Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
  • C08C19/00—Chemical modification of rubber
  • C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
  • C08C19/42—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups
  • C08C19/44—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups of polymers containing metal atoms exclusively at one or both ends of the skeleton
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B60—VEHICLES IN GENERAL
  • B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
  • B60C1/00—Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
  • B60C1/0016—Compositions of the tread
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
  • C08C19/00—Chemical modification of rubber
  • C08C19/25—Incorporating silicon atoms into the molecule
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L19/00—Compositions of rubbers not provided for in groups C08L7/00 - C08L17/00
  • C08L19/006—Rubber characterised by functional groups, e.g. telechelic diene polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L15/00—Compositions of rubber derivatives

Definitions

• the present invention relates to a specific functionalized diene elastomer.
• This functionalized elastomer has a reduced cold creep without degrading the properties of a reinforced rubber composition that contains it, including its hysteretic properties.
• EP 0 778 31 1, EP 0 786 493 or WO 9850462 has described a reinforced rubber composition based on a diene polymer functionalized at the chain end by a silanol function or a polysiloxane block having at least one at least one silanol end.
• This functionalized elastomer is not subject to penalizing structural modifications in the context of its subsequent use in a tire.
• the composition comprising such a functionalized elastomer also has good hysteresis properties.
• patent application WO 2009/077837 describes elastomers functionalized at one end of chain by a silanol function or a polysiloxane block having at least one silanol end, and functionalized at the other chain end. These elastomers are also described as being capable of being associated with star-shaped elastomers, particularly with silicon. However, the associations illustrated lead to a reinforced rubber composition whose compromise of properties implemented and hysteresis is not satisfactory for an application in pneumatic.
• the Mooney drop of the elastomer is not without effect on the properties of the elastomer and leads more particularly to a tendency for the elastomer to have a significant cold flow.
• This creep or cold flow reflects the ability of the elastomers to flow under a load equal to their own weight, especially when samples or balls of these elastomers are stacked on top of one another in storage crates. .
• cold creep can cause significant disadvantages during transportation and storage of elastomers.
• the object of the present invention is to provide an elastomer which gives a reinforced rubber composition good hysteresis properties and implementation for application in pneumatic, while having a reduced cold flow in view of a better hold when storing rubber. This results in a minimization of the risk that elastomer samples or bullets overflow crates, causing a collapse of the latter and opposing the extraction of elastomers.
• a functionalized diene elastomer composed of a diene elastomer functionalized at one end of a chain only by a silanol function or a polysiloxane block having a silanol end and, to a certain extent, of a diene coupled or star diene elastomer, gives a rubber composition containing rubber properties, and in particular the hysteretic properties and implementation, quite satisfactory and acceptable for use in pneumatic , while having a significantly improved cold flow resistance.
• the rubber properties of this "
• composition is thus maintained at a level equivalent to those of compositions of the prior art based on a single elastomer functionalized at the chain end by a silanol function. This is all the more unexpected since one could expect an increase in the hysteresis and the implementation of the rubber composition in favor of the significant increase in cold creep resistance observed for the first time.
• functionalized diene elastomer which it comprises.
• the invention therefore relates to a diene elastomer functionalized at the chain end by a silanol function or a polysiloxane block having a silanol end and, to some extent, starred or coupled with tin.
• Another object of the invention is a rubber composition reinforced with at least one inorganic filler such as silica, comprising such a functionalized diene elastomer.
• the invention also relates to a tire which incorporates in at least one of its constituent elements a reinforced rubber composition according to the invention.
• the invention also relates to methods for reducing cold creep of a monofunctional diene elastomer carrying at one end of a chain a silanol function or a polysiloxane block having a silanol end, the other end being free of any functionalization.
• composition based is meant a composition comprising the mixture and / or the reaction product of the various constituents used, some of these basic constituents being capable of or intended to react between they, at least in part, during the various phases of manufacture of the composition, in particular during its crosslinking or vulcanization.
• any range of values designated by the expression "between a and b" represents the range of values from more than a to less than b (i.e. terminals a and b excluded) while any range of values designated by the term “from a to b” means the range from a to b (i.e., including the strict limits a and b).
• the term functionalized diene elastomer a diene elastomer which comprises a group comprising one or more heteroatoms.
• This grouping can be at the end of the chain. It will then be said that the diene elastomer is functionalized at the end of the chain.
• This is generally an elastomer obtained by reacting a living elastomer with a functionalizing agent, that is to say any molecule that is at least monofunctional, the function being any type of chemical group known to those skilled in the art for reacting with a piece of living chain
• This group may be in the linear main elastomeric chain. It will be said that the diene elastomer is coupled or functionalized in the middle of the chain, as opposed to the position "at the end of the chain” and although the group is not precisely in the middle of the elastomeric chain. It is generally an elastomer obtained by reaction of a living elastomer on a coupling agent, that is to say any molecule at least difonfunctional, the function being any type of chemical group known to those skilled in the art to react with a piece of living chain.
• This group may be central to which n elastomeric chains (n> 2) are bonded forming a star structure of the elastomer. It will then be said that the diene elastomer is starred. It is generally an elastomer obtained by reaction of a living elastomer on a starzing agent, that is to say any multifunctional molecule, the function being any type of chemical group known to those skilled in the art to react with a piece of living chain
• a first object of the invention is therefore a functionalized diene elastomer characterized in that it is composed of 75 to 95% by weight of functional diene elastomer functionalized at the chain end by a silanol function or a polysiloxane block having a silanol end and from 5 to 25% by weight of star-diene or tin-coupled diene elastomers. These percentages refer to the total weight of the functionalized diene elastomer.
• the functionalized diene elastomer carrying at the end of the chain a silanol function or a polysiloxane block having a silanol end is It is present in the functionalized diene elastomer in proportions ranging from 75% to 95% by weight of the total weight of the functionalized elastomer, preferably from 75% to 90% by weight, more preferably from 75% to 85% by weight. % by weight, for example from 80% to 85% by weight.
• a preferential polysiloxane block having a silanol end are suitable those having the following general formula:
• R 1 and R 2 which are identical or different, represent an alkyl, cycloalkyl, aryl, alkaryl, aralkyl or vinyl group having from 1 to 10 carbon atoms, preferably an alkyl group having 1 to 6 carbon atoms, more preferably still and R 2 each represent a methyl radical.
• x is an integer ranging from 1 to 1500 and preferably from 1 to 50, more preferably still x is 1.
• the functionalized diene elastomer carrying a silanol function at the chain end or a silanol end polysiloxane block is monofunctional.
• the diene elastomer is functionalized at one end of the chain. The other end of the chain is free and has no function.
• the star-diene or tin-coupled diene elastomer is present in the functionalized elastomer in an amount of 5% to 25% by weight of the total weight of the functionalized elastomer, preferably ranging from 10 to 10% by weight. % to 25% by weight, more preferably still 15 to 25% by weight, for example 15 to 20% by weight.
• the star-diene or tin-coupled diene elastomer is present in the functionalized elastomer in an amount of 5% to 25% by weight of the total weight of the functionalized elastomer, preferably ranging from 10 to 10% by weight. % to 25% by weight, more preferably still 15 to 25% by weight, for example 15 to 20% by weight.
• the star-diene elastomer or coupled with tin the compromise cold creep of the elastomer / rubber properties of the rubber composition is penalized because of the increase in hysteresis .
• the diene elastomer is advantageously starred with tin, that is to say that the tin atom is linked to n chains.
• elastomers (n> 2) forming a star structure of the elastomer. More preferably still, four elastomeric chains are linked to tin; which results in a star-shaped elastomer with four branches.
• diene elastomer capable of being used in accordance with the invention is meant any homopolymer obtained by polymerization of a conjugated diene monomer having from 4 to 12 carbon atoms, any copolymer obtained by copolymerization of one or several conjugated dienes with each other or with one or more vinylaromatic compounds having 8 to 20 carbon atoms.
• conjugated dienes 1,3-butadiene, 2-methyl-1,3-butadiene, 2,3-di (C 1 -C 5) alkyl-1,3-butadiene, such as for example 2,3-dimethyl-1,3-butadiene, 2,3-diethyl-1,3-butadiene, 2-methyl-3-ethyl-1,3-butadiene, 2-methyl-3-isopropyl- 1,3-butadiene, phenyl-1,3-butadiene, 1,3-pentadiene, 2,4-hexadiene, etc.
• vinylaromatic compounds are especially suitable styrene, ortho-, meta, para-methylstyrene, the commercial mixture "vinyltoluene", para-tertiobutylstyrene, methoxy styrene s, vinylmesitylene, divinylbenzene, vinylnaphthalene, etc ..
• the copolymers may contain between 99% and 20% by weight of diene units and from 1% to 80% by weight of vinylaromatic units.
• the functionalized diene elastomer according to the invention is preferably chosen from the group of highly unsaturated diene elastomers consisting of polybutadienes (B), synthetic polyisoprenes (IR), butadiene copolymers and isoprene copolymers. and mixtures of these elastomers.
• Such copolymers are more preferably chosen from butadiene-styrene copolymers (SBR). - o -
• the functionalized diene elastomer can have any micro structure which is a function of the polymerization conditions used.
• the elastomer can be block, random, sequenced, microsequenced, etc. and be prepared in dispersion or in solution.
• the micro structure of these elastomers may be determined by the presence or absence of a modifying and / or randomizing agent and the amounts of modifying and / or randomizing agent used.
• the functionalized diene elastomer having at the chain end a silanol function or a polysiloxane block having a silanol end and the stannous or tin-coupled diene elastomer may have the same or different micro-structure.
• polybutadienes having a content (mol%) in units -1.2 of between 4% and 80% or those having a content (mol%) of cis-1,4 greater than 80% polybutadienes having a content (mol%) in units -1.2 of between 4% and 80% or those having a content (mol%) of cis-1,4 greater than 80%, polyisoprenes, copolymers of butadiene-styrene and in particular those having a Tg (glass transition temperature, measured according to ASTM D3418) between -80 ° C. and 0 ° C. and more particularly between -70 ° C.
• Tg glass transition temperature
• styrene content between 5% and 60% by weight and more particularly between 20% and 50%, a content (mol%) in -1,2 bonds of the butadiene part of between 4% and 75%, a content (mol%) of trans-1,4 bonds of between 10% and 80%, butadiene-isoprene copolymers and especially those having an isoprene content of between 5% and 90% by weight and a Tg of -80 ° C to -40 ° C , isoprene-styrene copolymers and in particular those having a styrene content of between 5% and 50% by weight and a Tg of between -50 ° C. and 0 ° C.
• butadiene-styrene-isoprene copolymers are particularly suitable those having a styrene content of between 5% and 50% by weight and more particularly between 10% and 40%, an isoprene content of between 15% and 60% by weight and more particularly between 20% and 50%, a butadiene content of between 5% and 50% by weight and more particularly between 20% and 40%, a content (mol%) in units -1, 2 of the butadiene part of between 4% and 85%, a content (mol%) in trans-1,4 units of the butadiene part of between 6% and 80%, a content (mol%) in units -1,2 plus -3.4 of the isoprenic portion between 5% and 70% and a content (mol%) in trans units -1,4 of the isoprenic part of between 10% and 50%, and more generally any butadiene-styrene-isoprene copolymer having a Tg of between -70 ° C. and 0 ° C.
• the functionalized diene elastomer at the end of the chain and the star-diene or tin-coupled diene elastomers are, before their functionalization, of the same nature.
• non-identical elastomers which are considered in the tire field as similar elastomers due to comparable technical effects are also within the scope of the invention.
• the polymerization of diene monomers is initiated by an initiator.
• an initiator any known monofunctional anionic initiator can be used.
• an initiator containing an alkali metal such as lithium is used in a preferred manner.
• organolithium initiators are particularly suitable those having a carbon-lithium bond.
• an organolithium hydrocarbon initiator having no heteroatom Preferably, use will be made of an organolithium hydrocarbon initiator having no heteroatom.
• Representative compounds are aliphatic organoliths such as ethyllithium, n-butyllithium (n-BuLi), isobutyl lithium, polymethylenes dilithium such as 1,4-dilithiobutane, etc.
• the polymerization is, as known per se, preferably carried out in the presence of an inert solvent which may be for example an aliphatic or alicyclic hydrocarbon such as pentane, hexane, heptane, isooctane, cyclohexane or an aromatic hydrocarbon such as benzene, toluene, xylene.
• an inert solvent which may be for example an aliphatic or alicyclic hydrocarbon such as pentane, hexane, heptane, isooctane, cyclohexane or an aromatic hydrocarbon such as benzene, toluene, xylene.
• the polymerization can be carried out continuously or discontinuously.
• the polymerization is generally carried out at a temperature of between 20 ° C. and 120 ° C. and preferably in the region of 30 ° C. to 90 ° C. It is of course also possible to add at the end of the polymerization a transmetallation agent for modifying the reactivity of the living-chain end.
• the living diene elastomer resulting from the polymerization is then functionalized to prepare the functionalized diene elastomer according to the invention.
• the functionalized diene elastomer is mixed at the end of the chain with a silanol function or a polysiloxane block having a silanol end and diene starch or tin-coupled elastomer, in the appropriate proportions.
• the diene elastomer functionalized at the chain end by a silanol function or a polysiloxane block having a silanol end may advantageously be obtained according to the procedures described in patent application EP-A-0 778 31 1, the description of which is described in US Pat. is integrated by reference.
• the diene elastomer star or coupled to tin can be obtained in a manner known per se by reaction of a tin derivative on the living diene elastomer resulting from the polymerization.
• the preparation of such a star-diene elastomer is described, for example, in US Pat. No. 3,393,182.
• the two elastomers can be mixed in an inert solvent, for example an aliphatic or alicyclic hydrocarbon such as pentane, hexane, heptane, isooctane, cyclohexane or an aromatic hydrocarbon such as benzene. , toluene, xylene, which may be the same as the polymerization solvent.
• an inert solvent for example an aliphatic or alicyclic hydrocarbon such as pentane, hexane, heptane, isooctane, cyclohexane or an aromatic hydrocarbon such as benzene. , toluene, xylene, which may be the same as the polymerization solvent.
• the mixing will then be carried out at a temperature of between 20 ° C. and 120 ° C. and preferably in the region of 30 ° C. to 90 ° C.
• the living diene elastomer resulting from the polymerization step is subjected to the reaction of a coupling agent or dimer-based starch. tin and that of a functionalizing agent capable of introducing at the end of the polymer chain the silanol function or the polysiloxane block having a silanol end.
• cyclic polysiloxane type agents capable of introducing at the end of the polymer chain the silanol function or the polysiloxane block having a silanol end
• Cyclic polysiloxanes which may be mentioned are those corresponding to the formula: ⁇ ⁇
• R 1 and R 2 which are identical or different, represent an alkyl, cycloalkyl, aryl, alkaryl, aralkyl or vinyl group having from 1 to 10 carbon atoms,
• n an integer of value 3 to 8.
• cyclic polysiloxane compounds examples include hexamethylcyclotrisiloxane, trimethyltriethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and mixtures thereof.
• tin coupling or starring agents mention may be made of tin derivatives of formula SnRxX4-x, where x represents an integer of value 0 to 2, R representing an alkyl or cycloalkyl radical, aryl, alkaryl, aralkyl, vinyl having 1 to 10 carbon atoms, preferably an alkyl radical having 1 to 4 carbon atoms, and X is a halogen atom, preferably chlorine.
• dibutyl tin dichloride or tin tetrachloride the latter being very particularly preferred.
• the functionalization can be obtained with a functionalizing agent derived from tin that can respond to the general formula (X 1 i R 1 2 Sn) -O- (SnR 1 3 - y X 1) or (X 1! R 2 1 Sn) -O- (CH2) n -O- (SnR 3-yl 1 1 X y), where y represents an integer of 0 or 1, R 1 represents an alkyl, cycloalkyl, aryl, alkaryl or vinyl having 1 to 12 carbon atoms, preferably butyl, X 1 is a halogen atom, preferably chlorine, and n is an integer of 1 to 20, preferably 4.
• the functionalization of the living diene elastomer resulting from the polymerization step can be carried out at a temperature ranging from 30 to 120 ° C., in the presence initially of an appropriate amount of a tin-based agent for staring or coupling 5% to 25% by weight of the living diene elastomer. Then, in "
• a second step the remaining living chains of the diene elastomer obtained after the first step are functionalized by adding a functionalizing agent capable of introducing at the end of the polymer chain the silanol function or the polysiloxane block having one end. silanol and reaction with this agent.
• the functionalization reaction of the diene elastomer is then stopped by the deactivation of the remaining living chains and by reaction of the chain ends SiO "with a proton donor compound to yield the functionalized diene elastomer according to the invention.
• the functionalized diene elastomer according to the invention has improved cold creep resistance. Which induces a better behavior during storage and transportation of this rubber.
• the functionalized diene elastomer according to the invention may be advantageously used in a rubber composition reinforced with at least one inorganic filler such as silica, which it maintains the dynamic properties and implementation at a satisfactory level for a tire application.
• This rubber composition is also the subject of the invention.
• the rubber composition is based on at least one reinforcing filler comprising an inorganic filler, and an elastomer matrix comprising the functionalized diene elastomer described above.
• the functionalized diene elastomer according to the invention is present in the rubber composition in proportions ranging from 10 to 100 phr.
• the functionalized diene elastomer is present in the elastomer matrix in a majority weight fraction.
• major weight fraction means the highest weight fraction of the matrix, preferably a weight fraction of at least 50%.
• the weight fraction refers to the total weight of the elastomer matrix.
• the diene elastomer functionalized according to the invention is then present in the elastomer matrix in an amount ranging from 50 to 100 phr, preferably 60 to 100 phr.
• the elastomer matrix may also comprise, in addition to the functionalized diene elastomer defined above, at least one diene elastomer conventionally used in tires such as natural rubber or a synthetic elastomer, or another functionalized diene elastomer, coupled or starry.
• This or these other diene elastomers are present in the matrix in proportions ranging from 0 to 90 phr, or even, according to the variant above, in proportions ranging from 0 to 50 phr.
• the rubber composition according to the invention further comprises the elastomer matrix, at least one reinforcing filler comprising an inorganic filler.
• inorganic filler is meant in the present application, by definition, any inorganic or mineral filler regardless of its color and origin (natural or synthetic), also called “white” charge, “clear” charge or “ non-black filler “(” non-black filler ”) as opposed to carbon black, capable of reinforcing on its own, with no other means than an intermediate coupling agent, a rubber composition intended for the manufacture of tires, in particular other terms capable of replacing, in its reinforcing function, a conventional carbon black of pneumatic grade; such a filler is generally characterized, in known manner, by the presence of hydroxyl groups (-OH) on its surface.
• inorganic filler is also meant any mixture of these fillers.
• the reinforcing inorganic filler is, wholly or at least predominantly, silica (SiO 2 ).
• the silica used may be any reinforcing silica known to those skilled in the art, in particular any precipitated or fumed silica having a BET surface and a CTAB specific surface area both less than 450 m 2 / g, even if the highly dispersible precipitated silicas are preferred.
• As reinforcing inorganic filler mention may also be made of mineral fillers of the aluminous type, in particular alumina (Al 2 O 3) or
• reinforcing inorganic filler is indifferent, whether in the form of powder, microbeads, granules, or beads.
• reinforcing inorganic filler is also understood to mean mixtures of different reinforcing inorganic fillers, in particular of highly dispersible silicas as described above.
• the reinforcing inorganic filler can be cut (mixed) with an organic filler, such as carbon black, thus constituting the reinforcing filler of the composition according to the invention.
• this reinforcing filler consists mainly of the reinforcing inorganic filler, that is to say that the proportion of inorganic filler is greater than 50% by weight of the total weight of the filler. the load, the maximum being 100%.
• the reinforcing filler consists of 70% to 100% by weight of the inorganic filler.
• carbon blacks are suitable for all carbon blacks, including blacks of the type HAF, ISAF, SAF, FF, FEF, GPF and S F conventionally used in the rubber composition for tires (so-called pneumatic grade black).
• the reinforcing carbon blacks of the 100, 200 or 300 series for example blacks NI 15, N134, N234, N326, N330, N339, N347, N375, are also more particularly mentioned.
• coarser blacks such as blacks N550 or N683.
• the carbon blacks could for example already be incorporated into the rubber in the form of a masterbatch.
• organic fillers other than carbon blacks
• the weight fraction of this carbon black in said reinforcing filler is preferably chosen less than or equal to 30% relative to the total weight of the filler. reinforcing, more preferably less than 20%.
• the composition according to the invention comprises from 35 to 200 phr of reinforcing filler.
• the level of reinforcing filler is between 40 and 140 phr, more preferably between 50 and 130 phr, the optimum being, in known manner, different according to the particular applications concerned; especially in the tire the level of reinforcement expected on a bicycle tire, for example, is of course less than that required on a tire capable of driving at high speed in a sustained manner, for example a motorcycle tire, a tire for a passenger vehicle or for utility vehicle such as Truck.
• a coupling agent or bonding agent
• a coupling agent at least bifunctional intended to ensure a sufficient connection, chemical and / or physical, between the inorganic filler and diene elastomer, in particular organosilanes or bifunctional polyorganosiloxanes.
• polysulfide silanes called “symmetrical” or “asymmetrical” according to their particular structure, are used, as described for example in the applications WO03 / 002648 (or US 2005/016651) and WO03 / 002649 (or US 2005 / 016650).
• x is an integer of 2 to 8 (preferably 2 to 5);
• a ' is a divalent hydrocarbon radical (preferably C 1 -C 6 alkylene groups or C 6 -C 12 arylene groups, plus especially alkylene Q-Qo, especially Ci-C 4 , especially propylene);
• radicals R'1 substituted or unsubstituted, identical or different, represent alkyl CrQg cycloalkyl, C 5 - IC8 aryl or C 6 -C 8 (preferably alkyl, Ci-C 6 ; cyclohexyl or phenyl, in particular alkyl groups, C 4, more particularly methyl and / or ethyl).
• radicals R '2 substituted or unsubstituted, identical or different, represent an alkoxy group or cycloalkoxy Qg Q-C5-C18 (preferably a group selected from Q-Cg alkoxyls cycloalkoxyls C 5 - C 8 , more preferably still a group selected from C 1 -C 4 alkoxyls, in particular methoxyl and ethoxyl).
• polysulphurized silanes By way of examples of polysulphurized silanes, mention may be made more particularly of bis (3-trimethoxysilylpropyl) polysulfides or of bis (3-triethoxysilylpropyl) polysulfides. Among these compounds, bis (3-triethoxysilylpropyl) tetrasulfide, abbreviated as TESPT, or bis (triethoxysilylpropyl) disulfide, abbreviated as TESPD, is especially used.
• TESPT bis (3-triethoxysilylpropyl) tetrasulfide
• TESPD bis (triethoxysilylpropyl) disulfide
• polysulfides especially disulfides, trisulfides or tetrasulfide s
• polysulfides especially disulfides, trisulfides or tetrasulfide s
• tetrasulfide bis- monoethoxydimethylsilylpropyl as described in patent application WO 02/083782 (or US 2004/132880).
• a coupling agent other than the poly (sulfonated) alkoxysilane mention may be made in particular of bifunctional POSS (polyorganosiloxanes) or else hydroxysilane polysulfides as described in patent applications WO 02/30939 (or US Pat. No. 6,774,255) and WO 02/31041 (or US 2004/051210), or else silanes or POSS bearing functional azo-dicarbonyl groups, such as described for example in patent applications WO 2006/125532, WO 2006/125533, WO 2006/125534.
• bifunctional POSS polyorganosiloxanes
• hydroxysilane polysulfides as described in patent applications WO 02/30939 (or US Pat. No. 6,774,255) and WO 02/31041 (or US 2004/051210)
• silanes or POSS bearing functional azo-dicarbonyl groups such as described for example in patent applications WO 2006/125532, WO 2006/125533, WO 2006/1255
• the level of coupling agent is advantageously less than 20 phr, it being understood that it is generally desirable to use the least possible amount. Its content is preferably between 0.5 and 12 phr, more preferably between 3 and 10 phr. Typically, the level of coupling agent is at least 0.5% and at most 15% by weight relative to the amount of inorganic filler, preferably at most 12% and more particularly at most 10%.
• the rubber compositions in accordance with the invention may also contain, in addition to the coupling agents, coupling activators, inorganic charge-covering agents or, more generally, processing aid agents capable of 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 implement in the green state.
• the rubber compositions in accordance with the invention may also comprise all or part of the usual additives usually used in elastomer compositions intended for the manufacture of tires, such as, for example, pigments, non-reinforcing fillers, such as anti-ozone waxes, chemical anti-ozonants, anti-oxidants, anti-fatigue agents, plasticizing agents, reinforcing or plasticizing resins, acceptors (for example phenolic novolac resin) or methylene donors (for example HMT or H3M) as described for example in the application WO 02/10269, a crosslinking system based on either sulfur, or sulfur and / or peroxide and / or bismaleimide donors, vulcanization accelerators, activators vulcanization.
• additives usually used in elastomer compositions intended for the manufacture of tires such as, for example, pigments, non-reinforcing fillers, such as anti-ozone waxes, chemical anti-ozonants, anti-oxidants, anti-fatigue agents,
• compositions of the invention may also comprise, as preferential non-aromatic or very weakly aromatic plasticizing agent, at least one compound chosen from the group consisting of naphthenic and paraffinic oils.
• the overall plasticizer content is preferably at least 10 and at most 100 phr, more preferably at most 80 phr, or even at most 70 phr.
• the composition comprises a plasticizer system composed of at least one MES or TDAE oil and at least one high Tg resin, each of the components being present for example in amounts ranging from 5 to 35 phr.
• the rubber composition according to the invention may be prepared according to a process which comprises at least the following steps:
• thermomechanical working time (sometimes referred to as a "non-productive" phase) of the necessary basic constituents, with the exception of the crosslinking composition, said composition comprising the elastomer matrix and a reinforcing filler, and
• the rubber composition thus obtained can then advantageously be extruded or calendered in a manner known per se, in the desired form, to manufacture semi-finished products such as treads.
• This process may also comprise, prior to carrying out the steps (i) and (ii) above, the steps of the preparation of the elastomer matrix and more particularly those of the preparation of the functionalized diene elastomer according to the invention. .
• the invention also relates to a tire which incorporates in at least one of its constituent elements a reinforced rubber composition according to the invention, and more particularly the invention relates to semi-finished articles of a tire. who understand this composition. Due to the cold creep resistance which characterizes the functionalized diene elastomer according to the invention, it will be noted that the storage and transport of this elastomer are substantially improved with respect to an elastomer without a star.
• the use of the rubber composition comprising the functionalized diene elastomer according to the invention, for the manufacture of a tread provides the tire containing a rolling resistance of a suitable level.
• the invention therefore more particularly relates to a tire tread which is such that it comprises a reinforced rubber composition according to the invention or which is such that it consists exclusively of this composition.
• the invention also relates to a method for reducing cold creep of a monofunctional diene elastomer carrying at one end of a chain a silanol function or a polysiloxane block having a silanol end, the other end being free of any functionalization.
• This process consists in conditioning the elastomer beforehand, modifying it by adding a diene coupled or star-diene elastomer in a proportion of 5 to 35% by weight relative to the weight of the monofunctional diene elastomer, in order to obtain a functionalized diene elastomer of which 75% to 95% by weight carries at one end of a chain a silanol function or a polysiloxane block having a silanol end, the other end being free of any functionalization, and 5% and 25% by weight is star-shaped or coupled with tin.
• the invention also relates to a process for reducing cold creep of a monofunctional diene elastomer carrying at one end of a chain a silanol function or a polysiloxane block having a silanol end, the other end being free from any functionalization.
• This process consists, during the synthesis of the diene elastomer, at the end of the polymerization stage, of coupling or starring of 5 to 25% by weight of the live elastomer with a tin-based compound then to functionalize 75 to 95% by weight of living elastomer remaining 2Q with a functionalization agent capable of introducing the silanol function or a polysiloxane block having a silanol end.
• Mn number-average molecular weight
• Mw weight average molecular weight
• the macromolecules are physically separated according to their respective sizes in the inflated state, in columns filled with a porous stationary phase.
• the polymer sample is solubilized in tetrahydrofuran at a concentration of about 1 g / l. Then the solution is filtered on 0.45 ⁇ porosity filter before injection.
• the injected volume of the polymer sample solution is 100 ⁇ .
• the detector is a differential refractometer "WATERS” whose model is “2410”. Chromatographic data exploitation software is used, whose trade name is WATERS EMPOWER.
• the calculated average molar masses relate to a calibration curve produced for SBRs of the following micro structure: 25% by mass of styrene-type units, 23% by mass of type-1,2 units and 50% by mass of type-1 units. 4 trans.
• the 1 H- 29 Si 2D NMR spectrum makes it possible to verify the nature of the function by virtue of the chemical shift values of the silicon nuclei and the protons in the neighborhood 2 J (via 2 links). It uses a coupling constant value 2 Jm-29Si of 8 Hz.
• the chemical shift of the silicon of the species SBR (CH 3 ) 2 SiOH at the end of the chain is about 1 1-12 ppm.
• the samples are solubilized in carbon disulfide (CS 2 ).
• 100 L of deuterated cyclohexane (C 6 D 12 ) are added for the lock signal.
• the NMR analyzes are carried out on a BRUKER 500 MHz spectrometer equipped with a BBI 5 mm broadband probe. For the quantitative 1H NMR experiment, the sequence uses a 30 ° pulse and a 2 second repetition time.
• the elastomer is solubilized in CDCl 3 at a concentration of about 75 g / L.
• the inherent viscosity is determined by measuring the flow time t of the polymer solution and the flow time to toluene in a capillary tube. In a Ubbelhode tube (capillary diameter 0.46 mm, capacity 18 to 22 ml), placed in a bath thermostated at 25 ⁇ 0.1 ° C, the flow time of toluene and that of the polymer solution at 0.1 g / dl are measured.
• t flow time of the toluene solution of polymer in seconds
• t 0 toluene flow time in seconds
• the die has a diameter of 6.35 mm and a thickness of 0.5 mm.
• the cold-flow apparatus is a cylindrical cut, pierced at the bottom. About 40g ⁇ 4g of previously prepared gum (2 cm in thickness and 52 mm in diameter) are placed in this device. On the rubber disc, a calibrated piston of 1 kg ( ⁇ 5 g) is positioned. The assembly is then placed in an oven, thermally stabilized at 100 ° C. ⁇ 0.5 ° C.
• the result of the test is the weight of gum weighed in grams.
• 32.5 l reactor equipped with a turbine-type stirrer is continuously fed with cyclohexane, butadiene, styrene and tetrahydrofurfuryl ethyl ether, in accordance with mass flow rates of 100/1 1 / 3.2 / 0.037, respectively. .
• 200 micromoles of n-butyllithium (n-BuLi) per 100 g of monomers are introduced at the line inlet in order to neutralize the protic impurities introduced by the various constituents present in the line inlet.
• 530 ⁇ of n-BuLi per 100 g of monomers are introduced.
• the different flow rates are adjusted so that the average residence time in the reactor is 40 minutes.
• the temperature is maintained at 80 ° C.
• the conversion rate which is measured on a sample taken at the outlet of the reactor, is 98%.
• the copolymer thus treated is separated from its solution by a steam stripping operation, and then dried on a roll tool at 100 ° C. for 20 minutes, to obtain the functionalized SiOH functional copolymer at the end of the chain.
• the ML viscosity of this copolymer A is 53.
• the molecular weight of the copolymer, determined by conventional SEC, is 123,000 g / mol, the Ip is 2.0.
• the SBR block of this copolymer A contains 25% of styrene (by weight) and, for its butadiene part, 58% of vinyl units, 21% of 1,4 cis units and 21% of 1,4 trans units.
• copolymer B which is carried out according to the operating conditions described in test 1, except that tin tetrachloride is added in place of hexamethylcyclotrisiloxane, 265 micromoles per 100 g of tetrachloride monomers of tin in solution in cyclohexane.
• the ML viscosity of copolymer B is 104.
• the molecular weight of the copolymer, determined by conventional SEC, is 209,000 g / mol, the Ip is 2.1.
• the SBR block of this copolymer B contains 25% of styrene (by weight) and, for its butadiene part, 58% of vinyl units, 21% of 1,4 cis units and 21% of 1,4 trans units.
• Hardness SHO E A measurements made according to DIN 53505. The results are in relative data: an increase compared to the control at 100 indicates an increased rigidity.
• the dynamic properties AG * and tan ( ⁇ ) max are measured on a viscoanalyzer (Metravib VA4000) according to ASTM D 5992-96.
• the response of a sample of vulcanized composition (cylindrical specimen 2 mm thick and section 79 mm 2 ), subjected to sinusoidal stress in alternating simple shear, at the frequency of 10 Hz, under normal conditions is recorded.
• temperature (23 ° C) according to ASTM D 1349-99.
• a peak-to-peak deformation amplitude sweep of 0.1% to 50% (forward cycle) followed by 50% to 0.1% (return cycle) is performed.
• the results exploited are the complex dynamic shear modulus (G *) and the loss factor tan ⁇ .
• the SBR C, SBR D, SBR E and SBR F elastomers were used for the preparation of tread-like rubber compositions C, D, E and F, each comprising silica as a reinforcing filler.
• compositions C, D, E and F has the following formulation (expressed in phr: parts per hundred parts of elastomer):
• compositions are performed, firstly, by a thermomechanical work, then, in a second finishing time, by mechanical work.
• thermomechanical working step is carried out for 4 to 5 minutes, until a maximum temperature of about 160 ° C. falls.
• thermomechanical work is thus achieved, it being specified that the average speed of the pallets during this first time is 50 rpm.
• compositions thus obtained are then calendered, either in the form of plates (with a thickness ranging from 2 to 3 mm) or thin rubber sheets, for the measurement of their physical or mechanical properties, or in the form of directly usable profiles, after cutting and / or assembly to the desired dimensions, for example as semi-finished products for tires, in particular for treads.
• the crosslinking is carried out at 150 ° C for 40 min.
• the cold flow resistance of the functionalized diene elastomer significantly improves by increasing the level of tin-starred copolymer in the rubber composition with respect to a composition B which does not does not contain any.
• compositions C, D and E there is a retention of tan ( ⁇ ) max at acceptable values, despite the increase in the level of star-stanned copolymer at the expense of the end-functionalized copolymer by a silanol function.
• compositions C, D and E comprising respectively in their elastomer matrix 5%, 10% and 20% of a star-bound copolymer. 'tin.

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