JPH0236292A - Friction material - Google Patents
Friction materialInfo
- Publication number
- JPH0236292A JPH0236292A JP18575288A JP18575288A JPH0236292A JP H0236292 A JPH0236292 A JP H0236292A JP 18575288 A JP18575288 A JP 18575288A JP 18575288 A JP18575288 A JP 18575288A JP H0236292 A JPH0236292 A JP H0236292A
- Authority
- JP
- Japan
- Prior art keywords
- fibers
- rubber
- glass
- glass fiber
- resin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000002783 friction material Substances 0.000 title claims abstract description 26
- 239000003365 glass fiber Substances 0.000 claims abstract description 51
- 239000000835 fiber Substances 0.000 claims abstract description 46
- 229920001971 elastomer Polymers 0.000 claims abstract description 32
- 239000005060 rubber Substances 0.000 claims abstract description 32
- 239000011230 binding agent Substances 0.000 claims abstract description 22
- 239000011347 resin Substances 0.000 claims abstract description 18
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 239000000945 filler Substances 0.000 claims abstract description 10
- 239000004744 fabric Substances 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 31
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract description 4
- 239000011521 glass Substances 0.000 abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 3
- 239000004760 aramid Substances 0.000 abstract description 3
- 229920003235 aromatic polyamide Polymers 0.000 abstract description 3
- 229910002804 graphite Inorganic materials 0.000 abstract description 3
- 239000010439 graphite Substances 0.000 abstract description 3
- 239000002759 woven fabric Substances 0.000 abstract description 3
- 229920000049 Carbon (fiber) Polymers 0.000 abstract description 2
- 244000043261 Hevea brasiliensis Species 0.000 abstract description 2
- 239000005909 Kieselgur Substances 0.000 abstract description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract description 2
- 239000004917 carbon fiber Substances 0.000 abstract description 2
- 239000000919 ceramic Substances 0.000 abstract description 2
- 229920003052 natural elastomer Polymers 0.000 abstract description 2
- 229920001194 natural rubber Polymers 0.000 abstract description 2
- 239000000377 silicon dioxide Substances 0.000 abstract description 2
- 229920003051 synthetic elastomer Polymers 0.000 abstract description 2
- 239000005061 synthetic rubber Substances 0.000 abstract description 2
- 239000000758 substrate Substances 0.000 abstract 2
- 229920002943 EPDM rubber Polymers 0.000 abstract 1
- 229920006282 Phenolic fiber Polymers 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 229920003048 styrene butadiene rubber Polymers 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 12
- 239000011162 core material Substances 0.000 description 8
- 239000005011 phenolic resin Substances 0.000 description 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000003431 cross linking reagent Substances 0.000 description 5
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- 235000014692 zinc oxide Nutrition 0.000 description 2
- 244000226021 Anacardium occidentale Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000002253 acid Substances 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
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 235000020226 cashew nut Nutrition 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- REQPQFUJGGOFQL-UHFFFAOYSA-N dimethylcarbamothioyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SC(=S)N(C)C REQPQFUJGGOFQL-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000005340 laminated glass Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 238000010068 moulding (rubber) Methods 0.000 description 1
- 210000002445 nipple Anatomy 0.000 description 1
- 239000010466 nut oil Substances 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical compound [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野1
本発明は、自動車等の乾式クラッチフェーシング、湿式
タラツチフ1−シング、またはブレーキパッド等に使用
することができる摩擦材に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field 1] The present invention relates to a friction material that can be used for dry clutch facings, wet clutch facings, brake pads, etc. of automobiles.
[従来の技術1
従来自動車のクラッチフェーシングに使用される摩擦材
としては、ガラス長繊維を基材とし、フィラー、および
結合剤として樹脂やゴムを用いたレジンモールドタイプ
、ゴムモールドタイプ等が知られている。[Prior art 1] Conventional friction materials used for automobile clutch facings include resin mold types and rubber mold types, which are based on long glass fibers and use resin or rubber as fillers and binders. ing.
そしてその摩擦性能を向上させるために繊維基材の改良
についての種々の提案がある。特にゴムモールド系のも
のは、回転バースト強度が低いとされている。そのため
例えば、嵩高加工を施したガラス繊維を繊維基材とした
り、ガラス長繊維のチョツプドストランドまたはミルド
ファイバーの特定の長さのものをV&維単基材したり、
芳香族ポリアミド繊維とガラス繊維とを混合した繊H塁
材としたものの開示があるが、まだ充分満足できるもの
は得られていない(特開昭56−167934号公報、
特開昭51−87549号公報、特開昭59−4538
3号公報)。There are various proposals for improving the fiber base material in order to improve its friction performance. In particular, rubber mold type tires are said to have low rotational burst strength. For this reason, for example, bulk-processed glass fiber may be used as a fiber base material, or chopped strands of long glass fibers or milled fibers of a specific length may be used as a V&fiber base material.
Although there is a disclosure of a fiber H base material made of a mixture of aromatic polyamide fiber and glass fiber, a fully satisfactory material has not yet been obtained (Japanese Patent Application Laid-open No. 167934/1983,
JP-A-51-87549, JP-A-59-4538
Publication No. 3).
[発明が解決しようとする課題]
上記の摩擦材においては、繊n基材の長繊維の長さが混
合や、成形加工時に折れて短くなったりして均一に分散
しなかったりして繊N塁材として充分に作用しないこと
が多い。また、長m帷tm雑基材として用いた場合には
、成形時に4M雑の被覆が充分におこなわれず、使用時
に繊維が露出して摩擦材の性能を低下させる。そのため
得られる(f棒材、特に短繊維を繊維基材に用いたクラ
ッチフェーシングにおいては、回転バースト強度が低下
する傾向を有する。[Problems to be Solved by the Invention] In the above-mentioned friction material, the length of the long fibers of the fiber N base material may be broken or shortened during mixing or molding processing, and may not be uniformly dispersed. It often does not function well as a base material. Furthermore, when used as a long m-width tm miscellaneous base material, the 4M miscellaneous coating is not sufficiently performed during molding, and the fibers are exposed during use, reducing the performance of the friction material. For this reason, the rotational burst strength tends to decrease in the clutch facings obtained using f rods, especially short fibers as the fiber base material.
そこで本発明は上記の種々の点に鑑み繊維基材の構成を
特定することにより摩擦材の回転バースト強度をより向
上させて、減らない、滑らない、壊れない、というクラ
ッチフェーシングの3要素をバランスよく保持した摩擦
材とすることを技術的課題とする。Therefore, in view of the various points mentioned above, the present invention further improves the rotational burst strength of the friction material by specifying the structure of the fiber base material, and balances the three elements of the clutch facing: not decreasing, not slipping, and not breaking. The technical challenge is to create a friction material that holds well.
[yI題を解決するための手段]
本発明の摩擦材は、繊維基材と、フィラー、樹脂または
ゴムの結合剤で構成されている摩擦材であって、
前記繊t4M材の少なくとも一部として、直径が20μ
m以下のガラス繊維からなり織目の間隙が1〜3mmの
ガラス繊維織物がS振部に対して平行に配置され使用さ
れていることを特徴とする。[Means for Solving the yI Problem] The friction material of the present invention is a friction material composed of a fiber base material and a filler, a resin, or a rubber binder, and includes at least a portion of the fiber T4M material. , diameter is 20μ
The present invention is characterized in that a glass fiber fabric made of glass fibers having a diameter of 1 to 3 mm and having a weave gap of 1 to 3 mm is used and arranged parallel to the S vibration section.
本発明の繊維基材は、少なくともその一部にガラス繊維
織物を用いその織目の間隙を1〜31とした平織、斜文
織、朱子織等の織物組織を有する。The fiber base material of the present invention has a woven structure such as a plain weave, a twill weave, and a satin weave, in which at least a portion thereof is made of glass fiber fabric, and the gaps between the weaves are 1 to 31.
その結果、II維基材と結合剤との親和性ならびその絡
み合いによる補強効果により、繊維基材の織目の間隙に
結合剤が充分に浸透して繊維基材と結合剤とが一体とな
るため、その摩擦材の回転バスト強度を向上させること
ができる。As a result, due to the affinity between the II fiber base material and the binder and the reinforcing effect due to their entanglement, the binder sufficiently penetrates into the gaps between the textures of the fiber base material and the fiber base material and the binder become integrated. , the rotational bust strength of the friction material can be improved.
このガラス繊H織物は、直径が20μm以下のガラスu
A維で形成され、その織目の間隙を1〜3mmになるよ
うに織られて樹脂などで11目の間隙が移動しないよう
に固定されている。このガラス繊維織物は、通常の方法
で織られたもので、使用するガラス繊維の形態はロービ
ング、撚糸、そのほか加工されものであってもよい。This glass fiber H fabric has a diameter of 20 μm or less.
It is made of A fiber, woven so that the gaps between the weaves are 1 to 3 mm, and fixed with resin or the like so that the gaps between the 11 stitches do not move. This glass fiber fabric is woven by a conventional method, and the glass fibers used may be in the form of roving, twisting, or other processed materials.
ガラス繊維織物の織目の間隙が1 mn+未満であると
、結合剤との付着浸透および絡み合いが不十分で、摩擦
材としての物性を充分に付与することができない。一方
その織目の間隙が3mmを超えると、結合剤が浸透しす
ぎてuA維基材の織目の形状が変形して間隙にばらつき
ができ摩擦材としての性能を低下させるとともに回転バ
ースト強度も低下するので好ましくない。また、このガ
ラス!!帷の直径が20μmを超えると織物への加工が
しにくくなり好ましくない。If the gap between the weave of the glass fiber fabric is less than 1 m+, adhesion and penetration with the binder and entanglement will be insufficient, and sufficient physical properties as a friction material cannot be imparted. On the other hand, if the gap between the weaves exceeds 3 mm, the binder will penetrate too much and the shape of the weave of the uA fiber base material will be deformed, causing variations in the gap, reducing its performance as a friction material and reducing its rotational burst strength. Therefore, it is not desirable. Also, this glass! ! If the diameter of the strip exceeds 20 μm, it becomes difficult to process it into a fabric, which is not preferable.
このガラス繊m織物は一枚で使用することもできるが、
特にゴムモールド系の場合にはこのガラス繊維織物を芯
材として両面をゴムモールド材で被覆しても、またはこ
のガラス繊維織物を複数枚積層して用いることが回転バ
ースト強度を高めるために好ましい。尚、このガラス繊
維織物には、前もって加工用の樹脂が含浸され織目の間
隙は固定されていることがこのましい。またこのゴムモ
ールド材で被覆したガラス繊維織物は、FJ擦而面対し
網目が平行に配置されて摩擦材が形成されている。そし
てこの織物が円盤状に形成してクラッチフェーシングを
成形するのがバースト強度を高めるのにこのましい。This glass fiber M fabric can be used as a single piece, but
In particular, in the case of a rubber mold type, it is preferable to use this glass fiber fabric as a core material and cover both sides with a rubber mold material, or to use a plurality of sheets of this glass fiber fabric in a stacked manner in order to increase the rotational burst strength. It is preferable that this glass fiber fabric is impregnated with a processing resin in advance to fix the gaps between the weaves. Furthermore, the glass fiber fabric coated with this rubber molding material has meshes arranged parallel to the FJ rubbing surface to form a friction material. In order to increase the burst strength, it is preferable to form the clutch facing by forming this fabric into a disk shape.
さらにこの繊M基材には、ガラス繊H織物の外にガラス
繊維の短繊維や、無機繊維のセラミックス繊維、シリカ
繊維、アルミナ繊維等の短繊維や、有機繊維の芳香族ポ
リアミド繊維、ポリアミドイミド繊維、フェノール樹脂
系、炭素繊維等の短繊維を添加することができる。In addition to the glass fiber H fabric, this fiber M base material also includes short fibers such as short glass fibers, inorganic fibers such as ceramic fibers, silica fibers, and alumina fibers, and organic fibers such as aromatic polyamide fibers and polyamide-imide fibers. Short fibers such as fibers, phenol resin type fibers, and carbon fibers can be added.
結合剤として使用されるゴムとしては、SBR。The rubber used as a binder is SBR.
NBR,EPDMlNRX rR,f fR等の合成ゴ
ムまたシよ天然ゴムを用いることができる。また上記の
ゴムに架橋剤を添加して架橋ゴムとすることができる。Synthetic rubber such as NBR, EPDMlNRX rR, f fR, etc. or natural rubber can be used. Further, a crosslinked rubber can be obtained by adding a crosslinking agent to the above rubber.
架橋剤としては、硫黄、酸化亜鉛などを用いることがで
きる。As the crosslinking agent, sulfur, zinc oxide, etc. can be used.
そのほか樹脂結合剤としては、フェノール樹脂系、メラ
ミン樹脂系のもの等が用いられ、通常フェノール樹脂系
のものが用いられる。またこの樹脂結合剤として、カシ
ューナツツオイル、ポリビニルブチラール、植物油、メ
ラミン、エポキシ化合物等で変性した変性フェノール樹
脂を用いてもよい。なお、フェード現客がおきにくい点
では無変性フェノール樹脂が好ましい。In addition, as the resin binder, a phenol resin type, a melamine resin type, etc. are used, and a phenol resin type is usually used. Further, as the resin binder, a modified phenol resin modified with cashew nut oil, polyvinyl butyral, vegetable oil, melamine, an epoxy compound, etc. may be used. In addition, unmodified phenolic resin is preferable in that it is less prone to fading.
フィラーとしては、炭酸カルシウム、硫酸バリウム、珪
藻土、二硫化モリブデン、黒鉛、カーボンブラック等を
用いることができる。As the filler, calcium carbonate, barium sulfate, diatomaceous earth, molybdenum disulfide, graphite, carbon black, etc. can be used.
本発明においては、前記以外に、架橋助剤、有機フィラ
ーを含むことができる。この架橋助剤としては、活性亜
鉛華またはカシュウ変性レジン等を用いることができる
。架橋促進剤としては、チウラム系のTMTM、TMT
D、スルフェンアミド系のcz、oz等を用いることが
できる。In the present invention, a crosslinking aid and an organic filler may be included in addition to the above. As this crosslinking aid, active zinc white or cashew-modified resin can be used. As a crosslinking accelerator, thiuram-based TMTM, TMT
D, sulfenamide-based cz, oz, etc. can be used.
[発明の作用および効!$!]
本発明の摩擦材は、繊維基材の少なくとも一部として直
径が20μm以下のガラス繊維からなり織目の間隙が1
〜3mmIIIIlのガラス繊維織物が使用されている
。[Action and effect of invention! $! ] The friction material of the present invention is made of glass fibers having a diameter of 20 μm or less as at least a part of the fiber base material, and has a weave gap of 1.
~3 mm III glass fiber fabric is used.
そしてこのガラス繊維織物の織目に結合剤が充分に含浸
されるため、織目の間隙が1〜3mll1であることが
必要である。そして、結合剤とガラス繊維織物とが織目
の間隙を介して互いに絡み合って補強しあうため回転バ
ースト強度を、従来の短繊維を分散させたものより格段
に向上させる。この場合の結合剤は、ゴムの場合でもI
jA脂の場合においても同様に回転バースト強度が向ト
する。In order to sufficiently impregnate the binder into the weaves of this glass fiber fabric, it is necessary that the gaps between the weaves be 1 to 3 ml. Since the binder and the glass fiber fabric intertwine and reinforce each other through the gaps between the weaves, the rotational burst strength is significantly improved compared to the conventional structure in which short fibers are dispersed. The binder in this case is I
In the case of jA fat, the rotational burst strength is similarly increased.
[実施例] 以下実施例により本発明を説明する。[Example] The present invention will be explained below with reference to Examples.
(実施例1)
本実施例の摩擦材は、ガラスJMI!織物にゴムを付着
させて複数枚積層して形成したものであり第1表に示す
配合成分およびその配合υj合で形成した。まず、フィ
ラーおよびゴムからなる結合剤をガラス繊維織物を主体
とする繊維基材に含浸させて成形して熱処理など通常の
製造方法で摩擦材のクラッチフエシングを形成した。(Example 1) The friction material of this example was glass JMI! It was formed by laminating a plurality of fabrics with rubber attached to them, and was formed using the ingredients shown in Table 1 and their blends υj. First, a fiber base material mainly made of glass fiber fabric was impregnated with a binder consisting of a filler and rubber, and then molded to form a clutch facing of a friction material using a conventional manufacturing method such as heat treatment.
結合剤のゴムA (SBR1架橋剤(硫黄)、架橋助剤
(D、Z)繊維長さ30manのガラス繊維入り)また
はゴムB (SBR,架橋剤(硫黄)繊維長さ5mmの
ガラス繊維入り)に無はフィラーの硫酸バリウムと黒鉛
とを配合して用いた。繊維基材としては、直径が6μm
のガラス繊維チョップと、直径が6μmのガラス繊維の
織物で織目の間隙が100mのガラス繊維織物を用いた
。このガラス繊維織物の繊維基材は、第1表に示すよう
に複数枚重ねて積層して用いた。Binder Rubber A (SBR1 crosslinking agent (sulfur), crosslinking aids (D, Z) containing glass fiber with a fiber length of 30 man) or Rubber B (SBR, crosslinking agent (sulfur) containing glass fiber with a fiber length of 5 mm) The filler barium sulfate and graphite were used in combination. The fiber base material has a diameter of 6 μm.
A glass fiber chop having a diameter of 6 μm and a glass fiber fabric having a weave gap of 100 m were used. The fiber base material of this glass fiber fabric was used by stacking a plurality of sheets as shown in Table 1.
そこでまずガラス繊維入を除いた結合剤とフィラとを第
1表に示す配合量を夫々秤ωして配合し、加圧ニーダ−
を用いてゴム練りをおこない、続いてニップルロールを
用いて架橋剤とガラス[tとを配合して混練した。次い
でこれらを溶媒のトルエンを用いてフィラーと結合剤と
を溶解分散させた。Therefore, first, the binder and filler excluding the glass fiber were weighed and blended in the amounts shown in Table 1, and then
Rubber kneading was carried out using a roller, and then the crosslinking agent and glass [t] were mixed and kneaded using a nipple roll. Next, the filler and binder were dissolved and dispersed using toluene as a solvent.
ガラス繊維織物は所定の円盤状(外径2QQmlllΦ
、内径150mmΦ)に形成した。(ガラス繊維織物8
0重量部に、ゴムと馴染み性をよくするための熱硬化性
樹脂のメラミン変性フェノール樹脂20重量部が含浸さ
れ乾燥した後、所定の寸法に打法いて形成したものであ
る)。この円盤状に形成されたガラス繊維織物へのゴム
の付着は、前記の溶媒のトルエンに溶解分散したゴム成
分をロルコーティング法でおこなった。ゴムの付Itの
調整は、溶媒中のゴム濃度でおこなうか、ロール絞りの
さいの、ロール間隔で調整できる。ゴムを付着させたガ
ラス繊維織物を60〜90℃の条件下でプレキュアをお
こない、あわせて脱溶媒をおこなった。ついでこのゴム
を付着してブレキュアざぜたガラス繊組織物を数枚積層
しく第1表に示寸枚数で)、温度165℃、圧力90
kg/ cII12で加圧成形した。ついでこれを23
0℃×5 Hr sの条件下に43いて熱処理をおこな
い、さらに表面を研磨し防錆処理をして同一形状の各ク
ラッチフェーシングNo1〜5を作製した。The glass fiber fabric has a predetermined disc shape (outer diameter 2QQmlllΦ
, an inner diameter of 150 mmΦ). (Glass fiber fabric 8
0 parts by weight is impregnated with 20 parts by weight of a melamine-modified phenol resin, which is a thermosetting resin to improve compatibility with rubber, and after drying, it is formed by punching into predetermined dimensions). Rubber was attached to the disk-shaped glass fiber fabric by a roll coating method using a rubber component dissolved and dispersed in the above-mentioned solvent, toluene. The rubber adhesion It can be adjusted by adjusting the rubber concentration in the solvent or by adjusting the roll interval during roll squeezing. The glass fiber fabric to which the rubber was attached was precured under conditions of 60 to 90°C, and at the same time, the solvent was removed. Next, several sheets of glass fiber tissue to which this rubber had been adhered and precured were laminated (with the dimensions shown in Table 1) at a temperature of 165°C and a pressure of 90°C.
Pressure molded at kg/cII12. Then this is 23
Clutch facings Nos. 1 to 5 having the same shape were produced by heat treatment under conditions of 0° C. x 5 hours for 43 hours, and further surface polishing and antirust treatment.
比較例として、ガラス繊H織物を使用しなでゴムモール
ドのクラッチフェーシング比較例NO1〜2を作成した
。As comparative examples, comparative examples Nos. 1 and 2 of rubber-molded clutch facings were created using glass fiber H fabric.
(実施例2)
この摩lr!材は、ガラス繊tI!織物を芯材とし両面
に従来のゴムモールド系摩擦材を圧着して形成したもの
である。(Example 2) This polish! The material is glass fiber! It is formed by using a woven fabric as the core material and pressing conventional rubber mold type friction materials on both sides.
実施例1のゴムAおよびゴムBに無機フィシとして硫酸
バリウムと黒鉛とガラス長繊維とを第2表に示すυノ合
に配合して実施例1に示す所定の形状のゴムモールド系
摩擦材(No7〜12)を形成した。A rubber mold type friction material ( Nos. 7 to 12) were formed.
ガラス繊維織物は、第2表に示す繊維径と織目間隙のも
のを用い、所定の円盤形状に形成した。The glass fiber fabrics had fiber diameters and weave gaps shown in Table 2, and were formed into a predetermined disc shape.
なお、このガラス繊維織物には、フェノール樹脂が20
虫吊%含浸されている。In addition, this glass fiber fabric contains 20% of phenolic resin.
It is impregnated with insect suspension.
次いでこのガラス繊維織物を、芯材とし前記のゴムモー
ルド系摩擦材でサンドイッチ状に挟み、実施例1と同様
に加圧熱処理をおこなってクラッチフェーシングを得た
。尚、芯材はこの場合は一枚であるが必要に応じて複数
枚用いてもよい。Next, this glass fiber fabric was sandwiched between the rubber molded friction materials described above as a core material, and subjected to pressure heat treatment in the same manner as in Example 1 to obtain a clutch facing. In this case, only one core material is used, but a plurality of core materials may be used if necessary.
比較例として前記のゴムAおよびゴムBを用いガラス繊
維織物をもちいないでゴムモールド摩擦材の比較例No
3〜4作成した。As a comparative example, Comparative Example No. 1 is a rubber molded friction material using the above-mentioned Rubber A and Rubber B without using glass fiber fabric.
I created 3-4.
(実施例3)
実施例1のゴムの代りに樹脂成分A(フエノル樹脂住人
ジュレズTR−311)または樹脂成分[3(フェノー
ル樹脂住人ジュレズTR8645)を結合剤として用い
、無機フィラーとしてll1lI酸バリウムを用いさら
に基N基材のガラス繊維チョップを況合し、実施例2と
同様にしてレジンモールド系の[γ振材を作成した。本
実廠例のレジンモールドの摩擦材は、ガラス繊維織物を
芯材としてその両面をレジンモールド系のI!i!If
f材で被覆したものである。第3表のN013〜15に
その組成をボす。(Example 3) Instead of the rubber in Example 1, resin component A (phenolic resin resident Jurez TR-311) or resin component [3 (phenolic resin resident Jurez TR8645) was used as a binder, and barium ll1lI acid was used as an inorganic filler. A resin-molded [γ vibration material] was prepared in the same manner as in Example 2 by using a glass fiber chop as a base material. The friction material of the resin mold in this example is made of glass fiber fabric as the core material, and both sides of it are made of resin mold type I! i! If
It is covered with f material. The compositions are listed in Nos. 013 to 15 in Table 3.
比較例としてガラス繊維織物を芯材として使用していな
いレジンモールド系のクラッチフェーシング比較例NO
5〜6を作製した。Comparative example No. 1 of a resin-molded clutch facing that does not use glass fiber fabric as a core material.
5 and 6 were produced.
(評価結果)
フルザイズダイナモ試験機を用い前記実施例No1〜1
5および比較例No1〜6のクラッチフェーシングにつ
いての性能評価をおこなった。クラッチフェーシングの
寸法は、Φ200X 140×3.5111m1イナー
シャ0.2kg−m−5ec2回転数″!800r’p
m、300℃における継合回数2000回の条件でおこ
なった。そして摩擦係数、摩耗率(X10−4mI13
/kg−m) 、回転バースト強度(rpm)を測定し
た。その結果を第1〜3表に示した。なお、回転バース
ト強度としては200℃でおこなった。(Evaluation results) Using a full-size dynamo tester, the above Examples Nos. 1 to 1
Performance evaluation was performed on the clutch facings of No. 5 and Comparative Examples Nos. 1 to 6. The dimensions of the clutch facing are Φ200X 140×3.5111m1 Inertia 0.2kg-m-5ec2 Revolutions''!800r'p
The test was carried out under the conditions of 2000 joints at 300°C. And friction coefficient, wear rate (X10-4mI13
/kg-m), and the rotational burst strength (rpm) was measured. The results are shown in Tables 1-3. Note that the rotational burst strength was 200°C.
実施例NO1〜5および比較例1〜2の摩擦係数および
摩耗率は、はぼ同一であるが、回転バースト強度は、N
O1〜5は14000以上あるが、比較例No1はi
1500、No2は8200Lかなく本実施例が著しく
向上していることを示している(第1表)。The friction coefficient and wear rate of Examples Nos. 1 to 5 and Comparative Examples 1 to 2 are almost the same, but the rotational burst strength is
There are more than 14,000 O1-5, but Comparative Example No.1 is i
1500, and No. 2 was only 8200L, indicating that this example was significantly improved (Table 1).
実施例2の芯材にガラス繊維織物をもちいた場合におい
ても、実施例No6〜12と比較例N。Even when glass fiber fabric was used as the core material in Example 2, Examples Nos. 6 to 12 and Comparative Example N.
3〜4と比べると実施例が14000あるのに対して、
比較例では高くても115o○であり、本発明の摩擦材
の回転バースト強度が優れていることを示している(第
2表)。Compared to 3-4, there are 14,000 examples,
In the comparative example, it was 115° at the most, indicating that the rotational burst strength of the friction material of the present invention is excellent (Table 2).
、またレジンモールド系についても実施例No13〜1
5と、比較例No5〜6とを比較すると実施例が120
00〜11500であるのに対して、比較例では600
0〜6500であり格段に向上していることを示してい
る(第3表)。, Also regarding the resin mold system, Example Nos. 13 to 1
5 and Comparative Examples Nos. 5 to 6, the example is 120.
00 to 11500, whereas in the comparative example it was 600.
0 to 6500, indicating a significant improvement (Table 3).
なお、レジンモールド系はガラス814H物の積層枚数
が一枚であるため、ゴムモールド系のものより回転バー
スト強度の絶対値が低い。ガラス繊N織物の81層枚数
が6枚前後で回転バースト強度は、はぼ一定になると推
測される。In addition, since the resin mold system has one laminated glass 814H material, the absolute value of the rotational burst strength is lower than that of the rubber mold system. It is estimated that the rotational burst strength becomes approximately constant when the number of 81-layer glass fiber N fabrics is around six.
Claims (1)
で構成されている摩擦材であつて、 前記繊維基材の少なくとも一部として、直径が20μm
以下のガラス繊維からなり織目の間隙が1〜3mmのガ
ラス繊維織物が摩擦面に対して平行に配置され使用され
ていることを特徴とする摩擦材。(1) A friction material composed of a fiber base material and a filler, resin, or rubber binder, wherein at least a portion of the fiber base material has a diameter of 20 μm.
A friction material characterized in that a glass fiber fabric made of the following glass fibers and having a weave gap of 1 to 3 mm is used and arranged parallel to a friction surface.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18575288A JPH0236292A (en) | 1988-07-26 | 1988-07-26 | Friction material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18575288A JPH0236292A (en) | 1988-07-26 | 1988-07-26 | Friction material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0236292A true JPH0236292A (en) | 1990-02-06 |
Family
ID=16176248
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18575288A Pending JPH0236292A (en) | 1988-07-26 | 1988-07-26 | Friction material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0236292A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2244061A (en) * | 1990-05-15 | 1991-11-20 | Ferodo Ltd | Friction material for railway disc brake pads |
WO2003064883A1 (en) * | 2002-01-25 | 2003-08-07 | Glasline Friction Technologies, Inc. | Composite friction elements and pultrusion method of making |
JP2008144773A (en) * | 2006-12-06 | 2008-06-26 | Akebono Brake Ind Co Ltd | Friction material and its manufacturing method |
CN101870438A (en) * | 2010-06-21 | 2010-10-27 | 临安华龙摩擦材料有限公司 | Friction brake disk of double-speed electric-block and preparation method thereof |
CN103320091A (en) * | 2013-05-27 | 2013-09-25 | 湖北飞龙摩擦密封材料股份有限公司 | A friction product |
CN104099065A (en) * | 2014-07-04 | 2014-10-15 | 青岛基宏汽车部件有限公司 | Copper-free rubbing material and preparation method thereof |
CN112228483A (en) * | 2019-11-06 | 2021-01-15 | 晋江凯燕新材料科技有限公司 | Modified organic filling material for friction material and preparation process thereof |
-
1988
- 1988-07-26 JP JP18575288A patent/JPH0236292A/en active Pending
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2244061A (en) * | 1990-05-15 | 1991-11-20 | Ferodo Ltd | Friction material for railway disc brake pads |
GB2244061B (en) * | 1990-05-15 | 1992-12-23 | Ferodo Ltd | Friction materials for railway disc brake pads |
WO2003064883A1 (en) * | 2002-01-25 | 2003-08-07 | Glasline Friction Technologies, Inc. | Composite friction elements and pultrusion method of making |
JP2008144773A (en) * | 2006-12-06 | 2008-06-26 | Akebono Brake Ind Co Ltd | Friction material and its manufacturing method |
CN101870438A (en) * | 2010-06-21 | 2010-10-27 | 临安华龙摩擦材料有限公司 | Friction brake disk of double-speed electric-block and preparation method thereof |
CN103320091A (en) * | 2013-05-27 | 2013-09-25 | 湖北飞龙摩擦密封材料股份有限公司 | A friction product |
CN104099065A (en) * | 2014-07-04 | 2014-10-15 | 青岛基宏汽车部件有限公司 | Copper-free rubbing material and preparation method thereof |
CN112228483A (en) * | 2019-11-06 | 2021-01-15 | 晋江凯燕新材料科技有限公司 | Modified organic filling material for friction material and preparation process thereof |
CN112228483B (en) * | 2019-11-06 | 2022-05-17 | 晋江市凯燕新材料研究院股份有限公司 | Modified organic filling material for friction material and preparation process thereof |
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