PNEUMATIC TIRE AND METHOD FOR MANUFACTURING THE SAME, AND TIRE VULCANIZING BLADDER

Abstract

A method for manufacturing a pneumatic tire uses a tire vulcanizing bladder including a plurality of vent lines, and is characterized in that the pneumatic tire includes an inner liner on an inner surface thereof, the inner liner has an SIBS layer containing a styrene-isobutylene-styrene triblock copolymer, the SIBS layer has a thickness of more than or equal to 0.05 mm and less than or equal to 0.6 mm, the SIBS layer contains more than or equal to 0.5% by mass and less than or equal to 40% by mass of a polymer obtained by polymerization of a monomer unit having 4 carbon atoms, and the vent lines each include a first vent line at a part corresponding to from a tire bead toe part to a tire buttress part, and a second vent line at a part corresponding to from the tire buttress part to a tire crown part.

Claims

1. A pneumatic tire manufactured using a tire vulcanizing bladder, wherein said pneumatic tire includes an inner liner including a plurality of vent lines on an inner surface thereof, said inner liner having a styrene-isobutylene-styrene (SIBS) layer containing a styrene-isobutylene-styrene triblock copolymer, said SIBS layer having a thickness of more than or equal to 0.05 mm and less than or equal to 0.6 mm, and a styrene-isobutylene (SIB) layer containing an SIB diblock copolymer, said SIB layer having a thickness of more than or equal to 0.01 mm and less than or equal to 0.3 mm, and said vent lines each including a first vent line extending from a tire bead toe part to a tire buttress part and a second vent line extending from said tire buttress part to a tire crown part, wherein said SIB diblock copolymer is linear and has a weight-average molecular weight of equal to or more than 40,000 and less than or equal to 120,000 and a styrene unit content of equal to or more than 10% by mass and less than or equal to 35% by mass, a radially outer end of each first vent line is connected to a radially inner end of a respective second vent line, said first vent line and said second vent line have a shape of a convex part having a width of more than or equal to 0.5 mm and less than or equal to 3.0 mm formed on a surface of the inner liner on a side in contact with the vulcanizing bladder during the tire manufacturing process and a depth of more than or equal to 0.1 mm and less than or equal to 2.0 mm from the surface of the inner liner on a side in contact with the vulcanizing bladder during the tire manufacturing process, said first vent line and said second vent line having a convex part cross-sectional area of more than or equal to 0.025 mm.sup.2 and less than or equal to 6.0 mm.sup.2, said first vent line has an angle of more than or equal to 60 and less than or equal to 90 with respect to a tangent to a part corresponding to said tire bead toe part, and said second vent line includes a vent line 4b1 having an angle of .sub.1 and a vent line 4b2 having an angle of .sub.2 with respect to the tangent to the part corresponding to the tire bead toe part, the angle .sub.1 has an angle of more than or equal to 40 and less than or equal to 90 with respect to the tangent to the part corresponding to the tire bead toe part, the angle .sub.2 has an angle of more than 90 and less than or equal to 140 with respect to the tangent to the part corresponding to the tire bead toe part, and the angle , the angle .sub.1, and the angle .sub.2 have magnitudes satisfying a >.sub.1, .sub.1<.sub.2, and .sub.2>.

2. The pneumatic tire according to claim 1, wherein said SIBS layer contains more than or equal to 0.5% by mass and less than or equal to 40% by mass of a polymer obtained by polymerization of a monomer unit having 4 carbon atoms.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0026] FIG. 1 is a schematic cross sectional view of the right half of a pneumatic tire in accordance with one embodiment of the present invention.

[0027] FIG. 2 is a view showing a tire vulcanizing bladder in accordance with one embodiment of the present invention.

[0028] FIG. 3 is a schematic cross sectional view of vent lines in accordance with one embodiment of the present invention.

[0029] FIG. 4 shows views of the vent lines in accordance with one embodiment of the present invention.

[0030] FIG. 5 shows schematic cross sectional views of the vent lines in accordance with one embodiment of the present invention.

[0031] FIG. 6 shows views of the vent lines in accordance with one embodiment of the present invention.

[0032] FIG. 7 is a schematic cross sectional view of a polymer sheet in accordance with one embodiment of the present invention.

[0033] FIG. 8 is a schematic cross sectional view of a polymer laminate in accordance with one embodiment of the present invention.

[0034] FIG. 9 is a schematic cross sectional view of a polymer laminate in accordance with one embodiment of the present invention.

[0035] FIG. 10 is a schematic cross sectional view of a polymer laminate in accordance with one embodiment of the present invention.

[0036] FIG. 11 is a schematic cross sectional view of a polymer laminate in accordance with one embodiment of the present invention.

DESCRIPTION OF EMBODIMENTS

[0037] <Pneumatic Tire>

[0038] A structure of a pneumatic tire manufactured by a manufacturing method in accordance with the present invention will be described with reference to FIG. 1. A pneumatic tire 101 in accordance with the present invention is used for passenger cars, trucks and buses, and heavy-duty equipment. Pneumatic tire 101 has a crown part 102, a tire buttress part 110 continuing to a side edge of crown part 102, a sidewall part 103, and a bead part 104. Further, a bead core 105 is embedded in bead part 104. Also provided are a carcass 106 arranged to extend from one bead part 104 to the other bead part with each of opposite ends being folded back to latch bead core 105, and a belt layer 107 composed of two plies on an outer side of carcass 106 at the crown part. An inner liner 109 extending from one bead part 104 to the other bead part is disposed on a tire radial inner side of carcass 106. The two plies of belt layer 107, each being made of a steel cord or a cord of aramid fiber or the like, are arranged so that the cords intersect with each other and each form an angle of usually 5 to 30 with respect to a tire circumferential direction. Regarding the carcass, organic fiber cords made of polyester, nylon, aramid or the like are arranged at an angle of about 90 with respect to the tire circumferential direction, and a bead apex 108 extending from the top end of bead core 105 toward the sidewall is disposed in a region surrounded by the carcass and the folded part thereof. It is noted that an insulation may be disposed between inner liner 109 and carcass 106.

[0039] Inner liner 109 includes a part 109a corresponding to from a bead toe part 104a to tire buttress part 110, and a part 109b corresponding to from tire buttress part 110 to crown part 102. During tire vulcanization, part 109a of inner liner 109 corresponding to from bead toe part 104a to tire buttress part 110 comes into contact with first vent lines of a vulcanizing bladder described later, and part 109b of the inner liner corresponding to from tire buttress part 110 to tire crown part 102 comes into contact with second vent lines of the vulcanizing bladder described later.

[0040] The pneumatic tire manufactured using the vulcanizing bladder including a plurality of vent lines has inner liner 109 including a plurality of vent lines. In inner liner 109, first vent lines are formed from bead toe part 104a to tire buttress part 110, and second vent lines are formed from tire buttress part 110 to tire crown part 102. The first and second vent lines each have the shape of a convex part formed on a surface of the inner liner on a side in contact with the vulcanizing bladder. Since such a convex part is formed corresponding to a groove in the vulcanizing bladder, the convex part has a width of more than or equal to 0.5 mm and less than or equal to 3.0 mm, and a height of more than or equal to 0.1 mm and less than or equal to 2.0 mm. The convex part of the first and second vent lines has a cross sectional area of more than or equal to 0.025 mm.sup.2 and less than or equal to 6.0 mm.sup.2. The first vent line has an angle of more than or equal to 60 and less than or equal to 90 with respect to a tangent to a part corresponding to the tire bead toe part, the second vent line has an angle of more than or equal to 40 and less than or equal to 90 with respect to the tangent to the part corresponding to the tire bead toe part, and angle and angle have magnitudes satisfying .

[0041] In addition, the inner liner at least has an SIBS layer containing a styrene-isobutylene-styrene triblock copolymer, and the SIBS layer has a thickness of more than or equal to 0.05 mm and less than or equal to 0.6 mm. Such an SIBS layer preferably contains more than or equal to 0.5% by mass and less than or equal to 40% by mass of a polymer obtained by polymerization of a monomer unit having 4 carbon atoms. Inner liner 109 may include at least one of an SIS layer containing a styrene-isoprene-styrene triblock copolymer and an SIB layer containing a styrene-isobutylene diblock copolymer, in addition to the SIBS layer. When the SIS layer or the SIB layer is included, the SIS layer and the SIB layer have a total thickness of more than or equal to 0.01 mm and less than or equal to 0.3 mm.

[0042] The inner liner may have the SIBS layer and at least one of the SIS layer and the SIB layer, the SIS layer and the SIB layer may have a total thickness of more than or equal to 0.01 mm and less than or equal to 0.3 mm, and at least one of the SIBS layer, the SIS layer, and the SIB layer may contain more than or equal to 0.5% by mass and less than or equal to 40% by mass of a polymer obtained by polymerization of a monomer unit having 4 carbon atoms. The SIBS layer, the SIS layer, and the SIB layer will be described later.

[0043] By manufacturing the pneumatic tire using the tire vulcanizing bladder including the plurality of vent lines for the inner liner composed of the SIBS layer or the inner liner composed of the SIBS layer and the SIS layer and/or the SIB layer as described above, it is possible to manufacture a pneumatic tire which discharges gas between the bladder and an inner surface of the tire without damaging the inner liner in a tire vulcanization step, and exhibits excellent performance in the air-in phenomenon, flex crack adjustment, rolling resistance, and steering stability.

[0044] Hereinafter, the tire vulcanizing bladder used to manufacture the pneumatic tire in accordance with the present invention will be described.

[0045] <Tire Vulcanizing Bladder>

[0046] The vent lines of the tire vulcanizing bladder used in a method for manufacturing the pneumatic tire in accordance with the present invention will be described with reference to FIGS. 2 to 5. In FIG. 2, flange parts 2a, 2b are provided at both ends of a tire vulcanizing bladder 1, and a plurality of vent lines 4 are provided from one flange part 2a to the other flange part 2b.

[0047] Vent lines 4 each include a first vent line 4a at a part corresponding to from the tire bead toe part to the tire buttress part, and a second vent line 4b at a part corresponding to from the tire buttress part to the tire crown part. A dotted line B indicates a boundary between first vent lines 4a and second vent lines 4b.

[0048] In FIG. 3, first vent line 4a has angle of more than or equal to 60 and less than or equal to 90, preferably more than or equal to 80 and less than or equal to 90, with respect to a tangent T to a part A of the bladder corresponding to the tire bead toe part. When angle is less than 60, there is a large difference between a direction in which the bladder contracts and a direction of the vent lines, which may cause flaws resulting from rubbing of the bladder and the inner liner. It is noted that, concerning angle , since the maximum angle with respect to tangent T is 90, a value exceeding 90 is indicated as 180(the value exceeding)90. Accordingly, also in the case where angle is more than 90 and less than or equal to 120, angle satisfies the condition of more than or equal to 60 and less than or equal to 90.

[0049] Preferably, angle has a magnitude changed depending on material characteristics of a thermoplastic elastomer forming the inner liner of the tire. For example, when the thermoplastic elastomer has a low melting point, and a phenomenon in which the thermoplastic elastomer is softened is considerably observed at the time of completion of the vulcanization step during manufacturing of the tire, angle preferably has a larger magnitude. On the other hand, when the thermoplastic elastomer has a high melting point, and flaws resulting from rubbing of the bladder and the inner liner are less likely to occur, angle can have a smaller magnitude.

[0050] Second vent line 4b has angle of more than or equal to 40 and less than or equal to 90, preferably more than or equal to 45 and less than or equal to 90, with respect to tangent T to part A of the bladder corresponding to the tire bead toe part (indicated in FIG. 3 as an angle with respect to a line T parallel to tangent T). When angle is less than 40, there is a large difference between the direction in which the bladder contracts and the direction of the vent lines, which may cause flaws resulting from rubbing of the bladder and the inner liner. It is noted that, concerning angle , since the maximum angle with respect to tangent T is 90, a value exceeding 90 is indicated as 180(the value exceeding)90. Accordingly, also in the case where angle is more than 90 and less than or equal to 140, angle satisfies the condition of more than or equal to 40 and less than or equal to 90.

[0051] Preferably, angle has a magnitude smaller than 90 to prevent disturbance of arrangement of carcass cords in the tire buttress part.

[0052] Angle and angle have magnitudes satisfying . When angle and angle have magnitudes satisfying <, the gas between the inner surface of the tire and the bladder may not be fully discharged during the tire vulcanization step. FIGS. 4(a) to 4(e) show exemplary vent lines satisfying the condition for angle and angle .

[0053] FIG. 4(a) shows the vent lines when angle is 90 and angle is 90.

[0054] FIG. 4(b) shows the vent lines when angle is 90 and angle is 60.

[0055] FIG. 4(c) shows the vent lines when angle is 90 and angle is 40.

[0056] FIG. 4(d) shows the vent lines when angle is 60 and angle is 60.

[0057] FIG. 4(e) shows the vent lines when angle is 60 and angle is 40.

[0058] Shapes of a groove cross section of first vent line 4a and second vent line 4b will be described with reference to FIG. 5. In FIG. 5, a double arrow line W indicates a width of the groove cross section of the vent line, and a double arrow line H indicates a depth of the groove cross section of the vent line. A shaded area S indicates a groove cross sectional area of the vent line, and a double arrow line D indicates a distance between two adjacent vent lines.

[0059] In the present specification, the width of the groove cross section of the first and second vent lines means a width of the groove cross section on the same plane as a mold-side surface of the bladder. Accordingly, even if the shape of the groove cross section of the first and second vent lines is, for example, substantially semicircular or substantially triangular, and the width of the groove cross section of the first and second vent lines have different magnitudes depending on the distance from the surface of the bladder, the width of the groove cross section of the first and second vent lines means the width on the same plane as the mold-side surface of the bladder.

[0060] The width of the groove cross section of the first and second vent lines is more than or equal to 0.5 mm and less than or equal to 3.0 mm, and preferably more than or equal to 0.5 mm and less than or equal to 2.0 mm. When the width of the groove cross section of the first and second vent lines is less than 0.5 mm, lines having the shape of a convex part formed in the inner liner corresponding to a concave part for the bladder vent lines have a low strength, which may cause flaws resulting from rubbing of the bladder and the inner liner. On the other hand, when the width of the groove cross section of the first and second vent lines is more than 3.0 mm, the convex part formed in the inner liner corresponding to the concave part for the bladder vent lines has a larger volume, and weight saving of the tire may not be able to be achieved.

[0061] Here, the depth of the groove cross section of the first and second vent lines means a distance from the same plane as the mold-side surface of the bladder, at a part having the greatest distance in the vertical direction from the surface of the bladder. Accordingly, when the shape of the groove cross section of the first and second vent lines is, for example, substantially semicircular or substantially triangular, and the depth from the surface of the bladder is not constant, the depth of the groove cross section of the first and second vent lines means the distance at the part having the greatest distance from the surface of the bladder. Specifically, when the shape of the groove cross section of the first and second vent lines is substantially semicircular, the depth of the groove cross section of the first and second vent lines is indicated by double arrow line H in FIG. 5(b) or 5(e). When the shape of the groove cross section of the first and second vent lines is substantially triangular, the depth of the groove cross section of the first and second vent lines is indicated by double arrow line H in FIG. 5(c) or 5(f).

[0062] The depth of the groove cross section of the first and second vent lines is more than or equal to 0.1 mm and less than or equal to 2.0 mm, and preferably more than or equal to 0.5 mm and less than or equal to 1.5 mm. When the depth of the groove cross section of the first and second vent lines is less than 0.1 mm, the gas between the inner surface of the tire and the bladder may not be fully discharged during the tire vulcanization step. On the other hand, when the depth of the groove cross section of the first and second vent lines is more than 2.0 mm, the convex part formed in the inner liner corresponding to the concave part for the bladder vent lines has a larger volume, and weight saving of the tire may not be able to be achieved.

[0063] The groove cross sectional area of the first and second vent lines means an area of a part surrounded by a line forming a groove and a line connecting both ends of the line forming the groove on the same plane as the mold-side surface of the bladder, in the groove cross section. For example, when a description is given with reference to FIG. 5(a), groove cross sectional area S of the first and second vent lines is an area of a part surrounded by a line l.sub.1 forming a groove and a line l.sub.2 connecting both ends of the line forming the groove on the same plane as the surface of the bladder, in the groove cross section.

[0064] The groove cross sectional area of the first and second vent lines is more than or equal to 0.025 mm.sup.2 and less than or equal to 6.0 mm.sup.2, and preferably more than or equal to 0.05 mm.sup.2 and less than or equal to 5.0 mm.sup.2. When the groove cross sectional area of the first and second vent lines is less than 0.025 mm.sup.2, the gas between the inner surface of the tire and the bladder may not be fully discharged during the tire vulcanization step. On the other hand, when the groove cross sectional area of the first and second vent lines is more than 6.0 mm.sup.2, the convex part formed in the inner liner corresponding to the concave part for the bladder vent lines has a larger volume, and weight saving of the tire may not be able to be achieved.

[0065] The distance between two adjacent vent lines is not particularly limited as long as the gas between the inner surface of the tire and the bladder is fully discharged during the tire vulcanization step. The distance between two adjacent vent lines is preferably, for example, more than or equal to 2.0 mm and less than or equal to 6.0 mm, and more preferably more than or equal to 2.5 mm and less than or equal to 5.0 mm. When the distance between two adjacent vent lines is less than 2.0 mm, the convex part formed in the inner liner corresponding to the concave part for the bladder vent lines has a larger volume, and weight saving of the tire may not be able to be achieved. On the other hand, when the distance between two adjacent vent lines is more than 6.0 mm, the gas between the inner surface of the tire and the bladder may not be fully discharged during the tire vulcanization step.

[0066] Preferably, the shape of the groove cross section of the first and second vent lines is, for example, substantially rectangular shown in FIG. 5(a), substantially semicircular shown in FIG. 5(b), or substantially triangular shown in FIG. 5(c). Further, the shape of the groove cross section of the first and second vent lines can be, for example, substantially rectangular, substantially semicircular, or substantially triangular with corners rounded and chamfered as shown in FIGS. 5(d) to 5(f).

[0067] Vent lines having the second vent lines different in form from the first and second vent lines fabricated above will be described with reference to FIG. 6.

[0068] The second vent lines shown in FIGS. 6(a) and 6(b) each include a vent line 4b.sub.1 having an angle of .sub.1 and a vent line 4b.sub.2 having an angle of .sub.2 with respect to tangent T to part A of the bladder corresponding to the tire bead toe part (indicated in FIGS. 6(a) and 6(b) as angles with respect to line T parallel to tangent T). The effect of discharging gas can be enhanced by forming two second vent lines having different angles with respect to tangent T.

[0069] When angle .sub.1 and angle .sub.2 have magnitudes satisfying .sub.1.sub.2, angle .sub.1 has an angle of more than or equal to 40 and less than or equal to 90, preferably more than or equal to 45 and less than or equal to 90, with respect to tangent T to part A of the bladder corresponding to the tire bead toe part. On the other hand, when measured in the same direction as angle .sub.1, angle .sub.2 has an angle of more than 90 and less than or equal to 140, preferably more than 90 and less than or equal to 135, with respect to tangent T.

[0070] Angle of the first vent line with respect to tangent T to part A of the bladder corresponding to the tire bead toe part, angle .sub.1, and angle .sub.2 have magnitudes satisfying .sub.1 and .sub.2. When the relation among the magnitudes of angle , angle .sub.1, and angle .sub.2 is not satisfied, the gas between the inner surface of the tire and the bladder may not be fully discharged during the tire vulcanization step.

[0071] FIGS. 6(a) and 6(b) show exemplary vent lines satisfying the above condition for angle , angle .sub.1, and angle .sub.2. FIG. 6(a) shows the vent lines when angle is 90, angle .sub.1 is 40, and angle .sub.2 is 140. FIG. 6(b) shows the vent lines when angle is 60, angle .sub.1 is 40, and angle .sub.2 is 140.

[0072] <Inner Liner>

[0073] The inner liner used for the pneumatic tire in accordance with the present invention may be a single-layer polymer sheet as shown in FIG. 7, or a multi-layer polymer laminate as shown in FIGS. 8 to 11. Both in the case where the inner liner is a single-layer polymer sheet and in the case where the inner liner is a multi-layer polymer laminate, the first vent lines are formed from bead toe part 104a to tire buttress part 110, and the second vent lines are formed from tire buttress part 110 to tire crown part 102.

[0074] <Inner Liner Composed of Single-layer Polymer Sheet>

[0075] As shown in FIG. 7, a polymer sheet 10a is made of an SIBS layer 11a containing a styrene-isobutylene-styrene triblock copolymer (hereinafter also referred to as SIBS).

[0076] (SIBS Layer)

[0077] SIBS layer 11a contains more than or equal to 0.5% by mass and less than or equal to 40% by mass of a polymer obtained by polymerization of a monomer unit having 4 carbon atoms. When the content of the polymer obtained by polymerization of a monomer unit having 4 carbon atoms is less than 0.5% by mass, vulcanization adhesive strength with the carcass or the insulation may be reduced, and when the content of the polymer is more than 40% by mass, air permeation resistance may be reduced, further reducing viscosity, which may cause deterioration in extrusion moldability. The content of the polymer is preferably more than or equal to 5% by mass and less than or equal to 20% by mass. On the other hand, the content of the SIBS in SIBS layer 11a is preferably more than or equal to 60% by mass and less than or equal to 99.5% by mass. When the content of the SIBS is less than 60% by mass, air permeation resistance may be reduced, and when the content of the SIBS is more than 99.5% by mass, vulcanization adhesive strength with the carcass or the insulation may be reduced. Therefore, both the cases are not preferred. The content of the SIBS is more preferably more than or equal to 80% by mass and less than or equal to 95% by mass.

[0078] The SIBS layer may contain a rubber component and sulfur, in addition to the SIBS described above. By adding a rubber component and sulfur to the SIBS and mixing them by heating, the rubber component and sulfur produce a vulcanization reaction during mixing by heating to form a sea-island structure in which the SIBS serves as a matrix (sea), and the rubber component serves as an island.

[0079] The SIBS layer having the sea-island structure has air shutoff properties originating in a matrix phase composed of the SIBS. Further, the rubber component constituting an island phase has tackiness before vulcanization with an adjacent member containing a rubber component, and vulcanization adhesiveness with the adjacent member because of the vulcanization reaction produced with the rubber component of the adjacent member during mixing by heating. Therefore, when the SIBS layer is used for the inner liner, the inner liner has excellent air shutoff properties, and has tackiness before vulcanization and vulcanization adhesiveness with the adjacent member.

[0080] Further, the SIBS content in a polymer component contained in the SIBS layer is preferably more than or equal to 5% by mass and less than or equal to 40% by mass. When the SIBS content is less than 5% by mass, air shutoff properties of the polymer sheet may deteriorate. On the other hand, when the SIBS content is more than 40% by mass, vulcanization adhesive strength with an adjacent member may be insufficient. The SIBS content is more preferably more than or equal to 10% by mass and less than or equal to 30% by mass of the polymer component, from the viewpoint of ensuring air shutoff properties. Preferably, the SIBS layer contains a polymer component containing, in addition to the SIBS described above, more than or equal to 60% by mass and less than or equal to 95% by mass of a rubber component of at least one kind selected from the group consisting of natural rubber, isoprene rubber, and butyl rubber, and more than or equal to 0.1 part by mass and less than or equal to 5 parts by mass of sulfur with respect to 100 parts by mass of the polymer component.

[0081] The thickness of SIBS layer 11a is more than or equal to 0.05 and less than or equal to 0.6 mm. When the thickness of SIBS layer 11a is less than 0.05 mm, the SIBS layer may be broken by a pressing pressure during vulcanization of a green tire in which the polymer sheet is used as the inner liner, and thus an air leak phenomenon may occur in the resultant tire. On the other hand, when the thickness of SIBS layer 11a is more than 0.6 mm, tire weight increases and fuel efficiency performance deteriorates. The thickness of SIBS layer 11a is more preferably more than or equal to 0.05 mm and less than or equal to 0.4 mm.

[0082] SIBS layer 11a can be obtained by a conventional method of forming a thermoplastic resin and a thermoplastic elastomer into a sheet. For example, SIBS layer 11a can be obtained by performing extrusion molding or calender molding on the SIBS.

[0083] With reference to FIG. 1, when polymer sheet 10a is used as inner liner 109 in pneumatic tire 101, SIBS layer 11a can be vulcanization-bonded with carcass 106 in the tire vulcanization step. Therefore, resultant pneumatic tire 101 can prevent the air-in phenomenon and have excellent air permeation resistance, since inner liner 109 is satisfactorily bonded with a rubber layer of carcass 106.

[0084] (Styrene-Isobutylene-Styrene Triblock Copolymer: SIBS)

[0085] Because of an isobutylene block of an SIBS, a polymer sheet containing the SIBS has excellent air permeation resistance. Therefore, when a polymer sheet containing an SIBS is used for an inner liner, a pneumatic tire having excellent air permeation resistance can be obtained.

[0086] Further, the SIBS has excellent durability since a molecular structure other than those of aromatic molecules is completely saturated and therefore deterioration and hardening are suppressed. Therefore, when a polymer sheet containing the SIBS is used for the inner liner, a pneumatic tire having excellent durability can be obtained.

[0087] When a pneumatic tire is manufactured by using a polymer sheet containing the SIBS for the inner liner, a halogenated rubber having high specific gravity (for example, halogenated butyl rubber), which has been conventionally used to impart air permeation resistance, is not used, since air permeation resistance can be ensured by containing the SIBS. Even if the halogenated rubber is used, the amount of use can be reduced. This enables weight saving of the tire and achieves the effect of improving fuel efficiency.

[0088] Although there is no particular limitation on the molecular weight of the SIBS, the weight-average molecular weight obtained by a GPC measurement is preferably more than or equal to 50,000 and less than or equal to 400,000 in view of fluidity, the molding step, rubber elasticity, and the like. When the weight-average molecular weight is less than 50,000, tensile strength and tensile elongation may decrease. When the weight-average molecular weight is more than 400,000, extrusion moldability may deteriorate. Therefore, both the cases are not preferred.

[0089] The SIBS usually contains more than or equal to 10% by mass and less than or equal to 40% by mass of a styrene unit. Since air permeation resistance and durability become more satisfactory, the content of the styrene unit in the SIBS is preferably more than or equal to 10% by mass and less than or equal to 30% by mass.

[0090] In the SIBS, a molar ratio of an isobutylene unit to a styrene unit (isobutylene unit/styrene unit) is preferably from 40/60 to 95/5 in view of the rubber elasticity of the copolymer. In the SIBS, the polymerization degree of each block is preferably from about 10,000 to 150,000 for an isobutylene block, and preferably from about 5,000 to 30,000 for a styrene block, in view of rubber elasticity and handling. When the polymerization degree of each block is less than 10,000, the SIBS becomes a liquid, and thus is not preferable.

[0091] The SIBS can be obtained by a conventional polymerization method for a vinyl-based compound and, for example, can be obtained by a living cationic polymerization method.

[0092] Japanese Patent Laying-Open No. 62-048704 and Japanese Patent Laying-Open No. 64-062308 disclose that living cationic polymerization of isobutylene with other vinyl compounds can be performed, and a polyisobutylene-based block copolymer can be manufactured by using isobutylene and other compounds as the vinyl compounds. In addition, a method for manufacturing a vinyl compound polymer by a living cationic polymerization method is described, for example, in U.S. Pat. No. 4,946,899, U.S. Pat. No. 5,219,948, and Japanese Patent Laying-Open No. 03-174403.

[0093] The SIBS does not have a double bond other than an aromatic double bond in the molecule and therefore has higher stability to ultraviolet rays than a polymer having a double bond in the molecule, such as polybutadiene, resulting in satisfactory weatherability.

[0094] (Rubber Component)

[0095] The SIBS layer may contain a rubber component. The rubber component provides the thermoplastic elastomer with tackiness before vulcanization with an adjacent member containing a rubber component. Further, because of the vulcanization reaction with sulfur, the rubber component can provide the thermoplastic elastomer with vulcanization adhesiveness with an adjacent member such as the carcass or the insulation.

[0096] The rubber component contains at least one kind selected from the group consisting of natural rubber, isoprene rubber, and butyl rubber, and particularly preferably contains natural rubber from the viewpoint of breaking strength and adhesiveness.

[0097] The content of the rubber component is preferably more than or equal to 60% by mass and less than or equal to 95% by mass of the polymer component in the SIBS layer. When the content of the rubber component is less than 60% by mass, the viscosity of the thermoplastic elastomer increases to cause deterioration in extrusion moldability, so that when fabricating the polymer sheet for the inner liner, the polymer sheet may not be able to be made thin. On the other hand, when the content of the rubber component is more than 95% by mass, air shutoff properties of the polymer sheet may deteriorate. The content of the rubber component is more preferably more than or equal to 70% by mass and less than or equal to 90% by mass of the polymer component, from the viewpoint of tackiness before vulcanization and vulcanization adhesiveness.

[0098] (Sulfur)

[0099] The SIBS layer can contain sulfur. As sulfur, sulfur generally used in the rubber industry for vulcanization may be used, and it is preferable to use insoluble sulfur. As used herein, insoluble sulfur refers to sulfur obtained by heating and rapidly cooling natural sulfur S.sub.8, and polymerizing it so as to become Sx (x=100,000 to 300,000). The use of insoluble sulfur can prevent blooming that would usually occur when sulfur is used as a rubber vulcanization agent.

[0100] The content of sulfur is preferably more than or equal to 0.1 part by mass and less than or equal to 5 parts by mass with respect to 100 parts by mass of the polymer component. When the content of sulfur is less than 0.1 part by mass, the vulcanization effect of the rubber component cannot be achieved. On the other hand, when the content of sulfur is more than 5 parts by mass, the hardness of the thermoplastic elastomer increases, and when the polymer sheet is used for the inner liner, the durability performance of the pneumatic tire may deteriorate. The content of sulfur is more preferably more than or equal to 0.3 part by mass and less than or equal to 3.0 parts by mass.

[0101] (Additive)

[0102] The SIBS layer can contain additives such as stearic acid, zinc oxide, an antioxidant, and a vulcanization accelerator.

[0103] Stearic acid functions as a vulcanization assistant for the rubber component. The content of stearic acid is preferably more than or equal to 1 part by mass and less than or equal to 5 parts by mass with respect to 100 parts by mass of the polymer component. When the content of stearic acid is less than 1 part by mass, the effect as a vulcanization assistant cannot be achieved. On the other hand, when the content of stearic acid is more than 5 parts by mass, the viscosity of the thermoplastic elastomer may be reduced, and the breaking strength may be reduced. Therefore, both the cases are not preferred. The content of stearic acid is more preferably more than or equal to 1 part by mass and less than or equal to 4 parts by mass.

[0104] Zinc oxide functions as a vulcanization assistant for the rubber component. The content of zinc oxide is preferably more than or equal to 0.1 part by mass and less than or equal to 8 parts by mass with respect to 100 parts by mass of the polymer component. When the content of zinc oxide is less than 0.1 part by mass, the effect as a vulcanization assistant cannot be achieved. On the other hand, when the content of zinc oxide is more than 8 parts by mass, the hardness of the thermoplastic elastomer increases, and when the polymer sheet is used for the inner liner, the durability performance of the pneumatic tire may deteriorate. The content of zinc oxide is more preferably more than or equal to 0.5 part by mass and less than or equal to 6 parts by mass.

[0105] An antioxidant has the function of preventing a series of degradations called aging, such as oxidation degradation, thermal degradation, ozone degradation, and fatigue degradation. Antioxidants are classified into a primary antioxidant composed of amines or phenols and a secondary antioxidant composed of sulfur compounds or phosphites. The primary antioxidant has the function of supplying hydrogen to various polymer radicals to stop a chain reaction of autooxidation, and the secondary antioxidant exhibits a stabilizing effect by turning hydroxyperoxide into stable alcohol.

[0106] The antioxidant includes amines, phenols, imidazoles, phosphors, thioureas, and the like.

[0107] Amines include phenyl--naphthylamine, 2,2,4-trimethyl-1,2-dihydroquinoline polymer, 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline, p, p-dioctyldiphenylamine, p,p-dicumyldiphenylamine, N,N-di-2-naphthyl-p-phenylenediamine, N,N-diphenyl-p-phenylenediamine, N-phenyl-N-isopropyl-p-phenylenediamine, N-phenyl-N-1,3-dimethylbutyl-p-phenylenediamine, N-(1,3-dimethylbutyl)-N-phenyl-p-phenylenediamine, and the like.

[0108] Phenols include 2,6-di-tert-butyl-4-methylphenol, 2,6-di-tert-butyl-4-methylphenol, styrenated methylphenol, 2,2-methylene bis (4-ethyl-6-tert-butylphenol), 2,2-methylene bis (4-methyl-6-tert-butylphenol), 4,4-butylidenebis (3-methyl-6-tert-butylphenol), 4,4-thiobis (3-methyl-6-tert-butylphenol), 2,5-di-tert-butyl-hydroquinone, 2,5-di-tert-amyl hydroquinone, and the like.

[0109] Imidazoles include 2-mercaptobenzimidazole, zinc salt of 2-mercaptobenzimidazole, nickel dibutyldithiocarbamate, and the like.

[0110] In addition, phosphors such as tris (nonylphenyl) phosphite, thioureas such as 1,3-bis (dimethylaminopropyl)-2-thiourea and tributyl thiourea, an antiozonant wax, and the like may be used.

[0111] One kind of the above-mentioned antioxidants may be used solely, or two or more kinds may be used in combination. Particularly, it is preferable to use N-(1,3-dimethylbutyl)-N-phenyl-p-phenylenediamine.

[0112] The content of the antioxidant is preferably more than or equal to 0.1 part by mass and less than or equal to 5 parts by mass with respect to 100 parts by mass of the polymer component. When the content of the antioxidant is less than 0.1 part by mass, the antioxidant effect cannot be achieved. On the other hand, when the content of the antioxidant is more than 5 parts by mass, the blooming phenomenon will occur in a thermoplastic resin composition. The content of the antioxidant is more preferably more than or equal to 0.3 part by mass and less than or equal to 4 parts by mass.

[0113] As the vulcanization accelerator, thiurams, thiazoles, thioureas, dithiocarbamates, guanidines, sulfenamides, and the like can be used.

[0114] Thiurams include tetramethylthiuram monosulfide, tetramethylthiuram disulfide, tetraethylthiuram disulfide, tetrabutylthiuram disulfide, dipentamethylenethiuram tetrasulfide, and the like.

[0115] Thiazoles include 2-mercaptobenzothiazole, dibenzothiazyl disulfide, N-cyclohexylbenzothiazole, N-cyclohexyl-2-benzothiazole sulfenamide, N-oxydiethylene-2-benzothiazole sulfenamide, N-tert-butyl-2-benzothiazole sulfenamide, N,N-dicyclohexyl-2-benzothiazole sulfenamide, N-tert-butyl-2-benzothiazolylsulfenamide, and the like.

[0116] Thioureas include N,N-diethylthiourea, ethylenethiourea, trimethylthiourea, and the like.

[0117] Dithiocarbamates include zinc dimethyldithiocarbamate, zinc diethyldithiocarbamate, zinc dibutyldithiocarbamate, sodium dimethyldithiocarbamate, sodium diethyldithiocarbamate, copper dimethyldithiocarbamate, iron (III) dimethyldithiocarbamate, selenium diethyldithiocarbamate, tellurium diethyldithiocarbamate, and the like.

[0118] Guanidines include di-o-tolylguanidine, 1,3-diphenylguanidine, 1-o-tolylbiguanide, di-o-tolylguanidine salt of dicatecholborate, and the like.

[0119] Sulfenamides include N-cyclohexyl-2-benzothiazyl sulfenamide, and the like.

[0120] One kind of the above-mentioned vulcanization accelerators may be used solely, or two or more kinds may be used in combination. Particularly, it is preferable to use dibenzothiazyl disulfide.

[0121] The content of the vulcanization accelerator is preferably more than or equal to 0.1 part by mass and less than or equal to 5 parts by mass with respect to 100 parts by mass of the polymer component. When the content of the vulcanization accelerator is less than 0.1 part by mass, the vulcanization acceleration effect cannot be achieved. On the other hand, when the content of the vulcanization accelerator is more than 5 parts by mass, the hardness of the thermoplastic resin composition increases, and when the polymer sheet is used for the inner liner, the durability performance of the pneumatic tire may deteriorate. In addition, the raw material cost of the thermoplastic resin composition increases. The content of the vulcanization accelerator is more preferably more than or equal to 0.3 part by mass and less than or equal to 4 parts by mass.

[0122] (Polymer Obtained by Polymerization of Monomer Unit Having 4 Carbon Atoms)

[0123] SIBS layer 11a preferably contains a polymer obtained by polymerization of a monomer unit having 4 carbon atoms. The polymer contains a low molecular weight component, which can improve unvulcanization tack strength and vulcanization adhesive strength of the SIBS layer with another polymer sheet or rubber layer without degrading air permeation resistance originating in the SIBS. Therefore, using SIBS layer 11a containing that polymer for an inner liner part of the tire can improve adhesive strength with an adjacent rubber layer constituting a carcass or insulation, and prevent the air-in phenomenon between the inner liner and the carcass or between the inner liner and the insulation. Further, by improving vulcanization adhesive strength between the inner liner and the carcass or between the inner liner and the insulation as described above, interlayer rigidity can be enhanced, and thus steering stability can be improved.

[0124] The number-average molecular weight of the polymer obtained by polymerization of a monomer unit having 4 carbon atoms obtained by a GPC measurement is preferably more than or equal to 300 and less than or equal to 3,000, and more preferably more than or equal to 500 and less than or equal to 2,500. The weight-average molecular weight of that polymer obtained by a GPC measurement is preferably more than or equal to 700 and less than or equal to 100,000, and more preferably more than or equal to 1,000 and less than or equal to 80,000. The viscosity-average molecular weight of that polymer obtained by a FCC measurement is preferably more than or equal to 20,000 and less than or equal to 70,000, and more preferably more than or equal to 30,000 and less than or equal to 60,000.

[0125] The polymer obtained by polymerization of a monomer unit having 4 carbon atoms includes polybutene, polyisobutylene, and so forth.

[0126] Polybutene is a copolymer having a molecular structure of long chain hydrocarbon mainly composed of isobutene as a monomer unit, with normal butene being further used, and obtained by causing them to react with each other. Hydrogenated polybutene may also be used as polybutene.

[0127] Polyisobutylene is a copolymer having a molecular structure of long chain hydrocarbon composed of isobutene as a monomer unit and obtained by polymerization thereof

[0128] <Inner Liner Composed of Polymer Laminate>

Embodiment 1

[0129] FIG. 8 is a schematic cross sectional view showing an exemplary polymer laminate used for the inner liner in accordance with the present invention.

[0130] A polymer laminate 10b in accordance with the present embodiment has an SIBS layer 11b containing an SIBS and an SIS layer 12b containing a styrene-isoprene-styrene triblock copolymer (hereinafter also referred to as SIS). SIBS layer 11b has a thickness of more than or equal to 0.05 mm and less than or equal to 0.6 mm, as with the above.

[0131] (SIS Layer)

[0132] The SIS layer can be obtained by mixing the SIS, sulfur, and other additives with a Banbury mixer, and then forming the mixture into a sheet by a conventional method of forming a thermoplastic elastomer into a sheet, such as extrusion molding or calender molding.

[0133] The thickness of SIS layer 12b is more than or equal to 0.01 mm and less than or equal to 0.3 mm. When the thickness of SIS layer 12b is less than 0.01 mm, SIS layer 12b may be broken by a pressing pressure during vulcanization of a green tire in which the polymer sheet is used as the inner liner, and thus vulcanization adhesive strength may decrease. On the other hand, when the thickness of SIS layer 12b is more than 0.3 mm, tire weight increases and fuel efficiency performance deteriorates. The thickness of SIS layer 12b is more preferably more than or equal to 0.05 mm and less than or equal to 0.2 mm. The SIS layer can be obtained by forming the SIS into a sheet by a conventional method of forming a thermoplastic resin or a thermoplastic elastomer into a sheet, such as extrusion molding or calender molding.

[0134] With reference to FIG. 1, when polymer laminate 10b is used as inner liner 109 of pneumatic tire 101, if a surface in which SIBS layer 11b exists is arranged toward a tire radial innermost side, and a surface in which SIS layer 12b exists is arranged toward a tire radial outer side so as to contact carcass 106, SIS layer 12b and carcass 106 can be vulcanization-bonded in the tire vulcanization step. Therefore, the resultant pneumatic tire 101 can prevent the air-in phenomenon and have further excellent air permeation resistance and durability, since inner liner 109 is satisfactorily bonded with the rubber layer of carcass 106.

[0135] (Styrene-Isobutylene-Styrene Triblock Copolymer: SIBS)

[0136] As the SIBS and the polymer obtained by polymerization of a monomer unit having 4 carbon atoms, those as described above can be used. Therefore, the styrene-isoprene-styrene triblock copolymer will be described below.

[0137] (Styrene-Isoprene-Styrene Triblock Copolymer: SIS)

[0138] Since an isoprene block of a styrene-isoprene-styrene triblock copolymer is a soft segment, a polymer sheet containing the SIS is easily vulcanization-bonded with a rubber component. Therefore, when the polymer sheet containing the SIS is used for the inner liner, the inner liner is excellent in adhesiveness with an adjacent rubber constituting a carcass or an insulation, for example, and thus a pneumatic tire that can prevent the air-in phenomenon and present excellent durability can be obtained.

[0139] Although there is no particular limitation on the molecular weight of the SIS, the weight-average molecular weight obtained by the GPC measurement is preferably more than or equal to 100,000 and less than or equal to 290,000 in view of rubber elasticity and moldability. When the weight-average molecular weight is less than 100,000, tensile strength may decrease. When the weight-average molecular weight is more than 290,000, extrusion moldability may deteriorate. Therefore, both the cases are not preferred.

[0140] The content of a styrene unit in the SIS is preferably more than or equal to 10% by mass and less than or equal to 30% by mass in view of tackiness, adhesiveness, and rubber elasticity.

[0141] In the SIS, a molar ratio of an isoprene unit to a styrene unit (isoprene unit/styrene unit) is preferably from 90/10 to 70/30. In the SIS, the polymerization degree of each block is preferably from about 500 to 5,000 for an isoprene block, and preferably from about 50 to 1,500 for a styrene block, in view of rubber elasticity and handling.

[0142] The SIS can be obtained by a conventional polymerization method for a vinyl-based compound and, for example, can be obtained by a living cationic polymerization method.

[0143] (Polymer Obtained by Polymerization of Monomer Unit Having 4 Carbon Atoms)

[0144] When the polymer laminate includes SIBS layer 11b and SIS layer 12b as described above, at least one of SIBS layer 11b and SIS layer 12b contains more than or equal to 0.5% by mass and less than or equal to 40% by mass of the polymer obtained by polymerization of a monomer unit having 4 carbon atoms. Specifically, this applies to the cases in which: (a) SIBS layer 11b contains that polymer and SIS layer 12b does not; (b) SIBS layer 11b does not contain that polymer and SIS layer 12b does; and (c) both of SIBS layer 11b and SIS layer 12b contain that polymer. Among the cases (a) to (c), the case (c) is preferable in terms of high adhesive strength.

[0145] When SIBS layer 11b contains the polymer obtained by polymerization of a monomer unit having 4 carbon atoms, the content of each of the SIBS and the polymer is preferably more than or equal to 0.5% by mass and less than or equal to 40% by mass.

[0146] When SIS layer 12b contains the polymer obtained by polymerization of a monomer unit having 4 carbon atoms, the content of the polymer is preferably more than or equal to 0.5% by mass and less than or equal to 40% by mass. When the content of the polymer is less than 0.5% by mass, vulcanization adhesive strength with the carcass or the insulation may be reduced, and when the content of the polymer is more than 40% by mass, air permeation resistance may be reduced, further reducing viscosity, which may cause deterioration in extrusion moldability. Therefore, both the cases are not preferred. The content of the polymer is more preferably more than or equal to 5% by mass and less than or equal to 20% by mass. On the other hand, the SIS content in SIS layer 12b is preferably more than or equal to 60% by mass and less than or equal to 99.5% by mass. When the SIS content is less than 60% by mass, viscosity may be reduced, which may cause deterioration in extrusion moldability, and when the SIS content is more than 99.5% by mass, vulcanization adhesive strength with the carcass or the insulation may be reduced. Therefore, both the cases are not preferred. The SIS content is more preferably more than or equal to 80% by mass and less than or equal to 95% by mass.

Embodiment 2

[0147] FIG. 9 is a schematic cross sectional view showing an exemplary polymer laminate used for the inner liner in accordance with the present invention.

[0148] A polymer laminate 10c in accordance with the present embodiment has an SIBS layer 11c containing an SIBS and an SIB layer 13c containing a styrene-isobutylene diblock copolymer (hereinafter also referred to as SIB). Preferably, SIBS layer 11c has a thickness of more than or equal to 0.05 mm and less than or equal to 0.6 mm, as with the above.

[0149] (SIB Layer)

[0150] The SIB layer in accordance with the present embodiment can be obtained by mixing the SIB, sulfur, and other additives with a Banbury mixer, and then forming the mixture into a sheet by a conventional method of forming a thermoplastic resin or a thermoplastic elastomer into a sheet, such as extrusion molding or calender molding.

[0151] The thickness of SIB layer 13c is preferably more than or equal to 0.01 mm and less than or equal to 0.3 mm. When the thickness of SIB layer 13c is less than 0.01 mm, SIB layer 13c may be broken by a pressing pressure during vulcanization of a green tire in which the polymer sheet is used as the inner liner, and thus vulcanization adhesive strength may decrease. On the other hand, when the thickness of SIB layer 13c is more than 0.3 mm, tire weight increases and fuel efficiency performance deteriorates. The thickness of SIB layer 13c is more preferably more than or equal to 0.05 mm and less than or equal to 0.2 mm. The SIB layer can be obtained by forming the SIB into a sheet by a conventional method of forming a thermoplastic resin or a thermoplastic elastomer into a sheet, such as extrusion molding or calender molding.

[0152] With reference to FIG. 1, when polymer laminate 10c is used as inner liner 109 of pneumatic tire 101, if a surface in which SIBS layer 11c exists is arranged toward the tire radial innermost side, and a surface in which SIB layer 13c exists is arranged toward the tire radial outer side so as to contact carcass 106, SIB layer 13c and carcass 106 can be vulcanization-bonded in the tire vulcanization step. Therefore, the resultant pneumatic tire 101 can prevent the air-in phenomenon and have further excellent air permeation resistance and durability, since inner liner 109 is satisfactorily bonded with the rubber layer of carcass 106.

[0153] (Styrene-Isobutylene-Styrene Triblock Copolymer: SIBS)

[0154] As the SIBS and the polymer obtained by polymerization of a monomer unit having 4 carbon atoms, those as described above can be used. Hereinafter, the styrene-isobutylene diblock copolymer will be described.

[0155] (Styrene-Isobutylene Diblock Copolymer: SIB)

[0156] Since an isobutylene block of a styrene-isobutylene diblock copolymer is a soft segment, a polymer sheet containing the SIB is easily vulcanization-bonded with a rubber component. Therefore, when the polymer sheet containing the SIB is used for the inner liner, the inner liner is excellent in adhesiveness with an adjacent rubber constituting a carcass or an insulation, for example, and thus a pneumatic tire that can prevent the air-in phenomenon and present excellent durability can be obtained.

[0157] It is preferable to use one having a linear chain as the SIB in view of rubber elasticity and adhesiveness.

[0158] Although there is no particular limitation on the molecular weight of the SIB, the weight-average molecular weight obtained by the GPC measurement is preferably more than or equal to 40,000 and less than or equal to 120,000 in view of rubber elasticity and moldability. When the weight-average molecular weight is less than 40,000, tensile strength may decrease. When the weight-average molecular weight is more than 120,000, extrusion moldability may deteriorate. Therefore, both the cases are not preferred.

[0159] The content of a styrene unit in the SIB is preferably more than or equal to 10% by mass and less than or equal to 35% by mass in view of tackiness, adhesiveness, and rubber elasticity.

[0160] In the SIB, a molar ratio of an isobutylene unit to a styrene unit (isobutylene unit/styrene unit) is preferably from 90/10 to 65/35. In the SIB, the polymerization degree of each block is preferably from about 300 to 3,000 for an isobutylene block, and preferably from about 10 to 1,500 for a styrene block, in view of rubber elasticity and handling.

[0161] The SIB can be obtained by a conventional polymerization method for a vinyl-based compound and, for example, can be obtained by a living cationic polymerization method.

[0162] International Publication No. WO 2005/033035 discloses a manufacturing method in which methylcyclohexane, n-butyl chloride, and cumyl chloride are charged in a stirrer, cooled to 70 C. and thereafter reacted for 2 hours, and then the reaction is terminated by adding a large amount of methanol, and the reaction product is vacuum-dried at 60 C. to obtain an SIB.

[0163] (Polymer Obtained by Polymerization of Monomer Unit Having 4 Carbon Atoms)

[0164] At least one of SIBS layer 11c and SIB layer 13c contains more than or equal to 0.5% by mass and less than or equal to 40% by mass of the polymer obtained by polymerization of a monomer unit having 4 carbon atoms. Specifically, this applies to the cases in which: (a) SIBS layer 11c contains that polymer and SIB layer 13c does not; (b) SIBS layer 11c does not contain that polymer and SIB layer 13c does; and (c) both of SIBS layer 11c and SIB layer 13c contain that polymer. Among the cases (a) to (c), the case (c) is preferable in terms of high adhesive strength.

[0165] When SIBS layer 11c contains the polymer obtained by polymerization of a monomer unit having 4 carbon atoms, the content of each of the SIBS and the polymer is preferably more than or equal to 0.5% by mass and less than or equal to 40% by mass.

[0166] When SIB layer 13c contains the polymer obtained by polymerization of a monomer unit having 4 carbon atoms, the content of the polymer is preferably more than or equal to 0.5% by mass and less than or equal to 40% by mass. When the content of the polymer is less than 0.5% by mass, vulcanization adhesive strength with the carcass or the insulation may be reduced, and when the content of the polymer is more than 40% by mass, air permeation resistance may be reduced, further reducing viscosity, which may cause deterioration in extrusion moldability. Therefore, both the cases are not preferred. The content of the polymer is more preferably more than or equal to 5% by mass and less than or equal to 20% by mass. On the other hand, the SIB content in SIB layer 13c is preferably more than or equal to 60% by mass and less than or equal to 99.5% by mass. When the SIB content is less than 60% by mass, viscosity may be reduced, which may cause deterioration in extrusion moldability, and when the SIB content is more than 99.5% by mass, vulcanization adhesive strength with the carcass or the insulation may be reduced. Therefore, both the cases are not preferred. The SIB content is more preferably more than or equal to 80% by mass and less than or equal to 95% by mass.

[0167] Instead of the SIS layer in Embodiment 1 and the SIB layer in Embodiment 2, an elastomer layer composed of a thermoplastic elastomer may be provided. Such an elastomer layer can contain a thermoplastic elastomer of at least one kind selected from the group consisting of: a styrene-butadiene-styrene triblock copolymer; a styrene-isoprenebutadiene-styrene triblock copolymer; a styrene-ethylenebutene-styrene triblock copolymer; a styrene-ethylenepropylene-styrene triblock copolymer; a styrene-ethyleneethylenepropylene-styrene triblock copolymer; and a styrene-butadienebutylene-styrene triblock copolymer. It is noted that these thermoplastic elastomers may be epoxy-modified thermoplastic elastomers having an epoxy group.

[0168] The SIS layer, the SIB layer, and the elastomer layer described above can contain additives such as stearic acid, zinc oxide, an antioxidant, and a vulcanization accelerator.

[0169] The content of stearic acid is preferably more than or equal to 1 part by mass and less than or equal to 5 parts by mass with respect to 100 parts by mass of a polymer component. When the content of stearic acid is less than 1 part by mass, vulcanization may not occur. On the other hand, when the content of stearic acid is more than 5 parts by mass, the breaking strength of a thermoplastic resin composition may deteriorate. The content of stearic acid is more preferably more than or equal to 1 part by mass and less than or equal to 4 parts by mass.

[0170] The content of zinc oxide is preferably more than or equal to 0.1 part by mass and less than or equal to 8 parts by mass with respect to 100 parts by mass of the polymer component. When the content of zinc oxide is less than 0.1 part by mass, vulcanization may not occur. On the other hand, when the content of zinc oxide is more than 8 parts by mass, the hardness of the thermoplastic resin composition may increase, and durability may deteriorate. The content of zinc oxide is more preferably more than or equal to 0.5 part by mass and less than or equal to 6 parts by mass.

[0171] The content of the antioxidant is preferably more than or equal to 0.1 part by mass and less than or equal to 5 parts by mass with respect to 100 parts by mass of the polymer component. When the content of the antioxidant is less than 0.1 part by mass, the antioxidant effect may not be able to be achieved. On the other hand, when the content of the antioxidant is more than 5 parts by mass, the blooming phenomenon may occur. The content of the antioxidant is more preferably more than or equal to 0.3 part by mass and less than or equal to 4 parts by mass.

[0172] The content of the vulcanization accelerator is preferably more than or equal to 0.1 part by mass and less than or equal to 5 parts by mass with respect to 100 parts by mass of the polymer component. When the content of the vulcanization accelerator is less than 0.1 part by mass, the vulcanization acceleration effect may not be able to be achieved. On the other hand, when the content of the vulcanization accelerator is more than 5 parts by mass, the hardness of the thermoplastic resin composition may increase, and durability may deteriorate. In addition, the raw material cost of the thermoplastic resin composition increases. The content of the vulcanization accelerator is more preferably more than or equal to 0.3 part by mass and less than or equal to 4 parts by mass.

Embodiment 3

[0173] FIG. 10 is a schematic cross sectional view showing an exemplary polymer laminate used for the inner liner in accordance with the present invention.

[0174] A polymer laminate 10d in accordance with the present embodiment has an SIBS layer 11d containing an SIBS, an SIS layer 12d containing an SIS, and an SIB layer 13d containing an SIB. SIBS layer 11d, SIS layer 12d, and SIB layer 13d are stacked in the above order. Further, in addition to SIBS layer 11d, SIS layer 12d, and SIB layer 13d, a rubber composition layer made of, for example, urethane rubber or silicone rubber can be included. In this case, the rubber composition layer is preferably arranged between SIBS layer 11d and SIS layer 12d, between SIBS layer 11d and SIB layer 13d, or between SIS layer 12d and SIB layer 13d.

[0175] The thickness of SIBS layer 11c is preferably more than or equal to 0.05 mm and less than or equal to 0.6 mm. SIS layer 12d and SIB layer 13d have a total thickness of more than or equal to 0.01 mm and less than or equal to 0.3 mm. When the total thickness of SIS layer 12d and SIB layer 13d is less than 0.01 mm, SIS layer 12d and SIB layer 13d may be broken by a pressing pressure during vulcanization of a green tire in which the polymer sheet is used as the inner liner, and thus vulcanization adhesive strength may decrease. On the other hand, when the total thickness of SIS layer 12d and SIB layer 13d is more than 0.3 mm, tire weight increases and fuel efficiency performance deteriorates. The total thickness of SIS layer 12d and SIB layer 13d is more preferably more than or equal to 0.05 mm and less than or equal to 0.2 mm.

[0176] With reference to FIG. 1, when polymer laminate 10d is used as inner liner 109 of pneumatic tire 101, if a surface in which SIBS layer 11d exists is arranged toward the tire radial innermost side, and a surface in which SIB layer 13d exists is arranged toward the tire radial outer side so as to contact carcass 106, SIB layer 13d and carcass 106 can be vulcanization-bonded in the tire vulcanization step. Therefore, the resultant pneumatic tire 101 can prevent the air-in phenomenon and have further excellent air permeation resistance and durability since inner liner 109 is satisfactorily bonded with the rubber layer of carcass 106.

[0177] As the SIBS, the SIS, the SIB, and the polymer obtained by polymerization of a monomer unit having 4 carbon atoms, those as described above can be used.

[0178] (Polymer Obtained by Polymerization of Monomer Unit Having 4 Carbon Atoms)

[0179] In the present embodiment, at least one of SIBS layer 11d, SIS layer 12d, and SIB layer 13d contains more than or equal to 0.5% by mass and less than or equal to 40% by mass of the polymer obtained by polymerization of a monomer unit having 4 carbon atoms. Specifically, this applies to the cases in which: (a) only SIBS layer 11d contains that polymer; (b) only SIS layer 12d contains that polymer; (c) only SIB layer 13d contains that polymer; (d) SIBS layer 11d and SIS layer 12d contain that polymer, and SIB layer 13d does not; (e) SIBS layer 11d and SIB layer 13d contain that polymer, and SIS layer 12d does not; (0 SIS layer 12d and SIB layer 13d contain that polymer, and SIBS layer 11d does not; and (g) all of SIBS layer 11d, SIS layer 12d, and SIB layer 13d contain that polymer. Among the cases (a) to (g), the case (d) is preferable in terms of high adhesive strength and low cost.

[0180] When SIBS layer 11d contains the polymer obtained by polymerization of a monomer unit having 4 carbon atoms, the content of each of the SIBS and the polymer can be made similar to that of the polymer sheet described above.

[0181] When SIS layer 12d and SIB layer 13d contain the polymer obtained by polymerization of a monomer unit having 4 carbon atoms, the content of each of the SIS and the polymer can be made similar to that in Embodiments 1 and 2.

Embodiment 4

[0182] FIG. 11 is a schematic cross sectional view showing an exemplary polymer laminate used for the inner liner in accordance with the present invention.

[0183] A polymer laminate 10e in accordance with the present embodiment has an SIBS layer 11e containing an SIBS, an SIB layer 13e containing an SIB, and an SIS layer 12e containing an SIS. SIBS layer 11e, SIB layer 13e, and SIS layer 12e are stacked in the above order. At least one of SIBS layer 11e, SIS layer 12e, and SIB layer 13e contains more than or equal to 0.5% by mass and less than or equal to 40% by mass of a polymer obtained by polymerization of a monomer unit having 4 carbon atoms.

[0184] Polymer laminate 10e in accordance with the present embodiment can be configured similarly to the counterpart of Embodiment 3 except that the SIS layer and the SIB layer are stacked in the different order.

[0185] <Method for Manufacturing Polymer Laminate>

[0186] The polymer laminate in accordance with one embodiment of the present invention can be obtained by coextrusion of pellets of an SIBS, an SIS, and an SIB with a T-die extruder. Further, the SIBS layer, the SIS layer, and the SIB layer can be obtained by lamination extrusion such as laminate extrusion or coextrusion of the SIBS layer, the SIS layer, and the SIB layer in the order described in, for example, any one of Embodiments 2 to 4.

[0187] When the SIBS layer contains the SIBS, a rubber component, and sulfur, the respective ingredients are charged into a twin-screw extruder and kneaded under the conditions of about 150 to 280 C. and 50 to 300 rpm, thereby obtaining pellets of a thermoplastic elastomer in which the SIBS, the rubber component, sulfur, and various additives as necessary are dynamically crosslinked. The obtained pellets are charged into a T-die extruder to obtain a polymer sheet of desired thickness.

[0188] In the twin-screw extruder, the SIBS serves as the matrix phase, and the rubber component serves as the island phase and is dispersed. Further, in the twin-screw extruder, the rubber component reacts with the additive component, and the rubber component serving as the island phase produces a crosslinking reaction. Since the rubber component is dynamically crosslinked in the twin-screw extruder, it is called dynamic crosslinking. Even if the rubber component is dynamically crosslinked in the twin-screw extruder, the shear viscosity of the whole system is low and extrusion molding is possible since the matrix phase of the system is composed of a thermoplastic resin component.

[0189] In the pellets of the dynamically-crosslinked thermoplastic elastomer obtained with the twin-screw extruder, the rubber component is crosslinked, however, the thermoplastic elastomer component of the matrix phase holds plasticity, and serves to produce plasticity of the whole system. Therefore, the thermoplastic elastomer also exhibits plasticity in T-die extrusion, and thus can be molded into a sheet shape.

[0190] Further, since the rubber component is crosslinked in the pellets of the dynamically-crosslinked thermoplastic elastomer, the thermoplastic elastomer of the inner liner can be prevented from penetrating into the cords of a carcass layer even when the pneumatic tire is heated while the pneumatic tire is manufactured using the polymer sheet fabricated from the pellets as the inner liner.

[0191] <Method for Manufacturing Pneumatic Tire>

[0192] The pneumatic tire in accordance with the present invention can be manufactured by the following method.

[0193] A green tire in which the polymer sheet or the polymer laminate fabricated above is used for the inner liner part is fabricated. In the case of using the polymer laminate, the polymer laminate is arranged toward the tire radial outer side such that the second layer contacts the carcass or the insulation. With such an arrangement, the second layer can be vulcanization-bonded with an adjacent member such as the carcass or the insulation in the tire vulcanization step. Therefore, the resultant pneumatic tire can have excellent air permeation resistance and durability since the inner liner is satisfactorily bonded with the adjacent member.

[0194] Then, it is preferable to mount the green tire in a mold, press the green tire by applying heat and pressure at 150 to 180 C. for 3 to 50 minutes using the tire vulcanizing bladder for forming the pneumatic tire in accordance with the present invention, cool the bladder at 50 to 120 C. for 10 to 300 seconds without removing the tire from the vulcanizing mold, and thereafter remove the tire from the vulcanizing mold.

[0195] In the pneumatic tire, the polymer sheet or the polymer laminate described above is used for the inner liner. Since the SIBS, the SIS, the SIB, and the like constituting the polymer sheet or the polymer laminate are thermoplastic elastomers, they are softened in the mold when heated to 150 to 180 C., for example, in the step of obtaining the vulcanized tire. The softened thermoplastic elastomer has higher reactivity than in the solid state, and is thus fused with an adjacent member. That is, the inner liner in contact with the outside surface of the expanding bladder is softened by heating and fused with the bladder. When an attempt is made to remove the vulcanized tire from the mold in a state where the inner liner is fused with the outside surface of the bladder, the inner liner peels off the insulation or the carcass adjacent thereto, causing the air-in phenomenon. Further, the tire may be deformed in shape.

[0196] Therefore, by rapidly cooling the temperature inside the bladder at 120 C. or lower for 10 or more seconds while maintaining the pressurized state without opening the vulcanizing mold after the pressurization and vulcanization, the thermoplastic elastomer used for the inner liner can be solidified. When the thermoplastic elastomer is solidified, fusing of the inner liner with the bladder is eliminated, and thus releasability when removing the vulcanized tire from the mold is improved.

[0197] The cooling temperature is preferably from 50 to 120 C. When the cooling temperature is lower than 50 C., it is necessary to prepare a special cooling medium, which may degrade productivity. When the cooling temperature is higher than 120 C., the thermoplastic elastomer may not be sufficiently cooled, which causes the inner liner to be still fused with the bladder upon opening of the mold, giving rise to the air-in phenomenon. The cooling temperature is more preferably from 70 to 100 C.

[0198] The cooling time is preferably from 10 to 300 seconds. When the cooling time is less than 10 seconds, the thermoplastic elastomer may not be sufficiently cooled, which causes the inner liner to be still fused with the bladder upon opening of the mold, giving rise to the air-in phenomenon. When the cooling time is more than 300 seconds, productivity deteriorates. The cooling time is more preferably from 30 to 180 seconds.

[0199] The step of cooling the vulcanized tire is preferably performed by cooling the inside of the bladder. Since a cavity exists inside the bladder, it is possible to introduce a cooling medium controlled to the cooling temperature into the bladder generally after completion of the vulcanization step, without reducing the pressure inside the bladder.

[0200] When the processing advances to the cooling step after completion of applying heat and pressure, it is preferable to advance to the cooling step without reducing the pressure inside the bladder. This is because, when the pressure inside the bladder is reduced after completion of applying heat and pressure, the thermoplastic elastomer is softened, and thus a reduction in pressure may cause a change in gauge, deformation, or occurrence of a void. It is noted that it is also possible to carry out the step of cooling the vulcanized tire by disposing a cooling structure in the mold, in addition to cooling the inside of the bladder.

[0201] It is preferable to use, as a cooling medium, at least one selected from the group consisting of air, steam, water, and oil. Of these, water having excellent cooling efficiency is preferably used.

EXAMPLES

Examples 1 to 35, Comparative Examples 1 to 9

[0202] (Fabrication of Polymer Sheet and Polymer Laminate)

[0203] The respective ingredients in accordance with formulations shown in Table 1 were charged into a twin-screw extruder (screw diameter: 50 mm; L/D: 30; cylinder temperature: 200 C.), and kneaded at 200 rpm to obtain pellets (Manufacturing Examples 1 to 8). The obtained pellets were charged into a co-extruder (cylinder temperature: 200 C.) to manufacture polymer sheets or polymer laminates having structures shown in Tables 3 to 6.

TABLE-US-00001 TABLE 1 Manufacturing examples 1 2 3 4 5 6 7 Formulation SIBS (*1) 100 100 100 (parts SIS (*2) 100 100 by mass) SIB (*3) 100 100 Polyisobutylene (*4) 0.5 40 0.5 40 (*1) SIBS: SIBSTAR 102T manufactured by Kaneka Corporation (a styrene-isobutylene-styrene triblock copolymer, weight-average molecular weight of 100,000, styrene unit content of 25% by mass, Shore A hardness of 25) (*2) SIS: D1161JP manufactured by Kraton Performance Polymers Inc. (a styrene-isoprene-styrene triblock copolymer, weight-average molecular weight of 150,000, styrene unit content of 15% by mass) (*3) SIB: In a 2 L reaction vessel equipped with a stirrer, 589 mL of methylcyclohexane (dried over molecular sieves), 613 mL of n-butyl chloride (dried over molecular sieves), and 0.550 g of cumyl chloride were charged. After cooling the reaction vessel to 70 C., 0.35 mL of -picoline (2-methylpyridine) and 179 mL of isobutylene were added. Further, 9.4 mL of titanium tetrachloride was added to start polymerization, and then the solution was reacted for 2.0 hours while being stirred at 70 C.. Next, 59 mL of styrene was added into the reaction vessel and the reaction was continued for 60 minutes, and then the reaction was terminated by adding a large amount of methanol. After removing the solvent and the like from the reaction solution, a polymer was dissolved in toluene and washed twice with water. This toluene solution was added to the methanol mixture, thereby precipitating the polymer, and the resultant polymer was dried at 60 C. for 24 hours to obtain a styrene-isobutylene diblock copolymer (weight-average molecular weight of 70,000, styrene unit content of 15% by mass) (*4) Polyisobutylene: Tetrax 3T manufactured by Nippon Oil Corporation (weight-average molecular weight of 49,000, viscosity-average molecular weight of 30,000)

[0204] <Manufacturing of Pneumatic Tire>

[0205] Each obtained polymer sheet or polymer laminate was used for the inner liner part of a pneumatic tire to prepare a green tire. It is noted that the polymer laminate was arranged so that the first layer was located at the radial innermost side of the green tire and the second layer contacted a carcass layer of the green tire. The green tire was subjected to press molding in a mold at 170 C. for 20 minutes, using a tire vulcanizing bladder having bladder vent lines in the shape shown in Tables 3 to 6, and cooled at 100 C. for 3 minutes without opening the vulcanizing mold and without reducing the pressure inside the bladder. Thereafter, the vulcanized tire was removed from the mold to manufacture the vulcanized tire of 195/65R15 size, and thus a pneumatic tire was obtained.

[0206] Using the obtained pneumatic tire, the following evaluations were performed.

[0207] ((a) Vulcanization Adhesive Strength of First Layer)

[0208] The first layer and the carcass layer as well as the first layer and an unvulcanized rubber sheet of the second layer were bonded together, and were heated at 170 C. for 20 minutes to obtain a sample for measuring vulcanization adhesive strength. Peel force was measured in a tensile peel test as vulcanization adhesive strength. The obtained value was expressed as an index by the following equation, for vulcanization adhesive strength of the first layer in each example and each comparative example, using the value in Example 1 as a reference value (100). It shows that the greater the value, the greater the vulcanization adhesive strength, which is preferable.

(vulcanization adhesive strength index)=(vulcanization adhesive strength in each example and each comparative example)/(vulcanization adhesive strength in Example 1)100

[0209] ((b) Flaws in Inner Liner)

[0210] Flaws in the inner liner on the inside of the vulcanized tire were visually examined, and judged on the following criteria. It is noted that the sizes of the flaws are not taken into consideration.

[0211] A: In appearance, per tire, the number of flaws in the inner liner was 0.

[0212] B: In appearance, per tire, the number of flaws in the inner liner was one or more.

[0213] ((c) Presence or Absence of Air-In Portions)

[0214] The inside of the tire after the vulcanization and cooling steps was examined, and evaluated on the following criteria.

[0215] A: In appearance, per tire, the number of air-in portions with a diameter of 5 mm or less and the number of air-in portions with a diameter of more than 5 mm were both 0.

[0216] B: In appearance, per tire, the number of air-in portions with a diameter of 5 mm or less was one to three, and the number of air-in portions with a diameter of more than 5 mm was 0.

[0217] C: In appearance, per tire, the number of air-in portions with a diameter of 5 mm or less was four or more, or the number of air-in portions with a diameter of more than 5 mm was one or more.

[0218] ((d) Flex Crack Growth Index)

[0219] In a tire durability driving test, it was evaluated whether the inner liner was broken or peeled off. The manufactured pneumatic tire of 195/65R15 size was mounted on a JIS standard rim 156JJ, and the inside of the tire was monitored under the conditions of a tire internal pressure of 150 KPa, which is lower than usual, a load of 600 kg, a speed of 100 km/hour, and a driving distance of 20,000 km, to measure the number of cracked/peeled portions. The obtained value was expressed as an index by the following equation, for flex crack growth in each example and each comparative example, using the value in Example 1 as a reference value (100). It shows that the greater the value, the more excellent the flex crack growth resistance.

(flex crack growth index)=(the number of cracked/peeled portions in Example 1)/(the number of cracked/peeled portions in each example and each comparative example)100

[0220] ((e) Rolling Resistance)

[0221] The manufactured pneumatic tire of 195/65R15 size was mounted on a JIS standard rim 156JJ, and rolling resistance was measured while driving the tire at room temperature (38 C.) under the conditions of a load of 3.4 kN, an air pressure of 230 kPa, and a speed of 80 km/hour, using a rolling resistance tester manufactured by KOBE STEEL, LTD. The obtained value was expressed as an index by the following equation, for rolling resistance in each example and each comparative example, using the value in Example 1 as a reference value (100). It shows that the greater the value, the smaller the rolling resistance, which is preferable.

(rolling resistance index)=(rolling resistance in Example 1)/(rolling resistance in each example and each comparative example)100

[0222] ((f) Steering Stability)

[0223] The pneumatic tire was mounted onto all wheels of a Japanese vehicle (FF 2000 cc), and the vehicle was driven around a test course to evaluate steering stability by a driver's sensory evaluation. On that occasion, relative evaluation was conducted on a scale of 10, with the value in Example 1 being set to 6. It shows that the greater the value, the more excellent the steering stability.

[0224] (Overall Judgment)

[0225] Criteria for overall judgment are as shown in Table 2.

TABLE-US-00002 TABLE 2 (a) (c) (d) Vulcanization (b) Presence Flex (e) adhesive Flaws or absence crack Rolling (f) Overall Judgment strength of in inner of air-in growth resistance Steering judgment criteria first layer liner portions index index stability A All of (a) to 100 or A A, B 100 or 100 or 6 or (f) satisfy more more more more conditions on the right. B Any one of (a) less than B C less less less to (f) satisfies a 100 than than than 6 corresponding 100 100 condition on the right. If a plurality of judgments are made, a judgment with lower evaluation is adopted. (Evaluation Results) Results are shown in Tables 3 to 6.

TABLE-US-00003 TABLE 3 Examples 1 2 3 4 5 6 7 8 9 10 11 12 13 Poly- First Man- 4 4 4 4 4 4 4 5 4 4 4 4 4 mer Layer ufac- Lami- turing nate example Struc- Thick- 0.6 0.5 0.5 0.5 0.5 0.5 0.3 0.3 0.3 0.3 0.3 0.3 0.3 ture ness (mm) Sec- Man- 6 6 6 6 6 6 6 6 6 6 6 ond ufac- (a) turing Layer example Thick- 0.1 0.1 0.05 0.1 0.05 0.05 0.05 0.05 0.05 0.05 0.05 ness (mm) Sec- Man- 7 7 7 ond ufac- (b) turing Layer example Thick- 0.1 0.1 0.05 ness (mm) Blad- Shape of groove sub- sub- sub- sub- sub- sub- sub- sub- sub- sub- sub- sub- sub- der cross section stan- stan- stan- stan- stan- stan- stan- stan- stan- stan- stan- stan- stan- Vent tially tially tially tially tially tially tially tially tially tially tially tially tially Line rectan- rectan- rectan- rectan- rectan- rectan- rectan- rectan- rectan- rectan- rectan- rectan- rectan- gular gular gular gular gular gular gular gular gular gular gular gular gular Width of groove 0.5 0.5 0.5 0.5 0.5 3.0 0.5 0.5 0.5 0.5 0.5 0.5 3.0 cross section (mm) Depth of groove 0.1 0.1 0.1 0.1 0.1 2.0 0.1 0.1 0.1 0.1 0.1 0.1 2.0 cross section (mm) Groove cross 0.05 0.05 0.05 0.05 0.05 6.00 0.05 0.05 0.05 0.05 0.05 0.05 6.0 sectional area (mm.sup.2) Angle () 90 90 90 90 90 90 90 90 90 60 60 90 90 Angle or 90 90 90 90 90 90 90 90 45 60 45 40/140 40/140 Angle (.sub.1/.sub.2) () Eval- Vulcanization 100 140 110 140 140 110 110 110 110 110 110 110 110 uation adhesive strength of first layer Flaws in inner A A A A A A A A A A A A A liner layer Presence B B B B B B B A A B B A A or absence of air-in portions Flex crack 100 105 120 120 120 135 155 160 130 130 130 135 125 growth index Rolling 100 100 105 105 105 104 107 107 105 105 105 105 103 resistance index Steering stability 6.0 8.5 7.0 8.5 8.5 7.0 6.5 6.5 6.5 6.5 6.5 6.5 6.5 Overall judgment A A A A A A A A A A A A A

TABLE-US-00004 TABLE 4 Examples 14 15 16 17 18 19 20 21 22 23 24 Polymer First Layer Manufacturing 4 4 4 4 4 4 4 4 4 4 4 Laminate example Structure Thickness (mm) 0.5 0.5 0.5 0.5 0.3 0.3 0.3 0.3 0.3 0.3 0.3 Second Manufacturing 6 6 6 6 6 6 6 6 6 6 (a) Layer example Thickness (mm) 0.1 0.05 0.1 0.05 0.05 0.05 0.05 0.05 0.05 0.05 Second Manufacturing 7 7 (b) Layer example Thickness (mm) 0.1 0.05 Bladder Shape of groove cross section sub- sub- sub- sub- sub- sub- sub- sub- sub- sub- sub- Vent Line stan- stan- stan- stan- stan- stan- stan- stan- stan- stan- stan- tially tially tially tially tially tially tially tially tially tially tially semi- semi- semi- semi- semi- semi- semi- semi- semi- semi- semi- circular circular circular circular circular circular circular circular circular circular circular Width of groove 0.5 0.5 0.5 3.0 0.5 0.5 0.5 0.5 0.5 0.5 3.0 cross section (mm) Depth of groove 0.1 0.1 0.1 2.0 0.1 0.1 0.1 0.1 0.1 0.1 2.0 cross section (mm) Groove cross 0.04 0.04 0.04 5.0 0.04 0.04 0.04 0.04 0.04 0.04 5.0 sectional area (mm.sup.2) Angle () 90 90 90 90 90 90 90 60 60 90 90 Angle or Angle (.sub.1/.sub.2) () 90 90 90 90 90 60 45 60 45 40/140 40/140 Eval- Vulcanization adhesive 110 140 140 110 110 110 110 110 110 110 110 uation strength of first layer Flaws in inner liner layer A A A A A A A A A A A Presence or absence B B B B B A A B B A A of air-in portions Flex crack growth index 125 125 125 140 155 165 135 135 135 140 130 Rolling resistance index 106 106 106 105 108 108 105 105 105 105 103 Steering stability 7.0 8.5 8.5 7.0 6.5 6.5 6.5 6.5 6.5 6.5 6.5 Overall judgment A A A A A A A A A A A

TABLE-US-00005 TABLE 5 Examples 25 26 27 28 29 30 31 32 33 34 35 Poly- First Man- 4 4 4 4 4 4 4 4 4 4 4 mer Layer ufac- Lami- turing nate example Struc- Thick- 0.5 0.5 0.5 0.5 0.3 0.3 0.3 0.3 0.3 0.3 0.3 ture ness (mm) Sec- Man- 6 6 6 6 6 6 6 6 6 6 ond ufac- (a) turing Layer example Thick- 0.1 0.05 0.1 0.05 0.05 0.05 0.05 0.05 0.05 0.05 ness (mm) Sec- Man- 7 7 ond ufac- (b) turing Layer example Thick- 0.1 0.05 ness (mm) Blad- Shape of groove subs- subs- subs- subs- subs- subs- subs- subs- subs- subs- subs- der cross section tan- tan- tan- tan- tan- tan- tan- tan- tan- tan- tan- Vent tially tially tially tially tially tially tially tially tially tially tially Line trian- trian- trian- trian- trian- trian- trian- trian- trian- trian- trian- gular gular gular gular gular gular gular gular gular gular gular Width of groove 0.5 0.5 0.5 3.0 0.5 0.5 0.5 0.5 0.5 0.5 3.0 cross section (mm) Depth of groove 0.1 0.1 0.1 2.0 0.1 0.1 0.1 0.1 0.1 0.1 2.0 cross section (mm) Groove cross 0.025 0.025 0.025 3.0 0.025 0.025 0.025 0.025 0.025 0.025 3.0 sectional area (mm.sup.2) Angle () 90 90 90 90 90 90 90 60 60 90 90 Angle 90 90 90 90 90 60 45 60 45 40/140 40/140 or Angle (.sub.1/.sub.2) () Eval- Vulcanization 110 140 140 110 110 110 110 110 110 110 110 uation adhesive strength of first layer Flaws in inner A A A A A A A A A A A liner layer Presence B B B B B A A B B A A or absence of air-in portions Flex crack 120 120 120 135 155 160 130 130 130 135 125 growth index Rolling 106 106 106 105 108 108 105 105 105 105 103 resistance index Steering 7.0 8.5 8.5 7.0 6.5 6.5 6.5 6.5 6.5 6.5 6.5 stability Overall judgment A A A A A A A A A A A

TABLE-US-00006 TABLE 6 Comparative Examples 1 2 3 4 5 6 7 8 9 Polymer First Mamfacturing 1 1 1 1 1 1 1 1 1 Laminate Layer example Structure Thickness 0.6 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 (mm) Second Manufacturing 2 2 2 2 2 2 2 (a) Layer example Thickness 0.1 0.1 0.1 0.1 0.1 0.1 0.1 (mm) Second Manufacturing 3 (b) Layer example Thickness 0.1 (mm) Bladder Shape of groove substan- substan- substan- substan- substan- substan- substan- substan- substan- Vent cross section tially tially tially tially tially tially tially tially tially Line rectangular rectangular rectangular rectangular rectangular rectangular rectangular semicircular triangular Width of groove 0.4 0.4 3.1 0.4 0.5 0.5 3.1 0.5 0.5 cross section (mm) Depth of groove 0.05 0.05 2.1 0.05 0.1 0.1 2.1 0.1 0.1 cross section (mm) Groove cross 0.02 0.02 6.51 0.02 0.05 0.05 6.51 0.04 0.025 sectional area (mm.sup.2) Angle () 90 90 90 90 60 50 90 60 60 Angle or 90 90 90 90 90 40 40/140 90 90 Angle (.sub.1/.sub.2) () Eval- Vulcanization 50 98 98 98 98 98 98 98 98 uation adhesive strength of first layer Flaws in inner liner layer B B B B B B B B B Presence or absence C C B C C C B C C of air-in portions Flex crack growth index 93 100 95 100 95 96 95 96 97 Rolling resistance index 93 100 95 100 97 96 95 98 98 Steering stability 5.5 5.5 5.5 5.5 5.5 5.5 5.5 5.5 5.5 Overall judgment B B B B B B B B B

[0226] (Comparison Between Examples 1 to 8 and Comparative Examples 1 to 4)

[0227] In the pneumatic tires manufactured in Examples 1 to 8, the first and second vent lines had a shape of a groove cross section having a width of more than or equal to 0.5 mm and less than or equal to 3.0 mm in a mold-side surface of the bladder and a depth of more than or equal to 0.1 mm and less than or equal to 2.0 mm from the mold-side surface of the bladder, and the first and second vent lines had a groove cross sectional area of more than or equal to 0.025 mm.sup.2 and less than or equal to 6.0 mm.sup.2.

[0228] In contrast, in the pneumatic tires manufactured in Comparative Examples 1, 2, and 4, the first and second vent lines had a shape of a groove cross section having a width of less than 0.5 mm in the mold-side surface of the bladder and a depth of less than 0.1 mm from the mold-side surface of the bladder, and the first and second vent lines had a groove cross sectional area of less than 0.025 mm.sup.2. Further, in the pneumatic tire manufactured in Comparative Example 3, the first and second vent lines had a shape of a groove cross section having a width of more than 3.0 mm in the mold-side surface of the bladder and a depth of more than 2.0 mm from the mold-side surface of the bladder, and the first and second vent lines had a groove cross sectional area of more than 6.0 mm.sup.2.

[0229] Thus, the pneumatic tires manufactured in Examples 1 to 8 exhibited excellent performance in the air-in phenomenon, flex crack adjustment, rolling resistance, and steering stability, when compared with those in Comparative Examples 1 to 4.

[0230] (Comparison Between Examples 1 to 8 and Comparative Example 5)

[0231] In the pneumatic tires manufactured in Examples 1 to 8, angle of the first vent line with respect to a tangent to a part corresponding to a tire bead toe part and angle of the second vent line with respect to the tangent to the part corresponding to the tire bead toe part satisfied , whereas in the pneumatic tire manufactured in Comparative Example 5, was not satisfied.

[0232] Thus, the pneumatic tires manufactured in Examples 1 to 8 exhibited excellent performance in the air-in phenomenon, flex crack adjustment, rolling resistance, and steering stability, when compared with that in Comparative Example 5.

[0233] (Comparison Between Examples 1 to 8 and Comparative Example 6)

[0234] In the pneumatic tires manufactured in Examples 1 to 8, angle of the first vent line with respect to the tangent to the part corresponding to the tire bead toe part was more than or equal to 60 and less than or equal to 90, whereas in the pneumatic tire manufactured in Comparative Example 6, angle of the first vent line with respect to the tangent to the part corresponding to the tire bead toe part was less than 60.

[0235] Thus, the pneumatic tires manufactured in Examples 1 to 8 exhibited excellent performance in the air-in phenomenon, flex crack adjustment, rolling resistance, and steering stability, when compared with that in Comparative Example 6.

[0236] (Comparison Between Examples 12 to 13 and Comparative Example 7)

[0237] In the pneumatic tires manufactured in Examples 12 to 13, the first and second vent lines had a shape of a groove cross section having a width of more than or equal to 0.5 mm and less than or equal to 3.0 mm in the mold-side surface of the bladder and a depth of more than or equal to 0.1 mm and less than or equal to 2.0 mm from the mold-side surface of the bladder, and the first and second vent lines had a groove cross sectional area of more than or equal to 0.025 mm.sup.2 and less than or equal to 6.0 mm.sup.2.

[0238] In contrast, in the pneumatic tire manufactured in Comparative Example 7, the first and second vent lines had a shape of a groove cross section having a width of more than 3.0 mm in the mold-side surface of the bladder and a depth of more than 2.0 mm from the mold-side surface of the bladder, and the first and second vent lines had a groove cross sectional area of more than 6.0 mm.sup.2.

[0239] Thus, the pneumatic tires manufactured in Examples 12 to 13 exhibited excellent performance in the air-in phenomenon, flex crack adjustment, rolling resistance, and steering stability, when compared with that in Comparative Example 7.

[0240] (Comparison Between Examples 14 to 24 and Comparative Example 8)

[0241] In the pneumatic tires manufactured in Examples 14 to 24, angle of the first vent line with respect to the tangent to the part corresponding to the tire bead toe part and angle of the second vent line with respect to the tangent to the part corresponding to the tire bead toe part satisfied , whereas in the pneumatic tire manufactured in Comparative Example 8, was not satisfied.

[0242] Thus, the pneumatic tires manufactured in Examples 14 to 24 exhibited excellent performance in the air-in phenomenon, flex crack adjustment, rolling resistance, and steering stability, when compared with that in Comparative Example 8.

[0243] (Comparison Between Examples 25 to 35 and Comparative Example 9)

[0244] In the pneumatic tires manufactured in Examples 25 to 35, angle of the first vent line with respect to the tangent to the part corresponding to the tire bead toe part and angle of the second vent line with respect to the tangent to the part corresponding to the tire bead toe part satisfied , whereas in the pneumatic tire manufactured in Comparative Example 9, was not satisfied.

[0245] Thus, the pneumatic tires manufactured in Examples 25 to 35 exhibited excellent performance in the air-in phenomenon, flex crack adjustment, rolling resistance, and steering stability, when compared with that in Comparative Example 9.

Examples 36 to 70, Comparative Examples 10 to 17

[0246] <Manufacturing of Polymer Laminate for Inner Liner>

[0247] The respective ingredients in accordance with formulations shown in Table 7 were charged into a twin-screw extruder (screw diameter: 50 mm; L/D: 30; cylinder temperature: 200 C.), and kneaded at 200 rpm to obtain pellets (Manufacturing Examples 9 to 15). The obtained pellets were charged into a co-extruder (cylinder temperature: 200 C.) to manufacture polymer laminates having structures shown in Tables 9 to 11.

TABLE-US-00007 TABLE 7 Manufacturing examples 8 9 10 11 12 13 14 15 Formu- IIR (*1) 60 95 lation NR (*2) 60 95 (parts SIBS (*3) 40 40 5 5 by SIS (*4) 100 100 mass) SIB (*5) 100 100 Stearic 3 3 3 3 3 3 acid (*6) Zinc oxide 5 5 5 5 5 5 (*7) Antioxidant 1 1 1 1 1 1 (*8) Vulcanization 1 1 1 1 1 1 (*9) accelerator Sulfur (*10) 0.5 0.5 0.5 0.5 0.5 0.5 (*1) IIR: Exxon chlorobutyl 1066 manufactured by Exxon Mobil Corporation (*2) NR: natural rubber TSR20 (*3) SIBS: SIBSTAR 102T manufactured by Kaneka Corporation (a styrene-isobutylene-styrene triblock copolymer, weight-average molecular weight of 100,000, styrene unit content of 25% by mass, Shore A hardness of 25) (*4) SIS: D1161JP manufactured by Kraton Performance Polymers Inc. (a styrene-isoprene-styrene triblock copolymer, weight-average molecular weight of 150,000, styrene unit content of 15% by mass) (*5) SIB: In a 2L reaction vessel equipped with a stirrer, 589 mL of methylcyclohexane (dried over molecular sieves), 613 mL of n-butyl chloride (dried over molecular sieves), and 0.550 g of cumyl chloride were charged. After cooling the reaction vessel to 70 C., 0.35 mL of -picoline (2-methylpyridine) and 179 mL of isobutylene were added. Further, 9.4 mL of titanium tetrachloride was added to start polymerization, and then the solution was reacted for 2.0 hours while being stirred at 70 C.. Next, 59 mL of styrene was added into the reaction vessel and the reaction was continued for 60 minutes, and then the reaction was terminated by adding a large amount of methanol. After removing the solvent and the like from the reaction solution, a polymer was dissolved in toluene and washed twice with water. This toluene solution was added to the methanol mixture, thereby precipitating the polymer, and the resultant polymer was dried at 60 C. for 24 hours to obtain a styrene-isobutylene diblock copolymer (weight-average molecular weight of 70,000, styrene unit content of 15% by mass) (*6) Stearic acid: Stearic Acid Lunac S30 manufactured by Kao Corporation (*7) Zinc oxide: Zinc White No. 1 manufactured by Mitsui Mining & Smelting Co., Ltd. (*8) Antioxidant: Noclac 6C (N-(1,3-dimethylbuty1)-N-phenyl-p-phenylenediamine) manufactured by Ouchi Shinko Chemical Industrial Co., Ltd. (*9) Vulcanization accelerator: Nocceler DM (di-2-benzothiazolyldisulfide) manufactured by Ouchi Shinko Chemical Industrial Co., Ltd. (*10) Sulfur: Sulfur Powder manufactured by Tsurumi Chemical Industry Co., Ltd.

[0248] <Manufacturing of Pneumatic Tire>

[0249] Each obtained polymer laminate was used for the inner liner part of a tire to prepare a green tire. It is noted that the polymer laminate was arranged so that the first layer was located at the radial innermost side of the green tire and the second layer contacted a carcass layer of the green tire. The green tire was subjected to press molding in a mold at 170 C. for 20 minutes, using a tire vulcanizing bladder having bladder vent lines in the shape shown in Tables 9 to 11, to manufacture a vulcanized tire of 195/65R15 size. After the vulcanized tire was cooled at 100 C. for 3 minutes, the vulcanized tire was removed from the mold to obtain a pneumatic tire.

[0250] Using the obtained pneumatic tire, the following evaluations were performed.

[0251] ((a) Flaws in Inner Liner Layer)

[0252] Flaws in the inner liner layer on the inside of the vulcanized tire were visually examined, and judged on the following criteria. It is noted that the sizes of the flaws are not taken into consideration.

[0253] A: In appearance, per tire, the number of flaws in the inner liner was 0.

[0254] B: In appearance, per tire, the number of flaws in the inner liner was one or more.

[0255] ((b) Presence or Absence of Air-In Portions)

[0256] The inside of the tire after the vulcanization and cooling steps was examined, and evaluated on the following criteria.

[0257] A: In appearance, per tire, the number of air-in portions with a diameter of 5 mm or less and the number of air-in portions with a diameter of more than 5 mm were both 0.

[0258] B: In appearance, per tire, the number of air-in portions with a diameter of 5 mm or less was one to three, and the number of air-in portions with a diameter of more than 5 mm was 0.

[0259] C: In appearance, per tire, the number of air-in portions with a diameter of 5 mm or less was four or more, or the number of air-in portions with a diameter of more than 5 mm was one or more.

[0260] ((c) Flex Crack Growth)

[0261] In a tire durability driving test, it was evaluated whether the inner liner was broken or peeled off. The manufactured pneumatic tire of 195/65R15 size was mounted on a JIS standard rim 156JJ, and the inside of the tire was monitored under the conditions of a tire internal pressure of 150 KPa, which is lower than usual, a load of 600 kg, a speed of 100 km/hour, and a driving distance of 20,000 km, to measure the number of cracked/peeled portions. The obtained value was expressed as an index by the following equation, for flex crack growth in each example and each comparative example, using the value in Example 69 as a reference value (100). It shows that the greater the value, the more excellent the flex crack growth resistance.

(flex crack growth index)=(the number of cracked/peeled portions in Example 69)/(the number of cracked/peeled portions in each example and each comparative example)100

[0262] ((d) Rolling Resistance)

[0263] The manufactured pneumatic tire of 195/65R15 size was mounted on a JIS standard rim 156JJ, and rolling resistance was measured while driving the tire at room temperature (38 C.) under the conditions of a load of 3.4 kN, an air pressure of 230 kPa, and a speed of 80 km/hour, using a rolling resistance tester manufactured by KOBE STEEL, LTD. The obtained value was expressed as an index by the following equation, for rolling resistance in each example and each comparative example, using the value in Example 69 as a reference value (100). It shows that the greater the value, the smaller the rolling resistance, which is preferable.

(rolling resistance index)=(rolling resistance in Example 69)/(rolling resistance in each example and each comparative example)100

[0264] Results are shown in Tables 9 to 11.

[0265] (Overall Judgment)

[0266] Criteria for overall judgment are as shown in Table 8.

TABLE-US-00008 TABLE 8 (a) Flaws (b) Presence (c) Flex (d) in inner or absence crack Rolling Overall Judgment liner of air-in growth resistance judgment criteria layer portions index index A All of (a) to A A or B 100 or 100 or (d) satisfy more more conditions on the right. B Any one B C less less of (a) to (d) than than satisfies a 100 100 corresponding condition on the right.

TABLE-US-00009 TABLE 9 Examples 36 37 38 39 40 41 42 43 Polymer First Manufacturing 9 9 9 9 9 8 9 9 Laminate Layer example Structure Thickness 0.5 0.5 0.5 0.5 0.3 0.3 0.3 0.3 (mm) Second Manufacturing 13 13 13 13 13 13 13 (a) Layer example Thickness 0.1 0.05 0.1 0.05 0.05 0.05 0.05 (mm) Second Manufacturing 15 15 (b) Layer example Thickness 0.1 0.05 (mm) Bladder Shape of groove substan- substan- substan- substan- substan- substan- substan- substan- Vent cross section tially tially tially tially tially tially tially tially Line rectangular rectangular rectangular rectangular rectangular rectangular rectangular rectangular Width of groove 0.5 0.5 0.5 3.0 0.5 0.5 0.5 0.5 cross section (mm) Depth of groove 0.1 0.1 0.1 2.0 0.1 0.1 0.1 0.1 cross section (mm) Groove cross 0.05 0.05 0.05 6.00 0.05 0.05 0.05 0.05 sectional area (mm.sup.2) Angle () 90 90 90 90 90 90 90 60 Angle or Angle (.sub.1/.sub.2) () 90 90 90 90 90 90 45 60 Evaluation Flaws in inner liner layer A A A A A A A A Presence or absence B B B B B A A B of air-in portions Flex crack growth index 120 120 120 135 155 160 130 130 Rolling resistance index 105 105 105 104 107 107 105 105 Overall judgment A A A A A A A A Examples 44 45 46 47 48 49 50 51 Polymer First Manufacturing 9 9 9 9 9 9 9 9 Laminate Layer example Structure Thickness 0.3 0.3 0.3 0.5 0.5 0.5 0.5 0.3 (mm) Second Manufacturing 13 13 13 13 13 13 13 (a) Layer example Thickness 0.05 0.05 0.05 0.1 0.05 0.1 0.05 (mm) Second Manufacturing 15 15 (b) Layer example Thickness 0.1 0.05 (mm) Bladder Shape of groove substan- substan- substan- substan- substan- substan- substan- substan- Vent cross section tially tially tially tially tially tially tially tially Line rectangular rectangular rectangular semicircular semicircular semicircular semicircular semicircular Width of groove 0.5 0.5 3.0 0.5 0.5 0.5 3.0 0.5 cross section (mm) Depth of groove 0.1 0.1 2.0 0.1 0.1 0.1 2.0 0.1 cross section (mm) Groove cross 0.05 0.05 6.00 0.04 0.04 0.04 5.00 0.04 sectional area (mm.sup.2) Angle () 60 90 90 90 90 90 90 90 Angle or Angle (.sub.1/.sub.2) () 45 40/140 40/140 90 90 90 90 90 Evaluation Flaws in inner liner layer A A A A A A A A Presence or absence B A A B B B B B of air-in portions Flex crack growth index 130 135 125 125 125 125 140 155 Rolling resistance index 105 105 103 106 106 106 105 108 Overall judgment A A A A A A A A

TABLE-US-00010 TABLE 10 Examples 52 53 54 55 56 57 58 59 Polymer First Layer Manufacturing 9 9 9 9 9 9 9 9 Laminate example Structure Thickness 0.3 0.3 0.3 0.3 0.3 0.3 0.5 0.5 (mm) Second Manufacturing 13 13 13 13 13 13 13 (a) Layer example Thickness 0.05 0.05 0.05 0.05 0.05 0.05 0.1 (mm) Second Manufacturing 15 (b) Layer example Thickness 0.1 (mm) Bladder Shape of groove substan- substan- substan- substan- substan- substan- substan- substan- Vent cross section tially tially tially tially tially tially tially tially Line semicircular semicircular semicircular semicircular semicircular semicircular triangular triangular Width of groove 0.5 0.5 0.5 0.5 0.5 3.0 0.5 0.5 cross section (mm) Depth of groove 0.1 0.1 0.1 0.1 0.1 2.0 0.1 0.1 cross section (mm) Groove cross 0.04 0.04 0.04 0.04 0.04 5.00 0.025 0.025 sectional area (mm.sup.2) Angle () 90 90 60 60 90 90 90 90 Angle or Angle (.sub.1/.sub.2) () 60 45 60 45 40/140 40/140 90 90 Eval- Flaws in inner liner layer A A A A A A A A uation Presence or absence A A B B A A B B of air-in portions Flex crack growth index 165 135 135 135 140 130 120 120 Rolling resistance index 108 105 105 105 105 103 106 106 Overall judgment A A A A A A A A 60 61 62 63 64 65 66 67 Polymer First Layer Manufacturing 9 9 9 9 9 9 9 9 Laminate example Structure Thickness 0.5 0.5 0.3 0.3 0.3 0.3 0.3 0.3 (mm) Second Manufacturing 13 13 13 13 13 13 13 13 (a) Layer example Thickness 0.05 0.1 0.05 0.05 0.05 0.05 0.05 0.05 (mm) Second Manufacturing 15 (b) Layer example Thickness 0.05 (mm) Bladder Shape of groove substan- substan- substan- substan- substan- substan- substan- substan- Vent cross section tially tially tially tially tially tially tially tially Line triangular triangular triangular triangular triangular triangular triangular triangular Width of groove 0.5 3.0 0.5 0.5 0.5 0.5 0.5 0.5 cross section (mm) Depth of groove 0.1 2.0 0.1 0.1 0.1 0.1 0.1 0.1 cross section (mm) Groove cross 0.025 3.00 0.025 0.025 0.025 0.025 0.025 0.025 sectional area (mm.sup.2) Angle () 90 90 90 90 90 60 60 90 Angle or Angle (.sub.1/.sub.2) () 90 90 90 60 45 60 45 40/140 Eval- Flaws in inner liner layer A A A A A A A A uation Presence or absence B B B A A B B A of air-in portions Flex crack growth index 120 135 155 160 130 130 130 135 Rolling resistance index 106 105 108 108 105 105 105 105 Overall judgment A A A A A A A A

TABLE-US-00011 TABLE 11 Examples Comparative Examples 68 69 70 10 11 12 13 14 15 16 17 Poly- First Manufacturing 9 9 9 9 9 9 9 9 9 9 9 mer Layer example Lami- Thickness 0.3 0.6 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 nate (mm) Struc- Second Manufacturing 13 13 13 13 13 13 13 13 13 ture (a) Layer example Thickness 0.05 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 (mm) Second Manufacturing 15 15 (b) Layer example Thickness 0.1 0.1 (mm) Shape of groove substan- substan- substan- substan- substan- substan- substan- substan- substan- substan- substan- cross section tially tially tially tially tially tially tially tially tially tially tially trian- rectan- rectan- rectan- rectan- rectan- rectan- rectan- rectan- semi - trian- gular gular gular gular gular gular gular gular gular circular gular Width of groove 3.0 0.50 0.50 0.40 3.10 0.40 0.50 0.50 3.10 0.50 0.50 cross section (mm) Bladder Depth of groove 2.0 0.10 0.10 0.05 2.10 0.05 0.10 0.10 2.10 0.10 0.10 Vent cross section (mm) Line Groove cross 3.00 0.05 0.05 0.02 6.51 0.02 0.05 0.05 6.51 0.04 0.025 sectional area (mm.sup.2) Angle () 90 90 90 90 90 90 60 50 90 60 60 Angle or 40/140 90 90 90 90 90 90 40 40/140 90 90 Angle (.sub.1/.sub.2) () Eval- Flaws in inner liner layer A A A B B B B B B B B uation Presence or absence A B B C B C C C B C C of air-in portions Flex crack growth index 125 100 105 100 95 100 95 96 95 96 97 Rolling resistance index 103 100 100 100 95 100 97 96 95 98 98 Overall judgment A A A B B B B B B B B

[0267] Examples 36 to 68 are tires manufactured using tire vulcanizing bladders in accordance with the present invention. The tires had no flaws in the inner liner layer, and was able to satisfactorily suppress occurrence of the air-in phenomenon. Further, the tires had an excellent flex crack growth resistance and a reduced rolling resistance.

[0268] Example 69 is a tire manufactured using a tire vulcanizing bladder in accordance with the present invention, having an inner liner including only a 0.6 mm-thick first layer. Although the tire had no flaws in the inner liner layer, an air-in phenomenon occurred therein.

[0269] Example 70 is a tire manufactured using a tire vulcanizing bladder in accordance with the present invention, having an inner liner including a 0.5 mm-thick first layer, a 0.1 mm-thick second (a) layer, and a 0.1 mm-thick second (b) layer. Although the tire had no flaws in the inner liner layer, an air-in phenomenon occurred therein. The tire had a good flex crack growth resistance, and had the same rolling resistance as that in Example 69.

[0270] Comparative Examples 9 to 15 are tires manufactured using tire vulcanizing bladders having vent lines with shapes which are outside of the scope of the present invention. The tires had flaws in the inner liner layer.

[0271] It should be understood that the embodiments and examples disclosed herein are illustrative and non-restrictive in every respect. The scope of the present invention is defined by the scope of the claims, rather than the description above, and is intended to include any modifications within the scope and meaning equivalent to the scope of the claims.

REFERENCE SIGNS LIST

[0272] 1: tire vulcanizing bladder; 2a, 2b: flange part; 4: vent line; 4a: first vent line; 4b: second vent line; 10a: polymer sheet; 10b, 10c, 10d, 10e: polymer laminate; 11a, 11b, 11c, 11d, 11e: SIBS layer; 12b, 12d, 12e: SIS layer; 13c, 13d, 13e: SIB layer; 20, 30, 40: polymer sheet; 21, 31, 41: first layer; 32, 42: second layer; 42a: second (a) layer; 42b: second (b) layer; 101: pneumatic tire; 102: crown part; 103: sidewall part; 104: bead part; 104a: bead toe part; 105: bead core; 106: carcass; 107: belt layer; 108: bead apex; 109: inner liner; 110: buttress part.