WO2020158695A1 - Stratifié - Google Patents

Stratifié Download PDF

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Publication number
WO2020158695A1
WO2020158695A1 PCT/JP2020/002876 JP2020002876W WO2020158695A1 WO 2020158695 A1 WO2020158695 A1 WO 2020158695A1 JP 2020002876 W JP2020002876 W JP 2020002876W WO 2020158695 A1 WO2020158695 A1 WO 2020158695A1
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WO
WIPO (PCT)
Prior art keywords
phr
rubber composition
sulfur
rubber
laminate according
Prior art date
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PCT/JP2020/002876
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English (en)
Inventor
Tomoya Sakurada
Original Assignee
Compagnie Generale Des Etablissements Michelin
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Publication of WO2020158695A1 publication Critical patent/WO2020158695A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B25/00—Layered products comprising a layer of natural or synthetic rubber
    • B32B25/02—Layered products comprising a layer of natural or synthetic rubber with fibres or particles being present as additives in the layer
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B25/00—Layered products comprising a layer of natural or synthetic rubber
    • B32B25/04—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B25/042—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material of natural rubber or synthetic rubber
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B25/00—Layered products comprising a layer of natural or synthetic rubber
    • B32B25/12—Layered products comprising a layer of natural or synthetic rubber comprising natural rubber
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B25/00—Layered products comprising a layer of natural or synthetic rubber
    • B32B25/16—Layered products comprising a layer of natural or synthetic rubber comprising polydienes homopolymers or poly-halodienes homopolymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/02—Physical, chemical or physicochemical properties
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/34—Silicon-containing compounds
    • C08K3/36—Silica
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/43—Compounds containing sulfur bound to nitrogen
    • C08K5/44—Sulfenamides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L21/00—Compositions of unspecified rubbers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/06—Copolymers with styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
    • B32B2262/02—Synthetic macromolecular fibres
    • B32B2262/0207—Elastomeric fibres

Definitions

  • the field of the invention is that of laminates intended in particular for articles, for example, tires, shoes, conveyors or caterpillar tracks, in more particular for tires, in still more particular for treads of tires, in especial for treads of tires capable of rolling over ground surface covered with snow, ice or the mixtures thereof.
  • rubber compositions to be tacky before curing is an important property to the rubber article (for example, a tire, a shoe or a caterpillar track) building. Indeed, for making the rubber articles, it is necessary to be able to apply the different layers of the article on each other and that these layers stick to each other before curing of the article, curing which will associate for crosslinking the layers to others.
  • This property of tack of the composition before curing is also called “tackiness” or “uncured tack” or “unvulcanized tack” or “green tack”.
  • micrometer order particles, millimeter order particles or the mixtures thereof are comprised of rubber compositions for various purposes, for example, improvement of grip on winter (snowy/icy) roads (Patent literature 1).
  • a specific laminate with rubber compositions intended in particular for a rubber article for example, a tire tread, a shoe sole, a conveyor belt and a caterpillar track tread, which allows an unexpectedly improved the tack of the rubber compositions with particles having a particle size.
  • each Tg DSC glass transition temperature
  • DSC Densilic Acid
  • any interval of values denoted by the expression “between a and b” represents the range of values of more than “a” and of less than “b” (i.e. the limits a and b excluded) whereas any interval of values denoted by the expression “from a to b” means the range of values going from “a” to “b” (i.e. including the strict limits a and b).
  • a tire has a geometry of revolution about an axis of rotation
  • the geometry of the tire is generally described in a meridian plane containing the axis of rotation of the tire, and the following definitions of directions of the tire are understood in the present application: - A radial direction is a direction perpendicular to the axis of rotation of the tire; - An axial direction is a direction parallel to the axis of rotation of the tire; - A circumferential direction is a direction perpendicular to the meridian plane.
  • a plane being perpendicular to the axis of rotation of the tire and passing through the middle of a tread surface of the tire is referred to as an equatorial plane of the tire.
  • Respective dimensions of a given element in the radial, axial and circumferential directions will also be denoted “radial thickness or height”, “axial width” and “circumferential length” of this element.
  • Expression “laterally” means “in the circumferential or axial direction”.
  • a first aspect of the invention is a laminate comprising at least two superposed portions comprising a first portion being made of a first rubber composition (FC) and a second portion being made of a second rubber composition (SC); wherein each of the rubber compositions is based on at least: an elastomer matrix; a reinforcing filler; and a crosslinking system based on at least one of sulfur (sulphur) or a sulfur-based vulcanization accelerator; wherein at least one of the first rubber composition (FC) or the second rubber composition (SC) is further based on particles having a particle size of between 200 and 5 mesh; wherein the amount in phr of sulfur in the first rubber composition (FC) is higher than that in the second rubber composition (SC), and wherein the amount in phr of sulfur-based vulcanization accelerator in the first rubber composition (FC) is lower than that in the second rubber composition (SC).
  • FC first rubber composition
  • SC second rubber composition
  • Mesh is defined as the number of holes per square inch of a screen used for sorting particles into different sizes. The higher the number of holes in the screen is, the smaller the hole size is.
  • the particles having the particle size of between 200 and 5 mesh can pass through a screen having 5 holes per square inch of screen, but cannot pass through a screen having 200 holes per square inch of screen.
  • Use may simply and preferably be made of an analysis of the particle size by mechanical sieving; the operation consists of sieving a defined amount of sample (for example 200 g) on a vibrating table for 30 min with different sieve diameters with meshes in accordance with ASTM E-10.
  • the amount in phr of sulfur is to say the amount of vulcanization sulfur content in phr.
  • the vulcanization sulfur may be sulfur, sulfur derived from a sulfur-donating agent or combinations thereof.
  • the specific laminate with the rubber compositions allows unexpectedly improved the tack of the rubber compositions with the particles having the particle size.
  • Each of the rubber compositions (FC and SC) of the tread of the tire according to the invention is based on each elastomer matrix.
  • the expression “highly unsaturated” diene elastomer is understood to mean in particular a diene elastomer having a content of units of diene origin (conjugated dienes) which is greater than 50%.
  • diene elastomer capable of being used in the compositions in accordance with the invention is understood in particular to mean: (a) - any homopolymer obtained by polymerization of a conjugated diene monomer, preferably having from 4 to 12 carbon atoms; (b) - any copolymer obtained by copolymerization of one or more conjugated dienes with one another or with one or more vinyl aromatic compounds preferably having from 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-butadienes, such as, for example, 2,3-dimethyl-1,3-butadiene, 2,3-diethyl-1,3-butadiene, 2-methyl-3-ethyl-1 ,3-butadiene or 2-methyl-3-isopropyl-1 ,3-butadiene, an aryl-1,3-butadiene, 1,3-pentadiene or 2,4-hexadiene.
  • 1,3-butadiene 1,3-butadiene, 2-methyl-1,3-butadiene, 2,3-di(C 1 -C 5 alkyl)-1,3-butadienes, such as, for example, 2,3-dimethyl-1,3-butadiene, 2,3-diethyl-1,3-butadiene, 2-methyl-3-ethyl-1 ,
  • vinylaromatic compounds styrene, ortho-, meta- or para-methylstyrene, the“vinyltoluene” commercial mixture, para-(tert-butyl) styrene, methoxystyrenes, chlorostyrenes, vinylmesitylene, divinylbenzene or vinylnaphthalene.
  • the copolymers are preferably selected from the group consisting of butadiene copolymers and combinations thereof, more preferably selected from the group consisting of styrene-butadiene copolymers (SBR), butadiene-isoprene copolymers (BIR), styrene-isoprene copolymers (SIR), styrene-butadiene-isoprene copolymers (SBIR) and combinations thereof, still more preferably selected from the group consisting of styrene-butadiene copolymers (SBR) and combinations thereof.
  • SBR styrene-butadiene copolymers
  • BIR butadiene-isoprene copolymers
  • SIR styrene-isoprene copolymers
  • SBIR styrene-butadiene-isoprene copolymers
  • the elastomer matrix comprises more than 50 phr and up to 100 phr, preferably 55 to 95 phr, more preferably 60 to 90 phr, still more preferably 65 to 85 phr, particularly 70 to 80 phr, of a first diene elastomer which is a styrene butadiene copolymer(s), preferably a solution styrene butadiene copolymer(s), and the elastomer matrix comprises no second diene elastomer or comprises less than 50 phr, preferably 5 to 45 phr, more preferably 10 to 40 phr, still more preferably 15 to 35 phr, particularly 20 to 30 phr, of a second diene elastomer which is different from the first diene
  • the second diene elastomer in the first rubber composition (FC), the second rubber composition (SC) or the both rubber compositions, preferably the both rubber compositions, the second diene elastomer is a polybutadiene(s) (BR) more preferably having a content (molar %) of 1,2-units of between 4% and 80% or those having a content (molar %) of cis-1,4-units of greater than 80%, more preferably greater than 90% (molar %), still more preferably greater than or equal to 96% (molar %).
  • BR polybutadiene(s)
  • the styrene-butadiene copolymer exhibits a styrene unit of less than 30% by weight (for example, between 3 and 30% by weight) per 100% by weight of the styrene-butadiene copolymer, preferably less than 27% by weight (for example, between 5 and 27% by weight), more preferably less than 23% by weight (for example, between 7 and 23% by weight), still more preferably less than 20% by weight (for example, between 10 and 20% by weight), particularly at most 18% by weight (for example, from 12 to 18%).
  • the styrene unit can be determined by 1H NMR method in accordance with ISO 21561.
  • Each of the rubber compositions (FC and SC) of the laminate according to the invention is based on a reinforcing filler.
  • a third aspect of the invention is the laminate according to the first aspect or the second aspect, wherein each of the rubber compositions (FC and SC) is such that the amount of the reinforcing filler is more than 0 phr and up to 250 phr, preferably 10 to 240 phr, more preferably 20 to 230 phr, still more preferably 30 to 220 phr, particularly 40 to 210 phr, more particularly 50 to 200 phr, still more particularly 60 to 190 phr, advantageously 70 to 180 phr, more advantageously 80 to 170 phr, still more advantageously 90 to 160 phr, still more advantageously 100 to 150 phr, especially 110 to 140 phr, especially 120 to 130 phr.
  • the reinforcing filler may comprise a reinforcing organic filler (for example, carbon black), a reinforcing inorganic filler (for instance, silica) or combinations thereof.
  • a reinforcing organic filler for example, carbon black
  • a reinforcing inorganic filler for instance, silica
  • Use may be made of any type of reinforcing filler known for its capabilities of reinforcing a rubber composition which can be used for the manufacture of the article, for example a reinforcing organic filler, such as carbon black, or a reinforcing inorganic filler, such as silica, with which a coupling agent is combined in a known way.
  • a reinforcing organic filler such as carbon black
  • a reinforcing inorganic filler such as silica
  • a fourth aspect of the invention is the laminate according to any one of the first to the third aspects, wherein each of the rubber compositions (FC and SC) is such that the reinforcing filler predominately comprises a reinforcing inorganic filler, that is, the reinforcing filler comprises more than 50% by weight of the reinforcing inorganic filler per 100% by weight of the reinforcing filler, preferably the reinforcing filler comprises more than 60%, more preferably more than 70%, still more preferably more than 80%, particularly more than 90%, by weight of the reinforcing inorganic filler per 100% by weight of the reinforcing filler.
  • filler should be understood here to mean any inorganic or mineral filler, whatever its color and its origin (natural or synthetic), also referred to as “white filler”, “clear filler” or even “non-black filler”, in contrast to carbon black, capable of reinforcing by itself alone, without means other than an intermediate coupling agent, a rubber composition intended for the manufacture of tires, in other words capable of replacing, in its reinforcing role, a conventional tire-grade carbon black; such a filler is generally characterized, in a known manner, by the presence of hydroxyl (-OH) groups at its surface.
  • -OH hydroxyl
  • this filler is unimportant, whether it is in the form of powder, microbeads, granules, beads or any other suitable densified form.
  • the reinforcing inorganic filler of the mixtures of various reinforcing inorganic fillers preferably of highly dispersible siliceous filler(s), aluminous filler(s) or both is described hereafter.
  • Mineral fillers of the siliceous type preferably silica (SiO 2 ), the aluminous type or both, preferably alumina (Al 2 O 3 ) are suitable in particular as the reinforcing inorganic fillers.
  • a fifth aspect of the invention is the laminate according to the fourth aspect, wherein each of the rubber compositions (FC and SC) is such that the reinforcing inorganic filler predominately comprises silica, that is, the reinforcing inorganic filler comprises more than 50% by weight of silica per 100% by weight of the reinforcing inorganic filler, preferably the reinforcing inorganic filler comprises more than 60%, more preferably more than 70%, still more preferably more than 80%, particularly more than 90%, more particularly 100%, by weight of silica per 100% by weight of the reinforcing inorganic filler.
  • the silica may be a type of silica or a blend of several silicas.
  • the silica used may be any reinforcing silica known to a person skilled in the art, in particular any precipitated or pyrogenic silica having a BET surface area and a CTAB specific surface area that are both less than 450 m 2 /g, preferably from 20 to 400 m 2 /g, more preferably 50 to 350 m 2 /g, still more preferably 100 to 300 m 2 /g, particularly between 150 and 250 m 2 /g, wherein the BET surface area is measured according to a known method, that is, by gas adsorption using the Brunauer-Emmett-Teller method described in “The Journal of the American Chemical Society”, Vol.
  • HDSs highly dispersible precipitated silicas
  • pyrogenic silicas for example, of “CAB-O-SIL S-17D” from Cabot, “HDK T40” from Wacker, “Aeroperl 300/30”, “Aerosil 380”, “Aerosil 150” or “Aerosil 90” from Evonik.
  • Such silica may be covered, for example, “CAB-O-SIL TS-530” covered with hexamethyldiasilazene or “CAB-O-SIL TS-622” covered with dimethyldichlorosilane from Cabot.
  • a reinforcing filler of another nature, in particular organic nature, such as carbon black might be used as filler equivalent to the reinforcing inorganic filler described in the present section, provided that this reinforcing filler is covered with an inorganic layer, such as silica, or else comprises, at its surface, functional sites, in particular hydroxyls, requiring the use of a coupling agent in order to form the connection between the filler and the elastomer.
  • an inorganic layer such as silica
  • the reinforcing filler comprises more than 0 and up to 240 phr, preferably between 10 and 230 phr, more preferably between 20 and 220 phr, still more preferably between 30 and 210 phr, particularly between 40 and 200 phr, more particularly between 50 and 190 phr, still more particularly preferably between 60 and 180 phr, advantageously between 70 and 170 phr, more advantageously between 80 and 160 phr, still more advantageously between 90 and 150 phr, especially between 100 and 140 phr, more especially between 110 and 130 phr, still more especially between 115 and 125 phr, of a reinforcing inorganic filler (for example, silica).
  • a reinforcing inorganic filler for example, silica
  • silane polysulfides referred to as “symmetrical” or “asymmetrical” depending on their particular structure, as described, for example, in applications WO 03/002648, WO 03/002649 and WO 2004/033548.
  • silane polysulfides correspond to the following general formula (I): (I) Z - A - Sx - A - Z , in which: - x is an integer from 2 to 8 (preferably from 2 to 5); - A is a divalent hydrocarbon radical (preferably, C 1 -C 18 alkylene groups or C 6 -C 12 arylene groups, more particularly C 1 -C 10 , in particular C 1 -C 4 , alkylenes, especially propylene); - Z corresponds to one of the formulae below: in which: - the R 1 radicals which are unsubstituted or substituted and identical to or different from one another, represent a C 1 -C 18 alkyl, C 5 -C 18 cycloalkyl or C 6 -C 18 aryl group (preferably, C 1 -C 6 alkyl, cyclohexyl or phenyl groups, in particular C 1 -C 4 alkyl groups, more particularly methyl, ethyl
  • the mean value of the "x" indices is a fractional number preferably of between 2 and 5, more preferably of approximately 4.
  • silane polysulfides of bis((C 1 -C 4 )alkoxyl(C 1 -C 4 )alkylsilyl(C 1 -C 4 )alkyl)polysulfides (in particular disulfides, trisulfides or tetrasulfides), such as, for example, bis(3-trimethoxysilylpropyl) or bis(3-triethoxysilylpropyl)polysulfides.
  • TESPT bis(3-triethoxysilylpropyl)tetrasulfide
  • TESPD bis(3-triethoxysilylpropyl)disulfide
  • silanes bearing at least one thiol (-SH) function referred to as mercaptosilanes
  • at least one blocked thiol function or both such as described, for example, in patents or patent applications US 6 849 754, WO 99/09036, WO 2006/023815, WO 2007/098080, WO 2008/055986 and WO 2010/072685.
  • the content of coupling agent may be from 0.5 to 15% by weight per 100% by weight of the reinforcing inorganic filler, preferably silica if each rubber composition is based on the reinforcing inorganic filler, preferably silica.
  • the amount of coupling agent is less than 30 phr (for example, between 0.1 and 30 phr), preferably less than 25 phr (for example, between 0.5 and 25 phr), more preferably less than 20 phr (for example, between 1 and 20 phr), still more preferably less than 15 phr (for example, between 1.5 and 15 phr) if each rubber composition is based on the reinforcing inorganic filler, preferably silica.
  • a sixth aspect of the invention is the laminate according to any one of the first to the fifth aspects, wherein each of the rubber compositions (FC and SC) is such that the reinforcing filler comprises less than 60 phr (for example, between 0 and 60 phr), preferably less than 50 phr (for example, between 0 and 50 phr), more preferably less than 40 phr (for example, between 0.5 and 40 phr), still more preferably less than 30 phr (for example, between 1.0 and 30 phr), particularly less than 20 phr (for example, between 1.5 and 20 phr), more particularly less than 10 phr (for example, between 2 and 10 phr), of carbon black.
  • the reinforcing filler comprises less than 60 phr (for example, between 0 and 60 phr), preferably less than 50 phr (for example, between 0 and 50 phr), more preferably less than 40 phr (for example, between
  • carbon blacks all carbon blacks conventionally used in tires (“tire-grade” blacks) are suitable, such as for example reinforcing carbon blacks of the 100, 200 or 300 series in ASTM grades (such as for example, the N115, N134, N234, N326, N330, N339, N347 or N375 blacks), or carbon blacks higher series, the 500, 600, 700 or 800 series in ASTM grades (such as for example the N550, N660, N683, N772, N774 blacks).
  • the carbon blacks might for example be already incorporated in an elastomer matrix, for instance, a diene elastomer, in the form of a masterbatch (see for example applications WO 97/36724 or WO 99/16600).
  • Each of the rubber compositions (FC and SC) of the laminate according to the invention is based on each crosslinking (or vulcanization) system based on sulfur and a sulfur-based vulcanization accelerator, wherein the amount in phr of sulfur in the first rubber composition (FC) is higher than that in the second rubber composition (SC), and wherein the amount in phr of sulfur-based vulcanization accelerator in the first rubber composition (FC) is lower than that in the second rubber composition (SC).
  • the crosslinking system may be further based on per oxide, bismaleimides, vulcanization activator, a vulcanization accelerator other than sulfur-based vulcanization accelerator or combinations thereof.
  • the vulcanization activators may be based on zinc (pure zinc, zinc derivatives (for example, zinc fatty acid salt), or combination thereof), fatty acid (in particular, stearic acid), or combinations thereof.
  • the vulcanization accelerator other than sulfur-based vulcanization accelerator may be based on guanidine derivatives (in particular diphenylguanidine), or combination thereof.
  • a seventh aspect of the invention is the laminate according to any one of the first to the sixth aspects, wherein the first rubber composition (FC) is such that the amount of sulfur is more than 1.5 phr (for example, between 1.5 and 15 phr), preferably more than 2.0 phr (for example, between 2.0 and 10 phr), more preferably more than 2.5 phr (for example, between 2.5 and 5 phr).
  • FC first rubber composition
  • the amount of sulfur in the second rubber composition (SC) is at most 1.5 phr (for example, more than 0 phr and up to 1.5 phr), preferably at most 1.0 phr (for example, more than 0 phr and up to 1.0 phr).
  • An eighth aspect of the invention is the laminate according to any one of the first to the seventh aspects, wherein the second rubber composition (SC) is such that the amount of sulfur-based vulcanization accelerator is more than 1.5 phr (for example, between 1.5 and 15 phr), preferably more than 2.0 phr (for example, between 2.0 and 10 phr), more preferably more than 2.5 phr (for example, between 2.5 and 5 phr).
  • SC second rubber composition
  • the amount of vulcanization in the first rubber composition (FC) is at most 1.5 phr (for example, more than 0 phr and up to 1.5 phr), preferably at most 1.0 phr (for example, more than 0 phr and up to 1.0 phr).
  • a ninth aspect of the invention is the laminate according to any one of the first to the eighth aspects, wherein each of the rubber compositions (FC and SC) is such that the sulfur-based vulcanization accelerator is selected from the group consisting of sulfenamide type sulfur-based vulcanization accelerators (for example, N-cyclohexyl-2-benzothiazole sulfenamide (abbreviated to “CBS”), N,N-dicyclohexyl-2 benzothiazolesulfenamide (“DCBS”), N-tert-butyl-2-benzothiazolesulfenamide (“TBBS”), N-tert-butyl-2 benzothiazolesulfenimide (“TBSI”)), thiazole type sulfur-based vulcanization accelerators (for example, 2-mercaptobenzothiazyl disulfide (abbreviated to “MBTS”)), thiuram type accelerators (for example, tetrabenzylthiuram disulfide (“TBZTD”)
  • a tenth aspect of the invention is the laminate according to the ninth aspect, wherein each of the rubber compositions (FC and SC) is such that the sulfur-based vulcanization accelerator predominately comprises a sulfenamide type sulfur-based vulcanization accelerator, that is, the sulfur-based vulcanization accelerator comprises more than 50% by weight of the sulfenamide type sulfur-based vulcanization accelerator per 100% by weight of the sulfur-based vulcanization accelerator, preferably the sulfur-based vulcanization accelerator comprises more than 60%, more preferably more than 70%, still more preferably more than 80%, particularly more than 90%, more particularly 100%, by weight of the sulfenamide type sulfur-based vulcanization accelerator per 100% by weight of the sulfur-based vulcanization accelerator.
  • At least one of the rubber compositions (FC and SC) of the laminate according to the invention is further based on particles having a particle size of between 200 and 5 mesh, preferably between 170 and 6 mesh, more preferably between 140 and 7 mesh, still more preferably between 120 and 8 mesh.
  • An eleventh aspect of the invention is the laminate according to any one of the first to the tenth aspects, wherein each of the rubber compositions is based on the rubber particles.
  • a twelfth aspect of the invention is the laminate according to any one of the first to the eleventh aspects, wherein the particle size is between 100 and 10 mesh, preferably between 80 and 10 mesh, more preferably between 70 and 10 mesh, still more preferably between 60 and 10 mesh, particularly between 50 and 10 mesh, in at least one of the first rubber composition (FC) or the second rubber composition (SC), preferably in each of the rubber compositions.
  • the particle size is between 100 and 10 mesh, preferably between 80 and 10 mesh, more preferably between 70 and 10 mesh, still more preferably between 60 and 10 mesh, particularly between 50 and 10 mesh, in at least one of the first rubber composition (FC) or the second rubber composition (SC), preferably in each of the rubber compositions.
  • a thirteenth aspect of the invention is the laminate according to any one of the first to the twelfth aspects, wherein the amount of particle is between 1 and 150 phr, preferably between 10 and 100 phr, in at least one of the first rubber composition (FC) or the second rubber composition (SC), preferably in each of the rubber compositions..
  • the particles are made of particles selected from the group consisting of potassium tetraborate, sodium tetraborate calcium tetraborate, potassium chloride, sodium chloride, zirconia bead, alkali feldspar, kureha microsphere, silica sand, porous silica bead, cellulose powder, porous cellulose bead, walnut hull, apricot kernel, peach kernel, corn ear core, oyster shells, chitin, polyvinyl alcohol powder, polyethylene resin, crumb rubber and combinations thereof, preferably selected from the group consisting of sodium chloride, porous cellulose bead, crumb rubber and combinations thereof, more preferably crumb rubber.
  • a fourteenth aspect of the invention is the laminate according to any one of the first to the thirteenth aspects, wherein the particles are crumb rubber particles, in at least one of the first rubber composition (FC) or the second rubber composition (SC), preferably in each of the rubber compositions.
  • the crumb rubber particles are defined as particles obtained by reducing scrap tire(s) or other rubber(s) into granules with reinforcing materials such as steel(s) or fiber(s) removed along with any other contaminants such as dust(s), glass(es), or rock(s).
  • “Rubber Chemistry and Technology” discloses many methods of grinding vulcanized or crosslinked rubber(s) into crumb rubber particles.
  • the crumb rubber particles are generated from scrap tires.
  • the crumb rubber particles are mechanically processed, cryogenically processed, or mechanically and cryogenically processed, that is, the crumb rubber particles is ground using a mechanical grinding process, a cryogenic process or the both processes.
  • the steel components are removed using a magnetic separator and the fiber components are separated by air classifiers or other separation equipment.
  • the mechanical grinding process uses a variety of grinding techniques, such as cracker mills, granulators, etc. to mechanically break down the rubber into small particles.
  • shredded rubber is frozen at an extremely low temperature then shattered into small particles.
  • Particular embodiments of the present invention use crumb rubber particles produced through a mechanical grinding process.
  • Other embodiments use crumb rubber particles produced using a cryogenic process.
  • Many crumb rubbers are commercially available and for example, a suitable crumb rubber for use in the present invention is available from Global Corporation or Nantong Huili Rubber Corporation.
  • the rubber compositions (FC and SC) of the laminates according to the invention may be based on all or a portion(s) of the usual additives generally used in the elastomer composition(s) intended in particular for laminates, in more particular articles (for example, tires, shoes or caterpillar tracks), in more particular for tires, in still more particular for snow tires or winter tires, such as, for example, protection agents, such as antiozone waxes, chemical antiozonants, antioxidants, plasticizing agent, tackifying resins, methylene acceptors (for example, phenolic novolak resin) or methylene donors (for example, hexamethylenetetramine (HMT) or hexamethoxymethylmelamine (H3M)).
  • protection agents such as antiozone waxes, chemical antiozonants, antioxidants, plasticizing agent, tackifying resins, methylene acceptors (for example, phenolic novolak resin) or methylene donors (for example, hexamethylenetetramine (H
  • compositions can be also based on coupling activators when a coupling agent is used, agents for covering the reinforcing inorganic filler or more generally processing aids capable, in a known way, by virtue of an improvement in the dispersion of the filler in the rubber matrix and of a lowering of the viscosity of the compositions, of improving their property of processing in the raw state;
  • these agents are, for example, hydrolysable silanes, such as alkylalkoxysilanes, polyols, polyethers, amines, or hydroxylated or hydrolysable polyorganosiloxanes.
  • a fifteenth aspect of the invention is the laminate according to any one of the first to the fourteenth aspects, wherein at least one of the first rubber composition (FC) or the second rubber composition (SC), preferably each of the rubber compositions, is further based on a plasticizing agent in order to soften the matrix by diluting the elastomer and the reinforcing filler.
  • FC first rubber composition
  • SC second rubber composition
  • the amount of the plasticizing agent is more than 30 phr, preferably more than 40 phr (for example, between 40 and 120 phr), more preferably more than 50 phr (for example, between 50 and 110 phr), still more preferably more than 60 phr (for example, between 60 and 100 phr), particularly between more than 70 phr (for example, between 70 and 90 phr).
  • a sixteenth aspect of the invention is the laminate according to the fifteenth aspect, wherein the plasticizing agent comprises a liquid plasticizer(s), a hydrocarbon resin(s) or combinations thereof, preferably comprise a liquid plasticizer(s) and a hydrocarbon resin(s).
  • the plasticizing agent comprises a liquid plasticizer(s), a hydrocarbon resin(s) or combinations thereof, preferably comprise a liquid plasticizer(s) and a hydrocarbon resin(s).
  • any extending oil whether of aromatic or non-aromatic nature, any liquid plasticizing agent known for its plasticizing properties with regard to elastomer matrix(es) (for instance, diene elastomer), can be used as the liquid plasticizer.
  • these plasticizers or these oils which are more or less viscous, are liquids (that is to say, as a reminder, substances that have the ability to eventually take on the shape of their container), as opposite to plasticizing hydrocarbon resin(s) which are by nature solid at ambient temperature (20°C) under atmospheric pressure.
  • the plasticizing agent comprises no liquid plasticizer or comprises at most 100 phr, preferably at most 90 phr, more preferably at most 80 phr, still more preferably at most 70 phr, particularly at most 60 phr, more particularly 10 to 60 phr, of a liquid plasticizer(s).
  • the vegetable oil(s) may be made of an oil selected from the group consisting of linseed, safflower, soybean, corn, cottonseed, turnip seed, castor, tung, pine, sunflower, palm, olive, coconut, groundnut and grapeseed oils, and combinations thereof, particularly sunflower oil(s), more particularly sunflower oil(s) containing more than 60%, still more particularly more than 70%, especially more than 80%, more especially more than 90%, still more especially 100%, by weight of oleic acid.
  • the hydrocarbon resin(s) are polymer well known by a person skilled in the art, which are essentially based on carbon and hydrogen, and thus miscible by nature in rubber composition(s), for instance, diene elastomer composition(s). They can be aliphatic or aromatic or also of the aliphatic/aromatic type, that is to say based on aliphatic monomers, aromatic monomers or both. They can be natural or synthetic and may or may not be petroleum-based (if such is the case, also known under the name of petroleum resins). They are preferably exclusively hydrocarbon, that is to say, that they comprise only carbon and hydrogen atoms.
  • the plasticizing agent comprises no hydrocarbon resin or comprises at most 100 phr, preferably at most 90 phr, more preferably at most 80 phr, still more preferably at most 70 phr, particularly at most 60 phr, more particularly 10 to 60 phr, of a hydrocarbon resin(s).
  • Use is more preferably made, among the above copolymer resins, of those selected from the group consisting of (D)CPD/ vinylaromatic copolymer resins, (D)CPD/terpene copolymer resins, (D)CPD/C 5 fraction copolymer resins, (D)CPD/C 9 fraction copolymer resins, terpene/vinylaromatic copolymer resins, terpene/phenol copolymer resins, C 5 fraction/vinyl-aromatic copolymer resins, C 9 fraction/vinylaromatic copolymer resins, and combinations thereof.
  • pene combines here, in a known way, the ⁇ -pinene, ⁇ -pinene and limonene monomers; use is preferably made of a limonene monomer, which compound exists, in a known way, in the form of three possible isomers: L-limonene (laevorotatory enantiomer), D-limonene (dextrorotatory enantiomer) or else dipentene, the racemate of the dextrorotatory and laevorotatory enantiomers.
  • the vinylaromatic compound is styrene or a vinylaromatic monomer resulting from a C 9 fraction (or more generally from a C 8 to C 10 fraction).
  • the vinylaromatic compound is the minor monomer, expressed as molar fraction, in the copolymer under consideration.
  • Each of the rubber compositions (FC and SC) of the laminates according to the invention may be manufactured in appropriate mixers using two successive preparation phases well known to a person skilled in the art: a first phase of thermomechanical working or kneading (referred to as “non-productive” phase) at high temperature, up to a maximum temperature of between 110°C and 190°C, preferably between 130°C and 180°C, followed by a second phase of mechanical working (referred to as “productive” phase) at a lower temperature, typically of less than 110°C, for example between 40°C and 100°C, finishing phase during which sulfur and the sulfur-based vulcanization accelerator in the crosslinking system are incorporated.
  • a first phase of thermomechanical working or kneading referred to as “non-productive” phase
  • productive phase a second phase of mechanical working
  • a process which can be used for the manufacture of each of such compositions comprises, for example and preferably, the following steps: - incorporating in the elastomer matrix(es), for instance, the diene elastomer(s), in a mixer, the reinforcing filler, the particles, during a first stage (referred to as a “non-productive” stage) everything being kneaded thermomechanically (for example in one or more steps) until a maximum temperature of between 110°C and 190°C is reached; - cooling the combined mixture to a temperature of less than 100°C; - subsequently incorporating, during a second stage (referred to as a “productive” stage), sulfur and the sulfur-based vulcanization accelerator in the crosslinking system; and - kneading everything up to a maximum temperature of less than 110°C.
  • the first (non-productive) phase is carried out in a single thermomechanical stage during which all the necessary constituents are introduced into an appropriate mixer, such as a standard internal mixer, followed, in a second step, for example after kneading for 1 to 2 minutes, by the other additives, optional additional filler-covering agents or processing aids, with the exception of sulfur and the sulfur-based vulcanization accelerator in the crosslinking system.
  • the total kneading time, in this non-productive phase is preferably between 1 and 15 min.
  • sulfur and the sulfur-based vulcanization accelerator in the crosslinking system are then incorporated at low temperature (for example, between 40°C and 100°C), generally in an external mixer, such as an open mill; the combined mixture is then mixed (the second (productive) phase) for a few minutes, for example between 2 and 15 min.
  • low temperature for example, between 40°C and 100°C
  • an external mixer such as an open mill
  • the final composition thus obtained is subsequently calendered, for example in the form of a sheet or of a plaque, in particular for laboratory characterization, or else extruded in the form of a rubber profiled element which can be used directly as a laminate or an article, for example, a tire tread, a shoe sole and a caterpillar track tread.
  • the laminate according to the invention it is possible to build a first layer of a homogeneous rubber composition, as the first rubber composition (FC), and a second layer of a homogeneous rubber composition, as the second rubber composition (SC), then to superpose the first layer onto the second layer or then to superpose the second layer onto the first layer, or to sandwich the other layer(s) or portion(s) between the first layer and the second layer, to get the laminate of the article.
  • FC first rubber composition
  • SC second layer of a homogeneous rubber composition
  • a nineteenth aspect of the invention is the laminate according to any one of the first to the eighteenth aspects, wherein the first portion is adjacent to the second portion.
  • a twentieth aspect of the invention is an article comprising a laminate according to any one of the first to the nineteenth aspects.
  • a twenty first aspect of the invention is the article according to the twentieth aspect, wherein the article is intended to contact with the ground.
  • a twenty second aspect of the invention is the article according to the twenty first aspect, wherein the first portion is arranged nearer to the ground than the second portion.
  • a twenty third aspect of the invention is the article according to the twenty first aspect, wherein the second portion is arranged nearer to the ground than the first portion.
  • a twenty fourth aspect of the invention is the article according to any one of the twentieth to the twenty third aspects, wherein at least one portion of the first portion or the second portion, preferably each of the portions, is intended to come into contact with the ground during the service life of article.
  • the service life means the duration to use the article (for example, the term from the new state to the final state of the article, in case of that the article is a tire, the final state means a state on reaching the wear indicator bar(s) in the tread of tire).
  • a twenty fifth aspect of the invention is the article according to twenty fourth aspect, wherein the portion intended to come into contact with the ground during the service life of the tire is made of the rubber composition further based on the particles.
  • a twenty sixth aspect of the invention is the article according to any one of the twentieth to the twenty fifth aspects, wherein the article is a tire, a shoe, a conveyor or a caterpillar track, preferably a tire, a shoe or a caterpillar track.
  • a twenty seventh aspect of the invention is the article according to the twenty sixth aspect, wherein the article is a tire.
  • the tires are particularly intended to equip passenger motor vehicles, including 4 ⁇ 4 (four-wheel drive) vehicles and SUV (Sport Utility Vehicles) vehicles, and industrial vehicles particularly selected from vans and heavy duty vehicles (i.e., bus or heavy road transport vehicles (lorries, tractors, trailers)).
  • passenger motor vehicles including 4 ⁇ 4 (four-wheel drive) vehicles and SUV (Sport Utility Vehicles) vehicles
  • industrial vehicles particularly selected from vans and heavy duty vehicles (i.e., bus or heavy road transport vehicles (lorries, tractors, trailers)).
  • a twenty eighth aspect of the invention is the article according to the twenty seventh aspect, wherein the article is a snow tire.
  • the snow tires classified in a category of use “snow”, identified by an inscription the alpine symbol (“3-peak-mountain with snowflake”), marked on their sidewalls, mean tires whose tread patterns, tread compounds, structures or both are primarily designed to achieve, in snow conditions, a performance better than that of normal tires intended for normal on-road use with regard to their abilities to initiate, maintain or stop vehicle motion.
  • a twenty ninth aspect of the invention is the article according to the twenty seventh aspect or the twenty eighth aspect, wherein the laminate is comprised in a tread of a tire.
  • a thirtieth aspect of the invention is the article according to any one of the twenty seventh to twenty ninth aspects, wherein the laminate is such that the superposed portions are radially superposed portions.
  • a thirty first aspect of the invention is the article according to the thirtieth aspect, wherein the laminate is such that the first portion is radially exterior to the second position.
  • the first portion may be a first layer of a homogeneous rubber composition, as the first rubber composition (FC)
  • the second portion may be a second layer of another homogeneous rubber composition, as the second rubber composition (SC).
  • the first layer is located to be intended to come into contact with the ground in the new state of the tire.
  • a thirty second aspect of the invention is the article according to the thirtieth aspect, wherein the laminate is such that the second portion is radially exterior to the first position.
  • the second portion may be a second layer of a homogeneous rubber composition, as the second rubber composition (SC)
  • the first portion may be a first layer of another homogeneous rubber composition, as the first rubber composition (FC).
  • the second layer is located to be intended to come into contact with the ground in the new state of the tire.
  • the invention relates to the rubber composition(s), to the laminate(s), to the article(s), to the tire (s) and the tire tread(s) described above, both in the raw state (i.e., before curing) and in the cured state (i.e., after crosslinking or vulcanization).
  • the three rubber compositions are based on a diene elastomer (SBR and BR) reinforced with a blend of silica (as a reinforcing inorganic filler) and carbon black, crumb rubber particles and a crosslinking system based on sulfur and N-dicyclohexyl-2-benzothiazolesulfenamide (as a sulfur-based vulcanization accelerator).
  • SBR and BR diene elastomer
  • silica as a reinforcing inorganic filler
  • carbon black crumb rubber particles
  • a crosslinking system based on sulfur and N-dicyclohexyl-2-benzothiazolesulfenamide
  • the formulations of the three rubber compositions are given at Table 1 with the content of the various products expressed in phr.
  • Each rubber composition was produced as follows: The reinforcing filler, the particles, the elastomer matrix and the various other ingredients, with the exception of sulfur and a sulfenamide type sulfur-based vulcanization accelerator (as a sulfur-based vulcanization accelerator) in the crosslinking system, were successively introduced into an internal mixer having an initial vessel temperature of approximately 60°C; the mixer was thus approximately 70% full (% by volume). Thermomechanical working (non-productive phase) was then carried out in one stage, which lasts in total approximately 3 to 4 minutes, until a maximum “dropping” temperature of 165°C was reached.
  • the rubber compositions thus obtained were subsequently calendered, either in the form of sheets (thickness of 2 to 3 mm) or of fine sheets of rubber, for the measurement of their physical or mechanical properties, or in the form of profiled elements which could be used directly, after cutting, assembling or both to the desired dimensions, for example as tire semi-finished products, in particular as tire treads.
  • two laminates (L-1: a reference, and L-2: an example according to the invention) comprising the first portion made of the first rubber compositions and the second rubber portions made of the second rubber compositions by superposition of the sheets of the rubber compositions (C-1, C-2 and C-3), as shown in Table 2, are compared.
  • test device based on the probe tack tester (ASTM D2979-95) was used.
  • An Instron tensile test machine comprising a fixed metallic jaw and a mobile metallic jaw was used. A first test specimen was stuck on the fixed metallic jaw. A second test specimen was stuck to the mobile jaw. The test specimens were cut into circular plates with a 45 mm diameter punch. The test specimens were made of mixing films on which plastic films were put in order to reinforce the mixing films. The mixing films were obtained by calendaring the unvulcanized mixtures with a thickness of 2 mm.
  • the principle of the measurement consisted in bringing the two mixing films into contact for 5 seconds by applying a compression force of 20 N. After this contact phase, the two mixing films were separated by driving the cross-member of the tensile test machine. The speed of displacement of the cross-member in this peeling phase was 1 mm/s. The displacement of the cross-member and the force were measured continuously as a function of time from the contact phase to the peeling phase. After the measurement of displacement of the cross-member and the force, each weight of mixing films adhering to each plastic film was measured. Each value of the heavier weight of mixing films adhering to the plastic film is reported in the table 2, in base 100 of the total weight of the mixing films to the both plastic films. The higher the value is, the higher better the tack is.
  • the measurements of tack were done with two test laminates (T-1: a reference, T-2: an example according to the invention).
  • the reference laminate (T-1) was such that the mixing films in the first test specimen and the second test specimen were made of C-1 as the first rubber composition (FC) and the second rubber composition (SC).
  • the example laminate according to the invention (T-2) was such that the mixing film in the first test specimen was made of C-2 as the first rubber composition (FC), and the mixing film in the second test specimen was made of C-3 as the second rubber composition (SC).
  • the specific laminate with rubber compositions intended in particular for a rubber article for example, a tire tread, a shoe sole and a caterpillar track tread, which allows an unexpectedly improved the tack of the rubber compositions of the laminate while maintaining the snow grip performance in the new state and the worn state.

Abstract

La présente invention concerne un stratifié qui comprend au moins deux parties superposées comprenant une première partie constituée d'une première composition de caoutchouc (FC) et une seconde partie constituée d'une seconde composition de caoutchouc (SC) ; chacune des compositions de caoutchouc étant basée sur au moins : une matrice élastomère ; une charge de renforcement ; et un système de réticulation basé sur le soufre ou/et un accélérateur de vulcanisation à base de soufre ; la première composition de caoutchouc (FC) et/ou la seconde composition de caoutchouc (SC) étant en outre basées sur des particules ayant une taille de particule comprise entre 200 et 5 mesh ; la quantité en phr de soufre dans la première composition de caoutchouc (FC) étant supérieure à celle dans la seconde composition de caoutchouc (SC), et la quantité en phr d'accélérateur de vulcanisation à base de soufre dans la première composition de caoutchouc (FC) étant inférieure à celle dans la seconde composition de caoutchouc (SC).
PCT/JP2020/002876 2019-01-28 2020-01-28 Stratifié WO2020158695A1 (fr)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021166166A1 (fr) * 2020-02-20 2021-08-26 Compagnie Generale Des Etablissements Michelin Composition de caoutchouc
WO2022162823A1 (fr) * 2021-01-28 2022-08-04 Compagnie Generale Des Etablissements Michelin Article, en particulier un pneu
WO2023121652A1 (fr) * 2021-12-21 2023-06-29 Compagnie Generale Des Etablissements Michelin Feuille de caoutchouc

Citations (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996037547A2 (fr) 1995-05-22 1996-11-28 Cabot Corporation Composes elastomeres incorporant des noirs de carbone traites au silicium
WO1997036724A2 (fr) 1996-04-01 1997-10-09 Cabot Corporation Nouveaux materiaux composites elastomeres, et procede et appareil s'y rapportant
WO1999009036A1 (fr) 1997-08-21 1999-02-25 Osi Specialties, Inc. Agents de couplage a base de mercaptosilanes bloques, utilises dans des caoutchoucs a charge
WO1999016600A1 (fr) 1997-09-30 1999-04-08 Cabot Corporation Melanges composites a base d'elastomere et procedes d'elaboration
WO1999028380A1 (fr) 1997-11-28 1999-06-10 Compagnie Generale Des Etablissements Michelin - Michelin & Cie Composition de caoutchouc pour pneumatiques, renforcee d'un noir de carbone revetu d'une couche alumineuse
WO2002031041A1 (fr) 2000-10-13 2002-04-18 Societe De Technologie Michelin Composition de caoutchouc comportant a titre d'agent de couplage un organosilane polyfonctionnel
WO2002030939A1 (fr) 2000-10-13 2002-04-18 Societe De Technologie Michelin Organosilane polyfonctionnel utilisable comme agent de couplage et son procede d'obtention
WO2002083782A1 (fr) 2001-04-10 2002-10-24 Societe De Technologie Michelin Pneumatique et bande de roulement comportant comme agent de couplage un tetrasulfure de bis-alkoxysilane
WO2003002649A1 (fr) 2001-06-28 2003-01-09 Societe De Technologie Michelin Bande de roulement pour pneumatique renforcee d'une silice a tres basse surface specifique
WO2003002648A1 (fr) 2001-06-28 2003-01-09 Societe De Technologie Michelin Bande de roulement pour pneumatique renforcee d'une silice a basse surface specifique
WO2003016387A1 (fr) 2001-08-13 2003-02-27 Societe De Technologie Michelin Composition de caoutchouc dienique pour pneumatique comprenant une silice specifique comme charge renforcante
WO2004033548A1 (fr) 2002-10-11 2004-04-22 Societe De Technologie Michelin Ceinture de pneumatique a base dune charge inorganique et d'un silane-polysulfure
US6849754B2 (en) 2001-08-06 2005-02-01 Degussa Ag Organosilicon compounds
WO2006023815A2 (fr) 2004-08-20 2006-03-02 General Electric Company Compositions cycliques de silanes mercaptofonctionnels bloquees derivees de diol
WO2006125533A1 (fr) 2005-05-26 2006-11-30 Societe De Technologie Michelin Compostion de cautchouc pour pneumatique comportant un agent de couplage organosilicique et un agent de recouvrement de charge inorganique
WO2006125532A1 (fr) 2005-05-26 2006-11-30 Societe De Technologie Michelin Composition de caoutchouc pour pneumatique comportant un agent de couplage organosiloxane
WO2006125534A1 (fr) 2005-05-26 2006-11-30 Societe De Technologie Michelin Composition de caoutchouc pour pneumatique comportant un systeme de couplage organosilicique
WO2007098080A2 (fr) 2006-02-21 2007-08-30 Momentive Performance Materials Inc. Composition de matière de charge non agglomérante à base de silane organofonctionnel
WO2008055986A2 (fr) 2006-11-10 2008-05-15 Rhodia Operations Procede de preparation d'alcoxysilanes (poly)sulfures et nouveaux produits intermediaires dans ce procede
WO2010072685A1 (fr) 2008-12-22 2010-07-01 Societe De Technologie Michelin Agent de couplage mercaptosilane bloque
WO2015016390A1 (fr) * 2013-07-31 2015-02-05 Compagnie Generale Des Etablissements Michelin Pneumatique possédant une bande de roulement comprenant des milli-particules
WO2015016388A1 (fr) * 2013-07-31 2015-02-05 Compagnie Generale Des Etablissements Michelin Pneu ayant une bande de roulement comprenant des milliparticules
WO2017104781A1 (fr) * 2015-12-17 2017-06-22 Compagnie Generale Des Etablissements Michelin Pneu comprenant une bande de roulement
WO2018079802A1 (fr) * 2016-10-31 2018-05-03 Compagnie Generale Des Etablissements Michelin Pneumatique comprenant une bande de roulement
WO2018110684A1 (fr) 2016-12-15 2018-06-21 Compagnie Generale Des Etablissements Michelin Pneumatique comprenant une bande de roulement
WO2018221630A1 (fr) * 2017-05-31 2018-12-06 Compagnie Generale Des Etablissements Michelin Pneu comprenant une bande de roulement

Patent Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996037547A2 (fr) 1995-05-22 1996-11-28 Cabot Corporation Composes elastomeres incorporant des noirs de carbone traites au silicium
WO1997036724A2 (fr) 1996-04-01 1997-10-09 Cabot Corporation Nouveaux materiaux composites elastomeres, et procede et appareil s'y rapportant
WO1999009036A1 (fr) 1997-08-21 1999-02-25 Osi Specialties, Inc. Agents de couplage a base de mercaptosilanes bloques, utilises dans des caoutchoucs a charge
WO1999016600A1 (fr) 1997-09-30 1999-04-08 Cabot Corporation Melanges composites a base d'elastomere et procedes d'elaboration
WO1999028380A1 (fr) 1997-11-28 1999-06-10 Compagnie Generale Des Etablissements Michelin - Michelin & Cie Composition de caoutchouc pour pneumatiques, renforcee d'un noir de carbone revetu d'une couche alumineuse
WO2002030939A1 (fr) 2000-10-13 2002-04-18 Societe De Technologie Michelin Organosilane polyfonctionnel utilisable comme agent de couplage et son procede d'obtention
US6774255B1 (en) 2000-10-13 2004-08-10 Michelin Recherche Et Technique, S.A. Polyfunctional organosilane usable as a coupling agent and process for the obtainment thereof
US20040051210A1 (en) 2000-10-13 2004-03-18 Jean-Claude Tardivat Rubber composition comprising a polyfunctional organosilane as coupling agent
WO2002031041A1 (fr) 2000-10-13 2002-04-18 Societe De Technologie Michelin Composition de caoutchouc comportant a titre d'agent de couplage un organosilane polyfonctionnel
WO2002083782A1 (fr) 2001-04-10 2002-10-24 Societe De Technologie Michelin Pneumatique et bande de roulement comportant comme agent de couplage un tetrasulfure de bis-alkoxysilane
US7217751B2 (en) 2001-04-10 2007-05-15 Michelin Recherche Et Technique S.A. Tire and tread comprising a bis-alkoxysilane tetrasulfide as coupling agent
WO2003002649A1 (fr) 2001-06-28 2003-01-09 Societe De Technologie Michelin Bande de roulement pour pneumatique renforcee d'une silice a tres basse surface specifique
WO2003002648A1 (fr) 2001-06-28 2003-01-09 Societe De Technologie Michelin Bande de roulement pour pneumatique renforcee d'une silice a basse surface specifique
US6849754B2 (en) 2001-08-06 2005-02-01 Degussa Ag Organosilicon compounds
WO2003016387A1 (fr) 2001-08-13 2003-02-27 Societe De Technologie Michelin Composition de caoutchouc dienique pour pneumatique comprenant une silice specifique comme charge renforcante
WO2004033548A1 (fr) 2002-10-11 2004-04-22 Societe De Technologie Michelin Ceinture de pneumatique a base dune charge inorganique et d'un silane-polysulfure
WO2006023815A2 (fr) 2004-08-20 2006-03-02 General Electric Company Compositions cycliques de silanes mercaptofonctionnels bloquees derivees de diol
WO2006125533A1 (fr) 2005-05-26 2006-11-30 Societe De Technologie Michelin Compostion de cautchouc pour pneumatique comportant un agent de couplage organosilicique et un agent de recouvrement de charge inorganique
WO2006125532A1 (fr) 2005-05-26 2006-11-30 Societe De Technologie Michelin Composition de caoutchouc pour pneumatique comportant un agent de couplage organosiloxane
WO2006125534A1 (fr) 2005-05-26 2006-11-30 Societe De Technologie Michelin Composition de caoutchouc pour pneumatique comportant un systeme de couplage organosilicique
WO2007098080A2 (fr) 2006-02-21 2007-08-30 Momentive Performance Materials Inc. Composition de matière de charge non agglomérante à base de silane organofonctionnel
WO2008055986A2 (fr) 2006-11-10 2008-05-15 Rhodia Operations Procede de preparation d'alcoxysilanes (poly)sulfures et nouveaux produits intermediaires dans ce procede
WO2010072685A1 (fr) 2008-12-22 2010-07-01 Societe De Technologie Michelin Agent de couplage mercaptosilane bloque
WO2015016390A1 (fr) * 2013-07-31 2015-02-05 Compagnie Generale Des Etablissements Michelin Pneumatique possédant une bande de roulement comprenant des milli-particules
WO2015016388A1 (fr) * 2013-07-31 2015-02-05 Compagnie Generale Des Etablissements Michelin Pneu ayant une bande de roulement comprenant des milliparticules
WO2017104781A1 (fr) * 2015-12-17 2017-06-22 Compagnie Generale Des Etablissements Michelin Pneu comprenant une bande de roulement
WO2018079802A1 (fr) * 2016-10-31 2018-05-03 Compagnie Generale Des Etablissements Michelin Pneumatique comprenant une bande de roulement
WO2018110684A1 (fr) 2016-12-15 2018-06-21 Compagnie Generale Des Etablissements Michelin Pneumatique comprenant une bande de roulement
WO2018221630A1 (fr) * 2017-05-31 2018-12-06 Compagnie Generale Des Etablissements Michelin Pneu comprenant une bande de roulement

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
THE JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 60, February 1938 (1938-02-01), pages 309

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021166166A1 (fr) * 2020-02-20 2021-08-26 Compagnie Generale Des Etablissements Michelin Composition de caoutchouc
WO2022162823A1 (fr) * 2021-01-28 2022-08-04 Compagnie Generale Des Etablissements Michelin Article, en particulier un pneu
WO2023121652A1 (fr) * 2021-12-21 2023-06-29 Compagnie Generale Des Etablissements Michelin Feuille de caoutchouc

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