• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to a tire for vehicles intended to carry heavy loads whose tread comprises a composition based on at least one elastomer matrix comprising a first diene elastomer and a styrene thermoplastic elastomer which represents at most 50% by weight of the elastomeric matrix, a reinforcing filler which comprises from 20 to 50 phr of a silica, which silica represents at least 50% by weight of the reinforcing filler which varies in a range from 25 to 60 phr, a coupling agent and a crosslinking system, which first diene elastomer is selected from the group consisting of polybutadienes, butadiene copolymers and mixtures thereof, which styrenic thermoplastic elastomer comprises at least one styrenic rigid segment and at least one diene flexible segment, which at least one a diene flexible segment comprises at least 20% by weight of conjugated diene units, the conjugated diene units may be all or partly hydrogenated.
    公开号:FR3015500A1
    申请号:FR1363150
    申请日:2013-12-20
    公开日:2015-06-26
    发明作者:Frederic Lemerle；Da Silva Jose Carlos Araujo
    申请人:Michelin Recherche et Technique SA Switzerland ；Compagnie Generale des Etablissements Michelin SCA；Michelin Recherche et Technique SA France；
    IPC主号:
    专利说明:

    [0001] The field of the present invention is that of tires for vehicles intended to carry heavy loads, in particular buses, trucks, agricultural vehicles, civil engineering vehicles. These tires are provided with treads which have, in relation to the tread thicknesses of the tires for light vehicles, in particular for passenger cars or vans, large thicknesses of rubber material. Typically the wearing part of the tread of a truck has a thickness of at least 15 mm, that of a civil engineering vehicle at least 30 mm, or up to 120 mm.
    [0002] During the running, a tread undergoes mechanical stresses and aggression resulting from direct contact with the ground. In the case of a tire mounted on a vehicle carrying heavy loads, the mechanical stresses and the aggressions suffered by the tire are amplified under the effect of the weight carried by the tire. This has the consequence that the crack initiators which are created in the tread under the effect of these stresses and these attacks, tend to spread more on the surface or inside the tread. The propagation of cracks in the tread can cause damage to the tread and thus reduce the life of the tread or the tire.
    [0003] A tire rolling on stony ground is very exposed to crack initiation. The very aggressive nature of the stony ground exacerbates not only this type of attack on the tread, but also its consequences on the tread. This is particularly true for tires fitted to civil engineering vehicles that typically operate in mines. This is also true for tires that are mounted on agricultural vehicles because of stony soil on arable land. The tires that equip heavy-duty vehicles of construction sites that circulate as much on stony soils as on bituminous soils, also know these same aggressions. Due to the two aggravating factors that are the weight carried by the tire and the aggressive nature of the taxiway, the crack propagation resistance of a tread of a tire for a civil engineering vehicle, an agricultural vehicle or a heavy-duty construction vehicle is crucial to minimizing the impact of tread damage. It is therefore important to have tires for heavy load vehicles, whose tread has a crack propagation resistance sufficiently high to minimize the effect of crack initiation on the life of the tread. rolling. To solve this problem, tire manufacturers, for example, use natural rubber in the treads because of the crack propagation resistance properties of natural rubber as mentioned in Table 3.7. Comparison of elastomers properties 162-163, Rubber Technology Handbook Hofmann, Hanser Publishers (1989).
    [0004] The Applicants have discovered that the combined use of a certain level of silica, a polybutadiene or a butadiene copolymer and a certain level of a specific thermoplastic elastomer in a tread makes it possible to improve the resistance to crack propagation of the tread of a vehicle tire for carrying heavy loads without substantial deterioration of other tread performance such as wear and rolling resistance. Thus, a first object of the invention is a tire for vehicles intended to carry heavy loads whose tread comprises a composition based on at least: an elastomer matrix comprising a first diene elastomer and a styrenic thermoplastic elastomer which represents at most 50% by weight of the elastomer matrix, which first diene elastomer is chosen from the group consisting of polybutadienes, butadiene copolymers and their mixtures, which thermoplastic styrene elastomer comprises at least one styrenic rigid segment and at least one flexible segment diene, wherein the at least one diene flexible segment comprises at least 20% by weight of conjugated diene units, the conjugated diene units being wholly or partly hydrogenated, a reinforcing filler which comprises from 20 to 50 phr of a silica, which silica represents at least 50% by weight of the reinforcing filler, the t with a reinforcing filler varying in a range from 25 to 60 phr, a coupling agent, a crosslinking system. The invention also relates to a method for preparing the tire according to the invention.
    [0005] I. MEASUREMENTS AND TESTS USED Resistance to crack propagation: The cracking speed was measured on specimens of rubber compositions, using a cyclic fatigue machine ("Elastomer Test System") of type 381, from MTS, as explained below. Resistance to cracking is measured by repeated tractions on a specimen initially accommodated (after a first traction cycle) and then scored. The tensile test piece consists of a parallelepiped-shaped rubber plate, for example a thickness of between 1 and 2 mm, a length of between 130 and 170 mm and a width of between 10 and 15 mm. the two lateral edges being each covered lengthwise by a cylindrical rubber bead (diameter 5 mm) allowing anchoring in the jaws of the traction machine. The test pieces thus prepared are tested in the new state. The test was conducted in air at a temperature of 20 ° C. After accommodation, 3 very fine cuts of between 15 and 20 mm in length are made using a razor blade, at mid-width and aligned along the length of the test piece, one at each end and one in the center of the latter, before starting the test. At each tensile cycle, the deformation rate of the specimen is adjusted automatically so as to keep the rate of energy restitution (amount of energy released during the progression of the crack) constant, at a value less than or equal to at about 500 J / m2. The crack propagation rate is measured in nanometers per cycle. Resistance to crack propagation will be expressed in relative units (u.r.) by dividing the speed of propagation of the control by that of the mixture, the speeds being measured at the same rate of energy release. A value greater than that of the control, arbitrarily set at 100, indicates an improved result, that is to say a higher resistance to the propagation of cracks. DETAILED DESCRIPTION OF THE INVENTION In the present description, unless expressly indicated otherwise, all the percentages (%) indicated are% by weight. The abbreviation "pce" means parts by weight per hundred parts of elastomers present in the elastomeric matrix, the elastomeric matrix designating all of the elastomers present in the rubber composition. On the other hand, any range of values designated by the expression "between a and h" represents the range of values greater than "a" and less than "h" (i.e., terminals a and b excluded). while any range of values designated by the expression "from a to h" means the range of values from "a" to "h" (i.e. including the strict limits a and b). By the term "composition-based" is meant in the present description a composition comprising the mixture and / or the reaction product in situ of the various constituents used, some of these basic constituents (for example the elastomer, the filler or other additive conventionally used in a rubber composition intended for the manufacture of tire) being capable of, or intended to react with one another, at least in part, during the different phases of manufacture of the composition intended for the manufacture of a tire .
    [0006] The elastomer matrix of the rubber composition has the essential feature of comprising a first diene elastomer selected from the group consisting of polybutadienes (BR), butadiene copolymers and mixtures thereof. Particularly suitable polybutadienes are those having a 1,2-unit content of between 4% and 80% by weight of the weight of the polybutadiene or those having a 1,4-cis bond content of at least 90%. % by mass of the mass of polybutadiene.
    [0007] As copolymers of butadiene are especially suitable copolymers of butadiene and styrene (SBR). The copolymers can be prepared in emulsion (ESBR) or in solution (SSBR). Mention may be made of butadiene-styrene copolymers and in particular those having a glass transition temperature Tg, measured according to ASTM D3418, between 0 ° C. and -90 ° C. and more particularly between -10 ° C. and -80 ° C., a styrene content of between 5% and 60% by weight and more particularly between 5% and 40%, a content (mol%) in -1,2 bonds of the butadiene part of between 4% and 75% of the butadiene part; a content (mol%) of trans-1,4 bonds of between 10% and 80% of the butadiene part. The first diene elastomer, whether it be a polybutadiene or a butadiene copolymer, may be modified with a modifying agent such as, for example, a coupling agent, starring agent or functionalization agent. As modifying agent, mention may be made of compounds comprising a C-Sn bond, or those comprising an amine, silanol or alkoxysilane function. Such elastomers are for example described in patents EP 0 778 311 B1, EP 0 890 607 B1 and EP 0 692 492 B1, EP 1 000 970 B1, EP 1 457 501 B1 or patent applications WO 2009/000750, WO 2009/133068.
    [0008] According to a preferred embodiment of the invention, the first diene elastomer is a polybutadiene, preferably having a 1,4-cis bond ratio greater than or equal to 90% by weight of the polybutadiene mass. This preferred embodiment of the invention may be combined with any one of the embodiments of the invention.
    [0009] According to one embodiment of the invention, the first diene elastomer represents at least 50% of the difference between the mass of the elastomer matrix and the mass of the styrenic thermoplastic elastomer, which is to say that the first diene elastomer has a weight fraction greater than or equal to 50% relative to the total mass of the non-thermoplastic elastomers of the elastomer matrix. According to this embodiment, for example, as an elastomer matrix, a mixture consisting of 40% by weight of the styrenic thermoplastic elastomer, 45% by weight of the first diene elastomer and 15% by weight of a second diene elastomer, the percentages being calculated on the basis of the total mass of the elastomeric matrix.
    [0010] According to another embodiment of the invention, the first diene elastomer represents at least 50% by weight of the elastomer matrix. According to this embodiment, for example, as an elastomer matrix, a mixture consisting of 40% by weight of the styrenic thermoplastic elastomer, 55% by weight of the first diene elastomer and 5% by weight is used. second diene elastomer, the percentages being calculated on the basis of the total mass of the elastomeric matrix. By a second diene elastomer (or indistinctly rubber), one or more elastomers consisting of at least a part (ie, a homopolymer or a copolymer) of monomeric diene units (monomers bearing two carbon-carbon double bonds) must be understood in known manner. carbon, conjugated or not), the second diene elastomer being different from the first diene elastomer and not being a styrenic thermoplastic elastomer.
    [0011] According to a preferred embodiment of the invention, only the first diene elastomer and the styrenic thermoplastic elastomer constitute the elastomer matrix, which means that the elastomer matrix contains no other elastomers than the first diene elastomer and the elastomer. thermoplastic styrenic.
    [0012] The styrenic thermoplastic elastomer comprises at least one styrenic rigid segment and at least one diene flexible segment comprising at least 20% by weight of conjugated diene units, the conjugated diene units being wholly or partly hydrogenated. The rigid and flexible segments can be arranged linearly, star or connected.
    [0013] A flexible segment refers to an elastomeric type polymer block, a rigid segment refers to a thermoplastic type polymer block. According to one embodiment of the invention, the styrenic thermoplastic elastomer is a diblock. The diblock comprises a single rigid styrenic segment connected to a single diene flexible segment.
    [0014] According to a preferred embodiment of the invention, the styrenic thermoplastic elastomer comprises at least two rigid styrenic segments. According to this preferred embodiment of the invention, generally at least two chain ends of the styrenic thermoplastic elastomer are each provided with a styrenic rigid segment and the styrenic rigid segments are connected by the one or more flexible diene segments. According to this preferred embodiment of the invention, the styrenic thermoplastic elastomer is preferably a triblock. The triblock then consists of two rigid styrenic segments and a flexible diene segment.
    [0015] In the case where the styrenic thermoplastic elastomer is a diblock, the denomination of "the at least one rigid segment" designates the rigid segment present in the styrenic thermoplastic elastomer. In the different cases of a diblock, for example in the case of a triblock, the name "the at least one rigid segment" designates the rigid segments present in the thermoplastic styrene elastomer.
    [0016] In the case where the styrenic thermoplastic elastomer is a diblock or a triblock, the denomination of "the at least one flexible segment" designates the flexible segment present in the styrenic thermoplastic elastomer. In cases where the styrenic thermoplastic elastomer is neither a diblock nor a triblock, the denomination of "the at least one flexible segment" designates the flexible segments present in the thermoplastic styrene elastomer. The at least one styrenic rigid segment is the homopolymer of a styrenic monomer or the block or random copolymer of several styrenic monomers or the copolymer of one or more styrenic monomers and another non-styrenic monomer such as 1,3-diene.
    [0017] By styrene monomer is to be understood in the present description styrene or substituted styrene. Examples of substituted styrenes that may be mentioned are methylstyrenes (for example, o-methylstyrene, m-methylstyrene or p-methylstyrene, alpha-methylstyrene, alpha-2-dimethylstyrene, alpha-4- dimethylstyrene or diphenylethylene), para-tert-butylstyrene, chlorostyrenes (e.g., o-chlorostyrene, m-chlorostyrene, p-chlorostyrene, 2,4-dichlorostyrene, 2,6-dichlorostyrene or , 4,6-trichlorostyrene), bromostyrenes (eg, o-bromostyrene, m-bromostyrene, p-bromostyrene, 2,4-dibromostyrene, 2,6-dibromostyrene or 2,4,6-dibromostyrene). tribromostyrene), fluorostyrenes (for example o-fluorostyrene, m-fluorostyrene, p-fluorostyrene, 2,4-difluorostyrene, 2,6-difluorostyrene or 2,4,6-trifluorostyrene) or para-hydroxy-styrene. According to a preferred embodiment of the invention, the at least one styrenic rigid segment has a glass transition temperature greater than 80 ° C. Preferably, the at least one styrenic rigid segment is polystyrene.
    [0018] The at least one diene flexible segment comprises at least 20% by weight of conjugated diene monomer units (also referred to as conjugated diene units). The at least one diene flexible segment can be the homopolymer of a conjugated diene or the random or block copolymer of several conjugated dienes or the copolymer of one or more conjugated dienes and at least one other non-diene monomer such as than a styrenic monomer. The proportion of conjugated diene units which form the diene flexible segment is preferably at least 50%, more preferably at least 60%, even more preferably at least 70% by weight of the weight of the diene flexible segment.
    [0019] Advantageously, it is at least 80% by weight of the mass of the diene flexible segment. These rates, whether preferential or not, apply to any of the embodiments of the invention. As conjugated diene units, 1,3-butadiene units and isoprene units are particularly suitable. The at least one diene flexible segment may be a polybutadiene, a polyisoprene or a copolymer of 1,3-butadiene and isoprene. The copolymer of 1,3-butadiene and isoprene may be of a block or random nature. Suitable thermoplastic styrene elastomers are diblock copolymers such as styrene / butadiene (SB), styrene / isoprene (SI), styrene / butadiene / isoprene (SBI) block copolymers or the mixture of these copolymers. In this designation the diene soft block is a random or block copolymer. Styrene / butadiene / styrene (SBS), styrene / isoprene / styrene (SIS), styrene / butadiene / isoprene / styrene (SBIS) copolymers or the mixture of these copolymers are particularly suitable as styrene thermoplastic elastomers. In this designation the diene soft block is a random or block copolymer. Particularly suitable is a styrene / butadiene / isoprene / styrene block copolymer (SBIS).
    [0020] According to a first variant of the invention, a fraction of the diene units of the at least one diene flexible segment is hydrogenated. It will be appreciated by those skilled in the art that it may equivalently use a styrenic thermoplastic elastomer whose double bonds of a fraction of the diene units of the diene soft segment will have been reduced in a single bond by a process other than hydrogenation. Among the methods which make it possible to reduce the double bonds of the diene units in single bond, mention may be made of reductions with aluminum hydride or with diimine, for example. According to a second variant of the invention, all the diene units of the at least one diene flexible segment is hydrogenated. It will be appreciated by those skilled in the art that it may equivalently use a styrenic thermoplastic elastomer whose double bonds of all of the diene units of the diene flexible segment will have been reduced in a single bond by a process other than hydrogenation. According to this second variant of the invention, the thermoplastic elastomer copolymers styrene / ethylene / butylene (SEB), styrene / ethylene / propylene (SEP), styrene / ethylene / ethylene / propylene (SEEP) or mixtures of these copolymers are suitable as thermoplastic elastomer . In this designation, the hydrogenated flexible diene block is a random or block copolymer. According to this second variant of the invention, the styrene / ethylene / butylene / styrene (SEBS), styrene / ethylene / propylene / styrene (SEPS), styrene / ethylene / ethylene / propylene / styrene block copolymers (SEEPS) are also suitable as thermoplastic elastomer ) or mixtures of these copolymers. In this designation, the hydrogenated flexible diene block is a random or block copolymer. Any of the embodiments of the invention applies to the first variant of the invention or to the second variant of the invention. Styrene thermoplastic elastomers are also suitable mixtures of a triblock copolymer mentioned above and a diblock copolymer mentioned above. Indeed, the triblock copolymer may contain a minority weight fraction of diblock copolymer consisting of a rigid styrenic segment and a diene flexible segment, the rigid block and the flexible block being respectively of the same chemical nature, in particular of the same microstructure, as the rigid and flexible blocks of the triblock. The presence of diblock copolymer in the triblock copolymer generally results from the synthesis process of the triblock copolymer which can lead to the formation of a secondary product such as the diblock copolymer. Most often the percentage of diblock copolymer in the triblock copolymer does not exceed 40% by weight of triblock copolymer. According to a preferred embodiment of the invention, the mass ratio of the at least one styrenic rigid segment is between 5 and 40% of the mass of the thermoplastic styrene elastomer. Below the minimum indicated, the thermoplastic nature of the styrenic thermoplastic elastomer is likely to decrease significantly while above the maximum recommended, the elasticity of the composition can be affected. For these reasons, the mass ratio of the at least one styrenic rigid segment in the styrenic thermoplastic elastomer is preferably in a range from 10 to 35%, more preferably from 10 to 20% of the mass of the thermoplastic elastomer. styrene. These levels, whether preferential or not, apply to any of the embodiments of the invention, especially when the polystyrene forms the at least one styrenic rigid segment of the thermoplastic styrene elastomer.
    [0021] The number-average molar mass (denoted Mn) of the styrenic thermoplastic elastomer is preferably between 50,000 and 500,000 g / mol, more preferably between 60,000 and 450,000 g / mol, more preferably between 80,000 and 300,000 g / mol. Advantageously it is between 100,000 and 200,000 g / mol. These preferred ranges of average molar mass values apply regardless of the embodiment of the invention. The molar mass is determined in a known manner by steric exclusion chromatography (SEC). The sample is first solubilized in tetrahydrofuran at a concentration of about 1 g / l; then the solution is filtered through a 0.45 μm porosity filter before injection. The equipment used is a chromatographic chain "WATERS alliance". The elution solvent is tetrahydrofuran, the flow rate 0.7 ml / min, the system temperature 35 ° C and the analysis time 90 min. A set of four WATERS columns in series, of trade names "STYRAGEL" ("HMW7", "HMW6E" and two "HT6E") is used. The injected volume of the solution of the polymer sample is 100 μl. The detector is a differential refractometer "WATERS P10-3243 - 9 - 2410" and its associated software for the exploitation of chromatographic data is the "WATERS MILLENIUM" system. The calculated average molecular weights relate to a calibration curve made with polystyrene standards.
    [0022] The styrenic thermoplastic elastomer is present in a mass proportion of at most 50% of the mass of the elastomer matrix of the rubber composition of the tread. Above the indicated maximum value, there is no more benefit on the crack propagation resistance of the rubber composition forming the tread of a tire intended to carry heavy loads. The level of the styrenic thermoplastic elastomer varies in a range preferably from 5 to 50%, more preferably from 10 to 45%, even more preferably from 20 to 45% by weight of the mass of the elastomer matrix. Advantageously, it varies from 25 to 45% by weight of the mass of the elastomer matrix. When the styrenic thermoplastic elastomer is a mixture of unsaturated thermoplastic styrene elastomers according to the invention, the rates indicated apply to the mixture and not to each of the styrenic thermoplastic elastomers. These rates, whether preferential or not, apply to any of the embodiments of the invention. According to a particular embodiment of the invention, the styrenic thermoplastic elastomer has a glass transition temperature below -20 ° C. This glass transition temperature is generally attributed to the glass temperature of the diene flexible segment of the styrenic thermoplastic elastomer. The glass transition temperature is measured by means of a Differential Scanning Calorimeter according to ASTM D3418 (1999). According to this particular embodiment of the invention, the styrenic thermoplastic elastomer has a Tg preferably less than -30 ° C, more preferably less than -40 ° C, even more preferably less than -50 ° C. The reinforcing filler may be any type of so-called reinforcing filler, known for its ability to reinforce a rubber composition that can be used for the manufacture of tires, for example an organic filler such as carbon black, a reinforcing inorganic filler such as silica which is associated in a known manner a coupling agent, or a mixture of these two types of charges. A reinforcing filler typically consists of nanoparticles whose average size (in mass) is less than one micrometer, generally less than 500 nm, most often between 20 and 200 nm, in particular and more preferably between 20 and 150 nm. According to the present invention, the reinforcing filler is present in an amount ranging from 25 to 60 phr. The reinforcing filler comprises a silica whose content varies from 20 to 50 phr and which represents at least 50% by weight of the reinforcing filler. By silica is meant one or more silicas. By silica, is to be understood here any silica capable of reinforcing on its own, without other means than an intermediate coupling agent, a rubber composition intended for the manufacture of pneumatic tires, in other words capable of replacing, in its reinforcing function, a conventional carbon black of pneumatic grade. As reinforcing silica is suitable any reinforcing silica known to those skilled in the art, especially any precipitated or fumed silica having a BET surface and a CTAB specific surface both less than 450 m 2 / g, preferably from 30 to 400 m 2 / g , especially between 60 and 300 m2 / g. An example of silica useful for the purposes of the invention is silica "Ultrasil VN3" marketed by the company Evonik. As highly dispersible precipitated silicas (called "HDS"), mention may be made, for example, of the "Ultrasil" 7000 and "Ultrasil" 7005 silicas of the Degussa company, the "Zeosil" 1165MP, 1135MP and 1115MP silicas of the Rhodia company. "Hi-Sil" silica EZ150G from the company PPG, the "Zeopol" silicas 8715, 8745 and 8755 from the Huber Company, the high surface area silicas as described in the application WO 03/016387. In the present discussion with respect to silica, the BET surface area is determined in a known manner by gas adsorption using the Brunauer-Emmett-Teller method described in "The Journal of the American Chemical Society" Vol. 60, page 309, February 1938, more precisely according to the French standard NF ISO 9277 of December 1996 (multipoint volumetric method (5 points) - gas: nitrogen - degassing: 1 hour at 160 ° C - relative pressure range p / po: 0.05 at 0.17). The CTAB specific surface is the external surface determined according to the French standard NF T 45-007 of November 1987 (method B). The physical state in which the silica is presented is indifferent, whether in the form of powder, microbeads, granules or beads.
    [0023] Those skilled in the art will understand that, as the equivalent filler of the reinforcing silica described in this paragraph, it would be possible to use a reinforcing filler of another nature, in particular organic such as carbon black, provided that this reinforcing filler would be covered with a silica layer requiring the use of a coupling agent to establish the bond between the filler and the elastomer. By way of example, mention may be made, for example, of carbon blacks for tires as described for example in documents WO 96/37547 and WO 99/28380. According to any embodiment of the invention, the silica preferably represents more than 50% by weight of the reinforcing filler. According to one embodiment of the invention, the reinforcing filler further comprises a carbon black. Carbon black means one or more carbon blacks. P10-3243 According to another embodiment of the invention, the reinforcing filler consists of a mixture of silica and carbon black. In this case, the rubber composition does not contain other reinforcing fillers than silica and carbon black.
    [0024] When the rubber composition contains a carbon black, the carbon black preferably has a BET surface area of at least 90 m 2 / g. As such are suitable black conventionally used in tires or their treads (so-called pneumatic grade black). Among these, more particularly include reinforcing carbon blacks of the series 100, 200, 300 (ASTM grade), such as blacks N115, N134, N234, N375. Preferably, the carbon black has a BET of at least 100 m 2 / g. The carbon blacks can be used in the isolated state, as commercially available, or in any other form, for example as a carrier for some of the rubber additives used. The carbon blacks could for example already be incorporated into an isoprene elastomer in the form of a masterbatch (see for example WO 97/36724 or WO 99/16600). The BET surface area of the carbon blacks is measured according to the D6556-10 standard [multipoint method (at least 5 points) - gas: nitrogen - relative pressure range P / PO: 0.1 to 0.3]. In order to couple the silica to the diene elastomer, a coupling agent is used in a well-known manner, in particular an at least bifunctional silane (or bonding agent) intended to ensure a sufficient chemical and / or physical connection between the inorganic filler (surface of its particles) and the diene elastomer. In particular, organosilanes or at least bifunctional polyorganosiloxanes are used.
    [0025] In particular, polysulfide silanes, called "symmetrical" or "asymmetrical" silanes according to their particular structure, are used, as described, for example, in claims WO 03/002648 (or US 2005/016651) and WO 00/002649 (or US 2005/016650). In particular, polysulphide silanes having the general formula (V) Z - A - Sx - A - Z (V) in which: - x is an integer of 2 to 8 ( preferably from 2 to 5); the symbols A, which may be identical or different, represent a divalent hydrocarbon radical (preferably a C1-C18 alkylene group or a C6-C12 arylene group, more particularly a C1-C10 alkylene, especially a C1-C4 alkylene, in particular propylene); the symbols Z, which are identical or different, correspond to one of the following three formulas: ## STR2 ## in which: ## STR2 ## the radicals R1, substituted or unsubstituted, which are identical to or different from each other, represent a C1-C18 alkyl, C5-C18 cycloalkyl or C6-C18 aryl group (preferably C1-C6 alkyl, cyclohexyl or phenyl groups, especially C1-C4 alkyl groups, more particularly methyl and / or ethyl). the radicals R2, substituted or unsubstituted, which are identical to or different from one another, represent a C1-C18 alkoxyl or a C5-C18 cycloalkoxyl group (preferably a group chosen from C1-C8 alkoxyls and C5-C8 cycloalkoxyls, plus still more preferably a group chosen from C1-C4 alkoxyls, in particular methoxyl and ethoxyl). In the case of a mixture of polysulfurized alkoxysilanes corresponding to formula (I) above, in particular common commercially available mixtures, the average value of "x" is a fractional number preferably of between 2 and 5, more preferably close to 4.
    [0026] But the invention can also be advantageously used for example with disulfide alkoxysilanes (x = 2). By way of examples of polysulphurized silanes, mention may be made more particularly of bis (C 1 -C 4) -alkyl (C 1 -C 4) -alkyl (C 1 -C 4) alkylsulfides (especially disulfides, trisulphides or tetrasulfides), as for example polysulfides of bis (3-trimethoxysilylpropyl) or bis (3-triethoxysilylpropyl). Among these compounds, bis (3-triethoxysilylpropyl) tetrasulfide, abbreviated TESPT, of formula [(C2H50) 3Si (CH2) 3S1 or bis (triethoxysilylpropyl) disulfide, abbreviated TESPD, of formula [( C2H50) 3Si (CH2) 3Sl2.
    [0027] As coupling agent other than polysulfurized alkoxysilane, there may be mentioned in particular bifunctional POSS (polyorganosiloxanes) or hydroxysilane polysulfides as described in patent applications WO 02/30939 (or US Pat. No. 6,774,255), WO 02 / 31041 (or US 2004/051210) or silanes or POSS carrying azodicarbonyl functional groups, as described for example in patent applications WO 2006/125532, WO 2006/125533, WO 2006/125534. The content of coupling agent is advantageously less than 10 phr, it being understood that it is generally desirable to use as little as possible. Typically the level of coupling agent is from 0.5% to 15% by weight relative to the amount of inorganic filler. Its level is preferably between 0 and 8 phr, more preferably in a range from 0.5 to 7.5 phr. This level is easily adjusted by those skilled in the art according to the level of inorganic filler used in the composition. The rubber composition in accordance with the invention may also contain, in addition to the coupling agents, coupling activators, inorganic charge-covering agents or, more generally, assisting agents for the implementation of the invention. in a known manner, by improving the dispersion of the filler in the rubber matrix and by lowering the viscosity of the compositions, to improve their ability to use in the green state, these agents being examples of hydrolysable silanes such as alkylalkoxysilanes (especially alkyltriethoxysilanes), polyols, polyethers (for example polyethylene glycols), primary, secondary or tertiary amines (for example trialkanolamines), hydroxylated or hydrolysable POSs, for example α,--dihydroxypolyorganosiloxanes (especially α,--dihydroxy-polydimethylsiloxanes), fatty acids such as, for example, stearic acid. The rubber composition may also comprise all or part of the usual additives usually used in elastomer compositions, for example plasticizers, pigments, protective agents such as anti-ozone waxes, chemical antiozonants, antioxidants, anti-fatigue, a crosslinking system, vulcanization accelerators or retarders, vulcanization activators. According to any embodiment of the invention, the crosslinking system is preferably based on sulfur, but it may also be based on sulfur donors, peroxide, bismaleimides or their mixtures. The rubber composition can be manufactured in suitable mixers, using two successive preparation phases well known to those skilled in the art: a first phase of work or thermomechanical mixing (so-called "non-productive" phase) at high temperature, up to at a maximum temperature of between 130 ° C. and 200 ° C., followed by a second mechanical working phase (so-called "productive" phase) to a lower temperature, typically less than 110 ° C., for example between 40 ° C. ° C and 100 ° C, finishing phase during which is incorporated the crosslinking system.
    [0028] The process for producing the tire according to the invention comprises, for example, the following steps: adding, during a first so-called non-productive step to the first diene elastomer, the styrenic thermoplastic elastomer, the reinforcing filler, the coupling agent by thermomechanically kneading until reaching a maximum temperature of between 130 and 200 ° C, - cooling the assembly to a temperature below 70 ° C, - then incorporating the crosslinking system, - kneading everything to a temperature maximum of less than 90 ° C to obtain a mixture, and then calender or extrude the resulting mixture to form a tread. Whatever the embodiment of the invention, the tire according to the invention is preferably a tire for vehicles off the road, that is to say, which rolls on stony ground such as civil engineering vehicles, construction heavy vehicles, or agricultural vehicles. The tire is in particular a tire for a civil engineering vehicle whatever the embodiment of the invention. The invention relates to the tires previously described both in the green state (that is to say, before firing) and in the fired state (that is to say, after crosslinking or vulcanization).
    [0029] P10-3243
    权利要求:
    Claims (24)
    [0001]
    REVENDICATIONS1. Tire for vehicles intended to carry heavy loads whose tread comprises a composition based on at least: an elastomer matrix comprising a first diene elastomer and a styrene thermoplastic elastomer which represents at most 50% by weight of the elastomer matrix which first diene elastomer is selected from the group consisting of polybutadienes, butadiene copolymers and mixtures thereof, which styrenic thermoplastic elastomer comprises at least one styrenic rigid segment and at least one diene flexible segment, which at least one flexible segment diene comprises at least 20% by weight of conjugated diene units, the conjugated diene units may be entirely or partly hydrogenated, a reinforcing filler which comprises from 20 to 50 phr of a silica, which silica represents at least 50% by weight of mass of the reinforcing filler, the rate of reinforcing filler varying in one do from 25 to 60 phr, - a coupling agent, - a crosslinking system.
    [0002]
    2. The tire of claim 1 wherein the first diene elastomer is at least 50% of the difference between the mass of the elastomeric matrix and the mass of the styrenic thermoplastic elastomer.
    [0003]
    3. A tire according to any one of claims 1 to 2 wherein the first diene elastomer is at least 50% by weight of the elastomeric matrix.
    [0004]
    4. A tire according to any one of claims 1 to 3 wherein the elastomeric matrix consists of a mixture of the first diene elastomer and the styrenic thermoplastic elastomer.
    [0005]
    5. A tire according to any one of claims 1 to 4 wherein the styrenic thermoplastic elastomer content is 5 to 50% by weight, preferably 10 to 45% by weight, more preferably 20 to 45% by weight, more preferably 25 to 45% by weight of the mass of the elastomeric matrix.
    [0006]
    A tire according to any one of claims 1 to 5 wherein the at least one rigid styrenic segment has a glass transition temperature of greater than 80 ° C.
    [0007]
    A tire according to any one of claims 1 to 6 wherein the at least one styrenic rigid segment is polystyrene. P10-3243 35- 16 -
    [0008]
    A tire according to any one of claims 1 to 7 wherein the conjugated diene units of the at least one diene flexible segment are 1,3-butadiene units or isoprene units.
    [0009]
    9. A tire according to any one of claims 1 to 8 wherein the styrenic thermoplastic elastomer is a diblock having a single rigid styrenic segment connected to a single diene flexible segment.
    [0010]
    10. A tire according to claim 9 wherein the styrenic thermoplastic elastomer is a block copolymer styrene / butadiene (SB), styrene / isoprene (SI), styrene / butadiene / isoprene (SBI) or the mixture of these copolymers.
    [0011]
    A tire according to any one of claims 1 to 8 wherein the styrenic thermoplastic elastomer comprises at least two rigid styrenic segments.
    [0012]
    12. A tire according to claim 11 wherein the styrenic thermoplastic elastomer is a triblock consisting of two rigid styrenic segments and a diene flexible segment.
    [0013]
    A tire according to claim 12 wherein the styrenic thermoplastic elastomer is a styrene / butadiene / styrene block copolymer (SBS), styrene / isoprene / styrene (SIS), styrene / butadiene / isoprene / styrene (SBIS) or the mixture of these copolymers.
    [0014]
    14. A tire according to any one of claims 1 to 13 wherein a fraction of the conjugated diene units of the at least one diene flexible segment is hydrogenated.
    [0015]
    15. A tire according to any one of claims 1 to 13 wherein all of the conjugated diene units of the at least one diene flexible segment is hydrogenated.
    [0016]
    The tire according to claims 9 and 15 wherein the styrenic thermoplastic elastomer is a styrene / ethylene / butylene (SEB), styrene / ethylene / propylene (SEP), styrene / ethylene / ethylene / propylene (SEEP) block copolymer or mixed.
    [0017]
    A tire according to claims 12 and 15 wherein the styrenic thermoplastic elastomer is a styrene / ethylene / butylene / styrene block copolymer (SEBS), styrene / ethylene / propylene / styrene (SEPS), styrene / ethylene / ethylene / propylene / styrene (SEEPS) or their mixture.
    [0018]
    18. A tire according to any one of claims 1 to 17 wherein the styrenic thermoplastic elastomer has a glass transition temperature of less than -20 ° C, preferably less than -30 ° C. P10-3243- 17 -
    [0019]
    19. A tire according to claim 18 wherein the styrenic thermoplastic elastomer has a glass transition temperature of less than -40 ° C, preferably less than -50 ° C.
    [0020]
    20. A tire according to any one of claims 1 to 19 wherein the reinforcing filler comprises a carbon black having a BET specific surface preferably of at least 90 m 2 / g, more preferably at least 100 m 2 / g.
    [0021]
    21. The tire of claim 20 wherein the reinforcing filler consists of a mixture of carbon black and silica.
    [0022]
    22. A tire according to any one of claims 1 to 21 wherein the tire is a tire off the road.
    [0023]
    23. The tire of claim 22 wherein the tire is a tire for a civil engineering vehicle.
    [0024]
    24. A method for manufacturing the tire according to any one of claims 1 to 23 which comprises the following steps: - adding in a first step said to be unproductive to the first diene elastomer, the styrenic thermoplastic elastomer, the reinforcing filler, the coupling agent, thermomechanically kneading until reaching a maximum temperature of between 130 and 200 ° C, - cooling the assembly to a temperature below 70 ° C, - then incorporate the crosslinking system, - kneading the whole up to a maximum temperature below 90 ° C to obtain a mixture, - then calender or extrude the resulting mixture to form a tread. 30 P10-3243
    类似技术:
    公开号 | 公开日 | 专利标题
    EP3310586B1|2020-04-29|Tyre for vehicles intended to bear heavy loads
    EP3083807B1|2020-02-05|Tire tread comprising a thermoplastic elastomer
    FR3015500A1|2015-06-26|PNEUMATIC FOR VEHICLES INTENDED TO WEAR HEAVY LOADS
    EP3099742B1|2020-04-15|Tyre provided with a tread comprising a thermoplastic elastomer
    EP3310585B1|2019-04-17|Tyre provided with a tread comprising a diene elastomer and thermoplastic elastomer system
    EP3152066A1|2017-04-12|Tyre with low rolling resistance
    EP2547728B1|2014-07-02|Tire and rubber composition containing a grafted polymer.
    WO2015091929A1|2015-06-25|Tire for vehicle bearing heavy loads
    EP3393823B1|2021-12-01|Tire for vehicles transporting heavy loads comprising a new tread
    EP3310584B1|2020-03-11|Tyre provided with a tread comprising a diene elastomer, a thermoplastic elastomer and a thermoplastic resin having polyphenylene ether patterns
    WO2015185395A1|2015-12-10|Tyre with low rolling resistance
    EP2524002A1|2012-11-21|Rubber composition including a polar thermoplastic elastomer including an alkylacrylate unit
    EP3099486B1|2018-01-03|Multilayer laminate for a tyre
    WO2015091922A1|2015-06-25|Tyre for vehicles intended to carry heavy loads
    EP3642050B1|2021-05-19|Pneumatic tyre for a vehicle carrying heavy loads, comprising a new tread
    WO2015091923A1|2015-06-25|Tire for vehicles bearing heavy loads
    EP2758466B1|2016-07-06|Off-road tyre tread
    EP2576684A1|2013-04-10|Pneumatic tire the crown of which is provided with an inner layer reducing rolling noise
    WO2019077272A1|2019-04-25|Rubber composition comprising a polyphenylene ether resin as a plasticiser
    EP3083273B1|2018-07-11|Tire for bicycle
    FR3056595A1|2018-03-30|TIRE TREAD COMPRISING A THERMOPLASTIC ELASTOMER
    FR3060585A1|2018-06-22|TIRE TREAD COMPRISING A MODIFIED ELASTOMER
    同族专利:
    公开号 | 公开日
    BR112016014503B1|2021-07-27|
    WO2015091933A1|2015-06-25|
    BR112016014503A2|2018-05-15|
    US20160312014A1|2016-10-27|
    FR3015500B1|2016-01-15|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    FR2954333A1|2009-12-23|2011-06-24|Michelin Soc Tech|PNEUMATIC HAVING THE TOP ZONE PROVIDED WITH A SUB-LAYER COMPRISING A THERMOPLASTIC ELASTOMER|
    WO2011161222A1|2010-06-23|2011-12-29|Societe De Technologie Michelin|Rubber composition comprising a thermoplastic filler and compatibilizer|
    FR2943065B1|2009-03-16|2011-04-22|Michelin Soc Tech|RUBBER COMPOSITION|
    CN102190822B|2010-03-17|2014-10-29|住友橡胶工业株式会社|Tire rubber composition and heavy-load tire|
    US8188355B2|2010-07-01|2012-05-29|Brian Eugene Tochilin|Adjustable depth snare drum|
    US8945906B2|2010-07-06|2015-02-03|University Of Maryland Baltimore County|Organic biofilm substrata as a microbial inoculum delivery vehicle for bioaugmentation of persistent organic pollutants in contaminated sediments and soils|EP3007909A4|2013-06-15|2017-03-01|Ronald Thompson|Annular ring and non-pneumatic tire|
    CA2976055A1|2015-02-04|2016-08-11|Advancing Mobility, Llc.|Non-pneumatic tire and other annular devices|
    FR3037593A1|2015-06-18|2016-12-23|Michelin & Cie|PNEUMATIC FOR VEHICLES INTENDED TO WEAR HEAVY LOADS|
    FR3045636B1|2015-12-22|2017-12-29|Michelin & Cie|TIRE FOR VEHICLE CARRYING HEAVY LOADS COMPRISING A NEW BEARING BAND|
    FR3056595A1|2016-09-29|2018-03-30|Compagnie Generale Des Etablissements Michelin|TIRE TREAD COMPRISING A THERMOPLASTIC ELASTOMER|
    WO2018227276A1|2017-06-15|2018-12-20|Camso Inc.|Wheel comprising a non-pneumatic tire|
    法律状态:
    2015-12-21| PLFP| Fee payment|Year of fee payment: 3 |
    2016-12-22| PLFP| Fee payment|Year of fee payment: 4 |
    2017-12-21| PLFP| Fee payment|Year of fee payment: 5 |
    2019-09-27| ST| Notification of lapse|Effective date: 20190906 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1363150A|FR3015500B1|2013-12-20|2013-12-20|PNEUMATIC FOR VEHICLES INTENDED TO WEAR HEAVY LOADS|FR1363150A| FR3015500B1|2013-12-20|2013-12-20|PNEUMATIC FOR VEHICLES INTENDED TO WEAR HEAVY LOADS|
    PCT/EP2014/078701| WO2015091933A1|2013-12-20|2014-12-19|Tyre for vehicles intended to bear heavy loads|
    US15/105,918| US20160312014A1|2013-12-20|2014-12-19|Tire for vehicles intended to bear heavy loads|
    BR112016014503-8A| BR112016014503B1|2013-12-20|2014-12-19|PNEUMATIC FOR VEHICLES INTENDED TO CARRY HEAVY LOADS|
    [返回顶部]