JPS6357931A - High heat resistive frictional material - Google Patents
High heat resistive frictional materialInfo
- Publication number
- JPS6357931A JPS6357931A JP20348986A JP20348986A JPS6357931A JP S6357931 A JPS6357931 A JP S6357931A JP 20348986 A JP20348986 A JP 20348986A JP 20348986 A JP20348986 A JP 20348986A JP S6357931 A JPS6357931 A JP S6357931A
- Authority
- JP
- Japan
- Prior art keywords
- friction
- high heat
- fibers
- ceramic fiber
- ceramic
- 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
- 239000000463 material Substances 0.000 title abstract description 7
- 239000000835 fiber Substances 0.000 claims abstract description 28
- 239000000919 ceramic Substances 0.000 claims abstract description 18
- 239000000126 substance Substances 0.000 claims abstract description 4
- 239000011230 binding agent Substances 0.000 claims abstract description 3
- 239000002783 friction material Substances 0.000 claims description 18
- 239000003607 modifier Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 abstract description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 4
- 229920005989 resin Polymers 0.000 abstract description 3
- 239000011347 resin Substances 0.000 abstract description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 2
- 238000000465 moulding Methods 0.000 abstract description 2
- 239000000377 silicon dioxide Substances 0.000 abstract description 2
- 238000005299 abrasion Methods 0.000 abstract 1
- 229910052681 coesite Inorganic materials 0.000 abstract 1
- 229910052593 corundum Inorganic materials 0.000 abstract 1
- 229910052906 cristobalite Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 235000012239 silicon dioxide Nutrition 0.000 abstract 1
- 229910052682 stishovite Inorganic materials 0.000 abstract 1
- 229910052905 tridymite Inorganic materials 0.000 abstract 1
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 1
- 239000003365 glass fiber Substances 0.000 description 7
- 239000010425 asbestos Substances 0.000 description 6
- 229910052895 riebeckite Inorganic materials 0.000 description 6
- 239000000428 dust Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 229910001369 Brass Inorganic materials 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000010951 brass Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000005011 phenolic resin Substances 0.000 description 4
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 3
- 244000226021 Anacardium occidentale Species 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 235000020226 cashew nut Nutrition 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004760 aramid Substances 0.000 description 2
- 229920006231 aramid fiber Polymers 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
- 238000007664 blowing Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000012210 heat-resistant fiber Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 201000005202 lung cancer Diseases 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical group C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture 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
- 229920001187 thermosetting polymer Polymers 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、耐熱性の優れた摩擦材に関するものである。[Detailed description of the invention] [Industrial application field] The present invention relates to a friction material with excellent heat resistance.
従来、自動車、鉄道車両、各種産業用機械のブレーキに
用いられる摩擦材としてシよ、石綿、ガラス繊維、アラ
ミド繊維、スチール繊維などの繊維を主成分とした有機
系摩擦材が知られている。Conventionally, organic friction materials whose main components are fibers such as asbestos, glass fibers, aramid fibers, and steel fibers have been known as friction materials used in the brakes of automobiles, railway vehicles, and various industrial machines.
しかし、石綿の使用に関しては、その粉じんが肺ガンの
発生の原因であることが指摘されており問題がある。ま
た、石綿は700〜800℃で結晶水を放出した後は極
めて脆くなるため、これを主成分とする従来の摩擦材は
高温での摩擦係数の低下や耐摩耗性が低いという問題が
ある。However, there is a problem with the use of asbestos, as its dust has been shown to be a cause of lung cancer. Further, since asbestos becomes extremely brittle after releasing crystallization water at 700 to 800° C., conventional friction materials containing asbestos as a main component have problems such as a decrease in the coefficient of friction at high temperatures and low wear resistance.
ガラス繊維は耐熱性が低く300℃付近から軟化を始め
以後温度の上昇とともに粘度が低下し溶融状態になるた
め、これを主成分とする摩擦材は高温での摩擦係数、耐
摩耗性などが低いという問題がある。Glass fiber has low heat resistance and begins to soften at around 300°C, after which the viscosity decreases as the temperature rises and it becomes molten. Therefore, friction materials that have glass fiber as its main component have low friction coefficients and wear resistance at high temperatures. There is a problem.
アラミド繊維を始めとする各種有機繊維も200〜30
0℃で熱分解あるい:よ熔融するため、これを主成分と
する摩擦材はガラス繊維を使用したものと同様高温での
摩擦係数、耐摩耗性が低いという問題を有する
一方、これらの繊維に対しスチール繊維は耐熱性の点で
は前記各種繊維に比べ優れているが、これを主成分とす
る摩擦材は熱伝導率が高く、また錆の発生により摩擦、
摩耗特性に悪影Vを及ぼすという問題を有する。Various organic fibers including aramid fibers also range from 200 to 30%.
Because it thermally decomposes or melts at 0°C, friction materials based on it have the same problems as those using glass fibers, such as low friction coefficient and wear resistance at high temperatures. On the other hand, steel fibers are superior in terms of heat resistance compared to the above-mentioned various types of fibers, but friction materials containing steel fibers as a main component have high thermal conductivity and are susceptible to friction and corrosion due to the formation of rust.
This has the problem of adversely affecting the wear characteristics.
また、炭素繊維を主成分とするものは、高価であるだけ
でなく摩擦係数が低いという問題を有する。Further, those whose main component is carbon fiber have the problem of not only being expensive but also having a low coefficient of friction.
本発明は、前記従来技術の有する欠点を改善した高耐熱
摩擦材を提供することを目的とし、特許請求の範囲記載
の高耐熱摩擦材を提供することにより前記目的を達成す
るものである。An object of the present invention is to provide a highly heat-resistant friction material that improves the drawbacks of the prior art, and achieves the above object by providing a highly heat-resistant friction material as described in the claims.
セラミックファイバーは、−Cに高純度のシリカとアル
ミナを電気溶融し、その細流を高圧の空気で吹き飛ばす
ことにより繊維化したもので、この繊維は200〜30
0℃で軟化するガラス繊維あるいは分解、溶融する有機
繊維、さらには800℃付近で結晶水を放出し脆化する
石綿とは異なり、900℃付近から軟化を始めるがそれ
と同時に結晶化が始まるため軟化が停止し1000℃以
上の耐熱性を有する繊維径が平均2μ前後の極めて細い
ガラス質繊維である。さらにこのセラミックファイバー
Gこはショットと称する非繊維状ガラス粒が通常50w
t%程度ふくまれている。ショットは粒径44〜200
μと粗大なものが大半であるため、これを含むと摩擦対
面を傷付ける可能性が高い。従ってこれが問題となる場
合には、このショットを取り除きその含有率を20wt
%以下にすることが望ましい。本発明に使用するショッ
ト含有率が20vat%以下のセラミックファイバーを
得る方法について説明する。Ceramic fiber is made by electrically melting high-purity silica and alumina in -C and blowing out the trickle with high-pressure air.
Unlike glass fibers that soften at 0℃ or organic fibers that decompose and melt, and even asbestos that releases crystal water and becomes brittle at around 800℃, it starts to soften at around 900℃, but at the same time it begins to crystallize, so it softens. It is an extremely thin glassy fiber with an average fiber diameter of about 2 μm, which has a heat resistance of 1000° C. or higher. Furthermore, the non-fibrous glass grains called ceramic fiber G-shot are usually 50w.
This includes approximately t%. Shot has a particle size of 44-200
Most of the particles are coarse and coarse, so if they are included, there is a high possibility that they will damage the friction surface. Therefore, if this becomes a problem, remove this shot and reduce its content to 20wt.
% or less. A method for obtaining ceramic fibers having a shot content of 20 vat % or less used in the present invention will be described.
所定量のSiO□とA1.O,を電気溶融し、その細流
を高速の空気流あるいは、高速回転ローターの遠心力で
吹き飛ばすことにより得られる繊維を水中シこ投入し攪
拌してセラミックファイバーのスラリーを作成する。次
にこのスラリーを円筒容器に徐々に導びくと同時に、こ
の容器の側壁より加圧水を送り込み、うず流を発生させ
、そのうす流の中でセラミックファイバーをほぐしショ
ットを分雛する。絡みがほぐされたセラミックファイバ
ーのスラリーをうす流の中心部から順次、流出させ移動
しているエンドレスのスクリーン上に導びき繊維を捕集
する。このようにして得られたセラミックファイバーは
例えば粒径が44μ以上でショット含有量が0.1 w
t%、あるいは18ut%である。A predetermined amount of SiO□ and A1. A slurry of ceramic fibers is created by electrolytically melting O, and blowing off the resulting stream with a high-speed air stream or the centrifugal force of a high-speed rotating rotor. Next, this slurry is gradually introduced into a cylindrical container, and at the same time pressurized water is pumped through the side wall of the container to generate a swirling flow, which loosens the ceramic fibers and separates the shots. A slurry of disentangled ceramic fibers is sequentially flowed out from the center of the thin stream and guided onto a moving endless screen to collect the fibers. The ceramic fiber thus obtained has a grain size of 44μ or more and a shot content of 0.1 w.
t% or 18ut%.
化学成分はSingが35wt%未満ではショット含有
率が極端に多くなり、65wt%を越えると耐熱性が低
下するので5i(h 35〜65wt%の範囲内にす
る必要がある。As for the chemical components, if Sing is less than 35 wt%, the shot content will be extremely high, and if Sing is more than 65 wt%, the heat resistance will decrease, so 5i (h) must be within the range of 35 to 65 wt%.
本発明の高耐熱摩擦材におけるセラミックファイバーの
配合割合は20〜10wt%とすることができる。The blending ratio of ceramic fibers in the highly heat-resistant friction material of the present invention can be 20 to 10 wt%.
本発明に用いる有機結合剤は、セラミックファイバー、
摩擦調整剤などを相互に団結するもので主にフェノール
樹脂などの熱硬化性樹脂が望ましい。その配合割合は1
0〜30wL%とすることができる。The organic binder used in the present invention includes ceramic fiber,
It is preferably a thermosetting resin such as phenol resin, which binds together friction modifiers and the like. The mixing ratio is 1
It can be 0 to 30 wL%.
摩擦調整剤としては、カシューダスト、ゴム粉末硫酸バ
リウム、炭酸カルシウム、グラファイト、二硫化モリブ
デン、銅、真ちゅう、アルミニウムなどの粉末が望まし
い。それらの配合割合は5〜30wt%とすることがで
きる。As the friction modifier, powders such as cashew dust, rubber powder barium sulfate, calcium carbonate, graphite, molybdenum disulfide, copper, brass, and aluminum are preferable. Their blending ratio can be 5 to 30 wt%.
次に、本発明の高耐熱摩擦材の代表的な製造方法につい
て述べる。セラミックファイバー、樹脂、摩擦調整剤を
所定の割合にて混合した後200〜400kg/cdの
圧力にて予備成型する。その後、この予備成型体を14
0〜180℃に加熱された金型に入れ150〜350k
g/ crAの圧力にて5〜10分間、加圧成型した後
170〜250℃の温度で5時間以上アフターキュアー
する。Next, a typical manufacturing method of the highly heat-resistant friction material of the present invention will be described. After mixing ceramic fiber, resin, and friction modifier in a predetermined ratio, the mixture is preformed at a pressure of 200 to 400 kg/cd. Thereafter, this preformed body was
Place in a mold heated to 0-180℃ for 150-350k
After pressure molding at a pressure of g/crA for 5 to 10 minutes, it is after-cured at a temperature of 170 to 250°C for 5 hours or more.
このようにして得られる本発明の高耐熱摩擦材は、耐熱
性性の極めて高いセラミックファイバーが配合されてい
るため耐摩耗性、摩擦係数の安定性などに優れるという
特許を有する。以下、本発明を実施例について説明する
。The highly heat-resistant friction material of the present invention obtained in this manner has a patent that it has excellent wear resistance, stability of friction coefficient, etc. because it contains ceramic fibers with extremely high heat resistance. Hereinafter, the present invention will be explained with reference to examples.
去止斑上
化学成分がSiO□52wt%、 AZ20348wj
%で、ショット含有率がO,1wt%のセラミックファ
イバーとフェノール樹脂、真ちゅう粉末、カーボン粉末
、カシューダストを第1表に示す容積比率になるように
混合し、プレスにて400kg/cnの圧力にて予備成
形した後、150℃で200 kg / ctAの圧力
で10分間加圧成型した。次に170℃で7時間アフタ
ーキュアーし本発明の高耐熱摩擦材を得た。これを所定
サイズに切断、研磨し摩擦摩耗テスト用試験片とした。The chemical component on the plaque is SiO□52wt%, AZ20348wj
%, and the shot content is O, 1 wt% ceramic fiber, phenolic resin, brass powder, carbon powder, and cashew dust are mixed at the volume ratio shown in Table 1, and pressed at a pressure of 400 kg/cn. After preforming at 150°C and a pressure of 200 kg/ctA for 10 minutes. Next, the material was after-cured at 170° C. for 7 hours to obtain a highly heat-resistant friction material of the present invention. This was cut to a predetermined size and polished to provide a test piece for friction and wear testing.
ル較■±
石綿とフェノール樹脂、真ちゅう粉末、カーボン粉末、
カシニーダストを第1表に示す容積比率になるよう混合
し実施例と同様の方法にて成型し試験片を作成した。Comparison ■± Asbestos and phenolic resin, brass powder, carbon powder,
Cassiny dust was mixed to the volume ratio shown in Table 1 and molded in the same manner as in the example to prepare a test piece.
ル較勇呈
Eガラスファイバーとフェノール樹脂、真ちゅう粉末、
カーボン粉末、カシューダストを第1表に示す容積比率
になるよう混合し、実施例と同様の方法にて成型し試験
片を作成した。Glass fiber and phenolic resin, brass powder,
Carbon powder and cashew dust were mixed in a volume ratio shown in Table 1, and molded in the same manner as in the example to prepare a test piece.
このようにして得た試験片をJIS D4411に規
定された方法に準じて摩i!!!係数及び摩耗量を測定
し、その結果を第2表に示す。The test piece thus obtained was polished according to the method specified in JIS D4411. ! ! The coefficient and wear amount were measured and the results are shown in Table 2.
第 1 表
第 2 表
〔発明の効果〕
以上のように本発明の高耐熱摩擦材は、セラミックファ
イバーと言う高耐熱性のファイバーを主成分としている
ため、高温でも摩擦係数が低下せず、摩耗量も少ないな
どの効果を有し、耐熱性の優れた摩擦材である。従って
熱的に厳しい条件下で使用される摩擦材として極めて優
れており、産業上有用なものである。Table 1 Table 2 [Effects of the Invention] As described above, since the highly heat-resistant friction material of the present invention has a highly heat-resistant fiber called ceramic fiber as its main component, the coefficient of friction does not decrease even at high temperatures, and it resists wear. It is a friction material with excellent heat resistance and has the effect of being small in amount. Therefore, it is extremely excellent as a friction material used under harsh thermal conditions and is industrially useful.
特許出願人 イ ビ デ ン 株式会社代表者 多
賀潤一部Patent applicant: Ibiden Co., Ltd. Representative: Jun Taga
Claims (1)
質的にAl_2O_3からなるセラミックファイバーと
有機結合剤と摩擦調整剤とからなることを特徴とする高
耐熱摩擦材。 2)前記セラミックファイバーは、その中に含有されて
いるショットの含有率が20%以下であることを特徴と
する特許請求の範囲第1項記載の高耐熱摩擦材。[Scope of Claims] 1) A highly heat-resistant friction material comprising ceramic fibers whose chemical components are SiO_235 to 65 wt% and the remainder substantially Al_2O_3, an organic binder, and a friction modifier. 2) The highly heat-resistant friction material according to claim 1, wherein the ceramic fiber has a shot content of 20% or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20348986A JPS6357931A (en) | 1986-08-28 | 1986-08-28 | High heat resistive frictional material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20348986A JPS6357931A (en) | 1986-08-28 | 1986-08-28 | High heat resistive frictional material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6357931A true JPS6357931A (en) | 1988-03-12 |
Family
ID=16475004
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20348986A Pending JPS6357931A (en) | 1986-08-28 | 1986-08-28 | High heat resistive frictional material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6357931A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013094113A1 (en) | 2011-12-23 | 2013-06-27 | ニチアス株式会社 | Bio-soluble inorganic fiber and method for producing same |
-
1986
- 1986-08-28 JP JP20348986A patent/JPS6357931A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013094113A1 (en) | 2011-12-23 | 2013-06-27 | ニチアス株式会社 | Bio-soluble inorganic fiber and method for producing same |
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