JPH06240233A - Wet friction material - Google Patents
Wet friction materialInfo
- Publication number
- JPH06240233A JPH06240233A JP5307193A JP5307193A JPH06240233A JP H06240233 A JPH06240233 A JP H06240233A JP 5307193 A JP5307193 A JP 5307193A JP 5307193 A JP5307193 A JP 5307193A JP H06240233 A JPH06240233 A JP H06240233A
- Authority
- JP
- Japan
- Prior art keywords
- friction material
- wet friction
- resin
- weight
- binder phase
- 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.)
- Withdrawn
Links
- 239000002783 friction material Substances 0.000 title claims abstract description 32
- 229920005989 resin Polymers 0.000 claims abstract description 28
- 239000011347 resin Substances 0.000 claims abstract description 28
- 239000011230 binding agent Substances 0.000 claims abstract description 19
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 11
- 239000000463 material Substances 0.000 claims abstract description 8
- 239000000945 filler Substances 0.000 claims abstract description 6
- 239000012784 inorganic fiber Substances 0.000 claims description 3
- 239000002657 fibrous material Substances 0.000 abstract description 6
- 230000002159 abnormal effect Effects 0.000 abstract description 5
- 239000004033 plastic Substances 0.000 abstract description 4
- 229920003023 plastic Polymers 0.000 abstract description 4
- 238000005979 thermal decomposition reaction Methods 0.000 abstract description 4
- 238000005299 abrasion Methods 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- 244000226021 Anacardium occidentale Species 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 235000020226 cashew nut Nutrition 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000003949 imides Chemical class 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 229920001721 polyimide Polymers 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004962 Polyamide-imide Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 229920006231 aramid fiber Polymers 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920002312 polyamide-imide Polymers 0.000 description 2
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy 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
- 150000001408 amides Chemical class 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000001816 cooling 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
- 150000002085 enols Chemical class 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000003607 modifier 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
- 229920003055 poly(ester-imide) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical class [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- ITRNXVSDJBHYNJ-UHFFFAOYSA-N tungsten disulfide Chemical compound S=[W]=S ITRNXVSDJBHYNJ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Braking Arrangements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、冷却効果と潤滑効果を
兼ねた潤滑油の存在の下で用いられる湿式摩擦材料に関
し、具体的には、例えばブレーキライニング,クラッチ
フェーシング,ディスクパットとして最適な湿式摩擦材
料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a wet friction material used in the presence of a lubricating oil having both a cooling effect and a lubricating effect, and more specifically, it is most suitable for a brake lining, a clutch facing and a disc pad. Wet friction material.
【0002】[0002]
【従来の技術】一般に、湿式摩擦材料は、有機系摩擦材
料と無機系摩擦材料に大別できる。この内、有機系摩擦
材料の代表的なものに、樹脂と繊維をマトリックスとす
る摩擦材料がある。有機系摩擦材料に使用される樹脂と
しては、エポキシ,塩化ビニール,ポリエチレン,ポリ
プロピレン,ポリアミド及びポリイミドがあり、具体的
に記載された代表的なものに、特開昭57−85877
号公報,特公平2−41559号公報及び特公平4−9
5622号公報がある。2. Description of the Related Art Generally, wet friction materials can be roughly classified into organic friction materials and inorganic friction materials. Among these, a typical organic friction material is a friction material having a resin and fibers as a matrix. Resins used for organic friction materials include epoxy, vinyl chloride, polyethylene, polypropylene, polyamide, and polyimide, and the representative ones specifically described are JP-A-57-85877.
Japanese Patent Publication No. 4-41559 and Japanese Patent Publication No. 4-9
There is a 5622 publication.
【0003】[0003]
【発明がを解決しようとする課題】樹脂の含有された有
機系摩擦材料としての特開昭57−85877号公報に
は、10〜40重量%の熱硬化性樹脂と摩擦性能調整剤
と有機系繊維とからなる摩擦材について記載されてい
る。同公報に記載されている熱硬化性樹脂としては、フ
ェノール,メラミン,尿素,エポキシ,ポリミイドが挙
げられる。As an organic friction material containing a resin, JP-A-57-85877 discloses a thermosetting resin of 10 to 40% by weight, a friction performance modifier, and an organic friction material. A friction material composed of fibers is described. Examples of the thermosetting resin described in the publication include phenol, melamine, urea, epoxy, and polymide.
【0004】また、特公平2−41559号公報には、
無機質繊維及び/又は無機質粒子5〜70重量%と、ポ
リアミド系重合体のパルプ状物質5〜70重量%と、固
体潤滑剤1〜30重量%とを主たる配合成分とし、かつ
ポリアミド繊維を実質的に含まない摩擦材用組成物につ
いて記載されている。Further, Japanese Patent Publication No. 2-41559 discloses that
Inorganic fibers and / or inorganic particles 5 to 70% by weight, polyamide polymer pulp-like substance 5 to 70% by weight, and solid lubricant 1 to 30% by weight as main compounding ingredients, and polyamide fibers substantially The composition for a friction material which is not included in the above is described.
【0005】さらに、特公平4−95622号公報に
は、ポリアミド繊維を含む繊維と粉体成分に、全体に対
して1〜5重量%のポリイミド樹脂と、他にフェノール
樹脂とでなる結合相を含浸させて成形されたクラッチフ
ェーシングについて記載されている。Further, in Japanese Examined Patent Publication (Kokoku) No. 4-95622, a binder phase composed of 1 to 5% by weight of a polyimide resin and a phenol resin is added to a fiber containing polyamide fiber and a powder component. An impregnated molded clutch facing is described.
【0006】これら3件の公報に代表される従来の樹脂
含有の摩擦材料を高負荷または高摺速の条件で使用する
と、樹脂の熱分解により摩擦材料の表面に塑性流動が起
こり、摩擦係数が低下し、さらに高い熱負荷が加わるこ
とにより異常摩耗となり、実用できなくなるという問題
がある。When the conventional resin-containing friction materials represented by these three publications are used under conditions of high load or high sliding speed, thermal decomposition of the resin causes plastic flow on the surface of the friction material, resulting in a friction coefficient. However, there is a problem that it becomes unusable due to abnormal wear due to a decrease in temperature and a higher heat load.
【0007】本発明は、上述のような問題を解決したも
ので、具体的には、高負荷または高摺速の条件において
も熱分解もしくは摩擦係数の低下あるいは異常摩耗の発
生を起こさせないような結合相で結合した高強度および
耐熱性に優れた湿式摩擦材料の提供を目的とするもので
ある。The present invention solves the above-mentioned problems, and more specifically, does not cause thermal decomposition, reduction in friction coefficient, or abnormal wear even under conditions of high load or high sliding speed. An object of the present invention is to provide a wet friction material which is bonded in a binder phase and has high strength and excellent heat resistance.
【0008】[0008]
【課題を解決するための手段】本発明者は、より高負荷
またはより高摺速の条件で実用できる湿式摩擦材料につ
いての検討を行っていた所、湿式摩擦材料の結合相とし
て使われている熱硬化性樹脂に、より大きく影響を受け
ること、熱硬化性樹脂といて、ビスアリルナジイミドを
用いると、熱分解および/または塑性流動の異常摩耗が
発生し難いという知見を得て、本発明を完成するに至っ
たものである。Means for Solving the Problems The present inventor has been investigating a wet friction material which can be put to practical use under a condition of a higher load or a higher sliding speed, and is used as a binder phase of the wet friction material. According to the present invention, it was found that the thermosetting resin is greatly affected, and that when the bisallylnadiimide is used as the thermosetting resin, thermal decomposition and / or abnormal wear of plastic flow is unlikely to occur. Has been completed.
【0009】本発明の湿式摩擦材料は、熱硬化性樹脂の
結合相5〜40重量%と、残り有機質または無機質の繊
維材料および充填材料とからなり、該結合相の50重量
%以上がビスアリルナジイミドでなることを特徴とする
ものである。The wet friction material of the present invention comprises 5 to 40% by weight of a binder phase of a thermosetting resin and the remaining organic or inorganic fiber material and a filler material, and 50% by weight or more of the binder phase is bis-ary. It is characterized by comprising lunadiimide.
【0010】本発明の湿式摩擦材料における熱硬化性樹
脂は、50重量%以上がビスアリルナジイミドからな
り、残りが例えばフェノール樹脂,エポキシ樹脂,フラ
ン樹脂,キシレン樹脂,ケトン樹脂,尿素樹脂,メラミ
ン樹脂,アニリン樹脂,イミド系樹脂,またはアミド系
樹脂を挙げることができる。これらの熱硬化性樹脂の
内、ビスアリルナジイミドと混在して用いる樹脂として
は、耐熱性の点からイミド系樹脂が好ましく、具体的に
は、特に、ポリイミド(ポリアミノビスマレイミド),
ポリアミドイミド,ポリエーテルイミド,ポリエステル
イミド,ベンゾイミダゾールイミド,ピロメイトイミ
ド,ケルイミド,サクシノイミドが好ましい。The thermosetting resin in the wet friction material of the present invention comprises 50% by weight or more of bisallylnadiimide, and the rest is, for example, phenol resin, epoxy resin, furan resin, xylene resin, ketone resin, urea resin, melamine. Resin, aniline resin, imide resin, or amide resin can be mentioned. Among these thermosetting resins, the resin used in combination with bisallylnadiimide is preferably an imide resin from the viewpoint of heat resistance, and specifically, polyimide (polyaminobismaleimide),
Polyamide imide, polyether imide, polyester imide, benzimidazole imide, pyromate imide, kelimide and succinimide are preferable.
【0011】この熱硬化性樹脂の結合相の他に含まれる
本発明の湿式摩擦材料の構成成分としての繊維材料は、
具体的には、例えばパルプ繊維,炭素繊維,ポリアミド
繊維,アラミド繊維,フェノール繊維,チタン酸カリウ
ム繊維,シリカ・アルミナ繊維,ガラス繊維,銅および
銅合金繊維,鉄および鉄合金繊維,炭化ケイ素ウイス
カ,カーボンウイスカーを挙げることができる。これら
の繊維材料は、60重量%以下、好ましくは5〜40重
量%含有されていればよく、この繊維材料の他に含まれ
る本発明の湿式摩擦材料の構成成分としての充填材料
は、具体的には、例えば黒鉛,二硫化モリブデン,二硫
化タングステン,鉛,ジルコンサンド,シリカ,カシュ
ーダスト,ゴム,セラミックス,硫酸バリウム,銅,鉄
の金属または合金を挙げることができる。これらの充填
材料は、80重量%以下含有されているものである。The fiber material as a constituent of the wet friction material of the present invention contained in addition to the binder phase of the thermosetting resin,
Specifically, for example, pulp fibers, carbon fibers, polyamide fibers, aramid fibers, phenol fibers, potassium titanate fibers, silica / alumina fibers, glass fibers, copper and copper alloy fibers, iron and iron alloy fibers, silicon carbide whiskers, Mention may be made of carbon whiskers. These fibrous materials may be contained in an amount of 60% by weight or less, preferably 5 to 40% by weight, and the filling material as a constituent component of the wet friction material of the present invention contained in addition to this fibrous material is specifically Examples of the metal or alloy include graphite, molybdenum disulfide, tungsten disulfide, lead, zircon sand, silica, cashew dust, rubber, ceramics, barium sulfate, copper and iron. These filling materials are contained in an amount of 80% by weight or less.
【0012】本発明の湿式摩擦材料における結合相が5
重量%未満になると、結合相としての役割が弱くなって
強度低下が顕著になること、逆に結合相が40重量%を
超えて多くなると、弾力性が乏しくなることおよび摩擦
時に結合相の塑性流動性が大きくなって、摩擦係数を顕
著に低下させることになる。また、結合相中に存在する
ビスアリルナジイミドが50重量%未満になると、高負
荷または高摺速において異常摩耗を起こしやすくなる。
従って、湿式摩擦材料全体の5〜40重量%を結合相と
し、この結合相中の50重量%がビスアリルナジイミド
と定めたものである。In the wet friction material of the present invention, the binder phase is 5
If the amount is less than 10% by weight, the role of the binder phase becomes weak and the strength is significantly reduced. On the contrary, if the amount of the binder phase exceeds 40% by weight, the elasticity becomes poor and the plasticity of the binder phase during friction. The fluidity increases, and the friction coefficient is significantly reduced. If the amount of bisallylnadiimide present in the binder phase is less than 50% by weight, abnormal wear is likely to occur at high load or high sliding speed.
Therefore, 5 to 40% by weight of the total wet friction material is defined as the binder phase, and 50% by weight of the binder phase is defined as bisallylnadimide.
【0013】[0013]
【作用】本発明の湿式摩擦材料は、結合相と繊維材料と
充填材料の組合わせでもって、全体の10〜50体積%
が気孔となるようにし、かつ気孔を均一に分散させるこ
とにより耐熱性を損うことなく適当な弾力性を引き出さ
せているという作用をしている。The wet friction material of the present invention comprises 10 to 50% by volume of the total amount of the combination of the binder phase, the fiber material and the filler material.
The pores are made uniform and the pores are evenly dispersed so that appropriate elasticity can be obtained without impairing heat resistance.
【0014】また、別の見方をすると、本発明の湿式摩
擦材料は、気孔を有するにもかかわらず、50重量%以
上のビスアリルナジイミドを含む結合相が最適な弾力性
と摩擦係数を兼備させるように作用しているものであ
る。From a different point of view, the wet friction material of the present invention has pores, but the binder phase containing 50% by weight or more of bisallylnadiimide has optimum elasticity and friction coefficient. It is acting to let you.
【0015】[0015]
【実施例1】市販されている平均直径5〜25μm,平
均長さ0.1〜1.0mmのアラミド繊維,チタン酸カ
リウム繊維,カーボン繊維と、NBR,硫酸バリウム,
膨張化黒鉛,カシューダスト,シリカの充填材料と、フ
ェノール樹脂,カシュー樹脂,ポリアミノビスマレイミ
ド樹脂,ビスアリルナジイミド樹脂([C37H34N
2O4] n)を用いて、表1の如く配合した。Example 1 Commercially available average diameter 5 to 25 μm, flat
Aramid fiber with a uniform length of 0.1 to 1.0 mm, titanium titanate
Lithium fiber, carbon fiber, NBR, barium sulfate,
Expanded graphite, cashew dust, silica filler,
Enol resin, cashew resin, polyaminobismaleimi
Resin, bisallyl nadimide resin ([C37H34N
2OFour] n) was used and blended as shown in Table 1.
【0016】表1の配合試料をV型ミキサーにより混合
した後、外径335mm,内径283mm,深さ5mm
の金型に充填してプレス成形した。After mixing the formulation samples shown in Table 1 with a V-type mixer, the outer diameter was 335 mm, the inner diameter was 283 mm, and the depth was 5 mm.
It was filled in the mold of No. 1 and press-molded.
【0017】得られた成形体を表1に併記した条件で焼
成して、本発明品1〜4および比較品1〜4を得た。The obtained molded bodies were fired under the conditions shown in Table 1 to obtain the products 1 to 4 of the present invention and the comparative products 1 to 4.
【0018】こうして得た本発明品1〜4および比較品
1〜4の抗折強度および気孔率を測定し、その結果を表
1に併記した。The bending strength and the porosity of the products 1 to 4 of the present invention and the comparative products 1 to 4 thus obtained were measured, and the results are also shown in Table 1.
【0019】次に、本発明品1〜4および比較品1〜4
を用いて、摺速48m/sec,吸収エネルギー10k
gfm/cm2で1万サイクルの耐久性試験を行い、そ
のときのサイクル数と動摩擦係数の関係を求めて表2
に、サイクル数と摩耗率の関係を求めて表3に示した。Next, products 1 to 4 of the present invention and comparative products 1 to 4
With a sliding speed of 48 m / sec and absorbed energy of 10 k
A durability test of 10,000 cycles was performed at gfm / cm 2 , and the relationship between the number of cycles and the dynamic friction coefficient at that time was obtained and Table 2
Table 3 shows the relationship between the number of cycles and the wear rate.
【0020】[0020]
【表1】 [Table 1]
【0021】[0021]
【表2】 [Table 2]
【0022】[0022]
【表3】 [Table 3]
【0023】[0023]
【発明の効果】本発明の湿式摩擦材料は、従来の湿式摩
擦材料である比較品に比べて、抗折強度および気孔率が
同等ではあるが、高負荷、高摺速における耐久性試験に
おける動摩擦係数および摩耗率が顕著に優れるという効
果を有している。EFFECTS OF THE INVENTION The wet friction material of the present invention has the same bending strength and porosity as the conventional wet friction material, but the dynamic friction in the durability test under high load and high sliding speed. It has an effect that the coefficient and the wear rate are remarkably excellent.
Claims (1)
と、残り有機質または無機質の繊維材料と充填材料とか
らなる摩擦材料において、該結合相の50重量%以上が
ビスアリルナジイミドでなることを特徴とする湿式摩擦
材料。1. A thermosetting resin binder phase in an amount of 5 to 40% by weight.
And a remaining friction material composed of an organic or inorganic fiber material and a filler material, wherein 50% by weight or more of the binder phase is bisallylnadiimide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5307193A JPH06240233A (en) | 1993-02-18 | 1993-02-18 | Wet friction material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5307193A JPH06240233A (en) | 1993-02-18 | 1993-02-18 | Wet friction material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06240233A true JPH06240233A (en) | 1994-08-30 |
Family
ID=12932589
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5307193A Withdrawn JPH06240233A (en) | 1993-02-18 | 1993-02-18 | Wet friction material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06240233A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1123602C (en) * | 2000-03-13 | 2003-10-08 | 中国科学院化学研究所 | Refractory antiwear polyimide as sealing material and its preparing process and application |
WO2006116474A2 (en) | 2005-04-26 | 2006-11-02 | Borgwarner Inc. | Friction material |
WO2009123042A1 (en) * | 2008-03-31 | 2009-10-08 | 宇部興産株式会社 | Friction material and resin composition for friction material |
US7749562B1 (en) | 2004-07-26 | 2010-07-06 | Borgwarner Inc. | Porous friction material comprising nanoparticles of friction modifying material |
US8021744B2 (en) | 2004-06-18 | 2011-09-20 | Borgwarner Inc. | Fully fibrous structure friction material |
CN102911595A (en) * | 2012-11-02 | 2013-02-06 | 东华大学 | Benzimidazole-type humidity-sensitive high-molecular coating material and preparation method and application thereof |
US8397889B2 (en) | 2008-03-12 | 2013-03-19 | Borgwarner Inc. | Frictional device comprising at least one friction plate |
WO2016039485A1 (en) * | 2014-09-12 | 2016-03-17 | 東洋製罐グループホールディングス株式会社 | Fiber-reinforced polyimide resin molded article and method for producing same |
-
1993
- 1993-02-18 JP JP5307193A patent/JPH06240233A/en not_active Withdrawn
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1123602C (en) * | 2000-03-13 | 2003-10-08 | 中国科学院化学研究所 | Refractory antiwear polyimide as sealing material and its preparing process and application |
US8021744B2 (en) | 2004-06-18 | 2011-09-20 | Borgwarner Inc. | Fully fibrous structure friction material |
US7749562B1 (en) | 2004-07-26 | 2010-07-06 | Borgwarner Inc. | Porous friction material comprising nanoparticles of friction modifying material |
WO2006116474A2 (en) | 2005-04-26 | 2006-11-02 | Borgwarner Inc. | Friction material |
EP1874850A4 (en) * | 2005-04-26 | 2008-06-18 | Borgwarner Inc | Friction material |
US8397889B2 (en) | 2008-03-12 | 2013-03-19 | Borgwarner Inc. | Frictional device comprising at least one friction plate |
WO2009123042A1 (en) * | 2008-03-31 | 2009-10-08 | 宇部興産株式会社 | Friction material and resin composition for friction material |
JP2009242656A (en) * | 2008-03-31 | 2009-10-22 | Ube Ind Ltd | Friction material and resin composition for friction material |
US8748509B2 (en) | 2008-03-31 | 2014-06-10 | Ube Industries, Ltd. | Friction material and resin composition for friction material |
CN102911595A (en) * | 2012-11-02 | 2013-02-06 | 东华大学 | Benzimidazole-type humidity-sensitive high-molecular coating material and preparation method and application thereof |
WO2016039485A1 (en) * | 2014-09-12 | 2016-03-17 | 東洋製罐グループホールディングス株式会社 | Fiber-reinforced polyimide resin molded article and method for producing same |
US10406765B2 (en) | 2014-09-12 | 2019-09-10 | Toyo Seikan Group Holdings, Ltd. | Fiber-reinforced polyimide resin molded article and production process therefor |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100571526B1 (en) | Fibrous base material for use in a non-asbestos, non-metallic friction material, non-asbestos friction material, non-asbestos, non-metallic friction material, and process for producing a non-asbestos, non-metallic friction material | |
KR100918511B1 (en) | Friction material with nanoparticles of friction modifying layer | |
US5707905A (en) | Fibrous base material for a friction lining material comprising less fibrillated aramid fibers and synthetic graphite | |
JP3535579B2 (en) | Unsaturated friction material containing powdered silicone resin and powdered phenolic resin and method for producing the same | |
JP2003503555A (en) | Bismuth sulfide-containing solid lubricants for use in brake linings | |
JP2005113130A (en) | High performance and highly durable deposit friction material | |
JP2005121221A (en) | Mixed deposit friction material | |
KR100347086B1 (en) | Friction pads for use in disc brakes | |
US6265071B1 (en) | Brake unit including brake disc and brake lining | |
JPH09176333A (en) | Fibrous lining material containing aramid having slight fibrillation and synthetic graphite | |
JPH06240233A (en) | Wet friction material | |
JPH06102782B2 (en) | Brake lining | |
JPH108035A (en) | Non-asbestos-based friction material | |
JPH059458A (en) | Wet friction material | |
JPH108036A (en) | Non-asbestos-based friction material | |
EP0488159B1 (en) | Non-asbestos friction material | |
US20050072637A1 (en) | Friction pairing for parking brakes in motor vehicles | |
JPH01145371A (en) | Highly wear-resistant c-b4c-based sliding member | |
JPS5813684A (en) | Friction material | |
JPH07115958B2 (en) | Carbon fiber reinforced carbon composite material with high friction coefficient | |
JP2000290636A (en) | Friction material | |
JPH0343485A (en) | Friction material | |
JP2000034468A (en) | Wet friction material | |
JP3865265B2 (en) | Friction material | |
JPH108033A (en) | Non-asbestos-based friction material |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A300 | Withdrawal of application because of no request for examination |
Free format text: JAPANESE INTERMEDIATE CODE: A300 Effective date: 20000509 |