The present invention relates to a pneumatic tire including an inner liner layer formed of a thermoplastic resin or a thermoplastic elastomer composition containing a blend of a thermoplastic resin and an elastomer. More specifically, the present invention relates to a pneumatic tire which is tree from air inclusion in bead parts and thus prevents curing failure attributable to the air inclusion.
Recently, it is proposed that a. film layer formed of a thermoplastic resin or a thermoplastic elastomer composition containing a blend of a thermoplastic resin and an elastomer be disposed as an inner liner layer on a tire inner surface.
In such a pneumatic tire, a carcass layer is laid between a pair of bead parts. An inner liner layer is disposed at a tire cavity side of the carcass layer. A tie rubber layer is interposed between the carcass layer and the inner liner layer to improve the adhesiveness between the two. Moreover, when chafers are provided to protect the respective bead parts, an end portion, on a tire cavity side, of each chafer is inserted between the carcass layer and the inner liner layer (see, for example, Patent Document 1).
However, when the end portion, on the tire cavity side, of the chafer 9 is disposed between the inner liner layer 7 and the tie rubber layer 8, a step formed on the basis of the thickness of the chafer 9 is likely to form air inclusion at a spot between the inner liner layer 7 and the tie rubber layer 8 in the bead part. If the air inclusion is present in the bead part in a high-temperature tire removed from the mold after curing, the inner liner layer 7 with a matrix of a thermoplastic resin expands in the air inclusion portion. This brings about a problem of curing failure.
Patent Document 1: Japanese patent application Kokai publication No. Hei 10-81108
An object of the present inventor is to provide a pneumatic tire: which has an inner liner layer formed of a thermoplastic resin or a thermoplastic elastomer composition containing a blend of a thermoplastic resin and an elastomer; and which, despite of this, is free from air inclusion in bead parts and is capable of preventing curing failure attributable to the air inclusion.
A pneumatic tire, of the present invention to accomplish the above object is a pneumatic tire including: a carcass layer laid between a pair of bead parts; an inner liner layer disposed at a tire cavity side of the carcass layer; a tie rubber layer interposed between the carcass layer and the inner liner layer; and chafers for protecting the respective bead parts, an end portion on a tire cavity side of each chafer being inserted between the carcass layer and the inner liner layer. The pneumatic tire is characterized in that: the inner liner layer is formed of a thermoplastic resin or a thermoplastic elastomer composition containing a blend of a thermoplastic resin and an elastomer; and the tie rubber layer is disposed between the inner liner layer and each chafer.
In the present invention, a pneumatic tire has an end portion, on a tire cavity side, of each chafer for protecting a corresponding bead part being inserted between a carcass layer and an inner liner layer. When the inner liner layer is formed of a thermoplastic resin or a thermoplastic elastomer composition, a tie rubber layer is disposed between the inner liner layer and the chafer. Thereby, air inclusion is prevented from being generated between the inner liner layer and the tie rubber layer in the bead part. Thus, the tire is capable of preventing curing failure attributable to the it inclusion.
In the present invention, the position of each lower end of the inner liner layer is preferably located outward of a corresponding bead toe in a tire radial direction. This is because of the following reason. An inner liner layer with a matrix of a thermoplastic resin has a higher rigidity than that formed of a butyl rubber. As a result, if the inner liner layer has such a dimension that the inner liner layer extends beyond the bead toe, a wrinkle is formed in the inner liner layer when a carcass layer is wound up around a bead core in building a tire. Meanwhile, the position of each lower end of the liner layer is preferably located within a region not more than 35% of a cross-sectional height of the tire. By this, the air permeation preventive function can be sufficiently demonstrated.
The position of each lower end of the tie rubber layer is preferably located at the same level as the position of the corresponding lower end of the inner liner layer, or located inward thereof in the tire radial direction. This makes it possible to more surely avoid air inclusion. In addition, a height ht measured in the tire radial direction from each bead toe to the position in the corresponding lower end of tine tie rubber layer and a height hb measured in the tire radial direction from the bead. toe to the position of an innermost diameter of the corresponding bead core preferably have a relationship of ht≧hb/2. This is because of the following reason. If a tie rubber layer generally not blended with an antioxidant is present in the vicinity of the bead toe without being covered with an inner liner layer, the physical properties of this portion are deteriorated through ozone degradation or the like. Thereby, the bead toe is easy to crack when the tire is fitted onto or removed from a rim. By satisfying the relationship of ht≧hb/2, it is possible to prevent the bead toe from cracking when the tire is fitted onto or removed from the rim. Furthermore, in order to prevent the bead toe from cracking when the tire is fitted onto or removed from the rim, it is effective to blend a rubber composition forming the tie rubber layer and an antioxidant.
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Hereinafter, a constitution of the present invention will be described in detail with reference to the attached drawings.
In
An inner liner layer 7 formed of thermoplastic resin or a thermoplastic elastomer composition is disposed at a tire cavity side of the carcass layer 4 in such manner that the inner liner layer 7 substantially covers the tire inner surface. Furthermore, a tie rubber layer 3 is interposed between the carcass layer 4 and the inner liner layer 7. Chafers 9 for protecting the respective bead carts 3 are each formed of a sheet member obtained by coating uniformly aligned reinforcing cords or reinforcing fabric with a rubber, a sheet member made of a rubber composition blended with short fibers, a sheet member made of a rubber composition superior in wear resistance to the peripheral rubber members, or the like. The thickness of the chafer 9 is normally set in a range of 0.3 mm. to 2.0 mm. The chafer 9 is disposed in a manner to cover an inner periphery side portion of the bead part 3 that comes into contact with a rim seat. An end portion, on a tire cavity side, of the chafer 9 is inserted between the carcass layer 4 and the inner liner layer 7. More specifically, as shown in
Meanwhile, in the tread part 1, multiple belt layers 10 are buried on an outer peripheral side of the carcass layer 4. These belt layers 10 are disposed in such a manner that: reinforcing cords thereof incline to a tire circumferential direction; and the reinforcing cords of one layer intersect the reinforcing cords of another layer. Furthermore, a belt reinforcing layer formed by continuously winding reinforcing cords in the tire circumferential direction may be disposed on an outer peripheral side of the belt layers 10.
In the pneumatic tire, the end portion, on the tire cavity side, of the chafer 9 for protecting the corresponding bead part 3 is inserted between the carcass layer 4 and the inner liner layer 7. Moreover, when the inner liner layer 7 is formed of the thermoplastic resin or the thermoplastic elastomer composition, the tie rubber layer 3 is disposed between the inner liner layer 7 and the chafer 9. Accordingly, the pneumatic tire prevents air inclusion from being generated between the inner liner layer 7 and the tie rubber layer 8 in the bead part 3. Thus, the tire, is capable of preventing curing failure attributable to such air inclusion.
In the pneumatic tire, as shown in
It is desirable that, as shown in
As shown in
The pneumatic tire can be obtained, for example, by: disposing a cylindrical inner liner layer around a making drum; bonding thereon tire constituent members such as a tie rubber layer, chafers, a carcass layer, bead cores, bead fillers, and side-wall rubbers to build a primary green tire; bonding thereto belt layers and a tread rubber while expanding the primary green tire in a toroidal shape to build a secondary green tire; and then curing the secondary green tire. Thus, the position 7e of the lower end of the inner liner layer 7 and the position Se of the lower end of the tie rubber layer 8 can be set arbitrarily based on the width (dimension in a drum axial direction) of each member.
As another approach to prevent the bead toe T from cracking when the tire is fitted onto or removed from the rim, it is effective to blend a rubber composition forming the tie rubber layer 8 with an antioxidant. Examples of such an antioxidant include para-phenylenediamines [for example, N-phenyl-N′-isopropyl-p-phenylenediamine, N-phenyl-N′-(1,3-dimethylbutyl)-p-phenylenediamine, and N,N′-diphenyl-p-phenylenediamine], diphenylamines [for example, alkylated diphenylamine mixtures], amine-ketone reaction products [for example, poly(1,2-dihydro-2,2,4-trimethylquinoline) and 6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline], imidazoles [for example, 2-mercaptobenzimidazole and 2-mercaptomethylbenzimidazole], monophenols [for example, mono(α-methylbenzyl)phenol, and 2,6-di-t-butyl-4-methylphenol], bisphenols [for example, 2,2′-methylenebis(4-methyl-6-t-butylphenol], special waxes [for example, paraffin waxes], and the like. Additionally, in the rubber composition forming the tie rubber layer 8, the amount of the antioxidant blended with 100 parts by weight of the rubber is desirably 8.0 to 5.0 parts by weight.
Hereinafter, the inner liner layer of the present invention will be described. The inner liner layer can he formed of a thermoplastic resin or a thermoplastic elastomer composition containing a blend of a thermoplastic resin and an elastomer.
Examples of the thermoplastic resin used in the present invention include polyamide resins [for example, nylon 6 (N6), nylon 66 (N66), nylon 46 (N46), nylon 11 (N11) , nylon 12 (N12), nylon 610 (N610), nylon 612 (N612), nylon 6/66 copolymers (N6/66), nylon 6/66/610 copolymers (N6/66/610), nylon MXD6, nylon 6T, nylon 6/6T copolymers, nylon 66/PP copolymers, and nylon 66/PPS copolymers], polyester resins [for example, aromatic polyesters such as polybutylene terephthalate (PBT), polyethylene terephthalate (PET), polyethylene isophthalate (PEI), polybutylene terephthalate/tetramethylene glycol copolymers, PET/PEI copolymers, polyarylate (PAR), polybutylene naphthalate (PBN), liquid crystal polyesters, and polyoxyalkylene diimide diacid/polybutylene terephthalate copolymers], polynitrile resins [for example, polyacrylonitrile (PAN), polymethacrylonitrile, acrylonitrile/styrene copolymers (AS), methacrylonitrile/styrene copolymers, and methacrylonitrile/styrene/butadiene copolymers], poly(meth)acrylate resins [for example, polymethyl methacrylate (PMMA), polyethyl methacrylate, ethylene-ethyl acrylate copolymers (EEA), ethylene-acrylic acid copolymers (EAA), and ethylene methylacrylate resins (EMA)], polyvinyl resins [for example, vinyl acetate (EVA), polyvinyl alcohol (PVA), vinyl alcohol/ethylene copolymers (EVOH), polyvinylidene chloride (PVDC), polyvinyl chloride (PVC), vinyl chloride/vinylidene chloride copolymers, and vinylidene chloride/methylacrylate copolymers], cellulose resins [for example, cellulose acetate and cellulose acetate butyrate], fluororesins [for example, polyvinylidene fluoride (PVDF), polyvinyl fluoride (PVF), polychlorofluoroethylene (PCTFE), and ethylene/tetrafluoroethylene copolymers (ETFE)], imide resins [for example, aromatic polyimide (PI)], and the like.
Examples of the elastomer used in the present invention include diene rubbers and their hydrogenated products [for example, NP, IR, epoxidized natural rubbers, SBR, BR (high-cis BR and low-cis PR) , NBR, hydrogenated NBR, and hydrogenated SBR], olefin rubbers [for example, ethylene propylene rubbers (EPDM, EPM), and maleic acid-modified ethylene propylene rubbers (M-EPM)], butyl rubber (IIR), copolymers of isobutylene and aromatic vinyl or diene monomer, acrylic rubbers (ACM), ionomers, halogen-containing rubbers [for example, Br-IIR, Cl-IIP, brominated isobutylene-p-methylstyrene copolymers (Br-IPMS), chloroprene rubbers (CR), hydrin rubbers (CHC, CHR), chlorosulfonated polyethylene (CSM), chlorinated polyethylene (CM), and maleic acid-modified chlorinated polyethylene (M-CM)], silicone rubbers (for example, methyl vinyl silicone rubbers, dimethyl silicone rubbers, and methylphenylvinyl silicone rubbers), sulfur-containing rubbers (for example, polysulfide rubbers), fluororubbers (for example, vinylidene fluoride rubbers, fluorine-containing vinyl ether rubbers, tetrafluoroethylene-propylene rubbers, fluorine-containing silicone rubbers, and fluorine-containing phosphazene rubbers), thermoplastic elastomers (for example, styrene elastomers, olefin elastomers, polyester elastomer, urethane elastomers, and polyamide elastomers), and the like.
In the thermoplastic elastomer composition used in the present invention, the component ratio or a thermoplastic resin component (A) to an elastomer component (B) may be appropriately set based on the balance between the thickness and the flexibility of the film layer. However, the preferable range is 10/90 to 90/10, further preferably 20/80 to 85/15 (in weight ratio).
The thermoplastic elastomer composition according to the present invention can be mixed with another polymer and a compounding agent such as a compatibilizer as a third component in addition to the above-described essential components (A) and (B). The purposes of mixing such a polymer are to improve the compatibility between the thermoplastic resin component and the elastomer component, to improve the film-molding processability of the material, to improve the heat resistance, to reduce cost, and so on. Examples of the material used for the polymer include polyethylene, polypropylene, polystyrene, ABS, SBS, polycarbonate, and the like.
The thermoplastic elastomer composition is obtained by melt-kneading the thermoplastic resin and the elastomer (uncured in the case of rubber) by use of a two-shaft kneading extruder or the like in advance; and dispersing the elastomer component in the thermoplastic resin forming a continuous phase. When the elastomer component is cured, a curing agent may be added during the kneading process to dynamically cure the elastomer. Although various compounding agents (except for the curing agent) may be added to the thermoplastic resin, or the elastomer component during the kneading process, it is preferable to premix the compounding agents before the kneading process. The kneader used for kneading the thermoplastic resin and the elastomer is not particularly limited. Examples of the kneader include a screw extruder, kneader, a banbury mixer, a two-shaft kneading extruder, and the like. Among these, a two-shaft kneading extruder is preferably used for kneading the resin component and the rubber component, and for dynamically kneading the rubber component. Furthermore, two or more types of kneaders may be used to successively knead the components. As the conditions for the melt kneading, it is desirable that the temperature should be equal to or higher than a temperature at which the thermoplastic resin melts. Meanwhile, the shear rate at the time of kneading a preferably 2500 to 7500 sec−1. The overall kneading time is 30 seconds to 10 minutes. When the curing agent is added, the curing time after the addition is preferably 15 seconds to 5 minutes. The thermoplastic elastomer composition produced by the above method is formed into a film by molding with a resin extruder or by calender molding. The film forming method may be a normal method by which the thermoplastic resin or the thermoplastic elastomer is formed into a film.
A thin film of the thermoplastic elastomer composition thus obtained has a structure in which tine elastomer is dispersed as a discontinuous phase in the matrix of the thermoplastic resin. By adopting the dispersed structure in such a state, it is possible to set the Young's modulus in a range of 1 to 500 MPa in the standard atmosphere specified by JIS K7100, and to provide an appropriate rigidity as tine tire constituent member.
The thermoplastic resin or the thermoplastic elastomer composition can be formed into a sheet or film to be buried in the tire as a single unit. Additionally, an adhesive layer may be stacked thereon to improve the adhesiveness to the adjacent rubber. Specific examples of an adhesive polymer forming the adhesive layer include: ultra-high-molecular-weight polyethylenes (UHMWPE) with a molecular weight of not less than one million, preferably not less than three million; acrylate copolymers, such as ethylene-ethyl acrylate copolymers (EEA), ethylene methyl acrylate resins (EMA), and ethylene acrylic-acid copolymers (EAA), as well as their maleic anhydride adducts; polypropylenes (PP) and their maleic-modified products; ethylene propylene copolymers and their maleic-modified products; polybutadiene resins and their anhydride maleic-modified products; styrene-butadiene-styrene copolymers (SBS); styrene-ethylene-butadiene-styrene copolymers (SEBS); fluoride-based thermoplastic resins; polyether-based thermoplastic resins; and the like. These can be molded into a sheet or film by a conventional method, for instance, by extrusion with a resin extruder. No specific restriction is imposed on the thickness of the adhesive layer. A smaller thickness of the adhesive layer serves better for the purpose of reducing the weight of the tire. It is preferable that the thickness thereof should be 5 μm to 150 μm.
Hereinabove, the preferable embodiment of the present invention has been described in detail. It should be understood, however, that various alterations, substitutions and replacements can be made within the range not departing from the spirit or scope of the present invention defined by the attached claims.
Pneumatic tires of Conventional Example and Examples 1 to 5 were prepared as follows. Each tire had a tire size of 225/40R18. Each tire included: a carcass layer laid between a pair of bead parts; an inner liner layer disposed at a tire cavity side of the carcass layer; a tie rubber layer interposed between the carcass layer and the inner liner layer; and chafers protecting the respective bead parts, an end portion on a tire cavity side of each chafer being inserted between the carcass layer and the inner liner layer. The inner liner layer was formed of a thermoplastic elastomer composition containing a blend of a thermoplastic resin (nylon 6,66) and an elastomer (brominated butyl rubber). The arrangement of the tie rubber layer and the chafers was made different among these examples. Note that: the thickness of the inner liner layer was 50 μm; the thickness of the tie rubber layer was 500 μm; and the thickness of the chafers was 0.7 mm.
In the tire of Conventional Example, each chafer was disposed between the tie rubber layer and the inner liner layer, as shown in
In the tire of Example 1, as shown in
In the tire of Example 2, as shown in
In the tire of Example 3, as shown in
In the tire of Example 4, as shown in
In the tire of Example 5, as shown in
These test tires were each evaluated on the curing failure and the durability of the bead. toe by the following testing methods. Table 1 shows the results.
For each of Conventional Example and Examples 1 to 5, 100 test tires were cured, and thereafter the inner surface side of each of the bead parts was visually observed. Thereby, the number of tires in which curing failure had occurred attributable to air inclusion was counted.
After left in a test room at a temperature of 50° C. and with an ozone concentration of 180 pphm for 2 weeks, each test tire was mounted on a wheel having a rim size of 18×8J, and was subjected to a 10,000-km running test using a drum testing machine under a condition in which: the tire was inflated with an air pressure of 240 kPa; and the maximum load for this air pressure was applied to the tire. After this running test, the test tire was removed from the rim. The inner surface side of each bead part was visually observed to evaluate the state of the bead toe. The evaluation results were indicated by “A” when the bead toe was not damaged at all, “B” when the bead toe was slightly damaged, and “C” when a large crack(s) was formed in the bead toe.
As learned from Table 1, any of the tires of Examples 1 to 5 had significant effects of prevention curing failure attributable to air inclusion in the bead parts comparison with the tires of Conventional Example. Examples 1 to 3 were favorable in the durability of the bead toe. With regard to Example 4, however, the durability of the bead toe was lowered because the position of each lower end of the tie rubber layer was at the same level as was the corresponding bead toe. Nevertheless, with regard to Example 5 with the same laminated structure as Example 4, the durability of the bead toe was improved because the rubber composition forming the tie rubber layer was blended with the antioxidant.
1 tread part
2 sidewall part
3 bead part
4 carcass layer
5 bead core
6 bead filler
7 inner liner layer
8 tie rubber layer
9 chafer
10 belt layer
Number | Date | Country | Kind |
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2008-287385 | Nov 2008 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP2009/068254 | 10/23/2009 | WO | 00 | 4/27/2011 |