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
  • C08C19/25—Incorporating silicon atoms into the molecule
• • 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
  • C08C19/30—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
• • 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
• • 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

Definitions

• the invention relates to a diene elastomer modified with functionalizing agents of di- and trialkoxy silane type having amino functional groups.
• the invention also relates to a method for preparing such a diene elastomer, a composition comprising it, and a semi-finished article and a tire comprising this composition.
• Patent FR2867477A1 which claims functionalization at the end of a chain with compounds of type e (dialkylaminoalkyl) trialkoxysilane and a rubber composition based on silica or carbon black. It is also possible to mention US Pat. No. 8071689B2 and US Pat. No. 8,101,30B2, which respectively claim, for one, functionalization at the end of a chain with a trialkoxysilane compound carrying a nitrogen group, the nitrogen atom being included in an aromatic heterocycle substituted or unsubstituted. substituted, and for the other, with an alkoxysilane carrying an amine function having at least one alkoxysilyl group and at least two tertiary amine groups.
• the strategy consists in adding the aminoalkoxysilane compound, preferably of the (aminoalkyl) trialkoxysilane type, in two stages during the functionalization stage: i) 1st addition in an amount such that the molar ratio n ((aminoalkyl) trialkoxysilane) / n (initiator based on alkali metal) is between 0.05 and 0.35, ii) then 2 nd addition in an amount such that the final molar ratio n ((aminoalkyl) trialkoxysilane) / n (metal-based initiator alkaline) is greater than or equal to 0.5.
• This process makes it possible to obtain a functional diene elastomer mixture comprising 40 to 80% by weight of functionalized elastomer at the end of the chain, 5 to 45% by weight of functionalized elastomer in the middle of the chain and 3 to 30% by weight. of star - shaped elastomer (3 - star stars).
• Patent EP0801078B1 may also be mentioned, claiming the addition of a carboxylic acid to the elastomer solution, with a molar ratio n (carboxylic acid) / n (anionic polymerization initiator) of between 0.8 and 1.2, before the stripping step in order to neutralize the basicity provided by the anionic polymerization initiator and to minimize the hydrolysis of the alkoxysilane groups.
• patent EP1198506B1 it is proposed to add a compound of the alkylalkoxysilane type (R 1 n Si (OR 2 ) 4 n) in the elastomer solution, before the stripping step, with a molar ratio n (R 1 Si (OR 2 ) 4- n) / n (Polymer-SiOR ') raised (20/1) to promote the reaction between the alkylalkoxysilane and the polymer which is in its hydrolysed form, Polymer-SiOH, by stripping .
• n R 1 Si (OR 2 ) 4- n
• n Polymer-SiOR '
• the object of the present invention is therefore to provide such a composition.
• One objective is in particular to propose a functionalized elastomer satisfactorily interacting with the reinforcing filler of a rubber composition containing it in order to reduce the hysteresis, while improving the processability and the storage stability of the Mooney viscosity of the elastomer.
• the invention therefore has obj and a modified diene elastomer comprising
• the subject of the invention is also a process for the synthesis of said modified diene elastomer.
• Another object of the invention is a reinforced rubber composition based at least on a reinforcing filler and an elastomeric matrix comprising at least said modified diene elastomer.
• 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 of values from a to b (ie including the strict limits a and b).
• the elastomeric species has an alkylalkoxysilane functional group, optionally partially or completely hydrolyzed to silano, carrying a primary, secondary or tertiary amine function, at one end of the chain, it will be said that the species is end functionalized. or chain end.
• the silicon atom of this group is directly linked to the chain of the diene elastomer and is substituted only by a single alkoxy group, in addition to the alkyl radical and the group comprising the amine function.
• the elastomeric species has an alkoxysilane functional group, optionally partially or completely hydrolyzed silano l, carrying a primary, secondary or tertiary amine function, within its elastomeric chain, the silicon atom of this group linking the two pieces of the chain of the diene elastomer, it is said that the elastomer is coupled or functionalized in the middle of the chain, as opposed to the "end of chain" position and although the grouping is not precisely in the middle of the elastomeric chain.
• silane functional group bearing a primary, secondary or tertiary amine function When a silane functional group bearing a primary, secondary or tertiary amine function is central to which three elastomer chains or branches are bonded forming a star structure of the elastomer, the species will then be said to be starred.
• the silicon atom of this group links the three branches of the modified diene elastomer to one another.
• 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 with one another, less in part, during the various phases of manufacture of the composition, in particular during its crosslinking or vulcanization.
• diene elastomer By diene elastomer, it is to be understood in a known way (one means one or more elastomers) derived at least in part (ie, a homopolymer or a copolymer) from monomers dienes (monomers bearing two carbon-carbon double bonds, conjugated or not). More particularly, the term "diene elastomer” is intended to mean any homopolymer obtained by polymerization of a conjugated diene monomer having 4 to 12 carbon atoms, or any copolymer obtained by copolymerization of one or more conjugated dienes with one another or with one or more compounds. vinylaromatic compounds having 8 to 20 carbon atoms.
• copolymers contain from 20% to 99% by weight of diene units, and from 1 to 80% by weight of vinylaromatic units.
• conjugated dienes which can be used in the process according to the invention, 1,3-butadiene, 2-methyl-1,3-butadiene, 2,3-di (C 1 to C 5 ) -alkyl-1 are especially suitable.
• 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 and 2,4-hexadiene, etc.
• vinylaromatic compounds are especially suitable styrene, ortho-, meta, para-methylstyrene, alpha-methylstyrene, the commercial mixture "vinyltoluene", para-tertiobutylstyrene, methoxystyrenes, vinylmesitylene, divinylbenzene and vinylnaphthalene etc.
• the diene elastomer of the invention is preferably chosen from the group of highly unsaturated diene elastomers consisting of polybutadienes (BR), synthetic polyisoprenes (IR) and butadiene copolymers, in particular butadiene copolymers and a vinyl aromatic monomer, isoprene copolymers and mixtures of these elastomers.
• BR polybutadienes
• IR synthetic polyisoprenes
• butadiene copolymers in particular butadiene copolymers and a vinyl aromatic monomer, isoprene copolymers and mixtures of these elastomers.
• Such copolymers are more particularly copolymers of butadiene-styrene (SBR), copolymers of isoprene-butadiene (BIR), copolymers of isoprene-styrene (SIR) and copolymers of isoprene-butadiene-styrene (SBIR) .
• SBR butadiene-styrene copolymers
• SBR butadiene-styrene copolymers
• E denotes the diene elastomer
• R denotes a linear or branched C 1 -C 10 and preferably C 1 -C 4 alkyl radical, more preferably a methyl radical,
• R 1 'de notes, according to the degree of hydrolysis, a hydrogen atom or a linear or branched C 1 -C 6, preferably C 1 -C 4, alkyl radical, more preferably a methyl or ethyl radical,
• R 2 ' is a divalent aliphatic hydrocarbon group, saturated or unsaturated, cyclic or non-cyclic, C 1 -C 18 , or aromatic C 6 -C 18, preferably linear C 1 -C 6 aliphatic, more preferably saturated linear aliphatic divalent hydrocarbon radical in d,
• R 3 'and R 4 ' which may be identical or different, represent a hydrogen atom or a linear or branched C 1 -C 18 and preferably C 1 -C 4 alkyl radical, more preferably a methyl or ethyl radical, or else R 3 and R 4 'together with N to which they are attached a heterocycle containing a nitrogen atom and at least one carbon atom, preferably 2 to 6 carbon atoms.
• At least one of the following four characteristics is respected and preferably the four:
• R represents a methyl radical
• Ri represents a hydrogen atom or a methyl or ethyl radical, preferably a hydrogen atom
• R 2 ' represents the divalent linear aliphatic hydrocarbon radical saturated with C3
• R 3 'and R 4' are identical or different, preferably identical, represent a methyl or ethyl radical, preferably methyl.
• the species (ii) functionalized in the middle of the chain by an alkoxysilane group, optionally partially or completely hydrolysed to silanol, carrying a primary, secondary or tertiary amine function, and whose silicon atom binds the two pieces of the chain preferably corresponds to the following formula (II):
• E denotes the diene elastomer
• R 1 denotes, according to the degree of hydrolysis, a hydrogen atom or a linear or branched alkyl radical, C 1 -C 6, preferably C 1 -C 4, more preferably a methyl or ethyl radical,
• R2 is a divalent aliphatic hydrocarbon group, saturated or unsaturated, cyclic or non-cyclic, C 1 -C 18 , or aromatic C 6 -C 18, preferably C 1 -C 18 linear aliphatic, more preferably the saturated linear aliphatic divalent hydrocarbon radical; ,
• R 3 and R 4 identical or different, represent a hydrogen atom or an alkyl radical, linear or branched -C C 18, preferably C 1 -C 4, more preferably methyl or ethyl, or R 3 and R 4 form with N to which they are bonded a heterocycle containing a nitrogen atom and at least one carbon atom, preferably from 2 to 6 carbon atoms.
• At least one of the following three characteristics is met and preferably the three:
• Ri represents a hydrogen atom or a methyl or ethyl radical, preferably a hydrogen atom
• R 2 represents the divalent linear aliphatic hydrocarbon radical saturated with C3,
• R 3 and R 4 identical or different, preferably identical, represent a methyl or ethyl radical, preferably methyl.
• the species (iii) stellate three branches containing a silane functional group, carrying a primary, secondary or tertiary amine function, and whose silicon atom binds the three branches of the chain, preferably corresponds to the formula (III ) next :
• the modified diene elastomer according to the invention may be prepared by a process including the modification of the elastomer by reacting a living diene elastomer with two appropriate functionalization. Such a process is also the object of the invention.
• the modified diene elastomer is obtained by the process comprising the following steps:
• step 2) addition to the living diene elastomer obtained in step 1) of a trialkoxysilane compound carrying a protected primary or protected secondary or tertiary amine function, the secondary ratio of trialkoxysilane carrying a protected primary amine function, secondary protected or tertiary / polymerization initiator ranging from 0.05 to 0.35, then
• step 3 adding to the solution of elastomer obtained at the end of step 2) an alkyldialcoxysilane compound carrying a protected primary or protected secondary or tertiary amine function, the alkyldialcoxysilane molar ratio carrying a function primary protected, secondary protected or tertiary amine / polymerization initiator used in step 1) being greater than or equal to 0.8.
• the polymerization of diene monomers is initiated by an initiator.
• an initiator any known mono functional anionic initiator can be used.
• an initiator containing an alkali metal such as lithium is used in a preferred manner.
• Suitable organolithium initiators include those having a carbon-lithium or nitrogen-lithium bond.
• Representative compounds are aliphatic organoliths such as ethyllithium, n-butyllithium (n-BuLi), isobutyl lithium, and the like. ; lithium amides obtained from a secondary amine and more particularly those obtained from a cyclic secondary amine, such as pyrrolidine or hexamethyleneimine.
• the polymerization is preferably carried out in the presence of an inert hydrocarbon solvent which may be, for example, an aliphatic or alicyclic hydrocarbon such as pentane, hexane, heptane, isopropanol or the like. octane, cyclohexane, methylcyclohexane or an aromatic hydrocarbon such as benzene, toluene, xylene.
• an inert hydrocarbon solvent which may be, for example, an aliphatic or alicyclic hydrocarbon such as pentane, hexane, heptane, isopropanol or the like.
• octane, cyclohexane, methylcyclohexane 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 150 ° C. and preferably in the region of 30 ° C. to 110 ° C.
• the second step of the process according to the invention consists of the modification of the living diene elastomer, obtained at the end of the anionic polymerization step, according to operating conditions favoring the star-branching and coupling reactions of the elastomer diene with a functionalization agent of trialkoxysilane type carrying a primary protected, secondary protected or tertiary amino function
• This trialkoxysilane compound carrying a protected, secondary protected or tertiary primary amine function preferably corresponds to the following formula (IV):
• the linear or branched R 1 "radicals which are identical to or different from each other, represent a C 1 -C 10 alkyl group, preferably a C 1 -C 4 alkyl group, more preferably a methyl or ethyl radical,
• R2 is a divalent aliphatic hydrocarbon group, saturated or unsaturated, cyclic or not, Ci-Cis, or aromatic C 6 -C 18, preferably linear aliphatic Ci-C 6 , more preferably the divalent linear aliphatic hydrocarbon radical saturated with C 3,
• R 5 and R 6 which may be identical or different, represent a trialkyl silyl radical, the alkyl groups, which may be identical or different, having from 1 to 4 carbon atoms, or a linear or branched C 1 -C 18 alkyl radical, preferably at C 1 -C 4, more preferably a methyl or ethyl radical, or else R 5 and R 6 form, with N to which they are bonded, a heterocycle containing a nitrogen atom and at least one carbon atom, preferably from 2 to 6 carbon atoms; carbon atoms.
• the functionalization agent may be chosen from 3 - (N, N - dimethylaminopropyl) trimethoxysilane, the 3 -
• the coupling agent is then 3 - (N, N-dimethylaminopropyl) trimethoxysilane.
• the functionalizing agent may be chosen from 3 - (N, N-methyltrimethylsilylaminopropyl) trimethoxysilane, 3 - (N, N-methyltrimethylsilylaminopropyl) triethoxysilane, and 3 - (N, N-ethyltrimethylsilylaminopropyl) trimethoxysilane.
• the coupling agent is then 3 - (N, N-methyltrimethylsilylaminopropyl) trimethoxysilane.
• the functionalizing agent may be chosen from 3 - (N, N-bistrimethylsilylaminopropyl) trimethoxysilane and 3 - (N, N-bistrimethylsilylaminopropyl) triethoxysilane.
• the coupling agent is then 3 - (N, N-bistrimethylsilylaminopropyl) trimethoxysilane.
• the mixture of the living diene polymer and the trialkoxysilane compound bearing a primary protected, secondary protected or tertiary amine function can be carried out by any appropriate means.
• the reaction time between the living diene polymer and aminotrialkoxysilane compound may be between 10 seconds and 2 hours.
• the second step of the process according to the invention leads to the formation of the species (ii) functionalized in the middle of the chain by an alkoxysilane group, optionally partially or completely hydrolyzed to silano, carrying a primary, secondary or secondary amine function.
• an alkoxysilane group optionally partially or completely hydrolyzed to silano, carrying a primary, secondary or secondary amine function.
• the species (iii) stellate three branches containing a silane functional group carrying a primary, secondary or tertiary amine function, and whose silicon atom binds the three branches of the chain.
• the third step of the process according to the invention consists in modifying the living diene elastomer according to operating conditions that favor an end-functionalization reaction of the diene elastomer with an alkyldialcoxysilane functionalization agent bearing a functional function.
• an alkyldialcoxysilane functionalization agent bearing a functional function bearing a functional function.
• This alkyl-dialkoxysilane compound carrying a protected, secondary protected or tertiary primary amine function has the following formula (V):
• R denotes a linear or branched C 1 -C 10, preferably C 1 -C 4, alkyl radical, more preferably a methyl radical,
• radicals R 1 '' which are identical to or different from each other, represent a linear or branched C 1 -C 10 and preferably C 1 -C 4 alkyl radical, more preferably a methyl or ethyl radical,
• R 2 ' is a divalent aliphatic hydrocarbon group, saturated or unsaturated, cyclic or not, Ci-Cis, or aromatic C 6 -C 18, preferably linear aliphatic C 1 -C 6 , more preferably the divalent aliphatic hydrocarbon radical linear saturated in C3,
• R7 and R8, which may be identical or different, represent a trialkyl silyl radical, identical or different alkyl groups having from 1 to 4 carbon atoms, or a radical alkyl, linear or branched, Ci-Cis, preferably Ci-C 4 , more preferably a methyl or ethyl radical, or R 7 and Rs form with N to which they are bonded a heterocycle containing a nitrogen atom and at least one carbon atom, preferably 2 to 6 carbon atoms.
• the functionalizing agent may be chosen from 3- (N, N-dimethylaminopropyl) (methyl) dimethoxysilane, 3- (N, N-dimethylaminopropyl) (methyl) diethoxysilane, 3- (N, N) diethylaminopropyl) (methyl) dimethoxysilane, 3- (N, N-diethylaminopropyl) (methyl) diethoxysilane, 3- (N, N-dipropylaminopropyl) (methyl) dimethoxysilane, 3- (N, N-dipropylaminopropyl) (methyl) ) diethoxysilane, 3- (N, N-dibutylaminopropyl) (methyl) dimethoxysilane, 3- (N, N-dibutylaminopropyl) (methyl) diethoxysilane, 3- (N, N-dipentylaminopropyl) (methyl) dimethoxysilane, 3-
• the coupling agent is then 3- (N, N-dimethylaminopropyl) (methyl) dimethoxysilane.
• the functionalization agent may be chosen from 3 - (N, N-methyltrimethylsilylaminopropyl) (methyl) dimethoxysilane, 3 - (N, N-methyltrimethylsilylaminopropyl) (methyl) diethoxysilane, 3 - (N N - ethyltrimethylsilylaminopropyl) (methyl) dimethoxysilane, 3 - (N, N - ethyltrimethylsilylaminopropyl) (methyl) diethoxysilane, 3 - (N, N - propyltrimethylsilylaminopropyl) (methyl) dimethoxysilane, 3 - (N, N - propyltrimethylsilylaminopropyl) (methyl) dimethoxysilane, 3 - (N, N - propyl
• the coupling agent is then 3 - (N, N-methyltrimethylsilylaminopropyl) (methyl) dimethoxysilane.
• the functionalizing agent may be chosen from 3 - (N, N-bistrimethylsilylaminopropyl) (methyl) dimethoxysilane and 3 - (N, N-bistrimethylsilylaminopropyl) (methyl) diethoxysilane.
• the coupling agent is then 3 - (N, N -bistrimethylsilylaminopropyl) (methyl) dimethoxysilane.
• the third step of the process according to the invention leads to the formation of the species (i) functionalized at the end of the chain by an alkylalkoxysilane group, optionally partially or completely hydrolysed in silano, bearing a primary, secondary or tertiary amine function, and bonded to the elastomer via the silicon atom.
• the process for synthesizing the modified diene elastomer according to the invention can be carried out in a manner known per se by the recovery steps of the modified elastomer.
• these steps comprise a stripping step in order to recover the elastomer from the previous steps in dry form.
• This stripping step may in particular have the effect of hydrolyzing all or part of the alkoxysilane hydro lysable functions of the modified diene elastomer to turn them into silano functions.
• these steps comprise a specific hydrolysis step dedicated to the hydrolysis of all or part of the alkoxysilane hydrolysable functions of the diene elastomer. modified to turn them into silano functions.
• This total or partial hydrolysis step may be carried out in a manner known per se, before a possible stripping step, by adding an acidic or basic compound.
• Such hydrolysis steps are described for example in EP 2 266 819 A 1.
• these steps comprise a specific step of deprotecting the primary amine or the secondary amine when at least one of the two functionalization agents used carries a protected primary or secondary amine function. .
• This step is implemented after the two functionalization steps, before a possible stripping step.
• it is possible to react the functionalized chains with the protected amino group with an acid, a base, a fluorinated derivative such as tetrabutylammonium fluoride, a silver salt such as silver nitrate, etc. to deprotect this or these function (s) amine.
• This deprotection step may have the effect of hydrolyzing all or part of the alkoxysilane hydro lysable functions of the modified diene elastomer to transform them into silano functions.
• the modified diene elastomer according to the invention is advantageously used in reinforced rubber compositions, especially for the manufacture of tires.
• another object of the invention is a reinforced rubber composition based on at least one reinforcing filler and an elastomeric matrix comprising at least one modified diene elastomer as described above. It should be understood that the rubber composition may comprise one or more of these modified diene elastomers according to the invention.
• the reinforced rubber composition according to the invention may be in the crosslinked state or in the uncrosslinked state, that is to say crosslinkable.
• the diene elastomer modified according to the invention can be, according to different variants, used alone in the composition or in blending with at least one other conventional diene elastomer, whether star-shaped, coupled, functionalized or not.
• this other diene elastomer used in the invention is chosen from the group of highly unsaturated diene elastomers consisting of polybutadienes (BR), synthetic polyisoprenes (IR), natural rubber (NR), butadiene copolymers, copolymers of isoprene and mixtures of these elastomers.
• Such copolymers are more preferably selected from the group consisting of butadiene-styrene copolymers (SBR), isoprene-butadiene copolymers (BIR), isoprene-styrene copolymers (SIR) and isoprene-copolymers.
• SBR butadiene-styrene copolymers
• BIR isoprene-butadiene copolymers
• SIR isoprene-styrene copolymers
• SBIR butadiene-styrene
• the elastomer matrix comprises predominantly the modified diene elastomer according to the invention.
• the conventional elastomer used in cutting is natural rubber and / or one or more diene polymers such as polybutadienes, polyisoprenes, butadiene-styrene or butadiene-styrene-isoprene copolymers
• this elastomer or these elastomers, modified or otherwise can then be present from 1 to 70 parts by weight per 100 parts of modified diene elastomer according to the invention.
• the elastomer matrix consists solely of the modified diene elastomer according to the invention.
• the rubber composition of the invention comprises, in addition to at least one elastomeric matrix as described above, at least one reinforcing filler.
• reinforcing filler known for its ability to reinforce a rubber composition that can be used for manufacturing tire treads, for example carbon black, a reinforcing inorganic filler such as silica with which it is associated with known manner a coupling agent, or a mixture of these two types of load.
• the rubber composition according to the invention may also comprise all or part of the usual additives normally used in elastomer compositions intended for the manufacture of tires, such as, for example, pigments, non-reinforcing fillers, coupling activators, agents and the like.
• protective agents such as anti-ozone waxes, chemical antiozonants, anti-oxidants, anti-fatigue agents, plasticizers, resins reinforcing or plasticizing agents, acceptors (for example novo lacquer phenolic resin) or methylene donors (for example HMT or H3M) as described for example in the application WO 02/1 0269, a crosslinking system based on of sulfur, either of sulfur and / or peroxide and / or bismaleimide donors, vulcanization accelerators, vulcanization activators.
• protective agents such as anti-ozone waxes, chemical antiozonants, anti-oxidants, anti-fatigue agents, plasticizers, resins reinforcing or plasticizing agents, acceptors (for example novo lacquer phenolic resin) or methylene donors (for example HMT or H3M) as described for example in the application WO 02/1 0269, a crosslinking system based on of sulfur, either of sulfur and / or peroxide and / or bismale
• the rubber composition according to the invention can then be calendered, for example in the form of a sheet, a plate or extruded, for example to form a rubber profile which can be used as a semi-finished rubber product intended for pneumatic.
• the invention also relates to a semi-finished article of rubber for a tire, comprising a rubber composition according to the invention, crosslinkable or crosslinked or consisting of such a composition. Due to the improvement of the hysteresis / processability compromise of a reinforced rubber composition according to the invention and the storage stability of the Mooney viscosity of the elastomer which enters into its composition, it will be noted that such a composition can constitute any semi-finished product of the tire and especially the tread.
• the invention thus finally has obj and a tire comprising a semi-finished article according to the invention, in particular a tread.
• the high resolution SEC technique is used to determine the mass percentages of the different chain populations present in a polymer sample.
• the apparatus used is a chromatographic chain "WATERS alliance 2695".
• the eluting solvent is tetrahydrofuran, the flow rate of 0.2 ml. min “1 , the system temperature of 35 ° C.
• a set of three identical columns in series is used (Shodex, length 300 mm, diameter 8 mm)
• the number of theoretical plates of the day of columns is greater to 22,000.
• the volume of the resolution the polymer sample is 50 ⁇ .
• the detector is a differential refractometer "WATERS 2414” and the chromatographic data exploitation software is the "WATERS EMPOWER" system.
• the calculated molar masses relate to a calibration curve produced for SBRs of microstructure as follows: 25% by weight of styrene type units, 23% by mass of 1,2 type units and 50% by mass of 1,4-trans type units.
• Mooney viscosities ML (i + 4) 100 ° C elastomers are measured according to ASTM D-1646.
• An oscillatory consistometer is used as described in ASTM D-1646.
• the Mooney plasticity measurement is carried out according to the following principle: the elastomer is molded in a cylindrical chamber heated to 100 ° C. After one minute preheating, the rotor rotates within the specimen at 2 rpm and the torque needed to maintain this movement after 4 minutes of rotation is measured.
• Tg glass transition temperatures
• NIR Near infrared spectroscopy
• the microstructure of elastomers is characterized by the technique of near infrared spectroscopy (NIR).
• NIR near-infrared spectroscopy
• the principle of the method is based on the Beer-Lambert law generalized to a multicomponent system. The method being indirect, it uses a multivariate calibration [Vilmin, F .; Dussap, C; Coste, N. Applied Spectroscopy 2006, 60, 619-29] carried out using standard elastomers of composition determined by 13 C NMR.
• the styrene content and the microstructure are then calculated from the NIR spectrum of a film. elastomer approximately 730 ⁇ thick.
• the acquisition of the spectrum is carried out in transmission mode between 4000 and 6200 cm “1 with a resolution of 2 cm " 1 , using a Bruker Tensor 37 Fourier transform infrared near-infrared spectrometer equipped with a cooled InGaAs detector. by Peltier effect.
• This level is determined by weighing a dried extract at 140 ° C., under the reduced pressure of 200 mmHg. 147 ml of a solution of 0.0516 mol ⁇ l "-1 (N, N-dimethylaminopropyl) trimethoxysilane in methylcyclohexane are added to the living polymer solution. After 15 minutes of reaction at 40 ° C., 190 ml of a solution of 3- (N, N-dimethylaminopropyl) (methyl) dimethoxysilane at 0.08 mol.L -1 in methylcyclohexane are then added to this polymer solution.
• the solution is antioxidized by the addition of 0.8 parts per hundred parts of elastomer (phr) of 4,4'-methylene-bis-2,6-tert-butylphenol and 0.2 part per hundred parts elastomer (phr) of N- (1,3-dimethylbutyl) -N'-phenyl-p-phenylenediamine
• elastomer (phr) 4,4'-methylene-bis-2,6-tert-butylphenol
• the mass percentage of chains functionalized at the end of the chain determined by the high-resolution SEC technique, is 50%, that of the functionalized chains in the middle of the chain is 20% and that of the 3-pointed star chains is 30%.
• the Mooney viscosity of polymer A is 70.
• the microstructure of this copolymer is determined by the NIR method: the mass ratio of 1,4-trans units is 22%, that of 1,4-cis units is 19% and that of 1,2 units is 59%. , each of these three rates pertaining to the butadiene units. The mass content of styrene is 27%.
• the glass transition temperature of this copolymer is -
• This level is determined by weighing a dried extract at 140 ° C., under the reduced pressure of 200 mmHg. 147 ml of a solution of 3- (N, N-dimethylaminopropyl) trimethoxysilane at 0.0516 mol.L 1 in methylcyclohexane are added to the living polymer solution. After a reaction time of 15 minutes at 40 ° C., 294 ml of a solution of 0.0516 mol.L -1 1 - (N, N-dimethylaminopropyl) trimethoxysilane in methylcyclohexane are then added to this polymer solution.
• the solution is antioxidized by the addition of 0.8 parts per hundred parts of elastomer (phr) of 4,4'-methylene-bis-2,6-tert-butylphenol and 0.2 part per hundred parts elastomer (phr) of N- (1,3-dimethylbutyl) -N'-phenyl-p-phenylenediamine
• elastomer (phr) 4,4'-methylene-bis-2,6-tert-butylphenol
• the mass percentage of chains functionalized at the end of the chain determined by the high-resolution SEC technique, is 50%, that of the functionalized chains in the middle of the chain is 20% and that of the 3-pointed star chains is 30%.
• the Mooney viscosity of polymer B is 72.
• the microstructure of this copolymer is determined by the NIR method: the mass ratio of 1,4-trans units is 21%, that of 1,4-cis units is 19% and that of 1,2 units is 60%. , each of these three rates pertaining to the butadiene units. The mass content of styrene is 28%.
• the glass transition temperature of this copolymer is -
• the polymer A, diene elastomer modified according to the invention undergoes no change in Mooney viscosity during the storage period spanning 60 days, unlike the control polymer B which sees its Mooney viscosity increase by 26 Mooney units. after 19 days of storage.

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• 2013
  • 2013-12-18 FR FR1362870A patent/FR3014872B1/fr not_active Expired - Fee Related
• 2014
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