Patent Grant
10968333
The present invention relates to polyfunctional coupling agents which can be used in particular for the coupling of reinforcing inorganic fillers and diene elastomers in rubber compositions intended, for example, for the manufacture of tyres.
It is known that, generally, in order to obtain the optimum reinforcing properties conferred by a filler, it is advisable for the latter to be present in the elastomeric matrix in a final form which is both as finely divided as possible and as homogeneously distributed as possible. In point of fact, such conditions can only be achieved in so far as the filler exhibits a very good ability, on the one hand, to be incorporated in the matrix during the mixing with the elastomer and to deagglomerate and, on the other hand, to disperse homogeneously in this matrix.
In an entirely known way, carbon black exhibits such abilities, which is not generally the case with inorganic fillers. This is because, for reciprocal affinity reasons, the inorganic filler particles have an unfortunate tendency to clump together in the elastomeric matrix. These interactions have the harmful consequence of limiting the dispersion of the filler and thus the reinforcing properties to a level substantially lower than that which it would be theoretically possible to achieve if all the (inorganic filler/elastomer) bonds capable of being created during the compounding operation were actually obtained. These interactions moreover tend to increase the consistency in the raw state of the rubber compositions and thus to make them more difficult to process than in the presence of carbon black.
Since fuel savings and the need to protect the environment have become a priority, it has, however, proved necessary to produce tyres having a reduced rolling resistance, without adversely affecting their wear resistance. This has been made possible in particular by virtue of the discovery of novel rubber compositions reinforced with specific inorganic fillers described as “reinforcing” which are capable of rivalling, from the reinforcing viewpoint, a conventional tyre-grade carbon black, while offering these compositions a lower hysteresis, which is synonymous with a lower rolling resistance for the tyres comprising them.
Such rubber compositions, comprising reinforcing inorganic fillers of siliceous or aluminous type, have, for example, been described in Patents or Patent Applications EP-A-0 501 227 (or U.S. Pat. No. 5,227,425), EP-A-0 735 088 (or U.S. Pat. No. 5,852,099), EP-A-0 810 258 (or U.S. Pat. No. 5,900,449), EP-A-0 881 252, WO99/02590, WO99/02601, WO99/02602, WO99/28376, WO00/05300 or WO00/05301.
Mention will in particular be made of the documents EP-A-0 501 227, EP-A-0 735 088 or EP-A-0 881 252, which disclose diene rubber compositions reinforced with highly dispersible precipitated silicas, such compositions making it possible to manufacture treads having a markedly improved rolling resistance, without affecting the other properties, in particular those of grip, endurance and wear resistance. Such compositions, exhibiting such a compromise in conflicting properties, are also described in Applications EP-A-0 810 258 and WO99/28376 with, as reinforcing inorganic fillers, specific highly-dispersible aluminous fillers (aluminas or aluminium (oxide) hydroxides), or also in Applications WO00/73372 and WO00/73373, which describe specific titanium oxides of the reinforcing type.
The use of these specific highly dispersible inorganic fillers, as predominant or non-predominant reinforcing filler, has admittedly reduced the difficulties in processing the rubber compositions comprising them but this processing nevertheless remains more difficult than for the rubber compositions conventionally comprising carbon black as filler.
In particular, it is necessary to use a coupling agent, also known as bonding agent, which has the role of providing the bonding between the surface of the inorganic filler particles and the elastomer, while facilitating the dispersion of this inorganic filler within the elastomeric matrix.
It should be remembered here that the term “coupling agent” (inorganic filler/elastomer) has to be understood as meaning, in a known way, an agent capable of establishing a satisfactory bond, of chemical and/or physical nature, between the inorganic filler and the diene elastomer; such an at least bifunctional coupling agent has, for example, the simplified general formula “Y—W—X”, in which:
The coupling agents should in particular not be confused with simple covering agents for inorganic filler which, in a known way, can comprise the Y functional group, active with regard to the inorganic filler, but are devoid of the X functional group, active with regard to the diene elastomer.
Coupling agents, in particular silica/diene elastomer coupling agents, have been described in a large number of documents, the most well-known being bifunctional organosilanes bearing at least one alkoxyl functional group as Y functional group and, as X functional group, at least one functional group capable of reacting with the diene elastomer, such as, for example, a sulfur-comprising functional group.
The Applicant Company has described, in its Patent EP 1 326 871, novel hydroxysilane coupling agents capable of overcoming the disadvantages of the mercaptosilane coupling agents as described in the publications FR-A-2 094 859 and GB-A-1 310 379, which bring about, for the compositions including them, problems of premature vulcanization, also known as “scorching”, and of excessive viscosity in the raw state. These novel hydroxysilane coupling agents also make it possible to overcome the disadvantages of alkoxysilane polysulfide coupling agents, as described in particular in the publications EP-A-1 043 357 and WO00/53671, especially TESPT (bis(3-triethoxysilylpropyl) tetrasulfide), which sort out the abovementioned disadvantages, but exhibit, however, the disadvantage of substantially slowing down the kinetics of vulcanization of the rubber compositions containing them, in comparison with that of the conventional compositions reinforced with carbon black.
The Applicant Company has continued these research studies and, after many years of research studies, has discovered that a specific functionalization of the coupling agent makes it possible to retain the rubber composition properties obtained with the first generation of abovementioned alkoxysilane coupling agents but also, surprisingly, that these novel coupling agents make it possible to improve the reinforcing and stiffness properties conferred on rubber compositions including them.
A subject-matter of the invention is thus an alkoxysilane polysulfide, of formula (I):
(R3O)3-n(R1)nSi—CH2—(R2)CH—Z—Sx—Z—HC(R2)—CH2—Si(R1)n(OR3)3-n
in which:
According to a favoured embodiment, the R3 groups each represent an ethoxy group, the polysulfide thus corresponding to the formula (OEt=ethoxy):
(EtO)3-n(R1)nSi—CH2—(R2)CH—Z—Sx—Z—HC(R2)—CH2—Si(R1)n(OEt)3-n
Advantageously, the R1 groups are chosen from C1-C6 alkyls, C5-C8 cycloalkyls and the phenyl radical, the Z groups being chosen from C1-C16 alkylenes and C6-C12 arylenes, and more preferably the R1 groups are chosen from C1-C3 alkyls, the Z groups being chosen from C1-C3 alkylenes.
According to a preferred embodiment of the invention, the polysulfide consists of a bis(2-methylpropane-1,3-diyl)(triethoxylsilane) polysulfide of formula:
According to another preferred embodiment of the invention, the polysulfide consists of a bis(2-methylpropane-1,3-diyl)(dimethylethoxylsilane) polysulfide of formula:
The invention also relates to a process for producing an ethoxysilane polysulfide of formula (I) which comprises the following stages:
The invention also relates to an elastomeric composition based on at least a diene elastomer, an inorganic filler as reinforcing filler and an alkoxysilane polysulfide as coupling agent, of formula (I):
(R3O)3-n(R1)nSi—CH2—(R2)CH—Z—Sx—Z—HC(R2)—CH2—Si(R1)n(OR3)3-n (I)
in which:
Finally, the invention relates to a tyre comprising a rubber composition as mentioned above.
Alkoxysilane Polysulfide of the Invention
The first subject-matter of the invention is an alkoxysilane polysulfide, of formula (I)
(R3O)3-n(R1)nSi—CH2—(R2)CH—Z—Sx—Z—HC(R2)—CH2—Si(R1)n(OR3)3-n (I)
in which:
Preferably, the R1 groups are chosen from C1-C6 alkyls, C5-C8 cycloalkyls and the phenyl radical, the Z groups being chosen from C1-C16 alkylenes and C6-C12 arylenes, and more preferably the R1 groups are chosen from C1-C3 alkyls, the Z groups being chosen from C1-C3 alkylenes.
According to a preferred alternative embodiment of the invention, the polysulfide corresponds to the formula (OEt=ethoxy):
(EtO)3-n(R1)nSi—CH2—(R2)CH—Z—Sx—Z—HC(R2)—CH2—Si(R1)n(OEt)3-n
and, more preferably still, the polysulfide corresponds to the formula (Me=methyl):
(EtO)3-n(Me)nSi—CH2-(Me)CH—Z—Sx—Z—HC(Me)-CH2—Si(Me)n(OEt)3-n
Preferably, the Z groups are chosen from methylene and ethylene.
The alkoxysilane polysulfides synthesized are in fact mixtures of polysulfides (for example from x=2 to x=9), with as consequence a mean value for x which is different from a whole value. The mean value targeted for x is preferably in a range extending from 2 to 6, more preferably in a range extending from 2 to 4.
According to a preferred embodiment of the invention, n is equal to 0 and preferably the polysulfide consists of a bis(2-methylpropane-1,3-diyl)(triethoxylsilane) polysulfide of formula:
According to another preferred embodiment of the invention, n is equal to 2 and preferably the polysulfide consists of a bis(2-methylpropane-1,3-diyl)(dimethylethoxylsilane) polysulfide of formula:
Process of Synthesis
The alkoxysilane polysulfide of formula (I) can be obtained by a process comprising the following stages:
with R1, R2 and Z as defined above;
with R3 as defined above;
According to an advantageous alternative to the process, the product C can be obtained by a hydrosilylation reaction of an alkene of formula R2—C(CH2)Z-Hal with a trialkoxyhydrosilane, as described, for example, by Mark D. Westmeyer in Application WO2005118598 or by Mark Paul Bowman in Application EP 0 669 338.
According to the preferred embodiment corresponding to an ethoxysilane polysulfide, the second stage of the above process is carried out as follows: an ethanolysis is carried out, in an inert organic solvent, on the product A in the presence of an organic or inorganic base, in order to trap the acid halide formed, and of ethanol, in order to obtain an alkoxysilane (product C′) of formula:
(EtO)3-n(R1)nSi—CH2—(R2)CH—Z-Hal
with R1, R2 and Z as defined above.
Advantageously, Hal is chlorine.
Preferably, the organic base intended to trap the acid halide formed is a tertiary amine.
According to an alternative embodiment of the process, the alkoxyl donor is used in excess with respect to the amount of product A.
Advantageously, the polysulfide is an ammonium or metal polysulfide (x≥2), of formula MnSx or M′Sx (M=alkali metal or NH4; M′=Zn or alkaline earth metal).
Preferably, it is a sodium polysulfide Na2Sx, preferably generated by the action of sulfur on Na2S.
More preferably still, the sulfidation stage is carried out in the aqueous phase or in a two-phase water/organic solvent medium, in the presence of a phase transfer catalyst and of a salt of formula M″Hal or M″2504 (M″ chosen from Li, Na and K; Hal chosen from F, Cl and Br).
Use as Coupling Agent
As indicated above, the compound of the invention, by virtue of its twofold functionality, has an advantageous industrial application as coupling agent intended, for example, to provide the bonding or adhesion between a reactive polymeric matrix (in particular a rubber matrix) and any material having a hydroxylated surface, in particular an inorganic material (for example, a glass fibre) or a metal material (for example, a wire made of carbon steel or of stainless steel).
Without this being limiting, it can be used in particular for the coupling of reinforcing inorganic or white fillers and diene elastomers, for example in rubber compositions intended for the manufacture of tyres. The term “reinforcing inorganic filler” is understood as meaning, in a known way, an inorganic or mineral filler, whatever its colour and its origin (natural or synthetic), also known as “white filler” or sometimes “clear filler”, in contrast to carbon black, this inorganic filler being capable of reinforcing, by itself alone, without means other than an intermediate coupling agent, a rubber composition intended for the manufacture of tyres, in other words capable of replacing, in its reinforcing role, a conventional tyre-grade carbon black filler.
Thus, the invention also relates to elastomeric compositions based on at least a diene elastomer, an inorganic filler as reinforcing filler and an ethoxysilane polysulfide as coupling agent, of formula (I) as mentioned above.
Advantageously, the diene elastomer is selected from the group consisting of polybutadienes, natural rubber, synthetic polyisoprenes, butadiene copolymers, isoprene copolymers and the mixtures of these elastomers.
For such a use, the diene elastomer is then preferably selected from the group of highly unsaturated diene elastomers consisting of polybutadienes (BRs), synthetic polyisoprenes (IRs), natural rubber (NR), butadiene/styrene copolymers (SBRs), butadiene/isoprene copolymers (BIRs), butadiene/acrylonitrile copolymers (NBRs), isoprene/styrene copolymers (SIRs), butadiene/styrene/isoprene copolymers (SBIRs) and the mixtures of these elastomers.
When the ethoxysilane polysulfide of the invention is intended for coupling (inorganic filler/diene elastomer) in a rubber composition forming, for example, all or a portion of a passenger vehicle tyre tread, the diene elastomer is then preferably an SBR or a blend (mixture) of SBR and of another diene elastomer, such as BR, NR or IR. In the case of an SBR elastomer, use is made in particular of an SBR having a styrene content of between 20% and 30% by weight, a content of vinyl bonds of the butadiene part of between 15% and 65%, a content of trans-1,4-bonds of between 15% and 75% and a glass transition temperature (Tg—measured according to Standard ASTM D3418-82) of between −20° C. and −55° C., this SBR copolymer, preferably prepared in solution (SSBR), optionally being used as a mixture with a polybutadiene (BR) preferably having more than 90% of cis-1,4-bonds.
When the tread is intended for a utility tyre, such as a heavy duty vehicle tyre, the diene elastomer is then preferably an isoprene elastomer, that is to say a diene elastomer selected from the group consisting of natural rubber (NR), synthetic polyisoprenes (IRs), the various isoprene copolymers and the mixtures of these elastomers; it is then more preferably natural rubber or a synthetic polyisoprene of the cis-1,4-type having a content (mol %) of cis-1,4-bonds of greater than 90%, more preferably still of greater than 98%.
The ethoxysilane polysulfides of the invention have proved to be sufficiently effective by themselves alone for the coupling of a diene elastomer and a reinforcing inorganic filler, such as silica, used in particular as predominant reinforcing filler. Preferably, the content of reinforcing filler will be chosen between 10 and 200 phr, more preferably between 30 and 150 phr, in particular greater than 50 phr, and more preferably still between 60 and 140 phr.
Preferably, the ethoxysilane polysulfides are used at a content of greater than 1 phr (parts by weight per hundred parts of elastomer), more preferably of between 2 and 20 phr. They can advantageously constitute the sole coupling agent present in rubber compositions reinforced with inorganic filler and intended for the manufacture of tyres.
Mention will be made, as reinforcing inorganic filler, of mineral fillers of the siliceous type, in particular silica (SiO2), or of the aluminous type, in particular alumina (Al2O3), or of aluminium (oxide) hydroxides, or also of reinforcing titanium oxides, as described in the abovementioned patents or patent applications.
Highly dispersible precipitated silicas (HDSs) are preferred, in particular when the invention is employed in the manufacture of tyres exhibiting a low rolling resistance; mention may be made, as examples of such silicas, of the Ultrasil 7000 silicas from Evonik, the Zeosil 1165MP, 1135MP, 1115MP and Premium 200MP silicas from Solvay, the Hi-Sil EZ150G silica from PPG or the Zeopol 8715, 8745 and 8755 silicas from Huber.
The reinforcing inorganic filler can be used also combined with a reinforcing organic filler, in particular carbon black.
The amount of carbon black present in the total reinforcing filler can vary within wide limits; it is preferably less than that of the reinforcing inorganic filler. Advantageously, carbon black is used in a very low proportion, with a content of between 2 and 20 phr and preferably at a content of less than 10 phr.
Such rubber compositions also comprise, in a known way, a crosslinking system, preferably a vulcanization system, that is to say a system based on sulfur (or on a sulfur-donating agent) and on a primary vulcanization accelerator. Additional to this base vulcanization system are various known secondary vulcanization accelerators or vulcanization activators, such as zinc oxide, stearic acid or equivalent compounds, or guanidine derivatives (in particular diphenylguanidine), incorporated during the first non-productive phase and/or during the productive phase, as described subsequently.
The sulfur is used at a preferred content of between 0.5 and 12 phr, in particular between 1 and 10 phr. The primary vulcanization accelerator is used at a preferred content of between 0.5 and 10 phr, more preferably of between 0.5 and 5.0 phr.
According to a preferred alternative embodiment of the invention, zinc and any zinc derivative, such as ZnO, are excluded among the secondary vulcanization accelerators or vulcanization activators used or they can be used in accordance with the 0.5 phr maximum of zinc in the composition, and preferably less than 0.3 phr. Furthermore, according to another preferred alternative form, guanidine derivatives, such as diphenylguanidine, are excluded.
The rubber compositions in accordance with the invention can also comprise all or a portion of the normal additives customarily used in elastomer compositions intended for the manufacture of tyres, in particular of treads, such as, for example, plasticizers or extender oils, whether the latter are aromatic or non-aromatic in nature, pigments, protective agents, such as antiozone waxes, chemical antiozonants or antioxidants, anti-fatigue agents, reinforcing resins, methylene acceptors (for example, phenolic novolak resin) or methylene donors (for example, HMT or H3M), such as described, for example, in Application WO 02/10269, a crosslinking system based either on sulfur or on sulfur-donating agents and/or on peroxide and/or on bismaleimides, vulcanization accelerators or vulcanization activators.
Manufacture of the Rubber Compositions
The rubber compositions of the invention are manufactured in appropriate mixers, using two successive phases of preparation according to a general procedure well known to a person skilled in the art: a first phase of thermomechanical working or kneading (sometimes described as “non-productive” phase) at high temperature, up to a maximum temperature of between 130° C. and 200° C., preferably between 145° C. and 185° C., followed by a second phase of mechanical working (sometimes described as “productive” phase) at a lower temperature, typically of less than 120° C., for example between 60° C. and 100° C., during which finishing phase the crosslinking or vulcanization system is incorporated.
It is possible to envisage one or more additional stages targeted at preparing masterbatches of elastomer and of reinforcing filler which are intended to be introduced during the first working phase.
The compositions thus obtained are subsequently calendered in the form of plaques (thickness of 2 to 3 mm) or of thin sheets of rubber, for the measurement of their physical or mechanical properties, or extruded in order to form profiled elements which can be used directly, after cutting and/or assembling to the desired dimensions, for example as semi-finished products for tyres, in particular as tyre treads.
The implementational examples which follow present in particular the synthesis of bis(2-methylpropane-1,3-diyl)(triethoxyl silane) (product B1) and of bis(2-methylpropane-1,3-diyl)(dimethylethoxylsilane) (product B2), illustrated by
This compound can be obtained by applying, to triethoxyhydrosilane, the procedure described, for example, by Mark D. Westmeyer in Application WO2005118598 or by Mark Paul Bowman in Application EP 0 669 338, i.e. a hydrosilylation reaction, catalysed by a ruthenium complex, with an alkene of formula R2—C(CH2)Z-Hal.
The reaction is carried out in a 2-litre round-bottomed flask equipped with a temperature control system, with a reflux condenser, with a mechanical stirrer and with a dropping funnel. The equipment is purged beforehand with nitrogen for 1 hour.
Sulfur (10.41 g), sodium sulfide nonahydrate (44.48 g) and sodium chloride (33.14 g) are added to a two-phase mixture of water (665.0 g) and toluene (126.3 g). The temperature of the mixture is brought to 80° C. and the medium is stirred at this temperature for 120 minutes. The reaction medium becomes red from the time of the dissolution of the salts.
Tetrabutylammonium chloride (9.94 g, in solution at 50% in toluene) is added at 86° C. Immediately afterwards, a solution of chloroisobutyltriethoxysilane (61.0 g) in toluene (457 g) is placed in the dropping funnel and is added dropwise. The addition lasts 2 hours and the temperature of the reaction medium is maintained between 84 and 86° C. After the end of the addition, the reaction medium is stirred for an additional 3 hours at 85° C. An analysis of the mixture by gas chromatography makes it possible to confirm the complete consumption of the starting chloroisobutyltriethoxysilane.
The temperature of the reaction medium is slowly brought back to ambient temperature. The aqueous phase is separated. 800 ml of water are added to the organic phase. The mixture is stirred at ambient temperature and then the aqueous and organic phases are separated. This washing is repeated six times so that the pH of the phase is equal to 7.
The organic phase is concentrated under at 30° C. at a pressure of less than 1 mm/Hg (affected by this pressure in 40 minutes). The oil obtained is concentrated under 1 mm/Hg at 30° C. for 1 h 30. 40 g of a brown oil are obtained.
The NMR spectrum of the product B1 obtained is presented in
The reaction is carried out in a 2-litre round-bottomed flask equipped with a temperature control system, with a reflux condenser, with a mechanical stirrer and with a dropping funnel. The equipment is purged beforehand with nitrogen for 1 hour.
Sulfur (10.33 g), sodium sulfide nonahydrate (44.49 g) and sodium chloride (33.45 g) are added to a two-phase mixture of water (365.0 g) and toluene (115.8 g). The temperature of the mixture is brought to 80° C. and the medium is stirred at this temperature for 120 minutes. The reaction medium becomes red from the time of the dissolution of the salts.
Tetrabutylammonium chloride (10.5 g, in solution at 50% in toluene) is added at 86° C. Immediately afterwards, a solution of chloroisobutyldimethylethoxysilane (47.67 g) in toluene (449.91 g) is placed in the dropping funnel and is added dropwise. The addition lasts 2 hours and the temperature of the reaction medium is maintained between 84 and 86° C. After the end of the addition, the reaction medium is stirred for an additional 3 hours at 85° C. An analysis of the mixture by gas chromatography makes it possible to confirm the complete consumption of the starting chloroisobutyldimethylethoxysilane.
The temperature of the reaction medium is slowly brought back to ambient temperature. The aqueous phase is separated. 800 ml of water are added to the organic phase. The mixture is stirred at ambient temperature and then the aqueous and organic phases are separated. This washing is repeated six times so that the pH of the phase is equal to 7.
The organic phase is concentrated under at 30° C. at a pressure of less than 1 mm/Hg (affected by this pressure in 40 minutes). The oil obtained is concentrated under 1 mm/Hg at 30° C. for 1 h 30. 39 g of a brown oil are obtained.
The NMR spectrum of the product B2 obtained is presented in
Preparation of the Rubber Compositions
The tests which follow are carried out in the following way: the diene elastomer (or the mixture of diene elastomers, if appropriate), the reinforcing filler, the coupling agent and then the various other ingredients, with the exception of the vulcanization system, are introduced into an internal mixer which is 70% filled and which has an initial vessel temperature of approximately 60° C. Thermomechanical working is then carried out (non-productive phase) in one or two stages (total duration of the kneading equal to approximately 7 min), until a maximum “dropping” temperature of approximately 165° C. is reached. The mixture thus obtained is recovered and cooled and then sulfur and sulfenamide accelerator are added on an external mixer (homofinisher) at 30° C., everything being mixed (productive phase) for 3 to 4 minutes.
The compositions thus obtained are subsequently calendered in the form of plaques (thickness of 2 to 3 mm) or of thin sheets of rubber, for the measurement of their physical or mechanical properties, or extruded in order to form profiled elements which can be used directly, after cutting and/or assembling to the desired dimensions, for example as semi-finished products for tyres, in particular as tyre treads.
Measurements and Tests Used
The rubber compositions are characterized, before and after curing, as indicated below.
Tensile Tests
These tests make it possible to determine the elasticity stresses and the properties at break. Unless otherwise indicated, they are carried out in accordance with French Standard NF T 46-002 of September 1988. The nominal secant moduli (or apparent stresses, in MPa) are measured in second elongation (i.e. after an accommodation cycle at the extension rate provided for the measurement itself) at 10% elongation (denoted M10), 100% elongation (denoted M100) and 300% elongation (denoted M300). The breaking stresses (in MPa) and the elongations at break (in %) are also measured. All these tensile measurements are carried out under the standard conditions of temperature and hygrometry according to French Standard NF T 40-101 (December 1979).
Rheometry
The measurements are carried out at 150° C. with an oscillating disc rheometer, according to Standard DIN 53529—Part 3 (June 1983). The change in the rheometric torque, ΔTorque, as a function of the time describes the change in the stiffening of the composition as a result of the vulcanization reaction. The measurements are processed according to Standard DIN 53529—Part 2 (March 1983): T0 is the induction period, that is to say the time necessary for the start of the vulcanization reaction; Tα (for example T99) is the time necessary to achieve a conversion of α %, that is to say α % (for example 99%) of the difference between the minimum (TMin) and maximum (TMax) torques. The conversion rate constant, denoted K (expressed in min−1), which is first order, calculated between 30% and 80% conversion, which makes it possible to assess the vulcanization kinetics, is also measured.
Test
The aim of this test is to demonstrate the improved performance qualities of compositions in accordance with the invention, compared with a conventional composition using TESPT.
Three compositions in accordance with the process explained in the preceding section, based on SBR, reinforced predominantly with silica, are thus prepared, which compositions differ from one another in the nature of their coupling agent, these coupling agents being used in an isomolar silicon content, and in the presence or the absence of zinc oxide (ZnO), as follows:
It should be remembered that TESPT is bis(3-triethoxysilylpropyl) tetrasulfide, of formula [(C2H5O)3Si(CH2)3S2]2; it is sold, for example, by Evonik under the name Si69 (or X50S when it is supported at 50% by weight on carbon black) or also by Witco under the name Silquest A1289 (in both cases, commercial mixture of polysulfides Sx with a mean value for x which is approximately 4).
The expanded formula for TESPT is:
Likewise, the silane disulfide coupling agent bis(triethoxysilylpropyl) disulfide, such as sold by Evonik under the reference Si75, is well known.
The formulation of the four compositions (contents of the various products expressed in phr) and their properties after curing (approximately 30 min at 150° C.) are given in Tables 1 and 2 respectively.
It is found, in the light of Table 2, surprisingly, that the compositions C3 and C4 in accordance with the invention exhibit reinforcing (M300/M100) properties which are significantly improved in comparison with the two control compositions C1 and C2 and also a marked improvement in the processability (Tmin). Surprisingly, it is found that these improvements in performance qualities for the compositions in accordance with the invention take place equally well in compositions with ZnO as in compositions without ZnO.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1662583 | Dec 2016 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/FR2017/053471 | 12/8/2017 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2018/109335 | 6/21/2018 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 4595740 | Panster | Jun 1986 | A |
| 5227425 | Rauline | Jul 1993 | A |
| 5534592 | Halasa | Jul 1996 | A |
| 5852099 | Vanel | Dec 1998 | A |
| 5900449 | Custodero et al. | May 1999 | A |
| 5977238 | Labauze | Nov 1999 | A |
| 6013718 | Cabioch et al. | Jan 2000 | A |
| 6156822 | Materne et al. | Dec 2000 | A |
| 6313205 | Chiron et al. | Nov 2001 | B1 |
| 6344506 | Vasseur | Feb 2002 | B2 |
| 6420488 | Penot | Jul 2002 | B1 |
| 6503973 | Robert et al. | Jan 2003 | B2 |
| 6536492 | Vasseur | Mar 2003 | B2 |
| 6747087 | Custodero et al. | Jun 2004 | B2 |
| 6765045 | Daniel et al. | Jul 2004 | B1 |
| 6774255 | Tardivat et al. | Aug 2004 | B1 |
| 6815473 | Robert et al. | Nov 2004 | B2 |
| 6835769 | Custodero et al. | Dec 2004 | B2 |
| 6890981 | Luginsland | May 2005 | B1 |
| 7135517 | Simonot et al. | Nov 2006 | B2 |
| 7199175 | Vasseur | Apr 2007 | B2 |
| 7202295 | Simonot et al. | Apr 2007 | B2 |
| 7256233 | Simonot et al. | Aug 2007 | B2 |
| 7312264 | Gandon-Pain | Dec 2007 | B2 |
| 7425313 | Custodero et al. | Sep 2008 | B2 |
| 7488768 | Tardivat et al. | Feb 2009 | B2 |
| 7659417 | Guennouni | Feb 2010 | B2 |
| 7820771 | Lapra et al. | Oct 2010 | B2 |
| 7900667 | Vasseur | Mar 2011 | B2 |
| 8344063 | Marechal et al. | Jan 2013 | B2 |
| 8394903 | Marechal | Mar 2013 | B2 |
| 8455584 | Robert et al. | Jun 2013 | B2 |
| 8492479 | Robert et al. | Jul 2013 | B2 |
| 9303148 | Cambon et al. | Apr 2016 | B2 |
| 20010034389 | Vasseur | Oct 2001 | A1 |
| 20010036991 | Robert et al. | Nov 2001 | A1 |
| 20010039308 | Custodero et al. | Nov 2001 | A1 |
| 20010056138 | Vasseur | Dec 2001 | A1 |
| 20020004549 | Custodero et al. | Jan 2002 | A1 |
| 20020183436 | Robert et al. | Dec 2002 | A1 |
| 20030202923 | Custodero et al. | Oct 2003 | A1 |
| 20030212185 | Vasseur | Nov 2003 | A1 |
| 20040030017 | Simonot et al. | Feb 2004 | A1 |
| 20040051210 | Tardivat et al. | Mar 2004 | A1 |
| 20050171264 | Simonot et al. | Aug 2005 | A1 |
| 20060009564 | Simonot et al. | Jan 2006 | A1 |
| 20060089445 | Gandon-Pain | Apr 2006 | A1 |
| 20070112120 | Vasseur | May 2007 | A1 |
| 20080132644 | Lapra et al. | Jun 2008 | A1 |
| 20090131572 | Cambon et al. | May 2009 | A1 |
| 20090270558 | Gandon-Pain et al. | Oct 2009 | A1 |
| 20100184912 | Marechal et al. | Jul 2010 | A1 |
| 20100216935 | Boswell et al. | Aug 2010 | A1 |
| 20100249270 | Robert et al. | Sep 2010 | A1 |
| 20100252156 | Robert et al. | Oct 2010 | A1 |
| 20110251354 | Marechal | Oct 2011 | A1 |
| 20110319646 | Boswell et al. | Dec 2011 | A1 |
| 20180282525 | Sato et al. | Oct 2018 | A1 |
| 20190233618 | Seeboth et al. | Aug 2019 | A1 |
| Number | Date | Country |
|---|---|---|
| 1474824 | Feb 2004 | CN |
| 1478125 | Feb 2004 | CN |
| 1993416 | Jul 2007 | CN |
| 101331141 | Dec 2008 | CN |
| 0098947 | Jan 1984 | EP |
| 0501227 | Sep 1992 | EP |
| 0669338 | Aug 1995 | EP |
| 0735088 | Oct 1996 | EP |
| 0810258 | Dec 1997 | EP |
| 0881252 | Dec 1998 | EP |
| 1002836 | May 2000 | EP |
| 1043357 | Oct 2000 | EP |
| 1127909 | Aug 2001 | EP |
| 1326871 | Jul 2003 | EP |
| 1326914 | Jun 2006 | EP |
| 2094859 | Feb 1972 | FR |
| 2740778 | May 1997 | FR |
| 2765882 | Jan 1999 | FR |
| 1310379 | Mar 1973 | GB |
| 9736724 | Oct 1997 | WO |
| 9902590 | Jan 1999 | WO |
| 9902601 | Jan 1999 | WO |
| 9902602 | Jan 1999 | WO |
| 9916600 | Apr 1999 | WO |
| 9928376 | Jun 1999 | WO |
| 0005300 | Feb 2000 | WO |
| 0005301 | Feb 2000 | WO |
| 0053671 | Sep 2000 | WO |
| 0073372 | Dec 2000 | WO |
| 0073373 | Dec 2000 | WO |
| 0192402 | Dec 2001 | WO |
| 0210269 | Feb 2002 | WO |
| 02053634 | Jul 2002 | WO |
| 2004003067 | Jan 2004 | WO |
| 2004056915 | Jul 2004 | WO |
| 2004096865 | Nov 2004 | WO |
| 2005118598 | Dec 2005 | WO |
| 2006013056 | Feb 2006 | WO |
| 2006069792 | Jul 2006 | WO |
| 2006069793 | Jul 2006 | WO |
| 2008141702 | Nov 2008 | WO |
| 2009000750 | Dec 2008 | WO |
| 2009000752 | Dec 2008 | WO |
| 2010072761 | Jul 2010 | WO |
| 2017033815 | Mar 2017 | WO |
| Entry |
|---|
| US 5,191,205 A1, 02/2001, Micouin et al. (withdrawn) |
| International Search Report dated Feb. 22, 2018 in corresponding PCT/FR2017/053471 (4 pages). |
| S. Brunauer, et al., “Adsorption of Gases in Multimolecular Layers”, J. Am. Chem. Soc., vol. 60, pp. 309-319 (1938). |
| R. Mildenberg, et al., Hydrocarbon Resins, VCH, New York, chapter 5 (1997). |
| Number | Date | Country | |
|---|---|---|---|
| 20190359791 A1 | Nov 2019 | US |
