WO2017195676A1 - Composition de caoutchouc et pneu la mettant en œuvre - Google Patents

Composition de caoutchouc et pneu la mettant en œuvre Download PDF

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WO2017195676A1
WO2017195676A1 PCT/JP2017/017052 JP2017017052W WO2017195676A1 WO 2017195676 A1 WO2017195676 A1 WO 2017195676A1 JP 2017017052 W JP2017017052 W JP 2017017052W WO 2017195676 A1 WO2017195676 A1 WO 2017195676A1
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styrene
butadiene
component
rubber composition
weight
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PCT/JP2017/017052
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English (en)
Japanese (ja)
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関根　優子
芦浦　誠
史 八柳
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横浜ゴム株式会社
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    • 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
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/02—Elements
    • C08K3/04—Carbon
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/34—Silicon-containing compounds
    • C08K3/36—Silica
    • 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

Definitions

  • the present invention relates to a rubber composition in which processability and tensile elongation at break are improved to the conventional level and a pneumatic tire using the rubber composition.
  • Patent Document 1 a pneumatic tire using a rubber composition blended with a styrene-butadiene copolymer having a specific arrangement of styrene units and silica as a tread has a wet skid resistance, a rolling resistance and an abrasion resistance at the same time. State that you are satisfied. However, since this rubber composition cannot always improve the tensile elongation at break and processability sufficiently, it cannot satisfy the demands of the customers.
  • Patent Document 2 the ozonolysis product of a styrene-butadiene copolymer is analyzed by gel permeation chromatography (GPC), the content ratio of the long chain styrene block to the total amount of styrene, the content of a single chain with one styrene unit. It is described that the ratio is measured.
  • the long chain styrene block is 5% by weight or less
  • the single chain having one styrene unit is 50% by weight or more
  • the total styrene content is styrene-butadiene based on the total styrene content in the styrene-butadiene copolymer.
  • a styrene-butadiene copolymer is described that is 10-30% by weight of the copolymer.
  • the rubber composition comprising this styrene-butadiene copolymer has not necessarily been able to sufficiently improve its rubber strength, tensile elongation at break and processability.
  • the analysis by GPC in Patent Document 2 shows that the ozonolysis product of the styrene-butadiene copolymer can be fractionated based on the number of styrene units and a chain consisting only of styrene units, but 1 of butadiene in the ozonization product. The number of units derived from 2-bond cannot be identified. Further, the analysis by GPC described in Patent Document 2 calculates the ratio of the amount of styrene in the decomposed product to the total amount of styrene, and does not accurately quantify the amount of each decomposed product.
  • An object of the present invention is to provide a rubber composition in which processability and tensile elongation at break are improved to the conventional level or more.
  • the rubber composition of the present invention that achieves the above object is a rubber composition comprising a diene rubber containing at least one styrene-butadiene copolymer and a reinforcing filler, wherein the at least one styrene-butadiene is used.
  • the styrene-butadiene copolymer component comprising a copolymer has the following characteristics (1) to (4).
  • the content of bound styrene is 5 to 50% by weight
  • one 1,2-bonded butadiene-derived unit is included in 100 mol% of the total of decomposition components containing styrene-derived units and / or 1,2-bonded butadiene-derived units.
  • the decomposition component V1 contained is less than 25 mol%.
  • styrene-derived units in a total of 100 mol% of decomposition components containing styrene-derived units and / or 1,2-bonded butadiene-derived units 5 mol% or more of the decomposition component S2V1 containing two benzene and one 1,2-bonded butadiene-derived unit (4)
  • the vinyl content of the butadiene portion is 50% or more
  • the rubber composition of the present invention has (1) a content of bound styrene of 5 to 50% by weight, and (2) among components obtained by ozonolysis, styrene-derived units and / or 1,2-bonded.
  • the decomposition component V1 containing one 1,2-bonded butadiene-derived unit is less than 25 mol%.
  • the diene rubber may contain at least one diene rubber other than the above-described styrene-butadiene copolymer.
  • the reinforcing filler may be at least one selected from silica and carbon black.
  • the rubber composition described above is suitable for use in pneumatic tires, particularly for cap treads.
  • This pneumatic tire is superior in tire durability to the conventional level, and is excellent in productivity and can stably produce a high-quality tire.
  • FIG. 1 is an example of a calibration curve showing the correlation between the concentration of the standard sample and the ionic strength.
  • FIG. 2 is an example of another calibration curve showing the correlation between the concentration of the standard sample and the ionic strength.
  • FIG. 3 is an explanatory diagram showing the relationship between the chain component and the slope of the calibration curve and the estimated slope of the calibration curve.
  • FIG. 4 is an explanatory diagram showing a relationship between another chain component and the slope of the calibration curve and the estimated slope of the calibration curve.
  • FIG. 5 is an explanatory diagram showing the relationship between yet another chain component and the slope of the calibration curve and the estimated slope of the calibration curve.
  • FIG. 6 is a partial cross-sectional view in the tire meridian direction showing an example of an embodiment of a pneumatic tire using the rubber composition of the present invention.
  • FIG. 6 is a cross-sectional view showing an example of an embodiment of a pneumatic tire using a rubber composition.
  • the pneumatic tire includes a tread portion 1, a sidewall portion 2, and a bead portion 3.
  • two carcass layers 4 in which reinforcing cords extending in the tire radial direction are arranged at predetermined intervals in the tire circumferential direction between the left and right bead portions 3 and embedded in the rubber layer are extended.
  • the portion is folded back from the inner side in the tire axial direction so as to sandwich the bead filler 6 around the bead core 5 embedded in the bead portion 3.
  • An inner liner layer 7 is disposed inside the carcass layer 4.
  • a belt cover layer 9 is disposed on the outer peripheral side of the belt layer 8.
  • tread portion 1 is formed by tread rubber layers 10a and 10b.
  • the tread rubber layers 10a and 10b are a cap tread and a base tread, and can preferably be constituted by the rubber composition of the present invention.
  • the rubber composition of the present invention comprises a diene rubber and a reinforcing filler.
  • the diene rubber necessarily contains at least one styrene-butadiene copolymer.
  • a polymer component comprising at least one styrene-butadiene copolymer may be referred to as a “styrene-butadiene copolymer component”.
  • the styrene-butadiene copolymer component satisfies all the following characteristics (1) to (4).
  • the content of bound styrene is 5 to 50% by weight
  • one 1,2-bonded butadiene-derived unit is included in 100 mol% of the total of decomposition components containing styrene-derived units and / or 1,2-bonded butadiene-derived units.
  • the decomposition component V1 contained is less than 25 mol%.
  • styrene-derived units in a total of 100 mol% of decomposition components containing styrene-derived units and / or 1,2-bonded butadiene-derived units 5 mol% or more of the decomposition component S2V1 containing two benzene and one 1,2-bonded butadiene-derived unit (4)
  • the vinyl content of the butadiene portion is 50% or more
  • the styrene-butadiene copolymer component is composed of a single styrene-butadiene copolymer
  • the styrene-butadiene copolymer needs to satisfy all the characteristics (1) to (4) described above.
  • the styrene-butadiene copolymer component when the styrene-butadiene copolymer component is composed of a blend of a plurality of styrene-butadiene copolymers, the styrene-butadiene copolymer component as a whole has all of the characteristics (1) to (4) described above. It is necessary to satisfy. As long as the styrene-butadiene copolymer component as a whole satisfies all of the properties (1) to (4), each styrene-butadiene copolymer constituting the blend has the above-mentioned (1) to (4). It may or may not satisfy all the characteristics.
  • the styrene-butadiene copolymer constituting the blend satisfies all the properties (1) to (4).
  • the rubber composition has excellent processability and tensile elongation at break. Can be a thing.
  • the styrene-butadiene copolymer component has (1) a content of bound styrene of 5 to 50% by weight, preferably 10 to 40% by weight.
  • a content of bound styrene of 5 to 50% by weight, preferably 10 to 40% by weight.
  • the glass transition temperature (Tg) of the styrene-butadiene copolymer component rises, the balance of viscoelastic properties is deteriorated, and the heat generation is increased. . That is, the balance between hysteresis loss and wet skid characteristics deteriorates.
  • the styrene content of the styrene-butadiene copolymer component is measured by 1 H-NMR.
  • the styrene-butadiene copolymer component used in the present invention is measured by a mass spectrometer after the decomposition component obtained by ozonolysis is separated by liquid chromatogram in two stages using two columns having different characteristics. (Hereafter, it may be described as “LC ⁇ LCMS analysis”).
  • LC ⁇ LCMS analysis the composition and amount of the ozonolysis component can be analyzed in more detail, and the 1,2-bonded butadiene-derived unit can be quantified in addition to the styrene-derived unit in the ozonolysis component.
  • the styrene-butadiene copolymer is a copolymer of styrene and butadiene, and includes a styrene repeating unit (styrene unit) and a butadiene repeating unit (butadiene unit).
  • the butadiene unit consists of a portion where butadiene is polymerized with 1,2-bonds (a repeating unit of ethylene having a vinyl group in the side chain) and a portion where butadiene is polymerized with a 1,4-bond (a repeating unit of 2-butylene divalent groups). Consists of.
  • the portion polymerized by 1,4-bond is composed of a repeating unit of trans-2-butylene structure and a repeating unit of cis-2-butylene structure.
  • the styrene-butadiene copolymer When the styrene-butadiene copolymer is subjected to ozonolysis, the butadiene portion polymerized by 1,4-bonds is cleaved. Further, the vinyl group in the side chain of the butadiene moiety polymerized by 1,2-bond is oxidized to a hydroxymethyl group. Thereby, in the styrene-butadiene copolymer, a repeating unit sandwiched between two butadiene units polymerized by two adjacent 1,4-bonds is generated as an ozonolysis component.
  • a compound represented by the following general formula (I) is obtained.
  • the compound represented by the general formula (I) is referred to as “ozone decomposition component V1”.
  • the direction of linking with adjacent units may be head-to-tail bond or head-to-head bond, and the head-to-tail bond / head-to-head bond represented by the chemical formula shall be replaced with each other. .
  • ozone decomposition component S2V1 a decomposition component composed of two styrene-derived units and one butadiene-derived unit polymerized by 1,2-bond.
  • the compound represented by the general formula (II) is selected from the order of arrangement of two styrene-derived units and one 1,2-bonded butadiene-derived unit, head-to-tail bond / head-to-head bond, and the order thereof. It is intended to include compounds wherein at least one of the different compounds.
  • the portion sandwiched between two butadiene units polymerized by two adjacent 1,4-bonds is obtained by ozonolysis, wherein styrene-derived units and / or 1,2-bonded butadiene-derived units are hydroxyethyl groups at both ends. It is generated as a decomposition component sandwiched between. Further, 1,4-butanediol is formed from a repeating portion in which two or more butadiene units polymerized by 1,4-bonds are continuous.
  • the styrene-butadiene copolymer component used in the present invention is (2) among the components obtained by ozonolysis and styrene-derived units and / or 1
  • the decomposition component V1 containing one 1,2-bonded butadiene-derived unit is less than 25 mol% in a total of 100 mol% of the decomposition components containing 1,2-bonded butadiene-derived units.
  • the decomposition component containing one 1,2-bonded butadiene-derived unit means the ozonolysis component V1 containing only one 1,2-bonded butadiene-derived unit as described above.
  • the number of moles of each decomposition component is determined.
  • the total number of moles of the decomposition component containing the styrene-derived unit and / or 1,2-bonded butadiene-derived unit produced by ozonolysis is calculated, and this is defined as 100 mol% of the ozonolysis component.
  • the amount of the decomposition component V1 containing one 1,2-bonded butadiene-derived unit is less than 25 mol%, preferably 10 mol% or more and less than 25 mol%, in 100 mol% of the ozonolysis component.
  • the ozonolysis component V1 By making the ozonolysis component V1 less than 25 mol%, the tensile elongation at break of the rubber composition can be made excellent. Moreover, the viscosity of a rubber composition can be made small and it can be made the thing excellent in processability.
  • the styrene-butadiene copolymer component used in the present invention includes (3) two styrene-derived units and 1,2-bond when the decomposition component obtained by ozonolysis is measured by LC ⁇ LCMS analysis.
  • the decomposition component S2V1 containing one butadiene-derived unit is 5 mol% or more, preferably 6 to 12 mol%.
  • the ozonolysis component S2V1 is an ozonolysis component containing only two styrene-derived units and one 1,2-bonded butadiene-derived unit as described above, and the ozonolysis component S2V1 includes the decomposition component represented by the general formula (II). Equivalent to.
  • the number of moles of the decomposition component represented by the general formula (II) is obtained.
  • the styrene-derived units are divided into two and 1, 2, -The ozonolysis component S2V1 consisting of one unit of butadiene-derived bonds must be at least 5 mol%.
  • the present invention is the number of moles of the ozonolysis component S1 containing only one styrene-derived unit and the ozonolysis component S2V1 containing two styrene-derived units and one 1,2-bonded butadiene-derived unit.
  • the analysis is performed individually by LC ⁇ LCMS analysis.
  • the conditions for measuring the ozonolysis component by LC ⁇ LCMS analysis can be as follows.
  • Liquid chromatograph Comprehensive two-dimensional LC Nexera-e (manufactured by Shimadzu Corporation)
  • Mass spectrometer LCMS-8040 or LCMS-8050 (both manufactured by Shimadzu Corporation)
  • First dimension column two columns (A) whose stationary phase is a polymer gel (Shodex Mspak GF-310 2D manufactured by Showa Denko KK, inner diameter: 2.0 mm, length 150 mm, particle size 5 ⁇ m) and the stationary phase is a polymer One column (B) (Super HZ 1000 manufactured by Tosoh Corporation, inner diameter: 2.0 mm, length 250 mm, particle size 3 ⁇ m), which is a gel, is connected in series, and a total of three are used in series.
  • A whose stationary phase is a polymer gel (Shodex Mspak GF-310 2D manufactured by Showa Denko KK, inner diameter: 2.0
  • Injection volume 1 ⁇ L (sample solution) (Concentration: 10 mg / mL)
  • Mobile phase THF Flow rate: 0.02 mL / min
  • Second dimension column Column (A) whose core is a core-shell polymer gel modified with octadecyl group (Kinetex C18 manufactured by Phenomenex, inner diameter: 3.0 mm, length 50 mm, particle size 2.6 ⁇ m)
  • Mobile phase A: water: methanol 1: 1
  • Mobile phase B Methanol flow rate: 2.0 mL / min
  • Time program B conc.
  • a commercially available sample may be used as the standard sample, or a sample obtained by separating and collecting from the SBR ozone decomposition product and calculating the purity by NMR or the like may be used.
  • a standard sample can be prepared as follows.
  • a solution-polymerized SBR having a styrene content of 36% by weight and a vinyl content in butadiene of 42% was subjected to ozonolysis treatment, LC-9104 (preparative GPC) manufactured by Nippon Analytical Industrial Co., Ltd., and four low-molecular columns (JAIGEL-1H, JAIGEL -H, 2 units each) were used to fractionate a total of 7 components of S1, S1V1, S2, S2V1, S3, S3V1, and V1 with chloroform solvent, and the purity was calculated by NMR to obtain a standard sample.
  • Polybutadiene having a vinyl content of 70% is subjected to ozonolysis treatment, using a column (VP-ODS 150 mm ⁇ 4.6 mm) with an HPLC system Prominence manufactured by Shimadzu Corporation, using mobile phase A as water and mobile phase B as methanol.
  • a column VP-ODS 150 mm ⁇ 4.6 mm
  • HPLC system Prominence manufactured by Shimadzu Corporation
  • mobile phase A as water
  • mobile phase B mobile phase B as methanol.
  • the elution time of the component was confirmed by mass spectrometry ionization conditions APCI + in a 40 minute gradient measurement of 20% B-100% B at a flow rate of 1 mL / min and an injection volume of 0.2 ⁇ L, and then V1, V2, and V3
  • the purity was calculated by NMR and used as a standard sample.
  • LC ⁇ LCMS analysis can be performed by the following operation.
  • LCMS-8040 product name
  • LCMS-8050 product name
  • Shimadzu Corporation is used, and the standard sample obtained as described above is measured in the APCI positive MS mode.
  • FIGS. 1 and FIG. 2 symbols such as “S1V1”, “V1”, and “S2” represent the number of 1,2-bonded butadiene-derived units and the number of styrene-derived units of the compound showing the calibration curve.
  • the symbol “S1V1” indicates that the compound has one 1,2-bonded butadiene-derived unit and one styrene-derived unit.
  • the calibration curve differs depending on the number of styrene-derived units and the number of 1,2-bonded butadiene-derived units contained in the compound.
  • the amount of change in the slope of the calibration curve when the number of styrene chains increases by one from the calibration curve of S1 to S3 is calculated, and the chain component Sn ( The slope of n ⁇ 4) was estimated.
  • the slope of the calibration curve was estimated by the same method. The estimated slope of the calibration curve is shown in FIG.
  • the detection result of the mass spectrometer was analyzed using the analysis software ChromSquare (manufactured by Shimadzu Corporation), and the elution time of the primary column was represented by the horizontal axis, the elution time of the secondary column was represented by the vertical axis, and the signal intensity was represented by contour lines.
  • ChromSquare manufactured by Shimadzu Corporation
  • the elution time of the primary column was represented by the horizontal axis
  • the elution time of the secondary column was represented by the vertical axis
  • the signal intensity was represented by contour lines.
  • a two-dimensional chromatogram was created.
  • components with very short elution times such as S2V1 and S1V1 can be separated, so identification of the chain structure of styrene-derived units and 1,2-linked butadiene-derived units in the sample Became possible.
  • the styrene-butadiene copolymer component used in the present invention has (4) a vinyl content in the butadiene portion of 50% or more, preferably 50 to 65%.
  • a vinyl content in the butadiene portion is measured by 1 H-NMR.
  • the content of the styrene-butadiene copolymer component having the characteristics (1) to (4) is preferably 40% by weight or more, more preferably 60 to 100% by weight, and still more preferably 100% by weight of the diene rubber. 80 to 100% by weight.
  • 40% by weight or more of the styrene-butadiene copolymer component specified by the characteristics (1) to (4) the tensile elongation at break of the rubber composition is excellent and the moldability is improved. can do.
  • the rubber composition of the present invention can contain a diene rubber other than the styrene-butadiene copolymer component that satisfies all the characteristics (1) to (4).
  • diene rubbers such as natural rubber (NR), polyisoprene rubber (IR), polybutadiene rubber (low cis BR), high cis BR, high trans BR (trans bond content of butadiene part 70 to 95%), styrene -Isoprene copolymer rubber, butadiene-isoprene copolymer rubber, solution polymerization random styrene-butadiene-isoprene copolymer rubber, emulsion polymerization random styrene-butadiene-isoprene copolymer rubber, emulsion polymerization styrene-acrylonitrile-butadiene copolymer rubber, acrylonitrile- Examples thereof include butadiene copolymer rubber
  • the content of the other diene rubber is preferably 60% by weight or less, more preferably 0 to 40% by weight, and further preferably 0 to 20% by weight in 100% by weight of the diene rubber.
  • various physical properties such as wear resistance can be improved.
  • the rubber composition of the present invention contains a diene rubber and a reinforcing filler.
  • reinforcing fillers include carbon black, silica, clay, aluminum hydroxide, calcium carbonate, mica, talc, aluminum hydroxide, aluminum oxide, titanium oxide, barium sulfate, and other inorganic fillers, cellulose, lecithin, lignin, An organic filler such as a dendrimer can be exemplified. Among these, it is preferable to blend at least one selected from carbon black and silica.
  • the rubber composition By adding carbon black to the rubber composition, the rubber composition can have excellent wear resistance and rubber strength.
  • the blending amount of carbon black is not particularly limited, but is preferably 10 to 100 parts by weight, more preferably 25 to 80 parts by weight with respect to 100 parts by weight of the diene rubber.
  • carbon black such as furnace black, acetylene black, thermal black, channel black and graphite may be blended.
  • furnace black is preferable, and specific examples thereof include SAF, ISAF, ISAF-HS, ISAF-LS, IISAF-HS, HAF, HAF-HS, HAF-LS, and FEF.
  • SAF SAF
  • ISAF ISAF-HS
  • ISAF-LS ISAF-LS
  • IISAF-HS IISAF-HS
  • HAF HAF-HS
  • HAF-LS HAF-LS
  • FEF FEF
  • the rubber composition can be made excellent in low heat build-up and wet grip performance.
  • the blending amount of silica is not particularly limited, but is preferably 10 to 150 parts by weight, more preferably 40 to 100 parts by weight with respect to 100 parts by weight of the diene rubber.
  • silica examples include silica usually used in rubber compositions for tire treads, such as wet silica, dry silica, carbon-silica (dual phase filler) with silica supported on the surface of carbon black, and silane coupling.
  • Silica treated with a compound reactive or compatible with both silica and rubber, such as an agent or polysiloxane, can be used.
  • wet method silica mainly containing hydrous silicic acid is preferable.
  • the compounding amount of the reinforcing filler containing silica and / or carbon black is preferably 10 to 150 parts by weight, more preferably 40 to 100 parts by weight with respect to 100 parts by weight of the diene rubber.
  • the blending amount of the reinforcing filler is less than 10 parts by weight, sufficient reinforcing performance cannot be obtained, and the rubber hardness and tensile strength at break are insufficient.
  • the blending amount of the reinforcing filler exceeds 150 parts by weight, the exothermic property increases and the tensile breaking elongation decreases. In addition, wear resistance is deteriorated and workability is also deteriorated.
  • the rubber composition of the present invention is preferable because the low heat build-up and wear resistance are further improved by blending a silane coupling agent with silica.
  • a silane coupling agent By compounding a silane coupling agent with silica, the dispersibility of silica is improved and the reinforcement with the diene rubber is further enhanced.
  • the silane coupling agent is preferably added in an amount of 2 to 20% by weight, more preferably 5 to 15% by weight, based on the amount of silica. When the compounding amount of the silane coupling agent is less than 2% by weight of the silica weight, the effect of improving the dispersibility of silica cannot be obtained sufficiently. On the other hand, if the silane coupling agent exceeds 20% by weight, the diene rubber component tends to be gelled, so that a desired effect cannot be obtained.
  • the silane coupling agent is not particularly limited, but a sulfur-containing silane coupling agent is preferable.
  • a sulfur-containing silane coupling agent is preferable.
  • 2006-249069 such as VP Si363 manufactured by the company, 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, bis (3-diethoxymethylsilylpropyl) tetrasulfide, dimethoxy Methylsilylpropyl
  • the silane coupling agent is an organosilicon compound.
  • organosilicon compound polysiloxane, polysiloxane side chain, or both ends, one end, or both side chains and both ends are amino groups, epoxy groups, carbinol groups, or mercapto.
  • Silicone oil introduced with one or more organic groups such as a group, carboxyl group, hydrogen group, polyether group, phenol group, silanol group, acrylic group, methacryl group or long chain alkyl group, condensed with one or more organic silanes
  • Examples include silicone oligomers obtained by reaction. Of these, bis- (3-triethoxysilylpropyl) tetrasulfide and bis (3-triethoxysilylpropyl) disulfide are preferable.
  • the rubber composition of the present invention includes a vulcanization or cross-linking agent, a vulcanization accelerator, an anti-aging agent, a processing aid, a plasticizer, a liquid polymer, a thermosetting resin, a thermoplastic, Various compounding agents generally used in rubber compositions for tire treads such as resins can be blended. Such a compounding agent can be kneaded by a general method to form a rubber composition, which can be used for vulcanization or crosslinking. The compounding amounts of these compounding agents can be the conventional general compounding amounts as long as they do not contradict the purpose of the present invention.
  • the tire tread rubber composition can be prepared by mixing the above-described components using a known rubber kneading machine such as a Banbury mixer, a kneader, or a roll.
  • the vulcanization or cross-linking agent is not particularly limited.
  • sulfur such as powdered sulfur, precipitated sulfur, colloidal sulfur, insoluble sulfur, and highly dispersible sulfur; halogen such as sulfur monochloride and sulfur dichloride.
  • Sulfur peroxide organic peroxides such as dicumyl peroxide and ditertiary butyl peroxide.
  • sulfur is preferable, and powder sulfur is particularly preferable.
  • the mixing ratio of the vulcanizing agent is usually in the range of 0.1 to 15 parts by weight, preferably 0.3 to 10 parts by weight, more preferably 0.5 to 5 parts by weight with respect to 100 parts by weight of the diene rubber. is there.
  • the vulcanization accelerator is not particularly limited, and examples thereof include N-cyclohexyl-2-benzothiazylsulfenamide, Nt-butyl-2-benzothiazolesulfenamide, N-oxyethylene-2-benzothiazolesulfuramide.
  • Sulfenamide vulcanization accelerators such as phenamide, N-oxyethylene-2-benzothiazole sulfenamide, N, N′-diisopropyl-2-benzothiazole sulfenamide; diphenyl guanidine, diortolyl guanidine, ortho Guanidine vulcanization accelerators such as trilbiguanidine; thiourea vulcanization accelerators such as diethylthiourea; thiazole vulcanization accelerators such as 2-mercaptobenzothiazole, dibenzothiazyl disulfide, and 2-mercaptobenzothiazole zinc salt; Tetramethylthiura Thiuram vulcanization accelerators such as monosulfide and tetramethylthiuram disulfide; Dithiocarbamate vulcanization accelerators such as sodium dimethyldithiocarbamate and zinc diethyldithiocarbamate; Sodium isopropylxanthate, zinc
  • xanthogenic acid-based vulcanization accelerators Of these, those containing a sulfenamide vulcanization accelerator are particularly preferred. These vulcanization accelerators are used alone or in combination of two or more.
  • the blending amount of the vulcanization accelerator is preferably 0.1 to 15 parts by weight, more preferably 0.5 to 5 parts by weight with respect to 100 parts by weight of the diene rubber.
  • the anti-aging agent is not particularly limited, but 2,2,4-trimethyl-1,2-dihydroquinoline polymer, p, p'-dioctyldiphenylamine, N, N'-diphenyl-p-phenylenediamine, N- Amine-based antioxidants such as phenyl-N'-1,3-dimethylbutyl-p-phenylenediamine, 2,6-di-t-butyl-4-methylphenol, 2,2'-methylenebis (4-methyl- 6-t-butylphenol) and the like. These anti-aging agents are used alone or in combination of two or more.
  • the blending amount of the antioxidant is preferably 0.1 to 15 parts by weight, more preferably 0.5 to 5 parts by weight with respect to 100 parts by weight of the diene rubber.
  • the processing aid is not particularly limited.
  • higher fatty acids such as stearic acid, higher fatty acid amides such as stearamide, aliphatic higher amines such as stearylamine, aliphatic higher alcohols such as stearyl alcohol, Fatty acid such as glycerin fatty acid ester and partial ester of polyhydric alcohol, fatty acid metal salt such as zinc stearate, zinc oxide and the like can be used.
  • the blending amount is appropriately selected, but the blending amount of the higher fatty acid, aliphatic higher amide, higher alcohol, and fatty acid metal salt is preferably 0.05 to 15 parts by weight, more preferably 100 parts by weight of the diene rubber. Is 0.5 to 5 parts by weight.
  • the compounding amount of zinc oxide is preferably 0.05 to 10 parts by weight, more preferably 0.5 to 3 parts by weight with respect to 100 parts by weight of the diene rubber.
  • the plasticizer used as the compounding agent is not particularly limited, but for example, aroma-based, naphthenic, paraffinic, silicone-based extending oils are selected depending on the application.
  • the amount of the plasticizer used is usually in the range of 1 to 150 parts by weight, preferably 2 to 100 parts by weight, and more preferably 3 to 60 parts by weight per 100 parts by weight of the diene rubber. When the amount of the plasticizer used is in this range, the dispersing effect of the reinforcing agent, tensile strength, wear resistance, heat resistance and the like are balanced to a high value.
  • other plasticizers include diethylene glycol, polyethylene glycol, and silicone oil.
  • thermosetting resin is not particularly limited, and examples thereof include resorcin-formaldehyde resin, phenol-formaldehyde resin, urea-formaldehyde resin, melamine-formaldehyde resin, phenol derivative-formaldehyde resin, and specifically m-3.
  • thermosetting resins that cure or become high molecular weight by heating or by giving heat and methylene donor, other guanamine resins, diallyl phthalate
  • thermosetting resins include resins, vinyl ester resins, phenol resins, unsaturated polyester resins, furan resins, polyimide resins, polyurethane resins, melamine resins, urea resins, and epoxy resins.
  • the thermoplastic resin is not particularly limited.
  • a polystyrene resin a polyethylene resin, a polypropylene resin, a polyester resin, a polyamide resin, a polycarbonate resin, a polyurethane resin, a polysulfone resin
  • examples include polyphenylene ether resins and polyphenylene sulfide resins.
  • aromatic hydrocarbon resins such as styrene- ⁇ -methylstyrene resin, indene-isopropenyltoluene resin, coumarone-indene resin, dicyclopentadiene resin, main raw materials are 1,3-pentadiene, pentene, methylbutene, etc.
  • hydrocarbon resins such as petroleum resins, alkylphenol resins, modified phenol resins, terpene phenol resins, terpene resins, and aromatic modified terpene resins.
  • the rubber composition of the present invention has improved the workability and the tensile elongation at break to the conventional level, so that the durability of the pneumatic tire is improved to the conventional level and a high-quality tire with excellent productivity is obtained. It can be produced stably.
  • the rubber composition of the present invention is a cross-section of a cap tread portion, an under tread portion, a sidewall portion, a bead filler portion of a pneumatic tire, a cord covering rubber such as a carcass layer, a belt layer, and a belt cover layer, and a run flat tire. It can be suitably used for a crescent-shaped side reinforcing rubber layer, a rim cushion portion, and the like.
  • styrene-butadiene copolymers were blended at the blending ratio shown in Table 1 to prepare a styrene-butadiene copolymer component, and (1) bound styrene content (% by weight), (2) 1, 2- mol% of ozonolysis component V1 containing one bonded butadiene-derived unit, (3) mol% of ozonolysis component S2V1 containing two styrene-derived units and one 1,2-linked butadiene-derived unit, And (4) vinyl content (% by weight) of the butadiene portion was measured.
  • the (1) bound styrene content of the styrene-butadiene copolymer component and (4) the vinyl content of the butadiene moiety were measured by 1 H-NMR.
  • the conditions for ozonolysis of the styrene-butadiene copolymer component were as described above.
  • the mole% of component S2V1 was measured based on the conditions described above for LC ⁇ LCMS analysis.
  • Eight types of rubber composition comprising the styrene-butadiene copolymer component (blend of a plurality of styrene-butadiene copolymers) shown in Table 1 and other diene rubbers, with the compounding agent shown in Table 2 as a common compound.
  • the products (Examples 1 to 5, Comparative Examples 1 to 3) were mixed with the components excluding sulfur and the vulcanization accelerator for 6 minutes using a 1.7 L closed Banbury mixer, and discharged from the mixer at 150 ° C. And cooled to room temperature. Thereafter, the mixture was again mixed for 3 minutes using a 1.7 liter closed Banbury mixer, and after release, a rubber composition was prepared by mixing sulfur and a vulcanization accelerator with an open roll.
  • the Mooney viscosity of the obtained rubber composition was evaluated by the following measuring method.
  • the obtained rubber composition was vulcanized at 160 ° C. for 30 minutes using a predetermined mold to prepare a vulcanized rubber test piece.
  • the tensile elongation at break was evaluated by the following measuring method.
  • Mooney viscosity The Mooney viscosity (ML 1 + 4 ) of the rubber composition is determined using a Mooney viscometer in accordance with JIS K6300 using an L-shaped rotor, preheating time 1 minute, rotor rotation time 4 minutes, temperature 100 ° C., The measurement was performed under the condition of 2 rpm. The obtained results are shown in the “Mooney viscosity” column of Table 1 as an index with Comparative Example 1 as 100. The smaller the “Mooney viscosity” index, the lower the Mooney viscosity and the better the moldability.
  • NS116 NS116 manufactured by Nippon Zeon Co., Ltd., bound styrene content of 20.9% by weight, vinyl content of 63.8%
  • non-oil-extended product NS570 NS570 manufactured by Nippon Zeon Co., Ltd., bound styrene content of 40.6% by weight
  • E581 E581 manufactured by Asahi Kasei Chemicals Corporation, a bound styrene content of 35.6% by weight, and a vinyl content of 41.
  • Vulcanization accelerator-1 Sunseller CM-PO (CZ) manufactured by Sanshin Chemical Co., Ltd.
  • Vulcanization accelerator-2 Sunseller DG (DPG) manufactured by Sanshin Chemical Co., Ltd.
  • the ozonolysis component V1 containing one 1,2-bonded butadiene-derived unit was 25 mol% or more, two styrene-derived units, and one 1,2-bonded butadiene-derived unit. Therefore, the Mooney viscosity is large and the moldability is inferior.
  • the styrene-butadiene copolymer component contained 25 mol% or more of an ozonolysis component V1 containing one 1,2-bonded butadiene-derived unit, two styrene-derived units, and 1, Since the ozonolysis component S2V1 containing one 2-bonded butadiene-derived unit is less than 5 mol%, the Mooney viscosity is large, the molding processability is inferior, and the tensile elongation at break is small.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Tires In General (AREA)

Abstract

L'invention concerne une composition de caoutchouc ayant une meilleure aptitude au façonnage et un allongement amélioré à la rupture par rapport aux niveaux précédents. La composition de caoutchouc contient une charge renforçante et un caoutchouc diène. Le caoutchouc diène comprend un constituant copolymère de styrène-butadiène comprenant au moins un copolymère de styrène-butadiène et satisfaisant aux exigences suivantes : (1) la teneur en styrène lié est de 5 à 50 % en poids, (2) des constituants obtenus par ozonolyse, parmi un total de 100 % en mole des constituants de décomposition comprenant des unités dérivées du butadiène 1,2-conjugué et/ou des unités dérivées du styrène, le constituant de décomposition (V1) qui contient une unité dérivée du butadiène 1,2-conjugué représente moins de 25 % en mole, (3) des constituants obtenus par ozonolyse, parmi un total de 100 % en mole des constituants de décomposition comprenant des unités dérivées du butadiène 1,2-conjugué et/ou des unités dérivées du styrène, le constituant de décomposition (S2V1) qui comprend deux unités dérivées du styrène et une unité dérivée du butadiène 1,2-conjugué représente au moins 5 % mole et (4) la teneur en vinyle de la fraction de butadiène est d'au moins 50 %.
PCT/JP2017/017052 2016-05-10 2017-04-28 Composition de caoutchouc et pneu la mettant en œuvre WO2017195676A1 (fr)

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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07300511A (ja) * 1994-12-02 1995-11-14 Asahi Chem Ind Co Ltd 改良されたゴム状重合体組成物
JP2000038423A (ja) * 1998-07-24 2000-02-08 Jsr Corp 共役ジオレフィン系共重合ゴムおよびゴム組成物
JP2000178378A (ja) * 1998-10-07 2000-06-27 Jsr Corp 油展ゴム及びゴム組成物
US20030100660A1 (en) * 2001-10-31 2003-05-29 David John Zanzig Tire with component comprised of a blend of polybutadiene-rich rubber composition which contains a minor portion of styrene-rich styrene/isoprene elastomer
JP2010280853A (ja) * 2009-06-05 2010-12-16 Bridgestone Corp ゴム組成物およびそれを用いた空気入りタイヤ
WO2016147961A1 (fr) * 2015-03-13 2016-09-22 横浜ゴム株式会社 Composition de caoutchouc et pneu l'utilisant
JP2016183219A (ja) * 2015-03-25 2016-10-20 住友ゴム工業株式会社 ゴム組成物およびタイヤ
WO2017057758A1 (fr) * 2015-09-30 2017-04-06 大塚化学株式会社 Additif pour conférer une faible accumulation de chaleur à un composant de caoutchouc

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07300511A (ja) * 1994-12-02 1995-11-14 Asahi Chem Ind Co Ltd 改良されたゴム状重合体組成物
JP2000038423A (ja) * 1998-07-24 2000-02-08 Jsr Corp 共役ジオレフィン系共重合ゴムおよびゴム組成物
JP2000178378A (ja) * 1998-10-07 2000-06-27 Jsr Corp 油展ゴム及びゴム組成物
US20030100660A1 (en) * 2001-10-31 2003-05-29 David John Zanzig Tire with component comprised of a blend of polybutadiene-rich rubber composition which contains a minor portion of styrene-rich styrene/isoprene elastomer
JP2010280853A (ja) * 2009-06-05 2010-12-16 Bridgestone Corp ゴム組成物およびそれを用いた空気入りタイヤ
WO2016147961A1 (fr) * 2015-03-13 2016-09-22 横浜ゴム株式会社 Composition de caoutchouc et pneu l'utilisant
JP2016183219A (ja) * 2015-03-25 2016-10-20 住友ゴム工業株式会社 ゴム組成物およびタイヤ
WO2017057758A1 (fr) * 2015-09-30 2017-04-06 大塚化学株式会社 Additif pour conférer une faible accumulation de chaleur à un composant de caoutchouc

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