JPH08134269A - Vibration-insulating rubber composition - Google Patents
Vibration-insulating rubber compositionInfo
- Publication number
- JPH08134269A JPH08134269A JP6279541A JP27954194A JPH08134269A JP H08134269 A JPH08134269 A JP H08134269A JP 6279541 A JP6279541 A JP 6279541A JP 27954194 A JP27954194 A JP 27954194A JP H08134269 A JPH08134269 A JP H08134269A
- Authority
- JP
- Japan
- Prior art keywords
- vibration
- rubber
- rubber composition
- copolymer
- vibration rubber
- 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
Abstract
Description
【0001】[0001]
【産業上の利用分野】各種の振動及び騒音の防止用ゴム
防振ゴム組成物に関する。TECHNICAL FIELD The present invention relates to a rubber anti-vibration rubber composition for preventing various vibrations and noises.
【0002】[0002]
【従来の技術】従来より、振動及び騒音の防止のために
防振ゴムが使用され、各所で防振効果が図られている。
ほとんどの防振ゴムにおいて要求される特性としては、
低周波で高歪み領域ではtanδが大きく、高周波で低
歪み領域では動倍率(動的弾性率と静的弾性率の比)が
低いことが理想的である。従って、防振ゴムのゴム材料
としてもtanδが大きく、動倍率が低いものが求めら
れるが、tanδが大きいことと低動倍率であることは
二律背反の関係にあり、どちらかの特性を優先させた、
またはバランスさせたゴム材料を防振ゴム用に使用する
のが現状である。このような理想的な特性を得るために
エチレングリコール等の液体を封入する等の構造上で工
夫をしている。2. Description of the Related Art Conventionally, anti-vibration rubber has been used to prevent vibration and noise, and anti-vibration effects have been achieved in various places.
The properties required for most anti-vibration rubber are:
Ideally, tan δ is large in the low-frequency and high-strain region, and the dynamic magnification (ratio of the dynamic elastic modulus and the static elastic modulus) is low in the high-frequency and low-strain region. Therefore, a rubber material having a large tan δ and a low dynamic magnification is also required as a rubber material for the anti-vibration rubber, but a large tan δ and a low dynamic magnification are in a trade-off relationship, and either characteristic is prioritized. ,
Alternatively, a balanced rubber material is currently used as a vibration-proof rubber. In order to obtain such ideal characteristics, a structure is devised such as enclosing a liquid such as ethylene glycol.
【0003】液体を封入して、上記理想的な特性を持た
せた防振ゴムは、構造が複雑になるため製造するのに手
間がかかり、部品数も増えるため非常に高価になる。ま
た、液体封入防振ゴムでは、液体の共振を利用してta
nδを出している為、液体の共振の出る方向のみしか高
いtanδの特性が得られないという欠点がある。The anti-vibration rubber which is filled with a liquid and has the above-mentioned ideal characteristics is complicated because of its complicated structure, which is troublesome to manufacture, and the number of parts increases, which makes it very expensive. In addition, in the liquid-filled anti-vibration rubber, ta
Since nδ is obtained, there is a disadvantage that a high tanδ characteristic can be obtained only in the direction in which the liquid resonance appears.
【0004】[0004]
【発明が解決しようとする課題】本発明は、上記問題点
を改良して、tanδが大きく、しかも動倍率が低い防
振ゴム用として理想方向の特性を持つゴム材料を提供す
ることにある。SUMMARY OF THE INVENTION It is an object of the present invention to improve the above problems and provide a rubber material having ideal directional characteristics for a vibration-proof rubber having a large tan δ and a low dynamic magnification.
【0005】[0005]
【課題を解決するするための手段】本発明者らは、前記
課題を解決する為に鋭意検討を行った結果、イソブチレ
ンとパラメチルスチレンとの共重合物でパラメチルスチ
レンの一部を臭素化した共重合体を使用することによ
り、上記目的の防振ゴム組成物を得ることに成功し、本
発明を完成するに至ったのである。即ち、本発明の防振
ゴム組成物はイソブチレンとパラメチルスチレンとの共
重合物で、パラメチルスチレンの一部を臭素化した共重
合体を使用することを特徴とするものである。尚、上記
パラメチルスチレンの一部を臭素化した共重合体とは、
通常臭素の重量%が、前記ポリマー全体を100重量%
とした場合に対して0.8〜2重量%程度臭素化された
ものである。Means for Solving the Problems As a result of intensive studies for solving the above problems, the present inventors have found that a part of paramethylstyrene is brominated with a copolymer of isobutylene and paramethylstyrene. By using the above copolymer, the anti-vibration rubber composition for the above purpose was successfully obtained, and the present invention was completed. That is, the anti-vibration rubber composition of the present invention is a copolymer of isobutylene and paramethylstyrene, and is characterized by using a copolymer obtained by brominated a part of paramethylstyrene. Incidentally, the copolymer brominated part of the para-methylstyrene,
Usually, the weight% of bromine is 100% by weight of the whole polymer.
The content of brominated is about 0.8 to 2% by weight.
【0006】本発明のポリマーは、単独もしくはジエン
系ゴムとのブレンドにて効果が見られる。ブレンドする
ゴムとして、天然ゴム、IR、SBR、BR等全てのジ
エン系ゴムで可能である。ブレンド比としては、特に制
限はないが、10重量部未満であると本ポリマーの特徴
(高ロス低動倍)が明確に発現しない。又、防振ゴムと
しては、疲労性が良好であることが望まれるが、ジエン
系のブレンドゴムとして天然ゴムもしくはイソプレンゴ
ムを適用することにより疲労性を維持できる。The polymer of the present invention is effective alone or in a blend with a diene rubber. As the rubber to be blended, all diene rubbers such as natural rubber, IR, SBR and BR can be used. The blending ratio is not particularly limited, but if it is less than 10 parts by weight, the characteristics of the present polymer (high loss and low dynamic ratio) will not be clearly exhibited. Further, it is desired that the anti-vibration rubber has good fatigue property, but the fatigue property can be maintained by applying natural rubber or isoprene rubber as the diene-based blend rubber.
【0007】本発明においては、上記ポリマーの他に通
常防振ゴム用の配合剤として使用される。例えば補強
剤、軟化剤、老化防止剤、加硫剤、加硫促進剤、加硫助
剤、分散剤、加工助剤等を適宜配合することが出来る。In the present invention, in addition to the above polymers, it is usually used as a compounding agent for anti-vibration rubber. For example, a reinforcing agent, a softening agent, an antiaging agent, a vulcanizing agent, a vulcanization accelerator, a vulcanization aid, a dispersant, a processing aid and the like can be appropriately added.
【0008】以下、実施例、比較例を示して、本発明を
更に詳細を説明するが、本発明はこれらの実施例に何ら
限定されるものではない。Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.
【0009】[0009]
【表1】 [Table 1]
【表2】 [Table 2]
【表3】 [Table 3]
【表4】 (注)ポリマー:「XP−50・グレード89−1」(エクソン化学社製)[Table 4] (Note) Polymer: "XP-50 grade 89-1" (manufactured by Exxon Chemical Co.)
【0010】表1、3の配合組成(配合単位:重量部)
に従い、防振ゴム組成物を調整した。この防振ゴム組成
物を加硫後におけるゴムの硬度、強伸度、静的弾性率、
損失係数、動倍率、疲労性を測定した結果を表2、4に
示す。Blend composition of Tables 1 and 3 (blending unit: parts by weight)
The anti-vibration rubber composition was prepared according to. Hardness of rubber after vulcanization of this anti-vibration rubber composition, high elongation, static elastic modulus,
Tables 2 and 4 show the results of measuring the loss coefficient, the dynamic magnification, and the fatigue resistance.
【0011】上記硬度、強伸度、静的弾性率、損失係
数、動倍率、疲労性は下記の方法により測定した。 (1)硬度、強伸度 JIS K6301により準拠して測定した。 (2)静的弾性率、損失係数、動倍率。 厚さ2mm、幅5mmの試料を用いて測定する。静的弾
性率は15%伸ばした時の応力から算出した。動倍率は
15%伸ばした状態で周波数15Hz、振幅2%及び周
波数100Hz、振幅0.2%、それぞれの正弦的振幅
を加えた時の応力から算出した動的弾性率と静的弾性率
の比より求めた。損失係数は15%伸ばした状態で周波
数15Hz、振幅2%、及び周波数100Hz、振幅
0.2%それぞれの正弦的振幅を加えた時の応力とおく
れ角から算出した。 (3)疲労性は、試験サンプルは、図2に示される防振
ゴム金具1(材質:SPCC−SD)に接着処理(ブラ
スト処理後、接着剤として下塗りケムロック205、上
塗りケムロック220、いずれもロード社製を塗布)を
行い、各ゴム組成物を用いて標準形状防振ゴムA(長さ
40mm、直径36mm)を加硫作成した。そのサンプ
ルを、図3のように25℃雰囲気下で剪断方向に0±5
0%(3Hz)の定歪み繰り返し振幅を与え、1cmの
クラック発生までの回数を評価した。The hardness, the strength and elongation, the static elastic modulus, the loss coefficient, the dynamic ratio, and the fatigue resistance were measured by the following methods. (1) Hardness and strong elongation Measured according to JIS K6301. (2) Static elastic modulus, loss coefficient, dynamic ratio. The measurement is performed using a sample having a thickness of 2 mm and a width of 5 mm. The static elastic modulus was calculated from the stress when stretched by 15%. The ratio of dynamic elastic modulus and static elastic modulus calculated from the stress when the dynamic magnification is 15%, the frequency is 15 Hz, the amplitude is 2% and the frequency is 100 Hz, the amplitude is 0.2%, and the respective sinusoidal amplitudes are applied. I asked more. The loss coefficient was calculated from the stress and the lag angle when the sinusoidal amplitude of 15 Hz, the amplitude of 2%, and the sinusoidal amplitude of 100 Hz and the amplitude of 0.2% were applied in the state of being extended by 15%. (3) Fatigue test, the test sample is adhered to the anti-vibration rubber fitting 1 (material: SPCC-SD) shown in FIG. 2 (after blasting, both the undercoat Chemlock 205 and the overcoat Chemlock 220 are loaded as an adhesive. Manufactured by the company) was applied, and a standard shape vibration-proof rubber A (length 40 mm, diameter 36 mm) was vulcanized using each rubber composition. The sample was subjected to 0 ± 5 in the shearing direction at 25 ° C. as shown in FIG.
A constant strain repetitive amplitude of 0% (3 Hz) was given, and the number of times until a crack of 1 cm was generated was evaluated.
【0012】[実施例]実施例1〜5は、天然ゴムと前
記共重合体のブレンド比を変えたものである。比較例1
はポリマーを天然ゴム100にした配合ゴムである。比
較例2〜6は、表1の配合の通り防振ゴム用として使用
される一般的な配合である。それぞれのゴムの特性は表
2に示す。また、それぞれのゴム材料の動倍率とtan
δとの関係を図1に示す。[Examples] In Examples 1 to 5, the blending ratio of the natural rubber and the copolymer was changed. Comparative Example 1
Is a compounded rubber in which the polymer is 100. Comparative Examples 2 to 6 are general formulations used for anti-vibration rubbers as shown in Table 1. The properties of each rubber are shown in Table 2. Also, the dynamic magnification and tan of each rubber material
The relationship with δ is shown in FIG.
【0013】防振ゴム材料としては、tanδが大き
く、動倍率が低いもの、即ち図1での右下の方向ものが
理想的である。前記共重合体をブレンドすることによ
り、tanδが大きく、動倍率が低い理想的な特性を示
している。この特徴は、前記共重合体のブレンド比を多
くすればする程顕著であり、前記共重合体のみの配合が
最もtanδが大きく、動倍率が低くなっている。ま
た、比較例7、8は、ジエン系のブレンドゴムとしてS
BR、BRをブレンドしたものである。動特性はtan
δが大きく動倍率が低い理想的なものになっているが、
疲労性はNRをブレンドした系(実施例3)に比べて劣
っている。従って、疲労性が厳しいところで使用する防
振ゴムへの適用はNRブレンドが適している。As the vibration-proof rubber material, a material having a large tan δ and a low dynamic magnification, that is, a material in the lower right direction in FIG. 1, is ideal. By blending the above-mentioned copolymer, tan δ is large and ideal dynamic characteristics are low. This characteristic becomes more remarkable as the blending ratio of the copolymer is increased, and the blending of only the copolymer has the largest tan δ and the low dynamic magnification. In Comparative Examples 7 and 8, S was used as a diene blend rubber.
It is a blend of BR and BR. Dynamic characteristics are tan
Although it is an ideal one with a large δ and a low dynamic magnification,
Fatigue is inferior to the NR blended system (Example 3). Therefore, the NR blend is suitable for application to the anti-vibration rubber used in a place where fatigue is severe.
【0014】[0014]
【発明の効果】以上により、防振ゴムとしてイソブチレ
ンとパラメチルスチレンとの共重合体でパラメチルスチ
レンの一部を臭素化した共重合体を用いることによりt
anδが大きく動倍率の低い防振ゴム組成物が提供され
る。As described above, the use of a copolymer of isobutylene and paramethylstyrene in which a part of paramethylstyrene is brominated as the anti-vibration rubber makes it possible to obtain t
An anti-vibration rubber composition having a large an δ and a low dynamic magnification is provided.
【図1】通常及び本発明に係る各種防振ゴム用組成物の
動倍率/tanδ(実施例、比較例)を示す関係図。FIG. 1 is a relational diagram showing dynamic magnification / tan δ (examples and comparative examples) of various anti-vibration rubber compositions according to the present invention.
【図2】各防振ゴム用組成物の疲労性測定試験サンプル
を示す防振ゴムの概略断面図である。FIG. 2 is a schematic cross-sectional view of anti-vibration rubbers showing a fatigue resistance measurement test sample of each anti-vibration rubber composition.
【図3】疲労試験方法を示す該略図である。FIG. 3 is a schematic diagram showing a fatigue test method.
1 防振ゴム金具 2 防振用ゴム 1 Anti-vibration rubber fittings 2 Anti-vibration rubber
Claims (4)
共重合物でパラメチルスチレンの一部を臭素化した共重
合体(ポリマー)を使用することを特徴とする防振ゴム
組成物。1. An anti-vibration rubber composition comprising a copolymer of isobutylene and paramethylstyrene, wherein a part of paramethylstyrene is brominated.
してなることを特徴とする請求項1記載の防振ゴム組成
物。2. The anti-vibration rubber composition according to claim 1, wherein the polymer and the diene rubber are blended.
比が上記ポリマ−/ジエン系ゴム=10/90〜100
/0であることを特徴とする請求項1又は2項に記載の
防振ゴム組成物。3. The blend ratio of the polymer and the diene rubber is the polymer / diene rubber = 10/90 to 100.
The anti-vibration rubber composition according to claim 1 or 2, wherein the anti-vibration rubber composition is / 0.
R)もしくはイソプレンゴム(IR)をブレンドしてな
ることを特徴とする請求項2乃至3記載の防振ゴム用組
成物。4. The natural rubber (N
R) or isoprene rubber (IR) is blended, The composition for antivibration rubbers of Claim 2 thru | or 3 characterized by the above-mentioned.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27954194A JP3329599B2 (en) | 1994-11-14 | 1994-11-14 | Anti-vibration rubber composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27954194A JP3329599B2 (en) | 1994-11-14 | 1994-11-14 | Anti-vibration rubber composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH08134269A true JPH08134269A (en) | 1996-05-28 |
JP3329599B2 JP3329599B2 (en) | 2002-09-30 |
Family
ID=17612436
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27954194A Expired - Lifetime JP3329599B2 (en) | 1994-11-14 | 1994-11-14 | Anti-vibration rubber composition |
Country Status (1)
Country | Link |
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JP (1) | JP3329599B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001074964A1 (en) * | 2000-04-05 | 2001-10-11 | Kaneka Corporation | Vibration damper composition |
US8609774B2 (en) | 2010-08-25 | 2013-12-17 | Daikin Industries, Ltd. | Belt |
US8754161B2 (en) | 2010-08-25 | 2014-06-17 | Daikin Industries, Ltd. | Complex-shaped fluororubber formed product |
US9006328B2 (en) | 2010-08-25 | 2015-04-14 | Daikin Industries, Ltd. | Fluororubber composition |
US9045614B2 (en) | 2010-08-25 | 2015-06-02 | Daikin Industries, Ltd. | Fluororubber composition |
US9068653B2 (en) | 2010-08-25 | 2015-06-30 | Daikin Industries, Ltd. | Sealing material |
US11054066B2 (en) | 2010-08-25 | 2021-07-06 | Daikin Industries, Ltd. | Hose |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03281663A (en) * | 1990-03-30 | 1991-12-12 | Shin Etsu Chem Co Ltd | Vibrationproof rubber |
JPH05507517A (en) * | 1990-06-08 | 1993-10-28 | エクソン・ケミカル・パテンツ・インク | Composition for tire tread |
JPH05508435A (en) * | 1990-07-18 | 1993-11-25 | エクソン・ケミカル・パテンツ・インク | Composition for tire inner liner |
JPH061882A (en) * | 1992-06-17 | 1994-01-11 | Yokohama Rubber Co Ltd:The | Rubber composition for sidewall |
JPH06207051A (en) * | 1993-01-12 | 1994-07-26 | Bridgestone Corp | Vibrationproof rubber composition |
-
1994
- 1994-11-14 JP JP27954194A patent/JP3329599B2/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03281663A (en) * | 1990-03-30 | 1991-12-12 | Shin Etsu Chem Co Ltd | Vibrationproof rubber |
JPH05507517A (en) * | 1990-06-08 | 1993-10-28 | エクソン・ケミカル・パテンツ・インク | Composition for tire tread |
JPH05508435A (en) * | 1990-07-18 | 1993-11-25 | エクソン・ケミカル・パテンツ・インク | Composition for tire inner liner |
JPH061882A (en) * | 1992-06-17 | 1994-01-11 | Yokohama Rubber Co Ltd:The | Rubber composition for sidewall |
JPH06207051A (en) * | 1993-01-12 | 1994-07-26 | Bridgestone Corp | Vibrationproof rubber composition |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001074964A1 (en) * | 2000-04-05 | 2001-10-11 | Kaneka Corporation | Vibration damper composition |
US7241837B2 (en) | 2000-04-05 | 2007-07-10 | Kaneka Corporation | Vibration damper composition |
US8609774B2 (en) | 2010-08-25 | 2013-12-17 | Daikin Industries, Ltd. | Belt |
US8754161B2 (en) | 2010-08-25 | 2014-06-17 | Daikin Industries, Ltd. | Complex-shaped fluororubber formed product |
US9006328B2 (en) | 2010-08-25 | 2015-04-14 | Daikin Industries, Ltd. | Fluororubber composition |
US9045614B2 (en) | 2010-08-25 | 2015-06-02 | Daikin Industries, Ltd. | Fluororubber composition |
US9068653B2 (en) | 2010-08-25 | 2015-06-30 | Daikin Industries, Ltd. | Sealing material |
US11054066B2 (en) | 2010-08-25 | 2021-07-06 | Daikin Industries, Ltd. | Hose |
Also Published As
Publication number | Publication date |
---|---|
JP3329599B2 (en) | 2002-09-30 |
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