JP2001011263A - Vibrationproof rubber composition - Google Patents
Vibrationproof rubber compositionInfo
- Publication number
- JP2001011263A JP2001011263A JP11184694A JP18469499A JP2001011263A JP 2001011263 A JP2001011263 A JP 2001011263A JP 11184694 A JP11184694 A JP 11184694A JP 18469499 A JP18469499 A JP 18469499A JP 2001011263 A JP2001011263 A JP 2001011263A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- sulfur
- vulcanization accelerator
- epdm
- hardness
- 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
Links
Landscapes
- Vibration Prevention Devices (AREA)
- Springs (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、防振ゴム組成物に
関する。更に詳しくは、一定値以下の硬さおよび動倍率
を有する加硫物を与え得る防振ゴム組成物に関する。TECHNICAL FIELD The present invention relates to a vibration-proof rubber composition. More specifically, the present invention relates to an anti-vibration rubber composition capable of providing a vulcanizate having a hardness and a dynamic magnification of a certain value or less.
【0002】[0002]
【従来の技術】ブチルゴム(イソブチレン-イソプレン共
重合ゴム)は、衝撃吸収性や振動減衰性にすぐれている
ので、防振ゴム材料として広く用いられている。このよ
うな用途に用いられる場合、支持部品の更なる軽量化に
伴い、製品(マウント)に低いバネ定数が求められるよ
うになるため、加硫物の硬さが低いことが求められてい
る。2. Description of the Related Art Butyl rubber (isobutylene-isoprene copolymer rubber) is widely used as an anti-vibration rubber material because of its excellent shock absorption and vibration damping properties. When used in such an application, a low spring constant is required for a product (mount) with a further reduction in the weight of the support component, and therefore, the hardness of the vulcanized product is required to be low.
【0003】ブチルゴムの低硬度化は、一般に可塑剤の
添加によって行われているが、加工性の点からその添加
量の上限は約50phr程度とされており、このような改質
方法には限界がみられる。また、可塑剤の添加による低
硬度化では、加硫物の動倍率が2.0をこえ、防振材料と
しての製品機能を満足させなくなる。[0003] The lowering of the hardness of butyl rubber is generally carried out by adding a plasticizer, but the upper limit of the amount added is about 50 phr from the viewpoint of processability. Is seen. In addition, when the hardness is reduced by adding a plasticizer, the dynamic magnification of the vulcanized product exceeds 2.0, and the product function as a vibration damping material cannot be satisfied.
【0004】[0004]
【発明が解決しようとする課題】本発明の目的は、一定
値以下の硬さおよび動倍率を有し、防振材料として好適
に使用される加硫物を与え得る防振ゴム組成物を提供す
ることにある。SUMMARY OF THE INVENTION It is an object of the present invention to provide a vibration-insulating rubber composition having a hardness and a dynamic magnification of not more than a certain value and capable of providing a vulcanized product suitably used as a vibration-proof material. Is to do.
【0005】[0005]
【課題を解決するための手段】かかる本発明の目的は、
ブチルゴム、ムーニー粘度ML1+8(100℃)が約50〜100のE
PDMおよびイオウ系加硫促進剤を含有する防振ゴム組成
物によって達成される。SUMMARY OF THE INVENTION The object of the present invention is as follows.
Butyl rubber, Mooney viscosity ML 1 + 8 (100 ° C) E of about 50-100
This is achieved by an anti-vibration rubber composition containing PDM and a sulfur-based vulcanization accelerator.
【0006】[0006]
【発明の実施の形態】EPDM(約90〜50重量部)およびブチ
ルゴム(約10〜50重量部)よりなるEPDMリッチのブレンド
ゴムにカーボンブラックを配合したゴム組成物は公知で
あり、それの加硫物がラジエータパッキン等として使用
されることは知られているが(特開昭63-68684号公報)、
それの加硫はEPDMリッチということもあって有機過酸化
物によって行われている。DETAILED DESCRIPTION OF THE INVENTION A rubber composition obtained by blending carbon black with an EPDM-rich blend rubber comprising EPDM (about 90 to 50 parts by weight) and butyl rubber (about 10 to 50 parts by weight) is known. Although it is known that sulphate is used as a radiator packing or the like (JP-A-63-68684),
Its vulcanization is done with organic peroxide, partly due to its EPDM richness.
【0007】本発明においては、一般にブチルゴム100
重量部に対して特定のムーニー粘度を有するEPDMが約20
〜100重量部、好ましくは約20〜60重量部というブチル
ゴムリッチのブレンドゴムとして用いられ、それの加硫
もイオウ系の加硫促進剤を用いて行われている。In the present invention, butyl rubber 100 is generally used.
EPDM with a specific Mooney viscosity of about 20 parts by weight
It is used as a butyl rubber-rich blend rubber of about 100 parts by weight, preferably about 20 to 60 parts by weight, and its vulcanization is also carried out using a sulfur-based vulcanization accelerator.
【0008】ブチルゴムにブレンドされて用いられるEP
DMとしては、ムーニー粘度ML1+8(100℃)が約50〜100、
好ましくは約50〜60のものが用いられる。ムーニー粘度
がこれ以下のものを用いると、加工性が不具合となり、
一方これ以上のムーニー粘度のものを用いると、ブチル
ゴムとの相溶性に欠けるようになる。EP used by blending with butyl rubber
As DM, Mooney viscosity ML 1 + 8 (100 ° C) is about 50-100,
Preferably about 50 to 60 are used. If the Mooney viscosity is less than this, the workability becomes defective,
On the other hand, if a material having a Mooney viscosity higher than this is used, the compatibility with butyl rubber will be lacking.
【0009】これらのブレンドゴムには、その加硫物の
低粘度化を達成させるために、ブチルゴム100重量部当
り約200重量部以下、好ましくは約20〜100重量部の可塑
剤を添加して用いることが好ましい。可塑剤としては、
セバシン酸、アゼライン酸、アジピン酸等の脂肪族ジカ
ルボン酸またはフタル酸等の芳香族ジカルボン酸のブチ
ル、2-エチルブチル、2-エチルヘキシル、オクチル、イ
ソオクチル、イソデシル等のジエステルが用いられる。In order to reduce the viscosity of the vulcanizate, a plasticizer of about 200 parts by weight or less, preferably about 20 to 100 parts by weight, is added to 100 parts by weight of butyl rubber. Preferably, it is used. As a plasticizer,
Diesters of aliphatic dicarboxylic acids such as sebacic acid, azelaic acid and adipic acid or aromatic dicarboxylic acids such as phthalic acid such as butyl, 2-ethylbutyl, 2-ethylhexyl, octyl, isooctyl and isodecyl are used.
【0010】以上の各成分に加えて、カーボンブラッ
ク、2価金属の酸化物または水酸化物あるいはハイドロ
タルサイト類等の受酸剤、加工助剤、その他必要な配合
剤が添加された組成物は、酸化亜鉛等の加硫剤およびイ
オウ系の加硫促進剤、より具体的にはチウラム系または
チアゾール系の加硫促進剤を用いて加硫が行われる。A composition containing, in addition to the above components, an acid acceptor such as carbon black, an oxide or hydroxide of a divalent metal or hydrotalcite, a processing aid, and other necessary additives. The vulcanization is carried out using a vulcanizing agent such as zinc oxide and a sulfur-based vulcanization accelerator, more specifically a thiuram-based or thiazole-based vulcanization accelerator.
【0011】チウラム系またはチアゾール系の加硫促進
剤としては、次のようなものが用いられる。 チウラム系加硫促進剤: R1R2:同一または異なるC3〜C8アルキル基 x:1〜4 y:1〜2 M:原子価nのZn、Cu、Fe、Teなどの金属 R:C3〜C8のアルキル基 M:Zn、Cu、Fe、Teなどの2価の金属 X:水素原子 シクロヘキシル基、アルキル基などによって置換された
N-モノ置換 アミノ基、ジシクロヘキシル基、オキシジエチレン基、
ジアルキル基などによって置換されたN-ジ置換アミノ基
(-NR1R2) アルキル基、アルキルフェニル基、アルキルベンジル基
などによってN-ジ置換されたチオカルバモイル基(-CS-N
R3R4)The following thiuram-based or thiazole-based vulcanization accelerators are used. Thiuram vulcanization accelerator: R 1 R 2 : the same or different C 3 -C 8 alkyl groups x: 1-4 y: 1-2 M: metals such as Zn, Cu, Fe, Te with valence n R: alkyl group of C 3 ~C 8 M: Zn, Cu, Fe, 2 -valent metal such as Te X: a hydrogen atom cyclohexyl, which is substituted by an alkyl group
N-monosubstituted amino group, dicyclohexyl group, oxydiethylene group,
N-disubstituted amino group substituted by dialkyl group etc.
(-NR 1 R 2 ) a thiocarbamoyl group N-disubstituted by an alkyl group, an alkylphenyl group, an alkylbenzyl group (-CS-N
R 3 R 4 )
【0012】これらの各成分を用いての組成物の調製
は、インターミックス、ニーダ等を用いる密閉式の場合
には、加硫剤および加硫促進剤以外の各成分を一括投入
し、約10〜20分間混練した後加硫剤および加硫促進剤を
投入し、約3分後に排出することによって行われ、また
オープンロールを用いる場合には、ブレンドゴムをロー
ルに巻き付け、加硫剤および加硫促進剤以外の各成分を
添加した後、最後に加硫剤および加硫促進剤を添加する
ことによって行われる。[0012] In the case of a closed type using an intermix, a kneader, or the like, the composition using these components is prepared by simultaneously charging each component other than the vulcanizing agent and the vulcanization accelerator, and adding about 10%. After kneading for about 20 minutes, a vulcanizing agent and a vulcanization accelerator are charged and discharged after about 3 minutes.If an open roll is used, the blended rubber is wound around a roll, and the vulcanizing agent and the vulcanizing agent are vulcanized. After adding each component other than a sulfur accelerator, it is performed by finally adding a vulcanizing agent and a vulcanization accelerator.
【0013】このようにして調製された組成物の加硫
は、約150〜200℃で約5〜20分間行われるプレス加硫に
よって行われる。The vulcanization of the composition thus prepared is carried out by press vulcanization performed at about 150 to 200 ° C. for about 5 to 20 minutes.
【0014】[0014]
【発明の効果】ブチルゴムに可塑剤を配合した場合に
は、その加硫物の硬さ(JIS A)を約20程度に迄するのが
限界であったが、ブチルゴムに特定のムーニー粘度を有
するEPDMをブレンドし、更に好ましくはそこに可塑剤を
加えてイオウ系の加硫促進剤を用いて加硫することによ
り、その硬さを17以下とし、しかも動倍率が2.0以下の
加硫物が得られるようになる。According to the present invention, when a plasticizer is blended with butyl rubber, the limit of the hardness (JIS A) of the vulcanized product is limited to about 20, but the butyl rubber has a specific Mooney viscosity. EPDM is blended, and more preferably, by adding a plasticizer thereto and vulcanizing using a sulfur-based vulcanization accelerator, the hardness is reduced to 17 or less, and a vulcanizate having a dynamic magnification of 2.0 or less is obtained. Will be obtained.
【0015】このように、硬さおよび動倍率の低い加硫
物を与える本発明の防振ゴム組成物は、CD-ROMマウン
ト、DVD-ROMマウント等の防振ゴム材料の成形材料とし
て有効に用いることができる。As described above, the anti-vibration rubber composition of the present invention, which provides a vulcanizate having a low hardness and low dynamic magnification, can be effectively used as a molding material for anti-vibration rubber materials such as CD-ROM mounts and DVD-ROM mounts. Can be used.
【0016】[0016]
【実施例】次に、実施例について本発明を説明する。Next, the present invention will be described with reference to examples.
【0017】 実施例1 ブチルゴム(エクソン社製品HT10-66) 100重量部 EPDM(DMSジャパン製品ケルタン314) 20 〃 [ML1+8(100℃)53] ジ(2-エチルヘキシル)セバケート 60 〃 HAFカーボンブラック 10 〃 ステアリン酸 1 〃 テトラメチルチウラムジサルファイド促進剤 1 〃 ジベンゾチアジルジサルファイド促進剤 1 〃 酸化マグネシウム 0.5 〃 酸化亜鉛 5 〃 以上の各配合成分をニーダで混練し、180℃で6分間のプ
レス加硫を行った。加硫物について、常態物性(JIS K-6
301準拠)および動倍率Kd(50Hz)/Kstの測定を行った。Example 1 Butyl Rubber (HT10-66 manufactured by Exxon) 100 parts by weight EPDM (Keltan 314 manufactured by DMS Japan) 20 20 [ML 1 + 8 (100 ° C) 53] di (2-ethylhexyl) sebacate 60〃 HAF carbon Black 10 ス テ Stearic acid 1 〃 Tetramethylthiuram disulfide accelerator 1 〃 Dibenzothiazyl disulfide accelerator 1 マ グ ネ シ ウ ム Magnesium oxide 0.5 亜 鉛 Zinc oxide 5 〃 Knead the above ingredients with a kneader and mix at 180 ° C for 6 minutes. Press vulcanization was performed. Regarding the vulcanized product, normal physical properties (JIS K-6
301) and dynamic magnification Kd (50 Hz) / Kst.
【0018】実施例2 実施例1において、EPDMとしてDMSジャパン製品ケルタン
4703[ML1+8(100℃)95]が同量用いられた。Example 2 In Example 1, DMS Japan product Keltan was used as EPDM.
4703 [ML 1 + 8 (100 ° C) 95] was used in the same amount.
【0019】実施例3 実施例2において、EPDM量を50重量部に、また可塑剤量
を100重量部にそれぞれ変更した。Example 3 In Example 2, the amount of EPDM was changed to 50 parts by weight, and the amount of plasticizer was changed to 100 parts by weight.
【0020】実施例4 実施例2において、EPDM量を100重量部に、また可塑剤量
を200重量部にそれぞれ変更した。Example 4 In Example 2, the amount of EPDM was changed to 100 parts by weight and the amount of plasticizer was changed to 200 parts by weight.
【0021】比較例 実施例1において、EPDMを用いずに、可塑剤量を40重量
部に変更した。Comparative Example In Example 1, the amount of the plasticizer was changed to 40 parts by weight without using EPDM.
【0022】以上の各実施例および比較例における測定
結果は、次の表に示される。 表 測定項目 実-1 実-2 実-3 実-4 比較例 [常態物性] 硬さ (JIS A) 16 16 10 4 18 引張強さ (MPa) 4.1 4.2 2.5 1.3 3.3 伸び (%) 800 780 870 950 600 100%モジュラス (MPa) 0.30 0.29 0.25 0.20 0.10 [動倍率] Kd(50Hz)/Kst 1.62 1.60 1.70 1.40 2.20The measurement results in the above Examples and Comparative Examples are shown in the following table. Table Measurement Items Actual-1 Actual-2 Actual-3 Actual-4 Comparative Example [Physical Properties] Hardness (JIS A) 16 16 10 4 18 Tensile Strength (MPa) 4.1 4.2 2.5 1.3 3.3 Elongation (%) 800 780 870 950 600 100% modulus (MPa) 0.30 0.29 0.25 0.20 0.10 [Dynamic magnification] Kd (50Hz) / Kst 1.62 1.60 1.70 1.40 2.20
フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) F16F 1/36 F16F 1/36 E 15/08 15/08 D Fターム(参考) 3J048 AA01 BB10 3J059 AA10 BC06 BC19 GA50 4J002 BB152 BB181 EH097 EH147 EV166 EV326 FD027 FD156 GM00 Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat II (Reference) F16F 1/36 F16F 1/36 E 15/08 15/08 DF Term (Reference) 3J048 AA01 BB10 3J059 AA10 BC06 BC19 GA50 4J002 BB152 BB181 EH097 EH147 EV166 EV326 FD027 FD156 GM00
Claims (3)
が約50〜100のEPDMおよびイオウ系加硫促進剤を含有し
てなる防振ゴム組成物。1. A butyl rubber, Mooney viscosity ML 1 + 8 (100 ° C.)
A rubber composition comprising about 50 to 100 EPDM and a sulfur-based vulcanization accelerator.
防振ゴム組成物。2. The anti-vibration rubber composition according to claim 1, further comprising a plasticizer.
(50Hz)/Kstが2.0以下の加硫物を与える請求項1または
2記載の防振ゴム組成物。3. The hardness (JIS A) is 17 or less, and the dynamic magnification Kd
3. The vibration-insulating rubber composition according to claim 1, which gives a vulcanizate having (50 Hz) / Kst of 2.0 or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11184694A JP2001011263A (en) | 1999-06-30 | 1999-06-30 | Vibrationproof rubber composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11184694A JP2001011263A (en) | 1999-06-30 | 1999-06-30 | Vibrationproof rubber composition |
Publications (1)
Publication Number | Publication Date |
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JP2001011263A true JP2001011263A (en) | 2001-01-16 |
Family
ID=16157751
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11184694A Pending JP2001011263A (en) | 1999-06-30 | 1999-06-30 | Vibrationproof rubber composition |
Country Status (1)
Country | Link |
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JP (1) | JP2001011263A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007169321A (en) * | 2005-12-19 | 2007-07-05 | Yamauchi Corp | Rubber vibration isolator and composition therefor |
WO2017094653A1 (en) * | 2015-11-30 | 2017-06-08 | 株式会社ブリヂストン | Rubber composition |
CN108250598A (en) * | 2017-12-29 | 2018-07-06 | 广州市骏怡汇汽车科技有限公司 | A kind of fire-retardant shock-absorption sound-insulation material and preparation method thereof |
Citations (7)
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JPS6323940A (en) * | 1986-07-16 | 1988-02-01 | Nok Corp | Rubber composition |
JPS6368684A (en) * | 1986-09-09 | 1988-03-28 | Nok Corp | Radiator packing and heat exchanger using the same |
JPH07324167A (en) * | 1994-05-31 | 1995-12-12 | Bridgestone Corp | Vibration-damping material |
JPH08239500A (en) * | 1995-02-28 | 1996-09-17 | Nitto Denko Corp | Vibration-damping material |
JPH09263702A (en) * | 1995-10-30 | 1997-10-07 | Bridgestone Corp | Anti-vibration thermoplastic material |
JPH10221930A (en) * | 1997-02-07 | 1998-08-21 | Arai Pump Mfg Co Ltd | Sponge rubber composition and production of sponge rubber roller |
JPH1180459A (en) * | 1997-09-01 | 1999-03-26 | Sumitomo Chem Co Ltd | Rubber composition for sponge, and manufacture of sponge rubber and sponge roller |
-
1999
- 1999-06-30 JP JP11184694A patent/JP2001011263A/en active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6323940A (en) * | 1986-07-16 | 1988-02-01 | Nok Corp | Rubber composition |
JPS6368684A (en) * | 1986-09-09 | 1988-03-28 | Nok Corp | Radiator packing and heat exchanger using the same |
JPH07324167A (en) * | 1994-05-31 | 1995-12-12 | Bridgestone Corp | Vibration-damping material |
JPH08239500A (en) * | 1995-02-28 | 1996-09-17 | Nitto Denko Corp | Vibration-damping material |
JPH09263702A (en) * | 1995-10-30 | 1997-10-07 | Bridgestone Corp | Anti-vibration thermoplastic material |
JPH10221930A (en) * | 1997-02-07 | 1998-08-21 | Arai Pump Mfg Co Ltd | Sponge rubber composition and production of sponge rubber roller |
JPH1180459A (en) * | 1997-09-01 | 1999-03-26 | Sumitomo Chem Co Ltd | Rubber composition for sponge, and manufacture of sponge rubber and sponge roller |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007169321A (en) * | 2005-12-19 | 2007-07-05 | Yamauchi Corp | Rubber vibration isolator and composition therefor |
WO2017094653A1 (en) * | 2015-11-30 | 2017-06-08 | 株式会社ブリヂストン | Rubber composition |
US10766213B2 (en) | 2015-11-30 | 2020-09-08 | Bridgestone Corporation | Rubber composition |
CN108250598A (en) * | 2017-12-29 | 2018-07-06 | 广州市骏怡汇汽车科技有限公司 | A kind of fire-retardant shock-absorption sound-insulation material and preparation method thereof |
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