WO2009125842A1 - 重荷重用タイヤ - Google Patents
重荷重用タイヤ Download PDFInfo
- Publication number
- WO2009125842A1 WO2009125842A1 PCT/JP2009/057367 JP2009057367W WO2009125842A1 WO 2009125842 A1 WO2009125842 A1 WO 2009125842A1 JP 2009057367 W JP2009057367 W JP 2009057367W WO 2009125842 A1 WO2009125842 A1 WO 2009125842A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- rubber
- trbr
- mass
- bmi
- belt
- Prior art date
Links
- 229920001971 elastomer Polymers 0.000 claims abstract description 108
- 239000005060 rubber Substances 0.000 claims abstract description 108
- 229920003192 poly(bis maleimide) Polymers 0.000 claims abstract description 50
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000011248 coating agent Substances 0.000 claims abstract description 36
- 238000000576 coating method Methods 0.000 claims abstract description 36
- 239000000203 mixture Substances 0.000 claims abstract description 36
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 34
- 239000010959 steel Substances 0.000 claims abstract description 34
- 229920001194 natural rubber Polymers 0.000 claims abstract description 7
- 244000043261 Hevea brasiliensis Species 0.000 claims abstract description 6
- 229920003052 natural elastomer Polymers 0.000 claims abstract description 6
- 229920003049 isoprene rubber Polymers 0.000 claims abstract 2
- 239000005062 Polybutadiene Substances 0.000 claims description 13
- 238000004073 vulcanization Methods 0.000 claims description 11
- 229920002857 polybutadiene Polymers 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000010030 laminating Methods 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 238000000926 separation method Methods 0.000 abstract description 24
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 37
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 8
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 7
- 230000035882 stress Effects 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
- 239000011324 bead Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000006229 carbon black Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 4
- 230000032683 aging Effects 0.000 description 3
- 229920005549 butyl rubber Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000003712 anti-aging effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- SQBBHCOIQXKPHL-UHFFFAOYSA-N tributylalumane Chemical compound CCCC[Al](CCCC)CCCC SQBBHCOIQXKPHL-UHFFFAOYSA-N 0.000 description 2
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 2
- 239000004636 vulcanized rubber Substances 0.000 description 2
- UFFVWIGGYXLXPC-UHFFFAOYSA-N 1-[2-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1N1C(=O)C=CC1=O UFFVWIGGYXLXPC-UHFFFAOYSA-N 0.000 description 1
- IPJGAEWUPXWFPL-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC(N2C(C=CC2=O)=O)=C1 IPJGAEWUPXWFPL-UHFFFAOYSA-N 0.000 description 1
- AQGZJQNZNONGKY-UHFFFAOYSA-N 1-[4-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=C(N2C(C=CC2=O)=O)C=C1 AQGZJQNZNONGKY-UHFFFAOYSA-N 0.000 description 1
- XAZPKEBWNIUCKF-UHFFFAOYSA-N 1-[4-[4-[2-[4-[4-(2,5-dioxopyrrol-1-yl)phenoxy]phenyl]propan-2-yl]phenoxy]phenyl]pyrrole-2,5-dione Chemical compound C=1C=C(OC=2C=CC(=CC=2)N2C(C=CC2=O)=O)C=CC=1C(C)(C)C(C=C1)=CC=C1OC(C=C1)=CC=C1N1C(=O)C=CC1=O XAZPKEBWNIUCKF-UHFFFAOYSA-N 0.000 description 1
- YNSSPVZNXLACMW-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)-3-ethyl-5-methylphenyl]methyl]-2-ethyl-6-methylphenyl]pyrrole-2,5-dione Chemical compound C=1C(C)=C(N2C(C=CC2=O)=O)C(CC)=CC=1CC(C=C1CC)=CC(C)=C1N1C(=O)C=CC1=O YNSSPVZNXLACMW-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- REQPQFUJGGOFQL-UHFFFAOYSA-N dimethylcarbamothioyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SC(=S)N(C)C REQPQFUJGGOFQL-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229920005555 halobutyl Polymers 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000010058 rubber compounding Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 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
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
-
- 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
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3415—Five-membered rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T152/00—Resilient tires and wheels
- Y10T152/10—Tires, resilient
- Y10T152/10495—Pneumatic tire or inner tube
- Y10T152/10765—Characterized by belt or breaker structure
- Y10T152/1081—Breaker or belt characterized by the chemical composition or physical properties of elastomer or the like
Definitions
- the present invention relates to a tire for a large vehicle, and in particular, a tire for a heavy load vehicle in which a belt layer formed by embedding a steel cord in a covering rubber is disposed radially outward of a crown portion of a carcass ply formed of a radial cord layer. It is about.
- a tire In recent years, with the increase in size of vehicles, tires that can withstand heavy loads are required.
- a tire includes a belt layer formed by laminating a plurality of layers made of a steel cord and a coating rubber covering the steel cord, and imparts load resistance, traction resistance, and the like to the tire. .
- a tire having such a belt layer is likely to generate belt end separation. This belt end separation is caused by fatigue of the belt end rubber due to dynamic interlaminar shear strain applied by the load, driving force, braking force and lateral force applied to the tire in addition to the interlaminar shear strain due to the tire air pressure. is there.
- the belt layer is devised such as changing various mechanical structures or rubber component configurations, while maintaining the load resistance, traction resistance, and crack resistance of the tire, Proposals have been made to improve heat separation resistance and cut separation resistance.
- a radial tire has been proposed in which the belt layer has five or more layers and a specific coating rubber is used for the main trunk layer and the protective layer to improve the heat separation resistance and cut separation resistance of the entire tire (Patent Document). 1). Further, the belt layer is composed of four layers having different widths, the steel cords of the constituent layers are inclined with respect to the equator plane of the tire, the inclination directions of the steel cords of adjacent layers are the same direction or the opposite direction, and the tires of each layer Proposed heavy-duty radial tires with improved separation resistance while maintaining wear resistance, traction resistance, cut resistance, etc. by configuring belt layers with different lengths in the width direction. (Patent Document 2 and Patent Document 3).
- a pair of left and right belt end cushion rubbers are disposed at both ends of at least two layers of the rubber-coated cord layers forming the main cross belt, and at least two of the cushion rubbers located on the same end side.
- a heavy-duty pneumatic radial tire is proposed in which the cushion rubbers are partially overlapped with each other in the tire width direction, and the deviation width of the overlapped cushion rubber in the tire width direction is in a specific size range. (Patent Document 4).
- a large-sized tire having heat resistance, durability, and crack resistance having a rubber composition having durability and a belt layer made of the rubber composition that maintains high elasticity even during long-term vulcanization of a large tire.
- Radial tires for vehicles have also been proposed. That is, a belt using a rubber composition in which transpolybutadiene and N, N′-diphenylmethane bismaleimide, which is a heat-resistant cross-linking agent, are combined in a specific ratio and used as a steel cord coating rubber A radial tire provided with a layer (Patent Document 5).
- JP 7-32815 A Japanese Patent Laid-Open No. 5-8607 JP-A-6-127213 Japanese Patent Laid-Open No. 11-32224 JP 2003-63205 A
- the crack at the belt end portion may occur due to the separation between the rubber-rubber of the coating rubber of the plurality of belt layers and the separation between the steel cord and the coating rubber in one layer.
- steel cord coating rubber the adhesion between steel cord and rubber is important, and the rubber composition used for the coated rubber may be added with an adhesion promoter for adhesion or a relatively large amount of sulfur. Yes.
- adhesiveness not only adhesiveness but also properties such as high hardness, low exothermic property, high rupture physical property, good aging physical property, low flex cracking property, etc. are required. Of these, the hardness can be increased.
- the object of the present invention is that the belt structure of a heavy-duty tire is almost the same as that of a conventional tire, and the increase in the weight of rubber is minimized, so that cracks caused by the separation between the steel cord at the belt end and the coating rubber are reduced. It is an object of the present invention to provide a heavy duty tire that can prevent generation and progress.
- the present invention relates to a carcass comprising a bead core provided on a pair of right and left bead portions, a radial cord layer extending from the crown portion to both bead portions via both sidewall portions, wound around the bead core and anchored to the bead portion.
- a heavy-duty tire comprising a ply, a belt and a tread disposed radially outward of the crown portion of the carcass ply, wherein the belt is formed by laminating a rubber-coated cord layer in which a steel cord is embedded in a coating rubber
- the separation of the steel cord and the coating rubber at the end of the rubber-coated cord layer and the end of the belt is to be prevented.
- the belt end separation is achieved by the steel cord moving in the belt due to the dynamic shear stress applied by the load, driving force, braking force and lateral force applied to the tire in addition to the interlaminar shear strain due to the tire air pressure. Separation occurs from the rubber at the end, and the separation develops inside.
- the present invention is a rubber other than a coating rubber in which a steel cord containing a specific proportion of transpolybutadiene and bismaleimide as a heat-resistant crosslinking agent is embedded in the end portion of the rubber-coated cord layer. It is covered with the composition.
- the end portion may be covered with the rubber composition by one rubber-coated cord layer or all of a plurality of layers.
- the steel cord may be covered with a conventional coating rubber while leaving the end portion, and only the end portion of the steel cord may be covered directly with the rubber composition. You may coat
- the present invention by covering the end portion of the rubber-coated steel cord of the tire belt with a rubber having high hardness, it is possible to prevent the occurrence and development of cracks caused by the separation between the steel cord and the coating rubber. Has an effect.
- the coating rubber composition for coating the steel cord of the tire belt used in the present invention comprises, for example, at least one of natural rubber and diene-based synthetic rubber such as polybutadiene and polyisoprene, and 5.0 phr of sulfur and carbon
- the rubber contains 55.0 phr of N330 carbon black, and other rubber compounding agents such as an adhesion aid, a vulcanization accelerator, and an antioxidant.
- a steel cord is coated with the above-described coating rubber composition to form a belt, and the end portion thereof is further coated so as to be wrapped with a hard end coating rubber composition from above the coating, Alternatively, only the end portion of the steel cord is not covered with the coating rubber composition, and the end portion of the rubber-coated cord layer is covered so as to be wrapped with the end-covering rubber composition.
- the rubber composition for covering the end portion for covering the end portion of the steel cord used in the present invention contains natural rubber and polyisoprene, and preferably contains 50% by mass or more of natural rubber. This is because if it is less than 50% by mass, the adhesive properties and rubber breaking properties may be deteriorated.
- SBR styrene / butadiene rubber
- BR polybutadiene
- IIR butyl rubber
- X-IIR halogenated butyl rubber
- EPDM ethylene / propylene / diene rubber
- SBR polystyrene
- the vinyl bond content of the butadiene portion is 35 to 85% by mass and the amount of bonded styrene is 30% by mass or less.
- the heat aging resistance of the rubber can be improved by setting it to at least%, and the fracture characteristics of the rubber can be maintained by setting it to 85% or less.
- the adhesive fall can be suppressed by making the amount of bond styrene into 30 mass% or less.
- the rubber composition for end coating of the present invention contains trans polybutadiene (TRBR) and bismaleimide (BMI) in addition to the above rubber components.
- TRBR trans polybutadiene
- BMI bismaleimide
- Bismaleimide increases the hardness of the rubber without sacrificing the low heat build-up and deterioration resistance of the rubber because the bismaleimide is polymerized with each other and the diene polymer such as natural rubber is directly crosslinked without sulfur. Can be made.
- the strain applied to the belt end is reduced and the separation of the rubber-steel cord is prevented by transferring the strain from the rubber-steel cord to the rubber-rubber.
- the hardness of the end can be increased without increasing the hardness of the coating rubber, and the end separation can be effectively reduced. Can be deterred. Even when transpolybutadiene (TRBR) and bismaleimide (BMI) are contained in the coating rubber, the separation of the rubber-steel cord can be prevented, and the rubber composition is applied to the rubber-coated cord layer and the belt end. By covering the object, separation at the end can be prevented.
- TRBR transpolybutadiene
- BMI bismaleimide
- the bismaleimide that can be used in the present invention is not particularly limited, but a bismaleimide represented by the following general formula can be used. (Wherein R represents an aromatic group having 6 to 18 carbon atoms or an alkyl aromatic group having 7 to 24 carbon atoms, and x and y each independently represents an integer of 0 to 3)
- Suitable bismaleimides include N, N′-1,2-phenylene bismaleimide, N, N′-1,3-phenylene bismaleimide, N, N′-1,4-phenylene bismaleimide, N, N ′. -1,4-xylylene bismaleimide, N, N ′-(4,4′-diphenylmethane) bismaleimide, 2,2-bis [4- (4-maleimidophenoxy) phenyl] propane, bis (3-ethyl- 5-methyl-4-maleimidophenyl] methane and the like can be exemplified, and N, N ′-(4,4′-diphenylmethane) bismaleimide is particularly preferable. More than one species can be included.
- the transpolybutadiene used in the rubber composition for covering an end of the present invention a commercially available product or a product obtained by synthesis may be used.
- a production method there can be mentioned a method in which a butadiene monomer is polymerized by contacting it with a quaternary catalyst of nickel boroacylate, tributylaluminum, triphenyl phosphite and trifluoroacetic acid in a solvent.
- the trans polybutadiene preferably has a trans bond content of 82% by mass to 98% by mass, and more preferably 86% to 98% from the viewpoint of effects. Further, when the mass average molecular weight is 30,000 to 200,000, the processability when unvulcanized can be improved, and the fracture resistance of the vulcanized rubber can be maintained.
- the blending amount of bismaleimide (BMI) and trans polybutadiene (TRBR) is determined by combining BMI and TRBR per 100 parts by weight of the rubber component from the viewpoints of compatibility with the rubber component, fracture resistance of the vulcanized rubber, heat generation, and the like. 0.1 part by mass to 10.0 parts by mass, and more than 25% of TRBR with respect to the total of BMI and TRBR, 0.1 parts by mass ⁇ TRBR + BMI ⁇ 10.0 parts by mass TRBR / (TRBR + BMI) ⁇ 25% This also includes the case of TRBR 100% in which BMI is not included.
- the total amount of BMI and TRBR is 0.1 to 7.0 parts by weight, more preferably 1.0 to 7.0 parts by weight per 100 parts by weight of the rubber component.
- TRBR is preferably 50% or more with respect to the total of BMI and TRBR.
- the amount of BMI is 0 to 6.0 parts by mass, preferably 0.1 to 4.0 parts by mass with respect to 100 parts by mass of the rubber component.
- the crack resistance tends to be lowered, and BMI tends to remain unreacted in the rubber composition after vulcanization. In some cases, the effect of increasing the heat aging resistance by generating a stable crosslinked form is impaired.
- the blending amount of TRBR contained in the rubber component is 25% by mass or more of the total amount with BMI. If it is less than 25%, the tan ⁇ of the tire will increase and the hysteresis loss will increase, so that sufficient improvement in crack resistance will not be seen for the high tensile stress at 100% elongation of the rubber.
- the rubber composition for end coating used in the present invention may contain various components usually used in the rubber industry in addition to the rubber component and BMI and TRBR.
- various components include reinforcing fillers such as carbon black and silica, and inorganic fillers such as calcium carbonate, vulcanization accelerators, anti-aging agents, zinc oxide, stearic acid, softeners, and ozone.
- inorganic fillers such as calcium carbonate, vulcanization accelerators, anti-aging agents, zinc oxide, stearic acid, softeners, and ozone.
- additives such as deterioration inhibitors.
- thiazole vulcanization accelerators such as M (2-mercaptobenzothiazole), DM (dibenzothiazyl disulfide) and CZ (N-cyclohexyl-2-benzothiazylsulfenamide), TT Examples thereof include thiuram vulcanization accelerators such as (tetramethylthiuram sulfide) and guanidine vulcanization accelerators such as DPG (diphenylguanidine).
- the rubber composition for end coating of the present invention preferably has the following characteristics. That is, after vulcanization, the tensile stress at 100% elongation is 2.5 MPa (megapascal) or more, preferably 3.5 MPa or more.
- the tensile stress can be measured in accordance with JIS K6301-1995. If the tensile stress is too small, when used as a coating rubber, the strain of the belt layer at the time of constant stress, which is the input of the vehicle belt rubber of the tire, is increased, and the crack resistance tends to be lowered.
- the rubber composition for end coating of the present invention has a tan ⁇ of not more than 0.300, preferably not more than 0.250 when measured at a temperature of 25 ° C. under a strain of 2%.
- tan ⁇ is an index of hysteresis loss. The larger tan ⁇ , the higher the hysteresis loss and the greater the amount of heat generated. That is, when tan ⁇ increases, the heat resistance of the rubber composition tends to decrease.
- Tan ⁇ can be measured, for example, using a viscoelasticity measuring apparatus (a spectrometer manufactured by Toyo Seiki Co., Ltd.) under a condition of frequency: 52 Hz.
- a heavy-duty tire according to the present invention uses the above-described end covering rubber composition for covering an end of a belt layer, and further includes an end portion of a steel cord coated with a steel cord coating rubber. It may be coated so as to be wrapped with an end covering rubber composition from above, or only the end portion of the steel cord is not covered with the coating rubber composition, but is covered so as to be wrapped with the end covering rubber composition.
- the belt has a coated cord layer.
- the steel cord may be any steel cord that has been conventionally used in the tire industry.
- the belt of the present invention may have other layers in addition to the steel cord and the coating rubber.
- the heavy load tire having the belt of the present invention is a tire used for a large vehicle, particularly a large construction vehicle, but can also be used for other heavy load vehicles.
- Example 1 to 8 and Comparative Examples 1 to 5 A rubber-coated cord layer in which a steel cord is embedded in the coating rubber composition shown in Table 1 is prepared, and the end portion is covered with 20 mm or more so as to be wrapped with each end coating rubber composition shown in Table 2.
- a tire having a belt obtained by laminating four layers was produced. About the rubber composition for edge part covering, each composition was knead
- the transpolybutadiene used in the rubber composition shown in Table 2 was prepared as follows. ⁇ Preparation of trans polybutadiene> A stainless steel reaction vessel equipped with a thermometer, a stirrer, a pressurizer, and an injection spout was prepared, and the inside of the vessel was replaced with nitrogen gas.
- TR-BR crystalline transpolybutadiene
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Abstract
Description
スチールコードコーティングゴムは、スチールコードとゴムの接着性が重要であり、被覆ゴムに使用するゴム組成物には、接着のための接着プロモータを添加したり、硫黄を比較的多く配合したりしている。しかし、セパレーション防止には接着性のみならず、高硬度、低発熱性、高破断物性、老化物性が良好、屈曲亀裂性が低い等の性質が必要であり、これらのうち、硬度高くすることがより有効である。硬度を増加させるために、従来、カーボンブラックなどの充填剤の配合量を増加する、樹脂などを添加する、硫黄などの架橋剤の配合量を増加する、加硫促進剤の配合量を増加する等の手段が取られている。しかしながら、これらの方法では、硬度は増加するが、低発熱性、耐久性、作業性や接着性が低下するなどの問題がある。
本発明で用いるスチールコードの端部を被覆する端部被覆用ゴム組成物は、天然ゴムとポリイソプレンを含有するものであるが、天然ゴムを50質量%以上含有することが好ましい。50質量%未満では接着特性およびゴム破壊特性の低下を招くことがあるからである。ゴム成分の残部としては、スチレン・ブタジエンゴム(SBR)、ポリブタジエン(BR)、ブチルゴム(IIR)、ハロゲン化ブチルゴム(X-IIR)、エチレン・プロピレン・ジエンゴム(EPDM)等が使用できる。
ビスマレイミドは、ビスマレイミド同士が重合すること及び天然ゴムなどのジエン系ポリマー間を硫黄を介さずに直接架橋するため、ゴムの低発熱性および耐劣化性を損なうことなく、ゴムの硬度を増加させることができる。ゴムを硬くすることでベルト端にかかる歪みを小さくすると共に、歪みをゴム-スチールコードからゴム-ゴム間に移すことにより、ゴム-スチールコードのセパレーションを防止する。また、ゴム被覆コード層及びベルト端部にコーティングゴムとは別のゴム組成物を被覆することで、コーティングゴムの硬度を上げることなく、端部の硬度を上げ、端部のセパレーションを効果的に抑止することができる。なお、コーティングゴムにトランスポリブタジエン(TRBR)及びビスマレイミド(BMI)を含有させた場合でも、ゴム-スチールコードのセパレーションを防止することができ、さらに、ゴム被覆コード層及びベルト端部に該ゴム組成物を被覆することで端部のセパレーションを防止できる。
トランスポリブタジエンとしては、トランス結合含量が82質量%~98質量%であることが好ましく、効果の点から86%~98%がさらに好ましい。また、その質量平均分子量が30,000~200,000であるときに、未加硫時の加工性を改良できると共に、加硫ゴムの耐破壊特性も維持することができる。
0.1質量部≦TRBR+BMI≦10.0質量部
TRBR/(TRBR+BMI)≧25%
であり、これはBMIが含まれないTRBR100%の場合も含む。
好ましくはゴム成分100重量部あたり、BMIとTRBR合わせて0.1質量部~7.0質量部、より好ましくは1.0質量部~7.0質量部である。
また、好ましくはBMIとTRBRの合計に対してTRBRが50%以上である。
実施例1~8及び比較例1~5
表1に示す配合のコーティングゴム組成物にスチールコードを埋設したゴム被覆コード層を作製し、その端部を表2に示す配合の各端部被覆用ゴム組成物で包み込むように20mm以上被い、これを4層積層したベルトを有するタイヤを作製した。
端部被覆用ゴム組成物について、各組成物を混練し、145℃で60分間加硫を行い、得られた加硫物を次の方法で物性を評価した。また、タイヤの耐疲労破壊性についても下記の方法で評価した。
評価結果を表2に示す。
〈トランスポリブタジエンの調製〉
温度計、攪拌装置、加圧装置、注入注出口を備えたステンレス製反応容器を用意し、この容器内を窒素ガスで置換した。この容器にブタジエン/ヘキサン溶液(23.7質量%ブタジエン)4086g、0.84mol/Lニッケルボロアシレート(以下、NiOBと称する)のヘキサン溶液12.0ml、0.62mol/Lトリブチルアルミニウム(以下、TIBALと称する)ヘキサン溶液49ml、トリフェニルホスファイト(以下、TPPと称する)のヘキサン溶液(TPPの原液2.64mlをヘキサン25mlで溶解したもの)約27ml、及びトリフルオロ酢酸(以下、TFAと称する)のヘキサン溶液(TFA15.6mlをヘキサン25mlで溶解したもの)約40mlを注入し、均一に混合して、80℃で6時間重合反応を行った。なお、触媒のモル比は、NiOB/TIBAL/TPP/TFA=1/3/1/20であった。
その後、過剰のイソプロパノールと老化防止剤の入った容器に、この溶液を注入し、重合を停止し再沈した。さらに、これをろ過し、50℃にて真空乾燥し、結晶性トランスポリブタジエン(以下、「TR-BR」と略記する)を得た。得られたTR-BRのトランス結合含有量は92%、質量平均分子量3.2×104であった。
試料として得られた加硫物をJIS K6301-1995に従って測定した。
得られた加硫物の試験片について、粘弾性測定装置(東洋精機社製スペクトロメーター)を用い、温度25℃;歪み2%;及び周波数52Hzの条件下で測定した。
試供タイヤに対して、一定速度、ステップロード条件のドラムテストを行い、ドラムテスト終了後のベルト端からの亀裂長さを測定し、比較例1の亀裂長さを100として測定値の逆数の指数化を行った。指数値が大きいほど亀裂長さが短く、耐疲労破壊性に優れることを示す。
*1:カーボンブラックN330
*2:ノックラック6C(大内新興化学工業社製)
*3:ナフテン酸コバルト
*4:ノクセラーDZ(大内新興化学工業社製)
*5:N,N’-(4,4’-ジフェニルメタン)ビスマレイミド
Claims (9)
- ビードコア、カーカスプライ、カーカスプライのラジアル方向外側に配置されたベルトとトレッドを備え、該ベルトがスチールコードをコーティングゴム中に埋設してなるゴム被覆コード層が積層されてベルトが形成された重荷重用タイヤにおいて、少なくとも1層のゴム被覆コード層端部またはベルト端部を天然ゴムとイソプレンゴムを含むゴム成分100質量部に対してトランスポリブタジエン(TRBR)とビスマレイミド(BMI)を下記の配合量で含むゴム組成物で被覆することを特徴とする重荷重用タイヤ。
0.1質量部≦TRBR+BMI≦10.0質量部
TRBR/(TRBR+BMI)≧25% - トランスポリブタジエン(TRBR)とビスマレイミド(BMI)の配合量が
0.1質量部≦TRBR+BMI≦7.0質量部
である請求項1に記載の重荷重用タイヤ。 - トランスポリブタジエン(TRBR)とビスマレイミド(BMI)の配合量が
1.0質量部≦TRBR+BMI≦7.0質量部
である請求項2に記載の重荷重用タイヤ。 - ビスマレイミド(BMI)の配合量が
0.1質量部≦BMI≦4.0質量部
である請求項1~3のいずれかに記載の重荷重用タイヤ。 - トランスポリブタジエン(TRBR)がトランスポリブタジエン(TRBR)とビスマレイミド(BMI)の総量に対して
TRBR/(TRBR+BMI)≧50%
である請求項1~4のいずれかに記載の重荷重用タイヤ。 - トランスポリブタジエンが、トランス結合含量が82質量%~98質量%であり、かつ質量平均分子量が30,000~200,000である請求項1~6のいずれかに記載の重荷重用タイヤ。
- ゴム被覆コード層端部又はベルト端部を被覆するゴム組成物が、加硫後に、JIS K6301-1995に従い測定した100%伸長時の引張応力2.5MPa以上、25℃で歪2%、52Hzの条件で測定したときのtanδが0.30以下である請求項1~6のいずれかに記載の重荷重用タイヤ。
- 2層以上のゴム被覆コード層の端部を被覆した請求項1~8のいずれかに記載の重荷重用タイヤ。
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
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ES09731034T ES2433746T3 (es) | 2008-04-10 | 2009-04-10 | Neumático para cargas pesadas |
JP2010507284A JP5404610B2 (ja) | 2008-04-10 | 2009-04-10 | 重荷重用タイヤ |
EP09731034.6A EP2281697B1 (en) | 2008-04-10 | 2009-04-10 | Tire for heavy loads |
BRPI0925409A BRPI0925409B1 (pt) | 2008-04-10 | 2009-04-10 | pneu para carga pesada |
CN2009801195428A CN102046395A (zh) | 2008-04-10 | 2009-04-10 | 重负载用轮胎 |
US12/936,797 US8672010B2 (en) | 2008-04-10 | 2009-04-10 | Tire for heavy load |
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JP2008102210 | 2008-04-10 | ||
JP2008-102210 | 2008-04-10 |
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WO2009125842A1 true WO2009125842A1 (ja) | 2009-10-15 |
Family
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PCT/JP2009/057367 WO2009125842A1 (ja) | 2008-04-10 | 2009-04-10 | 重荷重用タイヤ |
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US (1) | US8672010B2 (ja) |
EP (1) | EP2281697B1 (ja) |
JP (1) | JP5404610B2 (ja) |
CN (1) | CN102046395A (ja) |
BR (1) | BRPI0925409B1 (ja) |
ES (1) | ES2433746T3 (ja) |
WO (1) | WO2009125842A1 (ja) |
Cited By (3)
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JP2011225678A (ja) * | 2010-04-16 | 2011-11-10 | Bridgestone Corp | ゴム組成物、ベルトコーティングゴム及び空気入りタイヤ |
WO2015079659A1 (ja) * | 2013-11-28 | 2015-06-04 | 株式会社ブリヂストン | 空気入りタイヤ |
JP2016041779A (ja) * | 2014-08-15 | 2016-03-31 | 株式会社ブリヂストン | タイヤ用ゴム組成物及びタイヤ |
Families Citing this family (3)
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JP5557945B1 (ja) * | 2013-05-01 | 2014-07-23 | 株式会社ブリヂストン | タイヤ製造方法 |
US10040315B2 (en) * | 2013-06-24 | 2018-08-07 | Bridgestone Corporation | Pneumatic tire |
US11104180B2 (en) * | 2016-04-08 | 2021-08-31 | The Yokohama Rubber Co., Ltd. | Pneumatic tire |
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- 2009-04-10 US US12/936,797 patent/US8672010B2/en not_active Expired - Fee Related
- 2009-04-10 WO PCT/JP2009/057367 patent/WO2009125842A1/ja active Application Filing
- 2009-04-10 EP EP09731034.6A patent/EP2281697B1/en not_active Not-in-force
- 2009-04-10 JP JP2010507284A patent/JP5404610B2/ja not_active Expired - Fee Related
- 2009-04-10 BR BRPI0925409A patent/BRPI0925409B1/pt not_active IP Right Cessation
- 2009-04-10 ES ES09731034T patent/ES2433746T3/es active Active
- 2009-04-10 CN CN2009801195428A patent/CN102046395A/zh active Pending
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Also Published As
Publication number | Publication date |
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BRPI0925409B1 (pt) | 2019-12-31 |
BRPI0925409A2 (ja) | 2018-05-29 |
CN102046395A (zh) | 2011-05-04 |
EP2281697A4 (en) | 2011-09-28 |
EP2281697A1 (en) | 2011-02-09 |
JPWO2009125842A1 (ja) | 2011-08-04 |
US8672010B2 (en) | 2014-03-18 |
US20110030870A1 (en) | 2011-02-10 |
JP5404610B2 (ja) | 2014-02-05 |
ES2433746T3 (es) | 2013-12-12 |
EP2281697B1 (en) | 2013-08-21 |
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