JPS633083A - Wet friction member - Google Patents
Wet friction memberInfo
- Publication number
- JPS633083A JPS633083A JP14554486A JP14554486A JPS633083A JP S633083 A JPS633083 A JP S633083A JP 14554486 A JP14554486 A JP 14554486A JP 14554486 A JP14554486 A JP 14554486A JP S633083 A JPS633083 A JP S633083A
- Authority
- JP
- Japan
- Prior art keywords
- friction
- fibers
- friction member
- base material
- potential
- 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
- 239000000835 fiber Substances 0.000 claims abstract description 53
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000000463 material Substances 0.000 claims abstract description 23
- 239000000945 filler Substances 0.000 claims abstract description 22
- 239000011230 binding agent Substances 0.000 claims abstract description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000003607 modifier Substances 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 abstract description 6
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 239000010425 asbestos Substances 0.000 description 7
- 229910052895 riebeckite Inorganic materials 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000010009 beating Methods 0.000 description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000005995 Aluminium silicate Substances 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
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 235000012211 aluminium silicate Nutrition 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
- 230000005540 biological transmission Effects 0.000 description 2
- 235000020226 cashew nut Nutrition 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- -1 for example Substances 0.000 description 2
- 239000003365 glass 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
- 230000013011 mating Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000013054 paper strength agent Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000000725 suspension Substances 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
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 101100136092 Drosophila melanogaster peng gene Proteins 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- KYNKUCOQLYEJPH-UHFFFAOYSA-N [K][Ti] Chemical compound [K][Ti] KYNKUCOQLYEJPH-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 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
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 229920003235 aromatic polyamide Polymers 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
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000010586 diagram Methods 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
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000010443 kyanite Substances 0.000 description 1
- 229910052850 kyanite Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011134 resol-type phenolic resin Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は自動車などの車両で用いられる湿式摩擦部材に
関する。本発明はたとえば、車両のトランスミッション
内で油中に浸した状態で用いられる動力伝達用の湿式摩
擦クラッチなどに利用することができる。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a wet friction member used in vehicles such as automobiles. The present invention can be used, for example, in a wet friction clutch for power transmission that is used in a vehicle transmission while being immersed in oil.
〔従来の技術]
従来この種の湿式摩擦部材は、繊維と充填材と51Mg
整剤と含水中で混合し、抄紙して基材とした後、結合剤
を含浸して硬化させることで製造されている。[Prior art] Conventionally, this type of wet friction member consists of fibers, fillers, and 51Mg.
It is manufactured by mixing a conditioning agent in water and making paper into a base material, then impregnating it with a binder and curing it.
この充填材および摩m調整剤はIff!性能の良否を決
定する重要な成分であり、抄紙した時に繊維に一体的に
定着されている必要がある。そこで従来、この充填材お
よび摩擦調整剤を繊維に定着させるには、例えばアスベ
ストを定着材料として用い、mHとのからみを利用して
定着するもの、あるいは硫閣バンドなどを配合し、充填
材および1γ■調整剤を凝集させることにより繊維間に
定着させるもの、またはカチオン型ポリマーなどのカチ
オン化剤を配合し徴111繊維の表面電位を下げること
により定着させるもの、などが知られている。This filler and friction modifier are Iff! It is an important component that determines the quality of paper and must be integrally fixed to the fibers when paper is made. Conventionally, in order to fix these fillers and friction modifiers to fibers, for example, asbestos is used as a fixing material, and something that fixes by utilizing the entanglement with mH, or a sulfur band is mixed, and the filler and There are known methods in which the 1γ■ regulator is fixed between the fibers by agglomerating it, or in which a cationizing agent such as a cationic polymer is blended to lower the surface potential of the 111 fibers.
[発明が解決しようとする問題点]
上記した種々の定着方法において、アスベストを使用し
た場合には、公害面での不具合があり、硫酸バンドを用
いたときには酸性抄紙のため変色などの紅時変化が生ず
る。またカチオン化剤を用いる場合には定着強度が小さ
いという不具合がある。[Problems to be solved by the invention] In the above-mentioned various fixing methods, when asbestos is used, there are problems in terms of pollution, and when sulfuric acid band is used, red changes such as discoloration occur due to acidic papermaking. occurs. Further, when a cationizing agent is used, there is a problem that the fixing strength is low.
本発明は上記事情に鑑みてなされたものであり、アスベ
ストを使用せず、新規な定着材料を使用した湿式P!J
l!’部材を提供するものである。The present invention was made in view of the above circumstances, and uses a new fixing material without using asbestos. J
l! 'It provides parts.
[問題点を解決するための手段]
本発明の湿式f@腔部材は、U&維と、粉状充填材と、
摩擦調整剤と、からなる基材と、
該基Hの該繊維、該充填材および該摩g!XgJ含水を
結合する結合剤と、かうなる湿式摩擦部材において、
該基材にはpH5,5の水中にお(ブるζ電位がプラス
電位のアルミナ繊維が含有されていることを特徴とする
。[Means for solving the problems] The wet type f@ cavity member of the present invention includes U&fiber, powdery filler,
a base material consisting of a friction modifier, the fibers of the group H, the filler and the friction modifier g! A binder that binds XgJ water and such a wet friction member are characterized in that the base material contains alumina fibers having a positive ζ potential in water with a pH of 5.5.
本発明の湿式摩擦部材の基体をなす繊維としては、従来
と同様、有m繊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、リンクバルブ、木材バル
ブ、合成バルブ、ポリエステル系繊維、アクリル系繊維
、脂[1/j族ボリフ7ミド4Bm、ポリビニルアルコ
ール変性繊維、ポリ塩化ビニル111、ポリプロピレン
繊維、芳香族ポリアミド繊維、カーボン$31 N 、
などを−種または複数種類混合して用いることができる
。また無titiIffとしては、チタン酎カリウム繊
維、ガラス繊維、カオリンXHN、シリカ繊維、ボーキ
サイトmi、カヤナイトIIN、ホウ素4M帷、マグネ
シア繊維、ロックウール繊維、金属!l雑などを一種ま
たは複数種類用いることができる。なお有機繊維は摩擦
部材中に10〜70重寸%とするのが望ましく、無IR
繊維は2〜50重屋%含有するように用いるのがよい。As the fibers forming the base of the wet friction member of the present invention, both organic fibers and inorganic fibers can be used, as in the past. Examples of organic fibers include link valves, wood valves, synthetic valves, polyester fibers, acrylic fibers, fat [1/j group borif 7mid 4Bm, polyvinyl alcohol modified fibers, polyvinyl chloride 111, polypropylene fibers, and aromatic polyamide fibers. , carbon $31 N,
It is possible to use one species or a mixture of two or more species. In addition, titanium potassium fiber, glass fiber, kaolin XHN, silica fiber, bauxite mi, kyanite IIN, boron 4M cloth, magnesia fiber, rock wool fiber, metal! One or more kinds of miscellaneous materials can be used. It is preferable that the organic fiber is 10 to 70% by weight in the friction member, and has no IR.
It is preferable to use the fiber in an amount of 2 to 50%.
充填材は従来と同様、有機充填材およびM機充填材のい
ずれも用いることができる。例えばシリカ、タルク、酸
化マグネシウム、カオリン、硫酸バリウム、生石灰、リ
ン酸カルシウム、炭酸カルシウム、ケイソウ土、などを
用いることができる。As the filler, either an organic filler or an M machine filler can be used as in the conventional case. For example, silica, talc, magnesium oxide, kaolin, barium sulfate, quicklime, calcium phosphate, calcium carbonate, diatomaceous earth, etc. can be used.
なお、この充填材は紙中に5〜550重量%含イjされ
るように構成するのが望ましい。Note that it is desirable that this filler be contained in the paper in an amount of 5 to 550% by weight.
摩擦調整剤は摩擦係数を向上したり安定化するためのち
ので、たとえばアルミニウム粉、銅粉、鉄粉などの金属
粉、ゴム粉、カシユーダスト、グラフフィト粉などであ
る。この摩擦調整剤は従来と同様5〜30重量%配合す
ることができる。Friction modifiers are used to improve or stabilize the coefficient of friction, and include, for example, metal powders such as aluminum powder, copper powder, and iron powder, rubber powder, cashew dust, and graphite powder. This friction modifier can be blended in an amount of 5 to 30% by weight as in the conventional case.
本発明の最大の特徴は4M緒中にζ電位がプラス電位の
アルミナuxmが含有されているところにある。なおこ
のζ電位はpH5,5の水中における条件下で測定され
るものであり、+20mV以上の電位を有することが望
ましい。The greatest feature of the present invention is that the 4M material contains alumina uxm whose ζ potential is a positive potential. Note that this ζ potential is measured under conditions in water of pH 5.5, and it is desirable to have a potential of +20 mV or more.
従来、たとえば特開昭57−85876@公報に、繊維
の一部にアルミナ繊維を用いたI?!擦部材が開示され
ている。しかしながらこの種のPJ際部材ではアルミナ
1!維は耐熱性U&維として用いられており、抄紙時の
充填材、摩擦調整剤の歩留り向上の目的には用いられて
いない。Conventionally, for example, in Japanese Patent Application Laid-Open No. 57-85876, I? ! A rubbing member is disclosed. However, for this type of PJ material, alumina is 1! The fibers are used as heat-resistant U&fibers, and are not used for the purpose of improving the yield of fillers and friction modifiers during paper making.
従来用いられている繊維および充填材のpH5゜5の水
中におけるζ電位は一般にマイナスである。The ζ potential of conventionally used fibers and fillers in water at pH 5.5 is generally negative.
たとえばガラス繊維は一59mVであり、アルミナシリ
カ!!紺は一4mVである。For example, glass fiber has a voltage of -59 mV, and alumina silica! ! Navy blue is -4 mV.
そこで本発明では、プラス電位のアルミナ繊維を使用す
ることにより繊維、充填材および11!擦調整剤とアル
ミナ繊維とを電気的に結合させ、以て定着するようにし
たものである。この意味においてアルミナ繊維のζ電位
が+20mVより小さい場合には定着作用が小さくなり
好ましくない。なお従来用いられているアスベストは+
27mVのζ電位を有しており、これが定着作用に寄与
しているものと推察される。しかしながらアスベストは
公害面で不具合があり、本発明者らは鋭意研究の結果、
ζ電位がプラスのアルミナ繊維が定着に良好な結果をあ
たえることを見出して本発明を完成したものである。Therefore, in the present invention, by using alumina fibers with a positive potential, fibers, fillers, and 11! The friction modifier and alumina fibers are electrically bonded and fixed together. In this sense, if the ζ potential of the alumina fiber is less than +20 mV, the fixing effect will be reduced, which is not preferable. In addition, asbestos that is conventionally used is +
It has a ζ potential of 27 mV, which is presumed to contribute to the fixing effect. However, asbestos has problems in terms of pollution, and as a result of intensive research, the present inventors found that
The present invention was completed by discovering that alumina fibers with a positive ζ potential give good results in fixing.
アルミナ繊維は直1!1〜5μm1長さ0.3重2鵬m
のものが望ましい。そしてこのアルミナat、 G[は
摩擦部材中に0.5〜15重邑%小部することが好まし
い。15千呈%を越えると相手材に対づる攻撃性が顕著
になるので望ましくない。Alumina fiber is straight 1! 1~5 μm 1 length 0.3 layer 2 Peng
Preferably. Preferably, this alumina at, G[ is contained in a small amount of 0.5 to 15% by weight in the friction member. If it exceeds 15,000%, the aggressiveness towards the mating material becomes noticeable, which is not desirable.
また、本発明の摩擦部材には、抄紙時の強度を増すため
にアクリル系樹脂、ポリアミド樹脂、ポリアクリルアミ
ド樹脂、メラミン樹脂などの紙力剤を0.1〜5重量%
用いることも好ましい。In addition, the friction member of the present invention contains 0.1 to 5% by weight of a paper strength agent such as acrylic resin, polyamide resin, polyacrylamide resin, or melamine resin in order to increase the strength during paper making.
It is also preferable to use
結合剤は抄紙された繊維、充填材、S原調含水などから
なる基材を一体的に結合するものであり、従来と同様に
フェノール樹脂、エポキシriAIn 、メラミン樹脂
、尿素樹脂、ポリイミド樹脂などを、抄紙された基材に
対して一般に20〜40重量%のR用いることができる
。また場合によって(よコロイダルシリカなどの無磯結
合剤を用いることもできる。The binder is used to integrally bind the base material made of paper-made fibers, fillers, S original water content, etc., and as in the past, phenol resin, epoxy riAln, melamine resin, urea resin, polyimide resin, etc. Generally, 20 to 40% by weight of R can be used based on the base material from which the paper is made. In some cases, a non-isolated binder such as colloidal silica may also be used.
本発明のme部材を製造するには、まず水中にIJA雑
を投入し、圧縮と回復を反復して叩解する。To manufacture the ME member of the present invention, first, IJA miscellaneous material is put into water and beaten by repeating compression and recovery.
次にアルミナ繊維を加え、次いで充bn材および摩擦調
整剤を投入する。このときU&維、充填材およびI#J
擦調整剤は一般にζ電位がマイナスであり、アルミナ繊
維はプラスであるために繊維と充填(イと摩擦調整剤は
アルミナ繊維に引付けられて定着する。そしてこの分散
液を抄紙機を用いて抄紙し、乾燥する。そして液状の結
合剤を含浸させた後、その結合剤を硬化させることによ
り本発明の摩擦部材を製造することができる。Next, the alumina fibers are added, followed by the filler material and friction modifier. At this time, U&fiber, filler and I#J
Friction modifiers generally have a negative ζ potential, and alumina fibers have a positive potential, so the friction modifiers are attracted to and fixed on the alumina fibers. The friction member of the present invention can be manufactured by making paper, drying it, impregnating it with a liquid binder, and then curing the binder.
[発明の作用および効果]
本発明の!1!m1重では、繊維中にζ電位がプラス電
位のアルミナsumを用いている。そして抄紙前の懸濁
状態の時に、ζ電位がマイナスのAI#1と充填材と摩
擦調整剤とはアルミナm維に引きつけられる。これによ
り充填材および摩擦調整剤が定着され、抄紙時の充填材
およびwe調整剤の歩留りが向上する。従って従来のよ
うにアスベストを使う必要がないので、充填材などの歩
留りは従来と同等に維持しつつ、かつ無公害のJ!J隙
部材を製造することができる。またl1A11バンドを
使う必要がないので変色など経時変化を少なくすること
もできる。[Actions and Effects of the Invention] The present invention! 1! In the m1 layer, alumina sum having a positive ζ potential is used in the fiber. When in a suspended state before papermaking, AI#1 with a negative ζ potential, the filler, and the friction modifier are attracted to the alumina m fibers. This fixes the filler and friction modifier, and improves the yield of the filler and we modifier during paper making. Therefore, there is no need to use asbestos as in the past, so the yield of fillers, etc. can be maintained at the same level as in the past, and J! A J gap member can be manufactured. Furthermore, since there is no need to use the 11A11 band, changes over time such as discoloration can be reduced.
[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)
リンクパルプ50重石部とアラミド繊維10型組部を6
000重伝部0水に投入し、ビータにてor+ s L
tc。次ニア)LtミtmNS a f f i l
I (eta、IC1社製、pH5,5の水中にお
けるζ電(Q +48 m V >を0.5重量部加え
、均一に混合した後カシューダスト15重φ部、チ、タ
ン酸カリウム5重量部、およびケイソウ土25重量部、
さらにアクリル系樹脂からなる紙力剤2小山部を加えて
均一に混合するまでビータを運転した。そしてこの懸濁
液を丸網抄紙機にて抄紙し、乾燥して坪量200(]/
m’、厚さ0.6mmのKm部材基材を得た。そしてこ
の基材にレゾール型フェノール樹脂を30重世%含浸さ
せ、180℃で20分加熱して実施例1の摩擦部材を得
た。(Example 1) Link pulp 50 weight parts and aramid fiber 10 type assembled parts 6
000 Judenbu 0 Put it in water and use the beater to or+s L
tc. Next Near) LtmitmNS a f f i l
I (eta, manufactured by IC1, 0.5 parts by weight of ζ electricity (Q +48 m V > in water with pH 5.5) was added and mixed uniformly, then 15 parts by weight of cashew dust, 5 parts by weight of potassium titanate , and 25 parts by weight of diatomaceous earth,
Furthermore, two small peaks of paper strength agent made of acrylic resin were added and the beater was operated until they were uniformly mixed. This suspension is then made into paper using a circular mesh paper machine and dried to a basis weight of 200 (]/
A Km member base material having a thickness of 0.6 mm and a thickness of 0.6 mm was obtained. This base material was impregnated with 30% resol type phenolic resin and heated at 180° C. for 20 minutes to obtain the friction member of Example 1.
得られた摩擦部材について歩留り率、動的摩擦係数およ
び耐剥離性を測定し表および図に示す。The yield rate, dynamic friction coefficient, and peeling resistance of the obtained friction member were measured and shown in the table and figure.
なお歩留り率は、マツフル炉にて600℃で1時間加熱
した後の残φと抄紙前の懸濁液中の配合物の中の無礪物
の割合との比により社用されるものである。また動的S
擦係数はSAE#2試験機によりATF油中で回転数3
600rpm、加重7゜2kg/Crn” 、イナーシ
?2.5kg・cm・sec’ 、温度120℃の条件
で行なった。また耐剥離性試験は、動的摩擦係数におけ
るイナーシャを3.5kg−cm−5ec2とすること
以外は動的摩擦係数の測定と同様に行ない、スポット剥
離が生じた時点の回転数を3111定した。The yield rate is determined by the ratio of the remaining φ after heating at 600°C for 1 hour in a Matsufuru furnace to the proportion of solids in the suspension before papermaking. . Also dynamic S
The friction coefficient was determined by SAE #2 test machine at 3 rotations in ATF oil.
The peeling resistance test was conducted under the following conditions: 600 rpm, a load of 7゜2 kg/Crn'', an inertia of ?2.5 kg・cm・sec', and a temperature of 120℃.The peeling resistance test was conducted under the following conditions: the inertia in the dynamic friction coefficient was set to 3.5 kg-cm- The measurement of the dynamic coefficient of friction was carried out in the same manner as in the measurement except that the coefficient of friction was set to 5ec2, and the rotational speed at the time when spot peeling occurred was fixed at 3111.
(実施例2)
アルミナ繊維を2重量部と覆ること以外は実施例1と同
様の配合で同様に叩解、抄紙し、結合剤を含浸固化させ
て実施例2の摩擦部材をIQ 1ζ。そして得られた摩
擦部材について実施例1と同様に歩留り率、動的a!擦
係数および耐剥離性試験を測定し結果を表および図に示
す。(Example 2) The friction member of Example 2 was prepared in the same manner as in Example 1 except that 2 parts by weight of alumina fiber was used, beaten and paper-made, and impregnated with a binder and solidified to obtain a friction member of Example 2 with an IQ of 1ζ. The yield rate and dynamic a! of the obtained friction member were the same as in Example 1. The friction coefficient and peel resistance test were measured and the results are shown in the table and figure.
(実施例3)
アルミナ繊維を10重小部とすること以外は実施例1と
同様の配合で同様に叩解、抄紙し、結合剤を含浸固化さ
せて実施例3のFJv1部材を得た。(Example 3) The FJv1 member of Example 3 was obtained by beating and paper-making in the same manner as in Example 1, except that the alumina fiber was used in an amount of 10 parts by weight, and then impregnated with a binder and solidified.
そしC1!′Iられた摩擦部材について実施例1と同様
に歩留り率、動的I!J擦係数および耐剥離性試験を測
定し結果を表および図に示す。Then C1! As in Example 1, the yield rate and dynamic I! The J friction coefficient and peel resistance test were measured and the results are shown in the table and figure.
(比較例1)
アルミナ繊維を用いずカチオン化定着剤(アラフィック
ス1001荒川化学工業株式会社製)を2重度部間合す
ること以外番よ実施例1と同様の配合で同様に叩解、抄
紙し、結合剤を含浸固化させて比較例1の摩擦部材を得
た。そして得られた摩擦部材について実施例1と同様に
歩留り率、動的摩擦係数および耐剥離性試験を測定し結
果を表および図に示す。(Comparative Example 1) Beating and papermaking were carried out in the same manner as in Example 1, except that no alumina fiber was used and a cationic fixing agent (Arafix 1001 manufactured by Arakawa Chemical Industry Co., Ltd.) was used in two parts. A friction member of Comparative Example 1 was obtained by impregnating and solidifying a binder. Then, the yield rate, dynamic friction coefficient, and peeling resistance test were measured for the obtained friction member in the same manner as in Example 1, and the results are shown in the table and the figure.
(比較例2)
アルミナ繊維を0.2重量部とすること以外は実施例1
と同様の配合で同様に叩解、抄紙し、結合剤を含浸固化
させて比較例2の摩擦部材を得た。(Comparative Example 2) Example 1 except that the alumina fiber was 0.2 parts by weight
A friction member of Comparative Example 2 was obtained by beating, paper-making, impregnating and solidifying a binder with the same formulation as above.
そして得られた摩擦部材について実施151111と同
様に歩留り率、動的摩擦係数および耐剥離性試験を測定
し結果を表および図に示す。Then, the yield rate, dynamic friction coefficient, and peeling resistance test were measured for the obtained friction member in the same manner as in Example 151111, and the results are shown in the table and the figure.
(比較例3)
アルミナ繊維を20重1部とすること以外は実施例1と
同様の配合で同様に叩解、抄紙し、結合剤を含浸同化さ
せて比較例3のa!家部材を1りた。(Comparative Example 3) The alumina fibers were used in the same manner as in Example 1 except that the alumina fiber was used at 20 weights and 1 part, the beating and paper making were carried out in the same manner, and the binder was impregnated and assimilated. I got one house part.
そして得られた摩擦部材について実施例1と同様に歩留
り率、動的摩擦係数および耐剥離性試験を測定し結果を
表および図に示す。Then, the yield rate, dynamic friction coefficient, and peeling resistance test were measured for the obtained friction member in the same manner as in Example 1, and the results are shown in the table and the figure.
(評価)
表より明らに本発明の実施例の摩擦部材は、比較例とほ
ぼ同等の歩留り率を有していることが明らかである。即
ち、アスベストや硫酸バンドを用いなくとも従来と同等
の定着性能を有している。(Evaluation) It is clear from the table that the friction members of the examples of the present invention have substantially the same yield rate as the comparative examples. In other words, it has the same fixing performance as the conventional one even without using asbestos or sulfuric acid band.
また図より明らかに、動的摩擦係数は実施例の摩擦部材
と比較例の摩擦部材とはほとんど同等であり、かつiN
J Mは比較例の摩擦部材の方が少ない回転数で発生し
ている。なお、比較例2ではアルミナ繊維が少ないので
歩留り率が低く、かつ耐剥離性が劣っており、比較例3
では相手材料が摩耗したために耐剥離性の測定がでさな
かった。Also, it is clear from the figure that the dynamic friction coefficients of the friction member of the example and the friction member of the comparative example are almost the same, and iN
JM occurs at a lower rotational speed in the friction member of the comparative example. In addition, Comparative Example 2 had a low yield rate and poor peeling resistance because of the small amount of alumina fiber, and Comparative Example 3
In this case, peeling resistance could not be measured because the mating material was worn.
すなわち本実施例のa!擦部材は、定着性能および動的
I!j!療係数を従来と同等に維持するとともに、公害
面の不具合が無く、さらに長期にわたって剥離の発生を
防IL することができる。In other words, a! of this example! The rubbing member improves fixing performance and dynamic I! j! In addition to maintaining the same therapeutic coefficient as before, there is no pollution problem, and the occurrence of IL peeling can be prevented for a long period of time.
第1図は動的摩擦係数の測定結果を示す線図であり、第
2図は耐剥離性試験の結果を示すグラフである。
特許出願人 アイシン化工株式会社代理人
弁理士 大川 宏
同 弁理士 丸山明夫FIG. 1 is a diagram showing the measurement results of the dynamic coefficient of friction, and FIG. 2 is a graph showing the results of the peeling resistance test. Patent applicant Aisin Kako Co., Ltd. agent
Patent Attorney Hirodo Okawa Patent Attorney Akio Maruyama
Claims (4)
基材と、 該基材の該繊維、該充填材および該摩擦調整剤を結合す
る結合剤と、からなる湿式摩擦部材において、 該基材にはpH5.5の水中におけるζ電位がプラス電
位のアルミナ繊維が含有されていることを特徴とする湿
式摩擦部材。(1) A wet friction member consisting of a base material made of fibers, a powdery filler, and a friction modifier, and a binder that binds the fibers, the filler, and the friction modifier of the base material. A wet friction member characterized in that the base material contains alumina fibers having a positive ζ potential in water of pH 5.5.
mV以上のζ電位を有する特許請求の範囲第1項記載の
湿式摩擦部材。(2) Alumina fiber is +20 in water with pH 5.5
The wet friction member according to claim 1, which has a ζ potential of mV or more.
されている特許請求の範囲第1項記載の湿式摩擦部材。(3) The wet friction member according to claim 1, wherein the base material contains 0.5 to 15% by weight of alumina fibers.
mmである特許請求の範囲第1項記載の湿式摩擦部材。(4) Alumina fiber has a diameter of 1 to 5 μm and a length of 0.3 to 2
The wet friction member according to claim 1, which is mm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61145544A JPH0623388B2 (en) | 1986-06-21 | 1986-06-21 | Wet friction member |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61145544A JPH0623388B2 (en) | 1986-06-21 | 1986-06-21 | Wet friction member |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS633083A true JPS633083A (en) | 1988-01-08 |
JPH0623388B2 JPH0623388B2 (en) | 1994-03-30 |
Family
ID=15387635
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61145544A Expired - Lifetime JPH0623388B2 (en) | 1986-06-21 | 1986-06-21 | Wet friction member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0623388B2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4985439A (en) * | 1972-08-30 | 1974-08-16 | ||
JPS62283228A (en) * | 1986-05-29 | 1987-12-09 | Toyota Motor Corp | Wet friction material for vehicle |
-
1986
- 1986-06-21 JP JP61145544A patent/JPH0623388B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4985439A (en) * | 1972-08-30 | 1974-08-16 | ||
JPS62283228A (en) * | 1986-05-29 | 1987-12-09 | Toyota Motor Corp | Wet friction material for vehicle |
Also Published As
Publication number | Publication date |
---|---|
JPH0623388B2 (en) | 1994-03-30 |
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