The method for manufacturing the wet friction material 1 of the present invention is, for example, as shown in FIG. A two-layer paper component 10 is used as a base material by pouring it onto a screen 6 to make paper, and pouring an aqueous dispersion 8 containing glass fiber or (and) pulp onto an undried paper web 7 to make paper. It is characterized by
、 〔作用〕
本発明の湿式摩擦材は、摩擦面側の層2が上記の各原料
の働き、特にフィブリッ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50%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65%では摩擦
材そのもの覧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5ミク
ロンm以下の気孔による気孔量が80%以上を占る。[Function] In the wet friction material of the present invention, the pores in the layer 2 on the friction surface side become minute and dispersed due to the action of the above-mentioned raw materials, especially the action of the fibrid fibers. When the porosity is less than 50%, oil retention and circulation are insufficient, and when the porosity is 65%, the mechanical strength of the friction material itself is insufficient. In contrast, the friction material of the present invention has a porosity of 40 to 75%, and moreover, 80% or more of the pores are pores of 5 microns or less.
したがって分散された微細な気孔部分を油が循環するの
で、冷却性が向上する。Therefore, since the oil circulates through the dispersed fine pores, cooling performance is improved.
また固定面側の層3は気孔径が比較的大きくなっている
から、油の吸収、放散が良く、摩擦面の層2側からの油
を良く循環する。そのため、冷却性が一層向上する。Furthermore, since the layer 3 on the fixed surface side has a relatively large pore diameter, oil absorption and dissipation are good, and oil from the layer 2 side on the friction surface is well circulated. Therefore, cooling performance is further improved.
しかも摩擦面側の層2と固定面側の層3とは連続的に抄
紙されるので、両者が一体的になっており、機械的強度
が高い。Moreover, since the layer 2 on the friction surface side and the layer 3 on the fixed surface side are made into paper continuously, they are integrated and have high mechanical strength.
以下、本発明の実施例を詳細に説明する。 Examples of the present invention will be described in detail below.
下記の第1表(配合表)に示す各原料で抄紙し、紙質基
材を得る。なお実施例1〜5は本発明を適用した湿式摩
擦材の例、比較例6〜8は本発明を適財外の例である。Paper is made using each raw material shown in Table 1 (composition table) below to obtain a paper base material. Examples 1 to 5 are examples of wet friction materials to which the present invention is applied, and Comparative Examples 6 to 8 are examples in which the present invention is not suitable.
(以下余白)
第1表:配合重量%
第2ばに示すように、長網式抄紙機により抄紙する。先
ず摩擦面側の層2を構成する各原料の水溶分散液5が無
終端長網6上に流出し、紙匹7の繊維が分散しながら除
水されてゆく、除水の途中で、固定面側のM3を構成す
る各原料の水溶分散液8が紙匹7上に流出し二層の紙質
成分10が形成される。二層の紙質成分10はプレスト
ロール16・16で圧空され、乾燥ドラム17と18で
乾燥されてから、ロール19に巻取られる。なお12は
ダンディロール、1371テーブルロール、14はサク
ションボックスである。第3図に示すように、ロール状
の紙質成分lOはカッタ20で裁断され、シート状にな
る。この紙質成分10にフェノール樹脂を配合表に記載
の重量比をスプレィ法により吹付けて含浸させ、加熱硬
化させると湿式摩擦材1が製造される。この湿式摩擦材
lを第4図に示すように円盤状に裁断し、第5図に示す
ように芯金22の両面に接着して湿式クラッチのフリク
ションプレートが完成する。なお第5図の例では摩擦材
lの表面には溝が設けられている、すなわち断面は第6
図に示すようになる。摩擦面側の層2はディスクロータ
23(鎖線示)に当接する。(The following is a margin) Table 1: Mixed weight % As shown in Table 2, paper is made using a fourdrinier paper machine. First, the aqueous dispersion 5 of each raw material constituting the layer 2 on the friction surface side flows onto the endless fourdrinier 6, and the fibers of the paper web 7 are dispersed and removed.During the water removal, they are fixed. The aqueous dispersion 8 of each raw material constituting the surface side M3 flows onto the paper web 7, forming a two-layer paper component 10. The two-layer paper component 10 is compressed by press rolls 16, 16, dried by drying drums 17 and 18, and then wound onto a roll 19. Note that 12 is a dandy roll, 1371 table roll, and 14 is a suction box. As shown in FIG. 3, the roll-shaped paper component IO is cut by a cutter 20 into a sheet. A wet friction material 1 is produced by impregnating this paper component 10 with a phenol resin in the weight ratio shown in the formulation table by spraying and curing by heating. This wet type friction material 1 is cut into a disk shape as shown in FIG. 4, and is adhered to both sides of the core metal 22 as shown in FIG. 5 to complete the friction plate of the wet type clutch. In the example shown in FIG. 5, grooves are provided on the surface of the friction material l, that is, the cross section is the sixth
The result will be as shown in the figure. The layer 2 on the friction surface side comes into contact with a disc rotor 23 (indicated by a chain line).
各個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、圧力が上るに従って細か
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。The porosity and pore diameter distribution of each wet friction material are 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.
第7図は摩擦面側の居2の気孔径に対する気孔量の分布
(気孔径分布)の曲線である。実線で示す■〜■の曲線
は、実施例1〜5および比較例6の摩擦材の気孔径分布
で、気孔率が55〜58%、気孔量がピークになるとき
(図示曲線の最大のとき)の気孔径が2.5ミクロンm
である。鎖線で示す■の曲線は、比較例7の摩擦材の気
孔径分布で、気孔率が55%、気孔量がピークになると
きの気孔径が!0ミクロンmである0点線で示す■の曲
線は、比較例8の摩擦材の気孔径分布で、気孔率が56
%、気孔量がピークになるときの気孔径が7ミクロンm
である。FIG. 7 is a curve of the distribution of the amount of pores (pore diameter distribution) with respect to the pore diameter of the groove 2 on the friction surface side. The curves ■ to ■ shown by solid lines are the pore size distributions of the friction materials of Examples 1 to 5 and Comparative Example 6, when the porosity is 55 to 58% and the pore amount is at its peak (at the maximum in the illustrated curve). ) has a pore diameter of 2.5 microns
It is. The curve (■) shown by the chain line is the pore size distribution of the friction material of Comparative Example 7, and the pore size when the porosity is 55% and the pore amount reaches its peak! The curve ■ shown by the 0 dotted line, which is 0 micron m, is the pore size distribution of the friction material of Comparative Example 8, and the porosity is 56.
%, the pore diameter when the pore volume reaches its peak is 7 microns.
It is.
第8図は固定面側の層3の気孔径分布の曲線である。実
線で示す■■の曲線は、実施例1および実施例2の摩擦
材の気孔径分布で、気孔率が60%である。鎖線で示す
■■の曲線は、実施例3および実施例4の摩擦材の気孔
径分布で、気孔率が63%である0点線で示す■の曲線
は、実施例5の摩擦材の気孔径分布で、気孔率が56%
である。各個で気孔量がピークになるときの気孔径は、
夫々lOミクロンm程度以上である。なお比較例6は固
定側の層がない、また比較例7および比較例8の固定面
側の層は、実施例1および実施例2の固定面側の層と同
一であるから、気孔径分布は実線で示す■■の曲線と同
一になる。FIG. 8 is a curve of the pore size distribution of the layer 3 on the fixed surface side. The solid curve ■■ represents the pore size distribution of the friction materials of Example 1 and Example 2, and the porosity is 60%. The ■■ curve shown by the chain line is the pore size distribution of the friction materials of Example 3 and Example 4, and the ■■ curve shown by the 0-dot line with a porosity of 63% is the pore size distribution of the friction material of Example 5. Distribution, porosity is 56%
It is. The pore diameter when the pore volume reaches its peak in each individual is
Each is about 10 microns or more. Note that Comparative Example 6 does not have a layer on the fixed side, and the layers on the fixed side of Comparative Examples 7 and 8 are the same as the layers on the fixed side of Examples 1 and 2, so the pore size distribution is the same as the curve shown by the solid line.
また各個の湿式摩擦材について摩擦係数(pd)。Also, the coefficient of friction (pd) for each wet friction material.
耐久性および耐熱性を測定する。試験片は上記各個の湿
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。Measure durability and heat resistance. The test piece used is one obtained by cutting each of the above wet friction materials into a predetermined size, and pasting the cut pieces with a metal center plate in between.
!!l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。! ! 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.
測定条件
摩擦面数:4、イナーシャ: 2.5Kg−cm・5e
c2゜回転数: 380Orpm 、面圧: 7.2K
g/cm2、油液中、油温度:120℃、
各個の摩擦係数の測定の結果は、第9図に示しである。Measurement conditions Number of friction surfaces: 4, inertia: 2.5Kg-cm・5e
c2° rotation speed: 380Orpm, surface pressure: 7.2K
g/cm2, in oil liquid, oil temperature: 120°C, and the results of measuring each friction coefficient are shown in FIG.
同図に示す摩擦係数(pd)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6〜8の摩擦材
とは略同等の摩擦係数(ルd)を示している。The coefficient of friction (pd) shown in the figure is the value at 100 to 2000 cycles, and the coefficient of friction is approximately stable during these cycles. The friction materials of Examples 1 to 5 and the friction materials of Comparative Examples 6 to 8 have approximately the same coefficient of friction (ru d).
摩擦面側の層2の気孔の径により耐久性にどの程度是異
ができるか、実施例2(ピーク気孔径2.5 ミクロン
m第7図参照)、比較例7(ピーク気孔径10ミクロン
m)および比較例8(ピーク気孔径7ミクロンm)の耐
久性を測定する。耐久性の測定は、摩擦係数の測定と同
じ<SAE#2摩擦試験機で1一定をする( q 、
m 25cal /cm2) 、摩擦係数(#Ld)が
初期安定時より1割落ちるときまで、または剥離がlθ
%発生するときまでの荷重サイクルが第1θ図に示しで
ある。同図に示されるように、摩擦面側の層2のピーク
気孔径が小さい方が耐久性に優れていることが解る。How much difference can be made in durability depending on the diameter of the pores in layer 2 on the friction surface side? ) and Comparative Example 8 (peak pore diameter 7 μm). Measuring durability is the same as measuring friction coefficient <1 constant using SAE #2 friction tester (q,
m25cal/cm2), until the coefficient of friction (#Ld) drops by 10% from the initial stable state, or until the peeling reaches lθ
The load cycle until % occurs is shown in Fig. 1θ. As shown in the figure, it can be seen that the smaller the peak pore diameter of the layer 2 on the friction surface side, the better the durability.
耐熱性の測定は、下記の測定条件により測定する。Heat resistance is measured under the following measurement conditions.
測定条件
摩擦面数:6.イナーシャ: 2.0Kg−cm・5e
c2、回転数: 3000〜8200rpm、荷重二制
動時間がl5ecになるように調整、油液:流Q 2.
5cc/cm2−sinシー?7ト吹出′し、(q 、
= 10〜45caJl /cm2)、油温度二80
℃
耐熱性の測定結果は下記第2表に示しである。Measurement conditions Number of friction surfaces: 6. Inertia: 2.0Kg-cm・5e
c2, rotation speed: 3000 to 8200 rpm, adjusted so that the load braking time is 15ec, oil liquid: flow Q 2.
5cc/cm2-sin sea? 7 pieces were blown out, (q,
= 10~45caJl/cm2), oil temperature 280
C. The measurement results of heat resistance are shown in Table 2 below.
耐熱性の判定は、摩擦係数(ILd)が初期安定時よ9
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。Judgment of heat resistance is based on the coefficient of friction (ILd) at initial stability of 9.
A period up to 10% drop or until peeling occurs is considered good.
第2表 耐熱性
A : 5000サイクルまで良好
B : 2000サイクルまで良好
c : 1oooサイクルまで良好
D : 100サイクルまで良好
E:波形くずれ
第2表に示すように、実施例1〜5の摩擦材は、比較例
6〜8の1tI擦材に比べて、耐熱性が向上している。Table 2 Heat resistance A: Good up to 5000 cycles B: Good up to 2000 cycles C: Good up to 100 cycles D: Good up to 100 cycles E: Waveform distortion As shown in Table 2, the friction materials of Examples 1 to 5 , the heat resistance is improved compared to the 1tI rubbing materials of Comparative Examples 6 to 8.
なお、上記の例は長網式抄造機を使用して紙質成分lO
を製造しているが、丸網式抄造機を使用して製造するこ
とも可能である。In addition, the above example uses a fourdrinier paper making machine to produce paper material lO
However, it is also possible to manufacture using a circular mesh paper machine.
〔発IJ1の効果〕
以上説明したように本発明の湿式摩擦材は、冷却性が向
上するので、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
、耐久性、耐熱性を向上させることができる。しかも健
康面で有害性のあるアスベストヲ含んでいない。[Effects of IJ1] As explained above, the wet friction material of the present invention has improved cooling properties, and therefore has excellent heat resistance and friction performance. Even when used in conventional locations, durability and heat resistance can be improved without changing the friction coefficient level. Furthermore, it does not contain asbestos, which is harmful to health.
また摩擦面側の層と固定面側の層とは連続的に抄紙され
るので、両者が一体的になっており1機械的強度が高い
、製造工程も簡易である。Furthermore, since the friction surface side layer and the fixed surface side layer are made into paper continuously, they are integrated, resulting in high mechanical strength and a simple manufacturing process.
第1図は本発明を適用する湿式摩擦材の断面図、第2図
は湿式摩擦材を製造する装置の実施例を示す概略構成図
、第3図書第4図は湿式摩擦材の製造工程を説明する図
、第5図フリクションプレートの分解斜視図、第6図は
湿式摩擦材とディスクロータとの関連を示す断面図、第
7図は摩擦面側の層の気孔径分布を示す図、第8図は固
定面側の層の気孔径分布を示す図、第9図は摩擦係数を
示す図、第10図は気孔径による耐久性の変化を示す図
である。
l 、 、湿式摩擦材 2 、、、、、摩擦面側の層
3・・・・固定面側の層 6・・・・・無終端長網7・
・・−・紙匹 5・8・・・・・水溶分散液io、
、、、、紙質成分 19.、、、、ロール20−・・
カッタ 22・・・・・芯金23・・・・・ディ
スクロータ
特許出願人 アイシン化工株式会社
回 トヨタ自動車株式会社
第10図 気孔柱1: J:5耐ス姓
〜
第9図
←−−寅掩例−−例 トー比戦例→
第7v4 情操面側の層
箪8図 固定面側め層Fig. 1 is a sectional view of a wet friction material to which the present invention is applied, Fig. 2 is a schematic configuration diagram showing an embodiment of an apparatus for manufacturing a wet friction material, and Fig. 4 of Fig. 3 shows the manufacturing process of a wet friction material. Figure 5 is an exploded perspective view of the friction plate; Figure 6 is a sectional view showing the relationship between the wet friction material and the disc rotor; Figure 7 is a diagram showing the pore size distribution of the layer on the friction surface side; FIG. 8 is a diagram showing the pore size distribution of the layer on the fixed surface side, FIG. 9 is a diagram showing the friction coefficient, and FIG. 10 is a diagram showing the change in durability depending on the pore diameter. 1. Wet friction material 2. Layer on friction surface side 3. Layer on fixed surface side 6. Endless fourdrinier 7.
... Paperfish 5.8 ... Aqueous dispersion io,
,,,Paper quality component 19. ,,,,roll 20-...
Cutter 22...Core 23...Disc rotor Patent applicant Aisin Kako Co., Ltd. Toyota Motor Corporation Figure 10 Pore column 1: J: 5 resistance ~ Figure 9←--Tora Example - Example Tor ratio battle example → 7th v4 Layer on the emotional side Figure 8 Layer on the fixed side
Claims (1)
面側の層は骨格部分を構成する繊維成分と無機質充填剤
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、該紙質基材の気孔率が50〜65%で
気孔径5ミクロンm以下の気孔が全気孔中の80%以上
を占め、固定面側の層は骨格部分を構成する繊維成分を
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40〜70%で気孔径5ミクロンm以上の気孔
が全気孔中の60%以上を占めることを特徴とする湿式
摩擦材。 2、前記摩擦面側の層は繊維成分の少なくとも一部とし
てフィブリッド繊維10〜50重量%を含み、かつ無機
質充填剤の粒径が5ミクロンm以下および摩擦調整剤の
粒径が50ミクロンm以下であり、前記固定面側の層は
繊維成分にガラス繊維または/およびパルプを含むこと
を特徴とする特許請求の範囲第1項記載の湿式摩擦材。 3、少なくとも一部にフィブリッド繊維を含む繊維成分
と無機質充填剤と摩擦調整剤を混合した水溶分散液を抄
紙網上に流して抄紙し、その抄紙をした未乾燥の紙匹上
にガラス繊維または/およびパルプを含む水溶分散液を
流して抄紙した2層の紙質成分を基材にすることを特徴
とする湿式摩擦材の製造方法。[Claims] 1. It has two layers: a layer on the friction surface side and a layer on the fixed surface side, and the layer on the friction surface side contains a fiber component constituting the skeleton, an inorganic filler, and a friction modifier. A paper base material made by wet papermaking is impregnated with a thermosetting resin, and the paper base material has a porosity of 50 to 65%, pores with a pore diameter of 5 microns or less account for 80% or more of the total pores, and are fixed. The surface layer is made of a paper base material made by wet papermaking of the fiber components that make up the skeleton, and is impregnated with a thermosetting resin.
A wet friction material characterized in that pores with a porosity of 40 to 70% and a pore diameter of 5 microns or more account for 60% or more of all pores. 2. The layer on the friction surface side contains 10 to 50% by weight of fibrid fibers as at least part of the fiber component, and the particle size of the inorganic filler is 5 microns or less and the particle size of the friction modifier is 50 microns or less. The wet friction material according to claim 1, wherein the layer on the fixed surface side contains glass fiber and/or pulp as a fiber component. 3. Paper is made by pouring an aqueous dispersion of a fiber component containing at least a portion of fibrid fibers, an inorganic filler, and a friction modifier onto a papermaking net, and glass fibers or A method for producing a wet friction material, characterized in that the base material is a two-layer paper component made by flowing an aqueous dispersion containing / and pulp.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30056786A JPH0721298B2 (en) | 1986-12-16 | 1986-12-16 | Wet friction material and manufacturing method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30056786A JPH0721298B2 (en) | 1986-12-16 | 1986-12-16 | Wet friction material and manufacturing method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63152735A true JPS63152735A (en) | 1988-06-25 |
JPH0721298B2 JPH0721298B2 (en) | 1995-03-08 |
Family
ID=17886391
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30056786A Expired - Fee Related JPH0721298B2 (en) | 1986-12-16 | 1986-12-16 | Wet friction material and manufacturing method thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0721298B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004092904A (en) * | 2002-08-30 | 2004-03-25 | Borgwarner Inc | Friction material having friction modifying layer |
-
1986
- 1986-12-16 JP JP30056786A patent/JPH0721298B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004092904A (en) * | 2002-08-30 | 2004-03-25 | Borgwarner Inc | Friction material having friction modifying layer |
Also Published As
Publication number | Publication date |
---|---|
JPH0721298B2 (en) | 1995-03-08 |
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