JP5919126B2 - Rubber composition and pneumatic tire using the same - Google Patents

Description

  The present invention relates to a rubber composition and a pneumatic tire using the rubber composition as an inner liner, and more particularly to a rubber composition for an inner liner excellent in air permeation resistance and bending resistance and a pneumatic tire using the same. It is.

  Conventionally, for the purpose of reducing the fuel consumption and weight of a tire, it has been proposed to improve the air permeation resistance of the tire inner liner and make the inner liner thinner. For example, it has been proposed to use a rubber composition filled with low carbon black at a high blending amount for the inner liner to make the inner liner thinner. There was a problem with durability.

In contrast, by using a rubber composition containing non-reinforcing and flat mica and clay for the inner liner, the air permeability is improved while maintaining the bending fatigue resistance and low temperature durability of the inner liner. It is known to improve. For example, Patent Literature 1 discloses a rubber composition for an inner liner in which 1 to 150 parts by mass of an organically treated layered clay mineral is blended with respect to 100 parts by mass of a solid rubber. Discloses a rubber composition for an inner liner in which a rubber component and a layered or plate-like mineral having an aspect ratio of 3 or more and less than 30 are blended.
However, by using a rubber composition using a non-reinforcing and flat mica or clay in a high blending amount, the air permeation resistance can be improved, but the elastic modulus tends to increase. When the elastic modulus is increased, the bending resistance is lowered, and there is a problem that durability as an inner liner cannot be sufficiently obtained.

JP 2003-335902 A International Publication No. 01/62846

  In the rubber composition containing a high amount of clay minerals such as mica and clay, the present invention prevents a decrease in flex resistance by suppressing an increase in the elastic modulus, and improves air permeation resistance. An object is to provide an improved rubber composition and a pneumatic tire using the rubber composition.

As a result of diligent studies to achieve the above object, the present inventor has specified a fatty acid and a specific softening agent when the rubber component contains a non-reinforcing and flat clay mineral such as mica or clay in a high blending amount. It has been found that the above object can be achieved by blending in an amount, and the present invention has been completed.
That is, the present invention
1. A rubber composition comprising 80 parts by mass or more of a layered or platy clay mineral (B), a fatty acid (C), and a softening agent (D) with respect to 100 parts by mass of the rubber component (A), The blending amount of the fatty acid (C) is 1 to 10 parts by mass with respect to 100 parts by mass of the rubber component (A), and the softening agent (D) is selected from naphthenic oil, paraffinic oil and aromatic oil A rubber composition comprising at least one selected from the group consisting of 10 parts by mass or less based on 100 parts by mass of the rubber component (A);
2. 2. The rubber composition according to 1 above, wherein the total amount of the fatty acid (C) and the softener (D) is 10 parts by mass or less with respect to 100 parts by mass of the rubber component (A).
3. Furthermore, the rubber composition according to 1 or 2 above, wherein 15 parts by mass or less of carbon black (E) is blended with 100 parts by mass of the rubber component (A).
4). The rubber composition according to any one of 1 to 3, wherein the rubber component (A) contains 80 to 100% by mass of a butyl rubber,
5. The rubber composition according to any one of the above 1 to 4, wherein the rubber composition is a rubber composition for an inner liner of a tire,
6). A pneumatic tire using the rubber composition according to any one of 1 to 5 as an inner liner,
I will provide a.

  According to the present invention, the rubber component (A) is blended with a non-reinforcing and flat layered or platy clay mineral (B) such as mica or clay in a high blending amount, and the fatty acid (C) and the softening agent ( By blending D), a rubber composition, particularly a rubber composition for an inner liner of a tire, which prevents a decrease in flex resistance by suppressing an increase in elastic modulus and improves air permeation resistance. A rubber composition suitable as a product and a pneumatic tire using the same are obtained.

It is a schematic diagram which shows the definition of the average aspect-ratio used for the layered or plate-like clay mineral (B) based on this invention.

The present invention is described in detail below.
[Rubber composition]
The rubber composition of the present invention is obtained by blending a rubber component (A) with a layered or plate-like clay mineral (B), a fatty acid (C), and a softening agent (D).

[Rubber component (A)]
The rubber component used in the rubber composition of the present invention is not particularly limited, but a diene rubber is preferable, and examples of the diene rubber include natural rubber (NR) and diene synthetic rubber. Here, as the diene-based synthetic rubber, polyisoprene rubber (IR), polybutadiene rubber (BR), styrene-butadiene copolymer rubber (SBR), acrylonitrile-butadiene rubber (NBR), chloroprene rubber (CR), butyl System rubber and the like. These rubber components may be used alone or in combination of two or more.

In the rubber composition of the present invention, the rubber component is preferably a butyl rubber. When the rubber component is a butyl rubber, the air permeation resistance of the rubber composition can be greatly improved, and the rubber composition is suitable for an inner liner of a tire. The butyl rubber is preferably 80 to 100% by mass and 20 to 0% by mass or less of the diene rubber, and 95 to 100% by mass of the butyl rubber and 5 to 0% by mass or less of the diene rubber. Is particularly preferred.
The butyl rubber includes not only butyl rubber (IIR) but also halogenated butyl rubber, and examples of the halogenated butyl rubber include chlorinated butyl rubber and brominated butyl rubber. Among these butyl rubbers, it is preferable to use halogenated butyl rubber because air permeation resistance can be improved.

[Layered or platy clay mineral (B)]
The layered or plate-like clay mineral (B) used in the rubber composition of the present invention is used for improving the air permeation resistance of the tire inner liner.
As the layered or plate-like clay mineral, either a natural product or a synthetic product can be used. Examples of the layered or plate-like clay mineral include water-containing composites of clay (for example, kaolin clay, sericite clay, calcined clay, etc.), mica, feldspar, silica and alumina. Examples of layered clay minerals include smectite clay minerals such as montmorillonite, saponite, hectorite, beidellite, stevensite, nontronite, vermiculite, halloysite, and swelling mica. These layered or plate-like clay minerals may be natural or synthesized. Moreover, these may be used individually by 1 type and may be used in combination of 2 or more type.

Of the layered or plate-like clay minerals (B) described above used in the present invention, organically layered clay minerals can also be preferably used as the layered clay mineral.
Here, the organized layered clay mineral refers to a layered clay mineral organized by organic onium ions. As this layered clay mineral, the above-mentioned smectite clay minerals such as montmorillonite, saponite, hectorite, beidellite, stevensite, nontronite, vermiculite, halloysite, and swelling mica can be used.

  The organically layered clay mineral may be a layered clay mineral that is swellable with respect to an organic solvent so that the organic onium salt molecules described later can easily enter between the layers of the clay mineral (so-called intercalation). preferable. By using such a swellable layered clay mineral, the organic onium salt sufficiently penetrates between the layers, and when kneading with rubber, further expansion of the layers due to the intrusion of rubber molecules leads to an expansion in the rubber matrix. The dispersion of the layered clay mineral is obtained on the nano order. From this point, among the layered clay minerals, mica having a large average particle diameter, particularly swellable mica is preferable. The layered clay mineral can be organically treated by treatment with an organic onium salt, and an ammonium salt is particularly preferred as the organic onium salt.

  Examples of the organic onium ion that organicizes the layered clay mineral include hexyl ammonium ion, octyl ammonium ion, 2-ethylhexyl ammonium ion, dodecyl ammonium ion, octadecyl ammonium ion, dioctyl dimethyl ammonium ion, trioctyl ammonium ion, and distearyl. Dimethyl ammonium ion, trimethyl octadecyl ammonium ion, dimethyl octadecyl ammonium ion, methyl octadecyl ammonium ion, trimethyl dodecyl ammonium ion, dimethyl dodecyl ammonium ion, methyl dodecyl ammonium ion, trimethyl hexadecyl ammonium ion, dimethyl hexadecyl ammonium ion, methyl hexadecyl ammonium ion Ion, and the like.

Further, as unsaturated and unsaturated organic onium ions, 1-hexenylammonium ion, 1-dodecenylammonium ion, 9-octadecenylammonium ion (oleylammonium ion), 9,12-octadecadienyl Ammonium ions (linol ammonium ions), 9,12,15-octadecatrienyl ammonium ions (linoleyl ammonium ions) and the like can also be used. Among the above-mentioned organically modified layered viscosity minerals, those organically formed with distearyldimethylammonium ions are particularly preferable. Organization of the layered clay mineral is obtained, for example, by immersing the clay mineral in an aqueous solution containing organic onium ions and then washing the clay mineral with water to remove excess organic onium ions. The organically modified layered clay mineral thus obtained is blended and kneaded with the rubber component, so that the layered clay mineral is dispersed in the rubber as nano-order fine particles and extremely effectively improves the air permeation resistance. It becomes possible.
For this reason, the above-mentioned organized layered clay mineral is blended with a rubber component having a glass transition temperature of −55 ° C. or less, in particular, so that the rubber composition satisfies both air permeation resistance and low temperature durability. Can be obtained.

As the clay mineral used as the rubber composition of the present invention, clay is particularly preferable among the layered or plate-like clay minerals (B) described above, and kaolin clay, sericite clay, fired clay, and surface treatment are performed. A plate-like clay such as silane-modified clay is preferable, and kaolin clay is particularly preferable. If the average particle diameter (average Stokes equivalent diameter) of the layered or plate-like viscosity mineral of the component (B) is too large, the bending fatigue resistance is lowered, so it is preferably 50 μm or less, and more preferably 0.2 to 30 μm. More preferably, a range of about 0.2 to 5 μm is more preferable, and a range of 0.2 to 2 μm is most preferable.
If the average aspect ratio of the lamellar or plate-like viscosity mineral (B) is 2 to 200, the plane of the lamellar or plate-like viscosity mineral particles in the inner liner is oriented in a direction crossing the thickness direction of the inner liner. As a result of blocking the air permeation path, good air permeation resistance is obtained, but the average aspect ratio is preferably 3 to 150, more preferably 5 to 100, still more preferably 5 to 50, and particularly preferably 5 to 30. As a result, better air permeation resistance can be obtained.
When the component (B) having an average aspect ratio exceeding 200 is used, the component (B) at the time of rubber kneading is not uniformly dispersed when the filling amount is increased. This is not preferable because it causes a decrease in permeability.
The average aspect ratio is determined as x / y from the average major axis x and the average thickness y as shown in FIG.

[Fatty acid (C)]
As the fatty acid (C) used in the rubber composition of the present invention, a fatty acid and / or a derivative thereof can be used. Fatty acids and / or derivatives thereof are not particularly limited, but palm oil, palm kernel oil, camellia oil, olive oil, almond oil, canola oil, peanut oil, rice sugar oil, cocoa butter, palm oil, soybean oil, cottonseed oil , Aliphatic carboxylic acids derived from vegetable oils such as sesame oil, linseed oil, castor oil, rapeseed oil, aliphatic carboxylic acids derived from animal oils such as beef tallow, aliphatic carboxylic acids chemically synthesized from petroleum, stearic acid, palmitic acid, myristic acid And lauric acid, caprylic acid, oleic acid, linoleic acid and the like. These fatty acids and / or derivatives thereof may be used alone or in combination of two or more. Among these fatty acids and / or derivatives thereof, it is particularly preferable to use stearic acid.

[Softener (D)]
As the softener (D) used in the rubber composition of the present invention, a softener (D) containing at least one selected from naphthenic oil, paraffinic oil and aromatic oil can be used. Among these, paraffinic oil and naphthenic oil are preferable. A softener (D) may be used individually by 1 type, and may use 2 or more types together.
The molecular weight distribution (Mw / Mn) of the paraffinic oil used as the softening agent (D) is preferably 1.1 to 2, more preferably 1.1 to 1.5, and the kinematic viscosity (40 ° C.) is preferable. Is 30 to 2,000 mm ² / sec. As paraffinic oils, commercial products such as “Diana Process Oil PW” manufactured by Idemitsu Kosan Co., Ltd., “Super Oil Y22” manufactured by Nippon Oil Corporation, “Lucanto (registered trademark) HC” manufactured by Mitsui Chemicals, Inc. Can be used.
The naphthenic oil used as the softening agent (D) may be hydrogenated or non-hydrogenated. As naphthenic oils, commercially available products such as “Diana Process Oil NS”, “Diana Process Oil NM”, “Diana Process Oil NR” manufactured by Idemitsu Kosan Co., Ltd. and “SNH” manufactured by Sankyo Oil Chemical Co., Ltd. Can be used.
Commercially available products such as “Diana Process Oil AC” manufactured by Idemitsu Kosan Co., Ltd. can be used as the aromatic oil used as the softening agent (D).

[Amount of layered or platy clay mineral (B), fatty acid (C) and softener (D) to rubber component (A)]
In the rubber composition of this invention, it is necessary to mix | blend 80 mass parts or more of a layered or plate-like clay mineral (B) with respect to 100 mass parts of rubber components (A). When the component (B) is less than 80 parts by mass, the air permeation resistance is lowered, and the performance when used as a tire is lowered. (B) The preferable compounding quantity of a component is 85-200 mass parts, More preferably, it is 90-160 mass parts.
In the rubber composition of this invention, the compounding quantity of a fatty acid (C) needs to be 1-10 mass parts with respect to 100 mass parts of rubber components (A). When the amount of the component (C) is less than 1 part by mass, the elastic modulus of the resulting rubber composition is increased and the flex resistance is unfavorable, and when it exceeds 10 parts by mass, the air permeation resistance is undesirably lowered. . (C) The preferable compounding quantity of a component is 1-5 mass parts.
In the rubber composition of this invention, the compounding quantity of a softener (D) needs to be 10 mass parts or less with respect to 100 mass parts of rubber components (A). When the component (D) exceeds 10 parts by mass, the air permeation resistance decreases, which is not preferable. (D) The preferable compounding quantity of a component is 0.5-5 mass parts.

  In the rubber composition of the present invention, the total amount of the fatty acid (C) and the softening agent (D) is 10 parts by mass or less, preferably 1 to 9 parts by mass with respect to 100 parts by mass of the rubber component (A). By blending so as to be, it is possible to prevent a decrease in air permeation resistance.

Moreover, in the rubber composition of this invention, carbon black (E) can be mix | blended. As carbon black, an arbitrary one can be appropriately selected from those conventionally used for reinforcing rubber compositions. For example, as a preferable carbon black, N539 (FEF-LS), N550 (FEF), N660 (GPF), N634 (GPF-LS), N642 (GPF-LS), N7524, N762 (SRF-LM-NS) ), N772, N774 (SRF-HM-NS), and the like. Carbon black preferably has the following colloidal characteristics. That is, the nitrogen adsorption specific surface area (N ₂ SA) is preferably 50 m ² / g or less, and more preferably 20 to 50 m ² / g. Further, dibutyl phthalate absorption (DBP) is preferably from 125 cm ^3/100 g or less, and more preferably be about 100~30cm ³ / 100g. Here, the nitrogen adsorption specific surface area (N ₂ SA) of the colloidal characteristics is a value measured according to JIS K 6217-2: 2001, and DBP is a value measured according to JIS K 6217-4: 2008.

When blending carbon black (E), it is desirable to blend so as to be 15 parts by mass or less with respect to 100 parts by mass of the rubber component (A).
When the blending amount of carbon black is 15 parts by mass or less, steric hindrance due to carbon black is less likely to occur. When the rubber composition of the present invention is used as an inner liner for tires, a layered or plate-like clay mineral ( B) can be regularly arranged in the tire circumferential direction. As a result, more excellent effects are obtained with respect to bending fatigue resistance and air permeation resistance. Moreover, the fall of reinforcement property and the fall of workability | operativity by a moist and chigile at the time of rubber composition conveyance can also be suppressed. The preferred amount of carbon black (C) is 3 to 15 parts by mass, particularly preferably 5 to 13 parts by mass.

  Further, in the rubber composition of the present invention, in order to improve the dispersibility of the layered or plate-like clay mineral (B) in the rubber, a dispersion improver such as a silane coupling agent or triethanolamine is added as desired. be able to. The addition amount is preferably 0.1 to 5 parts by mass per 100 parts by mass of the rubber component.

Furthermore, organic short fibers made of an organic polymer resin can be blended with the rubber composition of the present invention. Thus, by mix | blending an organic short fiber, the inner surface code | cord exposure which may arise when manufacturing the tire with the thin inner liner thickness can be suppressed efficiently. The average diameter of the organic short fibers is preferably 1 μm to 100 μm, and the average length is preferably about 0.1 mm to 0.5 mm. The organic short fibers may be blended as a composite (hereinafter sometimes referred to as FRR) obtained by kneading short fibers and an unvulcanized rubber component in advance.
The blending amount of such organic short fibers is preferably 0.3 to 15 parts by mass per 100 parts by mass of the rubber component. When the blending amount is 0.3 parts by mass or more, the effect of eliminating the inner surface cord exposure can be sufficiently obtained, and when the blending amount is 5 parts by mass or less, adverse effects on workability can be suppressed. The material of the organic short fiber is not particularly limited, and examples thereof include polyamides such as nylon 6, ny66, syndiotactic-1,2-polybutadiene, isotactic polypropylene, polyethylene, and the like. Polyamide is preferred. When organic short fibers are blended, an adhesion improver between rubber and fibers such as hexamethylenetetramine and resorcin can be further blended in order to increase the modulus of the resulting rubber composition.

  In addition to the above-mentioned compounding agents, the rubber composition of the present invention contains various chemicals usually used in the rubber industry, such as vulcanizing agents, vulcanization accelerators, anti-aging agents, scorch preventing agents, and zinc white. It can mix | blend in the range which does not impair the objective of invention.

The rubber composition of the present invention can be produced by a usual method. That is, the rubber component (A), the layered or plate-like clay mineral (B), the fatty acid (C), the softening agent (D), and a compounding agent that is appropriately used as necessary are kneaded using a kneader. .
When the total amount of the layered or plate-like clay mineral (B) and the carbon black (E) used as necessary is large (for example, exceeding 100 parts by mass), first, the rubber component (A), layered Alternatively, plate clay mineral (B) and carbon black (E), fatty acid (C), softener (D) and other compounding agents except for vulcanizing agent are sufficiently kneaded at high temperature, and then vulcanized. A method of adding an agent and kneading at a low temperature is preferred. In this case, high temperature kneading can be performed in two or more stages as required. When the total amount of layered or plate-like clay mineral (B) and carbon black (E) is small (for example, 100 parts by mass or less), step (a) for pre-kneading the rubber component (A) By introducing, power consumption can be reduced and productivity can be increased. In this case, a step of kneading the pre-kneaded rubber component (A) with the layered or plate-like clay mineral (B), carbon black (E), fatty acid (C), softener (D) and other compounding agents. In (b), it is preferable that all the compounding chemicals except for the vulcanizing agent are added at the same time and kneading is performed in one stage, so that productivity can be further improved. The step (a) and the step (b) are preferably performed continuously.

  The step (a) of preliminarily kneading the rubber component is a step of kneading only the rubber component (A) with a kneader such as a Banbury mixer. In the present invention, this mastication treatment is preferably performed for 10 seconds or more. By setting this mastication treatment time to 10 seconds or more, formation of agglomerates of layered or plate-like clay mineral (B) on the rotor surface in the subsequent kneading treatment step can be suppressed, and excellent resistance to vulcanization after vulcanization. Air permeability and bending fatigue resistance can be obtained. In addition, since the productivity decreases when the mastication treatment time is lengthened, the mastication treatment time is more preferably in the range of 10 seconds to 60 seconds. Further, if the kneading step is performed in one stage without performing the preliminary kneading step, agglomerates of layered or plate-like clay mineral (B) are likely to be formed on the rotor surface, and after vulcanization, air permeability resistance and bending resistance Fatigue may not be obtained sufficiently.

  The kneading treatment step (b) is performed by kneading at high temperature, and the above-mentioned layered or plate-like clay mineral (B), fatty acid (C), softening agent (D), and necessary The carbon black (E) used according to the above and other compounding agents excluding the vulcanizing agent are added and kneaded. This kneading step may be performed in one stage or may be performed in a plurality of stages. The kneading temperature is preferably about 80 to 150 ° C. In addition, the kneading time may be appropriately selected so as to achieve a uniform kneading state, but usually it may be performed in a kneading time of 1 to 30 minutes.

  The rubber composition after the kneading treatment step (b) is added with a vulcanizing agent and, if necessary, a vulcanization accelerator in order to perform the vulcanizing agent adding step (c). c) is performed. The temperature in this vulcanizing agent addition step (c) is usually kneaded at a temperature in the range of about 80 to 120 ° C. When the kneading temperature exceeds 120 ° C., vulcanization starts, which may cause a decrease in air permeation resistance and bending fatigue resistance of the vulcanized rubber composition, which is not desirable. The kneading time in the vulcanizing agent addition step (c) is usually performed within a range of about 1 to 10 minutes.

By using such a kneading method for the rubber composition of the present invention described above, the dispersibility of the layered or platy clay mineral (B) and the carbon black (E) used as necessary is good. Thus, a vulcanized rubber composition having excellent air permeation resistance, bending fatigue resistance, low temperature durability and the like can be produced with high productivity.
The type of the kneader is not particularly limited, and can be appropriately selected from those normally used in the rubber industry, such as a closed mixer such as a Banbury mixer and an intermix, and a roll mixer, but a closed kneader is preferable.
The rubber composition of the present invention thus obtained is suitably used as a rubber composition for tire inner liners. This rubber composition desirably has a dynamic elastic modulus at −20 ° C. and a strain amplitude of 0.1% after vulcanization of 800 MPa or less, more preferably 600 MPa or less.

The pneumatic tire of the present invention is produced by a normal method using the rubber composition as an inner liner. That is, if necessary, the rubber composition of the present invention obtained by blending various chemicals as described above is processed as an inner liner member in an unvulcanized state, and molded as a tire inner liner by a conventional manufacturing process. To process. The inner liner layer is vulcanized at a vulcanization temperature of 130 ° C. or higher after being molded as a tire.
In the rubber composition of the present invention, although the layered or platy clay mineral (B) has a high blending amount, the decrease in flex resistance of the rubber composition after vulcanization is suppressed, and the air permeation resistance is improved. Since it is excellent, a tire with excellent performance can be obtained.
Moreover, by using the rubber composition of the present invention for the inner liner of a tire, a tire having a thin inner liner, that is, a tire having a thin inner liner can be easily manufactured.

Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the following examples. Various physical property evaluation methods were performed by the following methods.
(1) Air permeability (air permeability resistance)
The rubber composition after vulcanization obtained in Examples 1 to 9 and Comparative Examples 1 to 7 was subjected to an air permeation coefficient at 60 ° C. using an air permeation tester M-C1 (manufactured by Toyo Seiki Co., Ltd.). Was measured. The air permeability of Comparative Example 1 was taken as 100, and the air permeability was shown as an index. The smaller the index, the smaller the air permeability and the better the air permeation resistance.
(2) Elastic modulus About the rubber composition after vulcanization obtained by Examples 1-9 and Comparative Examples 1-7, using the Toyo Seiki spectrometer, initial strain 5%, dynamic strain 1%, 50Hz, The dynamic storage elastic modulus (E ′) was measured at a measurement temperature of 25 ° C., and indexed with Comparative Example 1 as 100. The larger the index, the higher the elastic modulus.
(3) Bending fatigue resistance Rubber test pieces were prepared from the vulcanized rubber compositions obtained in Examples 1 to 9 and Comparative Examples 1 to 7 in accordance with the bending test method of JIS K6260: 2010, A bending test was performed, and the time until a 10 mm crack was generated in the test piece was measured (Table 1). The time of Comparative Example 1 is taken as 100, and is shown as an index. The larger the index, the better the bending fatigue resistance.

Examples 1 to 5 , 7 to 9 , Reference Example 1 and Comparative Examples 1 to 7
16 types of rubber compositions were prepared using the types and amounts of compounding agents shown in Table 1.
These rubber compositions were kneaded using a Banbury mixer in two stages of high temperature kneading (maximum temperature 140 ° C.) and low temperature kneading (maximum temperature 100 ° C.) to obtain an unvulcanized rubber composition. In the low temperature kneading, a vulcanization accelerator and sulfur were added and kneaded. The test piece obtained by calendering the obtained unvulcanized rubber composition was vulcanized at 160 ° C. for 50 minutes, and the obtained vulcanized test piece was subjected to air permeation resistance and elasticity. The rate and bending fatigue resistance were measured. The results are shown in Table 1.

[Note] In Table 1,
* 1: Trademark: “JSR BROMOBUTYL 2255” manufactured by JSR Corporation
* 2: N660, manufactured by Asahi Carbon Co., Ltd.
* 3: Flat clay [trademark: “POLYFIL DL” (aspect ratio: 10) manufactured by J, M, Huber, Inc.] (a flat clay has a large aspect ratio of kaolin clay)
* 4: Stearic acid * 5: Softener [paraffinic oil, paraffinic oil manufactured by Idemitsu Kosan Co., Ltd., trade name “Diana Process Oil PW-90”]
* 6: Vulcanization accelerator [Noxeller DM-P, trade name (di-2-benzothiazolyl disulfide) manufactured by Ouchi Shinsei Chemical Co., Ltd.]

[Evaluation results]
The rubber compositions of Examples 1 to 9 shown in Table 1 indicate that a rubber composition having a good balance between air permeation resistance and bending fatigue resistance is obtained. On the other hand, it can be seen that the rubber compositions of Comparative Examples 1 to 3 are inferior in bending fatigue resistance because no softener is used. Further, the rubber composition of Comparative Example 4 has a low amount of fatty acid, so that the bending fatigue resistance is lowered. Conversely, the rubber composition of Comparative Example 5 has an air permeation resistance when the amount of fatty acid is too large. It turns out that it has fallen. It can be seen that the air permeability resistance of the rubber composition of Comparative Example 6 is lowered when the softening agent is too much. It can be seen that the rubber composition of Comparative Example 7 has low air permeation resistance due to the small amount of clay.

  The rubber composition of the present invention is useful as a rubber composition for inner liners of various tires, and is used for passenger cars, light trucks, light passenger cars, light trucks and large vehicles (for trucks, buses, construction vehicles, etc.). It is suitably used as an inner liner for various pneumatic tires.

Claims (5)

A rubber composition comprising 80 parts by mass or more of a layered or platy clay mineral (B), a fatty acid (C), and a softening agent (D) with respect to 100 parts by mass of the rubber component (A), The blending amount of the fatty acid (C) is 1 to 7 parts by mass with respect to 100 parts by mass of the rubber component (A), and the softening agent (D) is selected from naphthenic oil, paraffinic oil and aromatic oil It comprises at least one member, 0.5 to 6 parts by der for the blending amount of the rubber component (a) 100 parts by mass of is, and, said fatty acid (C) and the softener (D) total amount blended is, the of the rubber component (a) 100 parts by mass of a rubber composition characterized der Rukoto 10 parts by mass or less. Moreover, the the rubber component (A) 100 parts by mass of a rubber composition according to claim 1, carbon black (E) by blending 15 parts by mass or less. The rubber composition according to claim 1 or 2 , wherein the rubber component (A) contains 80 to 100% by mass of a butyl rubber. The rubber composition according to any one of claims 1 to 3 , wherein the rubber composition is a rubber composition for an inner liner of a tire. A pneumatic tire using the rubber composition for the inner liner of any one of claims 1-4.

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