JPH08200411A - Brake piston - Google Patents
Brake pistonInfo
- Publication number
- JPH08200411A JPH08200411A JP7125431A JP12543195A JPH08200411A JP H08200411 A JPH08200411 A JP H08200411A JP 7125431 A JP7125431 A JP 7125431A JP 12543195 A JP12543195 A JP 12543195A JP H08200411 A JPH08200411 A JP H08200411A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- phenol resin
- brake piston
- brake
- 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.)
- Granted
Links
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D65/00—Parts or details
- F16D65/14—Actuating mechanisms for brakes; Means for initiating operation at a predetermined position
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D2125/00—Components of actuators
- F16D2125/02—Fluid-pressure mechanisms
- F16D2125/06—Pistons
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Braking Arrangements (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】
【構成】 フェノール樹脂、及び充填材として硅灰石、
ガラス繊維及び焼成クレーを含有するフェノール樹脂組
成物を成形してなるブレーキピストンであり、フェノー
ル樹脂の硬化触媒としてサリチル酸等の酸触媒を用いる
ことが好ましい。
【効果】 機械的強度、耐摩耗性及び耐ブレーキ液性に
優れ、且つ軽量であり、硬化触媒として酸触媒を用いる
と耐ブレーキ液性が一層向上する。(57) [Summary] [Structure] Phenolic resin and silica stone as filler
It is a brake piston formed by molding a phenol resin composition containing glass fiber and calcined clay, and it is preferable to use an acid catalyst such as salicylic acid as a curing catalyst for the phenol resin. [Effect] It is excellent in mechanical strength, abrasion resistance and brake fluid resistance and is lightweight, and when an acid catalyst is used as a curing catalyst, the brake fluid resistance is further improved.
Description
【0001】[0001]
【産業上の利用分野】本発明は、耐摩耗性、耐ブレーキ
液性及び耐熱性に優れたフェノール樹脂製ディスクブレ
ーキ用ブレーキピストンに関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a brake piston for a disc brake made of a phenol resin, which has excellent wear resistance, brake fluid resistance and heat resistance.
【0002】[0002]
【従来の技術】従来、ディスクブレーキ用ブレーキピス
トンはその使用環境から耐熱性、耐摩耗性、耐ブレーキ
液性、機械的強度等が要求される。これらの特性を満た
すため、セラミックや金属製のブレーキピストンが用い
られていた。また、懸かる特性からプラスチック材料で
はフェノール樹脂成形材料が用いられている。セラミッ
クや金属製のブレーキピストンは、固体の重量が重い、
加工に時間がかかる、コストが高い等の問題がある。こ
れに対し、フェノール樹脂成形材料では耐熱性、機械的
強度も良く成形品も安易に得られることからそのメリッ
トは非常に高い。しかし、このような特性を付与するた
め、従来は配合基材としてガラス繊維やシリカ等を配合
していた。この場合、機械的強度、耐熱性は向上するも
ののコストが高くなる上に、耐摩耗性が著しく低下す
る。2. Description of the Related Art Conventionally, brake pistons for disc brakes are required to have heat resistance, wear resistance, brake fluid resistance, mechanical strength, etc., depending on the environment in which they are used. In order to satisfy these characteristics, a brake piston made of ceramic or metal has been used. In addition, a phenolic resin molding material is used as a plastic material because of its outstanding characteristics. Brake pistons made of ceramic or metal have a heavy solid weight,
There are problems such as long processing time and high cost. On the other hand, the phenol resin molding material has excellent heat resistance and mechanical strength, and a molded product can be easily obtained, so that its merit is very high. However, in order to impart such characteristics, glass fibers, silica and the like have been conventionally compounded as compounding base materials. In this case, although the mechanical strength and heat resistance are improved, the cost is increased and the wear resistance is significantly reduced.
【0003】[0003]
【発明が解決しようとする課題】本発明は、従来のディ
スクブレーキ用ブレーキピストンとして使用されていた
セラミックや金属に代わり、機械的強度、耐熱性を損な
うことなく耐摩耗性、耐ブレーキ液性に優れたフェノー
ル樹脂からなるブレーキピストンを提供するものであ
る。DISCLOSURE OF THE INVENTION The present invention replaces ceramics and metals used as conventional brake pistons for disc brakes with wear resistance and brake fluid resistance without impairing mechanical strength and heat resistance. The present invention provides a brake piston made of an excellent phenolic resin.
【0004】[0004]
【課題を解決するための手段】本発明は、フェノール樹
脂、及び充填材として硅灰石、ガラス繊維及び焼成クレ
ーを配合してなるフェノール樹脂組成物を成形してなる
ブレーキピストンに関するものである。SUMMARY OF THE INVENTION The present invention relates to a brake piston formed by molding a phenol resin composition containing phenol resin and silica stone, glass fiber and calcined clay as a filler.
【0005】フェノール樹脂はノボラック型フェノール
樹脂またはレゾール型フェノール樹脂のいずれを使用し
てもよい。場合によっては、これら2種類を併用しても
よい。また、レゾール型フェノール樹脂としてはジメチ
レンエーテル型またはメチロール型のいずれを用いても
よい。また、ノボラック型フェノール樹脂を用いた場
合、硬化剤としてヘキサメチレンテトラミンまたは上記
記載のレゾール型フェノール樹脂を併用する。As the phenol resin, either a novolac type phenol resin or a resol type phenol resin may be used. Depending on the case, these two types may be used in combination. As the resol-type phenol resin, either dimethylene ether type or methylol type may be used. When a novolac type phenol resin is used, hexamethylenetetramine or the above-mentioned resol type phenol resin is used as a curing agent.
【0006】硅灰石は粒径10μm〜300μmが好ま
しい。10μm未満では組成物の成形材料化の際作業性
が悪くなり、また300μmを越えると成形時に配向が
生じ機械的強度に異方差がでることと、寸法精度も悪く
なるため好ましくない。硅灰石はフェノール樹脂100
重量部に対し、200〜350重量部配合することが好
ましい。200重量部未満では耐摩耗性、寸法精度が低
下し耐ブレーキ液性も低下する。350重量部を越える
と材料化の際作業性が悪くなることと、成形時の流動性
が悪くなり成形が困難になるため好ましくない。The silica stone preferably has a particle size of 10 μm to 300 μm. If it is less than 10 μm, workability is deteriorated when the composition is used as a molding material, and if it exceeds 300 μm, orientation occurs during molding, resulting in anisotropic difference in mechanical strength and poor dimensional accuracy, which is not preferable. Silica stone is phenolic resin 100
It is preferable to mix 200 to 350 parts by weight with respect to parts by weight. If it is less than 200 parts by weight, abrasion resistance and dimensional accuracy are lowered, and brake fluid resistance is also lowered. If it exceeds 350 parts by weight, the workability during materialization is poor and the fluidity at the time of molding is poor, making molding difficult.
【0007】また、機械的強度を維持・向上するためガ
ラス繊維を配合する。ガラス繊維の配合量はフェノール
樹脂100重量部に対し80〜120重量部配合するの
が好ましい。80重量部未満では機械的強度が不十分と
なり、120重量部を越えるとガラス繊維の配向により
機械的強度の異方差が生じたり、耐摩耗性が低下する、
寸法精度が悪くなるといった問題が生じるため好ましく
ない。更にその繊維長は500μm〜5mmが好まし
い。500μm未満では、ガラス繊維の特徴である高強
度化の効果が小さくなるため好ましくない。5mmを越
えると、成形材料の生産性が悪くなったり、成形品中で
の配向が強くなり機械的強度に異方差が生じたり寸法精
度が悪くなるため好ましくない。Further, glass fibers are blended in order to maintain and improve the mechanical strength. The glass fiber content is preferably 80 to 120 parts by weight with respect to 100 parts by weight of the phenol resin. If it is less than 80 parts by weight, the mechanical strength will be insufficient, and if it exceeds 120 parts by weight, the mechanical strength will be anisotropic due to the orientation of the glass fibers, and the abrasion resistance will be reduced.
This is not preferable because it causes a problem that the dimensional accuracy becomes poor. Furthermore, the fiber length is preferably 500 μm to 5 mm. When it is less than 500 μm, the effect of increasing the strength, which is a characteristic of glass fiber, becomes small, which is not preferable. If it exceeds 5 mm, the productivity of the molding material is deteriorated, the orientation in the molded product is increased, the mechanical strength is anisotropic, and the dimensional accuracy is deteriorated, which is not preferable.
【0008】更に、耐ブレーキ液性、耐熱性の向上のた
めに焼成クレーを配合する。焼成クレーは、フェノール
樹脂100重量部に対して20〜100重量部配合する
ことが好ましい。20重量部未満では耐ブレーキ液性、
耐熱性に対して効果が不十分である。また、100重量
部を越えると耐摩耗性が低下することから好ましくな
い。Further, in order to improve the resistance to brake fluid and the heat resistance, calcined clay is added. It is preferable to add 20 to 100 parts by weight of the baked clay to 100 parts by weight of the phenol resin. If less than 20 parts by weight, brake fluid resistance,
The effect on heat resistance is insufficient. Further, if it exceeds 100 parts by weight, abrasion resistance is deteriorated, which is not preferable.
【0009】耐ブレーキ液性をより向上させるために、
硬化触媒として、通常のアルカリ触媒に代えて酸触媒を
用いることが好ましい。従来のフェノール樹脂製ブレー
キピストンは、硬化触媒として通常アルカリ触媒を用い
ている。この場合、ブレーキ液に侵されやすくブレーキ
ピストンとしての耐久性に問題のある場合が生じたが、
酸触媒を使用することによりこの問題を解決することが
できた。酸触媒としてイミドジスルホン酸、ベンゼンス
ルホン酸、トルエンスルホン酸、サリチル酸、シュウ
酸、酢酸、及びこれらの酸性塩等が用いられる。これら
酸触媒は、フェノール樹脂100重量部に対して3〜1
0重量部用いるのが好ましい。3重量部未満では耐ブレ
ーキ液性の向上に効果が無く、20重量部を越えると硬
化が速くなりすぎ、成形に困難が生じる。In order to further improve the brake fluid resistance,
As the curing catalyst, it is preferable to use an acid catalyst instead of the usual alkali catalyst. Conventional phenol resin brake pistons usually use an alkali catalyst as a curing catalyst. In this case, there was a case where it was easily affected by the brake fluid and there was a problem with the durability as a brake piston.
This problem could be solved by using an acid catalyst. As the acid catalyst, imidodisulfonic acid, benzenesulfonic acid, toluenesulfonic acid, salicylic acid, oxalic acid, acetic acid, and acid salts thereof are used. These acid catalysts are used in an amount of 3 to 1 with respect to 100 parts by weight of the phenol resin.
It is preferable to use 0 part by weight. If it is less than 3 parts by weight, there is no effect in improving the resistance to brake fluid, and if it exceeds 20 parts by weight, curing will be too fast and molding will be difficult.
【0010】このような、フェノール樹脂と充填材から
なる組成に、硬化触媒、滑剤、着色剤等を加え、加熱混
練することにより成形材料を得る。更にこのような方法
により得られた成形材料を射出成形、移送成形、圧縮成
形等により成形しディスクブレーキ用ブレーキピストン
を得る。A molding material is obtained by adding a curing catalyst, a lubricant, a colorant and the like to the composition composed of the phenol resin and the filler and kneading with heating. Further, the molding material obtained by such a method is molded by injection molding, transfer molding, compression molding or the like to obtain a brake piston for a disc brake.
【0011】[0011]
【作用】本発明においては、用いられる硅灰石は針状結
晶であることからガラス繊維と同様な効果により機械的
強度に優れた特性を得ることが出来るばかりでなく、ガ
ラス繊維やシリカに比べ耐摩耗性に優れている。このた
め硅灰石を多量に配合しても機械的強度を下げることな
く、耐摩耗性を損なうことがない。また焼成クレー、又
は焼成クレーと酸触媒を用いることによりブレーキ液と
のpH緩衝効果によりブレーキ液中での寸法変化、重量
変化、強度劣化を抑えることが出来る。更に機械的強度
の維持・向上のために、耐摩耗性に影響のない範囲でガ
ラス繊維を配合する。このような配合により機械的強
度、耐摩耗性、耐ブレーキ液性、耐熱性に優れたフェノ
ール樹脂組成物製のディスクブレーキ用ブレーキピスト
ンを得ることが出来る。In the present invention, since the apatite used is acicular crystals, not only it is possible to obtain excellent characteristics in mechanical strength due to the same effect as glass fiber, but it is more advantageous than glass fiber and silica. It has excellent wear resistance. Therefore, even if a large amount of silica stone is mixed, the mechanical strength is not lowered and the wear resistance is not impaired. Further, by using calcined clay, or calcined clay and an acid catalyst, it is possible to suppress dimensional changes, weight changes, and strength deterioration in the brake liquid due to the pH buffering effect of the brake liquid. Furthermore, in order to maintain and improve the mechanical strength, glass fibers are blended within a range that does not affect wear resistance. With such a compounding, it is possible to obtain a brake piston for a disc brake, which is made of a phenol resin composition and which is excellent in mechanical strength, wear resistance, brake fluid resistance and heat resistance.
【0012】[0012]
【実施例】次に本発明を実施例及び比較例に基づいて説
明する。ここで「部」は「重量部」を示す。表1に示す
材料及び配合にて、加熱ロールにより混練して、フェノ
ール樹脂成形材料を得た。EXAMPLES Next, the present invention will be explained based on Examples and Comparative Examples. Here, "part" means "part by weight". The materials and formulations shown in Table 1 were kneaded with a heating roll to obtain a phenol resin molding material.
【0013】[0013]
【表1】 (注)ノボラック樹脂 数平均分量900 レゾール樹脂 数平均分量600 硅灰石 平均粒径50μm 焼成クレー 平均粒径5μm ガラス繊維 長さ2mm、径5μm シリカ 平均粒径3μm[Table 1] (Note) Novolak resin Number average quantity 900 Resol resin Number average quantity 600 Silica stone Average particle size 50 μm Firing clay Average particle size 5 μm Glass fiber length 2 mm, Diameter 5 μm Silica average particle size 3 μm
【0014】実施例1、2、3はフェノール樹脂をそれ
ぞれノボラック型、レゾール型、ノボラック型及びレゾ
ール型を用い、従来のフィラーであるシリカ(比較例
1、2)を硅灰石に置き換えた場合である。実施例4、
5、6は、実施例1、2、3の硬化触媒をそれぞれ消石
灰(アルカリ)から酸触媒(サリチル酸)に置き換えた
場合である。比較例3、4は実施例1、4の焼成クレー
を除いた場合である。各実施例及び比較例で得られた成
形材料について、強度試験、耐ブレーキ液性、耐熱性、
摩耗試験等の評価を行った。その結果を表2に示す。In Examples 1, 2 and 3, novolac type, resol type, novolac type and resol type phenolic resins were used, respectively, and silica (comparative examples 1 and 2) as a conventional filler was replaced with silica stone. Is. Example 4,
In Nos. 5 and 6, the curing catalysts of Examples 1, 2, and 3 are replaced with slaked lime (alkali) by an acid catalyst (salicylic acid). Comparative Examples 3 and 4 are cases where the baked clay of Examples 1 and 4 was removed. For the molding materials obtained in each Example and Comparative Example, strength test, brake fluid resistance, heat resistance,
An evaluation such as a wear test was performed. The results are shown in Table 2.
【0015】[0015]
【表2】 [Table 2]
【0016】〔測定方法〕 (1)曲げ強さ:JIS K 7203による。 (2)耐ブレーキ液性:ブレーキ液中で200℃で50
0時間処理後の曲げ強さ保持率、寸法変化率、重量変化
率を測定。 (3)耐熱性:雰囲気250℃で500時間で処理後の
曲げ強さ保持率、寸法変化率、重量変化率を測定した。 (3)耐摩耗性:滑り摩耗試験による(相手材;S55
C)[Measuring Method] (1) Bending Strength: According to JIS K7203. (2) Brake fluid resistance: 50 at 200 ° C in brake fluid
Bending strength retention rate, dimensional change rate, and weight change rate after 0 hour treatment were measured. (3) Heat resistance: The bending strength retention rate, the dimensional change rate, and the weight change rate were measured after treatment at 250 ° C. for 500 hours. (3) Wear resistance: According to a sliding wear test (counterpart material; S55
C)
【0017】[0017]
【発明の効果】本発明による硅灰石、ガラス繊維、及び
焼成クレーを用いたフェノール樹脂組成物を成形して得
られたブレーキピストンは、機械的強度、耐摩耗性及び
耐ブレーキ液性に優れ、且つ軽量である。特に、硬化触
媒として酸触媒を用いると、耐ブレーキ液性が一層向上
したブレーキピストンを得ることができる。The brake piston obtained by molding the phenol resin composition using silica stone, glass fiber and calcined clay according to the present invention is excellent in mechanical strength, wear resistance and brake fluid resistance. It is also lightweight. In particular, when an acid catalyst is used as the curing catalyst, a brake piston with further improved brake fluid resistance can be obtained.
Claims (5)
石、ガラス繊維及び焼成クレーを含有するフェノール樹
脂組成物を成形してなることを特徴とするブレーキピス
トン。1. A brake piston formed by molding a phenol resin composition containing a phenol resin and silica stone, glass fiber and calcined clay as a filler.
100重量部に対して3〜20重量部用いてなる請求項
1記載のブレーキピストン。2. The brake piston according to claim 1, wherein an acid catalyst is used as a curing catalyst in an amount of 3 to 20 parts by weight based on 100 parts by weight of the phenol resin.
部に対して200〜350重量部含有してなる請求項1
又は2記載のブレーキピストン。3. The silica stone is contained in an amount of 200 to 350 parts by weight with respect to 100 parts by weight of a phenol resin.
Or the brake piston according to 2.
重量部に対して80〜120重量部含有してなる請求項
1又は2記載のブレーキピストン。4. The phenolic resin 100 is used as the glass fiber.
The brake piston according to claim 1 or 2, comprising 80 to 120 parts by weight with respect to parts by weight.
重量部に対して20〜100重量部含有してなる請求項
1又は2記載のブレーキピストン。5. The phenolic resin 100 is used as the baked clay.
The brake piston according to claim 1 or 2, which is contained in an amount of 20 to 100 parts by weight with respect to parts by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7125431A JP3032136B2 (en) | 1994-11-22 | 1995-05-24 | Brake piston |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28844294 | 1994-11-22 | ||
| JP6-288442 | 1994-11-22 | ||
| JP7125431A JP3032136B2 (en) | 1994-11-22 | 1995-05-24 | Brake piston |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP31886895A Division JP3121751B2 (en) | 1995-12-07 | 1995-12-07 | Phenolic resin molding material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH08200411A true JPH08200411A (en) | 1996-08-06 |
| JP3032136B2 JP3032136B2 (en) | 2000-04-10 |
Family
ID=26461873
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7125431A Expired - Lifetime JP3032136B2 (en) | 1994-11-22 | 1995-05-24 | Brake piston |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3032136B2 (en) |
-
1995
- 1995-05-24 JP JP7125431A patent/JP3032136B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JP3032136B2 (en) | 2000-04-10 |
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