JP2017008161A - Anti-vibration rubber composition and anti-vibration rubber - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide vibration-proof rubber composition capable of shortening vulcanization time while maintaining operation easiness during vulcanization and providing a vibration-proof rubber excellent in durability, and the vibration-proof rubber excellent in durability.SOLUTION: There is provided a vibration-proof rubber composition containing diene rubber, a silane coupling agent represented by following general formula (1), carbon black and silica, and having a blending ratio of the carbon black (a) to the silica (b) [(a)/(b)] of 10/90 to 45/55 by mass. In the general formula (1), Rrepresents a hydrocarbon group having 1 to 12 carbon atoms, L represents a bivalent hydrocarbon group having 1 to 5 carbon atoms, Rto Reach represents independently a hydrocarbon group having 1 to 5 carbon atoms.SELECTED DRAWING: None

Description

  The present invention relates to an anti-vibration rubber composition and an anti-vibration rubber.

  Conventionally, for various purposes such as automobiles, torsional dampers, engine mounts, muffler hangers, etc. have been used for the purpose of preventing noise by absorbing vibrations when the engine is driven. Is used. The anti-vibration rubber used in such applications is required to have high fatigue resistance in addition to good heat resistance, good ozone resistance and low dynamic magnification.

For example, in Patent Document 1, in order to form a vulcanized rubber (anti-vibration / vibration isolation rubber product) having excellent vibration-proof performance and support performance, small compression set, and excellent heat aging resistance, The preparation of rubber compositions using specific silane coupling agent treated silica is disclosed.
Moreover, in Patent Document 2, in order to obtain a vibration-proof rubber composition that can achieve both low dynamic ratio and high durability, and a vibration-proof rubber obtained by curing the rubber composition, the vibration-proof rubber composition is used. The diene rubber contains carbon black and silica as fillers, and the blending ratio of carbon black (a) and silica (b) is (a) / (b) = 80/20 to 20/80. It is disclosed that the configuration is (mass ratio).

JP 2006-052105 A JP 2011-105870 A

When silica was included in the rubber composition, the vulcanization time was long and the production efficiency was liable to decrease. On the other hand, if the vulcanization time of the rubber composition is shortened in order to increase the production efficiency of the vibration proof rubber, the workability of rubber processing may be lowered.
The present invention provides an anti-vibration rubber composition capable of shortening the vulcanization time while maintaining workability at the time of vulcanization, and further obtaining an anti-vibration rubber having excellent durability, and curing the rubber composition. Therefore, it is an object to provide a vibration-proof rubber excellent in durability.

The present inventors maintain the ease of work during vulcanization by blending a silane coupling agent having a specific structure in a system comprising a diene rubber, carbon black having a specific blending ratio, and silica. Thus, the present inventors have found that a vibration-proof rubber composition can be obtained that can shorten the vulcanization time and obtain a vibration-proof rubber having excellent durability.
That is, the present invention is configured as follows.

<1> A diene rubber, a silane coupling agent represented by the following general formula (1), carbon black, and silica, and a blending ratio of the carbon black (a) and the silica (b) [(A) / (b)] is an anti-vibration rubber composition having a mass basis of 10/90 to 45/55.

In formula (1), R ¹ represents a hydrocarbon group having 1 to 12 carbon atoms, L represents a divalent hydrocarbon group having 1 to 5 carbon atoms, and R ^{2 to} R ⁴ are each independently carbon. The hydrocarbon group of number 1-5 is represented.

<2> The anti-vibration rubber composition according to <1>, wherein the carbon black is at least one selected from the group consisting of SRF, GPF, FEF, HAF, ISAF, SAF, FT, and MT.

<3> The anti-vibration rubber composition according to <1> or <2>, wherein natural rubber is used alone as the diene rubber.

<4> The anti-vibration rubber composition according to <1> or <2>, wherein natural rubber and butadiene rubber are used in combination as the diene rubber.

<5> An anti-vibration rubber obtained by curing the anti-vibration rubber composition according to any one of <1> to <4>.

  According to the present invention, an anti-vibration rubber composition capable of shortening the vulcanization time while maintaining workability during vulcanization and obtaining an anti-vibration rubber having excellent durability, and anti-vibration having excellent durability. Rubber can be provided.

It is a figure showing an example of the relationship between the vulcanization time of the rubber composition of this invention, and a torque.

<Anti-Vibration Rubber Composition>
The anti-vibration rubber composition of the present invention comprises a diene rubber, a silane coupling agent represented by the following general formula (1) (hereinafter sometimes referred to as “specific silane coupling agent”), and a specific blend It contains carbon black and silica having a specific ratio.

In formula (1), R ¹ represents a hydrocarbon group having 1 to 12 carbon atoms, L represents a divalent hydrocarbon group having 1 to 5 carbon atoms, and R ^{2 to} R ⁴ are each independently carbon. The hydrocarbon group of number 1-5 is represented.
The anti-vibration rubber composition of the present invention contains a specific silane coupling agent together with a diene rubber, carbon black and silica having a specific mixing ratio, and vulcanization time while maintaining workability during vulcanization. The reason why an anti-vibration rubber excellent in durability can be obtained is not clear, but is presumed to be due to the following reason.
When the anti-vibration rubber composition contains silica and a conventional general silane coupling agent, the vulcanization time of the anti-vibration rubber composition tends to be delayed due to the action of inhibiting the vulcanization reaction. It is in. Therefore, the anti-vibration rubber composition is hard to be cured, and the production efficiency of the anti-vibration rubber is likely to decrease.
On the other hand, the anti-vibration rubber composition of the present invention is considered to have the following effects by including a specific silane coupling agent, carbon black having a specific blending ratio, and silica.
1) Although the time until the vulcanization reaction starts hardly changes, the inhibitory effect on the vulcanization reaction is small. 2) The reactivity of the coupling reaction between rubber and silica is improved. 3) Since silica and carbon black have different polarities and are easily separated, the presence of carbon black together with silica improves the dispersion state of each other and improves the dispersion state of silica.
Due to the combined action of 1) to 3) and 1) to 3), the anti-vibration rubber composition of the present invention can shorten the vulcanization time while maintaining workability during vulcanization, and is durable. It is presumed that an anti-vibration rubber having excellent properties can be obtained.

The vulcanization characteristics of the vibration-insulating rubber composition of the present invention will be described with reference to the drawings.
FIG. 1 is a diagram showing an example of the relationship between the vulcanization time and torque of the rubber composition of the present invention. The graph shown in FIG. 1 is a curve in which the horizontal axis represents vulcanization time and the vertical axis represents torque. Between the lowest value (0%) and the highest value (100%) of the anti-vibration rubber composition, the torque of the anti-vibration rubber composition reaches 10% after the vulcanization of the anti-vibration rubber composition is started. The vulcanization time is T10, and the vulcanization time when the torque of the vibration-proof rubber composition reaches 90% is T90. The vulcanization time for starting the vulcanization of the vibration-proof rubber composition was indicated as t0.

Generally, when the time from t0 to T90 is short, the vulcanization time is short, and the production efficiency of the anti-vibration rubber is improved. Workability after vulcanization of the anti-vibration rubber composition depends on how long the torque of the anti-vibration rubber composition is kept low. Conventionally, if the vulcanization time is shortened, the anti-vibration rubber composition is cured. The time “T90-T10” between T90 and T10 in which the travel proceeds is narrowed, and T10 also tends to be narrowed from t0.
By making the anti-vibration rubber composition of the present invention the T90-T10 can be shortened while maintaining the T10-t0 long, the vulcanization time can be shortened without reducing workability. Can do.
Hereinafter, the anti-vibration rubber composition and anti-vibration rubber of the present invention will be described in detail.

[Diene rubber]
The anti-vibration rubber composition of the present invention contains a diene rubber.
As the diene rubber, known rubbers can be used, and are not particularly limited. For example, natural rubber (NR); butadiene rubber (BR), styrene-butadiene rubber (SBR), isoprene rubber, styrene -Diene-based synthetic rubber such as isoprene copolymer, chloroprene rubber, acrylonitrile-butadiene rubber, and acrylate butadiene rubber; natural rubber such as epoxidized natural rubber or diene-based synthetic rubber whose molecular chain terminal is modified .
The anti-vibration rubber composition of the present invention contains one or more of the above diene rubbers.
Among the above-described diene rubbers, it is preferable to include at least one selected from the group consisting of natural rubber, butadiene rubber, and styrene-butadiene rubber, and it is more preferable to include at least natural rubber. For example, the vibration-proof rubber composition of the present invention may contain natural rubber alone as diene rubber, or may contain natural rubber and butadiene rubber.
The anti-vibration rubber composition of the present invention may contain a rubber other than the diene rubber (other rubber), but from the viewpoint of not impairing the effects of the present invention, The diene rubber content is preferably 80% by mass or more, more preferably 90% by mass or more, still more preferably 95% by mass or more, and 100% by mass with respect to the total mass of the rubber. % Is particularly preferred.

Examples of other rubbers include acrylic rubber, ethylene-propylene rubber (EPR, EPDM), fluorine rubber, silicone rubber, urethane rubber, butyl rubber, etc. These may be used alone or in combination of two or more. Can be used together.
The content of other rubber in the total rubber is preferably 20% by mass or less, more preferably 10% by mass or less, based on the total mass of the rubber, from the viewpoint of not impairing the effects of the present invention. The content is more preferably 5% by mass or less, and particularly preferably 0% by mass.

〔Silane coupling agent〕
The anti-vibration rubber composition of this invention contains the silane coupling agent (specific silane coupling agent) represented by General formula (1). The anti-vibration rubber composition of the present invention contains a specific silane coupling agent together with diene rubber, carbon black and silica having a specific compounding ratio, while maintaining the work stability of the anti-vibration rubber composition, The crosslinking time can be shortened and the durability of the anti-vibration rubber can be improved.

In formula (1), R ¹ represents a hydrocarbon group having 1 to 12 carbon atoms, L represents a divalent hydrocarbon group having 1 to 5 carbon atoms, and R ^{2 to} R ⁴ are each independently carbon. The hydrocarbon group of number 1-5 is represented.

The hydrocarbon group having 1 to 12 carbon atoms represented as R ¹ is preferably a saturated aliphatic hydrocarbon group having 1 to 12 carbon atoms or an unsaturated aliphatic hydrocarbon group having 2 to 12 carbon atoms.
The saturated aliphatic hydrocarbon group may be linear, branched or cyclic, but is preferably linear or branched, and more preferably linear. Moreover, it is preferable that it is 3-10, and, as for carbon number of a saturated aliphatic hydrocarbon group, it is more preferable that it is 5-8. Examples of the saturated aliphatic hydrocarbon group having 1 to 12 carbon atoms include a methyl group, an ethyl group, a propyl group, a butyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, and a dodecyl group. .
The unsaturated aliphatic hydrocarbon group may be linear, branched or cyclic, but is preferably linear or branched, and more preferably linear. Moreover, it is preferable that it is 3-10, and, as for carbon number of an unsaturated aliphatic hydrocarbon group, it is more preferable that it is 5-8. Examples of the unsaturated aliphatic hydrocarbon group having 2 to 12 carbon atoms include vinyl group, butenyl group, hexenyl group, heptenyl group, octenyl group, nonenyl group, decenyl group, dodecenyl group and the like.

The divalent hydrocarbon group having 1 to 5 carbon atoms represented as L is a hydrocarbon group obtained by removing one hydrogen atom from a saturated aliphatic hydrocarbon group having 1 to 5 carbon atoms in R ¹ , or Examples thereof include hydrocarbon groups obtained by removing one hydrogen atom from an unsaturated aliphatic hydrocarbon group having 2 to 5 carbon atoms in R ¹ . Examples of the saturated aliphatic hydrocarbon group and the unsaturated aliphatic hydrocarbon group are as described above.
L is preferably a 2-4 divalent linear saturated aliphatic hydrocarbon group.

R ² to R 1 to 5 carbon atoms which is represented as a ^{4 R 1} is the hydrocarbon groups a saturated aliphatic hydrocarbon group having 1 to 5 carbon atoms, or, the number of carbon atoms in ^{R 1} is 2-5 non A saturated aliphatic hydrocarbon group is mentioned. Examples of the saturated aliphatic hydrocarbon group and the unsaturated aliphatic hydrocarbon group are as described above.
R ^{2 to} R ⁴ are preferably each independently a linear saturated aliphatic hydrocarbon group having 1 to 4 carbon atoms, and a linear saturated aliphatic hydrocarbon group having 2 to 3 carbon atoms. More preferably.
The anti-vibration rubber composition of the present invention can contain one or more specific silane coupling agents.

The anti-vibration rubber composition of the present invention may further contain one or more silane coupling agents other than the specific silane coupling agent. From the viewpoint of not impairing the effects of the present invention, the content of the other silane coupling agent is preferably 20% by mass or less with respect to the total of the specific silane coupling agent and the other silane coupling agent, More preferably, it is 10 mass% or less.
More preferably, the vibration-proof rubber composition of the present invention does not contain any other silane coupling agent (content is 0% by mass).

The compounding quantity of a specific silane coupling agent is 1-15 mass parts with respect to 100 mass parts of silica compounding quantities, Preferably it is 1-10 mass parts, More preferably, it is 5-9 mass parts. When the blending amount is 1 part by mass or more, silica is easily dispersed in the rubber composition, and the reinforcing property of the rubber composition can be improved. Generally, the vibration-proof rubber composition contains silica, and the durability of the vibration-proof rubber can be improved by increasing dispersibility with a silane coupling agent. However, if a large amount of silane coupling agent is used to increase the dispersibility of silica, the vulcanization speed increases and the time until the vulcanization reaction of the rubber composition starts is accelerated. It could not be used. On the other hand, the specific silane coupling agent hardly affects the time until the vulcanization reaction starts, and it is difficult to reduce workability. Therefore, more silane coupling agents can be used than before. The dispersibility of the silica rubber composition can be improved.
In addition, even if it mixes more than 15 mass parts, the effect corresponding to the compounding quantity may not be acquired, and it is preferable that it is 15 mass parts or less from an industrial and economical viewpoint.

〔Carbon black〕
The anti-vibration rubber composition of the present invention contains carbon black.
Carbon black functions as a reinforcing filler for the anti-vibration rubber composition, and can increase the elastic modulus and the damping property.
The iodine adsorption amount of carbon black is preferably 140 g / kg or less, and more preferably 120 g / kg or less, from the viewpoint of workability and durability.
The type of carbon black is not particularly limited, and examples thereof include carbon black such as SRF, GPF, FEF, HAF, ISAF, SAF, FT, and MT. Among them, SRF, GPF, FEF, HAF, ISAF, FT and MT are preferred, and SRF, GPF, FEF, HAF, FT and MT are more preferred. Moreover, these carbon blacks may be used individually by 1 type, and may use 2 or more types together.
The blending amount of carbon black is not particularly limited as long as the effect is not impaired.

〔silica〕
The anti-vibration rubber composition of the present invention contains silica having a nitrogen adsorption specific surface area (BET method) satisfying a range of 30 to 230 m ² / g.
Silica, together with carbon black, functions as a reinforcing filler for the anti-vibration rubber composition, and can increase the elastic modulus and increase the damping property.
When the BET specific surface area of silica is 230 m ² / g or less, the silica gel is easily dispersed in the rubber composition.
The blending amount of silica is not particularly limited as long as the effect is not impaired.

  The compounding ratio (a / b) of carbon black (a) and silica (b) is 10/90 to 45/55 on a mass basis from the viewpoint of achieving both low dynamic magnification and durability and improving workability. . Preferably it is 10 / 90-30 / 70, More preferably, it is 20 / 80-30 / 70.

  The anti-vibration rubber composition of the present invention may contain a compounding agent used in an ordinary anti-vibration rubber composition together with the above components. For example, various fillers other than carbon black and silica (for example, clay, calcium carbonate, etc.), sulfur as a vulcanizing agent, vulcanization accelerator, vulcanization acceleration aid, softeners such as various process oils, zinc white, The various compounding agents generally blended such as stearic acid, wax, and anti-aging agent can be listed.

  Known oils can be used and are not particularly limited. Specifically, process oils such as aromatic oils, naphthenic oils, and paraffin oils; vegetable oils such as palm oils; synthesis of alkylbenzene oils and the like Oil; castor oil can be used. These can be used individually by 1 type or in combination of 2 or more types.

In the present invention, from the viewpoint of accelerating vulcanization, vulcanization accelerating aids such as zinc white (ZnO) and fatty acids can be blended.
The fatty acid may be a saturated, unsaturated, linear or branched fatty acid, and is not particularly limited as the carbon number of the fatty acid. For example, the fatty acid has 1 to 30 carbon atoms, preferably 15 to 15 carbon atoms. 30 fatty acids, more specifically, cyclohexane acid (cyclohexanecarboxylic acid), naphthenic acid such as alkylcyclopentane having a side chain, hexanoic acid, octanoic acid, decanoic acid (including branched carboxylic acid such as neodecanoic acid), Saturated fatty acids such as dodecanoic acid, tetradecanoic acid, hexadecanoic acid, octadecanoic acid (stearic acid), unsaturated fatty acids such as methacrylic acid, oleic acid, linoleic acid, linolenic acid, resin acids such as rosin, tall oil acid, abietic acid, etc. Is mentioned. Another vulcanization accelerator may be used individually by 1 type, and may use 2 or more types together. In the present invention, zinc white and stearic acid can be preferably used.
The blending amount of the vulcanization acceleration aid is preferably 1 to 15 parts by mass, more preferably 2 to 10 parts by mass with respect to 100 parts by mass of the total rubber.

  As the anti-aging agent, known ones can be used, and are not particularly limited, and examples thereof include a phenol type anti-aging agent, an imidazole type anti-aging agent and an amine type anti-aging agent. The blending amount of these anti-aging agents is usually 0.5 to 10 parts by mass, preferably 1 to 5 parts by mass with respect to 100 parts by mass of the total rubber.

  When obtaining the anti-vibration rubber composition of the present invention, there is no particular limitation on the blending method of each of the above components, and all the component raw materials may be blended and kneaded at once, or divided into two or three stages. You may mix and knead | mix a component. In the kneading, a kneader such as a roll, an internal mixer, a Banbury rotor or the like can be used. Furthermore, when forming into a sheet shape, a strip shape, or the like, a known molding machine such as an extrusion molding machine or a press machine may be used.

<Anti-vibration rubber>
The anti-vibration rubber of the present invention is obtained by curing the anti-vibration rubber composition of the present invention having the above configuration.
There are no particular limitations on the vulcanization conditions for curing the vibration-proof rubber composition, but vulcanization conditions of usually 120 to 180 ° C. and 5 to 120 minutes can be employed.

[Examples 1 to 17, Comparative Examples 1 to 8]
Each component was knead | mixed with the compounding composition shown in following Table 1, the vibration-proof rubber composition of Examples 1-17 and Comparative Examples 1-8 was manufactured, and it was made to vulcanize-harden then, and the vibration-proof rubber was produced.
Vulcanization characteristics were evaluated from the vulcanization status of each vibration proof rubber composition, and the obtained vibration proof rubber was evaluated for basic properties of hardness, tensile strength and tensile elongation, and durability fatigue resistance. The results are shown in Tables 1 and 2.

1. Vulcanization characteristics of anti-vibration rubber composition Time required to reach 10% of the maximum torque by measuring the torque of the anti-vibration rubber composition at 155 ° C using a vibration vulcanization tester (curast meter) (T10) and the time (T90) required to reach 90% of the maximum torque were measured.
In Tables 1 and 2, T10 and T90-T10 of Comparative Example 1 are used as a reference, and T10 and T90-T10 of Comparative Example 1 when T10 and T90-T10 are 100 are shown by index display. The larger the index value of T10, the longer the time in which the torque of the anti-vibration rubber composition is small, and the better the work stability. However, if the index value of T10 is too large, the vulcanization time becomes long. On the other hand, the smaller the index value of T90-T10, the shorter the time during which the torque of the anti-vibration rubber composition increases, and the shorter the vulcanization time.

2. Basic Characteristics of Anti-Vibration Rubber Hardness (Hs), tensile strength (Tb) and tensile elongation (Eb) of anti-vibration rubber were measured and evaluated according to the following JIS standards. The evaluation results are shown in Tables 1 and 2.
[Hardness (Hs)] ... Conforms to JIS K 6253 (Type A) [Tensile strength (Tb)] ... Conforms to JIS K 6251 [Tensile elongation (Eb)] ... Conforms to JIS K 6251 Conform

3. Durability fatigue property of vibration-proof rubber About the vibration-proof rubber of an Example and a comparative example, 0-200% expansion | extension was repeated at 85 degreeC, and the frequency | count until it fractured was made into count. In Tables 1 and 2, the number of breaks “100” of Comparative Example 1 is shown as an index in reference.
The larger the index value, the better the fatigue durability.

The details of each component in Tables 1 and 2 are as follows.
1) Rubber and natural rubber (NR): “RSS # 1”

2) Silane coupling agent / Silane coupling agent 1
“NXT” manufactured by Momentive Performance Materials Japan GK, S- [3- (triethoxysilyl) propyl] octanethioate; a silane coupling agent represented by the general formula (1), 1), R ¹ is a linear saturated aliphatic hydrocarbon group having 7 carbon atoms, L is a divalent linear saturated aliphatic hydrocarbon group having 3 carbon atoms, R ² = R ³ = R ⁴ = ethyl group It is.
・ Silane coupling agent 2
Manufactured by Evonik Degussa; bis-3-triethoxysilylpropyltetrasulfide (TESPT)
・ Silane coupling agent 3
Momentive Performance Materials Japan GK “A-1891”; 3-mercaptopropyltriethoxysilane

3) Carbon Black / HAF: Asahi Carbon Co., Ltd., trade name “# 70”
(Iodine adsorption amount 82g / kg, DBP oil absorption amount 102ml / 100g)
・ ISAF: Asahi Carbon Co., Ltd., trade name “# 80”
(Iodine adsorption amount 121g / kg, DBP oil absorption 114ml / 100g)
・ SAF: Asahi Carbon Co., Ltd., trade name “# 110”
(Iodine adsorption amount 145g / kg, DBP oil absorption 113ml / 100g)
・ FEF: Asahi Carbon Co., Ltd., trade name “# 65”
(Iodine adsorption amount 43g / kg, DBP oil absorption amount 121ml / 100g)
・ FT: Asahi Carbon Co., Ltd., trade name “# 15”
(Iodine adsorption 11g / kg, DBP oil absorption 41ml / 100g)

4) Precipitated Silica “NIPSIL VN3” Nitrogen adsorption specific surface area (BET method) 180-230 m ² / g manufactured by Silica / Tosoh / Silica
・ Tosoh Silica Precipitated Silica “NIPSIL ER” Nitrogen adsorption specific surface area (BET method) 70-120 m ² / g
-Tosoh Silica's precipitated silica "NIPSIL E75" nitrogen adsorption specific surface area (BET method) 30-60 m ² / g

5) WAX
“Antilux 654” manufactured by Rhein Chemie

6) Anti-aging agent / RD: 2,2,4-trimethyl-1,2-dihydroquinoline polymer, “NOCRACK 224” manufactured by Ouchi Shinsei Chemical Co., Ltd.
6PPD: N-phenyl-N ′-(1,3-dimethylbutyl) -p-phenylenediamine, “NOCRACK 6C” manufactured by Ouchi Shinsei Chemical Co., Ltd.

7) Naphthenic oil "Diana Process Oil NS-100" manufactured by Idemitsu Kosan Co., Ltd.

8) Vulcanization accelerator, TBT: “ACCEL TBT” manufactured by Kawaguchi Chemical Co., Ltd.
NS: “NOCCELER NS-F” manufactured by Ouchi Shinsei Chemical Industry Co., Ltd.

As is apparent from Tables 1 and 2, the anti-vibration rubber compositions of the examples had an index value of T10 close to 100 and maintained work stability, while T90-T10 was small and the vulcanization time was shortened. Further, it was found that the fatigue resistance of the obtained vibration-proof rubber is superior to the conventional one, with the index value being close to 100 and maintaining the conventional performance or exceeding 100.
The anti-vibration rubber composition of Comparative Example 4 has a smaller index value of T90-T10 than the anti-vibration rubber composition of Comparative Example 1, and a larger index value of the number of breaks of the obtained anti-vibration rubber. The index value of T10 is also large, but since the value greatly exceeds 100 (115 or more), it can be seen that the vulcanization time is long.

  The composition of the present invention is suitably used for various anti-vibration rubber members, and the composition of the present invention can be used in combination with a metal member, a resin member, or the like. Specifically, for example, engine mounts, strut mounts, member mounts, suspension bushes, toe collect bushes, lower arm bushes, differential mounts, muffler hangers, spring seats, dynamic dampers, viscous rubber dampers, center support rubbers, etc. Preferably used.

Claims (5)

Diene rubber,
A silane coupling agent represented by the following general formula (1);
Carbon black,
An anti-vibration rubber composition containing silica and having a compounding ratio [(a) / (b)] of the carbon black (a) and the silica (b) of 10/90 to 45/55 on a mass basis.

Wherein (1), ^{R 1} represents a hydrocarbon group having 1 to 12 carbon atoms, L is a divalent hydrocarbon group having 1 to 5 carbon ^atoms, R 2 to R ⁴ are each independently, Represents a hydrocarbon group having 1 to 5 carbon atoms. ]   The anti-vibration rubber composition according to claim 1, wherein the carbon black is at least one selected from the group consisting of SRF, GPF, FEF, HAF, ISAF, SAF, FT, and MT.   The anti-vibration rubber composition according to claim 1 or 2, wherein natural rubber is used alone as the diene rubber.   The anti-vibration rubber composition according to claim 1 or 2, wherein natural rubber and butadiene rubber are used in combination as the diene rubber.   Anti-vibration rubber obtained by curing the rubber composition according to any one of claims 1 to 4.