JPH01238927A - Manufacture of clutch facing - Google Patents
Manufacture of clutch facingInfo
- Publication number
- JPH01238927A JPH01238927A JP6574288A JP6574288A JPH01238927A JP H01238927 A JPH01238927 A JP H01238927A JP 6574288 A JP6574288 A JP 6574288A JP 6574288 A JP6574288 A JP 6574288A JP H01238927 A JPH01238927 A JP H01238927A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- fibers
- glass fiber
- solid lubricant
- clutch
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 239000000835 fiber Substances 0.000 claims abstract description 50
- 239000003365 glass fiber Substances 0.000 claims abstract description 38
- 239000000314 lubricant Substances 0.000 claims abstract description 25
- 239000007787 solid Substances 0.000 claims abstract description 21
- 239000000463 material Substances 0.000 claims abstract description 17
- 239000000945 filler Substances 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 13
- 229920005989 resin Polymers 0.000 claims description 22
- 239000011347 resin Substances 0.000 claims description 22
- 229920001971 elastomer Polymers 0.000 claims description 20
- 239000005060 rubber Substances 0.000 claims description 20
- 229920001187 thermosetting polymer Polymers 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 235000011837 pasties Nutrition 0.000 claims description 3
- 238000005245 sintering Methods 0.000 claims description 2
- 239000010425 asbestos Substances 0.000 abstract description 16
- 229910052895 riebeckite Inorganic materials 0.000 abstract description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 6
- 239000010439 graphite Substances 0.000 abstract description 6
- 229910002804 graphite Inorganic materials 0.000 abstract description 6
- 239000006185 dispersion Substances 0.000 abstract description 5
- 238000004804 winding Methods 0.000 abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052982 molybdenum disulfide Inorganic materials 0.000 abstract description 2
- YPMOSINXXHVZIL-UHFFFAOYSA-N sulfanylideneantimony Chemical compound [Sb]=S YPMOSINXXHVZIL-UHFFFAOYSA-N 0.000 abstract description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000005011 phenolic resin Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 5
- 229920001568 phenolic resin Polymers 0.000 description 5
- 229920000459 Nitrile rubber Polymers 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 244000226021 Anacardium occidentale Species 0.000 description 3
- 244000043261 Hevea brasiliensis Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000004760 aramid Substances 0.000 description 3
- 229920003235 aromatic polyamide Polymers 0.000 description 3
- 235000020226 cashew nut Nutrition 0.000 description 3
- 229920003052 natural elastomer Polymers 0.000 description 3
- 229920001194 natural rubber Polymers 0.000 description 3
- 229920002857 polybutadiene Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 2
- 239000004312 hexamethylene tetramine 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
- 238000002156 mixing Methods 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- -1 bulbs Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000002557 mineral fiber Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 125000000914 phenoxymethylpenicillanyl group Chemical group CC1(S[C@H]2N([C@H]1C(=O)*)C([C@H]2NC(COC2=CC=CC=C2)=O)=O)C 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
Landscapes
- Braking Arrangements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
【発明の詳細な説明】
し産業上の利用分野」
本発明は自動車、産業機械などに用いられるクラッチフ
ェーシングの製造方法に閃する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention is directed to a method of manufacturing clutch facings used in automobiles, industrial machinery, etc.
し従来の技術 課題]
従来、クラッチフェーシングは主に石綿繊維からなるヤ
ーン状、テープ状、ロービング状、クロス状等の基材繊
維に、フェノール樹脂等の熱硬化性樹脂または天然ゴム
等のゴム材または熱硬化性樹脂とゴム材の混合物を含浸
させ、得られた基材繊維に、ゴム材、熱硬化性樹脂、加
硫剤、加硫促進剤、硬化剤、潤滑剤1、無機短繊維、摩
擦調整剤等をミキサー等で混合分散させ、得られるペー
スト状充填剤を付着させ、積層体状に予備成形した後、
金型などで加熱圧縮し、次に、後焼成を行なって硬化さ
せることにより製造されている。[Conventional Technology Issues] Conventionally, clutch facings have been made using base fibers mainly made of asbestos fibers in the form of yarn, tape, roving, cross, etc., and a thermosetting resin such as phenolic resin or a rubber material such as natural rubber. Alternatively, impregnating the resulting base fiber with a mixture of a thermosetting resin and a rubber material, a rubber material, a thermosetting resin, a vulcanizing agent, a vulcanization accelerator, a curing agent, a lubricant 1, an inorganic short fiber, After mixing and dispersing friction modifiers etc. with a mixer etc., adhering the resulting paste filler, and preforming it into a laminate,
It is manufactured by heating and compressing it in a mold, etc., and then hardening it by post-firing.
ところで、上述のようにして得られたクラッチフェーシ
ングは摩擦係数が低く、v1械的強度も弱く、クラッチ
フェーシングの寿命も短、)という欠点があった。By the way, the clutch facings obtained as described above had drawbacks such as a low coefficient of friction, low v1 mechanical strength, and a short lifespan of the clutch facings.
これらを補うために、最近、石綿&R雄とガラス繊維等
を組合わせ、上記と同様の方法でクラッチフェーシング
が製造されており、このクラッチフェーシングは機械的
強度に優れ、摩擦1系数が高く、寿命も長く、広く使用
されている。In order to compensate for these problems, clutch facings have recently been manufactured by combining asbestos & R male with glass fibers, etc., using the same method as above.This clutch facing has excellent mechanical strength, high friction coefficient 1, and long lifespan. It has also been widely used for a long time.
しかし、このような石綿繊維とガラス繊維とを組合わせ
たクラッチフェーシングはクラッチをエンゲージさせる
際に、鳴き(異音)が発生し、運転者等に不快感を与え
るのみならず、鳴きの振動により、クラッチ周辺部品に
悪影響を与える欠点があり、更に鳴きがひどくなると、
シャダー発生等の走行不具合を生ずることもある。この
欠点を改善するために、石綿繊維及びガラス繊維の全量
または1部を芳香族ポリアミド繊維、カーボン繊維等に
置き換える方法もあるが、いずれも高価となり、実用性
に乏しい。However, such a clutch facing made of a combination of asbestos fiber and glass fiber generates squeal (abnormal noise) when the clutch is engaged, which not only causes discomfort to the driver, but also causes noise due to the vibration of the squeal. , there is a drawback that it has a negative effect on the parts around the clutch, and if the squeal gets worse,
This may cause running problems such as shudder. In order to improve this drawback, there is a method of replacing all or part of the asbestos fibers and glass fibers with aromatic polyamide fibers, carbon fibers, etc., but these methods are both expensive and impractical.
本発明は上述のような従来のクラッチフェーシングに付
随する問題点を解決するためになされたちのて゛あり、
その目的はクラッチフェーシングを製造する際に、ガラ
ス繊維等の基材繊維の表面に予め固体潤滑剤を付着させ
た後、通常のクラッチフェーシング製造工程においてク
ラッチフェーシングを製造することにより、鳴き発生の
無いクラッチフェーシングを安価に提供することにある
。The present invention has been made to solve the problems associated with conventional clutch facings as described above.
The purpose of this is to prevent squealing by applying a solid lubricant to the surface of base fibers such as glass fibers before manufacturing clutch facings in the normal clutch facing manufacturing process. The purpose is to provide clutch facings at low cost.
[課題を解決するための手段]
従って、本発明は基材繊維に熱硬化性樹脂またはゴム材
または熱硬化性樹脂とゴム材の混合物を含浸し、次に、
熱硬化性樹脂または熱硬化性樹脂とゴム材の混合物を含
むペースト状充填材を付着させ、得られた基材1!維を
M増体状に予備成形し、得られた予備成形体を加熱圧縮
し、後焼成することからなるクラッチフェーシングの製
造方法において、少なくとも基材繊維として固体潤滑剤
を付着させたガラス繊維を使用することを特徴とするク
ラッチフェーシングの製造方法を提供するにある。[Means for Solving the Problems] Therefore, the present invention impregnates a base fiber with a thermosetting resin, a rubber material, or a mixture of a thermosetting resin and a rubber material, and then:
A base material 1 obtained by attaching a pasty filler containing a thermosetting resin or a mixture of a thermosetting resin and a rubber material! In a method for manufacturing a clutch facing, which comprises preforming fibers into an M-enhanced shape, heating and compressing the obtained preform, and post-sintering, glass fibers to which a solid lubricant is attached are used as at least the base fibers. The present invention provides a method for manufacturing a clutch facing.
1作 用]
以下、本発明に係るクラッチフェーシングの製造方法に
ついて詳細に記載する。1 Effect] Hereinafter, the method for manufacturing a clutch facing according to the present invention will be described in detail.
本発明方法によりクラッチフェーシングを製造する際に
使用する基材繊維には少なくともガラス繊維を使用する
。すなわち、基材繊維としてはガラス繊維を単独で使用
するか、またはガラス繊維と石綿繊維を併用することが
できるが、石綿u!I維の代わりに鉱滓繊維、金属繊維
、カーボン繊維、セラミック&a維等の無機繊維や芳香
族ポリアミド繊維、木綿、麻、レーヨン等の有機繊維の
IFIまたは2種以上を組合わせて使用してもよい。At least glass fiber is used as the base fiber used in manufacturing the clutch facing according to the method of the present invention. That is, as the base fiber, glass fiber can be used alone or glass fiber and asbestos fiber can be used together, but asbestos u! Instead of I-fiber, IFI of mineral fiber, metal fiber, carbon fiber, inorganic fiber such as ceramic & A-fiber, aromatic polyamide fiber, organic fiber such as cotton, hemp, rayon, etc. or a combination of two or more may be used. good.
本発明の特徴は基材繊維として使用するガラス繊維の表
面に固体潤滑剤を付着させることにある。A feature of the present invention is that a solid lubricant is attached to the surface of the glass fiber used as the base fiber.
本発明に使用することができる固体潤滑剤としては二硫
化モリブデン、黒鉛、硫化アンチモン等を挙げることが
できる。上述のような固体潤滑剤を水、アルコール、鉱
油、エステル、ケトン等の分散媒体に分散させた溶液の
中にガラス繊維を浸漬するか、または分散溶液をガラス
繊維に吹付けることにより固体潤滑剤をガラス繊維表面
に付着させることができる。この時調製する分散溶液中
の固体潤滑剤の濃度は0.1〜20重量%が望ましく、
分散溶液に接着剤を添加して潤滑剤の接着効果を高める
こともできる。使用できる接着剤としては、PVA、エ
ポキシ樹脂、酢酸ビニル樹脂等が挙げられ、その使用量
は分散溶液の0.1〜5重敏%程度である。固体潤滑剤
のガラス繊維への付着量は0.1重量%以上が望ましく
、付着量が0.1重速%未満では、固体潤滑剤での処理
効果かないために好ましくない。Examples of solid lubricants that can be used in the present invention include molybdenum disulfide, graphite, and antimony sulfide. A solid lubricant can be prepared by dipping the glass fibers in a solution in which the solid lubricant described above is dispersed in a dispersion medium such as water, alcohol, mineral oil, ester, ketone, etc., or by spraying the dispersion solution onto the glass fibers. can be attached to the glass fiber surface. The concentration of the solid lubricant in the dispersion solution prepared at this time is preferably 0.1 to 20% by weight,
An adhesive can also be added to the dispersion solution to enhance the adhesive effect of the lubricant. Examples of adhesives that can be used include PVA, epoxy resins, vinyl acetate resins, etc., and the amount used is about 0.1 to 5% by weight of the dispersion solution. The amount of solid lubricant attached to the glass fibers is preferably 0.1% by weight or more, and if the amount is less than 0.1% by weight, it is not preferable because the solid lubricant has no treatment effect.
更に、固体潤滑剤を付着させたガラス繊維をゴム溶液に
浸漬して処理することが好ましい、使用できるゴムとし
てはブタジェンゴム(BR)、スチレン−ブタジェンゴ
ム(SBR)、アクリロニトリル−ブタジェンゴム(N
BR)等の合成ゴム、または天然ゴムを挙げることがで
きる。これらのゴムはトルエン等の溶媒に溶かして溶液
とすることができる。0.5〜10重量%程度の濃度の
ゴム溶液に固体潤滑剤を付着させたガラス繊維を浸漬す
ることが望ましい、このようにしてガラス繊維にゴムを
付着させる。ゴムの付着量は0.5〜10重筐%程度が
好ましい。Further, it is preferable to treat glass fibers to which a solid lubricant has been attached by immersing them in a rubber solution. Rubbers that can be used include butadiene rubber (BR), styrene-butadiene rubber (SBR), and acrylonitrile-butadiene rubber (N
Synthetic rubber such as BR) or natural rubber can be mentioned. These rubbers can be dissolved in a solvent such as toluene to form a solution. It is desirable to immerse the glass fibers to which the solid lubricant is attached in a rubber solution having a concentration of about 0.5 to 10% by weight. In this way, the rubber is attached to the glass fibers. The amount of rubber adhered is preferably about 0.5 to 10 weight percent.
また、固体潤滑剤を付着させたガラス繊維にカシュー樹
脂、メラミン樹脂、フェノール樹脂等の熱硬化性樹脂を
メタノール、水、トルエン等の希釈溶剤で溶かした液状
樹脂を浸漬することにより処理することもできる。0.
5〜30重量%程度の濃度の液状樹脂に固体潤滑剤を付
着させたガラス繊維を浸漬することが望ましい、このよ
うにしてガラス繊維に液状樹脂を付着させる。樹脂の付
着量は0.5〜30重量%程度が好ましい、基材として
石綿繊維を併用する場合もガラス繊維と同様に上記の処
理を行なうことが望ましい0石綿繊維のこの処理は慣用
の前処理であり、通常行なわれている操作を使用するこ
とができる。なお、石線繊維以外の上述の繊維も同様の
前処理を行なうことができる。Alternatively, glass fibers coated with a solid lubricant can be treated by immersing them in a liquid resin made by dissolving a thermosetting resin such as cashew resin, melamine resin, or phenolic resin in a diluting solvent such as methanol, water, or toluene. can. 0.
It is desirable to immerse glass fibers with a solid lubricant attached thereto in a liquid resin having a concentration of about 5 to 30% by weight. In this way, the liquid resin is attached to the glass fibers. The amount of resin deposited is preferably about 0.5 to 30% by weight. Even when asbestos fibers are used as a base material, it is desirable to carry out the above treatment in the same way as glass fibers. This treatment for 0-asbestos fibers is a conventional pretreatment. , and can use commonly used operations. Note that the above-mentioned fibers other than the stone wire fibers can also be subjected to the same pretreatment.
上述のようにして処理したガラス繊維またはガラス繊維
と他の繊維を基材繊維とし、ヤーン状、テープ状、ロー
ビング状、クロス状等に加工する。The glass fibers treated as described above or the glass fibers and other fibers are used as base fibers and processed into yarns, tapes, rovings, cloths, etc.
得られた基材繊維加工品に次にペースト状充填剤をjD
圧付着させた後、ノズルを通して付着量を現制し、乾燥
する。屹燥後のペースト状充填剤の付着量は20%〜8
0%程度が好ましい、ペースト状充填剤は通常のクラッ
チフェーシング製造操作に用いるものであり、ゴム材例
えばスチレン−ブタジェンゴム(SBR)、アクリロニ
トリル−ブタジェンゴム(NBR)等の合成ゴム及び天
然ゴム、熱硬化性樹脂例えばフェノール樹脂、メラミン
樹脂、硬化剤例えばヘキサミン、加硫剤例えば硫黄、加
硫促進剤例えばDM、無機短繊維例えば石綿、摩擦:A
整剤例えばカシューダスト、潤滑剤例えば黒鉛、及び溶
剤例えばトルエン等よりなるものである。ペースト状充
填剤は安定した生産性及び1贋擦特性を維持する点を鑑
みて、ゴム材と熱硬化性樹脂の比率を熱硬化性樹脂10
0重社部に対してゴム材40〜200重量部を配合した
ものが望ましい、更に、ペースト状充填剤には通常成形
助剤として石綿、岩綿、ガラス組Eセラミック繊維等の
無機晦維または芳香族ポリアミド繊維、バルブ、レーヨ
ン等の有機繊維が添加されている。Next, a paste filler is added to the obtained base fiber processed product.
After applying pressure, measure the amount of adhesion through a nozzle and dry. The amount of paste filler attached after drying is 20% to 8
The paste filler, which is preferably about 0%, is used in normal clutch facing manufacturing operations, and is suitable for rubber materials such as synthetic rubbers such as styrene-butadiene rubber (SBR), acrylonitrile-butadiene rubber (NBR), natural rubbers, and thermosetting rubbers. Resin such as phenolic resin, melamine resin, curing agent such as hexamine, vulcanizing agent such as sulfur, vulcanization accelerator such as DM, inorganic short fiber such as asbestos, friction: A
It consists of a conditioner such as cashew dust, a lubricant such as graphite, and a solvent such as toluene. In order to maintain stable productivity and anti-failure properties, the paste filler has a ratio of rubber material to thermosetting resin of 10% to thermosetting resin.
It is preferable that 40 to 200 parts by weight of rubber material is blended into the pasty filler.Furthermore, inorganic fibers such as asbestos, rock wool, glass-combined ceramic fibers, or Organic fibers such as aromatic polyamide fibers, bulbs, and rayon are added.
このようにして得られたペースト状充填剤付着済基材繊
維加工品を積層体状に慣用の成形法例えば交錯巻き法、
ラセン巻き法等を使用して予備成形し、更に金型に入れ
、100〜200 kgr/ cm2の圧力下で150
〜200℃の温度条件下で加熱圧縮して成形する。成形
体を次に150〜200℃の条件下で3〜15時間にわ
たり後焼成を行ない、その後研摩してクラッチフェーシ
ング製品とすることができる。The paste-like filler-adhered base fiber processed product thus obtained is molded into a laminate using a conventional method such as a cross-winding method.
It is preformed using a helical winding method, etc., and then put into a mold and rolled under a pressure of 100 to 200 kgr/cm2.
It is molded by heating and compression under a temperature condition of ~200°C. The compact can then be post-fired at 150-200° C. for 3-15 hours and then polished to form a clutch facing product.
し実 施 例1
゛U扼−例」−
石綿繊維を10%液状フェノール樹脂で処理し、一方の
ガラス繊維を水に分散させた固体潤滑剤(黒鉛)の液に
浸漬乾燥し、0.5重量%付着させた後、8%の液状フ
ェノール樹脂で処理し、得られたロービング状の石綿繊
維及びガラス繊維を基材繊維とした。Example 1: Asbestos fibers were treated with 10% liquid phenol resin, one of the glass fibers was immersed in a liquid of solid lubricant (graphite) dispersed in water, and dried. After the weight percent was deposited, it was treated with 8% liquid phenol resin, and the obtained roving-like asbestos fibers and glass fibers were used as base fibers.
この基材繊維に下記に示す配合割合をもつペースト状充
填材を付着させた。A paste-like filler having the blending ratio shown below was attached to this base fiber.
無機短繊維(石綿60・04) 5重量%ゴム
(NBR) 15重量%樹脂(
フェノール:PR51778・住友デュレツ)25重量
%
硬化剤(ヘキサミン) 1重量%加硫
剤(硫黄) 9重J!t?6摩
擦調整剤(カシューダスト:8203−カシュー株)5
重量%
潤滑剤(黒鉛) 5重量%無機
充填材 351!iff%この
時のペースト状充填剤と基材m維の比率は重菫比で約1
:1に調整した。Inorganic short fiber (asbestos 60.04) 5% by weight Rubber (NBR) 15% by weight Resin (
Phenol: PR51778/Sumitomo Durets) 25% by weight Hardening agent (hexamine) 1% by weight Vulcanizing agent (sulfur) 9-layer J! T? 6 Friction modifier (cashew dust: 8203-cashew stock) 5
Weight% Lubricant (graphite) 5% by weight Inorganic filler 351! if% At this time, the ratio of the paste filler to the base material m fiber is approximately 1 in terms of heavy violet ratio.
: Adjusted to 1.
ペースト状充填剤を付着後、交錯巻きにより予備成形体
を得、更に150℃−150kyf / cm2で成形
した後、170℃−5時間の後焼成を行ない、研摩して
クラッチフェーシングを得た。After attaching the paste filler, a preform was obtained by cross-winding, further molded at 150° C. and 150 kyf/cm 2 , and then post-fired at 170° C. for 5 hours and polished to obtain a clutch facing.
得られたクラッチフェーシングの性能を以下の第1表に
記載する。The performance of the obtained clutch facings is shown in Table 1 below.
及獲月−L
基材繊維としてガラス繊維を2本使用し、2本のガラス
繊維とも、実施例1と同様の操作により固体潤滑剤とし
て黒鉛を0.5重量%付着させた後、3%の液状フェノ
ール樹脂で処理し、得られたロービング状のガラス繊維
に実施例1と同一のペースト状充填剤含付着、以下、実
施例1と同様の操作によりクラッチフェーシングを得た
。Oiyokutsuki-L Two glass fibers were used as the base fibers, and after adhering 0.5% by weight of graphite as a solid lubricant to both glass fibers by the same operation as in Example 1, 3% A clutch facing was obtained by applying the same paste filler as in Example 1 to the obtained roving-shaped glass fibers and following the same operations as in Example 1.
得られたクラッチフェーシングの性能を以下の第1表に
記載する。The performance of the obtained clutch facings is shown in Table 1 below.
ル鮮上
石綿繊維を10%液状フェノール樹脂で処理し、一方の
ガラス繊維は固体潤滑剤を付着させずに、8%の液状フ
ェノール樹脂で処理し、得られたロービング状の石綿繊
維及びガラス繊維に実施例1と同様のペースト状充填剤
を付着させ、以下、実施例1と同様の操作によりクラッ
チフェーシングを得た。 得られたクラッチフェーシン
グの性能を以下の第1表に記載する。The asbestos fibers were treated with 10% liquid phenolic resin, and one of the glass fibers was treated with 8% liquid phenolic resin without adhering a solid lubricant, resulting in roving-like asbestos fibers and glass fibers. A paste-like filler similar to that in Example 1 was applied to the clutch, and a clutch facing was obtained by the same operations as in Example 1. The performance of the obtained clutch facings is shown in Table 1 below.
比4U阻y工
実施例2と同様に基材繊維としてガラス繊維を2本使用
し、固体潤滑剤を付着させずに、3%の液状フェノール
樹脂で処理し、得られたローピンク状のガラス繊維に実
施例1と同様のペースト状充填剤を付着させ、以下、実
施例1と同様の操作によりクラッチフェーシングを得た
。Similar to Example 2, two glass fibers were used as base fibers and treated with 3% liquid phenol resin without adhering solid lubricant, resulting in a low pink glass. A paste filler similar to that in Example 1 was attached to the fibers, and a clutch facing was obtained by the same operations as in Example 1.
得られたクラッチフェーシングの性能を以下の[発明の
効果]
本発明方法により製造されたクラッチフェーシングは基
材繊維として使用するガラス繊維の表面には固体潤滑剤
が付着しており、これによって以下のような効果が得ら
れる。[Effects of the Invention] The clutch facings produced by the method of the present invention have a solid lubricant attached to the surface of the glass fiber used as the base fiber, and as a result, the performance of the obtained clutch facing is as follows. You can get an effect like this.
ガラス繊維表面の潤滑性が潰れているため、安定した摩
擦性能が継続的に得られ、更にクラッチ作動時の鳴き発
生がなくなり、クラッチ周辺部品への悪影響もなく、鳴
き音による運転者の不快感も解消され、走行不具合も生
じなくなる。Since the lubricity of the glass fiber surface is destroyed, stable friction performance is continuously obtained, and there is no squealing when the clutch is activated, and there is no negative effect on the parts around the clutch, and the squealing noise does not cause discomfort to the driver. This also eliminates the problem of running problems.
Claims (1)
脂とゴム材の混合物を含浸し、次に、熱硬化性樹脂また
は熱硬化性樹脂とゴム材の混合物を含むペースト状充填
材を付着させ、得られた基材繊維を積層体状に予備成形
し、得られた予備成形体を加熱圧縮し、後焼成すること
からなるクラッチフェーシングの製造方法において、少
なくとも基材繊維として固体潤滑剤を付着させたガラス
繊維を使用することを特徴とするクラッチフェーシング
の製造方法。The base fiber is impregnated with a thermosetting resin or a rubber material or a mixture of a thermosetting resin and a rubber material, and then a pasty filler containing a thermosetting resin or a mixture of a thermosetting resin and a rubber material is attached. In the clutch facing manufacturing method, which comprises preforming the obtained base fibers into a laminate shape, heating and compressing the obtained preform, and post-sintering, a solid lubricant is used at least as the base fibers. A method for manufacturing a clutch facing characterized by using attached glass fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6574288A JPH01238927A (en) | 1988-03-22 | 1988-03-22 | Manufacture of clutch facing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6574288A JPH01238927A (en) | 1988-03-22 | 1988-03-22 | Manufacture of clutch facing |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01238927A true JPH01238927A (en) | 1989-09-25 |
Family
ID=13295772
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6574288A Pending JPH01238927A (en) | 1988-03-22 | 1988-03-22 | Manufacture of clutch facing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01238927A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20000053699A (en) * | 1999-12-24 | 2000-09-05 | 윤기정 | Manufacturing method of fabric reinforced thermoset composite |
US10890226B2 (en) | 2015-10-20 | 2021-01-12 | Tribotecc Gmbh | Fiber for tribological applications |
-
1988
- 1988-03-22 JP JP6574288A patent/JPH01238927A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20000053699A (en) * | 1999-12-24 | 2000-09-05 | 윤기정 | Manufacturing method of fabric reinforced thermoset composite |
US10890226B2 (en) | 2015-10-20 | 2021-01-12 | Tribotecc Gmbh | Fiber for tribological applications |
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