WO2022259751A1 - タイヤ用ゴム組成物、トレッドゴム及びタイヤ - Google Patents
タイヤ用ゴム組成物、トレッドゴム及びタイヤ Download PDFInfo
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- WO2022259751A1 WO2022259751A1 PCT/JP2022/016941 JP2022016941W WO2022259751A1 WO 2022259751 A1 WO2022259751 A1 WO 2022259751A1 JP 2022016941 W JP2022016941 W JP 2022016941W WO 2022259751 A1 WO2022259751 A1 WO 2022259751A1
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- mass
- rubber
- resin
- rubber composition
- tire
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- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000010690 paraffinic oil Substances 0.000 description 1
- LVMTVPFRTKXRPH-UHFFFAOYSA-N penta-1,2-diene Chemical compound CCC=C=C LVMTVPFRTKXRPH-UHFFFAOYSA-N 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920002742 polystyrene-block-poly(ethylene/propylene) -block-polystyrene Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical compound [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- FBBATURSCRIBHN-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyldisulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSCCC[Si](OCC)(OCC)OCC FBBATURSCRIBHN-UHFFFAOYSA-N 0.000 description 1
- VTHOKNTVYKTUPI-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSSCCC[Si](OCC)(OCC)OCC VTHOKNTVYKTUPI-UHFFFAOYSA-N 0.000 description 1
- KLFNHRIZTXWZHT-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltrisulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSCCC[Si](OCC)(OCC)OCC KLFNHRIZTXWZHT-UHFFFAOYSA-N 0.000 description 1
- JSXKIRYGYMKWSK-UHFFFAOYSA-N trimethoxy-[2-(2-trimethoxysilylethyltetrasulfanyl)ethyl]silane Chemical compound CO[Si](OC)(OC)CCSSSSCC[Si](OC)(OC)OC JSXKIRYGYMKWSK-UHFFFAOYSA-N 0.000 description 1
- JTTSZDBCLAKKAY-UHFFFAOYSA-N trimethoxy-[3-(3-trimethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CO[Si](OC)(OC)CCCSSSSCCC[Si](OC)(OC)OC JTTSZDBCLAKKAY-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F136/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F136/02—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F136/04—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F136/06—Butadiene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/06—Copolymers with styrene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C1/00—Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
- B60C1/0016—Compositions of the tread
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/25—Incorporating silicon atoms into the molecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L45/00—Compositions of homopolymers or copolymers of compounds having no unsaturated aliphatic radicals in side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic or in a heterocyclic ring system; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
Definitions
- the present invention relates to a rubber composition for tires, tread rubber and tires.
- the present invention solves the above-mentioned problems of the prior art, and provides a tire rubber composition capable of achieving both a high level of tire grip performance and manufacturing workability, and a tread rubber comprising such a rubber composition.
- the task is to provide Another object of the present invention is to provide a tire that achieves both high levels of grip performance and manufacturing workability.
- the gist and configuration of the present invention for solving the above problems is as follows.
- tread rubber of the present invention is characterized by comprising the rubber composition for tires described above.
- the rubber composition for tires and the tread rubber which consists of this rubber composition which can make a tire grip performance and manufacturing workability compatible at a high level can be provided. Further, according to the present invention, it is possible to provide a tire that achieves both grip performance and manufacturing workability at a high level.
- the rubber composition for tires, the tread rubber and the tire of the present invention will be exemplified in detail below based on the embodiments thereof.
- the rubber composition for tires of the present invention contains a rubber component and a softener.
- the rubber component contains at least one selected from styrene-butadiene rubber and butadiene rubber, and the softening agent has a softening point exceeding 110° C. and and a hydrogenated resin having a weight average molecular weight of 200 to 1600 g/mol, and a terpene-based resin, wherein the hydrogenated resin and the terpene-based resin are represented by the following formula: Hydrogenated resin/terpene resin mass ratio ⁇ 1.4/1 is characterized by satisfying
- the rubber composition for tires of the present invention contains, as a rubber component, at least one selected from styrene-butadiene rubber and butadiene rubber, so that it has sufficient breaking properties as a rubber composition for tires. Further, the rubber composition for a tire of the present invention contains, as a softening agent, a hydrogenated resin having a softening point of over 110°C and a polystyrene-equivalent weight average molecular weight of 200 to 1600 g/mol, and a terpene resin. Therefore, by applying it to a tire, it is possible to improve the grip performance of the tire.
- 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, the rubber composition in an unvulcanized state adheres to the production equipment. can be suppressed to improve manufacturing workability. Therefore, the rubber composition for tires of the present invention can achieve both the grip performance of the tire and the manufacturing workability at a high level.
- the rubber composition for tires of the present invention contains a rubber component, the rubber component contains at least one selected from styrene-butadiene rubber (SBR) and butadiene rubber (BR), and further contains other rubber components. It's okay.
- the rubber component preferably contains both styrene-butadiene rubber (SBR) and butadiene rubber (BR).
- 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 100% by mass.
- the proportion of styrene-butadiene rubber (SBR) is preferably 70% by mass or more, more preferably 80% by mass or more, preferably 100% by mass or less, and more preferably 90% by mass or less.
- the proportion of butadiene rubber (BR) is preferably 0% by mass or more, more preferably 10% by mass or more, and preferably 30% by mass or less, further preferably 20% by mass or less.
- the rubber component may further contain other rubber, and the content of the other rubber in the rubber component is preferably 30% by mass or less, more preferably 20% by mass or less, and even more preferably 10% by mass or less, It may be 0% by mass.
- 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 singly or in combination of two or more.
- the rubber composition for tires of the present invention comprises a softening agent, the softening agent being a hydrogenated resin having a softening point exceeding 110° C. and a polystyrene-equivalent weight average molecular weight of 200 to 1600 g/mol, and a terpene-based resin. and, and may further contain other softening agent components.
- the hydrogenated resin and the terpene resin are represented by the following formula: Hydrogenated resin/terpene resin mass ratio ⁇ 1.4/1 meet.
- the hydrogenated resin/terpene resin mass ratio is preferably 1.4/1 or more, and grip from the viewpoint of 6/1 or less.
- the total content of the softening agent is preferably 30 parts by mass or more and 170 parts by mass or less with respect to 100 parts by mass of the rubber component.
- the total content of the softening agent is more preferably 60 parts by mass or more, still more preferably 80 parts by mass or more with respect to 100 parts by mass of the rubber component, from the viewpoint of tire grip performance. 140 parts by mass or less, and even more preferably 120 parts by mass or less per 100 parts by mass of the rubber component.
- the softening point of the hydrogenated resin is 110°C or lower, the tire to which the rubber composition is applied cannot be sufficiently reinforced.
- 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, and 126° C. or higher, from the viewpoint of tire breaking properties. is more preferable, and 128° C. or higher is even more preferable.
- 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, and 141° C. or lower from the viewpoint of tire grip performance. is more preferably 136° C. or lower.
- the polystyrene-equivalent weight average molecular weight of the hydrogenated resin is less than 200 g/mol, the hydrogenated resin precipitates from the tire, making it difficult to fully exhibit the effects of the hydrogenated resin, and 1600 g/mol. exceeds, the hydrogenated resin becomes difficult to be compatible with the rubber component.
- the polystyrene-equivalent weight average molecular weight of the hydrogenated resin is preferably 300 g/mol or more, and is 400 g/mol or more.
- the polystyrene-equivalent weight average molecular weight of the hydrogenated resin is more preferably 1570 g/mol or less, such as 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, and 1400 g/mol or less.
- the ratio (Ts HR /Mw HR ) of the softening point (Ts HR ) (unit: °C) of the hydrogenated resin to the polystyrene-equivalent weight average molecular weight (Mw HR ) (unit: g/mol) of the hydrogenated resin is 0. It is preferably 0.075 or more, more preferably 0.083 or more, more preferably 0.095 or more, more preferably 0.104 or more, and 0.125 or more. It is more preferably 0.135 or more, more preferably 0.14 or more, and still more preferably 0.141 or more. Also, the ratio (Ts HR /Mw HR ) is preferably 0.25 or less, more preferably 0.23 or less.
- the softening point and polystyrene-equivalent weight-average molecular weight of the hydrogenated resin can be determined by the methods described in Examples below.
- the content of the hydrogenated resin in the rubber composition is more preferably 20 parts by mass or more, particularly preferably 30 parts by mass or more, relative to 100 parts by mass of the rubber component. Further, from the viewpoint of low-temperature brittleness of the rubber composition, the content of the hydrogenated resin in the rubber composition is more preferably 70 parts by mass or less, particularly preferably 60 parts by mass or less, relative to 100 parts by mass of the rubber component. .
- Examples of the C5 - based resin include aliphatic petroleum resins obtained by ( co)polymerizing a C5 fraction obtained by pyrolysis of naphtha in the petrochemical industry.
- the C5 fraction usually contains olefinic hydrocarbons such as 1 - pentene, 2-pentene, 2-methyl-1-butene, 2-methyl-2-butene, 3-methyl-1-butene, 2-methyl- Diolefinic hydrocarbons such as 1,3-butadiene, 1,2-pentadiene, 1,3-pentadiene and 3-methyl-1,2-butadiene are included.
- a commercially available product can be used as the C5 - based resin.
- the C 5 -C 9 resin refers to a C 5 -C 9 synthetic petroleum resin, and examples of the C 5 -C 9 resin include petroleum-derived C 5 -C 11 fractions, AlCl 3 , Examples include solid polymers obtained by polymerization using a Friedel-Crafts catalyst such as BF3 , and more specifically, copolymers containing styrene, vinyl toluene, ⁇ -methylstyrene, indene, etc. as main components. is mentioned. As the C 5 -C 9 resin, a resin containing less C 9 or higher components is preferable from the viewpoint of compatibility with the rubber component.
- the phrase "lower amount of C9 or higher components” means that the C9 or higher components in the total amount of the resin are less than 50% by mass, preferably 40% by mass or less.
- a commercially available product can be used as the C 5 -C 9 based resin.
- the C9 resin refers to a C9 synthetic petroleum resin, and refers to a solid polymer obtained by polymerizing a C9 fraction using a Friedel - Crafts type catalyst such as AlCl3 or BF3 .
- Examples of C9 -based resins include copolymers mainly composed of indene, ⁇ -methylstyrene, vinyltoluene, and the like.
- the terpene-based resin is a solid resin obtained by blending turpentine oil obtained at the same time as rosin is obtained from a pine tree, or a polymer component separated from it, and polymerizing using a Friedel-Crafts-type catalyst. , ⁇ -pinene resin, ⁇ -pinene resin, and the like.
- Terpene-based resins also include terpene-aromatic compound-based resins, and representative examples of the terpene-aromatic compound-based resins include terpene-phenol resins and styrene-terpene resins.
- the dicyclopentadiene-based resin refers to a resin obtained by polymerizing dicyclopentadiene using a Friedel-Crafts-type catalyst such as AlCl 3 or BF 3 .
- the hydrogenated resin is selected from hydrogenated C 5 resins and hydrogenated C 5 -C 9 -based resin, hydrogenated dicyclopentadiene-based resin (hydrogenated DCPD-based resin), and hydrogenated terpene-based resin, preferably at least one selected from the group consisting of hydrogenated C5 - based resin and hydrogenated It is more preferably at least one selected from the group consisting of C 5 -C 9 based resins, more preferably hydrogenated C 5 based resins.
- the resin has at least a hydrogenated DCPD structure or a hydrogenated cyclic structure in the monomer.
- the hydrogenated resin may be used singly or in combination of two or more.
- the rubber composition for tires of the present invention contains a terpene-based resin.
- a rubber composition containing a terpene-based resin By applying a rubber composition containing a terpene-based resin to a tire, it is possible to improve the grip performance of the tire.
- the content of the terpene-based resin is preferably 5 parts by mass or more and 35 parts by mass or less with respect to 100 parts by mass of the rubber component.
- the content of the terpene-based resin in the rubber composition is 5 parts by mass or more with respect to 100 parts by mass of the rubber component, the effect of improving the grip performance of the tire increases. Low-temperature brittleness of the rubber composition deteriorates.
- the content of the terpene-based resin in the rubber composition is more preferably 5 parts by mass or more, and even more preferably 10 parts by mass or more with respect to 100 parts by mass of the rubber component. .
- the content of the terpene-based resin in the rubber composition is more preferably 35 parts by mass or less with respect to 100 parts by mass of the rubber component, and 30 parts by mass or less. is more preferable.
- the rubber composition for tires of the present invention may further contain other softening agents in addition to the hydrogenated resin and terpene-based resin described above.
- Other softening agents include thermoplastic resins other than the hydrogenated resins and terpene-based resins described above, and liquid softening agents such as oils and liquid polymers.
- thermoplastic resins other than the hydrogenated resins and terpene-based resins include C5-based resins, C9 - based resins, C5- C9 - based resins, rosin-based resins, dicyclopentadiene resins, and alkylphenol-based resins. be done.
- the oil is a general term for extender oil contained in the rubber component and liquid oil added as a compounding agent of the rubber composition, and petroleum softening oil such as aromatic oil, paraffin oil, naphthenic oil, etc. Agent; vegetable 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 extender oil:compounding oil is 1:1 to 10:1.
- liquid polymer is preferably liquid at 25°C (room temperature) and has a weight average molecular weight of 5,000 to 100,000.
- liquid polymers include liquid polybutadiene, liquid polyisoprene, liquid polystyrene-butadiene, and the like.
- the tire rubber composition of the present invention preferably contains carbon black.
- the carbon black can reinforce the rubber composition and improve the breaking properties of the rubber composition, and also contributes to further improvement of the grip performance of the tire to which the rubber composition is applied.
- the carbon black is not particularly limited, and includes, for example, GPF, FEF, HAF, ISAF, and SAF grade carbon black. These carbon blacks may be used singly or in combination of two or more.
- the tire rubber composition of the present invention preferably contains silica.
- the grip performance (especially wet grip performance) of a tire to which the rubber composition is applied can be further improved.
- 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.
- BET method nitrogen adsorption specific surface area
- the nitrogen adsorption specific surface area (BET method) of silica is preferably 100 m 2 /g or more, preferably 120 m 2 /g or more, and 140 m 2 /g or more. is preferably 150 m 2 /g or more, preferably 170 m 2 /g or more, preferably 180 m 2 /g or more, preferably 190 m 2 /g or more, It is more preferably 195 m 2 /g or more.
- the nitrogen adsorption specific surface area (BET method) of silica is preferably 300 m 2 /g or less, more preferably 280 m 2 /g or less, and 270 m 2 /g or less. 2 /g or less is more preferable.
- the silica preferably has a cetyltrimethylammonium bromide adsorption specific surface area (CTAB) of 150 m 2 /g or more, more preferably 150 to 300 m 2 /g, still more preferably 150 to 250 m 2 /g, particularly preferably is 150-220 m 2 /g.
- CTAB cetyltrimethylammonium bromide adsorption specific surface area
- the tire to which the rubber composition is applied can be sufficiently reinforced. Further, when the CTAB is 300 m 2 /g or less, 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.
- silica examples include wet silica (hydrous silicic acid), dry silica (anhydrous silicic acid), calcium silicate, aluminum silicate, etc. Among these, wet silica is preferable. These silicas may be used singly or in combination of two or more.
- the content of silica in the rubber composition is preferably 10 parts by mass or more, preferably 15 parts by mass or more, relative to 100 parts by mass of the rubber component. is more preferable.
- the content of silica in the rubber composition is preferably 110 parts by mass or less, more preferably 100 parts by mass or less per 100 parts by mass of the rubber component. more preferred.
- the rubber composition for tires of the present invention preferably contains both the above carbon book and silica.
- the total content of silica and carbon black is preferably 70 parts by mass or more and 140 parts by mass or less with respect to 100 parts by mass of the rubber component.
- the total content of silica and carbon black is 70 parts by mass or more with respect to 100 parts by mass of the rubber component, the effect of improving the grip performance of the tire is further increased. Abrasion resistance of the composition is improved.
- 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 from the viewpoint of tire grip performance. More preferably 120 parts by mass or less per 100 parts by mass of the components.
- the rubber composition for tires of the present invention may contain a styrenic thermoplastic elastomer (TPS).
- the styrenic thermoplastic elastomer (TPS) has a styrenic polymer block (hard segment) and a conjugated diene polymer block (soft segment), and the styrenic polymer portion forms physical crosslinks to form bridges. It becomes a hooking point, while the conjugated diene polymer block imparts rubber elasticity. Some or all of the double bonds of the conjugated diene-based polymer block (soft segment) may be hydrogenated.
- thermoplastic styrenic elastomer is thermoplastic, while the rubber component (preferably diene-based rubber) is not thermoplastic. Therefore, in this specification, thermoplastic styrenic elastomer (TPS) is not included in the rubber component.
- the content of the styrenic thermoplastic elastomer (TPS) is preferably in the range of 1 to 30 parts by mass with respect to 100 parts by mass of the rubber component.
- thermoplastic styrene elastomer examples include styrene/butadiene/styrene (SBS) block copolymers, styrene/isoprene/styrene (SIS) block copolymers, and styrene/butadiene/isoprene/styrene (SBIS) block copolymers.
- SBS styrene/butadiene/styrene
- SIS styrene/isoprene/styrene
- SBIS styrene/butadiene/isoprene/styrene
- polymers styrene/isoprene (SI) block copolymers, styrene/butadiene/isoprene (SBI) block copolymers, styrene/ethylene/butylene/styrene (SEBS) block copolymers, styrene/ethylene/propylene/styrene ( SEPS) block copolymers, styrene/ethylene/ethylene/propylene/styrene (SEEPS) block copolymers, styrene/ethylene/butylene (SEB) block copolymers, styrene/ethylene/propylene (SEP) block copolymers, Styrene/ethylene/ethylene/propylene (SEEP) block copolymers and the like are included.
- SI styrene/isoprene
- SB styrene/propylene/styrene
- SEB styrene/ethylene
- the rubber composition for tires of the present invention comprises the aforementioned rubber component, softening agent, carbon black, silica, styrenic thermoplastic elastomer, and, if necessary, various components commonly used in the rubber industry, such as Silane coupling agents, anti-aging agents, stearic acid, zinc oxide (zinc oxide), vulcanization accelerators, vulcanizing agents, etc. may be appropriately selected and contained within a range that does not impair the object of the present invention. . Commercially available products can be suitably used as these compounding agents.
- the rubber composition for tires of the present invention contains silica
- it preferably contains a silane coupling agent in order to improve the effect of the silica.
- the silane coupling agent include bis(3-triethoxysilylpropyl) tetrasulfide, bis(3-triethoxysilylpropyl) trisulfide, bis(3-triethoxysilylpropyl) disulfide, bis(2-triethoxysilyl).
- ethyl)tetrasulfide bis(3-trimethoxysilylpropyl)tetrasulfide, bis(2-trimethoxysilylethyl)tetrasulfide, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 2-mercaptoethyltri Methoxysilane, 2-mercaptoethyltriethoxysilane, 3-trimethoxysilylpropyl-N,N-dimethylthiocarbamoyl tetrasulfide, 3-triethoxysilylpropyl-N,N-dimethylthiocarbamoyl tetrasulfide, 2-triethoxysilyl ethyl-N,N-dimethylthiocarbamoyl tetrasulfide, 3-trimethoxysilylpropyl benzothiazolyl tetrasulf
- the content of the antioxidant is not particularly limited, and is preferably in the range of 0.1 to 15 parts by mass, more preferably 1 to 10 parts by mass, relative to 100 parts by mass of the rubber component.
- vulcanization accelerator examples include sulfenamide-based vulcanization accelerators, guanidine-based vulcanization accelerators, thiazole-based vulcanization accelerators, thiuram-based vulcanization accelerators, and dithiocarbamate-based vulcanization accelerators. . Moreover, sulfur etc. are mentioned as said vulcanizing agent.
- the total content of the vulcanization system (vulcanization package) containing the vulcanization accelerator, vulcanizing agent, and stearic acid is not particularly limited, and is in the range of 1 to 25 parts by mass with respect to 100 parts by mass of the rubber component. is preferred, and a range of 5 to 20 parts by mass is more preferred.
- the method for producing the rubber composition is not particularly limited. It can be manufactured by extrusion or the like. Further, vulcanized rubber can be obtained by vulcanizing the obtained rubber composition.
- the kneading conditions are not particularly limited, and various conditions such as the input volume of the kneading device, the rotation speed of the rotor, the ram pressure, the kneading temperature, the kneading time, the type of the kneading device, etc. It can be selected as appropriate.
- the kneading device include Banbury mixers, intermixes, kneaders, rolls, etc., which are usually used for kneading rubber compositions.
- heating conditions there are no particular restrictions on the heating conditions, and various conditions such as the heating temperature, heating time, and heating device can be appropriately selected according to the purpose.
- the heating device include a heating roll machine or the like which is usually used for heating the rubber composition.
- the extrusion conditions are also not particularly limited, and various conditions such as extrusion time, extrusion speed, extrusion equipment, and extrusion temperature can be appropriately selected according to the purpose.
- the extrusion device include an extruder or the like that is usually used for extrusion of a rubber composition.
- the extrusion temperature can be determined appropriately.
- the tread rubber of the present invention is characterized by comprising the rubber composition for tires described above. Since the tread rubber of the present invention is made of the above rubber composition for tires, it is possible to achieve both tire grip performance and manufacturing workability at a high level.
- the tread rubber of the present invention may be applied to new tires or retreaded tires.
- the tread rubber of the present invention is particularly suitable as a tread rubber for tires for two-wheeled vehicles.
- the tread rubber of the present invention is particularly suitable for motorcycle tires because high grip performance is required.
- a tire of the present invention is characterized by comprising the tread rubber described above. Since the tire of the present invention has the above tread rubber, it has both grip performance and manufacturing workability at a high level.
- the tire of the present invention is particularly suitable as a tire for two-wheeled vehicles.
- the tire of the present invention is particularly suitable for motorcycle tires because high grip performance is required.
- the softening point and weight average molecular weight of the hydrogenated resin are measured by the following methods.
- Softening point The softening point of the hydrogenated resin is measured according to JIS-K2207-1996 (ring and ball method).
- the temperature of the remaining polymer solution was maintained at 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 allowed to mix for 30 minutes. Thereafter, 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.
- the above modified polymer solution is added to 20 L of an aqueous solution adjusted to pH 10 with sodium hydroxide, the solvent is removed and condensation reaction is performed at 110° C. for 2 hours, and the mixture is dried with a roll at 110° C. to obtain the modified polymer. Obtained.
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Abstract
Description
また、本発明は、グリップ性能と、製造作業性とを高いレベルで両立したタイヤを提供することを更なる課題とする。
前記ゴム成分が、スチレン-ブタジエンゴム及びブタジエンゴムから選択される少なくとも1種を含み、
前記軟化剤は、軟化点が110℃を超え且つポリスチレン換算の重量平均分子量が200~1600g/molである水素添加樹脂と、テルペン系樹脂と、を含み、
前記水素添加樹脂とテルペン系樹脂とが、下記の式:
水素添加樹脂/テルペン系樹脂の質量比≧1.4/1
を満たすことを特徴とする。
また、本発明によれば、グリップ性能と、製造作業性とを高いレベルで両立したタイヤを提供することができる。
本発明のタイヤ用ゴム組成物は、ゴム成分と、軟化剤と、を含む。そして、本発明のタイヤ用ゴム組成物においては、前記ゴム成分が、スチレン-ブタジエンゴム及びブタジエンゴムから選択される少なくとも1種を含み、前記軟化剤は、軟化点が110℃を超え且つポリスチレン換算の重量平均分子量が200~1600g/molである水素添加樹脂と、テルペン系樹脂と、を含み、前記水素添加樹脂とテルペン系樹脂とが、下記の式:
水素添加樹脂/テルペン系樹脂の質量比≧1.4/1
を満たすことを特徴とする。
また、本発明のタイヤ用ゴム組成物は、軟化剤として、軟化点が110℃を超え且つポリスチレン換算の重量平均分子量が200~1600g/molである水素添加樹脂と、テルペン系樹脂と、を含むことで、タイヤに適用することで、タイヤのグリップ性能を向上させることができる。
また、本発明のタイヤ用ゴム組成物においては、水素添加樹脂/テルペン系樹脂の質量比を1.4/1以上とすることで、未加硫状態のゴム組成物が生産設備に密着することを抑制して、製造作業性を向上させることができる。
従って、本発明のタイヤ用ゴム組成物は、タイヤのグリップ性能と、製造作業性とを高いレベルで両立することが可能である。
本発明のタイヤ用ゴム組成物は、ゴム成分を含み、該ゴム成分は、スチレン-ブタジエンゴム(SBR)及びブタジエンゴム(BR)から選択される少なくとも1種を含み、更に他のゴム成分を含んでもよい。なお、ゴム成分は、スチレン-ブタジエンゴム(SBR)及びブタジエンゴム(BR)の両方を含むことが好ましい。
前記スチレン-ブタジエンゴム(SBR)及びブタジエンゴム(BR)は、未変性のものであっても、変性されたものであってもよく、また、未変性のものと、変性されたものとのブレンドであってもよい。
また、前記ゴム成分において、スチレン-ブタジエンゴム(SBR)の割合は、70質量%以上が好ましく、80質量%以上が更に好ましく、また、100質量%以下が好ましく、90質量%以下が更に好ましい。
また、前記ゴム成分において、ブタジエンゴム(BR)の割合は、0質量%以上が好ましく、10質量%以上が更に好ましく、また、30質量%以下が好ましく、20質量%以下が更に好ましい。
本発明のタイヤ用ゴム組成物は、軟化剤を含み、該軟化剤は、軟化点が110℃を超え且つポリスチレン換算の重量平均分子量が200~1600g/molである水素添加樹脂と、テルペン系樹脂と、を含み、更に他の軟化剤成分を含んでもよい。
ここで、前記水素添加樹脂と前記テルペン系樹脂とは、下記の式:
水素添加樹脂/テルペン系樹脂の質量比≧1.4/1
を満たす。
本発明のタイヤ用ゴム組成物は、水素添加樹脂を含み、該水素添加樹脂は、軟化点が110℃を超え、ポリスチレン換算の重量平均分子量が200~1600g/molである。かかる水素添加樹脂を含むゴム組成物をタイヤに適用することで、タイヤのグリップ性能を向上させることができる。
タイヤからの水素添加樹脂の析出を抑制し、タイヤ外観の低下を抑制する観点から、水素添加樹脂のポリスチレン換算の重量平均分子量は、300g/mol以上であることが好ましく、400g/mol以上であることが好ましく、500g/mol以上であることがより好ましく、550g/mol以上であることが好ましく、600g/mol以上であることがより好ましく、650g/mol以上であることがより好ましく、700g/mol以上であることが更に好ましい。また、ゴム成分への水素添加樹脂の相溶性を高め、水素添加樹脂による効果をより高める観点から、水素添加樹脂のポリスチレン換算の重量平均分子量は、1570g/mol以下であることがより好ましく、1530g/mol以下であることがより好ましく、1500g/mol以下であることがより好ましく、1470g/mol以下であることがより好ましく、1430g/mol以下であることがより好ましく、1400g/mol以下であることがより好ましく、1370g/mol以下であることがより好ましく、1330g/mol以下であることがより好ましく、1300g/mol以下であることがより好ましく、1200g/mol以下であることがより好ましく、1100g/mol以下であることがより好ましく、1000g/mol以下であることがより好ましく、950g/mol以下であることが更に好ましい。
なお、水素添加樹脂の軟化点及びポリスチレン換算の重量平均分子量は、後述する実施例に記載の方法で求めることができる。
水素添加樹脂の原料となる樹脂としては、C5系樹脂、C5-C9系樹脂、C9系樹脂、テルペン系樹脂(テルペン-芳香族化合物系樹脂を包含する)、ジシクロペンタジエン系樹脂等が挙げられ、これら樹脂は、1種単独で用いてもよいし、2種以上を組み合わせて用いてもよい。
なお、本明細書において、テルペン系樹脂を還元水素化して得られる樹脂は、水素添加樹脂に分類する。
C5留分には、通常1-ペンテン、2-ペンテン、2-メチル-1-ブテン、2-メチル-2-ブテン、3-メチル-1-ブテン等のオレフィン系炭化水素、2-メチル-1,3-ブタジエン、1,2-ペンタジエン、1,3-ペンタジエン、3-メチル-1,2-ブタジエン等のジオレフィン系炭化水素等が含まれる。なお、C5系樹脂は、市販品を利用することができる。
C5-C9系樹脂としては、C9以上の成分の少ない樹脂が、ゴム成分との相溶性の観点から好ましい。ここで、「C9以上の成分が少ない」とは、樹脂全量中のC9以上の成分が50質量%未満、好ましくは40質量%以下であることを言うものとする。C5-C9系樹脂は、市販品を利用することができる。
C9系樹脂としては、例えば、インデン、α-メチルスチレン、ビニルトルエン等を主成分とする共重合体等が挙げられる。
ここで、樹脂全量中のジシクロペンタジエン由来成分が50質量%以上の場合、C5-DCPD系樹脂はジシクロペンタジエン系樹脂に含まれるものとする。樹脂全量中のジシクロペンタジエン由来成分が50質量%未満の場合、C5-DCPD系樹脂はC5系樹脂に含まれるものとする。更に第三成分等が少量含まれる場合でも同様である。
前記水素添加樹脂は、1種単独で使用してもよいし、2種以上を組み合わせて使用してもよい。
本発明のタイヤ用ゴム組成物は、テルペン系樹脂を含む。テルペン系樹脂を含むゴム組成物をタイヤに適用することで、タイヤのグリップ性能を向上させることができる。
本発明のタイヤ用ゴム組成物は、上述の水素添加樹脂、テルペン系樹脂の他、他の軟化剤を更に含んでいてもよい。ここで、他の軟化剤としては、上述の水素添加樹脂及びテルペン系樹脂以外の熱可塑性樹脂や、オイル、液状ポリマー等の液状軟化剤成分が挙げられる。
本発明のタイヤ用ゴム組成物は、カーボンブラックを含むことが好ましい。該カーボンブラックは、ゴム組成物を補強して、ゴム組成物の破壊特性を向上させることができ、また、ゴム組成物を適用したタイヤのグリップ性能の更なる向上にも寄与する。
本発明のタイヤ用ゴム組成物は、シリカを含むことが好ましい。ゴム組成物がシリカを含む場合、ゴム組成物を適用したタイヤのグリップ性能(特には、ウェットグリップ性能)を更に向上させることができる。
また、前記シリカは、セチルトリメチルアンモニウムブロミド吸着比表面積(CTAB)が好ましくは150m2/g以上であり、より好ましくは150~300m2/g、より一層好ましくは150~250m2/g、特に好ましくは150~220m2/gである。CTABが150m2/g以上であると、該ゴム組成物を適用したタイヤを十分に補強できる。また、CTABが300m2/g以下であると、ゴム組成物の弾性率が高くなり過ぎず、該ゴム組成物を適用したタイヤのウェットグリップ性能が向上する。
本発明のタイヤ用ゴム組成物は、スチレン系熱可塑性エラストマー(TPS)を含んでもよい。該スチレン系熱可塑性エラストマー(TPS)は、スチレン系重合体ブロック(ハードセグメント)と、共役ジエン系重合体ブロック(ソフトセグメント)とを有し、スチレン系重合体部分が物理架橋を形成して橋かけ点となり、一方、共役ジエン系重合体ブロックがゴム弾性を付与する。共役ジエン系重合体ブロック(ソフトセグメント)の二重結合は、一部又は全部が水素化されていてもよい。
なお、スチレン系熱可塑性エラストマー(TPS)は、熱可塑性である一方、前記ゴム成分(好ましくは、ジエン系ゴム)は、熱可塑性ではない。そのため、本明細書においては、スチレン系熱可塑性エラストマー(TPS)は、前記ゴム成分に含めないものとする。スチレン系熱可塑性エラストマー(TPS)の含有量は、前記ゴム成分100質量部に対して1~30質量部の範囲が好ましい。
本発明のタイヤ用ゴム組成物は、既述のゴム成分、軟化剤、カーボンブラック、シリカ、スチレン系熱可塑性エラストマー、並びに、必要に応じて、ゴム工業界で通常使用される各種成分、例えば、シランカップリング剤、老化防止剤、ステアリン酸、酸化亜鉛(亜鉛華)、加硫促進剤、加硫剤等を、本発明の目的を害しない範囲内で適宜選択して含有していてもよい。これら配合剤としては、市販品を好適に使用することができる。
前記ゴム組成物の製造方法は、特に限定されるものではないが、例えば、既述のゴム成分及び軟化剤に、必要に応じて適宜選択した各種成分を配合して、混練り、熱入れ、押出等することにより製造することができる。また、得られたゴム組成物を加硫することで、加硫ゴムとすることができる。
本発明のトレッドゴムは、上記のタイヤ用ゴム組成物からなることを特徴とする。かかる本発明のトレッドゴムは、上記のタイヤ用ゴム組成物からなるため、タイヤのグリップ性能と、製造作業性とを高いレベルで両立することが可能である。
なお、本発明のトレッドゴムは、新品タイヤに適用してもよいし、更生タイヤに適用してもよい。
本発明のトレッドゴムは、二輪車用タイヤのトレッドゴムとして、特に好適である。二輪車用タイヤには、高いグリップ性能が要求されるため、本発明のトレッドゴムが特に好適である。
本発明のタイヤは、上記のトレッドゴムを具えることを特徴とする。かかる本発明のタイヤは、上記のトレッドゴムを具えるため、グリップ性能と、製造作業性とが高いレベルで両立されている。
本発明のタイヤは、二輪車用タイヤとして、特に好適である。二輪車用タイヤには、高いグリップ性能が要求されるため、本発明のタイヤが特に好適である。
水素添加樹脂の軟化点、重量平均分子量は、以下の方法で測定する。
水素添加樹脂の軟化点は、JIS-K2207-1996(環球法)に準拠して測定する。
以下の条件で、ゲル透過クロマトグラフィー(GPC)により、水添樹脂の平均分子量を測定し、ポリスチレン換算の重量平均分子量を算出した。
・カラム温度:40℃
・注入量:50μL
・キャリアー及び流速:テトラヒドロフラン 0.6mL/min
・サンプル調製:樹脂成分約2.5mgをテトラヒドロフラン10mLに溶解
比較例3以外は、表1に示す配合処方で、通常の混練り装置を用いて混練を行って、ゴム組成物を調製した。比較例3については、同様に混練を行い、ゴム組成物を調整する。
比較例3以外のゴム組成物に対して、以下の方法で、グリップ性能及び製造作業性を評価した。比較例3のゴム組成物については、以下の方法で、グリップ性能及び製造作業性を評価する。結果を表1に示す。
比較例3以外は、上島製作所製スペクトロメーターにて、周波数52Hz、初期歪2%、動歪1%、温度50℃でゴム組成物の損失正接(tanδ)を測定し、比較例1のtanδを100として、指数表示した。比較例3については、同様に指数表示する。指数値が大きい程、tanδが大きく、グリップ性能に優れることを示す。
比較例3以外は、未加硫状態のゴム組成物と金属との間の90℃での密着力を、タックメータを用いて測定し、比較例1の密着力の逆数を100として、指数表示した。比較例3については、同様に指数表示する。指数値が大きい程、密着力が小さく、製造作業性に優れることを示す。
*2 SBR: スチレン-ブタジエンゴム、スチレン単位の割合(結合スチレン量)=35.5質量%、旭化成社製、商品名「タフデンE581」、ゴム成分100質量部に対して伸展油(軟化剤、25℃で液状)37.5質量部を含む油展ゴム、上段にゴム成分の含有量、下段に伸展油の含有量を示す。
*3 カーボンブラック: 旭カーボン社製、商品名「旭#107」
*4 シリカ: セチルトリメチルアンモニウムブロミド吸着比表面積(CTAB)=191m2/g、窒素吸着比表面積(BET法)=245m2/g
*5 オイル: 軟化剤(25℃で液状)、JX日鉱日石エネルギー社製、商品名「A/O MIX」
*6 樹脂A: 水素添加樹脂(水添C5系樹脂)、Eastman社製、商品名「登録商標Impera E1780」、軟化点=130℃、重量平均分子量(Mw)=909g/mol
*7 樹脂B: テルペン系樹脂(テルペン-フェノール樹脂)、ヤスハラケミカル社製、商品名「YSポリスターS145」
*8 樹脂C: 水素添加樹脂及びテルペン系樹脂以外の樹脂(C9系樹脂)、ENEOS社製、商品名「日石ネオポリマー140」
*9 樹脂D: 水素添加樹脂及びテルペン系樹脂以外の樹脂(アルキルフェノール樹脂)、SI GROUP-RIBECOURT S.A.S社製、商品名「R7521P」
*10 シランカップリング剤: 信越化学工業社製、商品名「ABC-856」
*11 老化防止剤:精工化学社製の商品名「サンタイトA」と住友化学株式会社製の商品名「アンチゲン6C」とを含むトータル量
*12 加硫パッケージ: 加硫促進剤と硫黄とステアリン酸とを含むトータル量
窒素置換された5Lオートクレーブに、窒素下、シクロヘキサン2.4kg、1,3-ブタジエン300gを仕込んだ。これらに、予め触媒成分としてバーサチック酸ネオジム(0.09mmol)のシクロヘキサン溶液、メチルアルモキサン(以下「MAO」ともいう)(1.8mmol)のトルエン溶液、水素化ジイソブチルアルミニウム(以下「DIBAH」ともいう)(5.0mmol)およびジエチルアルミニウムクロリド(0.18mmol)のトルエン溶液と1,3-ブタジエン(4.5mmol)を50℃で30分間反応熟成させた触媒を仕込み、80℃で60分間重合を行った。1,3-ブタジエンの反応転化率は、ほぼ100%であった。この重合体溶液200gを抜き取り、2,4-ジ-tert-ブチル-p-クレゾール1.5gを含むメタノール溶液を添加し、重合停止させた後、スチームストリッピングにより脱溶媒し、110℃のロールで乾燥して、変性前重合体を得た。
さらに、残りの重合体溶液を温度60℃に保ち、3-グリシドキシプロピルトリメトキシシラン(4.5mmol)のトルエン溶液を添加し、30分間反応させた。続いて、テトラ2-エチルヘキシルチタネート(13.5mmol)のトルエン溶液を添加し、30分間混合させた。その後、2,4-ジ-tert-ブチル-p-クレゾール1.5gを含むメタノール溶液を添加し、変性重合体溶液2.5kgを得た。
次に、水酸化ナトリウムによりpH10に調整した水溶液20Lに上記変性重合体溶液を添加し、110℃で2時間、脱溶媒とともに縮合反応を行い、110℃のロールで乾燥して、変性重合体を得た。
一方、水素添加樹脂を含むものの、テルペン系樹脂を含まない比較例2、4、5のゴム組成物は、グリップ性能を向上させることができなかった。
Claims (8)
- ゴム成分と、軟化剤と、を含むタイヤ用ゴム組成物であって、
前記ゴム成分が、スチレン-ブタジエンゴム及びブタジエンゴムから選択される少なくとも1種を含み、
前記軟化剤は、軟化点が110℃を超え且つポリスチレン換算の重量平均分子量が200~1600g/molである水素添加樹脂と、テルペン系樹脂と、を含み、
前記水素添加樹脂と前記テルペン系樹脂とが、下記の式:
水素添加樹脂/テルペン系樹脂の質量比≧1.4/1
を満たすことを特徴とする、タイヤ用ゴム組成物。 - 前記水素添加樹脂の含有量が、前記ゴム成分100質量部に対して10質量部以上80質量部以下である、請求項1に記載のタイヤ用ゴム組成物。
- 前記軟化剤の総含有量が、前記ゴム成分100質量部に対して30質量部以上170質量部以下である、請求項1又は2に記載のタイヤ用ゴム組成物。
- 前記ゴム成分は、スチレン単位の割合が10質量%以上50質量%以下である、請求項1~3のいずれか一項に記載のタイヤ用ゴム組成物。
- 更にカーボンブラックを含む、請求項1~4のいずれか一項に記載のタイヤ用ゴム組成物。
- 更にシリカを含み、該シリカと前記カーボンブラックとの総含有量が、前記ゴム成分100質量部に対して70質量部以上140質量部以下である、請求項5に記載のタイヤ用ゴム組成物。
- 請求項1~6のいずれか一項に記載のタイヤ用ゴム組成物からなることを特徴とする、トレッドゴム。
- 請求項7に記載のトレッドゴムを具えることを特徴とする、タイヤ。
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JP2023527547A JPWO2022259751A1 (ja) | 2021-06-08 | 2022-03-31 | |
US18/562,505 US20240240003A1 (en) | 2021-06-08 | 2022-03-31 | Rubber composition for tires, tread rubber, and tire |
EP22819939.4A EP4353493A4 (en) | 2021-06-08 | 2022-03-31 | RUBBER COMPOSITION FOR TIRE, TREAD RUBBER, AND TIRE |
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WO2015079703A1 (ja) | 2013-11-27 | 2015-06-04 | 株式会社ブリヂストン | ゴム組成物及びタイヤ |
WO2016104142A1 (ja) * | 2014-12-24 | 2016-06-30 | 住友ゴム工業株式会社 | 空気入りタイヤ |
JP2017071682A (ja) * | 2015-10-06 | 2017-04-13 | 住友ゴム工業株式会社 | タイヤ用ゴム組成物 |
JP2019031659A (ja) * | 2017-08-04 | 2019-02-28 | 旭化成株式会社 | 変性共役ジエン系重合体組成物、及びタイヤ |
US20190144643A1 (en) * | 2016-09-30 | 2019-05-16 | Kolon Industries, Inc. | Composition for tire tread comprising resin alternative to process oil |
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JP7340919B2 (ja) * | 2018-11-07 | 2023-09-08 | Toyo Tire株式会社 | タイヤトレッド用ゴム組成物及び空気入りタイヤ |
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WO2015079703A1 (ja) | 2013-11-27 | 2015-06-04 | 株式会社ブリヂストン | ゴム組成物及びタイヤ |
WO2016104142A1 (ja) * | 2014-12-24 | 2016-06-30 | 住友ゴム工業株式会社 | 空気入りタイヤ |
JP2017071682A (ja) * | 2015-10-06 | 2017-04-13 | 住友ゴム工業株式会社 | タイヤ用ゴム組成物 |
US20190144643A1 (en) * | 2016-09-30 | 2019-05-16 | Kolon Industries, Inc. | Composition for tire tread comprising resin alternative to process oil |
JP2019031659A (ja) * | 2017-08-04 | 2019-02-28 | 旭化成株式会社 | 変性共役ジエン系重合体組成物、及びタイヤ |
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CN117413014A (zh) | 2024-01-16 |
EP4353493A1 (en) | 2024-04-17 |
EP4353493A4 (en) | 2024-10-02 |
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