Rubber composition for studless tires

Abstract

To provide a rubber composition for studless tires having improved on-ice performance.SOLUTION: A rubber composition for studless tires comprises diene rubber 100 pts.mass comprising butadiene rubber 30 mass% or more and natural rubber, blended with inorganic filler 20 pts.mass or more and water-insoluble lignin, which is bioethanol extraction residue lignin.SELECTED DRAWING: None

Description

Technical Field

[0001] The present invention relates to a studless tire rubber composition having excellent ice performance.

Background Art

[0002] For studless tires (pneumatic tires for ice and snow roads), it is required to achieve high levels of both ice performance and wet performance. As a configuration for improving ice performance, for example, by forming a large number of recesses in the tread rubber, it is known that a scraping action can be obtained by the recesses, and an action of repeatedly absorbing and separating the water film on the ice surface can be obtained by the recesses. Patent Documents 1 and 2 describe that by blending a water-soluble lignin derivative into a tread rubber composition for studless tires, the water-soluble lignin derivative in contact with water dissolves to form recesses (holes) on the tread surface.

[0003] However, the ice performance required by consumers for studless tires has been increasing, and it has been required to further improve the ice performance.

Prior Art Documents

Patent Documents

[0004]

Patent Document 1

Patent Document 2

Summary of the Invention

Problems to be Solved by the Invention

[0005] An object of the present invention is to provide a studless tire rubber composition having ice performance superior to the conventional level.

Means for Solving the Problems

[0006] The present invention, which achieves the above objective, is characterized by comprising 30% by mass or more of butadiene rubber, 100 parts by mass of a diene-based rubber containing natural rubber, 20 parts by mass or more of an inorganic filler, and water-insoluble lignin. [Effects of the Invention]

[0007] The rubber composition for studless tires of the present invention is a diene system containing butadiene rubber and natural rubber, to which an inorganic filler and water-insoluble lignin are blended, thereby enabling studless tires to perform on ice at a level superior to that of conventional tires.

[0008] The rubber composition for studless tires may contain 100 parts by mass of the diene rubber and 0.1 to 50 parts by mass of the water-insoluble lignin. The water-insoluble lignin may be bioethanol extraction residue lignin. Furthermore, the water-insoluble lignin may contain 5 to 50% by mass of sugars, and the average particle size of the water-insoluble lignin may be 1 to 100 μm.

[0009] Furthermore, the water-insoluble lignin may consist of an extract of an ethanol aqueous solution of bioethanol extraction residue lignin and / or the extraction residue of the ethanol aqueous solution of bioethanol extraction residue lignin. Moreover, the water-insoluble lignin may contain 50% by mass or more of the extraction residue of the ethanol aqueous solution of bioethanol extraction residue lignin. The ethanol aqueous solution may contain 50 to 70% by mass of ethanol.

[0010] The rubber hardness of the cured product of the rubber composition for studless tires should preferably be 60 or less at 0°C and -10°C.

[0011] A studless tire having a tread made of a rubber composition for studless tires can achieve ice performance that is superior to conventional levels. [Modes for carrying out the invention]

[0012] The rubber composition for studless tires of the present invention is composed of 100% by mass of diene rubber, 30% by mass or more of butadiene rubber, and natural rubber. The inclusion of butadiene rubber ensures flexibility at low temperatures and maintains and improves low-temperature characteristics. The butadiene rubber should be 30% by mass or more, preferably 35% by mass or more, and more preferably 40-60% by mass, of the 100% by mass of diene rubber. It is preferable to use butadiene rubber that is commonly used in rubber compositions for studless tires.

[0013] The rubber composition for studless tires contains natural rubber in 100% by mass of diene-based rubber. The inclusion of natural rubber improves strength while maintaining a low glass transition temperature. The amount of natural rubber is preferably 30% by mass or more, more preferably 35% by mass or more, and more preferably 40-60% by mass, of the 100% by mass of diene-based rubber. It is preferable to use natural rubber that is commonly used in rubber compositions for studless tires.

[0014] The rubber composition for studless tires may contain other diene rubbers besides butadiene rubber and natural rubber. Examples of other diene rubbers include styrene-butadiene rubber, acrylonitrile-butadiene rubber, butyl rubber, halogenated butyl rubber, and the like. These other diene rubbers can be used alone or in any blend. The content of the other diene rubbers is preferably 0 to 30% by mass, more preferably 0 to 20% by mass, based on 100% by mass of the diene rubber.

[0015] The rubber composition for studless tires is formulated by blending 20 parts by mass or more of an inorganic filler with 100 parts by mass of diene rubber. By blending an inorganic filler, the strength of the rubber composition can be increased, and tire durability can be ensured. The amount of inorganic filler blended is 20 parts by mass or more, preferably 30 parts by mass or more, and more preferably 40 to 80 parts by mass, per 100 parts by mass of diene rubber. Examples of inorganic fillers include inorganic fillers such as carbon black, silica, clay, calcium carbonate, mica, talc, aluminum hydroxide, aluminum oxide, titanium dioxide, and barium sulfate, as well as organic fillers such as cellulose, lecithin, lignin, and dendrimer. Among these, it is preferable to blend at least one selected from carbon black and silica.

[0016] By incorporating carbon black, the strength of the rubber composition can be improved. Suitable carbon blacks include furnace black, acetylene black, thermal black, channel black, and graphite. Among these, furnace black is preferred, with specific examples including SAF, ISAF, ISAF-HS, ISAF-LS, IISAF-HS, HAF, HAF-HS, HAF-LS, and FEF. These carbon blacks can be used individually or in combination of two or more. Surface-treated carbon blacks, obtained by chemically modifying these carbon blacks with various acid compounds, can also be used.

[0017] By incorporating silica, the low heat generation and wet grip performance of the rubber composition can be improved. As for the silica, silica commonly used in rubber compositions for studless tires can be used, such as wet-process silica, dry-process silica, or carbon-silica (dual-phase filler) in which silica is supported on a carbon black surface, or silica surface-treated with compounds that are reactive or compatible with both silica and rubber, such as silane coupling agents or polysiloxanes. Among these, wet-process silica with hydrated silicic acid as the main component is preferred.

[0018] The rubber composition of the present invention is preferable because its low heat generation and tensile elongation at break are further improved by incorporating a silane coupling agent together with silica. By incorporating a silane coupling agent together with silica, the dispersibility of silica is improved, and the reinforcing properties with the diene-based rubber are enhanced. The amount of silane coupling agent is preferably 2 to 20% by weight, more preferably 5 to 15% by weight, relative to the amount of silica. If the amount of silane coupling agent is less than 2% by weight of silica, the effect of improving silica dispersibility is not sufficiently obtained. Also, if the amount of silane coupling agent exceeds 20% by weight, the diene-based rubber component tends to gel easily, making it impossible to obtain the desired effect.

[0019] While there are no particular limitations on the silane coupling agent, sulfur-containing silane coupling agents are preferred, such as 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-mercaptopropyldimethoxymethylsilane, 3-mercaptopropyldimethylmethoxysilane, 2-mercaptoethyltriethoxysilane, 3-mercaptopropyltriethoxysilane, and VP from Evonik. Si363, etc., mercaptosilane compounds exemplified in Japanese Patent Publication No. 2006-249069, 3-trimethoxysilylpropylbenzothiazole tetrasulfide, 3-triethoxysilylpropylbenzothiazolyl tetrasulfide, 3-triethoxysilylpropyl methacrylate monosulfide, 3-trimethoxysilylpropyl methacrylate monosulfide, 3-trimethoxysilylpropyl-N,N-dimethylthiocarbamoyl tetrasulfide, 3-triethoxysilylpropyl-N,N-dimethylthiocarbamoyl tetrasulfide, 2-triethoxysilylethyl-N,N-dimethylthiocarbamoyl tetrasulfide Methylthiocarbamoyl tetrasulfide, bis(3-diethoxymethylsilylpropyl)tetrasulfide, dimethoxymethylsilylpropyl-N,N-dimethylthiocarbamoyl tetrasulfide, dimethoxymethylsilylpropylbenzothiazolyl tetrasulfide, 3-octanoylthiopropyltriethoxysilane, 3-propionylthiopropyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltris(2-methoxyethoxy)silane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, β-(3,Examples of silane coupling agents include 4-epoxycyclohexyl)ethyltrimethoxysilane, 3-aminopropyltrimethoxysilane, N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, and N-(β-aminoethyl)-γ-aminopropylmethyldimethoxysilane. Furthermore, silane coupling agents are organosilicon compounds, and examples of organosilicon compounds include polysiloxane, silicone oils in which one or more organic groups such as amino groups, epoxy groups, carbinol groups, mercapto groups, carboxyl groups, hydrogen groups, polyether groups, phenol groups, silanol groups, acrylic groups, methacrylic groups, or long-chain alkyl groups are introduced to the side chain or both ends or one end or both sides of the polysiloxane, and silicone oligomers obtained by condensation reactions of one or more organosilicans. Among these, bis-(3-triethoxysilylpropyl)tetrasulfide and bis(3-triethoxysilylpropyl)disulfide are preferred.

[0020] The rubber composition for studless tires of the present invention is characterized by the inclusion of water-insoluble lignin. By incorporating water-insoluble lignin, the water-insoluble lignin particles dispersed in the tire tread can impart surface roughness to the tire tread surface, thereby improving ice performance. The amount of water-insoluble lignin is preferably 0.1 to 50 parts by mass, more preferably 1 to 50 parts by mass, per 100 parts by mass of diene-based rubber. By incorporating 0.1 parts by mass or more of insoluble lignin, the scratching action of the insoluble lignin particles can be obtained. Furthermore, by limiting the amount of insoluble lignin to 50 parts by mass or less, the flexibility of the rubber can be maintained.

[0021] In the present invention, the water-insoluble lignin is preferably bioethanol extraction residue lignin. Conventionally used lignin sulfonic acid, lignin sulfonate, kraft lignin, etc. are water-soluble lignins, and these water-soluble lignins are obtained as by-products when producing pulp from plant resources by methods such as the sulfite pulp process and the kraft pulp process. In contrast, bioethanol extraction residue lignin is obtained as the residue after water extraction of bioethanol when producing bioethanol from plant resources, and it is water-insoluble lignin.

[0022] Lignin is a major component of grassy plant resources together with cellulose and hemicellulose. Generally, in grassy plant resources, cellulose is contained at 40 - 50%, hemicellulose at 15 - 25%, and lignin at 20 - 30%. For example, cellulose and hemicellulose in grassy plant resources can be hydrolyzed to produce glucose, and the obtained glucose can be fermented to produce bioethanol. The residue component obtained by separating the obtained bioethanol by water extraction contains water-insoluble lignin and saccharides. In the production process of bioethanol, since retting and denaturation using chemicals like in the pulp production process are not performed, water-insoluble lignin and saccharides can be obtained in the residue component. Also, lignin obtained by performing another solvent extraction on the residue component after water extraction of bioethanol can be used, that is, the solvent-soluble component of lignin extracted using another solvent on the water extraction residue component, or the solvent extraction residue component can also be used. As the other solvent, an organic solvent is preferred, and examples include methanol, ethanol, isopropyl alcohol, undecane, tetrahydrofuran, hexadecane, 2-ethoxyethanol, liquid paraffin, dimethylformamide, propylene glycol, dimethyl sulfoxide, diethylene glycol, ethylene glycol, diiodomethane, formamide, glycerin, etc.

[0023] As another solvent for further extracting the water-insoluble lignin obtained as a residue component after water extraction of bioethanol, an aqueous ethanol solution is preferred. The aqueous ethanol solution is an aqueous solution containing preferably 50 to 70% by mass, more preferably 55 to 65% by mass, and still more preferably 58 to 62% by mass of ethanol. That is, the water-insoluble lignin used in the present invention preferably consists of an extract of the bioethanol extraction residue lignin with an aqueous ethanol solution and / or an extraction residue of the bioethanol extraction residue lignin with an aqueous ethanol solution.

[0024] By making the water-insoluble lignin into an extract of the bioethanol extraction residue lignin with an aqueous ethanol solution and / or its extraction residue, the tensile breaking strength and / or the tensile breaking elongation of the rubber composition can be made more excellent. Further, the water-insoluble lignin preferably contains 50% by mass or more, more preferably 50 to 80% by mass, of the extraction residue of the bioethanol extraction residue lignin with an aqueous ethanol solution, and the tensile breaking strength and / or the tensile breaking elongation of the rubber composition can be made even more excellent.

[0025] The grassy plant resources for producing bioethanol are not particularly limited, and examples include bamboo, palm (trunk, empty fruit bunch, fruit fiber, and seed), sugarcane, bagasse (sugarcane and the press residue of high-biomass sugarcane), rice straw, wheat straw, corn (ear axis, stem and leaves, and residues such as corn stover, corn cob, and corn hull), sorghum, sweet sorghum, switchgrass, miscanthus, napier grass, and other Gramineae plants.

[0026] Examples of the method for producing bioethanol from grassy plant resources include the following methods. Cellulose and hemicellulose from plant powder are hydrolyzed using a catalyst to obtain oligosaccharides containing glucose and xylose, as well as cellulose. The temperature during this process is preferably between 150°C and 200°C. The "catalyst" is not specifically limited to any catalyst that decomposes or softens lignin and decomposes cellulose and hemicellulose. Examples include sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, sodium hydroxide, potassium hydroxide, and ammonia. These may be used individually or in combination. Among these, sulfuric acid is particularly preferred for industrial use because it is inexpensive and readily available.

[0027] The obtained oligosaccharides, including glucose and xylose, and cellulose can be further saccharified with enzymes and fermented with microorganisms to obtain bioethanol. The enzymes used refer to enzymes that break down hemicellulose and cellulose contained in grasses into monosaccharide units, and any enzyme possessing both cellulase and hemicellulase activity is acceptable. In addition, there are no special limitations on the microorganisms used, as long as they can produce fermentation products derived from the stems and leaves of grasses. Specifically, yeasts and bacteria are examples, and genetically modified microorganisms are also preferably used. The generated bioethanol is separated from the fermentation liquid by water extraction. By drying the residue of the fermentation liquid after the bioethanol has been extracted with water, a water-insoluble lignin powder can be obtained.

[0028] The water-insoluble lignin obtained above is a high-molecular-weight compound based on guaiacylpropane (G core), syringylpropane (S core), and hydroxyphenylpropane (H core) structures. Since it has not been modified with chemicals or other means, it has a high content of hydroxyl groups originating from the aforementioned G, S, and H cores. Furthermore, for example, the amount of S and G cores bonded (β-O-4 bond amount by the thioacidris method) is high.

[0029] Water-insoluble lignin preferably contains 5 to 50% by mass of sugars. The inclusion of sugars in water-insoluble lignin can further increase the strength of the rubber. The amount of sugars is preferably 5 to 50% by mass, more preferably 5 to 40% by mass, of 100% by mass of water-insoluble lignin. Examples of sugars contained in water-insoluble lignin include cellulose, hemicellulose, cellobiose, xylose, mannose, arabinose, galacturonic acid, oligosaccharides, glucose, furfural, 5-hydroxymethylfurfural, and the like.

[0030] The water-insoluble lignin preferably has an average particle size of 1 to 100 μm, more preferably 5 to 100 μm, and even more preferably 10 to 100 μm. By keeping the average particle size of the water-insoluble lignin within this range, the scratching action of the tread surface can be further enhanced. The average particle size of the water-insoluble lignin can be measured by microscopic observation.

[0031] The rubber composition for studless tires containing water-insoluble lignin preferably has a hardness of 60 or less at 0°C and a hardness of 60 or less at -10°C. By keeping the hardness of the rubber at 0°C and -10°C at 60 or less, flexibility can be maintained and ice performance can be improved. The hardness of the rubber at 0°C is more preferably 40 to 60, and even more preferably 45 to 60. The hardness of the rubber at -10°C is more preferably 40 to 60, and even more preferably 45 to 60. The hardness of the rubber at 0°C and -10°C shall be measured using a durometer of type A in accordance with JIS K6253.

[0032] In addition to the components mentioned above, the rubber composition of the present invention may contain various compounding agents commonly used in tire tread rubber compositions, such as vulcanizing or crosslinking agents, vulcanization accelerators, antioxidants, processing aids, plasticizers, liquid polymers, thermosetting resins, and thermoplastic resins, according to conventional methods. Such compounding agents can be mixed in a conventional manner to form a rubber composition, which can then be used for vulcanization or crosslinking. The amounts of these compounding agents can be conventional amounts, as long as they do not contradict the objectives of the present invention. The tire tread rubber composition can be prepared by mixing the above components using a known rubber mixing machine, such as a Banbury mixer, kneader, or roll.

[0033] The rubber composition for studless tires is suitable for forming the tread and sidewall portions of studless tires, and is particularly suitable for forming the tread portion of studless tires. The resulting studless tire can improve ice performance to a level beyond that of conventional tires.

[0034] The present invention will be further described below with reference to examples, but the scope of the present invention is not limited to these examples. [Examples]

[0035] Fourteen types of studless tire rubber compositions (Examples 1-8, Comparative Examples 1-6) were prepared, each having a common additive formulation as shown in Table 3 and the formulations shown in Tables 1 and 2. For each composition, the components excluding sulfur and vulcanization accelerator were weighed, mixed in a 1.7-liter sealed Banbury mixer for 5 minutes, and then the masterbatch was released from the mixer and cooled to room temperature. This masterbatch was then subjected to the same Banbury mixer, and sulfur and vulcanization accelerator were added and mixed to obtain the studless tire rubber composition. The amounts of each additive shown in Table 3 are expressed as parts by mass per 100 parts by mass of the diene-based rubber shown in Tables 1 and 2.

[0036] The rubber compositions for studless tires obtained above were vulcanized in molds of predetermined shapes at 170°C for 10 minutes to prepare evaluation samples. Using the obtained evaluation samples, the rubber hardness at 0°C and -10°C, ice performance, and tensile properties were measured by the following methods.

[0037] Rubber hardness at 0°C and -10°C Using the evaluation samples of the obtained studless tire rubber composition, the rubber hardness at 0°C and -10°C was measured using a Type A durometer in accordance with JIS K6253. The results are shown in the "Rubber Hardness (0°C)" and "Rubber Hardness (-10°C)" columns of Tables 1 and 2.

[0038] Ice performance The obtained rubber composition for studless tires was attached to a flat cylindrical rubber base and tested on an inside drum type ice friction tester at a temperature of -3.0°C and a load of 5.5 kg / cm². 2 The measurement was taken at approximately 0.54 MPa and a drum rotation speed of 20 km / h. The results obtained are listed in the "Ice Performance (-3.0℃)" column of Tables 1 and 2, using the value of Comparative Example 1 as an index to be set to 100. A higher index indicates better ice performance.

[0039] Tensile properties (tensile breaking strength and tensile breaking elongation) The obtained evaluation samples were cut into JIS No. 3 dumbbell-shaped test specimens in accordance with JIS K6251. Tensile breaking strength and tensile breaking elongation were measured in accordance with JIS K6251 and are shown in the "Breaking Strength" and "Breaking Elongation" columns of Tables 1 and 2.

[0040] [Table 1]

[0041] [Table 2]

[0042] [Table 3]

[0043] The types of raw materials used in Tables 1-3 are shown below. • NR: Natural rubber, STR20 • BR: Butadiene rubber, NIPOL BR1261, manufactured by Nippon Zeon Co., Ltd. • Carbon Black: Seast KHP, manufactured by Tokai Carbon Co., Ltd. • Silica: ZEOSIL 165GR, manufactured by Rhodia Corporation • Coupling agent: Silane coupling agent, Si69, manufactured by Evonik DeGussa. Lignin-1: Contains 30-40% by mass of water-insoluble lignin and sugars, which are bioethanol extraction residues, with an average particle size of 50 μm. Herbaceous biomass is pretreated by dilute sulfuric acid pulping, the resulting pretreated herbaceous biomass is saccharified with enzymes, yeast is added to the resulting saccharification product and fermented, the resulting fermentation product is separated into aqueous solution and solid components, and the resulting solid component is dried to obtain "Lignin-1". Lignin-2: Contains 30-40% by mass of water-insoluble lignin and sugars, which are bioethanol extraction residues, with an average particle size of 50 μm. The solid-liquid mixture obtained by stirring and mixing "Lignin-1" and a 60% by mass aqueous solution of ethanol was subjected to solid-liquid separation, and the resulting solid was dried to obtain "Lignin-2". Lignin-3: Contains 30-40% by mass of water-insoluble lignin and sugars, which are bioethanol extraction residues, with an average particle size of 50 μm. A solid-liquid mixture of "Lignin-1" and a 60% by mass aqueous solution of ethanol was stirred and mixed, and the solid-liquid mixture was separated, and the soluble components in the 60% by mass aqueous solution of ethanol were dried to obtain "Lignin-3". • Lignin-4: Water-soluble lignin, Pearllex NP, manufactured by Nippon Paper Industries, contains approximately 5% sugars by mass. • Oil: Extract No. 4S, manufactured by Showa Shell Sekiyu Co., Ltd. • Resin: A mixture of YS Resin TO-125 and YS Resin TO-105 (both manufactured by Yasuhara Chemical Co., Ltd.) • Stearic acid: Stearic acid YR, manufactured by NOF Corporation. • Zinc oxide: Three types of zinc oxide manufactured by Seido Chemical Industry Co., Ltd. • Sulfur: AkzoNobel Crystex HSOT20 • Vulcanization accelerator: Noxellar DZ manufactured by Ouchi Shinko Chemical Co., Ltd.

[0044] As is clear from Tables 1 and 2, the rubber compositions for studless tires of Examples 1 to 8 were confirmed to improve ice performance to a level equal to or higher than that of Comparative Example 1. The rubber compositions for studless tires in Comparative Examples 2 and 3 contain water-soluble lignin instead of water-insoluble lignin, so the improvement in ice performance is not sufficiently achieved. The rubber composition for studless tires in Comparative Example 4 contains less than 30% by mass of butadiene rubber, so it does not provide a sufficient improvement in ice performance. Comparative Example 5: The rubber composition for studless tires has less than 20 parts by mass of inorganic filler, resulting in inferior hardness and ice performance. Comparative Example 6: The rubber composition for studless tires has less than 20 parts by mass of inorganic filler, resulting in inferior hardness and ice performance.

Claims

1. A rubber composition for studless tires, characterized by comprising 30% by mass or more of butadiene rubber, 100 parts by mass of a diene-based rubber containing natural rubber, 20 parts by mass or more of an inorganic filler, and water-insoluble lignin.

2. The rubber composition for studless tires according to claim 1, characterized in that 0.1 to 50 parts by mass of the water-insoluble lignin is blended with 100 parts by mass of the diene rubber.

3. The rubber composition for studless tires according to claim 1 or 2, wherein the water-insoluble lignin is bioethanol extraction residue lignin.

4. The rubber composition for studless tires according to any one of claims 1 to 3, characterized in that the water-insoluble lignin contains 5 to 50% by mass of sugars.

5. The rubber composition for studless tires according to any one of claims 1 to 4, characterized in that the average particle size of the water-insoluble lignin is 1 to 100 μm.

6. The rubber composition for studless tires according to any one of claims 1 to 5, characterized in that the hardened product has a rubber hardness of 60 or less at 0°C and a rubber hardness of 60 or less at -10°C.

7. A method for producing a rubber composition for studless tires according to any one of Claims 1 to 6, characterized in that the water-insoluble lignin consists of an extract of an ethanol aqueous solution of bioethanol extraction residue lignin and / or the extraction residue of the ethanol aqueous solution of bioethanol extraction residue lignin.

8. The method for producing a rubber composition for studless tires according to claim 7, characterized in that the water-insoluble lignin contains 50% by mass or more of the extraction residue of the ethanol aqueous solution of the bioethanol extraction residue lignin.

9. The method for producing a rubber composition for studless tires according to claim 7 or 8, characterized in that the ethanol aqueous solution contains 50 to 70% by mass of ethanol.

10. A studless tire having a tread portion made of the rubber composition for studless tires described in any one of claims 1 to 6.

Images