JP2000239441A - High damping rubber composition - Google Patents

High damping rubber composition

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Publication number
JP2000239441A
JP2000239441A JP11048012A JP4801299A JP2000239441A JP 2000239441 A JP2000239441 A JP 2000239441A JP 11048012 A JP11048012 A JP 11048012A JP 4801299 A JP4801299 A JP 4801299A JP 2000239441 A JP2000239441 A JP 2000239441A
Authority
JP
Japan
Prior art keywords
rubber
butyl rubber
butyl
natural rubber
pts
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
Application number
JP11048012A
Other languages
Japanese (ja)
Inventor
Yoshiharu Kiyohara
好晴 清原
Shin Maezawa
慎 前澤
Atsushi Shimoda
篤史 下田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nitta Corp
Original Assignee
Nitta Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nitta Corp filed Critical Nitta Corp
Priority to JP11048012A priority Critical patent/JP2000239441A/en
Publication of JP2000239441A publication Critical patent/JP2000239441A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a rubber composition showing less temperature-dependent and high damping ratio of vibration energy (heq) by mixing butyl rubber as a material which maintains small temperature dependence and increases damping ratio with natural rubber as a basic material. SOLUTION: An amount of butyl rubber to be mixed with natural rubber is preferably not more than 50 pts.wt per 100 pts.wt. of a sum of the natural rubber and the butyl rubber. About 5-50 pts.wt. of a 9C-based hydrocarbon resin as a damping improver having a softening point of not more than 120 deg.C may be mixed with 100 pts.wt. of the sum of the natural rubber and the butyl rubber. The rubber composition is prepared by masticating each component by means of intermixing followed by simultaneously, adding fillers, mixing thereof uniformly and kneading a vulcanization accelerator and a vulcanization agent. The filler may be localized in the butyl rubber. It is possible to maintain small temperature dependence and increase damping ratio by localizing the filler in the butyl rubber of the compound in which the natural rubber contains the butyl rubber.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】この発明は、地震に対する免
震やその他の防振・制振などの各種の振動エネルギーを
吸収するための高減衰ゴム組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a high-damping rubber composition for absorbing various vibrational energies such as seismic isolation against vibration and other vibration proofing / damping.

【0002】[0002]

【従来の技術】近年、地震に対する免震やその他の防振
・制振などの各種の振動エネルギーを吸収する装置や機
械が注目されている。
2. Description of the Related Art In recent years, devices and machines that absorb various vibration energies, such as seismic isolation against earthquakes and other vibration proofing / damping, have attracted attention.

【0003】振動エネルギーを吸収するための有効な手
段として、高減衰ゴム組成物が脚光を浴びている。そし
て従来の高減衰ゴム組成物は機械的特性に優れた天然ゴ
ムを主成分とし、これに極性の高いハイスチレン配合S
BRゴム等をブレンドすることによって振動エネルギー
の減衰特性を得ていた。
As an effective means for absorbing vibrational energy, high damping rubber compositions have been spotlighted. The conventional high damping rubber composition is composed mainly of natural rubber having excellent mechanical properties, and a highly polar high styrene compounded S
By blending BR rubber or the like, a damping characteristic of vibration energy has been obtained.

【0004】しかし従来の高減衰ゴム組成物は、減衰率
heqを高くすると温度依存性もかなり大きくなってし
まうという問題があった。できるだけ減衰率heqが高
くて温度依存性が小さい材料が好ましい。
[0004] However, the conventional high damping rubber composition has a problem that when the damping rate heq is increased, the temperature dependency is considerably increased. It is preferable to use a material having as high an attenuation rate heq as possible and having a small temperature dependency.

【0005】なお、天然ゴムに粒子径の細かいカーボン
ブラックを多量に配合することにより高い減衰特性を得
ようとするものもあるが、これも弾性率の温度依存性が
大きくなってしまう。
[0005] In addition, there is an attempt to obtain high damping characteristics by blending a large amount of carbon black having a fine particle diameter into natural rubber, but this also increases the temperature dependence of the elastic modulus.

【0006】[0006]

【発明が解決しようとする課題】そこでこの発明は、従
来よりも振動エネルギーの減衰率heqが高くて温度依
存性が小さい高減衰ゴム組成物を提供しようとするもの
である。
SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a high-damping rubber composition having a higher damping rate heq of vibration energy and a lower temperature dependency than conventional ones.

【0007】[0007]

【課題を解決するための手段】前記課題を解決するため
この発明では次のような技術的手段を講じている。 この発明の高減衰ゴム組成物は、基剤としての天然
ゴムと温度依存性維持・兼減衰率増加剤としてのブチル
ゴムとを具備することを特徴とする。
In order to solve the above-mentioned problems, the present invention employs the following technical means. The high damping rubber composition of the present invention is characterized by comprising natural rubber as a base and butyl rubber as a temperature dependency maintaining / decay rate increasing agent.

【0008】この高減衰ゴム組成物は前記の構成を採用
したので、従来とほぼ同等の温度依存性であってもより
減衰率を大きくすることができる。 減衰率増加剤として前記天然ゴムとブチルゴムとの
合計100重量部に対して軟化点が120℃以下のC9
系炭化水素樹脂約5〜50重量部が配合されたこととし
てもよい。
[0008] Since the high damping rubber composition employs the above-described structure, the damping rate can be further increased even if the temperature dependency is substantially the same as that of the conventional one. C9 having a softening point of 120 ° C. or less based on 100 parts by weight of the total of the natural rubber and the butyl rubber as an attenuation rate increasing agent
About 5 to 50 parts by weight of the hydrocarbon resin may be blended.

【0009】温度依存性維持・兼減衰率増加剤としてブ
チルゴムを具備せしめるように構成した場合、軟化点が
約120℃以下のC9系炭化水素樹脂の配合が約5〜5
0重量部加えることでゴム組成物の減衰率を十分に向上
させることができる。C9系炭化水素樹脂は、タッキネ
スを上げるため加工性の点から少量入れるのが好まし
い。 天然ゴム、ブチルゴムの他に、補強剤(カーボンブ
ラック、シリカ)、軟化剤、プロセスオイル、可塑剤、
粘着付与剤、老化防止剤、加硫剤、加硫促進剤、加硫遅
延剤、樹脂その他の添加物を必要に応じて加えることが
できる。
When butyl rubber is provided as an agent for maintaining the temperature dependency and increasing the damping rate, the compounding ratio of the C9 hydrocarbon resin having a softening point of about 120 ° C. or less is about 5 to 5%.
By adding 0 parts by weight, the damping rate of the rubber composition can be sufficiently improved. It is preferable to add a small amount of C9-based hydrocarbon resin from the viewpoint of processability in order to increase tackiness. In addition to natural rubber and butyl rubber, reinforcing agents (carbon black, silica), softeners, process oils, plasticizers,
Tackifiers, antioxidants, vulcanizing agents, vulcanization accelerators, vulcanization retarders, resins and other additives can be added as needed.

【0010】[0010]

【発明の実施の形態】次のようにして高減衰ゴム組成物
を作成した。
DESCRIPTION OF THE PREFERRED EMBODIMENTS A high-damping rubber composition was prepared as follows.

【0011】実施例1〜9は下記に示す各成分をインタ
ーミックスを用い、ゴムの素練りをした後、充填剤を同
時投入し均一に混練りした。その後、加硫促進剤と加硫
剤はロールで練り込んだ。
In Examples 1 to 9, the following components were mixed using an intermix, rubber was masticated, and then a filler was simultaneously added and uniformly kneaded. Thereafter, the vulcanization accelerator and the vulcanizing agent were kneaded with a roll.

【0012】なお、ブチルゴムに充填剤を偏在させても
よい。天然ゴムにブチルゴムを具備させた同一配合で、
ブチルゴムに充填剤を偏在させると、温度依存性を維持
しつつさらに減衰を向上させることができる。
The filler may be unevenly distributed in the butyl rubber. With the same blend of natural rubber and butyl rubber,
When the filler is unevenly distributed in the butyl rubber, the attenuation can be further improved while maintaining the temperature dependency.

【0013】[0013]

【実施例】実施例1〜9の配合を表1に、比較例1〜5
の配合を表2に示す。
EXAMPLES Table 1 shows the formulations of Examples 1 to 9 and Comparative Examples 1 to 5
Is shown in Table 2.

【0014】[0014]

【表1】 なお表1中、ブチルゴム1は日本合成ゴム社製JSR
Butyl 065を、ブチルゴム2は日本合成ゴム社
製JSR Butyl 268を、ブチルゴム3は日本
合成ゴム社製JSR Butyl 365を、C9系炭
化水素樹脂は日本石油化学社製日石ネオポリマーE10
0表す。
[Table 1] In Table 1, butyl rubber 1 is JSR manufactured by Nippon Synthetic Rubber Co., Ltd.
Butyl 065, butyl rubber 2 was JSR Butyl 268 manufactured by Nippon Synthetic Rubber Co., Ltd., butyl rubber 3 was JSR Butyl 365 manufactured by Nippon Synthetic Rubber Co., Ltd.
0 is represented.

【0015】[0015]

【表2】 また表2中、BR01は日本合成ゴム社製ブタジエン・
ラバーを、JSR1503は日本合成ゴム社製スチレン
・ブタジエン・ラバーを、E−SBR 9550は日本
ゼオン社製スチレン・ブタジエン・ラバーを、ハイスチ
レンSBR 2057SSは日本ゼオン社製ハイスチレ
ンSBRを示す。
[Table 2] In Table 2, BR01 is a butadiene product manufactured by Nippon Synthetic Rubber Co., Ltd.
Rubber, JSR1503 indicates styrene-butadiene rubber manufactured by Japan Synthetic Rubber Co., Ltd., E-SBR 9550 indicates styrene-butadiene rubber manufactured by Zeon Corporation, and high styrene SBR 2057SS indicates high styrene SBR manufactured by Zeon Corporation.

【0016】次に、上記各サンプルを用いて以下の測定
を行った。
Next, the following measurements were performed using each of the above samples.

【0017】硬度(JIS.A)、引張強度(Kgf/c
m2 )、破断伸び(%)、静的剪断弾性率(Kgf/cm2
をJIS.K−6301に準じて測定した。図1に示す
試験サンプルを調整し、周波数0.5 Hz、変形量がゴム
厚みに対して約100%、剪断試験を行ったときの−1
0℃及び20℃における弾性率の比を求め、弾性の温度
依存比(−10℃/20℃)を算出した。なお図中、サ
ンプルの高減衰ゴム組成物は1で示す。また前記図1に
示す試験サンプルにより、公知の方法で150%変形時
の減衰率heq(%)を算出した。
Hardness (JIS.A), tensile strength (Kgf / c)
m 2 ), elongation at break (%), static shear modulus (Kgf / cm 2 )
To JIS. It measured according to K-6301. The test sample shown in FIG. 1 was prepared, the frequency was 0.5 Hz, the amount of deformation was about 100% with respect to the rubber thickness, and the shear test was -1.
The elastic modulus ratio at 0 ° C. and 20 ° C. was determined, and the temperature dependence of elasticity (−10 ° C./20° C.) was calculated. In the drawing, the sample high damping rubber composition is indicated by 1. The damping rate heq (%) at the time of 150% deformation was calculated from the test sample shown in FIG. 1 by a known method.

【0018】実施例の測定結果を表3に、比較例の測定
結果を表4に示す。
Table 3 shows the measurement results of the examples, and Table 4 shows the measurement results of the comparative examples.

【0019】[0019]

【表3】 [Table 3]

【0020】[0020]

【表4】 ブチルゴムの配合量が多くなり過ぎると引張強度と破断
伸びが低下する傾向が見られる。そこでブチルゴムの配
合量は、天然ゴムとブチルゴムとの合計100重量部に
対して約50重量部以下とすることがより好ましい。
[Table 4] If the amount of butyl rubber is too large, the tensile strength and the elongation at break tend to decrease. Therefore, the blending amount of butyl rubber is more preferably about 50 parts by weight or less based on 100 parts by weight of the total of natural rubber and butyl rubber.

【0021】表3及び表4のheq(%)と温度依存比
(−10℃/20℃)との関係のグラフを図2に示す。
このグラフに示されるように、この実施例の高減衰ゴム
組成物は比較例のものと同等の温度依存性であってもよ
り減衰率を大きくすることができる。
FIG. 2 is a graph showing the relationship between the heq (%) in Tables 3 and 4 and the temperature dependency ratio (-10 ° C./20° C.).
As shown in this graph, the high damping rubber composition of this example can increase the damping rate even with the same temperature dependency as that of the comparative example.

【0022】なお実施例7〜9は、5〜30部のC9系
炭化水素樹脂を配合したものである。図2のグラフ中の
実施例の側の直線に示されるように、実施例7〜9のh
eqと温度依存性の関係(横軸に対して寝ている方が良
い)は比較例よりも好ましい。このように、天然ゴムに
ブチルゴムをブレンドしC9系炭化水素樹脂を添加する
と、減衰と温度依存性のバランスが良い配合となる。
Examples 7 to 9 contain 5 to 30 parts of a C9 hydrocarbon resin. As shown by the straight line on the side of the example in the graph of FIG.
The relationship between eq and the temperature dependency (it is better to lie on the horizontal axis) is more preferable than the comparative example. As described above, when butyl rubber is blended with natural rubber and a C9-based hydrocarbon resin is added, a blend having a good balance between attenuation and temperature dependence is obtained.

【0023】[0023]

【発明の効果】この発明は上述のような構成であり、次
の効果を有する。
The present invention is configured as described above and has the following effects.

【0024】従来よりも振動エネルギーの減衰率heq
が高くて温度依存性が小さい高減衰ゴム組成物を提供す
ることができる。
The attenuation rate of vibration energy heq
And a high damping rubber composition having high temperature dependency and low temperature dependency can be provided.

【図面の簡単な説明】[Brief description of the drawings]

【図1】試験サンプルを説明する斜視図。FIG. 1 is a perspective view illustrating a test sample.

【図2】heq(%)と温度依存比(−10℃/20
℃)との関係を示すグラフ。
FIG. 2: Heq (%) and temperature dependence ratio (−10 ° C./20)
C).

【符号の説明】[Explanation of symbols]

1 高減衰ゴム組成物 1 high damping rubber composition

───────────────────────────────────────────────────── フロントページの続き (72)発明者 下田 篤史 奈良県大和郡山市池沢町172 ニッタ株式 会社奈良工場内 Fターム(参考) 4J002 AC01W BA01Y BB18X GR00 ────────────────────────────────────────────────── ─── Continuing from the front page (72) Inventor Atsushi Shimoda 172 Ikezawa-cho, Yamatokoriyama-shi, Nara Pref.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 基剤としての天然ゴムと温度依存性維持
・兼減衰率増加剤としてのブチルゴムとを具備すること
を特徴とする高減衰ゴム組成物。
1. A high-damping rubber composition comprising natural rubber as a base and butyl rubber as a temperature-dependent maintaining / decay rate increasing agent.
【請求項2】 減衰率増加剤として前記天然ゴムとブチ
ルゴムとの合計100重量部に対して軟化点が120℃
以下のC9系炭化水素樹脂約5〜50重量部を配合した
請求項1記載の高減衰ゴム組成物。
2. A softening point of 120 ° C. with respect to a total of 100 parts by weight of the natural rubber and butyl rubber as an attenuation rate increasing agent.
The high damping rubber composition according to claim 1, wherein about 5 to 50 parts by weight of the following C9 hydrocarbon resin is blended.
JP11048012A 1999-02-25 1999-02-25 High damping rubber composition Pending JP2000239441A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11048012A JP2000239441A (en) 1999-02-25 1999-02-25 High damping rubber composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11048012A JP2000239441A (en) 1999-02-25 1999-02-25 High damping rubber composition

Publications (1)

Publication Number Publication Date
JP2000239441A true JP2000239441A (en) 2000-09-05

Family

ID=12791405

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11048012A Pending JP2000239441A (en) 1999-02-25 1999-02-25 High damping rubber composition

Country Status (1)

Country Link
JP (1) JP2000239441A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002347022A (en) * 2001-05-23 2002-12-04 Bridgestone Corp Method for manufacturing rubber composition
JP2007063329A (en) * 2005-08-29 2007-03-15 Bridgestone Corp Highly damping rubber composition
JP2007063328A (en) * 2005-08-29 2007-03-15 Bridgestone Corp Highly damping rubber composition
KR100971188B1 (en) 2010-02-23 2010-07-20 주식회사 부흥시스템 Hi-attenuation vulcanized rubber and a elastomeric bearing using thereof
JP2019006846A (en) * 2017-06-20 2019-01-17 株式会社ブリヂストン Rubber composition and tire using the same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002347022A (en) * 2001-05-23 2002-12-04 Bridgestone Corp Method for manufacturing rubber composition
JP2007063329A (en) * 2005-08-29 2007-03-15 Bridgestone Corp Highly damping rubber composition
JP2007063328A (en) * 2005-08-29 2007-03-15 Bridgestone Corp Highly damping rubber composition
KR100971188B1 (en) 2010-02-23 2010-07-20 주식회사 부흥시스템 Hi-attenuation vulcanized rubber and a elastomeric bearing using thereof
JP2019006846A (en) * 2017-06-20 2019-01-17 株式会社ブリヂストン Rubber composition and tire using the same

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