JPWO2018105230A1 - Rubber composition and pneumatic tire - Google Patents

Abstract

The present invention is a rubber composition having a low rubber viscosity during kneading, excellent processability, excellent fuel economy and wear resistance, and good vulcanization productivity despite containing a white filler. And a pneumatic tire using the same. The present invention contains a rubber component, a white filler, and a compound represented by the following formula (1), and the rubber composition contains 5 to 200 parts by mass of the white filler with respect to 100 parts by mass of the rubber component. Related to things. In formula (1), X represents -CONH-. R1 represents an alkyl group having 7 to 23 carbon atoms or an alkenyl group having 7 to 23 carbon atoms. R2 represents an alkylene group having 1 to 3 carbon atoms. R3 and R4 each independently represent a hydrogen atom, an alkyl group having 1 to 3 carbon atoms, or a hydroxyalkyl group having 1 to 3 carbon atoms, and at least one is the hydroxyalkyl group. [Chemical 1]

Description

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

With recent social demands for energy saving, automobiles are required to have low heat generation (low fuel consumption) and wear resistance. In accordance with this requirement, the fuel efficiency and wear resistance of the tire rubber composition are also required. Under such circumstances, white fillers such as silica, aluminum hydroxide, alumina, and magnesium sulfate are frequently used in order to improve the fuel efficiency of the rubber composition for tires.

White fillers such as silica and fine particle aluminum hydroxide tend to bond and agglomerate particles during kneading or standing after kneading, the compounding viscosity becomes too high, extrusion processability In addition, there is a problem that the sheet processability of the kneaded product is deteriorated. Therefore, conventionally, improvement of processability of a rubber composition containing a white filler has been demanded.

On the other hand, conventionally, a method for improving the processability of a rubber composition containing a white filler such as silica has been reported. For example, Patent Document 1 shows a weak chemical reactivity to an elastic polymer and a polar terminal showing weak chemical reactivity to silica as a processing aid for improving the dispersion of silica in a rubber composition. An amide compound having a nonpolar terminal is disclosed, and a technique for adding the amide compound to a rubber composition containing silica is described. Patent Documents 2 to 5 describe techniques for adding fatty acid monoethanolamide or fatty acid diethanolamide to a rubber composition containing a white filler such as silica.

Special table 2003-533574 gazette International Publication No. 2013/070626 JP 2013-245265 A Japanese Unexamined Patent Publication No. 2014-167055 JP 2013-159653 A

However, fatty acid amide, fatty acid monoethanolamide or fatty acid diethanolamide, which has been used as a white filler dispersibility improver, can suppress aggregation of white filler such as silica, but the viscosity of rubber during kneading. The effect of reducing the viscosity is low, and it is not sufficient in terms of improving the dispersibility of the white filler in the rubber. Further, these conventional compounds are not sufficient in improving the rubber properties such as low fuel consumption (tan δ) and wear resistance of the rubber composition.

The present invention solves the above problems, and despite containing a white filler, the rubber viscosity during kneading is low, the processability is excellent, the fuel economy and wear resistance are excellent, and the vulcanization productivity Another object of the present invention is to provide an excellent rubber composition and a pneumatic tire using the same.

In order to disperse the white filler such as silica well in the rubber composition, it is necessary to make the white filler hydrophobic. For example, in the case of silica, there is a method of hydrophobizing silica by combining a silane coupling agent with silica. However, high specific surface area silica used in a tire rubber composition has cohesiveness. It is expensive and tends to form a structure including a rubber called an occluder rubber.

（式（１）中、Ｘは−ＣＯＮＨ−を表す。Ｒ^１は炭素数７〜２３のアルキル基又は炭素数７〜２３のアルケニル基を表す。Ｒ^２は炭素数１〜３のアルキレン基を表す。Ｒ^３とＲ^４はそれぞれ独立して、水素原子、炭素数１〜３のアルキル基又は炭素数１〜３のヒドロキシアルキル基を表し、少なくとも１つは前記ヒドロキシアルキル基である。）In order to improve the hydrophobization of the white filler, the present inventors have described “improvement of adsorptivity to the white filler” of a compound having both a hydrophobic group and an adsorption group for the white filler (for example, a surfactant) and From the viewpoint of improving the hydrophobizing power of the adsorbing compound itself, as a result of examining a new white filler dispersibility improving agent, the rubber composition containing the white filler adsorbs to the white filler. By blending a compound represented by the following formula (1) with high properties, the rubber viscosity during kneading can be reduced to improve processability, and the dispersibility of the white filler can be improved. It has been found that fuel economy, wear resistance and wet grip performance can be improved, and that good vulcanization productivity can be secured, and the present invention has been completed. In addition, wet grip performance can be improved by reducing the rubber viscosity during kneading and increasing the amount of silica after improving fuel efficiency.
That is, the present invention contains a rubber component, a white filler, and a compound represented by the following formula (1), and the content of the white filler with respect to 100 parts by mass of the rubber component is 5 to 200 parts by mass. The present invention relates to a rubber composition.

(In formula (1), X represents -CONH-. R ¹ represents an alkyl group having 7 to 23 carbon atoms or an alkenyl group having 7 to 23 carbon atoms. R ² represents an alkylene group having 1 to 3 carbon atoms. R ³ and R ⁴ each independently represent a hydrogen atom, an alkyl group having 1 to 3 carbon atoms, or a hydroxyalkyl group having 1 to 3 carbon atoms, and at least one is the hydroxyalkyl group.)

The compound represented by the formula (1) is preferably fatty acid amidoethylaminoethanol.

The rubber composition contains sulfur, and among the sulfur, the sulfur content derived from powdered sulfur having a sulfur content of 70% by mass or more is 1.5% by mass with respect to 100 parts by mass of the rubber component. It is preferably less than part.

The rubber composition preferably contains silica as the white filler.

The rubber composition is preferably a tire rubber composition.

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

According to the rubber composition of the present invention, despite being a rubber composition containing a white filler, the rubber viscosity during kneading is low, the processability is excellent, the fuel efficiency and wear resistance are excellent, and Further, it is possible to provide a rubber composition having good vulcanization productivity, and it is possible to efficiently provide a pneumatic tire excellent in low fuel consumption and wear resistance.

（式（１）中、Ｘは−ＣＯＮＨ−を表す。Ｒ^１は炭素数７〜２３のアルキル基又は炭素数７〜２３のアルケニル基を表す。Ｒ^２は炭素数１〜３のアルキレン基を表す。Ｒ^３とＲ^４はそれぞれ独立して、水素原子、炭素数１〜３のアルキル基又は炭素数１〜３のヒドロキシアルキル基を表し、少なくとも１つは前記ヒドロキシアルキル基である。）The rubber composition of the present invention contains a rubber component, a white filler, and a compound represented by the following formula (1), and the content of the white filler with respect to 100 parts by mass of the rubber component is 5 to 200 parts by mass. .

(In formula (1), X represents -CONH-. R ¹ represents an alkyl group having 7 to 23 carbon atoms or an alkenyl group having 7 to 23 carbon atoms. R ² represents an alkylene group having 1 to 3 carbon atoms. R ³ and R ⁴ each independently represent a hydrogen atom, an alkyl group having 1 to 3 carbon atoms, or a hydroxyalkyl group having 1 to 3 carbon atoms, and at least one is the hydroxyalkyl group.)

As described above, by blending the rubber composition containing the white filler with the compound represented by the above formula (1) having a high adsorptivity to the white filler, the above-mentioned occluder rubber is reduced. As a result, processability can be improved by reducing rubber viscosity during kneading, and further, low fuel consumption, wear resistance and vulcanization productivity can be improved by improving the dispersibility of the white filler.

This is estimated as follows. The compound represented by the above formula (1) expresses moderate polarity at two positions of the hydroxyl group of R ³ and / or R ⁴ located at the molecular end and the CONH group of X located near the center of the molecule, It is possible to moderately adsorb (interact) with the surface of the white filler (in particular, the hydroxy group on the surface of the white filler). Therefore, the surface of the white filler is covered with this compound, and the compound hydrophobizes the surface of the white filler, thereby promoting the dispersibility of the white filler and coagulating the white filler. Since it can suppress and the viscosity of a compound can be reduced, the dispersibility of the white filler in rubber | gum can be improved efficiently. As a result, the processability, wet grip performance, low fuel consumption, wear resistance and vulcanization productivity of the rubber composition can be improved.

Furthermore, it is estimated as follows. The compound represented by the above formula (1) is an amino group between -CONH- and an alkanol group, as compared with fatty acid monoethanolamide and fatty acid diethanolamide, which have been conventionally used as a dispersibility improving agent for white fillers. It is characterized by having. By having the amino group in the molecular chain, the adsorptivity to the surface of the white filler (particularly the hydroxy group on the silica surface where the silane coupling agent cannot be accessed) is improved, and the viscosity reduction effect of the formulation is excellent. The dispersibility of the white filler in the rubber can be further improved. Furthermore, since it has an alkyl group or an alkenyl group at the terminal and has the amino group and hydroxy group in the molecular chain, it can be adsorbed flexibly on silica, so that a modified group of a silane coupling agent or a modified polymer and silica Interaction and silica dispersibility can be synergistically improved.

The rubber component is not particularly limited, and isoprene-based rubber including natural rubber (NR) and polyisoprene rubber (IR), butadiene rubber (BR), styrene-butadiene copolymer rubber (SBR), styrene-isoprene-butadiene. Examples include diene rubber components such as copolymer rubber (SIBR), chloroprene rubber (CR), and acrylonitrile-butadiene copolymer rubber (NBR), butyl rubber, ethylene propylene diene rubber (EPDM), and urethane rubber. These rubber components may be used alone or in combination of two or more. Especially, it is preferable to contain SBR and BR from a viewpoint of the balance of low fuel consumption, abrasion resistance, durability, and wet grip performance.

The styrene butadiene rubber (SBR) is not particularly limited, and examples thereof include emulsion polymerization SBR (E-SBR), solution polymerization SBR (S-SBR) and the like, whether oil-extended or not oil-extended. Good. Of these, oil-extended and high-molecular weight SBR is preferable from the viewpoint of grip performance. Further, terminal-modified S-SBR and main chain-modified S-SBR with enhanced interaction force with the filler can also be used. These SBRs may be used alone or in combination of two or more.

The styrene content of SBR is preferably 16% by mass or more, more preferably 20% by mass or more, still more preferably 25% by mass or more, and particularly preferably 30% by mass or more from the viewpoint of grip performance. If the styrene content is too high, the styrene group is adjacent, the polymer becomes too hard, the cross-linking tends to be non-uniform, the blowability at high temperature running may be deteriorated, and the temperature dependency increases, The performance change with respect to the temperature change becomes large, and there is a tendency that a stable grip performance in the running / late period cannot be obtained well, so 60 mass% or less is preferable, 50 mass% or less is more preferable, and 45 mass%. The following is more preferable.
In the present specification, the styrene content of SBR is calculated by 1H-NMR measurement.

The vinyl content of SBR is preferably 10% or more, more preferably 15% or more, from the viewpoint of Hs and grip performance of the rubber composition. Moreover, from a viewpoint of grip performance, EB (durability), and abrasion resistance, 90% or less is preferable, 80% or less is more preferable, 70% or less is further more preferable, and 60% or less is especially preferable.
In addition, in this specification, the vinyl content (1,2-bond butadiene unit amount) of SBR can be measured by an infrared absorption spectrum analysis method.

SBR also preferably has a glass transition temperature (Tg) of −45 ° C. or higher, more preferably −40 ° C. or higher. The Tg is preferably 10 ° C. or lower, and more preferably 5 ° C. or lower from the viewpoint of preventing embrittlement cracks in the temperate winter season.
In the present specification, the glass transition temperature of SBR is a value measured by performing differential scanning calorimetry (DSC) in accordance with JIS K 7121 under the condition of a heating rate of 10 ° C./min.

The weight average molecular weight (Mw) of SBR is preferably 200,000 or more, more preferably 250,000 or more, and even more preferably 300,000 or more, from the viewpoints of low fuel consumption and wear resistance. In addition, from the viewpoint of filler dispersibility, that is, low fuel consumption and wear resistance, the weight average molecular weight is preferably 2 million or less, and more preferably 1.8 million or less.
In this specification, the weight average molecular weight of SBR is gel permeation chromatography (GPC) (GPC-8000 series, manufactured by Tosoh Corporation, detector: differential refractometer, column: TSKGEL SUPERMULTIPORE, manufactured by Tosoh Corporation). It can be determined by standard polystyrene conversion based on the measured value by HZ-M).

In the case of containing SBR, the content of SBR in 100% by mass of the rubber component is preferably 20% by mass or more, more preferably 30% by mass or more, and more preferably 50% by mass or more, because sufficient grip performance can be obtained. Is more preferable. Although an upper limit is not specifically limited, 100 mass% is preferable from a viewpoint of grip performance.

The BR is not particularly limited. For example, BR1220 manufactured by Nippon Zeon Co., Ltd., BR130B manufactured by Ube Industries, Ltd., BR150B having a high cis content such as BR150B, BR1250H manufactured by Nippon Zeon Co., Ltd. It is synthesized using a modified cis content BR, a BR containing syndiotactic polybutadiene crystals such as VCR412 and VCR617 manufactured by Ube Industries, and a rare earth element catalyst such as BUNA-CB25 manufactured by LANXESS. BR with high cis content can be used. These BR may use 1 type and may use 2 or more types together.

The cis 1,4-bond content (cis content) of BR is preferably 90% by mass or more, more preferably 93% by mass or more, and still more preferably 95% by mass or more from the viewpoint of durability and wear resistance.

The vinyl content of BR is preferably 1.8% by mass or less, more preferably 1.5% by mass or less, still more preferably 1.0% by mass or less, and 0.8% by mass from the viewpoints of durability and wear resistance. The following are particularly preferred:
In the present specification, the vinyl content (1,2-bonded butadiene unit amount) and cis content (cis-1,4-bonded butadiene unit amount) of BR can be measured by infrared absorption spectrum analysis.

When BR is contained, the content of BR in 100% by mass of the rubber component is preferably 10% by mass or more, more preferably 15% by mass or more, and more preferably 20% by mass or more from the viewpoints of wear resistance and low fuel consumption. Is more preferable. The content is preferably 70% by mass or less, more preferably 60% by mass or less, and 40% by mass or less for a tire requiring grip performance, from the viewpoints of wear resistance, grip performance, and fuel efficiency.

In the rubber composition of the present invention, the total content of SBR and BR is preferably 80% by mass or more, more preferably 90% by mass or more, and 100% by mass in 100% by mass of the rubber component. If it is less than 80% by mass, the effects of the present invention may not be sufficiently obtained.

Examples of the white filler include silica, aluminum hydroxide, alumina (aluminum oxide), magnesium sulfate, calcium carbonate, and talc. These white fillers can be used alone or in combination of two or more. You can also. Among them, a white filler having a COO group is preferable because the effects of the present invention can be obtained more suitably, and among them, it is excellent in wear resistance, durability, wet grip performance and low fuel consumption. It is preferable to contain silica and / or aluminum hydroxide.

The silica is not particularly limited, and examples thereof include dry process silica (anhydrous silicic acid), wet process silica (hydrous silicic acid) and the like. These may be used alone or in combination of two or more. Of these, wet-process silica is preferred because it has many silanol groups.

BET specific surface area (nitrogen adsorption specific surface _area, N 2 SA) of silica is dispersed, abrasion performance, in terms of wet grip performance and processability, preferably ^{70~300m 2 / g, 80~280m 2 /} g is More preferably, 90-250 m < ² > / g is still more preferable.
Incidentally, _N 2 SA of the silica in this specification is a value measured by the BET method in accordance with ASTM D3037-81.

In the case of containing silica, the content with respect to 100 parts by mass of the rubber component is preferably 20 parts by mass or more, more preferably 30 parts by mass or more, and still more preferably 40 parts by mass or more from the viewpoint of wet grip performance. Further, the content of silica is preferably 160 parts by mass or less, and more preferably 150 parts by mass or less, from the viewpoint of ensuring workability and fracture resistance (TB) that suppresses shrinkage associated with cooling after vulcanization.

BET specific surface area (nitrogen adsorption specific surface _area, N 2 SA) of the aluminum hydroxide, in terms of wet grip performance, preferably at least ^{5 m} 2 / g, more preferably at least ^{10m 2 / g, 12m 2 /} g or more further preferable. Further, BET specific surface area of aluminum hydroxide, the dispersibility of the aluminum hydroxide, re aggregation preventing, from the viewpoint of abrasion resistance, preferably from ^{60 m} 2 / g or less, more preferably ^{50m 2 / g, 40m 2 /} g The following is more preferable.
In addition, the BET specific surface area of the aluminum hydroxide in this specification is a value measured by BET method according to ASTM D3037-81.

The average particle diameter (D50) of aluminum hydroxide is preferably 0.1 μm or more, more preferably 0.2 μm or more, and more preferably 0.3 μm or more, from the viewpoints of dispersibility of aluminum hydroxide, prevention of reaggregation, and wear resistance. Further preferred. The average particle diameter (D50) of aluminum hydroxide is preferably 3.0 μm or less, more preferably 2.0 μm or less, from the viewpoint of wear resistance.
In addition, the average particle diameter (D50) in this specification is a particle diameter of 50% of the integrated mass value of the particle diameter distribution curve calculated | required with the particle diameter distribution measuring apparatus.

The content with respect to 100 parts by mass of the rubber component in the case of containing aluminum hydroxide is preferably 1 part by mass or more, more preferably 2 parts by mass or more, and still more preferably 3 parts by mass or more from the viewpoint of grip performance. The content of aluminum hydroxide is preferably 60 parts by mass or less, more preferably 55 parts by mass or less, and still more preferably 50 parts by mass or less from the viewpoint of wear resistance.

From the viewpoint of wet grip performance, the content of the white filler with respect to 100 parts by mass of the rubber component is 5 parts by mass or more, preferably 30 parts by mass or more, and more preferably 40 parts by mass or more. Further, the content of the white filler is 200 parts by mass or less, preferably 180 parts by mass or less, from the reason of ensuring break resistance (TB) that suppresses shrinkage associated with workability and cooling after vulcanization. More preferably, it is 150 parts by mass or less.

In the present invention, since the compound represented by the formula (1) is blended, the white filler is preferably dispersed in the rubber composition even if the content of the white filler is increased (even if it is 80 parts by mass or more). Better processability, low fuel consumption, wear resistance and vulcanization productivity can be obtained.

Silica is preferably used in combination with a silane coupling agent. 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) disulfide, bis (3-triethoxy (Silylpropyl) sulfide type such as tetrasulfide, 3-mercaptopropyltrimethoxysilane, NXT-Z100, NXT-Z45, NXT, etc. manufactured by Momentive (silane coupling agent having a mercapto group), vinyltriethoxysilane Vinyl type such as 3-aminopropyl triethoxysilane, glycidoxy type such as γ-glycidoxypropyltriethoxysilane, nitro type such as 3-nitropropyltrimethoxysilane, 3-chloropropyltrimethoxysilane Black System, and the like. These may be used alone or in combination of two or more. Of these, sulfide type and mercapto type are preferable from the viewpoints of strong binding strength with silica and excellent fuel efficiency. Use of a mercapto type is also preferable from the viewpoint that fuel efficiency and wear resistance can be suitably improved.

The content with respect to 100 parts by mass of silica in the case of containing a silane coupling agent is 4.0 parts by mass or more because the effect of improving the filler dispersibility and the effect of reducing the viscosity can be obtained. Preferably, it is 6.0 parts by mass or more. In addition, the content of the silane coupling agent is preferably 12 parts by mass or less, and is preferably 10 parts by mass or less because sufficient coupling effect and silica dispersion effect cannot be obtained and the reinforcing property is lowered. It is more preferable.

（式（１）中、Ｘは−ＣＯＮＨ−を表す。Ｒ^１は炭素数７〜２３のアルキル基又は炭素数７〜２３のアルケニル基を表す。Ｒ^２は炭素数１〜３のアルキレン基を表す。Ｒ^３とＲ^４はそれぞれ独立して、水素原子、炭素数１〜３のアルキル基又は炭素数１〜３のヒドロキシアルキル基を表し、少なくとも１つは前記ヒドロキシアルキル基である。）The rubber composition of the present invention contains a compound represented by the following formula (1).

(In formula (1), X represents -CONH-. R ¹ represents an alkyl group having 7 to 23 carbon atoms or an alkenyl group having 7 to 23 carbon atoms. R ² represents an alkylene group having 1 to 3 carbon atoms. R ³ and R ⁴ each independently represent a hydrogen atom, an alkyl group having 1 to 3 carbon atoms, or a hydroxyalkyl group having 1 to 3 carbon atoms, and at least one is the hydroxyalkyl group.)

In the formula (1), X represents —CONH— from the viewpoint that the polarity (electron withdrawing property) at the center of the molecule is increased and the production is easy.

R ¹ in the formula (1), the adsorption of the white filler, in terms of hydrophobic forces compound itself represented by the formula (1), an alkyl group carbon atoms or 7 to 23 carbon atoms 7-23 These alkyl groups and alkenyl groups may be linear, branched or cyclic, but are preferably linear. For example, octyl group, nonyl group, isononyl group, decyl group, undecyl group, dodecyl group, tridecyl group, isotridecyl group, tetradecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, henycosyl group, tricosyl group, etc. Alkenyl groups such as octenyl group, nonenyl group, decenyl group, heptadecenyl group and the like. The raw material of the compound is preferably lauric acid, tridecylic acid, myristic acid, palmitic acid, stearic acid, behenic acid, oleic acid, palm oil fatty acid, palm kernel oil fatty acid, palm oil fatty acid, hydrogenated palm oil. Fatty acids such as fatty acids, beef tallow fatty acids and hydrogenated beef tallow fatty acids, methyl esters of these fatty acids, and fats and oils such as coconut oil, palm kernel oil, palm oil, hydrogenated palm oil, beef tallow, hydrogenated beef tallow and the like.

When the number of carbon atoms of R ¹ in the formula (1) exceeds 23, the density of polar groups such as amino groups is lowered, and the polarity is lowered, so that the adsorption performance on the surface of the white filler tends to be lowered. On the other hand, when the carbon number of R ¹ is less than 7, the adsorption performance is excessive, and the bond between the silane coupling agent and the white filler (particularly silica) tends to be inhibited.
The reason that the effects of the present invention can be obtained more suitably, carbon atoms in the alkyl group and alkenyl group for ^{R 1,} preferably 9 to 21, more preferably 11 to 19, more preferably from 15 to 19.

R ¹ is preferably an alkenyl group because particularly good wear resistance can be obtained.

R ² in formula (1) is an alkylene group having 1 to 3 carbon atoms from the viewpoint of imparting an appropriate hydrophobic and hydrophilic amphoteric surface active function to the compound represented by formula (1). The group may be either linear or branched, but is preferably linear.

Examples of the alkylene group having 1 to 3 carbon atoms include a methylene group, an ethylene group, and a propylene group.

When the carbon number of R ² in the formula (1) exceeds 3, an appropriate hydrophobic / hydrophilic amphoteric surface active function cannot be imparted to the compound represented by the formula (1), and the surface of the white filler Adsorption performance tends to decrease.

R ³ and R ⁴ in the formula (1) are each independently a hydrogen atom or a carbon number of 1 to 3 from the viewpoint of the adsorptivity to the white filler at the end of the compound represented by the formula (1). Or an alkyl group having 1 to 3 carbon atoms, at least one of which is the hydroxyalkyl group.

The alkyl group having 1 to 3 carbon atoms may be linear, branched or cyclic, but is preferably linear. Examples of the alkyl group having 1 to 3 carbon atoms include a methyl group, an ethyl group, and a propyl group.

When the number of carbon atoms of the alkyl group exceeds 3, the density of polar groups such as amino groups and hydroxy groups is lowered, and the polarity is lowered, so that the adsorption performance to the surface of the white filler tends to be lowered.

The hydroxyalkyl group having 1 to 3 carbon atoms may be linear, branched or cyclic, but is preferably linear. Examples of the alkyl group of a hydroxyalkyl group having 1 to 3 carbon atoms (that is, an alkyl group having 1 to 3 carbon atoms) include a methyl group, an ethyl group, and a propyl group.

When the number of carbon atoms of the hydroxyalkyl group exceeds 3, the density of polar groups such as amino groups and hydroxy groups decreases, and the polarity decreases, so that the adsorption performance of the white filler on the surface tends to decrease.

As R ³ and R ^4, it is preferable that one is a hydrogen atom and the other is a hydroxyalkyl group because the effects of the present invention can be more suitably obtained. As a result, the amino group in the molecular chain is likely to be adsorbed on the surface of the white filler (particularly the hydroxy group on the surface of the white filler) in the same manner as the terminal hydroxy group, and the acidity generated by the white filler surface is easily neutralized. It is presumed to be.

Specific compounds represented by the formula (1) include, for example, oleic acid amidoethylaminoethanol, lauric acid amidoethylaminoethanol, stearic acid amidoethylaminoethanol, caprylic acid amidoethylaminoethanol, behenic acid amidoethylamino. Fatty acid amidoethylaminoethanol such as ethanol; fatty acid amidopropylaminopropanol such as oleic acid amidopropylaminopropanol, lauric acid amidopropylaminopropanol, stearic acid amidopropylaminopropanol, caprylic amidopropylaminopropanol, behenic acid amidopropylaminopropanol Oleic acid amide (N methyl) ethylaminoethanol, lauric acid amide (N methyl) ethylaminoethanol, stearic acid Fatty acid amides (N-methyl) ethylaminoethanol such as amide (N-methyl) ethylaminoethanol, caprylic acid amide (N-methyl) ethylaminoethanol, behenic acid amide (N-methyl) ethylaminoethanol; oleic acid amide ethylaminopropanol, laurin Fatty acid amidoethylaminopropanol such as amidoethylaminopropanol, amidoethylamino stearate, amidoethylaminopropanol caprylate, amidoethylaminopropanol behenate; amidopropylaminoethanol oleate, amidopropylaminoethanol laurate, stearic acid Fatty acid amino acids such as amidopropylaminoethanol, caprylic amidopropylaminoethanol, behenic acid amidopropylaminoethanol, etc. Propylamino ethanol; stearic acid amide (N ethanol) ethylamino ethanol, lauric acid amide methylamino ethanol, stearic acid amide methylamino ethanol, amido ethylamino methanol laurate, stearic acid amide ethylamino methanol and the like. These may be used alone or in combination of two or more. Of these, fatty acid amidoethylaminoethanol is preferred, and oleic acid amidoethylaminoethanol, lauric acid amidoethylaminoethanol, stearic acid amidoethylaminoethanol are more preferred, and olein is preferred because the effects of the present invention can be obtained more suitably. Acid amidoethylaminoethanol and stearic acid amidoethylaminoethanol are more preferable. In these compounds, the amino group in the molecular chain is easily adsorbed on the surface of the white filler (especially the hydroxy group on the surface of the white filler) in the same manner as the terminal hydroxy group, and neutralizes the acidity generated by the surface of the white filler. It is assumed that it is easy.
In addition, because the effect of the present invention can be obtained satisfactorily, the compound represented by the formula (1) includes unsaturated fatty acid amide ethylaminoethanol such as oleic acid amidoethylaminoethanol, stearic acid amidoethylaminoethanol and the like The combined use with a saturated fatty acid amidoethylaminoethanol is more preferable, and the combined use of oleic acid amidoethylaminoethanol and stearic acid amidoethylaminoethanol is more preferable.

The compound represented by the formula (1) can be synthesized by a known method. For example, a fatty acid and 2- (2-aminoethylamino) ethanol are mixed, heated at 120 ° C. to 180 ° C., and the produced water or methanol is added. By distilling off, fatty acid amidoethylaminoethanol can be obtained.

The content of the compound represented by the formula (1) with respect to 100 parts by mass of the rubber component appropriately interacts with the white filler, and when the silane coupling agent is blended, the silane coupling agent and the white filler ( In particular, since the viscosity reduction effect and the white filler dispersibility improvement effect are manifested without inhibiting the reaction of silica), that is, without imparting excessive lubricity to the surface of the white filler, 0. 5 mass parts or more are preferable, 1 mass part or more are more preferable, and 2 mass parts or more are still more preferable. Further, the content of the compound is preferably 10 parts by mass or less for the purpose of improving fuel economy, wet grip performance, and abrasion resistance without giving excessive lubricity to the surface of the white filler. The amount is more preferably at most 6 parts by mass, even more preferably at most 6 parts by mass.

The compound represented by the formula (1) may be used in combination with a fatty acid alcohol amide. Thereby, better wear resistance is obtained.

Examples of fatty acid alcohol amides include coconut oil fatty acid N-methylethanolamide, coconut oil fatty acid monoethanolamide, and coconut oil fatty acid diethanolamide. These may be used alone or in combination of two or more. Among these, coconut oil fatty acid N-methylethanolamide is preferable because the effects of the present invention can be more suitably obtained.

When the fatty acid alcohol amide is contained, the content of the fatty acid alcohol amide is preferably 0.1 parts by mass or more, more preferably 0.5 parts by mass or more, and more preferably 1 part by mass or more with respect to 100 parts by mass of the rubber component. Further preferred. The content is preferably 5 parts by mass or less, more preferably 4 parts by mass or less, and still more preferably 3 parts by mass or less. If it is in the said range, the effect of this invention will be acquired more suitably.
For the same reason, the total content of the compound represented by the formula (1) and the fatty acid alcohol amide is preferably 0.3 parts by mass or more, more preferably 0.5 parts by mass or more, and further preferably 1 part by mass or more. 2 parts by mass or more is particularly preferable. The total content is preferably 10 parts by mass or less, more preferably 8 parts by mass or less, and still more preferably 6 parts by mass or less.

In addition to the above components, the rubber composition according to the present invention includes compounding agents generally used in the production of rubber compositions, such as carbon black, resin components, oil, zinc oxide, stearic acid, anti-aging agents. , Waxes, vulcanizing agents, vulcanization accelerators, and the like can be appropriately blended.

The carbon black nitrogen adsorption specific surface area _(N 2 SA) of grip performance, in terms of wear resistance, and a ^{80 m} 2 / g or more, preferably 100 m ² / g or more, more preferably at least 120 m ² / g. _{Also, N} 2 SA, from the viewpoint of ensuring good filler dispersion, preferably from 600 meters ² / g or less, more preferably ^{450m 2 / g, 200m 2 /} g or less is more preferable.
Incidentally, _N 2 SA of carbon black, JIS K 6217-2: determined by the BET method in compliance with 2001.

When carbon black is contained, the content of carbon black with respect to 100 parts by mass of the rubber component is 3 parts by mass or more for the purpose of ensuring wear resistance and ultraviolet crack prevention performance. The preferred carbon black content varies depending on the tire member used and the grip performance, wear resistance, and fuel efficiency expected of the tire. In the case of a tire that ensures wet grip performance with silica, such as a tread portion of a general-purpose tire, the content of carbon black with respect to 100 parts by mass of the rubber component is preferably 5 to 30 parts by mass. Moreover, in the case of a tire that ensures dry grip performance and wear resistance with carbon black, such as a tread portion of a racing tire, the content of carbon black with respect to 100 parts by mass of the rubber component is preferably 40 to 180 parts by mass.

The rubber composition of the present invention preferably contains a vulcanization accelerator. There is no restriction | limiting in particular in the kind of vulcanization accelerator, The normally used thing can be used. Examples of the vulcanization accelerator include thiazole, thiuram, thiourea, guanidine, dithiocarbamic acid, aldehyde-amine or aldehyde-ammonia, imidazoline, or xanthate vulcanization accelerators. These vulcanization accelerators may be used alone or in combination of two or more. Among these, a thiazole vulcanization accelerator is preferable, and it is more preferable to use a thiazole vulcanization accelerator and a guanidine vulcanization accelerator in combination.

Examples of the thiazole vulcanization accelerator include N-tert-butyl-2-benzothiazolylsulfenamide (TBBS), N-cyclohexyl-2-benzothiazolylsulfenamide (CBS), N, N-dicyclohexyl. Sulfenamide vulcanization accelerators such as 2-benzothiazolylsulfenamide (DCBS); N-tert-butyl-2-benzothiazolylsulfenimide (TBSI), di-2-benzothiazolyl disulfide (DM), 2-mercaptobenzothiazole (M) and the like. Of these, sulfenamide vulcanization accelerators are preferred. Examples of the guanidine vulcanization accelerator include diphenyl guanidine, diort triguanidine, triphenyl guanidine and the like. These may be used alone or in combination of two or more.

When the rubber composition contains a vulcanization accelerator, the content of the vulcanization accelerator is not particularly limited and can be freely determined according to the desired vulcanization speed and crosslinking density. When the vulcanization accelerator is contained, the content of the vulcanization accelerator is preferably 0.5 to 10 parts by mass with respect to 100 parts by mass of the rubber component.

In this invention, since the compound represented by Formula (1) is mix | blended, the acidity of a rubber composition can be shifted to the alkali side. As a result, the amount of guanidine vulcanization accelerator can be reduced. The guanidine vulcanization accelerator shifts the rubber composition to alkalinity and promotes the reaction between the sulfenamide vulcanization accelerator and sulfur, while cutting the bond between silica and silane coupling agent produced by kneading. There is a risk that. Excess guanidine-based vulcanization accelerator alone or in combination with a sulfenamide-based vulcanization accelerator may form an insoluble white bloom, which may contaminate the tire appearance. On the other hand, in this invention, since the compounding quantity of a guanidine type | system | group vulcanization accelerator can be reduced, more favorable tire performance (for example, low fuel-consumption property, abrasion resistance) is obtained, and the external appearance of a tire also improves.

When the guanidine vulcanization accelerator is contained, the content of the guanidine vulcanization accelerator is preferably 0 to 3 parts by mass, more preferably 0.1 to 2.8 with respect to 100 parts by mass of the rubber component. Part by mass. Thereby, better tire performance (for example, low fuel consumption and wear resistance) is obtained, and the appearance of the tire is also improved.

In general, when the amount of sulfur is reduced, even if the amount of the vulcanization accelerator is increased, the initial vulcanization speed t10 becomes too slow and the vulcanization time needs to be extended. There is a tendency to get worse. On the other hand, in this invention, even if it reduces the compounding quantity of sulfur by mix | blending the compound represented by Formula (1), initial stage vulcanization speed t10 is ensured, ensuring Hs by the increase in a vulcanization accelerator. It can be maintained in a good range.

Examples of sulfur include powdered sulfur, sulfur polymer, liquid sulfur oligomer, and the like. In rubber compositions for treads containing silica, sulfur is usually powdered sulfur having an oil-treated sulfur content of 70% by mass or more. The content is generally 0.3 to 2.0 parts by mass with respect to 100 parts by mass of the rubber component. In addition, when the sulfur content is 0.3 to 1.4 parts by mass, the initial vulcanization rate t10 is remarkably slow, so that thiazole vulcanization accelerators and guanidine vulcanization accelerators that are usually used In addition, it is necessary to use a thiuram vulcanization accelerator such as TBZTD or ZTC. However, if a thiuram vulcanization accelerator is added, the wear resistance tends to deteriorate. On the other hand, in the present invention, the compound represented by the formula (1) can hydrophobize the silica surface and shift the acidity of the rubber composition to the alkali side. Therefore, a thiuram vulcanization accelerator is blended. Even if it is not, an appropriate initial vulcanization rate t10 can be obtained, and an appropriate crosslinking density, that is, an appropriate Hs can be obtained. Also, good abrasion resistance can be obtained by not incorporating a thiuram vulcanization accelerator.

As powdered sulfur, those having a sulfur content of 70 mass%, 80 mass%, 90 mass%, and 95 mass% are commercially available.
From the reason that the effects of the present invention can be obtained more suitably, the sulfur content of the powdered sulfur is preferably 70% by mass or more, more preferably 90% by mass or more, and still more preferably 95% by mass or more. Is 99% by mass or less, more preferably 98% by mass or less.
For the same reason, the oil content of powdered sulfur is preferably 1% by mass or more, more preferably 2% by mass or more, and preferably 30% by mass or less, more preferably 10% by mass or less, still more preferably. 5% by mass or less.

From the viewpoint of wear resistance and sulfur dispersibility, the sulfur content derived from powdered sulfur having a sulfur content of 70% by mass or more is preferably less than 1.5 parts by mass with respect to 100 parts by mass of the rubber component. More preferably, it is 1.3 parts by mass or less, and still more preferably 1.1 parts by mass or less. Moreover, from a viewpoint of co-crosslinking adhesiveness with an adjacent tire member, Preferably it is 0.3 mass part or more, More preferably, it is 0.4 mass part or more.

The rubber composition of the present invention may use a hybrid crosslinking agent as a crosslinking agent other than sulfur. The hybrid crosslinking agent is preferably an alkyl sulfide crosslinking agent such as 1,6-bis (N, N′-dibenzylthiocarbamoyldithio) hexane, and the content thereof is preferably 1 to 3 parts by mass.

The rubber composition of the present invention can be produced by a general method. For example, after kneading components other than the crosslinking agent and the vulcanization accelerator among the above components in a known kneader used in a general rubber industry such as a Banbury mixer, a kneader, and an open roll, Further, a crosslinking agent and a vulcanization accelerator can be added and further kneaded and then vulcanized.

The rubber composition of the present invention is used for tire members such as tire treads, under treads, carcass, sidewalls and beads, as well as rubber soles, anti-vibration rubbers, belts, hoses, and other industrial rubber products. be able to. In particular, since wet grip properties and wear resistance can be improved, it is preferably used as a rubber composition for tires and a rubber composition for shoe sole rubber, and a tire having a tread composed of the rubber composition of the present invention, the present invention. It is more preferable to use a shoe (sport shoe) having a sole rubber composed of the rubber composition.

The pneumatic tire of the present invention can be produced by a usual method using the rubber composition. That is, by extruding a rubber composition containing the above components in accordance with the shape of a tread or the like at an unvulcanized stage, and molding it with a tire molding machine by a normal method together with other tire members, Unvulcanized tires can be formed. A tire is obtained by heating and pressurizing the unvulcanized tire in a vulcanizer.

The pneumatic tire of the present invention is used as, for example, passenger car tires, truck / bus tires, motorcycle tires, high-performance tires, and the like. In addition, the high-performance tire in this specification is a tire that is particularly excellent in grip performance, and is a concept that includes a competition tire used in a competition vehicle.

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

＜化合物２＞：三洋化成工業（株）製の試作品（ステアリン酸アミドエチルアミノエタノール、下記式で表される化合物（式（１）で表される化合物））

＜化合物３＞：化合物１及び化合物２の混合物（混合比率（質量比）は化合物１：化合物２＝５０：５０）
＜化合物４＞：化合物１及び化合物２の混合物（混合比率（質量比）は化合物１：化合物２＝７５：２５）
＜化合物５＞：三洋化成工業（株）製の試作品（オレイン酸アミドプロピルアミノプロパノール、下記式で表される化合物（式（１）で表される化合物））
ＲＣＯＮＨＣＨ（ＣＨ_３）ＣＨ_２ＮＨＣＨ_２ＣＨ_２ＣＨ_２ＯＨ
Ｒ＝Ｃ_１７Ｈ_３３
＜化合物６＞：三洋化成工業（株）製のプロファンＡＢ−２０（ヤシ油脂肪酸モノエタノールアミド、下記式で表される化合物）

＜化合物７＞三洋化成工業（株）製の試作品（ヤシ油脂肪酸Ｎメチルエタノールアミド、下記式で表される化合物）

＜化合物８＞：三洋化成工業（株）製の試作品（ヤシ油脂肪酸ジエタノールアミド、下記式で表される化合物）

＜化合物９＞：ストラクトール社製のＥＦ４４（脂肪酸亜鉛）
＜化合物１０＞：化合物７及び化合物３の混合物（混合比率（質量比）は化合物７：化合物３＝５０：５０）
＜プロセスオイル＞：Ｈ＆Ｒ社製のＶｉｖａｔｅｃ５００（ＴＤＡＥオイル、Ｔｇ：−５８℃）
＜樹脂＞：ヤスハラケミカル（株）製の水添スチレンテルペン樹脂 Ｍ１２５（水添率：１１％、軟化点：１２３℃、Ｔｇ：６９℃、水酸基価：０ｍｇＫＯＨ／ｇ、ＳＰ値：８．５２）
＜酸化亜鉛＞：三井金属鉱業（株）製の酸化亜鉛２種
＜ステアリン酸＞：日油（株）製のステアリン酸「椿」
＜ハイブリッド架橋剤＞ランクセス社製のＫＡ９１８８（１，６−ビス（Ｎ，Ｎ’−ジベンジルチオカルバモイルジチオ）ヘキサン）
＜硫黄＞：細井化学工業（株）製のＨＫ−２００−５（オイル含有率５質量％、硫黄含有率９５質量％）
＜加硫促進剤１＞：大内新興化学工業（株）製のノクセラーＮＳ−Ｇ（ＴＢＢＳ、Ｎ−ｔｅｒｔ−ブチル−２−ベンゾチアジルスルフェンアミド）
＜加硫促進剤２＞：大内新興化学工業（株）製のノクセラーＤ（ＤＰＧ、１，３−ジフェニルグアニジン）Hereinafter, various chemicals used in Examples and Comparative Examples will be described together.
<SBR>: prepared by a method for producing SBR described later (S-SBR, oil extended 37.5 parts, styrene content: 41% by mass, vinyl content: 40%, Tg: -29 ° C., weight average molecular weight: 1.19 million)
<BR>: CB24 manufactured by LANXESS Co., Ltd. (High cis BR synthesized using an Nd-based catalyst, Tg: -110 ° C., cis content: 96 mass%, vinyl content: 0.7 mass%)
<Carbon black>: HP180 manufactured by Orion Engineered Carbons (N ₂ SA: 175 m ² / g, CTAB specific surface area: 181 m ² / g)
<Silica>: ULTRASIL VN3 manufactured by Evonik Degussa (N ₂ SA: 175 m ² / g)
<Aluminum hydroxide>: Ath # B manufactured by Sumitomo Chemical Co., Ltd. (average particle size: 0.6 μm, N ₂ SA: 15 m ² / g)
<Silane coupling agent 1>: Si75 (bis (3-triethoxysilylpropyl) disulfide) manufactured by Evonik Degussa
<Silane coupling agent 2>: NXT-Z45 (Mercapto silane coupling agent) manufactured by Momentive
<Wax>: Ozoace 0355 manufactured by Nippon Seiwa Co., Ltd.
<Anti-aging agent 1>: Antigen 6C (6PPD, N- (1,3-dimethylbutyl) -N′-phenyl-p-phenylenediamine) manufactured by Sumitomo Chemical Co., Ltd.
<Aging inhibitor 2>: NOCRACK 224 (TMQ, 2,2,4-trimethyl-1,2-dihydroquinoline polymer) manufactured by Ouchi Shinsei Chemical Co., Ltd.
<Compound 1>: Prototype manufactured by Sanyo Kasei Kogyo Co., Ltd. (Oleidoamidoethylaminoethanol, compound represented by the following formula (compound represented by formula (1)))

<Compound 2>: Prototype manufactured by Sanyo Chemical Industries Co., Ltd. (stearic acid amidoethylaminoethanol, compound represented by the following formula (compound represented by formula (1)))

<Compound 3>: Mixture of Compound 1 and Compound 2 (mixing ratio (mass ratio) is Compound 1: Compound 2 = 50: 50)
<Compound 4>: Mixture of Compound 1 and Compound 2 (mixing ratio (mass ratio) is Compound 1: Compound 2 = 75: 25)
<Compound 5>: Prototype manufactured by Sanyo Chemical Industries Co., Ltd. (amidopropylaminopropanol oleate, compound represented by the following formula (compound represented by formula (1)))
RCONHCH (CH ₃ ) CH ₂ NHCH ₂ CH ₂ CH ₂ OH
R = C ₁₇ H ₃₃
<Compound 6>: Prophan AB-20 (coconut oil fatty acid monoethanolamide, compound represented by the following formula) manufactured by Sanyo Chemical Industries, Ltd.

<Compound 7> Prototype manufactured by Sanyo Chemical Industries (coconut oil fatty acid N-methylethanolamide, compound represented by the following formula)

<Compound 8>: Prototype manufactured by Sanyo Kasei Kogyo Co., Ltd. (coconut oil fatty acid diethanolamide, compound represented by the following formula)

<Compound 9>: EF44 (fatty acid zinc) manufactured by Straktor
<Compound 10>: Mixture of Compound 7 and Compound 3 (mixing ratio (mass ratio) is Compound 7: Compound 3 = 50: 50)
<Process oil>: Vivatec 500 manufactured by H & R (TDAE oil, Tg: −58 ° C.)
<Resin>: Hydrogenated styrene terpene resin M125 manufactured by Yasuhara Chemical Co., Ltd. (hydrogenation rate: 11%, softening point: 123 ° C., Tg: 69 ° C., hydroxyl value: 0 mgKOH / g, SP value: 8.52)
<Zinc oxide>: Two types of zinc oxide manufactured by Mitsui Mining & Smelting Co., Ltd. <Stearic acid>: Stearic acid "Kashiwa" manufactured by NOF Corporation
<Hybrid crosslinking agent> KA9188 (1,6-bis (N, N'-dibenzylthiocarbamoyldithio) hexane manufactured by LANXESS)
<Sulfur>: HK-200-5 manufactured by Hosoi Chemical Co., Ltd. (oil content 5% by mass, sulfur content 95% by mass)
<Vulcanization accelerator 1>: Noxeller NS-G (TBBS, N-tert-butyl-2-benzothiazylsulfenamide) manufactured by Ouchi Shinsei Chemical Industry Co., Ltd.
<Vulcanization accelerator 2>: Noxeller D (DPG, 1,3-diphenylguanidine) manufactured by Ouchi Shinsei Chemical Co., Ltd.

Production method of SBR (1) Preparation of terminal modifier In a nitrogen atmosphere, 20.8 g of 3- (N, N-dimethylamino) propyltrimethoxysilane (manufactured by Amax Co.) was placed in a 250 mL volumetric flask, and further anhydrous hexane (Manufactured by Kanto Chemical Co., Inc.) was added to prepare a total volume of 250 mL.
(2) Preparation of SBR To a 30 L pressure-resistant vessel sufficiently purged with nitrogen, add 18 L of n-hexane, 800 g of styrene (manufactured by Kanto Chemical Co., Inc.), 1200 g of butadiene and 1.1 mmol of tetramethylethylenediamine, and rise to 40 ° C. Warm up. Next, 1.8 mL of 1.6 M butyl lithium (manufactured by Kanto Chemical Co., Inc.) was added, and the mixture was heated to 50 ° C. and stirred for 3 hours. Next, 4.1 mL of the terminal modifier was added and stirred for 30 minutes. After adding 15 mL of methanol and 0.1 g of 2,6-tert-butyl-p-cresol (manufactured by Ouchi Shinsei Chemical Co., Ltd.) to the reaction solution, 1200 g of TDAE was added and stirred for 10 minutes. Thereafter, the aggregate was recovered from the polymer solution by a steam stripping treatment. The obtained aggregate was dried under reduced pressure for 24 hours to obtain SBR1. The amount of bound styrene was 41% by mass, the vinyl content was 40%, Tg: -29 ° C, and Mw was 1.19 million.

Examples and Comparative Examples According to the formulation shown in Tables 1 and 2, chemicals other than sulfur, hybrid cross-linking agent and vulcanization accelerator were mixed for 5 minutes at a discharge temperature of 170 ° C using a 1.7 L closed Banbury mixer. A kneaded product was obtained by kneading. Furthermore, the obtained kneaded material was kneaded with the Banbury mixer at a discharge temperature of 150 ° C. for 4 minutes (remill). Next, using a biaxial open roll, sulfur and a vulcanization accelerator were added to the obtained kneaded product and kneaded for 4 minutes until reaching 105 ° C. to obtain an unvulcanized rubber composition. The obtained unvulcanized rubber composition was vulcanized and molded at 170 ° C. for 12 minutes at a pressure of 25 kgf / cm ² to prepare a test rubber composition.

Further, the unvulcanized rubber composition is extruded by an extruder equipped with a die having a predetermined shape, and is bonded together with other tire members to form an unvulcanized tire, which is pressed at 170 ° C. for 12 minutes. Test tires were produced by vulcanization. The following evaluation was performed about the obtained rubber composition for a test and the tire for a test. The results are shown in Tables 1 and 2.

<Viscosity index>
For each unvulcanized rubber composition, according to the Mooney viscosity measurement method according to JIS K 6300-1, “Unvulcanized rubber—physical properties—Part 1: Determination of viscosity and scorch time using Mooney viscometer” Mooney viscosity (ML1 + 4) was measured under a temperature condition of 130 ° C. The results are shown as an index with the Mooney viscosity of Comparative Example 1 as 61. The smaller the viscosity index, the lower the Mooney viscosity and the better the workability. Note that 65 or less is a performance target value.

<Initial vulcanization speed t10>
Each unvulcanized rubber composition was subjected to a vulcanization test at a measurement temperature of 160 ° C. using a vibration type vulcanization tester (curlastometer) described in JIS K6300, and time and torque plotted. A sulfur velocity curve was obtained. When the minimum value of the torque of the vulcanization rate curve is ML, the maximum value is MH, and the difference (MH−ML) is ME, time t10 (minute) to reach ML + 0.1ME was calculated. In addition, 2.0 to 3.6 minutes is set as the performance target value.

<Low fuel consumption index>
Using a viscoelastic spectrometer VES manufactured by Iwamoto Seisakusho, the loss tangent tan δ of each test rubber composition was measured under the conditions of a temperature of 50 ° C., a frequency of 10 Hz, an initial strain of 10%, and a dynamic strain of 2%. . The smaller tan δ, the lower the exothermic property and the better the fuel efficiency. The results were expressed as an index with the reciprocal of tan δ of Comparative Example 1 being 100. A larger index indicates better fuel efficiency. The fuel efficiency index is set to 100 or more as a performance target value.

<Abrasion resistance index>
Each test tire was mounted on a 2000 cc domestic FR vehicle and ran for a long run of 500 km at Okayama International Circuit.
Traveling mode: Severe handling to the extent that the tread main groove can be cut by 1 mm in 20 km traveling, including 8 sharp turns.
After running, the amount of remaining grooves in the tire tread rubber was measured (8.0 mm when new) and evaluated as wear resistance. The greater the average remaining groove amount of the main groove, the better the wear resistance. The results are shown as an index with the remaining groove amount of Comparative Example 1 as 100. It shows that it is excellent in abrasion resistance, so that an index | exponent is large. Note that the wear resistance index is 100 or more as a performance target value.

In the examples containing the rubber component, the white filler, and the compound represented by the above formula (1), the rubber viscosity during kneading is low even though the rubber composition contains the white filler. Excellent fuel efficiency, low fuel consumption, abrasion resistance and vulcanization productivity.

From the comparison between Comparative Examples 1 and 8, in the formulation not containing the compound represented by the above formula (1), when the amount of sulfur is reduced, an appropriate initial vulcanization speed t10 is maintained even if the vulcanization accelerator is increased. I couldn't. On the other hand, from the comparison of Examples 1 and 5, when the compound represented by the above formula (1) is contained, even if the amount of sulfur is reduced, the amount of the vulcanization accelerator is increased, so that appropriate Hs and low fuel consumption are achieved. Thus, it was possible to maintain an appropriate initial vulcanization speed t10 while ensuring wear resistance. Moreover, in the formulation containing the compound represented by the above formula (1), wear resistance was greatly improved by reducing the amount of sulfur.

Claims (6)

Containing a rubber component, a white filler, and a compound represented by the following formula (1),
The rubber composition whose content of the white filler is 5 to 200 parts by mass with respect to 100 parts by mass of the rubber component.

(In formula (1), X represents -CONH-. R ¹ represents an alkyl group having 7 to 23 carbon atoms or an alkenyl group having 7 to 23 carbon atoms. R ² represents an alkylene group having 1 to 3 carbon atoms. R ³ and R ⁴ each independently represent a hydrogen atom, an alkyl group having 1 to 3 carbon atoms, or a hydroxyalkyl group having 1 to 3 carbon atoms, and at least one is the hydroxyalkyl group.) The rubber composition according to claim 1, wherein the compound represented by the formula (1) is fatty acid amidoethylaminoethanol. Contains sulfur,
The content of a sulfur content derived from powdered sulfur having a sulfur content of 70% by mass or more of the sulfur is less than 1.5 parts by mass with respect to 100 parts by mass of the rubber component. Rubber composition. The rubber composition according to any one of claims 1 to 3, comprising silica as the white filler. It is a rubber composition for tires, The rubber composition in any one of Claims 1-4. The pneumatic tire which has a tire member produced using the rubber composition in any one of Claims 1-5.