JP2008163067A - Rubber composition - Google Patents

Rubber composition Download PDF

Info

Publication number
JP2008163067A
JP2008163067A JP2006350937A JP2006350937A JP2008163067A JP 2008163067 A JP2008163067 A JP 2008163067A JP 2006350937 A JP2006350937 A JP 2006350937A JP 2006350937 A JP2006350937 A JP 2006350937A JP 2008163067 A JP2008163067 A JP 2008163067A
Authority
JP
Japan
Prior art keywords
rubber
mass
parts
amine
rubber composition
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
Application number
JP2006350937A
Other languages
Japanese (ja)
Other versions
JP5170363B2 (en
Inventor
Takahiro Saito
崇浩 斉藤
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.)
Bridgestone Corp
Original Assignee
Bridgestone 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 Bridgestone Corp filed Critical Bridgestone Corp
Priority to JP2006350937A priority Critical patent/JP5170363B2/en
Publication of JP2008163067A publication Critical patent/JP2008163067A/en
Application granted granted Critical
Publication of JP5170363B2 publication Critical patent/JP5170363B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

<P>PROBLEM TO BE SOLVED: To provide a rubber composition satisfying both of good bonding property and ozone resistance by improving its ozone resistance and also preventing the reduction of the bonding property as much as possible. <P>SOLUTION: This rubber composition is characterized by containing at least 1 kind of natural rubber and a synthetic diene-based rubber, an amine-based anti-aging agent and silica gel, and also having 3 to 10 pts.mass content of the amine-based antioxidant based on 100 pts.mass rubber component. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、自動車などの防振ゴムとして好適に用いられるゴム組成物に関する。   The present invention relates to a rubber composition suitably used as a vibration-proof rubber for automobiles and the like.

自動車やその他の車両には種々の防振装置や防振部材が用いられており、これら防振装置や防振部材にゴム材料がしばしば用いられており、従来、このような防振ゴムとして用いられるゴム組成物としては、天然ゴムや合成ゴムのゴム成分に各種充填剤、加硫剤、加硫促進剤、老化防止剤などを添加配合して調製されている(特許文献1)。   Various anti-vibration devices and anti-vibration members are used in automobiles and other vehicles, and rubber materials are often used for these anti-vibration devices and anti-vibration members. Conventionally, they are used as such anti-vibration rubbers. The rubber composition is prepared by adding various fillers, vulcanizing agents, vulcanization accelerators, anti-aging agents and the like to the rubber components of natural rubber and synthetic rubber (Patent Document 1).

このようなゴム組成物には、大気中のオゾンとの接触によりゴム表面が荒れてしまい、防振ゴムとしての耐久性が劣化するとの課題がある。耐オゾン性は、カーボンブラックを過剰に添加したり、老化防止剤を増量することにより向上させることができるが、このようにカーボンブラックを多量に添加したり、老化防止剤を増量すると鋼材やアルミ材などの基材との接着性が低下し、防振装置に組み込む際やそのまま防振材として用いる場合などに支障をきたすことになる。   Such a rubber composition has a problem that the rubber surface is roughened by contact with ozone in the atmosphere, and durability as a vibration-proof rubber is deteriorated. The ozone resistance can be improved by adding excessive carbon black or increasing the amount of anti-aging agent. However, adding a large amount of carbon black or increasing the amount of anti-aging agent in this way can increase the resistance to steel and aluminum. Adhesiveness with a base material such as a material is lowered, which causes trouble when incorporated in a vibration isolator or when used as it is as a vibration isolator.

特開2006−131871号公報JP 2006-131871 A

本発明は、上記事情に鑑みなされたもので、耐オゾン性を向上させると共に、接着性の低下を可及的に防止して、良好な接着性と耐オゾン性とを両立させ、例えば防振ゴムのように鋼材やアルミ材等の基材に接着して使用するゴム部材などとして好適に用いられるゴム組成物を提供することを目的とする。   The present invention has been made in view of the above circumstances, and improves ozone resistance and prevents deterioration of adhesion as much as possible to achieve both good adhesion and ozone resistance. An object of the present invention is to provide a rubber composition that is suitably used as a rubber member or the like that is used by adhering to a base material such as steel or aluminum like rubber.

本発明者は、上記目的を達成するため、鋭意検討を行った結果、天然ゴムや合成ジエン系ゴムに添加剤の一としてアミン系老化防止剤を配合したゴム組成物において、シリカゲルを適量添加配合することにより、耐オゾン性向上のために上記アミン系老化防止剤の配合量を増量しても、鋼材やアルミ材に対する接着性を低下させることなく、良好に耐オゾン性を向上させ得ることを見出した。   As a result of intensive studies to achieve the above object, the present inventor has added a suitable amount of silica gel in a rubber composition in which an amine anti-aging agent is added as an additive to natural rubber or synthetic diene rubber. By improving the ozone resistance, it is possible to improve the ozone resistance satisfactorily without reducing the adhesion to steel and aluminum materials even if the amount of the amine-based anti-aging agent is increased. I found it.

即ち、従来、アミン系老化防止剤の添加量は、ゴム成分100質量部に対して0.5〜2質量部程度であり、それ以上増量すると接着性の大幅な低下が生じていたが、シリカゲルを例えばゴム成分100質量部に対して5〜100質量部添加配合することにより、アミン系老化防止剤の塩基成分がシリカゲルの酸性分に吸着され、老化防止剤の接着界面への移行が阻止されて、アミン系老化防止剤の添加量を従来は行われなかった3質量部以上に増量しても接着性を低下させることなく、鋼材やアルミ材との十分な接着性を維持したまま耐オゾン性を効果的に向上させ得ることを見出し、本発明を完成したものである。   That is, conventionally, the addition amount of the amine-based anti-aging agent is about 0.5 to 2 parts by mass with respect to 100 parts by mass of the rubber component. For example, by adding and blending 5 to 100 parts by mass with respect to 100 parts by mass of the rubber component, the base component of the amine-based anti-aging agent is adsorbed by the acidic component of the silica gel, and the migration of the anti-aging agent to the adhesion interface is prevented. In addition, even if the addition amount of the amine-based anti-aging agent is increased to 3 parts by mass or more which has not been conventionally performed, ozone resistance is maintained while maintaining sufficient adhesiveness with steel and aluminum materials without reducing adhesiveness. The present invention has been completed by finding that the properties can be effectively improved.

従って、本発明は、天然ゴム及び合成ジエン系ゴムから選ばれた少なくとも1種のゴム成分と、アミン系老化防止剤と、シリカゲルとを含有し、かつ上記アミン系老化防止剤の含有量が上記ゴム成分100質量部に対して3〜10質量部であることを特徴とするゴム組成物を提供するものである。   Therefore, the present invention contains at least one rubber component selected from natural rubber and synthetic diene rubber, an amine anti-aging agent, and silica gel, and the content of the amine anti-aging agent is the above. The rubber composition is provided in an amount of 3 to 10 parts by mass with respect to 100 parts by mass of the rubber component.

本発明によれば、上記アミン系老化防止剤の増量により耐オゾン性を大幅に向上とさせることができ、しかも該老化防止剤の増量による接着性の低下を招くことなく、良好な接着性を有するゴム組成物を得ることができ、耐オゾン性に優れると共に鋼材やアルミ材などとの良好な接着性を有し、防振ゴムなどとして好適に用いられるゴム組成物を提供される。   According to the present invention, the ozone resistance can be greatly improved by increasing the amount of the above-mentioned amine-based anti-aging agent, and good adhesiveness can be obtained without causing a decrease in adhesiveness due to the increase in the amount of the anti-aging agent. There is provided a rubber composition that is excellent in ozone resistance and has good adhesion to steel, aluminum, and the like, and is suitably used as a vibration-proof rubber.

以下、本発明につき更に詳しく説明する。
本発明のゴム組成物は、上述のように、天然ゴム及び合成ジエン系ゴムから選ばれた少なくとも1種のゴム成分と、アミン系老化防止剤と、シリカゲルとを含有してなるものである。
Hereinafter, the present invention will be described in more detail.
As described above, the rubber composition of the present invention contains at least one rubber component selected from natural rubber and synthetic diene rubber, an amine antioxidant, and silica gel.

ここで、上記ゴム成分としてより具体的には、天然ゴム、ブタジエンゴム(BR)、スチレンブタジエンゴム(SBR)、ブタジエン−アクリロニトリル共重合体ゴム(NBR)、イソプレンゴム(IR)、イソブチレン−イソプレン共重合体ゴム(IIR)クロロプレンゴム(CR)等の合成ジエン系ゴムが例示され、これらの1種又は2種以上を混合して用いることができ、場合によってはこれらの1種又は2種以上とエチレン−プロピレン−ジエン共重合体(EPDM)、アクリルゴム(ACM)、クロロスルホン化ポリエチレン(CSM)などの他のゴムを更に混合して用いることもできる。なお、特に制限されるものではないが、上記合成ジエン系ゴムの中でもSBR、BR、IRが特に好ましく用いられる。   More specifically, the rubber component includes natural rubber, butadiene rubber (BR), styrene butadiene rubber (SBR), butadiene-acrylonitrile copolymer rubber (NBR), isoprene rubber (IR), and isobutylene-isoprene. Synthetic diene rubbers such as polymer rubber (IIR) and chloroprene rubber (CR) are exemplified, and one or two or more of these may be used in combination. In some cases, one or two or more of these may be used. Other rubbers such as ethylene-propylene-diene copolymer (EPDM), acrylic rubber (ACM), and chlorosulfonated polyethylene (CSM) can be further mixed and used. Although not particularly limited, SBR, BR and IR are particularly preferably used among the synthetic diene rubbers.

上記アミン系老化防止剤としては、ジアリルアミン系老化防止剤、p−フェニレンジアミン系老化防止剤が好ましく用いられ、これらの1種又は2種以上を併用することができる。これら老化防止剤としてより具体的には、ジアリルアミン系老化防止剤としてはp,p’−ジオクチルジフェニルアミン、p,p’−ジクミルジフェニルアミンなどが例示され、またp−フェニレンジアミン系老化防止剤としてはN,N’−ジフェニル−p−フェニレンジアミン、N−フェニル−N’−イソプロピル−p−フェニレンジアミン、N−フェニル−N’−1,3−ジメチルブチル−p−フェニレンジアミン、N−フェニル−N’−(3−メタクリロイルオキシ−2−ヒドロキシプロピル)−p−フェニレンジアミンなどが例示される。これらの中でもN−フェニル−N’−イソプロピル−p−フェニレンジアミン、N−フェニル−N’−1,3−ジメチルブチル−p−フェニレンジアミンが特に好適に用いられる。   As said amine type | system | group antioxidant, a diallylamine type | system | group antioxidant and p-phenylenediamine type | system | group antioxidant are used preferably, These 1 type (s) or 2 or more types can be used together. More specifically, examples of these antiaging agents include p, p'-dioctyldiphenylamine, p, p'-dicumyldiphenylamine and the like as diallylamine antiaging agents, and examples of p-phenylenediamine antiaging agents. N, N′-diphenyl-p-phenylenediamine, N-phenyl-N′-isopropyl-p-phenylenediamine, N-phenyl-N′-1,3-dimethylbutyl-p-phenylenediamine, N-phenyl-N Examples include '-(3-methacryloyloxy-2-hydroxypropyl) -p-phenylenediamine. Among these, N-phenyl-N′-isopropyl-p-phenylenediamine and N-phenyl-N′-1,3-dimethylbutyl-p-phenylenediamine are particularly preferably used.

これらアミン系老化防止剤の配合量は、上記ゴム成分100質量部に対して、3〜10質量部、好ましくは5〜10質量部とされ、従来2質量部程度までであったアミン系老化防止剤配合量を大幅に増量して、耐オゾン性を大幅に向上させたものである。この場合、アミン系老化防止剤の配合量が3重量部未満であると十分な耐オゾン性を得ることができずに本発明の目的を十分に達成しえず、一方10質量部を超えると接着性の低下を十分に防止することができない場合があり、また10質量部を超えて添加しても特に効果の向上は見られない。   The compounding amount of these amine anti-aging agents is 3 to 10 parts by mass, preferably 5 to 10 parts by mass with respect to 100 parts by mass of the rubber component. The amount of the agent is greatly increased to greatly improve the ozone resistance. In this case, if the compounding amount of the amine-based anti-aging agent is less than 3 parts by weight, sufficient ozone resistance cannot be obtained, and the object of the present invention cannot be sufficiently achieved. In some cases, the decrease in adhesiveness cannot be sufficiently prevented, and even when added in an amount exceeding 10 parts by mass, no particular improvement in effect is observed.

次に、シリカゲルは、特に制限されるものではないが、BET法による窒素吸着比表面積が30〜240m2/g、特に80〜230m2/gであることが好ましく、このシリカゲルの添加により、上記アミン系老化防止剤の塩基成分をシリカゲルの酸性分が吸着して接着界面へのアミン系老化防止剤の移行を防止し、接着性低下を招くことなく、アミン系老化防止剤の増量を可能としたものである。なお、上記比表面積が240m2/gを超えると防振特性が低下する場合がある。 Next, the silica gel is not particularly limited, but the nitrogen adsorption specific surface area by the BET method is preferably 30 to 240 m 2 / g, particularly 80 to 230 m 2 / g. The base component of the amine anti-aging agent is adsorbed by the acidic component of the silica gel to prevent the amine anti-aging agent from migrating to the adhesive interface, and the amount of the amine anti-aging agent can be increased without causing a decrease in adhesion. It is a thing. In addition, when the specific surface area exceeds 240 m 2 / g, the vibration isolation characteristics may be deteriorated.

このシリカゲルの配合量は、特に制限されるものではないが、上記ゴム成分100質量部に対して、5〜100質量部、特に10〜50質量部とすることが好ましい。この場合、シリカゲルの配合量が5質量部未満であると十分な接着性低下の防止効果が得られない場合があり、また静バネ定数が低くなって防振ゴムとする場合には不適となる場合がある。一方、配合量が100質量部を超えると、組成物をゴムに混練することが困難になる場合がある。   The compounding amount of the silica gel is not particularly limited, but is preferably 5 to 100 parts by mass, particularly 10 to 50 parts by mass with respect to 100 parts by mass of the rubber component. In this case, if the blending amount of silica gel is less than 5 parts by mass, a sufficient effect of preventing adhesion deterioration may not be obtained, and it becomes unsuitable when the static spring constant is lowered to obtain a vibration-proof rubber. There is a case. On the other hand, when the amount exceeds 100 parts by mass, it may be difficult to knead the composition into rubber.

本発明のゴム組成物には、上記各成分の他に、必要に応じて加硫剤、加硫促進剤、耐熱老化防止剤、ワックス、着色剤、充填剤、可塑剤、軟化剤、粘着付与剤などの公知の添加剤を適宜添加配合することができる。   In addition to the above-mentioned components, the rubber composition of the present invention includes a vulcanizing agent, a vulcanization accelerator, a heat-resistant anti-aging agent, a wax, a colorant, a filler, a plasticizer, a softening agent, and tackifying as necessary. A known additive such as an agent can be appropriately added and blended.

上記加硫剤としては、例えば硫黄などが挙げられ、加硫促進剤としては、2−メルカプトベンゾチアゾール、ジベンゾチアジルジスルフィド、N−シクロヘキシル−2−ベンゾチアジルスルフェンアミド、N−t−ブチル−2−ベンゾチアジルスルフェンアミド、N−t−ブチル−2−ベンゾチアジルスルフェンイミド等のベンゾチアゾール系加硫促進剤;ジフェニルグアニジン等のグアニジン系加硫促進剤;テトラドデシルチウラウムジスルフィド、テトラオクチルチウラウムジスルフィド、テトラベンジルチウラウムジスルフィド等のチウラウム系加硫促進剤;その他ジアルキルジチオリン酸亜鉛などが例示される。また、充填剤としてはカーボンブラック、炭酸カルシウム、クレー、マイカなどが例示される。更に、ステアリン酸や亜鉛華などの公知の添加剤を配合することができる。   Examples of the vulcanizing agent include sulfur. Examples of the vulcanizing accelerator include 2-mercaptobenzothiazole, dibenzothiazyl disulfide, N-cyclohexyl-2-benzothiazylsulfenamide, and Nt-butyl. Benzothiazole vulcanization accelerators such as 2-benzothiazylsulfenamide and Nt-butyl-2-benzothiazylsulfenimide; guanidine vulcanization accelerators such as diphenylguanidine; tetradodecyl thiuram disulfide And thiouranium-based vulcanization accelerators such as tetraoctylthiouranium disulfide and tetrabenzylthiouranium disulfide; and other zinc dialkyldithiophosphates. Examples of the filler include carbon black, calcium carbonate, clay, mica and the like. Furthermore, known additives such as stearic acid and zinc white can be blended.

本発明のゴム組成物は、上記各成分を混練し、必要に応じて加熱することにより、製造される。この場合、混練操作は、従来から公知のロール、バンバリーミキサー、ニーダー等の混合装置を使用することができる。また、成形はプレス成形、トランスファー成形、主出成形など、成形する形状や成形物の用途などに応じて適宜選択することができる。また、本発明のゴム組成物は、耐オゾン性に優れかつ接着性も良好なものであり、鋼材やアルミ材からなる基材に接着させて使用される防振ゴムなどとして特に好適なものであるが、この場合接着剤としては、特に制限されるものではないが、フェノール樹脂系接着剤、エポキシ系接着剤、ハイパロン系接着剤、塩化ゴム系接着剤などが好適に用いられる。   The rubber composition of the present invention is produced by kneading the above components and heating as necessary. In this case, the kneading operation can use a conventionally known mixing device such as a roll, a Banbury mixer, a kneader or the like. Further, the molding can be appropriately selected according to the shape to be molded, the use of the molded product, such as press molding, transfer molding and main molding. Further, the rubber composition of the present invention has excellent ozone resistance and good adhesiveness, and is particularly suitable as a vibration-proof rubber used by being bonded to a base material made of steel or aluminum. In this case, the adhesive is not particularly limited, but a phenol resin adhesive, an epoxy adhesive, a hypalon adhesive, a chlorinated rubber adhesive, and the like are preferably used.

以下、実施例,比較例を示し、本発明をより具体的に説明するが、本発明は下記実施例に制限されるものではない。   EXAMPLES Hereinafter, although an Example and a comparative example are shown and this invention is demonstrated more concretely, this invention is not restrict | limited to the following Example.

[実施例1〜7、比較例1〜3]
下記、表1に示す配合成分を混練し、加硫して実施例1〜7及び比較例1〜3の10種のゴム組成物を得た。得られた各ゴム組成物につき、耐オゾン性及び接着性を下記の通り評価した。結果を表1に示す。
[Examples 1-7, Comparative Examples 1-3]
The following blending components shown in Table 1 were kneaded and vulcanized to obtain 10 types of rubber compositions of Examples 1 to 7 and Comparative Examples 1 to 3. About each obtained rubber composition, ozone resistance and adhesiveness were evaluated as follows. The results are shown in Table 1.

耐オゾン性
JIS K6259(1993)に従い、40℃、50pphm、0−20%伸張の条件で動的オゾン劣化試験を行い、24hr後、100hr後、200hr後の亀裂の状態をJIS K6259に規定の基準に従って評価した。
接着性
JIS K6256(1999)に従い、鋼材及びアルミ材に対する剥離試験を行って接着性を評価した。良否判定は、ゴム凝集破壊が生じたものを○(良)、それ以外の破壊が生じたものは×(否)とした。なお、表1中の「熱老化後」の値は、70℃に1000hr放置した後の結果である。
Ozone resistance In accordance with JIS K6259 (1993), a dynamic ozone degradation test was conducted under the conditions of 40 ° C., 50 pphm, and 0-20% elongation. Evaluated according to.
Adhesiveness According to JIS K6256 (1999), a peel test was performed on steel and aluminum materials to evaluate the adhesiveness. In the pass / fail judgment, the case where the rubber cohesive failure occurred was evaluated as ◯ (good), and the case where the other failure occurred was evaluated as x (failed). The values of “After heat aging” in Table 1 are the results after leaving at 70 ° C. for 1000 hours.

Figure 2008163067
RSS#1
天然ゴム Ribbed smoked Sheet 1号
Nipsil VN3
沈降式シリカ、BET比表面積180〜230m2/g(東ソー・シリカ(株)製)
6PPD(6C)
大内新興化学工業社製の老化防止剤(N−フェニル−N’−1,3−ジメチルブチル−p−フェニレンジアミン)
1PPD(3C)
大内新興化学工業社製の老化防止剤(N−フェニル−N’−イソプロピル−p−フェニレンジアミン)
RD
耐熱老化防止剤(大内新興化学工業社製)
CZ
加硫促進剤(大内新興化学工業社製)
Figure 2008163067
RSS # 1
Natural rubber Ribbed smoked Sheet No.1
Nipsil VN3
Precipitated silica, BET specific surface area 180-230 m 2 / g (manufactured by Tosoh Silica Co., Ltd.)
6PPD (6C)
Anti-aging agent (N-phenyl-N′-1,3-dimethylbutyl-p-phenylenediamine) manufactured by Ouchi Shinsei Chemical Co., Ltd.
1PPD (3C)
Anti-aging agent (N-phenyl-N'-isopropyl-p-phenylenediamine) manufactured by Ouchi Shinsei Chemical Co., Ltd.
RD
Heat aging inhibitor (manufactured by Ouchi Shinsei Chemical Co., Ltd.)
CZ
Vulcanization accelerator (Ouchi Shinsei Chemical Co., Ltd.)

上記表1の通り、アミン系老化防止剤(6PPD、1PPD)を3質量部以上、特に5質量部以上添加した実施例のゴム組成物は、耐オゾン性に優れ、しかもシリカゲル(Nipsil VN3)の配合により、鋼材及びアルミ材に対して良好な接着性を有している。これに対し、アミン系老化防止剤の配合量が1質量部と少ない比較例2,3のゴム組成物は、接着性は良好であるものの、耐オゾン性に劣り、アミン系老化防止剤を5質量部に増量した比較例1のゴム組成物は、耐オゾン性に優れるもののシリカゲルが配合されていないために接着性が大幅に低下している。   As shown in Table 1, the rubber compositions of the examples to which 3 parts by mass or more, particularly 5 parts by mass or more of the amine-based anti-aging agent (6PPD, 1PPD) are added are excellent in ozone resistance, and moreover the silica gel (Nipsil VN3). By blending, it has good adhesion to steel and aluminum. On the other hand, the rubber compositions of Comparative Examples 2 and 3 having a small compounding amount of the amine anti-aging agent of 1 part by mass are poor in ozone resistance but 5% of the amine anti-aging agent although the adhesiveness is good. Although the rubber composition of Comparative Example 1 increased in mass parts is excellent in ozone resistance, since the silica gel is not blended, the adhesiveness is greatly lowered.

このように、アミン系老化防止剤の増量により耐オゾン性を大幅に向上とさせることができ、しかもシリカゲルの添加により該老化防止剤の増量による接着性の低下を招くことなく、良好な接着性を有するゴム組成物が得られることを確認した。   Thus, the ozone resistance can be greatly improved by increasing the amount of the amine-based anti-aging agent, and good adhesion can be achieved without causing a decrease in the adhesiveness due to the increase in the amount of the anti-aging agent by adding silica gel. It was confirmed that a rubber composition having

Claims (7)

天然ゴム及び合成ジエン系ゴムの少なくとも1種のゴム成分と、アミン系老化防止剤と、シリカゲルとを含有し、かつ上記アミン系老化防止剤の含有量が上記ゴム成分100質量部に対して3〜10質量部であることを特徴とするゴム組成物。   It contains at least one rubber component of natural rubber and synthetic diene rubber, an amine anti-aging agent and silica gel, and the content of the amine anti-aging agent is 3 with respect to 100 parts by mass of the rubber component. A rubber composition characterized in that the content is from 10 to 10 parts by mass. 上記アミン系老化防止剤として、ジアリルアミン系老化防止剤及び/又はp−フェニレンジアミン系老化防止剤を含有する請求項1記載のゴム組成物。   The rubber composition according to claim 1, comprising a diallylamine-based antioxidant and / or a p-phenylenediamine-based antioxidant as the amine-based antioxidant. アミン系老化防止剤の含有量が、ゴム成分100質量部に対して5〜10質量部である請求項1又は2記載のゴム組成物。   The rubber composition according to claim 1 or 2, wherein the content of the amine-based antioxidant is 5 to 10 parts by mass with respect to 100 parts by mass of the rubber component. 上記合成ジエン系ゴムとして、スチレンブタジエンゴム、ブタジエンゴム及びイソプレンゴムから選ばれる1種又は2種以上を含有する請求項1記載のゴム組成物。   The rubber composition according to claim 1, comprising one or more selected from styrene butadiene rubber, butadiene rubber and isoprene rubber as the synthetic diene rubber. 上記シリカゲルが、BET法による窒素吸着比表面積が30〜240m2/gのシリカゲルである請求項1〜4のいずれか1項に記載のゴム組成物。 The rubber composition according to any one of claims 1 to 4, wherein the silica gel is a silica gel having a nitrogen adsorption specific surface area of 30 to 240 m 2 / g by a BET method. シリカゲルの含有量が、ゴム成分100質量部に対して5〜100質量部である請求項1〜5のいずれか1項に記載のゴム組成物。   The rubber composition according to any one of claims 1 to 5, wherein the content of silica gel is 5 to 100 parts by mass with respect to 100 parts by mass of the rubber component. 防振ゴムとして用いられるものである請求項1〜6のいずれか1項に記載のゴム組成物。   The rubber composition according to any one of claims 1 to 6, which is used as a vibration-proof rubber.
JP2006350937A 2006-12-27 2006-12-27 Rubber composition Active JP5170363B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006350937A JP5170363B2 (en) 2006-12-27 2006-12-27 Rubber composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2006350937A JP5170363B2 (en) 2006-12-27 2006-12-27 Rubber composition

Publications (2)

Publication Number Publication Date
JP2008163067A true JP2008163067A (en) 2008-07-17
JP5170363B2 JP5170363B2 (en) 2013-03-27

Family

ID=39692982

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006350937A Active JP5170363B2 (en) 2006-12-27 2006-12-27 Rubber composition

Country Status (1)

Country Link
JP (1) JP5170363B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102666705A (en) * 2009-11-18 2012-09-12 株式会社普利司通 Vibration isolating rubber composition and vibration isolating rubber
CN104311914A (en) * 2014-10-13 2015-01-28 安徽奥丰汽车配件有限公司 Automotive engine bush
CN106496662A (en) * 2016-10-25 2017-03-15 上海众力投资发展有限公司 A kind of car engine suspension rubber composition

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06136184A (en) * 1992-05-20 1994-05-17 Goodyear Tire & Rubber Co:The Sidewall composition of tire containing silica with low ph
JPH1081787A (en) * 1996-07-10 1998-03-31 Sumitomo Rubber Ind Ltd Vibration-damping member
JPH10310664A (en) * 1997-03-13 1998-11-24 Tokai Rubber Ind Ltd Rubber composition for structure support
JP2001206990A (en) * 2000-01-28 2001-07-31 Goodyear Tire & Rubber Co:The Endless rubber track and transporting means containing the track
JP2002301903A (en) * 2001-02-09 2002-10-15 Goodyear Tire & Rubber Co:The Tire with side wall of reinforced rubber
JP2006307156A (en) * 2005-01-28 2006-11-09 Showa Denko Kk Chloroprene-based polymer for vulcanized rubber and method for producing the same

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06136184A (en) * 1992-05-20 1994-05-17 Goodyear Tire & Rubber Co:The Sidewall composition of tire containing silica with low ph
JPH1081787A (en) * 1996-07-10 1998-03-31 Sumitomo Rubber Ind Ltd Vibration-damping member
JPH10310664A (en) * 1997-03-13 1998-11-24 Tokai Rubber Ind Ltd Rubber composition for structure support
JP2001206990A (en) * 2000-01-28 2001-07-31 Goodyear Tire & Rubber Co:The Endless rubber track and transporting means containing the track
JP2002301903A (en) * 2001-02-09 2002-10-15 Goodyear Tire & Rubber Co:The Tire with side wall of reinforced rubber
JP2006307156A (en) * 2005-01-28 2006-11-09 Showa Denko Kk Chloroprene-based polymer for vulcanized rubber and method for producing the same

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102666705A (en) * 2009-11-18 2012-09-12 株式会社普利司通 Vibration isolating rubber composition and vibration isolating rubber
US20120232208A1 (en) * 2009-11-18 2012-09-13 Bridgestone Corporation Vibration isolating rubber composition and vibration isolating rubber
EP2502960A4 (en) * 2009-11-18 2013-08-21 Bridgestone Corp Vibration isolating rubber composition and vibration isolating rubber
CN102666705B (en) * 2009-11-18 2016-04-06 株式会社普利司通 vibration damping rubber composition and vibration-proof rubber
US9315656B2 (en) * 2009-11-18 2016-04-19 Bridgestone Corporation Vibration isolating rubber composition and vibration isolating rubber
CN104311914A (en) * 2014-10-13 2015-01-28 安徽奥丰汽车配件有限公司 Automotive engine bush
CN106496662A (en) * 2016-10-25 2017-03-15 上海众力投资发展有限公司 A kind of car engine suspension rubber composition

Also Published As

Publication number Publication date
JP5170363B2 (en) 2013-03-27

Similar Documents

Publication Publication Date Title
JP2011105870A (en) Vibration-proof rubber composition and vibration-proof rubber
JP6112755B2 (en) Anti-vibration rubber composition and anti-vibration rubber
JP2010254872A (en) Rubber composition for vibration insulating rubber
JP5625227B2 (en) Rubber composition for liquid filled anti-vibration rubber
JP2017119873A (en) Vibration-proof rubber composition and vibration-proof rubber
WO2015186482A1 (en) Rubber vibration dampener composition and rubber vibration dampener
JP2007291295A (en) Water proofing nitrile rubber composition
JP5170363B2 (en) Rubber composition
JP6408905B2 (en) Anti-vibration rubber composition
JP2007224085A (en) Cross-linking rubber composition
JP6977420B2 (en) Anti-vibration rubber composition and anti-vibration rubber products
JP6754226B2 (en) Rubber composition, rubber composition for anti-vibration rubber products and anti-vibration rubber products
JP5401771B2 (en) Rubber composition
JP2018188532A (en) Chloroprene rubber composition and vulcanizate thereof
JP2011162585A (en) Rubber composition for vibration-damping rubber, and vibration-damping rubber
JPH10219033A (en) Rubber composition for high-attenuation support
JP2005089727A (en) Vulcanized rubber composition
JP6105426B2 (en) Anti-vibration rubber composition and anti-vibration rubber
JP2010143280A (en) Vibration control rubber composition and stabilizer bush of automobile using the same
KR100693448B1 (en) Tire sidewall rubber composition for high flexibility
JP2008069199A (en) Rubber composition for coating fixed cord and tire having carcass and/or belt using the same
JP5998490B2 (en) Rubber composition for air spring
JP2013155249A (en) Rubber composition for air spring
JP3593526B2 (en) Rubber composition and molded product thereof
JP2009279763A (en) Method for producing rubber vibration insulator and rubber vibration insulator

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20091201

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20110404

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20120912

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20121112

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20121205

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20121218

R150 Certificate of patent or registration of utility model

Ref document number: 5170363

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313111

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250