Tire rubber composition, tread rubber, and tire

Abstract

The problem of the present invention is to provide a rubber composition for a tire with which both tire gripping performance and manufacturing workability can be achieved at high levels. The solution to this problem is a rubber composition, for a tire, that includes a rubber component and a softening agent, and that is characterized in that: the rubber component includes at least one substance selected from styrene-butadiene rubbers and butadiene rubbers; the softening agent has a softening point of more than 110°C and includes a terpene-based resin and a hydrogenated resin having a weight average molecular weight of 200-1600 g / mol in terms of polystyrene; and the hydrogenated resin and the terpene-based resin satisfy the formula: mass ratio of hydrogenated resin / terpene-based resin ≥ 1.4 / 1.

Description

[Technical Field]

[0001] This invention relates to a rubber composition for tires, tread rubber, and tires. [Background technology]

[0002] Conventionally, there has been a desire to improve the grip performance of tire treads, and increasing the amount of softening agents such as resins and oils has been considered in order to improve grip performance. For example, Patent Document 1 below discloses that applying a rubber composition, which is made by compounding a thermoplastic resin and a silica-containing filler with a rubber component containing 70% by mass or more of natural rubber, to the tread rubber of a tire improves the braking performance (hereinafter abbreviated as "grip performance") of the tire on both dry and wet road surfaces. [Prior art documents] [Patent Documents]

[0003] [Patent Document 1] International Publication No. 2015 / 079703 [Overview of the project] [Problems that the invention aims to solve]

[0004] However, when a large amount of softening agent is added to the rubber composition, the unvulcanized rubber composition adheres to the production equipment, significantly worsening manufacturing efficiency. Therefore, there is a need for technology that can improve tire grip performance at a high level without compromising manufacturing efficiency.

[0005] Therefore, the object of the present invention is to solve the problems of the above-mentioned prior art and to provide a tire rubber composition that can achieve a high level of both tire grip performance and ease of manufacturing, and a tread rubber made from such a rubber composition. Furthermore, a further objective of the present invention is to provide a tire that achieves a high level of both grip performance and ease of manufacturing.

Means for Solving the Problem

[0006] The gist of the present invention for solving the above problems is as follows.

[0007] The rubber composition for a tire of the present invention is a rubber composition for a tire containing a rubber component and a softening agent, where the rubber component contains at least one selected from styrene-butadiene rubber and butadiene rubber, the softening agent contains a hydrogenated resin having a softening point exceeding 110°C and a weight average molecular weight in terms of polystyrene of 200 to 1600 g / mol, and a terpene resin, the hydrogenated resin and the terpene resin satisfy the following formula: Mass ratio of hydrogenated resin / terpene resin ≥ 1.4 / 1 and are characterized by this.

[0008] Further, the tread rubber of the present invention is characterized by being composed of the above rubber composition for a tire.

[0009] Further, the tire of the present invention is characterized by including the above tread rubber.

Advantages of the Invention

[0010] According to the present invention, it is possible to provide a rubber composition for a tire that can achieve both high grip performance and high manufacturing workability of a tire, and a tread rubber composed of such a rubber composition. Further, according to the present invention, it is possible to provide a tire that achieves both high grip performance and high manufacturing workability at a high level.

Embodiments for Carrying Out the Invention

[0011] Hereinafter, the rubber composition for a tire, the tread rubber, and the tire of the present invention will be exemplified and described in detail based on their embodiments.

[0012] <Rubber Composition for a Tire> The rubber composition for tires of the present invention contains a rubber component and a softening agent. In the rubber composition for tires of the present invention, the rubber component contains at least one selected from styrene-butadiene rubber and butadiene rubber, and the softening agent contains a hydrogenated resin having a softening point exceeding 110°C and a weight average molecular weight in terms of polystyrene of 200 to 1600 g / mol, and a terpene resin, and the hydrogenated resin and the terpene resin satisfy the following formula: Mass ratio of hydrogenated resin / terpene resin ≥ 1.4 / 1 and is characterized by this.

[0013] The rubber composition for tires of the present invention contains at least one selected from styrene-butadiene rubber and butadiene rubber as a rubber component, and thus has sufficient fracture properties as a rubber composition for tires. Further, the rubber composition for tires of the present invention contains a hydrogenated resin having a softening point exceeding 110°C and a weight average molecular weight in terms of polystyrene of 200 to 1600 g / mol, and a terpene resin as a softening agent, and thus can improve the grip performance of the tire when applied to the tire. Further, in the rubber composition for tires of the present invention, by setting the mass ratio of the hydrogenated resin / terpene resin to 1.4 / 1 or more, it is possible to suppress the adhesion of the unvulcanized rubber composition to the production equipment and improve the manufacturing workability. Therefore, the rubber composition for tires of the present invention can achieve both high grip performance and manufacturing workability of the tire.

[0014] [[ID=1...]] (Rubber component) The rubber composition for tires of the present invention contains a rubber component, and the rubber component contains at least one selected from styrene-butadiene rubber (SBR) and butadiene rubber (BR), and may further contain other rubber components. It is preferable that the rubber component contains both styrene-butadiene rubber (SBR) and butadiene rubber (BR).

[0015] Styrene-butadiene rubber (SBR) and butadiene rubber (BR) are relatively difficult to adhere to and have excellent fracture properties. Furthermore, styrene-butadiene rubber is highly effective in improving tire grip performance, while butadiene rubber is highly effective in improving abrasion resistance. Therefore, a rubber composition suitable for tire applications is obtained by including at least one selected from styrene-butadiene rubber (SBR) and butadiene rubber (BR) as the rubber component. The styrene-butadiene rubber (SBR) and butadiene rubber (BR) may be unmodified, modified, or a blend of unmodified and modified materials.

[0016] In the aforementioned rubber component, the total proportion of styrene-butadiene rubber (SBR) and butadiene rubber (BR) is preferably 70% by mass or more, more preferably 80% by mass or more, even more preferably 90% by mass or more, and may be 100% by mass. Furthermore, in the rubber component, the proportion of styrene-butadiene rubber (SBR) is preferably 70% by mass or more, more preferably 80% by mass or more, more preferably 100% by mass or less, and more preferably 90% by mass or less. Furthermore, in the rubber component, the proportion of butadiene rubber (BR) is preferably 0% by mass or more, more preferably 10% by mass or more, more preferably 30% by mass or less, and more preferably 20% by mass or less.

[0017] The rubber component preferably contains styrene units in a proportion of 10% by mass or more and 50% by mass or less. Here, the proportion of styrene units in the rubber component refers to the content of monomer units derived from styrene in the total rubber component. When the proportion of styrene units in the rubber component is 10% by mass or more, the effect of improving the grip performance of the tire is greatly enhanced, and when it is 50% by mass or less, the low-temperature embrittlement of the rubber composition is improved. The proportion of styrene units in the rubber component can be determined by infrared spectroscopy (Morello method).

[0018] The rubber component may further contain other rubbers, and the content of other rubbers in the rubber component is preferably 30% by mass or less, more preferably 20% by mass or less, even more preferably 10% by mass or less, and may be 0% by mass. Examples of such other rubbers include natural rubber (NR), isoprene rubber (IR), chloroprene rubber (CR), styrene-isoprene rubber (SIR), acrylonitrile-butadiene rubber (NBR), butyl rubber (IIR), halogenated butyl rubber, etc. These other rubbers may be used individually or in mixtures of two or more.

[0019] The aforementioned rubber component may be partially or entirely oil-distributed, and if the rubber component is oil-distributed, the spreading oil is classified as a softening agent as described later.

[0020] (Softener) The tire rubber composition of the present invention contains a softening agent, the softening agent comprising a hydrogenated resin having a softening point exceeding 110°C and a weight-average molecular weight in polystyrene terms of 200 to 1600 g / mol, and a terpene resin, and may further contain other softening agent components. Here, the hydrogenated resin and the terpene resin are defined by the following formula: Mass ratio of hydrogenated resin / terpene resin ≥ 1.4 / 1 It satisfies the condition.

[0021] If the hydrogenated resin content is less than 1.4 times the terpene resin content, the rubber composition adheres to the production equipment, resulting in poor manufacturing efficiency. From the viewpoint of suppressing adhesion of the rubber composition to the production equipment and improving manufacturing efficiency, the mass ratio of hydrogenated resin to terpene resin is preferably 1.4 / 1 or higher, and from the viewpoint of grip, it is preferably 6 / 1 or lower.

[0022] The aforementioned softening agent is a compounding agent that has the effect of softening the rubber composition, and specifically includes the hydrogenated resins and terpene resins mentioned above, as well as other thermoplastic resins and liquid softening agent components such as oils and liquid polymers. Here, the liquid softening agent components such as oils and liquid polymers are liquid at 25°C (room temperature).

[0023] The total content of the softener is preferably 30 parts by mass or more and 170 parts by mass or less per 100 parts by mass of the rubber component. When the total content of the softener is 30 parts by mass or more per 100 parts by mass of the rubber component, the effect of improving the grip performance of the tire is greatly enhanced, and when it is 170 parts by mass or less, the workability of the rubber composition is improved. From the viewpoint of tire grip performance, the total content of the softener is more preferably 60 parts by mass or more per 100 parts by mass of the rubber component, and even more preferably 80 parts by mass or more, and from the viewpoint of the workability of the rubber composition, it is more preferably 140 parts by mass or less per 100 parts by mass of the rubber component, and even more preferably 120 parts by mass or less.

[0024] -Hydrogenated resin- The rubber composition for tires of the present invention contains a hydrogenated resin, the hydrogenated resin having a softening point exceeding 110°C and a weight-average molecular weight of 200 to 1600 g / mol on a polystyrene basis. By applying such a rubber composition containing a hydrogenated resin to a tire, the grip performance of the tire can be improved.

[0025] If the softening point of the hydrogenated resin is 110°C or lower, it cannot adequately reinforce the tire to which the rubber composition is applied. From the viewpoint of tire fracture characteristics, the softening point of the hydrogenated resin is preferably 116°C or higher, more preferably 120°C or higher, more preferably 123°C or higher, more preferably 126°C or higher, and even more preferably 128°C or higher. Furthermore, from the viewpoint of tire grip performance, the softening point of the hydrogenated resin is preferably 160°C or lower, more preferably 150°C or lower, more preferably 145°C or lower, more preferably 141°C or lower, and even more preferably 136°C or lower.

[0026] Furthermore, if the weight-average molecular weight of the hydrogenated resin, calculated on a polystyrene basis, is less than 200 g / mol, the hydrogenated resin will precipitate from the tire, making it difficult to fully realize the effects of the hydrogenated resin. Conversely, if it exceeds 1600 g / mol, the hydrogenated resin will not be compatible with the rubber components. From the viewpoint of suppressing the precipitation of hydrogenated resin from the tire and suppressing the deterioration of the tire appearance, the weight-average molecular weight of the hydrogenated resin in terms of polystyrene is preferably 300 g / mol or more, more preferably 400 g / mol or more, more preferably 500 g / mol or more, more preferably 550 g / mol or more, more preferably 600 g / mol or more, more preferably 650 g / mol or more, and even more preferably 700 g / mol or more. Furthermore, from the viewpoint of improving the compatibility of the hydrogenated resin with the rubber component and further enhancing the effects of the hydrogenated resin, the weight-average molecular weight of the hydrogenated resin in terms of polystyrene is more preferably 1570 g / mol or less, more preferably 1530 g / mol or less, more preferably 1500 g / mol or less, more preferably 1470 g / mol or less, more preferably 1430 g / mol or less, more preferably 1400 g / mol or less, more preferably 1370 g / mol or less, more preferably 1330 g / mol or less, more preferably 1300 g / mol or less, more preferably 1200 g / mol or less, more preferably 1100 g / mol or less, more preferably 1000 g / mol or less, and even more preferably 950 g / mol or less.

[0027] The weight-average molecular weight (Mw) of the hydrogenated resin in terms of polystyrene. HR (Units are g / mol) Softening point (Ts) of hydrogenated resin HR The ratio (Ts) (unit is °C) HR / Mw HRThe ratio (Ts) is preferably 0.075 or higher, more preferably 0.083 or higher, more preferably 0.095 or higher, more preferably 0.104 or higher, more preferably 0.125 or higher, more preferably 0.135 or higher, more preferably 0.14 or higher, and even more preferably 0.141 or higher. HR / Mw HR ) is preferably 0.25 or less, and more preferably 0.23 or less. The softening point and weight-average molecular weight (in polystyrene equivalent) of the hydrogenated resin can be determined by the method described in the examples below.

[0028] The content of the hydrogenated resin is preferably 10 parts by mass or more and 80 parts by mass or less per 100 parts by mass of the rubber component. When the content of the hydrogenated resin in the rubber composition is 10 parts by mass or more per 100 parts by mass of the rubber component, the effect of improving the grip performance of the tire is greatly enhanced, on the other hand, when it exceeds 80 parts by mass, the low-temperature embrittlement of the rubber composition deteriorates. In contrast, when the content of the hydrogenated resin is 10 parts by mass or more and 80 parts by mass or less per 100 parts by mass of the rubber component, the grip performance of the tire to which the rubber composition is applied can be further improved while suppressing the deterioration of the low-temperature embrittlement of the rubber composition. From the viewpoint of tire grip performance, the content of the hydrogenated resin in the rubber composition is more preferably 20 parts by mass or more and particularly preferably 30 parts by mass or more per 100 parts by mass of the rubber component. Furthermore, from the viewpoint of low-temperature embrittlement of the rubber composition, the content of the hydrogenated resin in the rubber composition is more preferably 70 parts by mass or less and particularly preferably 60 parts by mass or less per 100 parts by mass of the rubber component.

[0029] The hydrogenated resins mentioned above refer to resins obtained by reducing and hydrogenating other resins. Examples of resins used as raw materials for hydrogenated resins include C5 resins, C5-C9 resins, C9 resins, terpene resins (including terpene-aromatic compound resins), and dicyclopentadiene resins. These resins may be used individually or in combination of two or more types. In this specification, resins obtained by reducing and hydrogenating terpene resins are classified as hydrogenated resins.

[0030] Examples of the aforementioned C5 resins include aliphatic petroleum resins obtained by (co)polymerizing C5 fractions obtained by the thermal decomposition of naphtha in the petrochemical industry. The C5 fraction typically contains olefinic hydrocarbons such as 1-pentene, 2-pentene, 2-methyl-1-butene, 2-methyl-2-butene, and 3-methyl-1-butene, as well as diolefinic hydrocarbons such as 2-methyl-1,3-butadiene, 1,2-pentadiene, 1,3-pentadiene, and 3-methyl-1,2-butadiene. Commercially available C5 resins can be used.

[0031] The aforementioned C5-C9 resin refers to a C5-C9 synthetic petroleum resin, and an example of a C5-C9 resin is a petroleum-derived C5-C9 resin. 11 Examples include solid polymers obtained by polymerizing fractions using Friedel-Crafts catalysts such as AlCl3 and BF3, and more specifically, copolymers mainly composed of styrene, vinyltoluene, α-methylstyrene, indene, etc. As for C5-C9 resins, resins with a low amount of C9 or higher components are preferred from the viewpoint of compatibility with rubber components. Here, "low amount of C9 or higher components" means that the amount of C9 or higher components in the total resin is less than 50% by mass, preferably 40% by mass or less. Commercially available C5-C9 resins can be used.

[0032] The aforementioned C9 resin refers to a C9 synthetic petroleum resin, specifically a solid polymer obtained by polymerizing a C9 fraction using a Friedel-Crafts type catalyst such as AlCl3 or BF3. Examples of C9 resins include copolymers mainly composed of indene, α-methylstyrene, vinyltoluene, etc.

[0033] The aforementioned terpene resins are solid resins obtained by polymerizing turpentine oil, which is obtained simultaneously when rosin is obtained from pine trees, or polymer components separated therefrom, using a Friedel-Crafts type catalyst. Examples include β-pinene resin and α-pinene resin. Terpene resins also include terpene-aromatic compound resins, and typical examples of such terpene-aromatic compound resins include terpene-phenol resin and styrene-terpene resin. Terpene-phenol resins can be obtained by reacting terpenes with various phenols using a Friedel-Crafts type catalyst, or by further condensation with formalin. Styrene-terpene resins can be obtained by reacting styrene with terpenes using a Friedel-Crafts type catalyst. There are no particular restrictions on the terpenes used as raw materials, but monoterpene hydrocarbons such as α-pinene and limonene are preferred, those containing α-pinene are more preferred, and α-pinene is particularly preferred.

[0034] The aforementioned dicyclopentadiene-based resin refers to a resin obtained by polymerizing dicyclopentadiene using, for example, a Friedel-Crafts type catalyst such as AlCl3 or BF3.

[0035] Furthermore, the resin used as a raw material for the hydrogenated resin may include, for example, a resin obtained by copolymerizing a C5 fraction with dicyclopentadiene (DCPD) (C5-DCPD resin). Here, if the dicyclopentadiene-derived component in the total resin is 50% by mass or more, the C5-DCPD resin is considered to be included in the dicyclopentadiene resin. If the dicyclopentadiene-derived component in the total resin is less than 50% by mass, the C5-DCPD resin is considered to be included in the C5 resin. The same applies even if a small amount of a third component or the like is included.

[0036] From the viewpoint of improving the compatibility between the rubber component and the hydrogenated resin and further improving the grip performance of the tire to which the rubber composition is applied, the hydrogenated resin is preferably at least one selected from the group consisting of hydrogenated C5 resins, hydrogenated C5-C9 resins, hydrogenated dicyclopentadiene resins (hydrogenated DCPD resins), and hydrogenated terpene resins, more preferably at least one selected from the group consisting of hydrogenated C5 resins and hydrogenated C5-C9 resins, and even more preferably a hydrogenated C5 resin. Furthermore, it is preferable that the resin has at least a hydrogenated DCPD structure or a hydrogenated cyclic structure in its monomer. The hydrogenated resin may be used alone or in combination of two or more types.

[0037] -Terpene resins- The rubber composition for tires of the present invention contains a terpene resin. By applying the rubber composition containing the terpene resin to a tire, the grip performance of the tire can be improved.

[0038] The aforementioned terpene resins are solid resins obtained by polymerizing turpentine oil, which is obtained simultaneously when rosin is obtained from pine trees, or polymer components separated therefrom, using a Friedel-Crafts type catalyst. Examples include β-pinene resin and α-pinene resin. Terpene resins also include terpene-aromatic compound resins, and a representative example of such terpene-aromatic compound resins is terpene-phenol resin. These terpene-phenol resins can be obtained by reacting terpenes with various phenols using a Friedel-Crafts type catalyst, or by further condensation with formalin. There are no particular restrictions on the terpenes used as raw materials, but monoterpene hydrocarbons such as α-pinene and limonene are preferred, those containing α-pinene are more preferred, and α-pinene is particularly preferred.

[0039] The content of the terpene resin is preferably 5 parts by mass or more and 35 parts by mass or less per 100 parts by mass of the rubber component. When the content of the terpene resin in the rubber composition is 5 parts by mass or more per 100 parts by mass of the rubber component, the effect of improving the grip performance of the tire is greatly enhanced, while when it exceeds 35 parts by mass, the low-temperature embrittlement of the rubber composition deteriorates. From the viewpoint of tire grip performance, the content of the terpene resin in the rubber composition is more preferably 5 parts by mass or more per 100 parts by mass of the rubber component, and even more preferably 10 parts by mass or more. Furthermore, from the viewpoint of low-temperature embrittlement of the rubber composition, the content of the terpene resin in the rubber composition is more preferably 35 parts by mass or less per 100 parts by mass of the rubber component, and even more preferably 30 parts by mass or less.

[0040] -Other softeners- The tire rubber composition of the present invention may further contain other softening agents in addition to the hydrogenated resin and terpene resin described above. Examples of other softening agents include thermoplastic resins other than the hydrogenated resin and terpene resin described above, as well as liquid softening components such as oils and liquid polymers.

[0041] Examples of thermoplastic resins other than the hydrogenated resins and terpene resins include C5 resins, C9 resins, C5-C9 resins, rosin resins, dicyclopentadiene resins, and alkylphenol resins.

[0042] Furthermore, the term "oil" refers to the general term for the extensible oil contained in the rubber component and the liquid oil added as a compounding agent to the rubber composition. Examples include petroleum-based softeners such as aromatic oils, paraffinic oils, and naphthenic oils; and plant-based softeners such as palm oil, castor oil, cottonseed oil, and soybean oil. Among these, petroleum-based softeners such as aromatic oils, paraffinic oils, and naphthenic oils are preferred. From the viewpoint of workability, the preferred mass ratio of extensible oil to compounding oil is 1:1 to 10:1.

[0043] In addition, the liquid polymer is preferably in a liquid state at 25°C (room temperature) and has a weight average molecular weight of 5,000 to 100,000. Examples of such liquid polymers include liquid polybutadiene, liquid polyisoprene, and liquid polystyrene-butadiene.

[0044] (Carbon black) The rubber composition for tires of the present invention preferably contains carbon black. The carbon black can reinforce the rubber composition and improve the fracture properties of the rubber composition, and also contributes to further improvement of the grip performance of tires to which the rubber composition is applied.

[0045] The carbon black is not particularly limited, and examples thereof include carbon blacks of GPF, FEF, HAF, ISAF, and SAF grades. These carbon blacks may be used alone or in combination of two or more.

[0046] From the viewpoints of the fracture properties of the rubber composition and the grip performance of tires to which the rubber composition is applied, the content of carbon black in the rubber composition is preferably 10 parts by mass or more, more preferably 20 parts by mass or more, based on 100 parts by mass of the rubber component. Also, from the viewpoint of the abrasion resistance of the rubber composition, the content of carbon black in the rubber composition is preferably 140 parts by mass or less, more preferably 130 parts by mass or less, based on 100 parts by mass of the rubber component.

[0047] (Silica) The rubber composition for tires of the present invention preferably contains silica. When the rubber composition contains silica, the grip performance (particularly wet grip performance) of tires to which the rubber composition is applied can be further improved.

[0048] The silica preferably has a nitrogen adsorption specific surface area (BET method) of 80 m 2 / g or more and less than 330 m 2 / g. When the nitrogen adsorption specific surface area (BET method) of the silica is 80 m 2If the amount is 1 / g or more, the tire to which the rubber composition is applied can be sufficiently reinforced. Also, if the specific surface area of ​​silica adsorbing nitrogen (BET method) is 330 m² 2 If the value is less than / g, the elastic modulus of the rubber composition does not become too high, and the wet grip performance of the tire to which the rubber composition is applied is improved. From the viewpoint of further improving the fracture characteristics of the tire, the nitrogen adsorption specific surface area (BET method) of silica is 100m 2 It is preferable that it be 120m or more. 2 It is preferable that it be 140m or more / g. 2 It is preferable that it be 150m or more / g. 2 It is preferable that it be 170m or more / g. 2 It is preferable that it be 180m or more / g. 2 It is preferable that it be 190m or more / g. 2 It is preferable that it be 195m or more / g 2 It is even more preferable that the nitrogen adsorption specific surface area of ​​silica be 300 m² or more. Furthermore, from the viewpoint of further improving the wet grip performance of the tire, the nitrogen adsorption specific surface area (BET method) of silica should be 300 m². 2 It is preferable that the amount be less than or equal to 280m 2 It is more preferable that it be less than or equal to / g, and 270m 2 It is even more preferable that the amount be less than or equal to / g. Furthermore, the silica preferably has a cetyltrimethylammonium bromide adsorption specific surface area (CTAB) of 150 m². 2 It is 150-300m or more 2 / g, more preferably 150-250m 2 / g, particularly preferably 150-220m 2 It is / g. CTAB is 150m 2 If the amount is 300m or more, the tire to which the rubber composition is applied can be sufficiently reinforced. 2 If the value is less than / g, the elastic modulus of the rubber composition does not become too high, and the wet grip performance of the tire to which the rubber composition is applied is improved.

[0049] Examples of the silica include wet silica (hydrated silica), dry silica (anhydrous silica), calcium silicate, and aluminum silicate, with wet silica being preferred among these. These silicas may be used individually or in combination of two or more.

[0050] From the viewpoint of tire grip performance (particularly wet grip performance), the silica content in the rubber composition is preferably 10 parts by mass or more, and more preferably 15 parts by mass or more, per 100 parts by mass of rubber component. Furthermore, from the viewpoint of wear resistance of the rubber composition, the silica content in the rubber composition is preferably 110 parts by mass or less, and more preferably 100 parts by mass or less, per 100 parts by mass of rubber component.

[0051] The rubber composition for tires of the present invention preferably contains both carbon black and silica as described above. Here, the total content of silica and carbon black is preferably 70 parts by mass or more and 140 parts by mass or less per 100 parts by mass of the rubber component. When the total content of silica and carbon black is 70 parts by mass or more per 100 parts by mass of the rubber component, the effect of improving the grip performance of the tire is further enhanced, and when it is 140 parts by mass or less, the wear resistance of the rubber composition is improved. Furthermore, from the viewpoint of tire grip performance, the total content of silica and carbon black is more preferably 80 parts by mass or more per 100 parts by mass of the rubber component, and from the viewpoint of wear resistance of the rubber composition, it is more preferably 120 parts by mass or less per 100 parts by mass of the rubber component.

[0052] (Styrene-based thermoplastic elastomer) The tire rubber composition of the present invention may contain a styrene-based thermoplastic elastomer (TPS). The styrene-based thermoplastic elastomer (TPS) has a styrene-based polymer block (hard segment) and a conjugated diene-based polymer block (soft segment), where the styrene-based polymer portion forms physical crosslinks and acts as a crosslinking point, while the conjugated diene-based polymer block imparts rubber elasticity. The double bonds of the conjugated diene-based polymer block (soft segment) may be partially or entirely hydrogenated. Note that styrene-based thermoplastic elastomer (TPS) is thermoplastic, while the rubber component (preferably diene rubber) is not. Therefore, in this specification, styrene-based thermoplastic elastomer (TPS) is not included in the rubber component. The content of styrene-based thermoplastic elastomer (TPS) is preferably in the range of 1 to 30 parts by mass per 100 parts by mass of the rubber component.

[0053] Examples of the styrene-based thermoplastic elastomer (TPS) include styrene / butadiene / styrene (SBS) block copolymer, styrene / isoprene / styrene (SIS) block copolymer, styrene / butadiene / isoprene / styrene (SBIS) block copolymer, styrene / isoprene (SI) block copolymer, styrene / butadiene / isoprene (SBI) block copolymer, styrene / ethylene / butylene / styrene (SEBS) block copolymer, styrene / ethylene / propylene / styrene (SEPS) block copolymer, styrene / ethylene / ethylene / propylene / styrene (SEEPS) block copolymer, styrene / ethylene / butylene (SEB) block copolymer, styrene / ethylene / propylene (SEP) block copolymer, and styrene / ethylene / ethylene / propylene (SEEP) block copolymer.

[0054] (Other ingredients) The rubber composition for tires of the present invention may contain the aforementioned rubber components, softeners, carbon black, silica, styrene-based thermoplastic elastomers, and, if necessary, various components commonly used in the rubber industry, such as silane coupling agents, antioxidants, stearic acid, zinc oxide (zinc oxide), vulcanization accelerators, vulcanizing agents, etc., selected appropriately within a range that does not impair the purpose of the present invention. Commercially available products can be suitably used as these compounding agents.

[0055] When the tire rubber composition of the present invention contains silica, it is preferable to include a silane coupling agent in order to improve the effect of the silica. The silane coupling agent may be bis(3-triethoxysilylpropyl)tetrasulfide, bis(3-triethoxysilylpropyl)trisulfide, bis(3-triethoxysilylpropyl)disulfide, bis(2-triethoxysilylethyl)tetrasulfide, bis(3-trimethoxysilylpropyl)tetrasulfide, bis(2-trimethoxysilylethyl)tetrasulfide, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 2-mercaptoethyltrimethoxysilane, 2-mercaptoethyltriethoxysilane, 3-trimethoxysilylpropyl-N,N-dimethylthiocarbamoyltetrasulfide, 3-triethoxysilylpropyl-N, Examples include N-dimethylthiocarbamoyl tetrasulfide, 2-triethoxysilylethyl-N,N-dimethylthiocarbamoyl tetrasulfide, 3-trimethoxysilylpropylbenzothiazolyl tetrasulfide, 3-triethoxysilylpropylbenzothiazolyl tetrasulfide, 3-triethoxysilylpropyl methacrylate monosulfide, 3-trimethoxysilylpropyl methacrylate monosulfide, bis(3-diethoxymethylsilylpropyl)tetrasulfide, 3-mercaptopropyldimethoxymethylsilane, dimethoxymethylsilylpropyl-N,N-dimethylthiocarbamoyl tetrasulfide, and dimethoxymethylsilylpropylbenzothiazolyl tetrasulfide. The content of the silane coupling agent is preferably in the range of 2 to 20 parts by mass, and more preferably in the range of 5 to 15 parts by mass, per 100 parts by mass of silica.

[0056] Examples of the aforementioned antioxidants include N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine (6C), 2,2,4-trimethyl-1,2-dihydroquinoline polymer (TMDQ), 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline (AW), and N,N'-diphenyl-p-phenylenediamine (DPPD). The content of the antioxidant is not particularly limited, but is preferably in the range of 0.1 to 15 parts by mass, and more preferably 1 to 10 parts by mass, per 100 parts by mass of the rubber component.

[0057] Examples of the vulcanization accelerator include sulfenamide-based vulcanization accelerators, guanidine-based vulcanization accelerators, thiazole-based vulcanization accelerators, thiram-based vulcanization accelerators, and dithiocarbamate-based vulcanization accelerators. Examples of the vulcanizing agent include sulfur. The total content of the vulcanization system (vulcanization package) containing the vulcanization accelerator, vulcanizing agent, and stearic acid is not particularly limited, but is preferably in the range of 1 to 25 parts by mass, and more preferably in the range of 5 to 20 parts by mass, per 100 parts by mass of the rubber component.

[0058] (Method for manufacturing rubber composition) The method for producing the rubber composition is not particularly limited, but for example, it can be produced by mixing the rubber components and softeners described above with various components as needed, and then kneading, heating, extruding, etc. Furthermore, the obtained rubber composition can be vulcanized to produce vulcanized rubber.

[0059] There are no particular restrictions on the mixing conditions, and various conditions such as the input volume of the mixing device, the rotation speed of the rotor, the ram pressure, as well as the mixing temperature, mixing time, and the type of mixing device can be appropriately selected according to the purpose. Examples of mixing devices include Banbury mixers, intermixes, kneaders, and rolls, which are commonly used for mixing rubber compositions.

[0060] There are no particular restrictions on the heat treatment conditions, and various conditions such as heat treatment temperature, heat treatment time, and heat treatment equipment can be appropriately selected according to the purpose. Examples of such heat treatment equipment include heat treatment roll machines commonly used for heat treatment of rubber compositions.

[0061] There are no particular restrictions on the extrusion conditions, and various conditions such as extrusion time, extrusion speed, extrusion equipment, and extrusion temperature can be appropriately selected according to the purpose. Examples of extrusion equipment include extruders typically used for extruding rubber compositions. The extrusion temperature can be determined as appropriate.

[0062] There are no particular restrictions on the apparatus, method, and conditions for performing the vulcanization, and they can be appropriately selected according to the purpose. Typical vulcanization apparatuses include molding vulcanizers using molds, which are commonly used for vulcanizing rubber compositions. The vulcanization temperature is typically around 100-190°C.

[0063] <Tread Rubber> The tread rubber of the present invention is characterized by comprising the above-described tire rubber composition. Because the tread rubber of the present invention comprises the above-described tire rubber composition, it is possible to achieve a high level of both tire grip performance and ease of manufacturing. The tread rubber of the present invention may be applied to new tires or to retreaded tires. The tread rubber of the present invention is particularly suitable as a tread rubber for motorcycle tires. Since motorcycle tires require high grip performance, the tread rubber of the present invention is particularly suitable.

[0064] <Tires> The tire of the present invention is characterized by comprising the above-described tread rubber. Because the tire of the present invention comprises the above-described tread rubber, it achieves a high level of both grip performance and ease of manufacturing. The tire of the present invention is particularly suitable as a tire for motorcycles. Since motorcycle tires require high grip performance, the tire of the present invention is particularly suitable.

[0065] The tire of the present invention may be obtained by molding an unvulcanized rubber composition and then vulcanizing it, depending on the type of tire to be applied, or by molding a semi-vulcanized rubber that has undergone a pre-vulcanization process, and then further vulcanizing it. The tire of the present invention is preferably a pneumatic tire, and as the gas to be filled into the pneumatic tire, in addition to ordinary air or air with adjusted oxygen partial pressure, an inert gas such as nitrogen, argon, or helium can be used. [Examples]

[0066] The present invention will be described in more detail below with reference to examples, but the present invention is not limited in any way to the following examples.

[0067] <Analysis Method for Hydrogenated Resins> The softening point and weight-average molecular weight of hydrogenated resins are measured by the following method.

[0068] (1) Softening point The softening point of hydrogenated resins is measured in accordance with JIS-K2207-1996 (ring-sphere method).

[0069] (2) Weight average molecular weight Under the following conditions, the average molecular weight of the hydrogenated resin was measured by gel permeation chromatography (GPC), and the weight-average molecular weight in terms of polystyrene was calculated. Column temperature: 40°C ·Injection volume: 50μL • Carrier and flow rate: Tetrahydrofuran 0.6 mL / min Sample preparation: Dissolve approximately 2.5 mg of resin component in 10 mL of tetrahydrofuran.

[0070] <Preparation of rubber composition> Except for Comparative Example 3, the rubber compositions were prepared by mixing using a conventional mixing device according to the formulations shown in Table 1. For Comparative Example 3, the rubber composition was prepared by mixing in the same manner.

[0071] <Evaluation of rubber compositions> The grip performance and workability of the rubber compositions other than Comparative Example 3 were evaluated using the following method. The grip performance and workability of the rubber composition of Comparative Example 3 were evaluated using the following method. The results are shown in Table 1.

[0072] (3) Grip performance Except for Comparative Example 3, the loss tangent (tanδ) of the rubber composition was measured using a spectrometer manufactured by Ueshima Seisakusho at a frequency of 52 Hz, initial strain of 2%, dynamic strain of 1%, and temperature of 50°C. The tanδ of Comparative Example 1 was set to 100, and the values ​​were expressed exponentially. Comparative Example 3 was expressed exponentially in the same manner. A larger exponential value indicates a larger tanδ and superior grip performance.

[0073] (4) Manufacturing workability Except for Comparative Example 3, the adhesion strength between the unvulcanized rubber composition and the metal at 90°C was measured using a tack meter and expressed as an index, with the reciprocal of the adhesion strength of Comparative Example 1 set to 100. Comparative Example 3 is expressed similarly as an index. A larger index value indicates lower adhesion strength and superior workability in manufacturing.

[0074] [Table 1]

[0075] *1 BR: Butadiene rubber, modified polymer synthesized by the following method *2 SBR: Styrene-butadiene rubber, percentage of styrene units (amount of bound styrene) = 35.5% by mass, manufactured by Asahi Kasei Corporation, product name "Toughden E581", oil-applied rubber containing 37.5 parts by mass of spreadable oil (softener, liquid at 25°C) per 100 parts by mass of rubber component, the upper row shows the content of rubber component, and the lower row shows the content of spreadable oil. *3 Carbon Black: Manufactured by Asahi Carbon Co., Ltd., product name "Asahi #107" *4 Silica: Cetyltrimethylammonium bromide adsorption specific surface area (CTAB) = 191 m² 2 / g, nitrogen adsorption specific surface area (BET method) = 245m 2 / g *5 Oil: Plasticizer (liquid at 25°C), manufactured by JX Nippon Oil & Energy Corporation, product name "A / O MIX" *6 Resin A: Hydrogenated resin (hydrogenated C5 resin), manufactured by Eastman, product name "Registered Trademark Impera E1780", softening point = 130°C, weight average molecular weight (Mw) = 909 g / mol *7 Resin B: Terpene resin (terpene-phenol resin), manufactured by Yasuhara Chemical Co., Ltd., product name "YS Polyster S145" *8 Resin C: Resin other than hydrogenated resin and terpene resin (C9 resin), manufactured by ENEOS, product name "Nisseki Neopolymer 140" *9 Resin D: Resin other than hydrogenated resin and terpene resin (alkylphenol resin), manufactured by SI GROUP-RIBECOURT S.A.S, product name "R7521P" *10 Silane coupling agent: Manufactured by Shin-Etsu Chemical Co., Ltd., product name "ABC-856" *11 Antioxidant: Total amount including the product named "Santite A" manufactured by Seiko Chemical Co., Ltd. and the product named "Antigen 6C" manufactured by Sumitomo Chemical Co., Ltd. *12 Vulcanization package: Total amount including vulcanization accelerator, sulfur and stearic acid

[0076] <Synthesis method of BR(*1)> In a 5L autoclave purged with nitrogen, 2.4 kg of cyclohexane and 300 g of 1,3-butadiene were charged under nitrogen. To these, a catalyst prepared by reacting 0.09 mmol of neodymium versatate in cyclohexane, 1.8 mmol of methyl almoxane (hereinafter also referred to as "MAO") in toluene, 5.0 mmol of diisobutylaluminum hydride (hereinafter also referred to as "DIBAH") in toluene, and 0.18 mmol of diethylaluminum chloride with 1,3-butadiene (4.5 mmol) at 50°C for 30 minutes was charged, and polymerization was carried out at 80°C for 60 minutes. The reaction conversion rate of 1,3-butadiene was approximately 100%. 200 g of this polymer solution was withdrawn, and a methanol solution containing 1.5 g of 2,4-di-tert-butyl-p-cresol was added to stop the polymerization. After that, the solvent was removed by steam stripping, and the solution was dried with a roller at 110°C to obtain the pre-modified polymer. Furthermore, the remaining polymer solution was kept at a temperature of 60°C, and a toluene solution of 3-glycidoxypropyltrimethoxysilane (4.5 mmol) was added and reacted for 30 minutes. Subsequently, a toluene solution of tetra-2-ethylhexyl titanate (13.5 mmol) was added and mixed for 30 minutes. After that, a methanol solution containing 1.5 g of 2,4-di-tert-butyl-p-cresol was added to obtain 2.5 kg of modified polymer solution. Next, the modified polymer solution was added to 20 L of an aqueous solution adjusted to pH 10 with sodium hydroxide, and a condensation reaction was carried out at 110°C for 2 hours with solvent removal. The modified polymer was then dried with a roller at 110°C to obtain the modified polymer.

[0077] Table 1 shows that the rubber composition of the example according to the present invention is superior in both grip performance and workability compared to the rubber composition of Comparative Example 1, in which the mass ratio of hydrogenated resin / terpene resin is less than 1.4 / 1. On the other hand, the rubber compositions of Comparative Examples 2, 4, and 5, which contained hydrogenated resins but did not contain terpene resins, were unable to improve grip performance.

Claims

1. A rubber composition for tires comprising a rubber component and a softening agent, The rubber component comprises at least one selected from styrene-butadiene rubber and butadiene rubber. The softening agent comprises a hydrogenated resin having a softening point exceeding 110°C and a weight-average molecular weight of 200 to 1600 g / mol on a polystyrene basis, and a terpene resin. The hydrogenated resin and the terpene resin are given by the following formula: 6 / 1 ≥ Mass ratio of hydrogenated resin / terpene resin ≥ 1.4 / 1 Satisfying the conditions, The hydrogenated resin content is 30 parts by mass or more and 80 parts by mass or less per 100 parts by mass of the rubber component. The content of the terpene resin is 5 parts by mass or more and 35 parts by mass or less per 100 parts by mass of the rubber component. The total content of the softening agent is 35 parts by mass or more and 170 parts by mass or less per 100 parts by mass of the rubber component. The hydrogenated resin is hydrogenated C ５ Resin systems and hydrogenated C ５ -C ９ A rubber composition for tires, characterized by being at least one selected from the group consisting of resins.

2. The rubber composition for tires according to claim 1, wherein the rubber component has a proportion of styrene units of 10% by mass or more and 50% by mass or less.

3. The tire rubber composition according to claim 1 or 2, further comprising carbon black.

4. The tire rubber composition according to claim 3, further comprising silica, wherein the total content of the silica and the carbon black is 70 parts by mass or more and 140 parts by mass or less per 100 parts by mass of the rubber component.

5. A tread rubber characterized by comprising the tire rubber composition described in any one of claims 1 to 4.

6. A tire characterized by comprising the tread rubber described in claim 5.

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