JPH05320372A - Resin composition for frictional material - Google Patents
Resin composition for frictional materialInfo
- Publication number
- JPH05320372A JPH05320372A JP13125892A JP13125892A JPH05320372A JP H05320372 A JPH05320372 A JP H05320372A JP 13125892 A JP13125892 A JP 13125892A JP 13125892 A JP13125892 A JP 13125892A JP H05320372 A JPH05320372 A JP H05320372A
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- phenol resin
- fibers
- friction material
- 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
Landscapes
- Reinforced Plastic Materials (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、摩擦材用樹脂組成物に
係わり、詳述すると自動車、鉄道車両、産業機械等の部
品として使用される金属繊維、無機繊維、有機繊維を基
材とする摩擦材料に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin composition for friction materials, and more specifically, it is based on metal fibers, inorganic fibers and organic fibers used as parts for automobiles, railway vehicles, industrial machines and the like. It relates to friction materials.
【0002】[0002]
【従来の技術】自動車、鉄道車両及び各産業用機械に
は、その制動のために摩擦材料が使用されている。この
摩擦材料は、結合剤にフェノール樹脂、ゴムを用い、金
属繊維、及びアスベスト、セラミックファイバーなどの
無機繊維、ポリイミド、ポリアミド、フェノール樹脂な
どの有機質繊維を基材とし、これに増摩剤、減摩剤とし
ての充填剤、添加剤を添加してなる複合材料から作られ
ている。この摩擦材料に要求される特性には、摩擦係
数、摩耗量、相手金属板に対する攻撃性、鳴きなどの摩
擦性能、並びに曲げ強度、剪断強度などがある。近年の
交通機関の高速化、車輌の大型化に伴い、摩擦材料は高
速下、高負荷下などのより過酷な条件下で使用されるよ
うになり、これらの条件下でも安定した制動効果を有す
ることが強く要求されている。また、摩擦性能に最も大
きく影響する要因は結合剤の選択にあるとされている。
この結合剤としては熱硬化性樹脂が広く使用されてお
り、耐熱性、耐摩耗性、価格などから一般的にフェノー
ル樹脂が使用されている。フェノール樹脂としては前記
諸性能を改善するために、柔軟性に優れるカシュ変性フ
ェノール樹脂、油変性フェノール樹脂、ゴム変性フェノ
ール樹脂、メラミン変性フェノール樹脂など各種変性樹
脂が検討されている。2. Description of the Related Art Friction materials are used for braking automobiles, railway vehicles and industrial machines. This friction material uses phenol resin and rubber as a binder, and uses metal fibers, inorganic fibers such as asbestos and ceramic fibers, and organic fibers such as polyimide, polyamide, and phenol resin as a base material. It is made of a composite material containing fillers and additives as a lubricant. The characteristics required of this friction material include the coefficient of friction, the amount of wear, the aggressiveness to the mating metal plate, the friction performance such as squeal, and the bending strength and the shear strength. With the recent increase in speed of transportation and the increase in size of vehicles, friction materials have come to be used under more severe conditions such as high speed and high load, and have a stable braking effect even under these conditions. Is strongly required. Further, it is said that the factor that most affects the friction performance is the selection of the binder.
A thermosetting resin is widely used as this binder, and a phenol resin is generally used because of its heat resistance, abrasion resistance, price, and the like. As the phenol resin, various modified resins such as cash-modified phenol resin, oil-modified phenol resin, rubber-modified phenol resin and melamine-modified phenol resin, which are excellent in flexibility, have been studied in order to improve the above-mentioned various performances.
【0003】[0003]
【発明が解決しようとする課題】しかし、これらは耐熱
性に劣るため過酷な条件下での使用においては制動性能
が不安定であり、鳴きが発生する。本発明は前記欠点の
ない摩擦材料に関するものであり、フェノール樹脂及び
結合アクリロニトリル量35%以上のNBRを主結合剤
としてなり、更に、周期率表第IIa族元素の塩化物を含
むことを特徴とするものである。However, since these are inferior in heat resistance, the braking performance is unstable and squeal occurs when used under severe conditions. The present invention relates to a friction material which does not have the above-mentioned drawbacks, which comprises a phenol resin and NBR having a bound acrylonitrile amount of 35% or more as a main binder, and further contains a chloride of a group IIa element of the periodic table. To do.
【0004】[0004]
【課題を解決するための手段】以下、本発明について具
体的に説明する。フェノール樹脂には、未変性タイプと
しては、ノボラック型フェノール樹脂、レゾール型フェ
ノール樹脂、ジメチレンエーテル型フェノール樹脂など
がある。また、エラストマ変性、カシュ変性、シリコー
ン変性、油変性などの変性樹脂があるが、耐熱性に優れ
た未変性タイプのノボラック型フェノール樹脂がよく、
未反応フェノール量が3重量%以下、好ましくは2重量
%以下が望ましい。未反応フェノール量が3重量%以上
では、硬化した摩擦材料中に低分子物が多く残るため、
過酷な条件下では摩擦係数が不安定となり、安定した制
動性能が得られない。オルト率は50%以上が好まし
く、60%以上が望ましい。オルト率が低いと硬化した
樹脂が硬くなるため柔軟性に劣り鳴きが悪くなる。ま
た、オルト率が50%以下では、硬化反応も遅いため、
成形時間を充分長くしないと摩擦材料中の樹脂の硬化状
態が不均一となり、安定した摩擦係数、摩耗率が得られ
なく、やはり過酷な条件下では安定した制動性能が得ら
れない。The present invention will be specifically described below. Examples of the unmodified type of the phenol resin include novolac type phenol resin, resol type phenol resin, and dimethylene ether type phenol resin. Also, there are modified resins such as elastomer modified, cache modified, silicone modified, oil modified, but unmodified novolac type phenolic resin with excellent heat resistance is often used.
It is desirable that the amount of unreacted phenol is 3% by weight or less, preferably 2% by weight or less. When the amount of unreacted phenol is 3% by weight or more, a large amount of low molecular weight substances remain in the hardened friction material.
Under severe conditions, the friction coefficient becomes unstable and stable braking performance cannot be obtained. The ortho ratio is preferably 50% or more, and more preferably 60% or more. If the ortho ratio is low, the cured resin becomes hard, resulting in poor flexibility and poor squealing. If the ortho ratio is 50% or less, the curing reaction is slow, so
If the molding time is not made sufficiently long, the cured state of the resin in the friction material becomes non-uniform, and stable friction coefficient and wear rate cannot be obtained, and also stable braking performance cannot be obtained under severe conditions.
【0005】このような樹脂を得る方法としては、石炭
酸、クレゾール、キシレノール、アルキルフェノールな
どのフェノール類とホルムアルデヒドなどのアルデヒド
類を塩化亜鉛、酢酸亜鉛などの触媒下で反応させる方法
がある。硬化剤としてのヘキサメチレンテトラミンの添
加量はフェノール樹脂に対し5重量%以上、12重量%
以下が望ましい。5重量%以下の添加量では架橋密度が
低過ぎるため、所望の剪断強度、曲げ強度が得られな
い。また、12重量%以上では、逆に未反応ヘキサメチ
レンテトラミンが残り摩擦係数が不安定となる。NBR
としては結合アクリロニトリル量が35%以上が望まし
く、好ましくは固形の粉末状が望ましい。As a method of obtaining such a resin, there is a method of reacting phenols such as carboxylic acid, cresol, xylenol, and alkylphenol with aldehydes such as formaldehyde in the presence of a catalyst such as zinc chloride or zinc acetate. Hexamethylenetetramine as a curing agent is added in an amount of 5% by weight or more and 12% by weight or more based on the phenol resin.
The following is desirable. If the amount added is less than 5% by weight, the crosslink density is too low, and the desired shear strength and bending strength cannot be obtained. On the other hand, if it is 12% by weight or more, unreacted hexamethylenetetramine remains, and the friction coefficient becomes unstable. NBR
It is desirable that the amount of bound acrylonitrile is 35% or more, preferably solid powder.
【0006】周期率表第IIa族元素の塩化物としては、
マグネシウム、カルシウム、バリウム、ストロンチウム
などの塩化物があり、これらの中で好ましくは塩化カル
シウム、塩化マグネシウム、塩化バリウム、塩化ストロ
ンチウムが望ましい。また添加量はフェノール樹脂に対
し、2重量%乃至15重量%が望ましい。The chlorides of Group IIa elements of the periodic table are as follows:
There are chlorides such as magnesium, calcium, barium and strontium. Among these, calcium chloride, magnesium chloride, barium chloride and strontium chloride are preferable. Further, the addition amount is preferably 2% by weight to 15% by weight with respect to the phenol resin.
【0007】基材については、鉄、銅、黄銅などの金属
繊維及びアスベスト繊維、セラミック繊維、ガラス繊
維、ウォラストナイト、人工鉱物質繊維などの無機質繊
維、ポリイミド繊維、ポリアミド繊維、フェノール繊維
などの有機質繊維などがある。これらの基材の中で金属
繊維が望ましい。また、他の基材としてアスベスト繊維
は公害の発生のため使用できないが、無機質繊維、又は
有機質繊維などの従来使用している基材を併用して使用
することができる。また、金属繊維としては、錆びの問
題のない銅繊維、黄銅繊維が望ましい。また、シリカな
どの増摩剤、黒鉛、三硫化アンチモン、二硫化モリブテ
ンなどの減摩剤など従来使用している無機質及びカシュ
樹脂などの有機質添加剤を単独又は併用して使用するこ
とができる。前記組成をナウタミキサなどで均一に混合
し、成形用粉体を得る。これを成形温度130℃乃至1
60℃、成形圧力39.4MPa乃至58.8MPaで
所定時間成形し、成形品を得る。この成形品を160℃
乃至220℃の温度で所定時間熱処理し、必要において
は、さらに400℃以上の温度でスコーチ処理を行う。
本発明は、これら製造法を特に前記方法に限定するもの
ではないが、望ましくは熱処理温度を180℃と低温で
行うか、又は低温から高温まで段階的に行うことが望ま
しい。すなわち、高温で熱処理すると未反応物などが飛
散し、充分な架橋構造が得られないが、低温で充分反応
させることにより、フェノール樹脂の架橋反応完結し、
熱に対し安定した構造となる。The base material includes metal fibers such as iron, copper and brass and asbestos fibers, ceramic fibers, glass fibers, wollastonite, inorganic fibers such as artificial mineral fibers, polyimide fibers, polyamide fibers and phenol fibers. There are organic fibers. Metal fibers are desirable among these substrates. Further, asbestos fibers cannot be used as other base materials due to the occurrence of pollution, but conventionally used base materials such as inorganic fibers or organic fibers can be used in combination. Further, as the metal fibers, copper fibers and brass fibers which do not cause a problem of rust are desirable. Also, conventionally used inorganic additives such as silica and other lubricants, graphite, antimony trisulfide, molybdenum disulfide and other lubricants, and organic additives such as cache resins can be used alone or in combination. The above composition is uniformly mixed with a Nauta mixer or the like to obtain a molding powder. Molding temperature 130 ℃ to 1
Molding is performed for a predetermined time at 60 ° C. and a molding pressure of 39.4 MPa to 58.8 MPa to obtain a molded product. This molded product at 160 ° C
Heat treatment is performed at a temperature of ˜220 ° C. for a predetermined time, and if necessary, scorch treatment is further performed at a temperature of 400 ° C. or higher.
In the present invention, these production methods are not particularly limited to the above-mentioned methods, but it is desirable to perform the heat treatment at a low temperature of 180 ° C. or to perform the heat treatment stepwise from a low temperature to a high temperature. That is, when heat-treated at a high temperature, unreacted substances and the like scatter, and a sufficient crosslinked structure cannot be obtained, but by sufficiently reacting at a low temperature, the crosslinking reaction of the phenol resin is completed,
The structure is stable against heat.
【0008】[0008]
【実施例】以下本発明の実施例を説明するが、本発明は
これに限定されるものではない。高オルト率ノボラック
型フェノール樹脂、アクリロニトリル結合量39%のN
BRを用い、ナウタミキサを用い、表1に示す組成の配
合物を均一に混合し、この混合物を160℃、39.2
MPaの条件下で成形用金型を用いて10分間成形し、
次いで180℃で4時間アフターベーキングして摩擦材
を作り、これらの鳴き特性を調べた。EXAMPLES Examples of the present invention will be described below, but the present invention is not limited thereto. High ortho novolak type phenol resin, N with acrylonitrile bond content of 39%
Using a BR and a Nauta mixer, the formulations having the compositions shown in Table 1 were uniformly mixed, and the mixture was heated at 160 ° C. for 39.2.
Molding for 10 minutes using a molding die under the condition of MPa,
Then, after-baking was performed at 180 ° C. for 4 hours to prepare a friction material, and the squeaking characteristics of these materials were investigated.
【0009】[0009]
【比較例】高オルト率ノボラック型フェノール樹脂、結
合アクリロニトリル量39%のNBRを用い、ナウタミ
キサを用い、表1に示す組成の配合物を実施例と同様な
方法で摩擦材を作製した。これらの摩擦材の鳴き特性を
表1に示す。COMPARATIVE EXAMPLE A friction material was prepared in the same manner as in the examples using the compound having the composition shown in Table 1 using a high ortho novolak type phenol resin, NBR having a bound acrylonitrile content of 39% and a Nauta mixer. The squealing characteristics of these friction materials are shown in Table 1.
【0010】本発明の実施例の摩擦材は、熱的に安定し
ているため鳴き特性に優れており、鳴きが発生しないこ
とが分かる。It can be seen that the friction materials of the examples of the present invention have excellent squealing characteristics because they are thermally stable, and no squealing occurs.
【0011】[0011]
【表1】 [Table 1]
【0012】[0012]
【発明の効果】本発明により、鳴きが発生しない摩擦材
用樹脂組成物が提供できる。According to the present invention, it is possible to provide a resin composition for a friction material which does not cause squeal.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 // C08J 5/10 CFB 7188−4F (C08L 9/02 61:00) (72)発明者 馬場 日男 茨城県下館市大字小川1500番地 日立化成 工業株式会社下館研究所内 (72)発明者 栗田 高明 茨城県下館市大字小川1500番地 日立化成 工業株式会社下館研究所内─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification number Office reference number FI technical display location // C08J 5/10 CFB 7188-4F (C08L 9/02 61:00) (72) Inventor Baba Hio, 1500 Ogawa, Shimodate, Ibaraki Prefecture, Shimodate Research Laboratory, Hitachi Chemical Co., Ltd. (72) Inventor Takaaki Kurita 1500, Ogawa, Shimodate City, Shimodate, Ibaraki Hitachi Shiseido Research Laboratory, Hitachi Chemical Co., Ltd.
Claims (3)
脂、(b)結合アクリロニトリル量35%以上のNB
R、(c)金属繊維を含み、(a)/(b)が重量比で
2乃至5で、(c)が20重量%以上からなる摩擦材用
樹脂組成物において、さらに周期率表IIa族元素の
(d)塩化物を含み、(d)が(a)に対し2重量%乃
至15重量%であることを特徴とする摩擦材用樹脂組成
物。1. An NB having (a) a phenol resin and (b) a bound acrylonitrile amount of 35% or more as essential components.
A resin composition for a friction material comprising R, (c) metal fibers, (a) / (b) in a weight ratio of 2 to 5, and (c) in an amount of 20% by weight or more, further comprising a periodic table IIa group. A resin composition for a friction material comprising (d) chloride of the element, wherein (d) is 2 wt% to 15 wt% with respect to (a).
60%以上で、かつ未反応フェノール量が3重量%以下
の高オルトノボラック型フェノール樹脂であることを特
徴とする摩擦材用樹脂組成物。2. A resin composition for a friction material, wherein the phenol resin according to claim 1 is a high ortho novolac type phenol resin having an ortho ratio of 60% or more and an unreacted phenol amount of 3% by weight or less. ..
維の単独、又は混合物であることを特徴とする摩擦材用
樹脂組成物。3. A resin composition for a friction material, wherein the metal fiber of claim 1 is a brass fiber or a copper fiber alone or as a mixture.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13125892A JPH05320372A (en) | 1992-05-25 | 1992-05-25 | Resin composition for frictional material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13125892A JPH05320372A (en) | 1992-05-25 | 1992-05-25 | Resin composition for frictional material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH05320372A true JPH05320372A (en) | 1993-12-03 |
Family
ID=15053717
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13125892A Pending JPH05320372A (en) | 1992-05-25 | 1992-05-25 | Resin composition for frictional material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH05320372A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6596789B2 (en) * | 1998-08-26 | 2003-07-22 | Nisshinbo Industries, Inc. | Non-asbestos friction materials |
-
1992
- 1992-05-25 JP JP13125892A patent/JPH05320372A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6596789B2 (en) * | 1998-08-26 | 2003-07-22 | Nisshinbo Industries, Inc. | Non-asbestos friction materials |
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