JP5415740B2 - Rubber composition and pneumatic tire - Google Patents

Description

The present invention relates to a rubber composition and a pneumatic tire.

Conventionally, vehicle fuel efficiency has been reduced by reducing the rolling resistance of tires (improving rolling resistance performance). However, in recent years, there has been an increasing demand for lower fuel consumption of vehicles, and the rubber composition for producing a tread with a high occupation ratio of tires among tire components is superior in low heat generation. Is required.

Natural rubber has high mechanical strength and excellent wear resistance, so it is used in various tire members such as treads. There was a problem that it was easy. Conventionally, as a technique to suppress the reversion of vulcanizable rubber compositions used in rubber products such as tires and improve the heat resistance, the amount of vulcanization accelerator compounded with sulfur as a vulcanizing agent is increased. And a method of blending a thiuram vulcanization accelerator as a vulcanization accelerator is known.

Further, as a crosslinking agent capable of forming a long-chain crosslinked structure represented by-(CH ₂ ) ₆ -S-, flexis-made PERKALINK 900, Duralink HTS, Bayer-made Vulcuren KA9188, and the like are known. It is known that the re-vulcanization of the rubber composition can be suppressed by adding the above crosslinking agent to the rubber composition. However, when these methods are used, reversion can be suppressed, but there has been a problem that the fuel economy and wet grip properties are lowered and the performance balance is deteriorated.

Patent Document 1 describes modified polybutadiene obtained by modifying polybutadiene with organoalkoxysilane or organoaloxysilane, and Patent Document 2 describes modified polybutadiene obtained by modifying polybutadiene with a diamine compound, which can improve performance such as wet skid resistance. It is described that it is useful as a rubber material. However, even if such modified polybutadiene is used, there is still room for improvement in terms of achieving both low heat generation performance and wet grip performance.

Patent Document 3 describes that vulcanization reversion can be suppressed by using a mixture of an aliphatic carboxylic acid and an aromatic carboxylic acid zinc salt together with silica or a silane coupling agent. However, even if this is used, it is not sufficient in terms of achieving the above-mentioned performance. Further, the use of styrene butadiene rubber as a rubber component has not been studied in detail.
Japanese Patent Laid-Open No. 2001-40001 JP 2007-31722 A JP 2007-321041 A

An object of the present invention is to solve the above-mentioned problems and to provide a rubber composition having excellent low heat build-up property and at the same time excellent wet grip properties, and a pneumatic tire using the rubber composition.

The present invention contains 1 to 8 parts by mass of a mixture of a zinc salt of an aliphatic carboxylic acid and a zinc salt of an aromatic carboxylic acid and 10 to 150 parts by mass of silica based on 100 parts by mass of the rubber component, The present invention relates to a rubber composition containing a styrene butadiene rubber whose rubber component is modified with a compound represented by the following formula (1).

（式中、Ｒ^１、Ｒ^２及びＲ^３は、同一若しくは異なって、アルキル基、アルコキシ基、シリルオキシ基、アセタール基、カルボキシル基、メルカプト基又はこれらの誘導体を表す。Ｒ^４及びＲ^５は、同一若しくは異なって、水素原子又はアルキル基を表す。ｎは整数を表す。）

(Wherein R ¹ , R ² and R ³ are the same or different and each represents an alkyl group, an alkoxy group, a silyloxy group, an acetal group, a carboxyl group, a mercapto group or a derivative thereof. R ⁴ and R ⁵ are (The same or different, and represents a hydrogen atom or an alkyl group. N represents an integer.)

The aliphatic carboxylic acid preferably has 4 to 16 carbon atoms.
The aromatic carboxylic acid is preferably benzoic acid, phthalic acid or naphthoic acid.

The silica is composed of silica (1) having an average primary particle diameter of 22 nm or more and silica (2) having an average primary particle diameter of less than 22 nm, and the average primary particle diameter of the silica (1) and (2) is represented by the following formula: ;
(Average primary particle diameter of silica (1)) / (Average primary particle diameter of silica (2)) ≧ 1.4
It is preferable to contain 10 parts by mass or more of the silica (1) and 5 parts by mass or more of the silica (2) with respect to 100 parts by mass of the rubber component.

The present invention also relates to a pneumatic tire having a tread produced using the rubber composition.

According to the present invention, a rubber using a styrene butadiene rubber modified with a specific compound as a rubber component, containing a predetermined amount of a mixture of a zinc salt of an aliphatic carboxylic acid and a zinc salt of an aromatic carboxylic acid and silica. Since it is a composition, by using the rubber composition as a tread, it is possible to provide a pneumatic tire having excellent low heat buildup and excellent wet grip properties.

The rubber composition of the present invention comprises 1 to 8 parts by mass of a mixture of a zinc salt of an aliphatic carboxylic acid and a zinc salt of an aromatic carboxylic acid and 10 to 150 parts by mass of silica based on 100 parts by mass of the rubber component. contains. The rubber component used in the rubber composition contains styrene butadiene rubber (modified SBR) modified with the compound represented by the above formula (1). By using the modified SBR, the above mixture and silica, excellent low heat generation performance can be obtained while maintaining good wet grip performance in the rubber composition.

In the compound represented by the above formula (1), R ¹ , R ² and R ³ are the same or different and are an alkyl group, an alkoxy group, a silyloxy group, an acetal group, a carboxyl group (—COOH), a mercapto group (— SH) or derivatives thereof. As said alkyl group, C1-C4 alkyl groups, such as a methyl group, an ethyl group, n-propyl group, isopropyl group, n-butyl group, t-butyl group, etc. are mentioned, for example. Examples of the alkoxy group include alkoxy groups having 1 to 8 carbon atoms such as methoxy group, ethoxy group, n-propoxy group, isopropoxy group, n-butoxy group and t-butoxy group (preferably having 1 to 6 carbon atoms). More preferably, C1-C4) etc. are mentioned. The alkoxy group includes a cycloalkoxy group (cycloalkoxy group having 5 to 8 carbon atoms such as cyclohexyloxy group) and an aryloxy group (aryloxy group having 6 to 8 carbon atoms such as phenoxy group and benzyloxy group). ) Is also included.

Examples of the silyloxy group include a silyloxy group substituted with an aliphatic group having 1 to 20 carbon atoms and an aromatic group (trimethylsilyloxy group, triethylsilyloxy group, triisopropylsilyloxy group, diethylisopropylsilyloxy group, t- Butyldimethylsilyloxy group, t-butyldiphenylsilyloxy group, tribenzylsilyloxy group, triphenylsilyloxy group, tri-p-xylylsilyloxy group, etc.).

Examples of the acetal group include groups represented by -C (RR ')-OR "and -O-C (RR')-OR". Examples of the former include a methoxymethyl group, an ethoxymethyl group, a propoxymethyl group, a butoxymethyl group, an isopropoxymethyl group, a t-butoxymethyl group, and a neopentyloxymethyl group. The latter includes a methoxymethoxy group, an ethoxy group, and the like. Methoxy group, propoxymethoxy group, i-propoxymethoxy group, n-butoxymethoxy group, t-butoxymethoxy group, n-pentyloxymethoxy group, n-hexyloxymethoxy group, cyclopentyloxymethoxy group, cyclohexyloxymethoxy group, etc. Can be mentioned. R ¹ , R ² and R ³ are preferably alkoxy groups. Thereby, both low exothermic property and high rubber strength can be suitably achieved.

Examples of the alkyl group for R ⁴ and R ⁵ include the same groups as the above alkyl group.

As n (integer), 1-5 are preferable. Thereby, low exothermic property and wet grip property can be combined suitably. Furthermore, n is more preferably 2 to 4, and most preferably 3. When n is 0, it is difficult to bond a silicon atom and a nitrogen atom, and when n is 6 or more, the effect as a modifier is reduced.

Specific examples of the compound represented by the above formula (1) include 3-aminopropyldimethylmethoxysilane, 3-aminopropylmethyldimethoxysilane, 3-aminopropylethyldimethoxysilane, 3-aminopropyltrimethoxysilane, 3-aminopropyltrimethoxysilane, Aminopropyldimethylethoxysilane, 3-aminopropylmethyldiethoxysilane, 3-aminopropyltriethoxysilane, 3-aminopropyldimethylbutoxysilane, 3-aminopropylmethyldibutoxysilane, dimethylaminomethyltrimethoxysilane, 2-dimethyl Aminoethyltrimethoxysilane, 3-dimethylaminopropyltrimethoxysilane, 4-dimethylaminobutyltrimethoxysilane, dimethylaminomethyldimethoxymethylsilane, 2-dimethylaminoethyldimethoxy Methylsilane, 3-dimethylaminopropyldimethoxymethylsilane, 4-dimethylaminobutyldimethoxymethylsilane, dimethylaminomethyltriethoxysilane, 2-dimethylaminoethyltriethoxysilane, 3-dimethylaminopropyltriethoxysilane, 4-dimethylaminobutyl Triethoxysilane, dimethylaminomethyldiethoxymethylsilane, 2-dimethylaminoethyldiethoxymethylsilane, 3-dimethylaminopropyldiethoxymethylsilane, 4-dimethylaminobutyldiethoxymethylsilane, diethylaminomethyltrimethoxysilane, 2- Diethylaminoethyltrimethoxysilane, 3-diethylaminopropyltrimethoxysilane, 4-diethylaminobutyltrimethoxysilane, diethylamino Tildimethoxymethylsilane, 2-diethylaminoethyldimethoxymethylsilane, 3-diethylaminopropyldimethoxymethylsilane, 4-diethylaminobutyldimethoxymethylsilane, diethylaminomethyltriethoxysilane, 2-diethylaminoethyltriethoxysilane, 3-diethylaminopropyltriethoxysilane 4-diethylaminobutyltriethoxysilane, diethylaminomethyldiethoxymethylsilane, 2-diethylaminoethyldiethoxymethylsilane, 3-diethylaminopropyldiethoxymethylsilane, 4-diethylaminobutyldiethoxymethylsilane, and the like. These may be used alone or in combination of two or more.

Examples of the method for modifying styrene butadiene rubber (SBR) with the compound represented by the above formula (1) (modifier) include the methods described in JP-B-6-53768, JP-B-6-57767, and the like. A conventionally known method can be used. For example, SBR may be brought into contact with a modifier, such as a method of polymerizing SBR and adding a predetermined amount of the modifier to the polymer rubber solution, a method of reacting by adding a modifier to the SBR solution, and the like. Can be mentioned.

The styrene butadiene rubber (SBR) to be modified is not particularly limited, and those commonly used in the tire industry can be used.

Examples of rubber components other than the modified SBR used in the rubber composition include diene rubbers, such as natural rubber (NR), epoxidized natural rubber (ENR), butadiene rubber (BR), and styrene butadiene rubber (SBR). , Isoprene rubber (IR), ethylene-propylene-diene rubber (EPDM), butyl rubber (IIR), halogenated butyl rubber (X-IIR), chloroprene rubber (CR), acrylonitrile (NBR), isomonoolefin and paraalkyl styrene Copolymer halides can be used. Of these, natural rubber is preferably used in combination with the modified SBR in terms of strength improvement.

The NR is not particularly limited, and for example, those commonly used in the tire industry such as SIR20, RSS # 3, TSR20, and the like can be used.

The rubber composition of the present invention contains a zinc salt of an aliphatic carboxylic acid and a zinc salt of an aromatic carboxylic acid. The zinc salt is effective in reversion, can also improve the processability of a composition containing silica, and can more effectively suppress reversion of a composition containing silica. . Thus, since the vulcanization return can be suppressed, good fuel efficiency can be obtained.

Aliphatic carboxylic acids include 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, sesame oil, linseed oil, castor oil , Carboxylic acid derived from vegetable oil such as rapeseed oil, aliphatic carboxylic acid derived from animal oil such as beef tallow, aliphatic carboxylic acid chemically synthesized from petroleum, etc. It is also possible to prepare for a decrease in the supply amount of oil, and furthermore, since the vulcanization return can be sufficiently suppressed, an aliphatic carboxylic acid derived from vegetable oil is preferable, and an aliphatic carboxylic acid derived from palm oil, palm kernel oil or palm oil is preferred. More preferred.

The aliphatic carboxylic acid preferably has 4 or more carbon atoms, more preferably 6 or more carbon atoms. If the aliphatic carboxylic acid has less than 4 carbon atoms, the dispersibility tends to deteriorate. The carbon number of the aliphatic carboxylic acid is preferably 16 or less, more preferably 14 or less, and still more preferably 12 or less. When the carbon number of the aliphatic carboxylic acid exceeds 16, there is a tendency that the vulcanization return cannot be sufficiently suppressed.

The aliphatic group in the aliphatic carboxylic acid may be a chain structure such as an alkyl group or a cyclic structure such as a cycloalkyl group.

Examples of the aromatic carboxylic acid include benzoic acid, phthalic acid, mellitic acid, hemimellitic acid, trimellitic acid, diphenic acid, toluic acid, and naphthoic acid. Of these, benzoic acid, phthalic acid, or naphthoic acid is preferable because reversion can be sufficiently suppressed.

Content ratio of zinc salt of aliphatic carboxylic acid and zinc salt of aromatic carboxylic acid in the mixture (molar ratio: zinc salt of aliphatic carboxylic acid / zinc salt of aromatic carboxylic acid, hereinafter referred to as content ratio) is 1/20 or more is preferable, 1/15 or more is more preferable, and 1/10 or more is still more preferable. If the content ratio is less than 1/20, it is not possible to consider the environment or prepare for a future reduction in the amount of oil supplied, and the dispersibility and stability of the mixture tend to deteriorate. The content ratio is preferably 20/1 or less, more preferably 15/1 or less, and still more preferably 10/1 or less. When the content ratio exceeds 20/1, there is a tendency that the vulcanization return cannot be sufficiently suppressed.

The zinc content in the mixture is preferably 3% by mass or more, and more preferably 5% by mass or more. If the zinc content in the mixture is less than 3% by mass, there is a tendency that the vulcanization return cannot be sufficiently suppressed. Moreover, 30 mass% or less is preferable and, as for the zinc content rate in a mixture, 25 mass% or less is more preferable. If the zinc content in the mixture exceeds 30% by mass, the workability tends to decrease and the cost increases unnecessarily.

Content of a mixture is 1 mass part or more with respect to 100 mass parts of rubber components, Preferably it is 2 mass parts or more, More preferably, it is 3 mass parts or more. When the content of the mixture is less than 1 part by mass, the effect of suppressing reversion is not sufficient, and it becomes difficult to obtain a sufficient improvement effect. The content of the mixture is 8 parts by mass or less, preferably 7 parts by mass or less, more preferably 5 parts by mass or less. When the content of the mixture exceeds 8 parts by mass, the tendency to bloom increases, and the improvement of the effect with respect to the added amount decreases, and the cost increases unnecessarily.

The rubber composition of the present invention contains silica. By blending silica with the modified SBR and the mixture, good low heat build-up and wet grip performance can be obtained. Examples of the silica include, but are not limited to, dry method silica (anhydrous silicic acid), wet method silica (anhydrous silicic acid), and the like, and wet method silica is preferable because it has many silanol groups. Silica may be used alone or in combination of two or more.

The content of the silica (the total amount when two or more types are used) is 10 parts by mass or more, preferably 20 parts by mass or more with respect to 100 parts by mass of the rubber component. When the content of silica is less than 10 parts by mass, sufficient effects due to the blending of silica cannot be obtained. The silica content is 150 parts by mass or less, preferably 120 parts by mass or less. If the silica content exceeds 150 parts by mass, it will be difficult to disperse the silica into the rubber, and the processability of the rubber will deteriorate.

When two or more types of silica are blended, silica (1) having an average primary particle size of 22 nm or more and silica (2) having an average primary particle size of less than 22 nm are used, and the silicas (1) and (2) are used. It is preferable that the average primary particle diameter satisfies the relationship of (average primary particle diameter of silica (1)) / (average primary particle diameter of silica (2)) ≧ 1.4. By using such silica together, the dispersion of silica is improved. The average primary particle diameter of silica (1) is preferably 2.0 times or more the average primary particle diameter of silica (2). If it is less than 1.4 times, the difference of the average primary particle diameter of two types of silica will become small, and there exists a tendency for the effect by blending two types of silica not to be acquired.

The contents of silica (1) and (2) preferably satisfy the following general formula.
(Content of silica (1)) × 0.03 ≦ (content of silica (2)) ≦ (content of silica (1)) × 14
The content of silica (2) is more preferably 0.15 times or more, and still more preferably 0.25 times or more of the content of silica (1). Further, the content of silica (2) is more preferably 7 times or less of the content of silica (1), and still more preferably 4 times or less. When the content of silica (2) is less than 0.03 times the content of silica (1), the steering stability tends to decrease, and when it exceeds 14 times, the rolling resistance tends to increase.
In addition, the content of the silica (1) is preferably 10 parts by mass or more and the content of the silica (2) is preferably 5 parts by mass or more with respect to 100 parts by mass of the rubber component.

The average primary particle diameter of silica in the present invention means an average value of values obtained by observing the minimum particle unit of silica constituting the aggregated structure as a circle and measuring the absolute maximum length of the minimum particle as the diameter of the circle. To do. For the average primary particle diameter of silica, for example, using a transmission electron microscope H-7100 manufactured by Hitachi, Ltd., the diameter of 100 primary particles is observed, and the average value of the diameters of the 100 primary particles is obtained. Obtained by.

The rubber composition of the present invention preferably contains a silane coupling agent together with silica such as silica (1) and (2).
As the silane coupling agent, any silane coupling agent conventionally used in combination with silica can be used in the rubber industry. For example, bis (3-triethoxysilylpropyl) tetrasulfide, bis (2-tri Ethoxysilylethyl) tetrasulfide, bis (4-triethoxysilylbutyl) tetrasulfide, bis (3-trimethoxysilylpropyl) tetrasulfide, bis (2-trimethoxysilylethyl) tetrasulfide, bis (4-trimethoxysilyl) Butyl) tetrasulfide, bis (3-triethoxysilylpropyl) trisulfide, bis (2-triethoxysilylethyl) trisulfide, bis (4-triethoxysilylbutyl) trisulfide, bis (3-trimethoxysilylpropyl) Trisulfi Bis (2-trimethoxysilylethyl) trisulfide, bis (4-trimethoxysilylbutyl) trisulfide, bis (3-triethoxysilylpropyl) disulfide, bis (2-triethoxysilylethyl) disulfide, bis (4 -Triethoxysilylbutyl) disulfide, bis (3-trimethoxysilylpropyl) disulfide, bis (2-trimethoxysilylethyl) disulfide, bis (4-trimethoxysilylbutyl) disulfide, 3-trimethoxysilylpropyl-N, N-dimethylthiocarbamoyl tetrasulfide, 3-triethoxysilylpropyl-N, N-dimethylthiocarbamoyl tetrasulfide, 2-triethoxysilylethyl-N, N-dimethylthiocarbamoyl tetrasulfide, 2-trime Xylylethyl-N, N-dimethylthiocarbamoyl tetrasulfide, 3-trimethoxysilylpropylbenzothiazolyl tetrasulfide, 3-triethoxysilylpropylbenzothiazole tetrasulfide, 3-triethoxysilylpropyl methacrylate monosulfide, 3- Sulfide type such as trimethoxysilylpropyl methacrylate monosulfide, mercapto type such as 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 2-mercaptoethyltrimethoxysilane, 2-mercaptoethyltriethoxysilane, vinyltri Vinyl series such as ethoxysilane and vinyltrimethoxysilane, γ-glycidoxypropyltriethoxysilane, γ-glycidoxypropyltrimethoxysila , Glycidoxy type such as γ-glycidoxypropylmethyldiethoxysilane, γ-glycidoxypropylmethyldimethoxysilane, nitro type such as 3-nitropropyltrimethoxysilane, 3-nitropropyltriethoxysilane, 3-chloropropyl Examples include chloro-based compounds such as trimethoxysilane, 3-chloropropyltriethoxysilane, 2-chloroethyltrimethoxysilane, and 2-chloroethyltriethoxysilane. Product names include Si69, Si75, Si363 (Degussa), NXT, NXT-LV, NXT-ULV, NXT-Z (GE). Of these, bis (3-triethoxysilylpropyl) disulfide is preferable. These silane coupling agents may be used alone or in combination of two or more.

The content of the silane coupling agent is preferably 3 parts by mass or more and more preferably 8 parts by mass or more with respect to 100 parts by mass of the total content of silica. If content of a silane coupling agent is less than 3 mass parts, there exists a tendency for fracture strength to fall large. Moreover, 15 mass parts or less are preferable, and, as for content of the said silane coupling agent, 10 mass parts or less are more preferable. When the content of the silane coupling agent exceeds 15 parts by mass, effects such as an increase in fracture strength and a reduction in rolling resistance due to the addition of the silane coupling agent tend not to be obtained.

You may mix | blend carbon black with the said rubber composition. Thereby, the intensity | strength of rubber | gum can be improved. As carbon black, GPF, FEF, HAF, ISAF, SAF, etc. can be used, for example.

When carbon black is used, the nitrogen adsorption specific surface area (N ₂ SA) of the carbon black is preferably 30 m ² / g or more, and more preferably 40 m ² / g or more. When N ₂ SA is less than 30 m ² / g, there is a tendency that sufficient reinforcing properties cannot be obtained. Further, N ₂ SA of carbon black is preferably 120 m ² / g or less, and more preferably 90 m ² / g or less. When N ₂ SA exceeds 120 m ² / g, the viscosity at the time of unvulcanization becomes very high, and the workability tends to deteriorate or the fuel consumption tends to deteriorate. The nitrogen adsorption specific surface area of carbon black is determined by the A method of JIS K6217.

The content of carbon black is preferably 5 parts by mass or more, more preferably 8 parts by mass or more with respect to 100 parts by mass of the rubber component. If the amount is less than 5 parts by mass, sufficient reinforcing properties tend not to be obtained. Further, the content of carbon black is preferably 30 parts by mass or less, more preferably 20 parts by mass or less with respect to 100 parts by mass of the rubber component. When it exceeds 30 parts by mass, heat generation tends to increase.

In the rubber composition of the present invention, in addition to the rubber component such as the modified SBR, a mixture, silica, a silane coupling agent, and carbon black, a compounding agent generally used for manufacturing a rubber composition, such as clay, is used. Reinforcing fillers, zinc oxide, stearic acid, various anti-aging agents, oils such as aroma oil, vulcanizing agents such as wax and sulfur, vulcanization accelerators, and the like can be appropriately blended.

As a method for producing the rubber composition of the present invention, a known method can be used. For example, the above components are kneaded using a rubber kneader such as an open roll or a Banbury mixer, and then vulcanized. Can be manufactured.

Although the rubber composition of the present invention can be used for each member of a tire, it can be suitably applied to a tread. The tread can be used for a tread having a single layer structure, but can also be used for a base tread having a multilayer structure (such as a two-layer structure including a cap tread and a base tread). The tread can be produced by pasting a sheet into a predetermined shape, or by inserting it into two or more extruders and forming it in two layers at the head outlet of the extruder.

The pneumatic tire of the present invention is produced by a usual method using the rubber composition. In other words, if necessary, the rubber composition is extruded into a tread shape in accordance with the unvulcanized rubber composition, molded in a normal manner on a tire molding machine, and pasted together with other tire members. In addition, after forming an unvulcanized tire, the tire can be manufactured by heating and pressing in a vulcanizer.

The tire of the present invention is suitably used as a passenger car tire, bus tire, truck tire, and the like.

The present invention will be specifically described based on examples, but the present invention is not limited to these examples.

Hereinafter, various chemicals used in Examples and Comparative Examples will be described together.
SBR (1): E15 manufactured by Asahi Kasei Chemicals Corporation (vinyl content: 64% by mass, non-modified)
SBR (2): modified styrene butadiene rubber manufactured by Sumitomo Chemical Co., Ltd. (vinyl content 58 mass%, R ¹ , R ² and R ³ = —OCH ₃ , R ⁴ and R ⁵ = —CH ₂ CH ₃ , n = 3)
NR: RSS # 3
Mixture of aliphatic carboxylic acid and aromatic carboxylic acid zinc salt: Activator 73A ((i) aliphatic carboxylic acid zinc salt: zinc of fatty acid (carbon number: 8 to 12) derived from palm oil) Salt, (ii) aromatic carboxylic acid zinc salt: zinc benzoate, content molar ratio: 1/1, zinc content: 17% by mass)
Silica (1): ULTRASIL 360 (average primary particle size: 28 nm) manufactured by Degussa Co., Ltd.
Silica (2): ULTRASIL VN3 manufactured by Degussa Co., Ltd. (average primary particle size: 15 nm)
Carbon black: Seast NH manufactured by Tokai Carbon Co., Ltd. (N ₂ SA74m ² / g)
Silane coupling agent: Si75 (bis (3-triethoxysilylpropyl) disulfide) manufactured by Degussa Corporation
Zinc oxide: Zinc Hana No. 1 manufactured by Mitsui Mining & Smelting Co., Ltd. Stearic acid: Stearic acid “Kashiwa” manufactured by Nippon Oil & Fats Co., Ltd.
Anti-aging agent: Antigen 6C (N- (1,3-dimethylbutyl) -N′-phenyl-p-phenylenediamine) manufactured by Sumitomo Chemical Co., Ltd.
Wax: Sunnock N manufactured by Ouchi Shinsei Chemical Industry Co., Ltd.
Aroma oil: Process X-140 manufactured by Japan Energy Co., Ltd.
Sulfur: Powder sulfur vulcanization accelerator manufactured by Karuizawa Sulfur Co., Ltd. (1): Noxeller CZ (N-cyclohexyl-2-benzothiazolylsulfenamide) manufactured by Ouchi Shinsei Chemical Co., Ltd.
Vulcanization accelerator (2): Noxeller D (N, N'-diphenylguanidine) manufactured by Ouchi Shinsei Chemical Industry Co., Ltd.

Examples 1 to 6 and Comparative Example 1
Various rubber compositions were obtained by kneading and blending according to the formulation shown in Table 1. Test tires (size: 195 / 65R15) in which these rubber compositions become tread parts were prepared and used for the following tests.

(Rolling performance)
A rolling resistance tester was used to measure the rolling resistance when the test tire was run at a rim (15 × 6JJ), internal pressure (230 kPa), load (3.43 kN), speed (80 km / h), and a comparative example. Expressed as an index when 1 is 100. A larger index is better.

(Wet grip performance)
The braking distance from the initial speed of 100 km / h was determined on the wet asphalt road surface. The result is expressed as an index. The larger the number, the better the wet skid performance (wet grip performance). The index was calculated by the following formula.
Wet skid performance = (braking distance of comparative example 1) ÷ (braking distance of each example or each comparative example) × 100

The tire of the example using the rubber composition containing the modified SBR, the above mixture and silica in the tread had good rolling resistance performance and wet grip performance, and the balance between both performances was good. On the other hand, in the tire of Comparative Example 1 in which SBR (non-modified) was used instead of modified SBR and no mixture was blended, both the rolling resistance performance and the wet grip performance were inferior.

Claims (6)

1 to 8 parts by mass of a mixture of a zinc salt of an aliphatic carboxylic acid and a zinc salt of an aromatic carboxylic acid, 10 to 150 parts by mass of silica, and a nitrogen adsorption specific surface area of 30 to 120 m with respect to 100 parts by mass of the rubber component ² / g containing 5-30 parts by mass of carbon black ,
A rubber composition comprising a styrene butadiene rubber in which the rubber component is modified with a compound represented by the following formula (1).

(Wherein R ¹ , R ² and R ³ are the same or different and each represents an alkyl group, an alkoxy group, a silyloxy group, an acetal group, a carboxyl group, a mercapto group or a derivative thereof. R ⁴ and R ⁵ are (The same or different, and represents a hydrogen atom or an alkyl group. N represents an integer.) The rubber composition according to claim 1, wherein the aliphatic carboxylic acid has 4 to 16 carbon atoms. The rubber composition according to claim 1 or 2, wherein the aromatic carboxylic acid is benzoic acid, phthalic acid or naphthoic acid. The silica is composed of silica (1) having an average primary particle diameter of 22 nm or more and silica (2) having an average primary particle diameter of less than 22 nm, and the average primary particle diameter of the silica (1) and (2) is represented by the following formula:
(Average primary particle diameter of silica (1)) / (Average primary particle diameter of silica (2)) ≧ 1.4
The filling,
The rubber composition according to any one of claims 1 to 3, comprising 10 parts by mass or more of the silica (1) and 5 parts by mass or more of the silica (2) with respect to 100 parts by mass of the rubber component. The rubber composition according to any one of claims 1 to 4, wherein the rubber component contains natural rubber. A pneumatic tire having a tread produced from the rubber composition according to any one of claims 1-5.