JPH02305884A - Seal member for oil seal and its manufacture - Google Patents
Seal member for oil seal and its manufactureInfo
- Publication number
- JPH02305884A JPH02305884A JP1126488A JP12648889A JPH02305884A JP H02305884 A JPH02305884 A JP H02305884A JP 1126488 A JP1126488 A JP 1126488A JP 12648889 A JP12648889 A JP 12648889A JP H02305884 A JPH02305884 A JP H02305884A
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- seal
- fine particles
- room temperature
- oil
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 34
- 229920000642 polymer Polymers 0.000 claims abstract description 119
- 239000010419 fine particle Substances 0.000 claims abstract description 43
- 238000007789 sealing Methods 0.000 claims abstract description 43
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 19
- 239000000463 material Substances 0.000 claims abstract description 19
- 239000007787 solid Substances 0.000 claims abstract description 15
- 238000002844 melting Methods 0.000 claims abstract description 6
- 230000008018 melting Effects 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims description 30
- 238000004073 vulcanization Methods 0.000 claims description 15
- 239000012298 atmosphere Substances 0.000 claims description 7
- 239000004793 Polystyrene Substances 0.000 abstract description 8
- 239000000203 mixture Substances 0.000 abstract description 7
- 229920002223 polystyrene Polymers 0.000 abstract description 7
- 229920000120 polyethyl acrylate Polymers 0.000 abstract description 4
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 238000004898 kneading Methods 0.000 description 36
- 238000000465 moulding Methods 0.000 description 20
- 239000000945 filler Substances 0.000 description 15
- 239000002245 particle Substances 0.000 description 12
- 229920001971 elastomer Polymers 0.000 description 11
- 239000005060 rubber Substances 0.000 description 11
- 150000002484 inorganic compounds Chemical class 0.000 description 9
- 229910010272 inorganic material Inorganic materials 0.000 description 9
- 239000004698 Polyethylene Substances 0.000 description 8
- 229920000573 polyethylene Polymers 0.000 description 8
- -1 polypropylene Polymers 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 4
- 238000001746 injection moulding Methods 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 229920002943 EPDM rubber Polymers 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 229920001973 fluoroelastomer Polymers 0.000 description 2
- 229920003049 isoprene rubber Polymers 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 101150096839 Fcmr gene Proteins 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
Landscapes
- Sealing With Elastic Sealing Lips (AREA)
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はオイルシール用シール部材およびその製造方法
に関し、特に、回転又は往復動する軸の外周に摺動して
軸の油側と大気側とをシールするオイルシール用シール
部材およびその製造方法に関するものである。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a sealing member for an oil seal and a method for manufacturing the same, and particularly to a sealing member for an oil seal that slides on the outer periphery of a rotating or reciprocating shaft and connects the oil side and the atmosphere side of the shaft. The present invention relates to a sealing member for an oil seal that seals an oil seal and a method for manufacturing the same.
〔従来技術および解決しようとする課題〕−aに、オイ
ルシールは、第3図に示すように、軸5の外側のハウジ
ング6に配設されて、回転又は往復動する軸5の外周に
摺動して軸5の油側と大気側とをシールする環状のシー
ルリップ部2を有する弾性材からなるシール部材1と、
このシール部材lのシールリップ部2に軸5への抱き締
め力を付与するばね3と、前記シール部材lに埋設され
てシール部材lを補強する金属環4とから構成されてい
る。[Prior art and problems to be solved]-a. As shown in FIG. a seal member 1 made of an elastic material and having an annular seal lip portion 2 that moves to seal the oil side and the atmosphere side of the shaft 5;
It is comprised of a spring 3 that applies a force to the seal lip portion 2 of the seal member 1 to hold it against the shaft 5, and a metal ring 4 that is embedded in the seal member 1 and reinforces the seal member 1.
そして、前記シール部材1は、従来、基材となるゴム材
1)に、充填剤12および加硫剤その他の助剤などを添
加し混練したものを加硫成形することにより製造されて
おり、オイルシールとしてのシールIIs能は、前記軸
5の外周に接触するシールリップ部2の摺動面の形態、
すなわち、その摺動面に表出する前記充填剤12の粒径
やその形状などにより左右されることが知られている。The sealing member 1 is conventionally manufactured by vulcanizing and kneading a rubber material 1) serving as a base material, adding a filler 12, a vulcanizing agent, and other auxiliary agents, and kneading the mixture. The ability of the seal IIs as an oil seal is determined by the shape of the sliding surface of the seal lip portion 2 that contacts the outer periphery of the shaft 5;
That is, it is known that it depends on the particle size and shape of the filler 12 exposed on the sliding surface.
〔中村研へ;日ゴム協誌、62゜74〜8.3(198
9)参照〕
一般に、前記充填剤12としては、偏平形状の天然の無
機化合物の微粒子が用いられているが、この無機化合物
の微粒子は、その粒径分布カ大きく、また、アスペクト
比も広い分布を持っており、このため無機化合物の微粒
子を充填剤12としてゴム剤1)中に分散配合したシー
ル部材lにあっては、そのシールリップ部2のIS動面
に表出する無機化合物の微粒子が均一な粒径およびアス
ペクト比を持っていないので、所望のシール性能を存す
るものを再現性よく加硫成形することが非常に困難であ
った。[To Nakamura Lab; Japan Rubber Association Journal, 62°74-8.3 (198
Refer to 9) Generally, flat-shaped natural inorganic compound fine particles are used as the filler 12, but these inorganic compound fine particles have a large particle size distribution and a wide aspect ratio distribution. Therefore, in a sealing member l in which fine particles of an inorganic compound are dispersed in the rubber material 1) as a filler 12, the fine particles of an inorganic compound exposed on the IS moving surface of the seal lip portion 2 are does not have a uniform particle size and aspect ratio, so it has been extremely difficult to vulcanize and mold with good reproducibility the desired sealing performance.
また、前記シール部材lを射出成形により製造する工程
は、第4図に示すように、1)+それぞれ計量したゴム
材1)と無機化合物の微粒子からなる充填剤12とをバ
ッチで混練するバッチ混練工程、(2)前記(1)の工
程で得られた混練物を冷却して加硫剤を投入してロール
で混練するロール混練工程、(3)前記(2)の工程で
得られた混練物を冷却して押出し機により押出し、帯状
の生地ゴムを得る工程、(4)前記+3)の工程で得ら
れた帯状の生地ゴムを射出成形機に入れ加硫成形する成
形工程とからなっている。As shown in FIG. 4, the step of manufacturing the sealing member l by injection molding is as follows: 1) + A batch of kneading the weighed rubber material 1) and a filler 12 made of fine particles of an inorganic compound in a batch. a kneading step, (2) a roll kneading step of cooling the kneaded material obtained in step (1) above, adding a vulcanizing agent and kneading it with a roll, (3) a step of kneading the kneaded material obtained in step (2) above. It consists of a step of cooling the kneaded material and extruding it with an extruder to obtain a band-shaped dough rubber, and (4) a molding step of putting the band-shaped dough rubber obtained in step +3 above into an injection molding machine and vulcanization molding. ing.
しかしながら、上記のようなシール部材lの製造工程に
あっては、前記(2)のロール混練工程において、人手
作業が必要になるとともに、そのロールに作業員が挟み
こまれる危険性が大きく、また、(3)の工程で製造し
た生地ゴムを次の(4)の工程の射出成形機に入れる際
に、生地ゴムの運搬、投入の作業もあって煩雑であり、
さらに、前記(2)〜(4)の工程において、ゴム材l
l中に化学的および物理的に安定化した状態で充填剤1
2を混練配合する操作は、熟練した作業員の経験とかん
とによって行われており、従来のシール部材lの製造工
程では、熟練した作fJ員の人手が多く必要であり、作
業の危険性も大きく、さらに、(1)〜(3)の工程は
約100分程度の長時間の工程であるため、その製造工
程の簡略化および短縮化が要求されているという問題点
を有していた。However, in the manufacturing process of the sealing member l as described above, manual labor is required in the roll kneading process of (2) above, and there is a large risk of workers getting caught in the rolls. , When putting the dough rubber manufactured in step (3) into the injection molding machine in the next step (4), the work of transporting and feeding the dough rubber is complicated,
Furthermore, in the steps (2) to (4), the rubber material l
Filler 1 in a chemically and physically stabilized state
The operation of kneading and blending 2 is carried out by skilled workers based on their experience and acumen.The conventional manufacturing process for sealing members requires a large number of skilled workers, and the work is dangerous. Furthermore, since steps (1) to (3) are long steps of about 100 minutes, there was a problem in that the manufacturing process needed to be simplified and shortened. .
本発明は上記のような従来のもののもつ問題点を解決し
たものであって、従来の天然の無機化合物の微粒子から
なる充填剤に代えて、室温でゴム状弾性を示すポリマー
中でミクロ分散相を形成する室温で固体のポリマーを充
填剤として用いて、その室温で固体のポリマーの微粒子
を前記ゴム状弾性を示すポリマー中に均一に分散すると
ともに、このミクロ分散相を所定の条件下で配向させる
ことにより、充填剤であるポリマーの微粒子の粒径、分
散状態およびアスペクト比などをその製造工程において
任意に制jII可能とし、混練から加硫成形まで一貫し
た製造工程で管理でき、製造工程を大幅に簡略化できる
オイルシール用シール部材およびその製造方法を提供す
ることを目的としている。The present invention solves the problems of the conventional methods as described above, and instead of the conventional filler consisting of fine particles of a natural inorganic compound, a micro-dispersed phase is used in a polymer that exhibits rubber-like elasticity at room temperature. Using a polymer that is solid at room temperature as a filler, fine particles of the polymer that is solid at room temperature are uniformly dispersed in the rubber-like elastic polymer, and this microdispersed phase is oriented under predetermined conditions. By doing so, it is possible to control the particle size, dispersion state, aspect ratio, etc. of the fine particles of the polymer that is the filler in the manufacturing process, and it is possible to control the manufacturing process from kneading to vulcanization molding in an integrated manner, making it possible to control the manufacturing process. It is an object of the present invention to provide a sealing member for an oil seal that can be greatly simplified and a method for manufacturing the same.
上記の目的を達成するために本発明のオイルシール用シ
ール部材は、回転又は往復動する軸の外周に摺動して軸
の油側と大気側とをシールするオイルシール用シール部
材であって、このオイルシール用シール部材は、室温で
固体である第1のポリマーの微粒子が、前記第1のポリ
マーと非相溶性の室温でゴム状弾性を示す第2のポリマ
ー中に、配向した状態で均一に分散されている手段を有
しており、また、本発明のオイルシール用シール部材の
製造方法は・回転又は往復動する軸の外周に摺動して軸
の油側と大気側とをシールするオイルシール用シール部
材の製造方法であって、室温で固体である第1のポリマ
ーと、この第1のポリマーと非相溶性の室温でゴム状弾
性を示す第2のポリマーとを両ポリマーの融点温度以上
で混練し、前記第1のポリマーの微粒子を第2のポリマ
ー中に均一に分散してミクロ分散相を形成した混練物を
調製し、続いて、この混練物に加硫剤を添加してさらに
混練し、次いで、この加硫剤添加混練物を成形型内で、
前記第1のポリマーの軟化点温度付近で剪断応力を作用
し、前記@2のポリマー中に均一に分散する第1のポリ
マーの微粒子を配向させた状態で加硫成形する手段を有
している。In order to achieve the above object, the seal member for an oil seal of the present invention is a seal member for an oil seal that slides on the outer periphery of a rotating or reciprocating shaft to seal the oil side and the atmosphere side of the shaft. This sealing member for an oil seal has fine particles of a first polymer that is solid at room temperature oriented in a second polymer that is incompatible with the first polymer and exhibits rubber-like elasticity at room temperature. The method of manufacturing the sealing member for an oil seal according to the present invention includes means for uniformly dispersing the oil seal, and the method for producing the sealing member for an oil seal of the present invention includes: a means for sliding on the outer periphery of a rotating or reciprocating shaft to connect the oil side and the atmospheric side of the shaft; A method for producing a sealing member for an oil seal that seals, wherein a first polymer that is solid at room temperature and a second polymer that is incompatible with the first polymer and exhibits rubber-like elasticity at room temperature are both polymers. to prepare a kneaded product in which fine particles of the first polymer are uniformly dispersed in a second polymer to form a microdispersed phase, and then a vulcanizing agent is added to this kneaded product. The vulcanizing agent is added and further kneaded, and then this vulcanizing agent-added kneaded product is placed in a mold.
The method includes means for applying shear stress near the softening point temperature of the first polymer to vulcanize and mold fine particles of the first polymer uniformly dispersed in the @2 polymer in an oriented state. .
本発明は上記の手段を採用したことにより、シール部材
は、母材となる室温でゴム状弾性を示す第2のポリマー
中に室温で固体の第1のポリマーの微粒子がほぼ均一な
粒径で、かつ、配向された状態で分散され、そのシール
部材の摺動面に表出する前記第1のポリマーの微粒子に
より、所定のシール機能を有することとなり、また、こ
のシール部材の製造に際しては、前記第2のポリマー中
における第1のポリマーの微粒子の粒径、分散状態およ
び配向状態を、その製造工程における混練時および成形
時の温度、時間、剪断応力などを1tIl′mすること
により任意に制御でき、所望のシール性能を付与するこ
とができることとなる。By adopting the above means, the present invention provides a sealing member in which fine particles of the first polymer, which is solid at room temperature, have a substantially uniform particle size in the second polymer, which is a base material and exhibits rubber-like elasticity at room temperature. , and the fine particles of the first polymer that are dispersed in an oriented state and exposed on the sliding surface of the sealing member have a predetermined sealing function, and when manufacturing this sealing member, The particle size, dispersion state, and orientation state of the fine particles of the first polymer in the second polymer can be arbitrarily adjusted by adjusting the temperature, time, shear stress, etc. during kneading and molding in the manufacturing process. This means that it is possible to control and provide desired sealing performance.
以下、図面に示す本発明の実施例について説明する。 Embodiments of the present invention shown in the drawings will be described below.
第1図には本発明のオイルシール用シール部材の製造工
程が示されていて、まず、室温で固体である第1のポリ
マーAの所定量と、室温でゴム状弾性を示す第2のポリ
マーBの所定量とをそれぞれ溶融化した状態でif!練
機の中に入れる。FIG. 1 shows the manufacturing process of the sealing member for an oil seal of the present invention. First, a predetermined amount of a first polymer A that is solid at room temperature and a second polymer that exhibits rubber-like elasticity at room temperature are prepared. If! in a state in which a predetermined amount of B and Put it in the kneading machine.
そして、上記の第1および第2のポリマーA1Bを、両
ポリマーA、Bの融点温度以上で車軸または2軸の混’
amで混練する第1の混練工程により、前記第1のポリ
マーAの微粒子が第2のポリマーB中に均一に分散した
ミクロ分散相を形成した混練物を調製する。Then, the first and second polymers A1B are heated to a temperature above the melting point temperature of both polymers A and B, and then
By the first kneading step of kneading with am, a kneaded product is prepared in which fine particles of the first polymer A form a microdispersed phase in which the fine particles of the first polymer A are uniformly dispersed in the second polymer B.
次いで、この第1の混練工程でU4i1シた混練物を所
定温度に降温した後、加硫剤を添加し、第2の混練工程
により混練する。Next, after the temperature of the kneaded product obtained by U4i1 in this first kneading step is lowered to a predetermined temperature, a vulcanizing agent is added and kneaded in a second kneading step.
さらに、この加硫剤を添加して混練した加硫剤混練物を
、プレス成形機、射出成形機などの成形機に入れ、前記
第1のポリマーAの軟化点温度付近に加熱した状態で剪
断応力を作用し、前記第2のポリマーB中に分散したミ
クロ分散相である第1のポリマーAの微粒子を配向させ
、その状態で加硫成形する。Furthermore, the vulcanizing agent kneaded product obtained by adding and kneading this vulcanizing agent is put into a molding machine such as a press molding machine or an injection molding machine, and sheared while being heated to around the softening point temperature of the first polymer A. Stress is applied to orient the fine particles of the first polymer A, which is a microdispersed phase dispersed in the second polymer B, and vulcanization molding is performed in this state.
上記の第1の混練工程から加硫成形工程の前までの時間
は、20〜30分程度である。The time from the first kneading step to before the vulcanization molding step is about 20 to 30 minutes.
上記の室温で固体の第1のポリマーAおよび室温でゴム
状弾性を示す第2のポリマーBは、それぞれ複数のポリ
マーからなってもよい。The first polymer A that is solid at room temperature and the second polymer B that exhibits rubber-like elasticity at room temperature may each be composed of a plurality of polymers.
前記第1のポリマー八と第2のポリマーBの組合せの例
としては、第1のポリマー八としてのポリスチレン(P
S)と第2のポリマーBとしてのポリエチルアクリレ
ート (PEA) 、第1のポリマーAとしてのポリプ
ロピレン(PP)と第2のポリマーBとしてのエチレン
−プロピレンゴム(EPDM)、第1のポリマーAとし
てのポリスチレン(P S)と第2のポリマーBとして
のポリジメチルシロキサン(PDMS)、第1のポリマ
=Aとしてのポリエチレン(PE)と第2のポリマーB
としてのイソプレンゴム(IR)またはブタジェンゴム
(BR)、第1のポリマーAとしてのポリエチレン(P
E) と第2のポリマーBとしてのエチレン−プロ
ピレンゴム(EPDM)、第1のポリマーAとしてのフ
ッ素ゴムとポリスチレンとの混合物と第2のポリマーB
としてのポリエチレン(PE)などが代表的なものとし
て挙げられる。As an example of the combination of the first polymer 8 and the second polymer B, polystyrene (P
S) and polyethyl acrylate (PEA) as the second polymer B, polypropylene (PP) as the first polymer A and ethylene-propylene rubber (EPDM) as the second polymer B, as the first polymer A polystyrene (PS) and polydimethylsiloxane (PDMS) as the second polymer B, polyethylene (PE) as the first polymer = A and second polymer B
isoprene rubber (IR) or butadiene rubber (BR) as first polymer A, polyethylene (P
E) and ethylene-propylene rubber (EPDM) as the second polymer B, a mixture of fluororubber and polystyrene as the first polymer A, and the second polymer B
Typical examples include polyethylene (PE).
また、上記の第1ポリマー八と第2のポリマーBとの混
合割合は、前記第2のポリマーB中に第1のポリマーA
の微粒子が相分離した状態で分散配合されてミクロ分散
相を形成する範囲であればいずれの割合でもよいが、両
ポリマーA、Bの合計量に対して第2のポリマーBの割
合が60重量部以上であり、好ましくは70!I!量部
以上であり、さらに好ましくは70〜85重量部である
。In addition, the mixing ratio of the first polymer 8 and the second polymer B is such that the first polymer A is in the second polymer B.
Any ratio may be used as long as the fine particles are dispersed and blended in a phase-separated state to form a micro-dispersed phase, but the ratio of the second polymer B to the total amount of both polymers A and B is 60% by weight. or more, preferably 70! I! The amount is at least 70 parts by weight, more preferably 70 to 85 parts by weight.
前記第1の混練工程における混練温度および剪断応力は
、第1のポリマーAと第2のポリマーBのそれぞれの溶
融状態における固有粘度お、よび目的とする第1のポリ
マーAの微粒子の粒径などを考慮して適宜の条件を選択
することができる。The kneading temperature and shear stress in the first kneading step are determined based on the intrinsic viscosity of each of the first polymer A and the second polymer B in their molten state, the target particle size of the first polymer A fine particles, etc. Appropriate conditions can be selected taking into consideration.
前記第1の混練工程の後、加硫剤を添加する前に混練物
・を所定温度に降温するが、この時の温度は混練物中の
第1のポリマーへの微粒子の分散状態が安定に保持され
るとともに、加硫剤を混練配合が可能な温度であり、降
温の方法は、前記第1のポリマーAの微粒子の凝集がお
きないように、徐々に降温するより短時間で降温するこ
とが好ましい。After the first kneading step, the temperature of the kneaded product is lowered to a predetermined temperature before adding the vulcanizing agent, and the temperature at this time is such that the state of dispersion of the fine particles in the first polymer in the kneaded product is stable. The temperature is maintained at a temperature at which the vulcanizing agent can be kneaded and blended, and the method of lowering the temperature is to lower the temperature in a short period of time rather than gradually lowering the temperature to prevent agglomeration of the fine particles of the first polymer A. is preferred.
したがって、加硫剤を添加した後の第2の混練工程にお
ける混練温度および剪断応力は、加硫剤を混練配合する
とともに、第1のポリマーAの微粒子の分散状態が保持
される範囲で適宜の条件を選択することができる。Therefore, the kneading temperature and shear stress in the second kneading step after adding the vulcanizing agent are determined as appropriate within the range where the vulcanizing agent is kneaded and the fine particles of the first polymer A are maintained in a dispersed state. Conditions can be selected.
前記加硫成形工程においては、前記第1のポリマーAの
軟化点温度付近に加熱した状態で加硫剤添加混練物に剪
断応力を作用するが、この時の剪断応力の大きさは、前
記第2のポリマーB中の第1のポリマーAの微粒子を配
向させる大きさであればよく、目的とする配向の程度に
応じて、温度などを考慮して適宜の大きさの剪断応力を
選択することができ、具体的な剪断応力を作用させる手
段としては、二輪または車軸押し出し成形機などを用い
て、成形機内に加硫剤In W物を装填する際の押出し
圧などによっても配向させることができ、また、シール
リップ部2の摺動面を形成する成形機内の部分を回転可
能としてその回転力により剪断応力を作用させてもよい
。In the vulcanization molding step, shear stress is applied to the vulcanizing agent-added kneaded product while it is heated to around the softening point temperature of the first polymer A, and the magnitude of the shear stress at this time is equal to It is sufficient that the shear stress has a size that orients the fine particles of the first polymer A in the polymer B of No. 2, and an appropriate size of shear stress should be selected depending on the desired degree of orientation and taking into account temperature, etc. As a specific means for applying shear stress, orientation can also be achieved by using a two-wheel or axle extrusion molding machine, and applying extrusion pressure when loading the vulcanizing agent InW into the molding machine. Alternatively, the portion within the molding machine that forms the sliding surface of the seal lip portion 2 may be made rotatable, and the shearing stress may be applied by the rotational force.
上記の工程で製造される本発明によるオイルシール用シ
ール部材にあっては、第1の混練工程で、母材となる室
温でゴム状弾性を示す第2のポリマーB中に室温で固体
の第1のポリマーAの微粒子が、第2図+alに示すよ
うに、ミクロ分散相としてほぼ均一な粒径で均一に分散
されており、次の第2の混練工程ではその状態が保持さ
れ、次いで、最後の加硫成形工程で前記第1のポリマー
Aの微粒子が変形して配向する剪断応力が作用して、第
2図山)に示すように、第1のポリマーAの微粒子が偏
平な一定のアスペクト比を有した状態となり、その状態
で加硫成形されるものであり、得られた本発明によるシ
ール部材lの摺動面には、第1のポリマーへの微粒子が
第2のポリマーB中に偏平に変形して配向された状態で
均一に分散しており、軸5の外周に摺動する際に所定の
安定したシール機能を有することとなる。In the sealing member for an oil seal according to the present invention manufactured by the above steps, in the first kneading step, the second polymer B, which is a base material and exhibits rubber-like elasticity at room temperature, is mixed with a polymer that is solid at room temperature. As shown in Fig. 2+al, the fine particles of Polymer A of No. 1 are uniformly dispersed as a microdispersed phase with a substantially uniform particle size, and this state is maintained in the next second kneading step, and then, In the final vulcanization molding step, shear stress that deforms and orients the fine particles of the first polymer A acts, causing the fine particles of the first polymer A to form flat, uniform shapes, as shown in Figure 2. In this state, the sliding surface of the obtained sealing member l according to the present invention has fine particles in the first polymer in the second polymer B. They are uniformly dispersed in a flatly deformed and oriented state, and have a predetermined and stable sealing function when sliding on the outer periphery of the shaft 5.
また、本発明のオイルシール用シール部材の製造方法に
あっては、従来の天然の無機化合物の微粒子を充填剤と
して含存したオイルシール用シール部材に比べて、オイ
ルシール用シール部材としてのシール性能を左右する充
填剤である第1のポリマーAの微粒子の粒径、分散状態
およびアスペクト比を、混練工程における温度、剪断応
力の大きさ、混練時間および加硫成形工程における剪断
応力の大きさなどを変化させることで確実に制御するこ
とができるので、熟練作業員の経験′やかんなどの不確
定要素がなく、品質が一定で安定したシール性能を有す
るシール部材を安定的に供給することができることとな
る。In addition, in the method of manufacturing a sealing member for an oil seal of the present invention, compared to a conventional sealing member for an oil seal containing fine particles of a natural inorganic compound as a filler, the sealing member as a sealing member for an oil seal is The particle size, dispersion state, and aspect ratio of the fine particles of the first polymer A, which is a filler that affects performance, are determined by the temperature in the kneading process, the magnitude of shear stress, the kneading time, and the magnitude of shear stress in the vulcanization molding process. Since it can be reliably controlled by changing the factors such as the experience of experienced workers, there are no uncertain factors such as kettle, etc., and it is possible to stably supply sealing members with constant quality and stable sealing performance. It becomes possible.
さらに、本発明のオイルシール用シール部材の製造工程
は、ロール状の混練物を人手によって運搬したり、成形
機中に搬入などの操作をする必要がなく、工程の無駄な
時間を省略でき、簡略化できるとともに、ロール混練時
におけるローラーによるまきこみゃ挟み込みの危険性が
ないので工程の安全性を向上でき、混練から加硫成形ま
で一貫した製造ラインで製造できるので、その製造工程
をロボットの導入などによる無人化が容易で、工程の大
幅な簡略化が可能となり、さらに、上記の第1の混練工
程から加硫成形工程の前までの時間は、20〜30分程
度であり、従来の製造工程に比べて大幅な工程短縮化が
可能である。Furthermore, the manufacturing process of the sealing member for oil seals of the present invention does not require operations such as manually transporting the roll-shaped kneaded material or carrying it into the molding machine, and wasteful time in the process can be omitted. Not only can it be simplified, but the safety of the process can be improved as there is no risk of the makikomya being caught between the rollers during roll kneading, and the process can be manufactured using an integrated production line from kneading to vulcanization molding, so it is possible to introduce robots into the manufacturing process. It is easy to unattend the manufacturing process, and the process can be greatly simplified. Furthermore, the time from the first kneading process to the vulcanization molding process is about 20 to 30 minutes, compared to conventional manufacturing. It is possible to significantly shorten the process compared to other processes.
また、前記第1のポリマーAとして、たとえば、低温特
性の良好な樹脂材料と耐摩耗特性の良好な樹脂材料との
2種類を混合したものを用いることにより、両特性にす
ぐれたシール部材を得ることも可能となる。Furthermore, by using, for example, a mixture of two types of resin materials, ie, a resin material with good low-temperature properties and a resin material with good wear resistance properties, as the first polymer A, a sealing member excellent in both properties can be obtained. It also becomes possible.
以下、実験例により本発明をさらに具体的に説明する。The present invention will be explained in more detail below using experimental examples.
実験例
前記第1のポリマーAとして、平均分子量?、75X1
0’の単分散ポリスチレン(融点約200℃、軟化点約
180℃) (東ソ社製)を20重■部と、第2のポリ
マーBとして、平均分子fit1.0XIO”の架橋サ
イトなしのポリエチルアクリレート(融点約1)0℃)
(日本メタトロン社製)を80重全部とを窒素雰囲気
下、200℃でそれぞれ溶融し、インターナルミキサー
にいれ、4Qrpmで約10分間、混練温度200℃で
混練した。(前記第1および第2のポリマーの総量はイ
ンターナルミキサーの容量の80%で行った。)
得られた混練物における第1のポリマーへの微粒子の粒
径は、光学顕微鏡観察により8〜20μmの範囲であり
、非相溶状態で前記第2のポリマーB中に第1のポリマ
ーAの微粒子がミクロ相分離構造を有していることを確
認した。Experimental example As the first polymer A, the average molecular weight? , 75X1
0' monodispersed polystyrene (melting point: about 200°C, softening point: about 180°C) (manufactured by Toso Corporation) and 20 parts by weight of the second polymer B, a polystyrene with an average molecular fit of 1.0XIO'' without crosslinking sites was prepared. Ethyl acrylate (melting point approx. 1) 0℃)
(manufactured by Nippon Metatron Co., Ltd.) and all 80 weights were melted at 200° C. under a nitrogen atmosphere, put into an internal mixer, and kneaded at 4 Q rpm for about 10 minutes at a kneading temperature of 200° C. (The total amount of the first and second polymers was 80% of the capacity of the internal mixer.) The particle size of the fine particles added to the first polymer in the obtained kneaded product was determined to be 8 to 20 μm by observation with an optical microscope. It was confirmed that the fine particles of the first polymer A had a microphase-separated structure in the second polymer B in an incompatible state.
次に、前記の混練物を100℃に降温した後、この混練
物に、加硫剤および加硫促進剤として、イオウ0.3重
量部、ステアリン酸ナトリウム0.5重量部、ステアリ
ン酸カリウム0.5重置部を添加し、100℃で10分
間混練した。Next, after the temperature of the kneaded product was lowered to 100°C, 0.3 parts by weight of sulfur, 0.5 parts by weight of sodium stearate, and 0 parts by weight of potassium stearate were added to the kneaded product as a vulcanizing agent and a vulcanization accelerator. .5 overlapping parts were added and kneaded at 100°C for 10 minutes.
次に、上記の加硫剤添加混練物を二軸またはJ4i軸押
し出し成形機に入れ、この二軸または車軸押し出し成形
機により、0.7kg/m以上(トルク値で)、好まし
くは0.7〜1.2kg/mの剪断応力を作用した後、
180℃で5分間加硫成形した。Next, the above-mentioned vulcanizing agent-added kneaded product is put into a twin-screw or J4i-shaft extrusion molding machine, and by this twin-screw or axle-shaft extrusion molding machine, the kneaded product with the addition of a vulcanizing agent is produced at a rate of 0.7 kg/m or more (in terms of torque value), preferably 0.7 kg/m or more. After applying a shear stress of ~1.2 kg/m,
Vulcanization molding was performed at 180°C for 5 minutes.
上記で得られた加硫成形物であるオイルシール用シール
部材1のシールリップ部2の断面および摺動面は、第2
図色)に示したように、室温でゴム状弾性を示す第2の
ポリマーB中に、室温で固体の第1のポリマーAの微粒
子が配向された状態で均一に分散されていた。The cross section and sliding surface of the seal lip portion 2 of the oil seal sealing member 1, which is the vulcanized product obtained above, are
As shown in Figure (color), fine particles of the first polymer A, which is solid at room temperature, were uniformly dispersed in an oriented state in the second polymer B, which exhibits rubber-like elasticity at room temperature.
本発明は上記のように構成したので、従来の天然の無機
化合物の微粒子を充填剤として含有したオイルシール用
シール部材に比べて、本発明のシール部材の摺動面には
、充填剤となる第1のポリマーの微粒子がほぼ均一な粒
径で分散され、かつ、配向された状態であるので、安定
したシール4!S1能を有するものであり、また、この
オイルシール用シール部材のシール性能を左右する充填
剤である第1のポリマーの微粒子の粒径、分散状態およ
びアスペクト比を、混練工程における温度、剪断応力の
大きさ、混練時間および加硫成形工程における剪断応力
などを変化することで確実に制御することができるので
、熟練作業員の経験やかんなどの不確定要素がなく、品
質が一定で安定したシール性能を有するシール部材を安
定的に供給することができるものであり、さらに、ロー
ル状のa練物を人手によって運搬したり、成形機中に搬
入などの扼作をする必要力λなくて工程の無駄な時間を
省略できて前略化できるとともに、ロール混練時におけ
るローラーによるまきこみゃ挟み込みなどの危険性がな
いので工程の安全性を向上できる。Since the present invention is configured as described above, the sliding surface of the seal member of the present invention contains a filler, compared to a conventional seal member for an oil seal containing fine particles of a natural inorganic compound as a filler. Since the fine particles of the first polymer are dispersed with a substantially uniform particle size and in an oriented state, a stable seal 4! The particle size, dispersion state, and aspect ratio of the first polymer fine particles, which have S1 properties and are the filler that influences the sealing performance of this oil seal sealing member, are controlled by the temperature and shear stress in the kneading process. It can be reliably controlled by changing the size, kneading time, and shear stress in the vulcanization process, so there are no uncertainties such as the experience of skilled workers, and a stable seal with constant quality can be achieved. It is possible to stably supply a sealing member with high performance, and furthermore, there is no need to manually transport the roll-shaped a mixture or carry it into the molding machine, which reduces the process time. Wasted time can be omitted and the process can be simplified, and the safety of the process can be improved since there is no danger of the makikomya being caught by the rollers during roll kneading.
また、混練から加硫成形まで一貫した製造ラインで製造
できるので、その製造工程はロボ−/ )の導入などに
よる無人化が容易で、工程の大幅な筒略化が可能となり
・さらに・従来の製造工程に比べて大幅な工程短縮化が
可能であるなどのすぐれた効果を有するものである。In addition, since it can be manufactured on an integrated production line from kneading to vulcanization molding, the manufacturing process can be easily automated by introducing robots/ ), making it possible to significantly simplify the process. It has excellent effects such as being able to significantly shorten the manufacturing process compared to the manufacturing process.
第1図は本発明のオイルシール用シール部材の製造工程
を示す工程説明図、第2図は本発明の方法により製造し
たオイルシール用シール部材の断面を光学顕微鏡で見た
模式図、第3図は−IWのオイルシールの構造を説明す
る図、第4図は従来のオイルシール用シール部材の製造
工程を説明する工程説明図である。
1・・・・・・シール部材
2・・・・・・シールリップ部
3・・・・・・ばね
4・・・・・・金属環
5・・・・・・軸
6・・・・・・ハウジング
A・・・・・・mlのポリマー
B・・・・・・第2のポリマー
1)・・・・・・ゴム材
12・・・・・・充填材(無機化合物)特 許 出
願 人
第1図
6智
第2図
(b)
琶こ勾方勤−
手続補正書(膀
■、事件の表示 平成 1年特許願 第12
6488号2、発明の名称 オイルシール用
シール部材およびその製造方法3、補正をする者
羽生との関係 特許出願人 。
住所 東京都港区芝大門1丁目12番15号
氏名 (名称) 株式会社エヌ・オー・ケー綜合技術
研究所4、代理人 ■1021鯨262−4761
)住所 東京都千代田区九段南3丁目8番
13号5、補正命令の日付 自発
7、補正の内容
(1)明細書の「特許請求の範囲」を男1賑の1lll
り補正する。
(2)同書第7頁第3行目の「状態で均一に分散」を[
4だ片で分ti!t、、Jと補正する。
(3)同書同頁第2行目の「中に均一に」を「中に」と
補正する。
(4) 同書同頁第2行目の「中に均一に」を「中に
」と補正する。
(5)同書第1)頁第1行目の「フン素ゴムとポリスチ
レンとの混合物」を「ポリスチレンまたはポリエチレン
」と補正する。
(6) 同書同頁第2行目の「ポリエチレン(PE)
Jを「フッ素ゴム」と補正する。
(7)同書第16頁第6行目の「架橋サイトなしの」を
「架橋サイトを有する」と補正する。
(8) 同書同頁第2行目〜第7行目の「ポリエチル
アクリレート」の後にr (PA401)Jを加入する
。
(9)同書第17頁第6行目〜第8行目のro、7に、
g/m以上〜0.7〜1.2kg/mlを「回転数14
Orpmで総エネルギーが300MJ/m’ Jと補正
する。
8、添付書類の目録
fl)別紙 ・・・・・・1通別紙
特許請求の範囲
(1) 回転又は往復動する軸(5)の外周に摺動し
て軸(5)の油側と大気側とをシールするオイルシール
用シール部材(1)であって、このオイルシール用シー
ル部材(1)は、室温で固体である第1のポリマー(A
)の微粒子が、前記第1のポリマー(A)と非相溶性の
室温でゴム状弾性を示す第2のポリマー(B)中に、配
向した状態で分散されていることを特徴とするオイルシ
ール用シール部材。
(2) 回転又は往復動する軸(5)の外周に摺動し
て軸(5)の油側と大気側とをシールするオイルシール
用シール部材(1)の製造方法であって、室温で固体で
ある第1のポリマー(A)と、この第1のポリマー(A
)と非相溶性の室温でゴム状弾性を示す第2のポリマ
ー(B)とを両ポリマー(A)、(B)の融点温度以上
で混練し、前記第1のポリマー(A>の微粒子を第2の
ポリマー(B)中に分散してミクロ分散相を形成した混
練物を調製し、続いて、この混練物に加硫剤を添加して
さらに混練し、次いで、この加硫剤添加混練物を成形型
内で、前記第1のポリマー(A)の軟化点温度付近で剪
断応力を作用し、前記第2のポリマー(B)中に分散す
る第1のポリマー(A)の微粒子を配向させた状態で加
硫成形することを特徴とするオイルシール用シール部材
の製造方法。FIG. 1 is a process explanatory diagram showing the manufacturing process of the sealing member for an oil seal of the present invention, FIG. The figure is a diagram illustrating the structure of the -IW oil seal, and FIG. 4 is a process explanatory diagram illustrating the manufacturing process of a conventional sealing member for an oil seal. 1... Seal member 2... Seal lip portion 3... Spring 4... Metal ring 5... Shaft 6...・Housing A...ml Polymer B...Second polymer 1)...Rubber material 12...Filler (inorganic compound) Patent application Figure 1, Figure 6, Figure 2 (b) Tsutomu Wako Magakata - Procedural amendment (bladder ■, case description, 1999 patent application No. 12)
6488 No. 2, Title of the invention Seal member for oil seals and method for manufacturing the same 3, Relationship with Amendr Hanyu Patent applicant. Address 1-12-15 Shiba Daimon, Minato-ku, Tokyo Name N.O.K. Research Institute of Technology 4, Agent ■1021 Kujira 262-4761
)Address: 8-13-5 Kudanminami 3-chome, Chiyoda-ku, Tokyo Date of amendment order Voluntary 7 Contents of amendment (1) The scope of claims in the specification
Correct. (2) In the same book, page 7, line 3, “uniformly dispersed in the state” [
Minute ti with 4 pieces! t, , J. (3) In the second line of the same page of the same book, "uniformly inside" is corrected to "inside." (4) In the second line of the same page of the same book, "uniformly inside" is corrected to "inside." (5) "Mixture of fluorine rubber and polystyrene" in the first line of page 1 of the same book is corrected to "polystyrene or polyethylene." (6) “Polyethylene (PE)” in the second line of the same page of the same book
Correct J to "fluororubber". (7) In the same book, page 16, line 6, "without a crosslinking site" is amended to "having a crosslinking site". (8) Add r (PA401)J after "polyethyl acrylate" in lines 2 to 7 of the same page of the same book. (9) In the same book, page 17, lines 6 to 8, ro, 7,
g/m or more ~ 0.7 to 1.2 kg/ml at "revolutions 14
Orpm corrects the total energy to 300 MJ/m'J. 8. List of attached documents fl) Attached sheet......1 attached sheet Claims (1) Sliding on the outer periphery of the rotating or reciprocating shaft (5), the oil side of the shaft (5) and the atmosphere A sealing member (1) for an oil seal sealing the sides, the sealing member (1) for an oil seal is made of a first polymer (A) that is solid at room temperature.
) are dispersed in an oriented state in a second polymer (B) that is incompatible with the first polymer (A) and exhibits rubber-like elasticity at room temperature. Seal material for use. (2) A method for manufacturing an oil seal seal member (1) that slides on the outer periphery of a rotating or reciprocating shaft (5) to seal the oil side and the atmosphere side of the shaft (5), the method comprising: A solid first polymer (A);
) and an incompatible second polymer (B) that exhibits rubber-like elasticity at room temperature are kneaded at a temperature higher than the melting point temperature of both polymers (A) and (B), and the fine particles of the first polymer (A>) are kneaded. A kneaded product is prepared by dispersing in the second polymer (B) to form a micro-dispersed phase, then a vulcanizing agent is added to this kneaded product and further kneaded, and then this vulcanizing agent addition kneading Shearing stress is applied to the object in a mold at a temperature near the softening point of the first polymer (A) to orient the fine particles of the first polymer (A) dispersed in the second polymer (B). A method for manufacturing a sealing member for an oil seal, characterized by vulcanization molding in a state of
Claims (2)
(5)の油側と大気側とをシールするオイルシール用シ
ール部材(1)であって、このオイルシール用シール部
材(1)は、室温で固体である第1のポリマー(A)の
微粒子が、前記第1のポリマー(A)と非相溶性の室温
でゴム状弾性を示す第2のポリマー(B)中に、配向し
た状態で均一に分散されていることを特徴とするオイル
シール用シール部材。(1) An oil seal seal member (1) that slides on the outer periphery of a rotating or reciprocating shaft (5) to seal the oil side and the atmosphere side of the shaft (5), the oil seal seal Member (1) includes fine particles of a first polymer (A) that is solid at room temperature in a second polymer (B) that is incompatible with the first polymer (A) and exhibits rubber-like elasticity at room temperature. A seal member for an oil seal, characterized in that the seal member is uniformly dispersed in an oriented state.
(5)の油側と大気側とをシールするオイルシール用シ
ール部材(1)の製造方法であって、室温で固体である
第1のポリマー(A)と、この第1のポリマー(A)と
非相溶性の室温でゴム状弾性を示す第2のポリマー(B
)とを両ポリマー(A)、(B)の融点温度以上で混練
し、前記第1のポリマー(A)の微粒子を第2のポリマ
ー(B)中に均一に分散してミクロ分散相を形成した混
練物を調製し、続いて、この混練物に加硫剤を添加して
さらに混練し、次いで、この加硫剤添加混練物を成形型
内で、前記第1のポリマー(A)の軟化点温度付近で剪
断応力を作用し、前記第2のポリマー(B)中に均一に
分散する第1のポリマー(A)の微粒子を配向させた状
態で加硫成形することを特徴とするオイルシール用シー
ル部材の製造方法。(2) A method for manufacturing an oil seal sealing member (1) that slides on the outer periphery of a rotating or reciprocating shaft (5) to seal the oil side and the atmosphere side of the shaft (5), the method comprising: A first polymer (A) that is solid and a second polymer (B) that is incompatible with the first polymer (A) and exhibits rubber-like elasticity at room temperature.
) are kneaded at a temperature higher than the melting point temperature of both polymers (A) and (B), and the fine particles of the first polymer (A) are uniformly dispersed in the second polymer (B) to form a microdispersed phase. Next, a vulcanizing agent is added to this kneaded material and further kneaded, and then this vulcanizing agent-added kneaded material is placed in a mold to soften the first polymer (A). An oil seal characterized in that vulcanization is performed in a state in which fine particles of the first polymer (A) are oriented and uniformly dispersed in the second polymer (B) by applying shear stress near a point temperature. A method for manufacturing a seal member for use.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1126488A JP2781204B2 (en) | 1989-05-19 | 1989-05-19 | Oil seal seal member and method of manufacturing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1126488A JP2781204B2 (en) | 1989-05-19 | 1989-05-19 | Oil seal seal member and method of manufacturing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02305884A true JPH02305884A (en) | 1990-12-19 |
| JP2781204B2 JP2781204B2 (en) | 1998-07-30 |
Family
ID=14936448
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1126488A Expired - Lifetime JP2781204B2 (en) | 1989-05-19 | 1989-05-19 | Oil seal seal member and method of manufacturing the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2781204B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07138489A (en) * | 1993-11-17 | 1995-05-30 | Bando Chem Ind Ltd | Bearing resin composition |
| WO2001005893A1 (en) * | 1999-07-19 | 2001-01-25 | Caterpillar Inc. | Seal material having anisotropic properties |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5147950A (en) * | 1974-10-22 | 1976-04-24 | Tatsuji Myashita | DANSEISEIKEISHIIRINGUZAI |
| JPS60141743A (en) * | 1983-12-28 | 1985-07-26 | Uchiyama Mfg Corp | Material composition for bearing sealant |
| JPS6479285A (en) * | 1987-09-21 | 1989-03-24 | Komatsu Mfg Co Ltd | Sealing material |
-
1989
- 1989-05-19 JP JP1126488A patent/JP2781204B2/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5147950A (en) * | 1974-10-22 | 1976-04-24 | Tatsuji Myashita | DANSEISEIKEISHIIRINGUZAI |
| JPS60141743A (en) * | 1983-12-28 | 1985-07-26 | Uchiyama Mfg Corp | Material composition for bearing sealant |
| JPS6479285A (en) * | 1987-09-21 | 1989-03-24 | Komatsu Mfg Co Ltd | Sealing material |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07138489A (en) * | 1993-11-17 | 1995-05-30 | Bando Chem Ind Ltd | Bearing resin composition |
| WO2001005893A1 (en) * | 1999-07-19 | 2001-01-25 | Caterpillar Inc. | Seal material having anisotropic properties |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2781204B2 (en) | 1998-07-30 |
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