JP2000230067A - Foamed rubber composition - Google Patents
Foamed rubber compositionInfo
- Publication number
- JP2000230067A JP2000230067A JP3241899A JP3241899A JP2000230067A JP 2000230067 A JP2000230067 A JP 2000230067A JP 3241899 A JP3241899 A JP 3241899A JP 3241899 A JP3241899 A JP 3241899A JP 2000230067 A JP2000230067 A JP 2000230067A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- microspheres
- pts
- dpt
- azc
- 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
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ベアリングシー
ル、ホィールシール、またはオイルシール等の密封材の
リップ摺動部分に凹凸を形成させ、シール性能を向上せ
しめるゴム組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a rubber composition for improving the sealing performance by forming irregularities on a lip sliding portion of a sealing material such as a bearing seal, a wheel seal or an oil seal.
【0002】[0002]
【従来の技術】シール性能を向上させる手段として従来
では、ゴム材にPTFE樹脂、グラファイト、モリブデ
ン、セルロース繊維等の添加剤を練り込む方法が知られ
ているが、物性低下、ロール加工性等まだまだ解決され
なければならない問題を多く抱えている。また、リップ
表面の改質される技術も検討されてきている。その方法
としては、 (1)リップ表面にフッ素コーティング処理する方法. (2)リップに螺旋状の溝を形成する方法. などが考えられている。2. Description of the Related Art Conventionally, as a means for improving sealing performance, there has been known a method of kneading additives such as PTFE resin, graphite, molybdenum, and cellulose fiber into a rubber material. There are many problems that need to be resolved. Also, techniques for modifying the lip surface have been studied. The method is as follows: (1) A method of applying a fluorine coating treatment to the lip surface. (2) A method of forming a spiral groove on the lip. And so on.
【0003】[0003]
【発明が解決しようとする課題】しかしながら前記のリ
ップ表面を改質する方法は下記に示すように様々な欠点
を表わす。すなわち、前記(1)のリップ表面にフッ素
コーティング処理する方法については、コスト面及び成
形方法に問題を有し、前記(2)のリップに螺旋状の溝
を形成する方法では、回転方向に左右があるためどうし
ても左右2タイプの製品を必要とし使用箇所に大きな制
限を与える。このようなことから本発明は、今回リップ
表面の改質手段で、簡単かつ物性的にも影響されず成形
し易い方法としてリップ表面にミクロの凹凸を形成させ
ることを考えてみた。However, the above-described method of modifying the lip surface presents various disadvantages as described below. That is, the method (1) of applying a fluorine coating to the lip surface has problems in terms of cost and molding method, and the method (2) of forming a spiral groove on the lip has a problem in the right and left directions of rotation. give a big limitation to the point-of-use and requires absolutely right and left two types of products for which there is. In view of the above, the present invention has conceived of forming micro unevenness on the lip surface as a method of modifying the lip surface easily and easily without being affected by physical properties.
【0004】[0004]
【課題を解決しようとする手段】本発明はシールのリッ
プ表面の改質方法として、ミクロの凹凸をシールのリッ
プに形成させるために、数々の発泡剤、マイクロスフェ
アを検討した結果、特定の発泡剤の組合せ及び特定のマ
イクロスフェアを用いることでシールのリップ面にミク
ロの凹凸を形成せしめるゴム組成物を見出した。According to the present invention, as a method of modifying the surface of a seal lip, a number of foaming agents and microspheres have been studied in order to form micro unevenness on the seal lip. We have found a rubber composition that can form micro unevenness on the lip surface of the seal by using a combination of agents and specific microspheres.
【0005】[0005]
【発明の実施の形態】従来、発泡剤として知られている
のは、 (a)無機発泡剤(重炭酸ナトリウム、亜硝酸アンモニ
ウム、等) (b)ニトロソ化合物…N,N´−ジニトロソペンタメ
チレンテトラミン(DPT)が一般 (c)アゾ化合物…アゾジカルボンアミド(AZC)、
アゾビスイソブチロニトリル(ABIN) (d)スルホニルヒドラジド化合物…ベンゼンスルホニ
ルヒドラジド(BSH)、トルエンスルホニルヒドラジ
ド(TSH)及びそれらの誘導体等がある。本発明の用
途から分解温度が180℃〜200℃の範囲で、かつ微
細で独立気泡を形成できるものに限定した。その条件に
合う発泡剤として前記(b)のDPTと前記(c)のA
ZCがある。ところがDPT単独で使用すると未加硫生
地が経時変化し、スコーチタイムが短くなり、発泡しな
くなり、AZC単独では逆に未加硫生地のスコーチタイ
ムが長くなり、加硫低下を引き起こす。そこでDPTと
AZCを併用することにより未加硫生地の経時変化を少
なくし、安定した微細で独立気泡を持つゴム加硫物を作
ることができる。DESCRIPTION OF THE PREFERRED EMBODIMENTS Conventionally known blowing agents include (a) inorganic blowing agents (sodium bicarbonate, ammonium nitrite, etc.) (b) nitroso compounds: N, N'-dinitrosopentamethylene Tetramine (DPT) is generally used. (C) Azo compound: azodicarbonamide (AZC),
Azobisisobutyronitrile (ABIN) (d) Sulfonyl hydrazide compound: benzenesulfonyl hydrazide (BSH), toluenesulfonyl hydrazide (TSH), derivatives thereof, and the like. For the purposes of the present invention, the decomposition temperature is limited to a range of 180 ° C. to 200 ° C. and is fine and capable of forming closed cells. As the blowing agent meeting the conditions, the DPT of (b) and the A of (c)
There is ZC. However, when DPT is used alone, the unvulcanized dough changes with time, the scorch time is shortened, and foaming is not performed. On the other hand, when AZC is used alone, the scorch time of the unvulcanized dough becomes longer, causing a reduction in vulcanization. Therefore, by using DPT and AZC together, it is possible to reduce the change with time of the unvulcanized dough and to produce a stable, fine, vulcanized rubber having closed cells.
【0006】また、中空マイクロスフェアとしてはかな
り以前から種々のものが工業化され、南九州に産出する
シラスを加工して得られるシラスバルーンや、ホウケイ
酸ガラスから得られるマイクロバルーン、アルミナバル
ーンなどの無機材料、カーボン組成のカーボンスフェア
や発泡剤とフェノール樹脂からなるフェノールバルーン
などの有機材料がある。Various hollow microspheres have been industrialized for a long time, and inorganic microspheres such as shirasu balloons obtained by processing shirasu produced in Minamikyushu, microballoons obtained from borosilicate glass, and alumina balloons. Materials include organic materials such as carbon spheres having a carbon composition and phenol balloons comprising a foaming agent and a phenol resin.
【0007】このような種々のマイクロスフェアを検討
した結果、ゴム加硫物の断面にミクロの凹凸を形成せし
めるのはエクスパーセル社のエクスパンセルのもので、
一番均一なものが得られた。このエクスパンセルは熱膨
張性のマイクロスフェアで、温度を上げると外殻のポリ
マー(塩化ビニリデン・アクリロニトリルコポリマー)
が軟化し、内包されたイソブタンがガス化し、真球で内
圧のない風船玉のごとく膨れ上がり、平均50μmの中
洞が形成される。特に発泡させる温度領域の高いDu5
51、091が最適である。[0007] As a result of studying such various microspheres, it is the Expancel manufactured by Expellcel that forms micro unevenness on the cross section of the rubber vulcanizate.
The most uniform one was obtained. The Expancel is a thermo-expandable microsphere. The polymer of the outer shell (vinylidene chloride / acrylonitrile copolymer) increases when the temperature is increased.
Is softened, the contained isobutane is gasified, and swells like a balloon ball with a true sphere and no internal pressure, forming a central cavity of 50 μm on average. Du5 with a particularly high temperature range for foaming
51 and 091 are optimal.
【0008】[0008]
【実施例】<実施例1> ニトリルゴム :100 ステアリンサン : 1 活性亜鉛化 : 5 老化防止剤ODP : 3 MAFカーボン : 60 可塑剤DOP : 10 硫黄 : 0.5 促進剤(A) : 2.0 促進剤(B) : 1.5 セルマイクA(DPT) : 1.5 AZC : 1.5EXAMPLES <Example 1> Nitrile rubber: 100 Stearin sun: 1 Active zincation: 5 Antioxidant ODP: 3 MAF carbon: 60 Plasticizer DOP: 10 Sulfur: 0.5 Accelerator (A): 2 0 Accelerator (B): 1.5 Cell microphone A (DPT): 1.5 AZC: 1.5
【0009】<実施例2> ニトリルゴム :100 ステアリンサン : 1 活性亜鉛化 : 5 老化防止剤ODP : 3 MAFカーボン : 60 可塑剤DOP : 10 硫黄 : 0.5 促進剤(A) : 2.0 促進剤(B) : 1.5 Du551 : 5<Example 2> Nitrile rubber: 100 Stearin sun: 1 Active zincation: 5 Antioxidant ODP: 3 MAF carbon: 60 Plasticizer DOP: 10 Sulfur: 0.5 Accelerator (A): 2.0 Accelerator (B): 1.5 Du551: 5
【0010】ドライ時の回転トルク値を従来のものと比
較して表1に示す。[0010] Table 1 shows the rotational torque value in the dry state in comparison with the conventional one.
【表1】 従来のものは回転数の増加と共に回転トルク値が低下
し、リップがシャフトにだんだん追随しなくなることを
示している。ところが、実施例のものは回転数に拘らず
ほとんど一定の値を維持している。リップの摺動面にミ
クロの凹凸が形成されることによって、接触面積が増大
してシャフトにより密着し、その結果高い回転トルク値
を保持していると考えられる。[Table 1] The prior art shows that the rotational torque value decreases with an increase in the number of revolutions, and the lip gradually stops following the shaft. However, in the case of the embodiment, almost constant value is maintained regardless of the rotation speed. It is considered that the formation of micro unevenness on the sliding surface of the lip increases the contact area and makes the shaft more closely contact with the shaft, and as a result, maintains a high rotational torque value.
Claims (1)
部に対して、(A)ジニトロソペンタメチレンテトラミ
ン(DPT)とアゾジカルボンアミド(AZC)をそれ
ぞれ1〜3重量部組合せ、(B)熱膨張性のマイクロス
フェアで、特にイソブタンを内包した塩化ビニリデン・
アクリロニトリルコポリマーで形成されたマイクロスフ
ェアー:5〜10重量部、(A)もしくは(B)どちら
かを含むことを特徴とした発泡ゴム組成物。1. A combination of (A) 1 to 3 parts by weight of dinitrosopentamethylenetetramine (DPT) and azodicarbonamide (AZC) with 100 parts by weight of synthetic rubber, particularly nitrile rubber, and (B) thermal expansion Microspheres, especially vinylidene chloride containing isobutane
A microsphere formed of an acrylonitrile copolymer: a foamed rubber composition characterized by containing 5 to 10 parts by weight, either (A) or (B).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3241899A JP3553811B2 (en) | 1999-02-10 | 1999-02-10 | Foam rubber composition for seal lip |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3241899A JP3553811B2 (en) | 1999-02-10 | 1999-02-10 | Foam rubber composition for seal lip |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000230067A true JP2000230067A (en) | 2000-08-22 |
JP3553811B2 JP3553811B2 (en) | 2004-08-11 |
Family
ID=12358411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3241899A Expired - Fee Related JP3553811B2 (en) | 1999-02-10 | 1999-02-10 | Foam rubber composition for seal lip |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3553811B2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001060896A2 (en) * | 2000-02-16 | 2001-08-23 | Qinetiq Limited | Foamed rubber structure and method of making the same |
CN102010533A (en) * | 2010-11-29 | 2011-04-13 | 江苏兴华胶带股份有限公司 | Method for preparing cellular structure rubber elastomer |
JP2012067235A (en) * | 2010-09-27 | 2012-04-05 | Sanwa Kako Co Ltd | Chloroprene rubber foam and method for producing the same |
CN103421218A (en) * | 2013-08-30 | 2013-12-04 | 安徽金科橡塑制品有限公司 | Rubber foam material and preparing method thereof |
CN103435868A (en) * | 2013-08-30 | 2013-12-11 | 安徽金科橡塑制品有限公司 | Formula of rubber foamed elastic pad and preparation method thereof |
-
1999
- 1999-02-10 JP JP3241899A patent/JP3553811B2/en not_active Expired - Fee Related
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001060896A2 (en) * | 2000-02-16 | 2001-08-23 | Qinetiq Limited | Foamed rubber structure and method of making the same |
WO2001060896A3 (en) * | 2000-02-16 | 2002-04-25 | Martin Paul Burke | Foamed rubber structure and method of making the same |
JP2012067235A (en) * | 2010-09-27 | 2012-04-05 | Sanwa Kako Co Ltd | Chloroprene rubber foam and method for producing the same |
CN102010533A (en) * | 2010-11-29 | 2011-04-13 | 江苏兴华胶带股份有限公司 | Method for preparing cellular structure rubber elastomer |
CN103421218A (en) * | 2013-08-30 | 2013-12-04 | 安徽金科橡塑制品有限公司 | Rubber foam material and preparing method thereof |
CN103435868A (en) * | 2013-08-30 | 2013-12-11 | 安徽金科橡塑制品有限公司 | Formula of rubber foamed elastic pad and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JP3553811B2 (en) | 2004-08-11 |
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