Patent Application
20090229726
The present invention relates to a tire for heavy loading. More specifically, the present invention relates to a tire for heavy loading which is excellent in an air holding property and a durability of a bead part and can stand use over a long period of time by disposing a member having an excellent oxygen permeation resistance and an excellent flexibility at least in the periphery of a bead centering on a bead toe part of the tire.
An inner liner layer comprising low gas permeable butyl base rubber such as a butyl rubber, a halogenated butyl rubber and the like as a principal component has so far been disposed up to the periphery of a toe tip in an inner face of a pneumatic tire in order to prevent air leaking and maintain a tire pressure at a fixed level. However, a rubber composition for an inner liner having a large content of the above butyl base rubbers shrinks to a large extent in an unvulcanized state, and it can not completely cover the toe rubber in a certain case. Oxygen filled in the tire brings about oxidative deterioration of rubber members disposed in the circumference of a bead part, whereby a crack growth resistance at a ply end and a durability of the toe rubber are reduced.
In order to solve the above problems, it is important in improving a tire durability to more surely protect a bead part and a toe tip from oxygen. The present inventors have filed Japanese Patent Application No. 338789/2000 for the purpose of inhibiting oxidative deterioration of a bead part and proposed to dispose a member blended with butyl base rubber such as a butyl rubber, a halogenated butyl rubber and the like having a good air permeation resistance at a toe part, whereby an effect of improving the durability has been obtained.
However, durability is more and more strongly required to tires in the market, and a reduction in a thickness of a gauge in an inner liner layer is desired to be further improved as social demand to energy saving is being increased in recent years. This is because members which have an excellent oxygen permeation resistance and a high flexibility and which can be reduced in a thickness of a gauge have not yet been found out.
On the other hand, it is known that an ethylene-vinyl alcohol copolymer (hereinafter abbreviated as EVOH) is excellent in a gas barriering property. An air permeation amount of EVOH is one hundredth or less of an inner liner rubber composition blended with butyl base rubber, and therefore the inner pressure holding property can be enhanced to a large extent even with a thickness of 50 μm or less. In addition thereto, the tire can be reduced in a weight. Accordingly, it is tried to use EVOH for an inner liner of a tire in order to improve an air permeability of the tire (refer to, for example, a patent document 1).
However, an elastic modulus of this EVOH is high to a large extent as compared with those of rubbers usually used for tires, and therefore breakage and cracks have been caused in a certain case by deformation in bending. Accordingly, when using an inner liner comprising EVOH, there has been involved therein the problem that an inner pressure holding property of a tire before use is enhanced to a large extent but an inner pressure holding property of the tire after use which is subjected to bending deformation in rolling of the tire is reduced in a certain case as compared with that of the tire before use.
An inner liner for an inner face of a tire prepared by using a resin composition comprising 60 to 99% by weight of an ethylene-vinyl alcohol copolymer having an ethylene content of 20 to 70 mole % and a saponification degree of 80% or more and 1 to 40% by weight of a hydrophobic surfactant is disclosed in order to solve the above problem (refer to, for example, a patent document 2). However, the flexibility is not necessarily sufficiently satisfactory.
Then, the present inventors have repeated researches of a material having a flexibility of a higher degree while holding a gas barriering property, and they have found that a modified ethylene-vinyl alcohol copolymer obtained by reacting 1 to 50 mass parts of an epoxy compound with 100 mass parts of an ethylene-vinyl alcohol copolymer having an ethylene unit of 25 to 50 mole % is excellent as a material for an inner liner (refer to, for example, a patent document 3).
Patent document 1: Japanese Patent Application Laid-Open No. 40207/1994
Patent document 2: Japanese Patent Publication Laid-Open No. 52904/2002
Patent document 3: Japanese Patent Publication Laid-Open No. 176048/2004
In light of the situation described above, an object of the present invention is to provide a tire for heavy loading which is excellent in an air holding property and a durability of a bead part and can stand use over a long period of time by disposing a member having an excellent oxygen permeation resistance and an excellent flexibility at least in the periphery of a bead centering on a bead toe part of the tire.
Intensive researches repeated by the present inventors in order to develop a pneumatic tire having the preferred properties described above have resulted in finding that the above object can be achieved by providing an air blocking layer in which an oxygen permeation amount is a certain value or lower and which is excellent in a flexibility at a specific place at least in the periphery of a bead centering on a bead toe part of the tire.
Further, it has been found that the above object can effectively be achieved by using a member having at least a layer comprising particularly a specific modified ethylene-vinyl alcohol copolymer as the air blocking layer described above.
The present invention has been completed based on the above findings.
That is, the present invention provides;
(1) a tire for heavy loading, wherein an air blocking layer having a thickness of 1 mm or less and an oxygen permeation amount of 3×10−13 cm3·cm/cm2·sec·Pa or less at 60° C. and 65% RH is provided on a whole outermost layer of a carcass layer so that an end of the air blocking layer is set within 100 mm from a toe tip of a bead part in a direction along a bead base line,
(2) a tire for heavy loading in which an inner surface is covered with an inner liner, wherein an air blocking layer having a thickness of 1 mm or less and an oxygen permeation amount of 3×10−13 cm3·cm/cm2·sec·Pa or less at 60° C. and 65% RH is provided on a whole outermost layer of an inner liner layer so that an end of the air blocking layer is set within 100 mm from a toe tip of a bead part in a direction along a bead base line,
(3) a tire for heavy loading in which an inner surface is covered with an inner liner, wherein an air blocking layer having a thickness of 1 mm or less and an oxygen permeation amount of 3×10−13 cm3·cm/cm2·sec·Pa or less at 60° C. and 65% RH is provided on a whole outermost layer of an inner liner layer so that an end of the air blocking layer is set within 10 mm from a toe end of a bead part in a direction along an inner surface of the tire,
(4) a tire for heavy loading in which an inner surface is covered with an inner liner, wherein an air blocking layer having a thickness of 1 mm or less and an oxygen permeation amount of 3×10−13 cm3·cm/cm2·sec·Pa or less at 60° C. and 65% RH is provided so that an end of the air blocking layer is set within 100 mm from a toe tip of a bead part in a direction along a bead base line; the other end thereof is overlapped partially with the inner liner; and the overlapped part is provided on an outermost layer of the inner liner layer,
(5) a tire for heavy loading in which an inner surface is covered with an inner liner, wherein an air blocking layer having a thickness of 1 mm or less and an oxygen permeation amount of 3×10−13 cm3·cm/cm2·sec·Pa or less at 60° C. and 65% RH is provided so that an end of the air blocking layer is set within 10 mm from a toe tip of a bead part in a direction along an inner surface of the tire; the other end thereof is overlapped partially with the inner liner; and the overlapped part is provided on an outermost layer of the inner liner layer,
(6) the tire for heavy loading as described in any of the above items (1) to (5), wherein a toe rubber is provided at a toe tip of the bead part, and a rubber composition in which 20 to 40 mass % of a rubber component comprises a butyl rubber and/or a halogenated butyl rubber is used for the above toe rubber,
(7) the tire for heavy loading as described in any of the above items (1) to (6), wherein the air blocking layer comprises at least one layer containing a modified ethylene-vinyl alcohol copolymer obtained by reacting 1 to 50 mass parts of an epoxy compound with 100 mass parts of an ethylene-vinyl alcohol copolymer having an ethylene unit of 25 to 50 mole %,
(8) the tire for heavy loading as described in the above item (7), wherein the epoxy compound is glycidol or epoxypropane,
(9) the tire for heavy loading as described in the above item (7) or (8), wherein the ethylene-vinyl alcohol copolymer having an ethylene unit of 25 to 50 mole % which is used for modification has a saponification degree of 90 mole % or more,
(10) the tire for heavy loading as described in any of the above items (7) to (9), wherein the layer containing the modified ethylene-vinyl alcohol copolymer is a layer having an oxygen permeation amount of 3×10−15 cm3·cm/cm2·sec·Pa or less at 6° C. and 65% RH,
(11) the tire for heavy loading as described in any of the above items (7) to (10), wherein the layer containing the modified ethylene-vinyl alcohol copolymer is a cross-linked layer,
(12) the tire for heavy loading as described in any of the above items (7) to (11), wherein the layer containing the modified ethylene-vinyl alcohol copolymer is a layer having a thickness of 50 μm or less,
(13) the tire for heavy loading as described in any of the above items (7) to (12), wherein the air blocking layer comprises the layer containing the modified ethylene-vinyl alcohol copolymer and a layer containing a rubber-like elastic body which is adjacent to the layer,
(14) the tire for heavy loading as described in the above item (13), wherein the air blocking layer is obtained by sticking the layer containing the modified ethylene-vinyl alcohol copolymer onto the layer containing the rubber-like elastic body via at least one adhesive layer,
(15) the tire for heavy loading as described in the above item (13) or (14), wherein the layer containing the rubber-like elastic body is a layer having an oxygen permeation amount of 3×10−12 cm3·cm/cm2·sec·Pa or less at 20° C. and 65% RH,
(16) the tire for heavy loading as described in any of the above items (13) to (15), wherein the layer containing the rubber-like elastic body is a layer containing a butyl rubber and/or a halogenated butyl rubber,
(17) the tire for heavy loading as described in any of the above items (13) to (16), wherein the layer containing the rubber-like elastic body is a layer containing a diene base rubber,
(18) the tire for heavy loading as described in any of the above items (13) to (17), wherein the layer containing the rubber-like elastic body is a layer containing a thermoplastic urethane base elastomer,
(19) the tire for heavy loading as described in any of the above items (13) to (18), wherein the air blocking layer is obtained by sticking layers containing different rubber-like elastic bodies via at least one adhesive layer and (20) the tire for heavy loading as described in any of the above items (13) to (19), wherein a thickness of the layer containing the rubber-like elastic body is 50 to 1500 μm in total.
The tire for heavy loading according to the present invention is a tire in which an air blocking layer is provided mainly in the periphery of a bead and in an outermost layer of a carcass layer or an inner liner layer. A position in which the above air blocking layer is provided includes five kinds of embodiments shown below.
The outermost layer shows a layer provided at a position brought into contact with air.
The air blocking layer used for the pneumatic tire of the present invention has a thickness of 1 mm or less and an oxygen permeation amount of 3×10−13 cm3·cm/cm2·sec·Pa or less, preferably 7×10−14 cm3·cm/cm2·sec·Pa or less and more preferably 3×10−14 cm3·cm/cm2·sec·pa or less at 60° C. and 65% RH. If the above oxygen permeation amount exceeds 3×10−13 cm3·cm/cm2·sec·Pa, the purpose of the present invention can not sufficiently be achieved.
A lower limit value of a thickness of the air blocking layer shall not specifically be restricted as long as the oxygen permeation amount at 60° C. and 65% RH satisfies 3×10−13 cm3·cm/cm2·sec·Pa or less, and it is usually about 10 μm.
The tire of the first embodiment is a tire for heavy loading in which the above air blocking layer is provided, as shown in
The above air blocking layer provided as shown in
The tire of the second embodiment is a tire for heavy loading in which the above air blocking layer is provided, as shown in
The tire of the third embodiment is a tire for heavy loading in which the above air blocking layer is provided, as shown in
Both of the second and third embodiments assume a two layer structure with an inner liner of a conventional butyl rubber base excluding a periphery of a bead, and not only a rise in a durability of the tire but also a reduction in a gauge of the above air blocking layer and inner liner layer becomes possible to make it possible to reduce a weight of the tire.
The tire of the fourth embodiment is a tire for heavy loading, wherein the above air blocking layer is provided, as shown in
The function of the bead part in the tire of the above embodiment is substantially the same as those of the tires in the first and second embodiments.
The tire of the fifth embodiment is a tire for heavy loading, wherein the above air blocking layer is provided, as shown in
The function of the bead part in the tire of the above embodiment is substantially the same as that of the tire in the third embodiment.
The above air blocking layer in both of the fourth and fifth embodiments is provided mainly in the periphery of the bead, and variation in the position of an end of the inner liner caused by the shrinkage of the inner liner in non-vulcanization is covered by overlapping one end of the above air blocking layer with the inner liner layer in both cases. In addition thereto, the toe rubber can be prevented from being deteriorated; the bead part is improved in a durability; and chipping of the toe in detaching a rim can be reduced
In the respective suitable examples of 4: rubber chafer, 5: inner liner layer and 6: toe rubber which are shown in
Next, a member constituting the above air blocking layer shall be explained.
Capable of being preferably given as the member described above is a member having at least one layer (hereinafter referred to as a modified ethylene-vinyl alcohol copolymer layer) containing a modified ethylene-vinyl alcohol copolymer obtained by reacting 1 to 50 mass parts of an epoxy compound with 100 mass parts of an ethylene-vinyl alcohol copolymer having an ethylene unit of 25 to 50 mole %. The above modification makes it possible to reduce an elastic modulus of an unmodified ethylene-vinyl alcohol copolymer to a large extent and makes it possible to improve the breaking property and a degree of causing cracks in bending
In the ethylene-vinyl alcohol copolymer used for the above modification, a content of the ethylene unit is preferably 25 to 50 mole %. From the viewpoint of obtaining the good flexibility and the good fatigue resistance, a content of the ethylene unit is more suitably 30 mole % or more, further suitably 35 mole % or more. Further, from the viewpoint of the gas barriering property, a content of the ethylene unit is more suitably 48 mole % or less, further suitably 45 mole % or less. When a content of the ethylene unit is less than 25 mole %, the flexibility and the fatigue resistance are likely to be deteriorated, and in addition thereto, the melt molding property is likely to be deteriorated as well. On the other hand, if the content exceeds 50 mole %, the gas barriering property is short in a certain case.
Further, a saponification degree of the ethylene-vinyl alcohol copolymer described above is preferably 90 mole % or more, more preferably 95 mole % or more, further preferably 98 mole % or more and most preferably 99 mole % or more. If the saponification degree is less than 90 mole %, the gas barriering property and the heat stability in producing a laminate are likely to be unsatisfactory.
A suitable melt flow rate (MFR) (190° C., under a load of 21.18 N) of the ethylene-vinyl alcohol copolymer used for the modifying treatment is 0.1 to 30 g/10 minutes, more suitably 0.3 to 25 g/10 minutes. In the case of the ethylene-vinyl alcohol copolymer having a melting point falling in the vicinity of 190° C. or exceeding 190° C., MFR is shown by a value obtained by measuring MFR under a load of 21.18 N at plural temperatures which are the melting point or higher and extrapolating them into 190° C. in a single logarithmic graph in which inverse numbers of an absolute temperature is on an axis of ordinate and in which a logarithm of MFR is plotted on an axis of abscissa.
having an axis of ordinate of inverse numbers of absolute temperatures and an axis of abscissa of logarithms of MFR.
The modifying treatment can be carried out by reacting preferably 1 to 50 mass parts, more preferably 2 to 40 mass parts and further preferably 5 to 35 mass parts of the epoxy compound with 100 mass parts of the unmodified ethylene-vinyl alcohol copolymer described above. In this case, a suitable solvent is advantageously used to carry out the reaction in a solution.
In the modifying treatment method carried out by a solution reaction, a solution of the ethylene vinyl alcohol copolymer is reacted with the epoxy compound in the presence of an acid catalyst or an alkali catalyst, whereby the modified ethylene-vinyl alcohol copolymer is obtained. The reaction solvent is preferably a polar aprotic solvent which is a good solvent for ethylene-vinyl alcohol copolymers, such as dimethylsulfoxide, dimethylformamide, dimethylacetamide and N-methylpyrrolidone. The reaction catalyst includes acid catalysts such as p-toluenesulfonic acid, methanesulfonic acid, trifluoromethanesulfonic acid, sulfuric acid and boron trifluoride and alkali catalysts such as sodium hydroxide, potassium hydroxide, lithium hydroxide and sodium methoxide. Among them, the acid catalysts are preferably used. The catalyst amount is suitably about 0.0001 to 10 mass parts per 100 mass parts of the ethylene-vinyl alcohol copolymer. Further, the modified ethylene-vinyl alcohol copolymer can be produced as well by dissolving the ethylene-vinyl alcohol copolymer and the epoxy compound in a reaction solvent to subject them to heat treatment.
The epoxy compound used for the modifying treatment shall not specifically be restricted, and it is preferably a monovalent epoxy compound. When it is a divalent or higher epoxy compound, cross-linking reaction with the ethylene-vinyl alcohol copolymer is caused to produce gel, lumps and the like, whereby a quality of the laminate is likely to be reduced. From the viewpoints of an easiness in producing the modified ethylene-vinyl alcohol copolymer, the gas barriering property, the flexibility and the fatigue resistance, the preferred monovalent epoxy compound includes glycidols and epoxypropane.
A melt flow rate (MFR) (190° C., under a load of 21.18 N) of the ethylene-vinyl alcohol copolymer used in the present invention shall not specifically be restricted, and from the viewpoint of obtaining the good gas barriering property, the good flexibility and the good fatigue resistance, it is preferably 0.1 to 30 g/10 minutes, more preferably 0.3 to 25 g/10 minutes and further preferably 0.5 to 20 g/10 minutes. In the case of modified EVOH having a melting point falling in a vicinity of 190° C. or exceeding 190° C., MFR is shown by a value obtained by measuring MFR under a load of 21.18 N at plural temperatures which are the melting point or higher and extrapolating them into 190° C. in a single logarithmic graph in which an inverse number of an absolute temperature is on an axis of ordinate and in which a logarithm of MFR is plotted on an axis of abscissa.
An oxygen permeation amount of the film layer in which the modified ethylene-vinyl alcohol copolymer used for the member constituting the above air blocking layer is used as a material is preferably 3×10−15 cm3·cm/cm2·sec·Pa or less, more preferably 7×10−16 cm3·cm/cm2·sec·Pa or less and further preferably 3×10−16 cm3·cm/cm2·sec·Pa or less at 60° C. and 65% RH.
In order to use the modified ethylene-vinyl alcohol copolymer for the member constituting the above air blocking layer, the modified ethylene-vinyl alcohol copolymer described above is usually molded into a film, a sheet and the like by melt molding. The melt molding method includes, for example, a T die method, an inflation method and the like. In this case, the melting temperature is, though varied depending on a melting point of the above copolymer and the like, preferably 150 to 170° C.
In the member constituting the above air blocking layer, the modified ethylene-vinyl alcohol copolymer layer is preferably cross-linked. If the above copolymer layer is not cross-linked, the modified ethylene-vinyl alcohol copolymer layer is notably deformed in a vulcanizing step for producing a pneumatic tire to make it impossible to maintain the homogeneous layer, so that a gas barriering property, a flexibility and a fatigue resistance of the air blocking layer are likely to be deteriorated.
A method for cross-linking the modified ethylene-vinyl alcohol copolymer shall not specifically be restricted, and the preferred method includes a method in which the above copolymer layer is irradiated with an energy beam.
The energy beam includes ionizing radiations such as a UV ray, an electron beam, an X-ray, an α-ray, a γ-ray and the like. An electron beam is preferred as an energy beam.
An irradiation method of an electron beam includes a method in which a film or a sheet obtained by molding the above copolymer is introduced into an electron beam irradiation apparatus and in which it is irradiated with the electron beam. A dose of the electron beam shall not specifically be restricted, and it preferably falls in a range of 10 to 60 Mrad. If a dose of the electron beam irradiated is lower than 10 Mrad, cross-linking is less liable to proceed. On the other hand, if a dose of the electron beam irradiated exceeds 60 Mrad, deterioration of the film or the sheet is liable to proceed. More suitably, a dose of the electron beam falls in a range of 20 to 50 Mrad.
The member constituting the above air blocking layer may be a molded matter of a single layer comprising the modified ethylene-vinyl alcohol copolymer layer described above or may be a multilayer structure having at least one modified ethylene-vinyl alcohol copolymer layer.
The above multilayer structure includes a structure comprising the above modified ethylene-vinyl alcohol copolymer layer and a layer (hereinafter referred to as a rubber-like elastic body layer) containing a rubber-like elastic body which is adjacent to the copolymer layer.
Further, it includes a structure obtained by sticking the modified ethylene-vinyl alcohol copolymer layer onto the rubber-like elastic body layer via at least one adhesive layer.
The ethylene-vinyl alcohol copolymer has a —OH group, and therefore it is relatively easy to secure adhesion with rubber. Use of, for example, an adhesive of a chlorinated rubber/isocyanate base for the adhesive layer makes it possible to secure adhesion with the rubber composition used for the tire.
The layer structure of the multilayer structure described above includes, for example, A/B1, B1/A/B1, A/Ad/B1, B1/Ad/A/Ad/B1, B1/A/B1/B2, B1/A/B1/Ad/B2 and the like, wherein the modified ethylene-vinyl alcohol copolymer layer is represented by A; the rubber-like elastic body layer is represented by B1 and B2 (B1 and B2 are different layers respectively); and the adhesive layer is represented by Ad. However, the layer structure shall not be restricted to the above structures.
Also, the respective layers may be single layers or may be multilayers in a certain case. Further, when the modified ethylene-vinyl alcohol copolymer layer, the rubber-like elastic body layer and the adhesive layer each are plural, the plural modified ethylene-vinyl alcohol copolymer layers may be the same or different; the plural rubber-like elastic body layers may be the same or different; and the plural adhesive layers may be the same or different.
A method for producing the multilayer structure shall not specifically be restricted and includes, for example, a method in which the rubber-like elastic body and the adhesive layer are melt-extruded onto the molded matter (a film, a sheet and the like) comprising the modified ethylene-vinyl alcohol copolymer, a method in which the modified ethylene-vinyl alcohol copolymer and the adhesive layer are melt-extruded onto the base material of the rubber-like elastic body in a manner contrary to the above, a method in which the modified ethylene-vinyl alcohol copolymer and the rubber-like elastic body (and if necessary, the adhesive layer) are coextrusion-molded, a method in which a molded matter obtained from the modified ethylene-vinyl alcohol copolymer and a film or a sheet of the rubber-like elastic body are laminated via the adhesive layer and a method in which a molded matter obtained from the modified ethylene-vinyl alcohol copolymer and a film or a sheet of the rubber-like elastic body (and if necessary, an adhesive layer) are stuck together on a drum in molding a tire.
In the member constituting the above air blocking layer, a thickness of the modified ethylene-vinyl alcohol copolymer layer is preferably 50 μm or less. If it exceeds 50 μm, the merit of a decrease in a weight of the inner liner using a butyl rubber, a halogenated butyl rubber and the like which are used at present is reduced. From the viewpoint of a gas barriering property, a flexibility and a fatigue resistance, a thickness of the modified ethylene-vinyl alcohol copolymer layer is more preferably 1 to 40 μm, further preferably 5 to 30 μm.
In the modified ethylene-vinyl alcohol copolymer layer in the multilayer structure described above, a flexibility and a fatigue resistance are enhanced by using the copolymer layer having a thickness of 50 μm or less, and breakage and cracks are less liable to be caused by bending deformation in rolling of the tire. Even it broken, peeling is less liable to be brought about, and cracking is less liable to be extended because of good adhesion of the above modified ethylene-vinyl alcohol copolymer layer with the rubber-like elastic body layer, so that large breakage and cracks are not brought about. When breakage and cracks are caused, a gas barriering property of broken and cracked parts produced in the modified ethylene-vinyl alcohol copolymer layer is supplemented by the rubber-like elastic body layer, and therefore oxygen can be inhibited from being permeated.
The rubber-like elastic body layer in the member constituting the above air blocking layer has preferably an oxygen permeation amount of 3×10−12 cm3·cm/cm2·sec·Pa or less at 60° C. and 65% RH from the viewpoint of a gas barriering property. It is more preferably 7×10−13 cm3·cm/cm2·sec·Pa or less.
A butyl rubber, a diene base rubber and the like are given as the suited examples of the rubber-like elastic body constituting the above rubber-like elastic body layer. The diene base rubber described above is suitably natural rubbers, butadiene rubbers and the like. From the viewpoint of the gas barriering property, a butyl rubber is preferably used as the rubber-like elastic body, and a halogenated butyl rubber is more preferably used. From the viewpoint of inhibiting cracks from being extended after the cracks described above are produced on the rubber-like elastic body layer, a composition containing a butyl rubber and a diene base rubber is preferably used as the rubber-like elastic body. Use of the above composition as the rubber-like elastic body makes it possible to inhibit oxygen well from being permeated even when fine cracks are produced on the rubber-like elastic body layer.
Further, a thermoplastic urethane base elastomer is preferably used from the viewpoints of a reduction in a thickness of the rubber-like elastic body, production of cracks and inhibition of extension thereof.
The thermoplastic urethane base elastomer (hereinafter abbreviated as TFU) described above is an elastomer having a urethane group (—NH-COO—) in a molecule, and it is produced by intermolecular reaction of three components of (1) polyol (long chain diol), (2) diisocyanate and (3) short chain diol. Polyol and short chain diol are subjected to addition reaction with diisocyanate to produce linear polyurethane. Among the above components, the polyol assumes a soft part (soft segment) in the elastomer, and the diisocyanate and the short chain diol assume a hard part (hard segment). The properties of TPU are under the control of the properties of the raw materials, the polymerization conditions and the blend ratios, and among them, the type of the polyol exerts an influence on the properties of TPU to a large extent. A large part of the basic characteristics of TPU is determined by the kind of the long chain diol, and a hardness thereof is controlled by a proportion of the hard segment.
The kind thereof includes (a) caprolactone type (polylactone ester polyol obtained by subjecting caprolactone to ring opening), (b) adipic acid type (=adipate type)<adipic acid ester polyol of adipic acid and glycol> and (c) PTMG (polytetramethylene glycol) type (=ether type)<polytetramethylene glycol obtained by ring-opening polymerization of tetrahydrofuran>.
The rubber-like elastic body layer in the member constituting the above air blocking layer has a thickness falling in a range of preferably 50 to 1500 μm in total. If the above thickness is less than 50 μm in total, a flexibility and a fatigue resistance of the air blocking layer are reduced, and breakage and cracks are liable to be caused by bending deformation in running of a tire. Further, cracking is liable to be extended. On the other hand, if the thickness exceeds 1500 μm in total, the merit of a reduction in a weight of a pneumatic tire which is used at present is reduced. From the viewpoint of a gas barriering property, a flexibility and a fatigue resistance of the air blocking layer and a reduction in a weight of the pneumatic tire, a thickness of the rubber-like elastic body layer is more preferably 100 to 1000 μm, further preferably 300 to 800 μm in total.
Next, the present invention shall be explained in further details with reference to examples, but the present invention shall by no means be restricted by these examples.
The characteristic values of the ethylenevinyl alcohol copolymer used for modification were measured according to methods shown below.
Calculated from a spectrum obtained by 1H-NMR (nuclear magnetic resonance) measurement (using “JNX GX-500 type” manufactured by JEOL Ltd.) using deuterated dimethylsulfoxide as a solvent.
A sample of an ethylene-vinyl alcohol copolymer was filled into a cylinder having an inner diameter of 9.65 mm and a length of 162 mm in Melt Indexer L244 (manufactured by Takara Industry Co., Ltd.) and molten at 109° C., and then a load of 21.18 N was evenly applied thereon by means of a plunger.
A resin amount (g/10 minutes) extruded per unit time from an orifice having a diameter of 2.1 mm provided in the center of the cylinder was measured, and this was designated as the melt flow rate. In the case of the ethylene-vinyl alcohol copolymer having a melting point falling in a vicinity of 190° C. or exceeding 190° C., MFR was shown by a value obtained by measuring MFR under a load of 21.18 N at plural temperatures which were the melting point or higher and extrapolating them into 190° C. in a single logarithmic graph in which an inverse number of the absolute temperature was on an axis of ordinate and in which a logarithm of MFR was plotted on an axis of abscissa.
A pressurized reaction bath was charged with 2 mass parts of an ethylene-vinyl alcohol copolymer (MRF: 5.5 g/10 minutes, 190° C. under a load of 21.18 N) having an ethylene unit content of 44 mole % and a saponification degree of 99.9 mole % and 8 mass parts of N-methyl-2-pyrrolidone, and the mixture was heated and stirred at 120° C. for 2 hours, whereby the ethylene-vinyl alcohol copolymer was completely dissolved. Glycidol 0.4 mass part as an epoxy compound was added thereto and then heated at 160° C. for 4 hours.
After finishing heating, a deposit was precipitated in 100 mass parts of distilled water and washed sufficiently with a large amount of distilled water to remove N-methyl-2-pyrrolidone and unreacted glycidol, whereby a modified ethylene-vinyl alcohol copolymer was obtained. Further, the modified ethylene-vinyl alcohol copolymer thus obtained was crushed to fine particles having a particle diameter of about 2 mm by means of a crusher and then washed again sufficiently with a large amount of distilled water. The particles obtained after washing were dried under vacuum at room temperature for 8 hours, and then they were molten at 200° C. and pelletized by means of a double shaft extruding machine.
A pressurized reaction bath was charged with 2 mass parts of an ethylene-vinyl alcohol copolymer (MRF: 5.5 g/10 minutes, 190° C. under a load of 21.18 N) having an ethylene unit content of 44 mole % and a saponification degree of 99.9 mole % and 8 mass parts of N-methyl-2-pyrrolidone, and the mixture was heated and stirred at 120° C. for 2 hours, whereby the ethylene-vinyl alcohol copolymer was completely dissolved. Epoxypropane 0.4 mass part as an epoxy compound was added thereto and then heated at 160° C. for 4 hours.
After finishing heating, a deposit was precipitated in 100 mass parts of distilled water and washed sufficiently with a large amount of distilled water to remove N-methyl-2-pyrrolidone and unreacted epoxypropane, whereby a modified ethylene-vinyl alcohol copolymer was obtained. Further, the modified ethylene-vinyl alcohol copolymer thus obtained was crushed to fine particles having a particle diameter of about 2 mm by means of a crusher and then washed again sufficiently with a large amount distilled water. The particles obtained after washing were dried under vacuum at room temperature for 8 hours, and then they were molten at 200° C. and pelletized by means of a double shaft extruding machine.
The pellets of the modified ethylene-vinyl alcohol copolymer I obtained in Production Example 1 were used to produce a film on the following extruding conditions by means of a film forming machine comprising a 40 mmφ extruding device (PLABOR GT-40-A manufactured by Plastic Engineering Laboratory) and a T die to obtain a single layer film 1 having a thickness of 20 μm. Type: single shaft extruding machine (non-bent type); L/D: 24; bore diameter: 40 mm φ; screw: single thread full flight type, surface: copper nitride; screw revolution: 40 rpm; dice: 550 mm width coat hanger die; lip gap: 0.3 mm; cylinder, die temperature setting: C1/C2/C3/adaptor/die=180/200/210/210/210 (° C.)
The modified ethylene-vinyl alcohol copolymer II (modified EVOH II) obtained in Production Example 2 and thermoplastic polyurethane (Kuramiron 3190 manufactured by Kuraray Co., Ltd.) as an elastomer were used to produce a three layer film 2 (thermoplastic polyurethane layer/modified EVOH II layer/thermoplastic polyurethane layer) on the following coextrusion molding conditions by means of a two-kind three-layer coextruding apparatus. The thicknesses of the respective layers were 20 μm for both the modified EVOH II layer and the thermoplastic polyurethane layer.
Layer structure: thermoplastic polyurethane/modified EVOH II/thermoplastic polyurethane (thickness: 20/20/20; unit: μm); extruding temperatures of the respective resins: C1/C2/C3/die=170/170/220/220° C.; extruding machine specifications of the respective resins: 25 mm φ extruding machine P25-18AC (manufactured by Osaka Seiki Working Co., Ltd.) for thermoplastic polyurethane, 20 mm φ extruding machine for modified EVOH II, labo machine ME type CO-EXT (manufactured by Toyo Seiki Seisaku-sho, Ltd.); T die specification: for 500 mm width two-kind three-layer (manufactured by Plastic Engineering Laboratory); temperature of cooling roll: 50° C.; receiving speed: 4 m/minute
The film 1 to the film 2 produced in Production Example 3 and Production Example 4 were evaluated for an oxygen permeation amount and a flexibility according to the following methods.
The respective films produced were subjected to humidity conditioning at 20° C. and 65% RH for 5 days.
Samples of the respective two films in which humidity conditioning was finished were used to measure oxygen permeation amounts under the condition of 20° C. and 65% RH by means of MOCON OX-TRAN 2/20 type manufactured by Modern Control Co., Ltd. according to a method described in JIS K7126 (isopiestic method) to determine the average value thereof.
Each film was cut to prepare 50 films of 21 cm×30 cm, and the respective films were subjected to humidity conditioning at 20° C. and 65% RH for 5 days. Then, they were bent at bending frequencies of 50 times, 75 times, 100 times, 125 times, 150 times, 175 times, 200 times, 225 times, 250 times, 300 times, 400 times, 500 times, 600 times, 700 times, 800 times, 1000 times and 1500 times according to ASTM F 392-74 by means of a gerbo flex tester manufactured by Rigaku Kogyo Co., Ltd., and then the number of pinholes was measured.
Measurement was carried out five times in the respective bending frequencies to set the average value thereof as the pinhole number. The measuring results were plotted, wherein the bending frequency (P) was allotted to an axis of abscissa, and the pinhole number was allotted to an axis of ordinate. A bending frequency (Np1) when the pinhole number was 1 was determined by extrapolation, and the significant number was set to the second digit. In the case of the films in which pinholes were not observed at a bending frequency of 1500 times, the bending frequency was increased thereafter by 500 times, and the bending frequency at which pinholes were observed was set as Npl.
An oxygen permeation amount of the film 1 was 2.6×10−16 cm3·cm/cm2·sec·Pa, and the excellent gas barriering property was shown.
Further, a flexibility of the film 1 was evaluated according to the method described above to find that Npl was 500 times and that the very excellent flexibility was shown.
An oxygen permeation amount of the film 2 was 2.6×10−16 cm3·cm/cm2·sec·Pa, and the excellent gas barriering property was shown.
Further, a flexibility of the film 2 was evaluated according to the method described above to find that Npl was 5000 times and that the very excellent flexibility was shown.
The films of kinds shown in Table 1 were used and subjected to cross-linking treatment by irradiating the respective films with an electron beam on the conditions of an accelerating voltage of 200 kV and an irradiating energy of 30 Mrad by means of an electron beam irradiating apparatus “Curetron EBC200-100 for production” manufactured by Nissin High Voltage Co., Ltd. “Metaloc R30M” manufactured by Toyo Kagaku Kenkyusho Co., Ltd. was applied as an adhesive on one surface of the cross-linked film obtained above and stuck on a place shown in Table 1 in a form shown in Table 1, and then a tire (11R22.5 14PR) for trucks and busses was produced by a conventional method.
The tire produced above was charged with oxygen at an air pressure of 900 kPa and left standing at 60° C. for one month, and then it was subjected to a drum test on the conditions of a load of 6270 kg and a speed 60 km/hour in order to confirm a durability of a bead part. The travel distance and the oxygen increasing amount in the rubber at the ply end part were measured. Both values were shown by indices, wherein values obtained in Comparative Example 1 were set as controls, and the results thereof are shown in Table 1. In the case of the travel distance, the tire having a larger index shows that it traveled a longer distance, and in the case of the oxygen increasing amount, the smaller numerical value shows the smaller increasing amount.
The oxygen increasing amount in the rubber at the ply end part was measured by means of “Varico EC III CHNSO element analyzer” manufactured by Nihon Siber Hegner Co., Ltd.
The same procedure as in Examples 1 to 5 was carried out, except that a three layer film was used as the film and that the inner liner layer using a butyl base rubber was not provided in the tire.
The same procedure as in Examples 1 to 6 was carried out, except that the films were not stuck. The results thereof are shown in Table 1.
“Whole surface” in the film disposing range shows a whole surface of an inner side in the inner liner layer.
In “Distance from the toe tip”, (−) shows the inner liner side, and (+) shows the rubber chafer side.
The present invention can provide a tire for heavy loading which is inhibited from being deteriorated due to permeation of oxygen to enhance a durability of a bead part and which can stand use over a long period of time by disposing a member having an excellent oxygen permeation resistance and an excellent flexibility at least in the periphery of a bead centering on a bead toe part of the tire.
Further, a conventional inner liner can be reduced in a thickness or removed, and the tire can be reduced in a weight.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2005-079616 | Mar 2005 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2006/303410 | 2/24/2006 | WO | 00 | 1/4/2008 |
