EP3102646A1 - Durch eine klebstoffzusammensetzung mit aromatischem aldehyd und polyphenol haftbar gemachtes verstärkungselement aus bronziertem metall - Google Patents

Durch eine klebstoffzusammensetzung mit aromatischem aldehyd und polyphenol haftbar gemachtes verstärkungselement aus bronziertem metall

Info

Publication number
EP3102646A1
EP3102646A1 EP15704499.1A EP15704499A EP3102646A1 EP 3102646 A1 EP3102646 A1 EP 3102646A1 EP 15704499 A EP15704499 A EP 15704499A EP 3102646 A1 EP3102646 A1 EP 3102646A1
Authority
EP
European Patent Office
Prior art keywords
aldehyde
reinforcing element
aromatic
copper
steel reinforcing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP15704499.1A
Other languages
English (en)
French (fr)
Inventor
Clément MICHOUD
David DOISNEAU
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Compagnie Generale des Etablissements Michelin SCA
Original Assignee
Michelin Recherche et Technique SA Switzerland
Compagnie Generale des Etablissements Michelin SCA
Michelin Recherche et Technique SA France
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Michelin Recherche et Technique SA Switzerland, Compagnie Generale des Etablissements Michelin SCA, Michelin Recherche et Technique SA France filed Critical Michelin Recherche et Technique SA Switzerland
Publication of EP3102646A1 publication Critical patent/EP3102646A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60CVEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
    • B60C9/00Reinforcements or ply arrangement of pneumatic tyres
    • B60C9/0007Reinforcements made of metallic elements, e.g. cords, yarns, filaments or fibres made from metal
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J107/00Adhesives based on natural rubber
    • C09J107/02Latex
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J109/00Adhesives based on homopolymers or copolymers of conjugated diene hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J109/00Adhesives based on homopolymers or copolymers of conjugated diene hydrocarbons
    • C09J109/06Copolymers with styrene
    • C09J109/08Latex
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J161/00Adhesives based on condensation polymers of aldehydes or ketones; Adhesives based on derivatives of such polymers
    • C09J161/04Condensation polymers of aldehydes or ketones with phenols only
    • C09J161/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • C09J161/12Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols with polyhydric phenols
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60CVEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
    • B60C9/00Reinforcements or ply arrangement of pneumatic tyres
    • B60C9/0007Reinforcements made of metallic elements, e.g. cords, yarns, filaments or fibres made from metal
    • B60C2009/0014Surface treatments of steel cords
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60CVEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
    • B60C9/00Reinforcements or ply arrangement of pneumatic tyres
    • B60C9/0007Reinforcements made of metallic elements, e.g. cords, yarns, filaments or fibres made from metal
    • B60C2009/0021Coating rubbers for steel cords

Definitions

  • the field of the present invention is that of metal reinforcing elements and adhesive compositions or "glues" intended to adhere such metal reinforcing elements to unsaturated rubber matrices such as those commonly used in semi-finished articles or products. made of rubber.
  • the present invention more particularly relates to steel reinforcing elements coated with adhesive layers based on a phenol-aldehyde resin, in particular to coated steel reinforcing elements capable of reinforcing tire structures.
  • Pneumatic steel reinforcing elements comprising one or more steel wire reinforcement elements, for example steel wires
  • steel wire reinforcement elements for example steel wires
  • adhesives known under the name "RFL” for resorcinol-formaldehyde-latex
  • RFL adhesives comprise, in a well known manner, a thermosetting phenolic resin obtained by the condensation of resorcinol with formaldehyde and one or more diene rubber latex in aqueous solution.
  • the RFL glues of EP2006341 ensure good adhesion of the coated steel wire (s) to rubber matrices without the latter being surface-treated, that is to say in the absence of a layer of a coating metal, for example a layer of brass.
  • the RFL glue requires the use of a halogenated polymer and a metal oxide.
  • this RFL adhesive requires the use of a rubber matrix comprising an acrylic rubber composition and thus does not allow satisfactory adhesion with any rubber matrix.
  • a reinforced steel reinforcing element comprising:
  • one or more filamentary reinforcing elements each comprising a steel core
  • the invention also relates to a method of manufacturing a coated steel reinforcing member comprising:
  • one or more filamentary reinforcing elements each comprising a steel core
  • the method according to the invention comprises a step of coating at least a portion of the layer of the copper-tin alloy coating of the or each wire reinforcing element with the adhesive layer comprising an adhesive composition as described above. .
  • the invention relates to the use, for the adhesion of a steel reinforcing element to a rubber matrix, of an adhesive composition forming an adhesive layer coating at least a portion of a layer of a coating of a copper-tin alloy coating at least a portion of each steel core of one or more filamentary reinforcing elements, the adhesive composition being as described above.
  • the invention also relates to a reinforced rubber composite of at least one coated steel reinforcing element as described above comprising a rubber matrix in which is embedded the coated steel reinforcing element.
  • Another object of the invention is a tire comprising at least one rubber composite as described above.
  • the invention therefore relates to any composite (article or semi-finished product) of rubber, in particular any tire, before or after firing (for crosslinking or final vulcanization), comprising a reinforced steel reinforcing element as described above.
  • the invention also relates to the use of the reinforcing element made of coated steel as described above as reinforcing element for semi-finished articles or products made of rubber, particularly tires, especially those intended to equip vehicles with tourism-type engines, SUVs ("Sport Utility Vehicles"), two-wheelers (especially bicycles, motorcycles), planes, such as industrial vehicles chosen from light trucks, "heavy trucks” - that is to say, metro, bus, road transport vehicles (trucks, tractors, trailers), off-the-road vehicles such as agricultural or civil engineering vehicles; other transport or handling vehicles.
  • SUVs Sport Utility Vehicles
  • two-wheelers especially bicycles, motorcycles
  • planes such as industrial vehicles chosen from light trucks, "heavy trucks” - that is to say, metro, bus, road transport vehicles (trucks, tractors, trailers
  • iene elastomer or indistinctly rubber is meant an elastomer derived at least in part (that is to say a homopolymer or a copolymer) from monomer (s) diene (s) (ie, carrier (s) two carbon-carbon double bonds, conjugated or not).
  • isoprene elastomer a homopolymer or copolymer of isoprene, in other words a diene elastomer selected from the group consisting of natural rubber (NR), synthetic polyisoprenes (IR), the various copolymers of isoprene and mixtures of these elastomers.
  • NR natural rubber
  • IR synthetic polyisoprenes
  • any range of values designated by the expression "between a and b" represents the range of values from more than a to less than b (i.e., terminals a and b excluded) while any range of values designated by the expression “from a to b” means the range from a to b (i.e., including the strict limits a and b).
  • composition based on a composition comprising the mixture and / or the reaction product of the various basic constituents used for this composition, some of them may be intended to react or susceptible to react with each other or with their surrounding chemical environment, at least in part, during the various phases of manufacture of the composition, the reinforcing element, the composites or finished articles, in particular during a cooking step.
  • the copper-tin alloy is generally known as bronze.
  • the copper-tin alloy comprises between 80% and 99.5% copper and between 0.5% and 20% tin by weight of the alloy.
  • a steel reinforcing element whose steel core is coated with a copper-tin alloy coating layer, ie bronze, is referred to as "tanned” and is referred to as a tanned steel reinforcing element.
  • the coated tanned steel reinforcement element according to the invention may comprise, in one embodiment, a single wire reinforcement element.
  • the tanned steel reinforcing member coated according to the invention comprises a plurality of wire reinforcing elements assembled together, for example by wiring or twisting.
  • the coated bronzed steel reinforcement elements comprising several wire reinforcing elements, for example, layered cables and multi-strand cables.
  • Each element of filament reinforcement is unitary, that is to say that the constituents of each element of filament reinforcement are inseparable from each other.
  • the adhesive layer coats at least a portion of the copper-tin alloy coating layer of the or each wire reinforcing member.
  • the adhesive layer may partially or completely coat the layer of the copper-tin alloy coating of the or each filament reinforcing member.
  • the adhesive layer may coat portions of the copper-tin alloy coating layer of that element or its screen.
  • the adhesive layer may coat the copper-tin alloy coating layer with a plurality of wire elements without coating other ones or coat only parts of the copper-tin alloy coating layer of some or all of the wire elements.
  • element of filial reinforcement is meant the elongated elements of great length relative to their cross section, whatever the shape of the latter, for example circular, oblong, rectangular or square, or even flat, this filament element may be rectilinear as not straight, for example twisted, or corrugated.
  • the diameter of each filament reinforcing element is preferably less than 5 mm, more preferably in a range from 0.1 to 0.5 mm. Mention may also be made of strips or strips which have a great length relative to their thickness.
  • the steel core is monolithic, that is to say that it comes for example from material or molding.
  • the steel may have a pearlitic, ferritic, austenitic, bainitic, martensitic microstructure or a microstructure derived from a mixture of these microstructures.
  • the steel comprises a carbon content ranging from 0.2% to 1% by weight and more preferably from 0.3% to 0.7% by weight.
  • the steel comprises a manganese content ranging from 0.3% to 0.7% by weight, a silicon content ranging from 0.1% to 0.3% by weight, and a phosphorus level of at most up to 0.045% inclusive of the mass, with a maximum sulfur content of up to 0.045% inclusive and a maximum nitrogen content of up to 0.008% inclusive.
  • the steel comprises at most 0.1% inclusive, preferably 0.05% inclusive, and more preferably 0.02% including mass bound vanadium and / or molybdenum.
  • the steel used comprises less than 0.5%, preferably not more than 0.05% inclusive, and more preferably not more than 0.02% inclusive of chromium.
  • the steel comprises at least 0.5% inclusive, preferably at least 5% inclusive, and more preferably at least 15% inclusive, inclusive of chromium.
  • a stainless steel comprises at least 2% inclusive, preferably at least 4% inclusive and more preferably at least 6% by weight nickel.
  • the copper-tin alloy coating layer directly covers at least a portion of the steel core of the or each wire reinforcing member.
  • the adhesive layer directly coats at least a portion of the copper-tin alloy coating layer of the or each wire reinforcing member.
  • the coated reinforcing element does not have a non-metallic intermediate layer which would be interposed between the layer of the copper-tin alloy coating of the or each wire reinforcing element and the adhesive layer comprising the composition. adhesive.
  • the adhesive layer directly coats a non-metallic adhesion interlayer directly coating at least a portion of the copper-tin alloy coating layer of the or each wire reinforcing member.
  • the non-metallic interlayer generally referred to as the adhesion primer, in combination with the adhesive layer comprising the adhesive composition, improves the adhesion of the coated tanned steel reinforcement element to the rubber matrix.
  • adhesion primers are those commonly used by those skilled in the art for pre-gluing certain textile fibers (polyester fibers, for example PET, aramid, aramid / nylon).
  • a primer based on blocked isocyanate By layer “directly” coating an object or coating “directly” covering an object, it is meant that the layer or coating is in contact with the object without any other object, in particular another layer or another coating being interposed between the two.
  • the adhesive composition therefore comprises at least one (i.e., one or more) phenol-aldehyde resin; this phenol-aldehyde resin is based on at least one (that is to say one or more) aromatic aldehyde and at least one (that is to say one or more) polyphenol, which constituents will be described in detail below.
  • the first component of the phenol-aldehyde resin is an aromatic aldehyde having at least one aldehyde function, comprising at least one aromatic ring.
  • the aromatic nucleus carries the aldehyde function.
  • the aromatic aldehyde carries at least two aldehyde functions.
  • the aromatic ring of the aromatic aldehyde carries two aldehyde functions, the latter being able to be in the ortho, meta or para position on the aromatic ring.
  • the aromatic nucleus of the aromatic aldehyde is a benzene nucleus.
  • this aromatic aldehyde is selected from the group consisting of 1,2-benzene-dicarboxaldehyde, 1,3-benzene-dicarboxaldehyde, 1,4-benzene-dicarboxaldehyde, 2-hydroxybenzene-1, 3,5-tricarbaldehyde, and mixtures of these compounds.
  • the aromatic polyaldehyde used is 1,4-benzenedicarboxaldehyde, also called terephthaldehyde, as a reminder of the chemical formula developed:
  • the aromatic aldehyde has formula (A):
  • X is N, S or O and R is -H or -CHO.
  • Aromatic aldehydes are derived from renewable resources and not from oil. Aromatic aldehydes are for example from the bio-resource or transformation products of the bio-resource.
  • the aromatic aldehyde is of general formula ( ⁇ '):
  • X represents O.
  • X represents O and R represents -H.
  • the aromatic aldehyde used is then of formula (B1):
  • X comprises N.
  • X represents NH.
  • the aromatic aldehyde used is of formula (Cl):
  • X represents NH.
  • the aromatic aldehyde used is of formula (Cl):
  • R represents -CHO in the variant of the aromatic aldehyde of formula (Cl) and the aromatic aldehyde obtained is then 2,5-lH-pyrroledicarboxaldehyde.
  • X represents NR1 with R1 representing an alkyl, aryl arylalkyl, alkylaryl or cycloalkyl group.
  • R1 representing an alkyl, aryl arylalkyl, alkylaryl or cycloalkyl group.
  • the aromatic aldehyde used is of formula (C2):
  • X comprises S.
  • R represents -CHO in the variant of the aromatic aldehyde of formula (D'I) and is then 2,5-thiophene dicarboxaldehyde.
  • X is SR 2 with R 2 being alkyl, aryl arylalkyl, alkylaryl or cycloalkyl.
  • the aromatic aldehyde used is of formula (D2):
  • X represents R3-S-R2 with R2, R3 each independently of each other an alkyl, aryl arylalkyl, alkylaryl or cycloalkyl group.
  • the aromatic aldehyde used is of formula (D3):
  • the phenol-aldehyde resin may comprise a mixture of the compounds indicated above, in particular a mixture of furfuraldehyde and 2,5-furanedicarboxaldehyde.
  • the composition is free of formaldehyde.
  • each aldehyde is preferentially different from formaldehyde.
  • the composition is then also preferably free of formaldehyde.
  • the or each aldehyde of the phenol-aldehyde resin is different from formaldehyde.
  • formaldehyde-free it is meant that the formaldehyde mass content by weight of the aldehyde (s) is strictly less than 1%.
  • the composition may comprise formaldehyde.
  • the composition then comprises a weight ratio of formaldehyde by total weight of the aldehyde (s) is less than or equal to 10%, preferably to 5% and more preferably to 2%.
  • the second component of the phenol-aldehyde resin is a polyphenol having one or more aromatic ring (s).
  • a polyphenol comprising a single aromatic ring
  • the latter carries two or three hydroxyl functions in the meta position with respect to each other (in the case of two functions) or with respect to each other. (in the case of three functions), the remainder of the aromatic ring being by definition unsubstituted; by this is meant that the other carbon atoms of the remainder of the aromatic ring (those other than carbon atoms bearing hydroxyl functions) carry a single hydrogen atom.
  • a polyphenol comprising several (two or more) aromatic rings
  • at least two of them are each carrying two or three hydroxyl functions in the meta position with respect to each other (in the case of two functions), or with respect to each other (in the case of three functions), it being understood that the two ortho positions of at least one of these hydroxyl functions are unsubstituted; by this is meant that the two carbon atoms located on both sides (in the ortho position) of the hydroxyl carbon atom (ie, bearing the hydroxyl function) carry a single hydrogen atom.
  • the polyphenol molecule comprises several aromatic rings
  • at least two of these aromatic nuclei are chosen from those of general formulas:
  • the polyphenol is for example a flavonoid, characterized for recall by a basic structure with 15 carbon atoms, formed by two benzene rings connected by three carbon atoms. More particularly, the flavonoid used is 2 ', 4', 3, 5, 7-pentahydroxyflavone, also called "Morin", of formula (V) below:
  • this compound is a polyphenol having two aromatic rings (of respective formulas IV-c and IV-d above), each of which is indeed carrying two hydroxyl functional groups in the meta position with respect to each other, the two ortho positions of at least one of these two hydroxyl functions being unsubstituted.
  • the polyphenol is for example phloroglucide, also called 2,4,6,3 ', 5' -biphenylpentol, of the following structural formula:
  • this compound is a polyphenol comprising two aromatic rings (of respective formulas IV-a and IV-b above), each of which is indeed carrying at least two (in this case, a carrier of two , the other carrier of three) hydroxyl functions meta position relative to each other, the two ortho positions of at least one of these two hydroxyl functions being unsubstituted.
  • the polyphenol is for example 2,2 ', 4,4'-tetrahydroxydiphenyl sulfide of the following structural formula:
  • the polyphenol is selected from the group consisting of phloroglucinol (III), 2,2 ', 4,4'-tetrahydroxydiphenyl sulfide (VII) and mixtures of these compounds.
  • III phloroglucinol
  • VII 4,4'-tetrahydroxydiphenyl sulfide
  • a latex is a stable dispersion of elastomer microparticles (s) suspended in an aqueous solution.
  • the unsaturated elastomer latexes that is to say bearing carbon-carbon double bonds, in particular diene elastomer, are well known to those skilled in the art.
  • the adhesive composition comprises an unsaturated elastomer latex.
  • the unsaturated elastomer of the latex is preferably a diene elastomer, more preferably a diene elastomer chosen from the group consisting of polybutadienes, butadiene copolymers, polyisoprenes, isoprene copolymers and mixtures of these elastomers. It is even more preferably selected from the group consisting of butadiene copolymers, vinylpyridine-styrene-butadiene terpolymers, natural rubber, and mixtures of these elastomers.
  • the adhesive composition and / or its phenol-aldehyde resin and / or its starting unsaturated elastomer latex may, of course, comprise all or part of the usual additives for adhesive compositions such as those used in conventional RFL glues; examples are bases such as ammonia, sodium hydroxide, potassium hydroxide or ammonium hydroxide, dyes, fillers such as carbon black or silica, antioxidants or other stabilizers.
  • the resin itself is prepared by gradually mixing the polyphenol and the aromatic aldehyde in a basic solvent such as a sodium hydroxide solution, preferably having a pH of between 9 and 13. more preferably between 10 and 12.
  • All the constituents are mixed with stirring for a variable time depending on the temperature used and the specific composition targeted, for example for a period which may vary between 1 min and 6 h, at a temperature between 15 ° C and 90 ° C, preferably between 20 ° C and 60 ° C.
  • the phenol-aldehyde resin thus precondensed is generally diluted in water to obtain an aqueous adhesive composition. Then, a latex or latices (if more) of unsaturated elastomer (s) are added to form the aqueous adhesive composition, according to a general procedure which is well known to those skilled in the art. field of RFL glues.
  • the constituents of the adhesive composition are added in the following order: water, any additives soaked in water (eg ammonia), latex (s) (in any order), phenol-aldehyde resin (diluted).
  • water any additives soaked in water (eg ammonia), latex (s) (in any order), phenol-aldehyde resin (diluted).
  • the mixture is mixed with stirring for 1 to 30 minutes, for example at 23 ° C.
  • the adhesive composition is generally stored at room temperature (23 ° C.) for a maturation time that can typically vary from 1 to several hours or even several days, before its final use.
  • the content of solids content of phenol-aldehyde resin preferably represents between 5 and 60%, more preferably between 10 and 30% by weight of the dry extract of adhesive composition.
  • the level of unsaturated elastomer (that is to say the solids content of the latex) is in turn preferably between 40 and 95%, more preferably between 70 and 90%, by weight of the extract. dry of the adhesive composition.
  • the weight ratio of polyphenol to aromatic aldehyde is preferably between 0.1 and 3, more preferably between 0.25 and 2.
  • the weight ratio of the resin solids content to the dry latex extract is preferably between 0.1 and 2.0, more preferably between 0.15 and 1.0.
  • the water content of the adhesive composition is preferably between 60 and 90%, more preferably between 60 and 85%.
  • the adhesive composition comprises a gelatin.
  • the gelatin slows down the dewetting of the wire reinforcing elements and thus to ensure better adhesion between the bronzed steel reinforcing element and the rubber matrix.
  • Gelatin means any mixture of proteins comprising products of the total or partial hydrolysis of collagen.
  • At least a portion of the steel core of the or each wire reinforcing element is coated with a layer of the copper-tin alloy coating, and then the layer of the copper alloy coating is coated.
  • the adhesive layer comprising the adhesive composition described above.
  • the step of coating by the layer of the copper-tin alloy coating can be carried out conventionally by several successive stages of immersion of the wire in lead, bronze, soda and acid baths, and then a step drying and finally a surface treatment step, for example using benzofuran.
  • the step of coating with the adhesive layer may be carried out by any suitable method, in particular by any known coating technique such as, for example, spraying, dip impregnation, scrolling in a bath or other equivalent thin-film deposition technique. or ultra-thin, or a combination of one or more of these techniques.
  • the weight of dry extract of the adhesive composition deposited on a kilogram of non-coated steel wire reinforcement element is preferably between 2 and 100 g, more preferably between 2 and 50 g, more preferably between 3 and 15 g. .
  • the coated bronzed steel reinforcing member undergoes a first heat treatment to remove any solvent or water, at a temperature of preferably between 110 ° C and 260 ° C, more preferably between 130 ° C and 250 ° C, for example by crossing a tunnel furnace, typically several meters long, such as those commonly used for heat treatment after gluing textile materials with RFL glue.
  • the anhydrous-coated tanned steel reinforcement element thus obtained undergoes a second heat treatment to complete the crosslinking of the adhesive composition, preferably led to air in a tunnel oven as described above.
  • the treatment temperature is preferably between 150 ° C and 350 ° C.
  • the treatment times are from a few seconds to a few minutes depending on the case (for example between 10 s and 10 min).
  • the thickness of the layer consisting of the adhesive composition coating the copper-tin alloy coating layer is in a range of values from 5 to 100 ⁇ , preferably from 5 to 50 ⁇ and more preferably from 10 to 35 ⁇ . ⁇ .
  • each wire reinforcement element may undergo processing steps, for example descaling, drawing in a humid medium or in a dry medium. or heat treatment. Examples of these processing steps are described in particular in documents US20100170624, US5535612 or JP2000219938. III - COMPOSITE
  • the present invention also relates to the use, for the adhesion of the tanned steel reinforcing element to a rubber matrix, of the adhesive composition described above, for forming a reinforced rubber composite of such an element which constitutes another object of the invention.
  • This rubber composite may be prepared according to a method comprising at least the following steps: in a first step, combining at least a portion of the coated steel reinforcing element coated according to the invention with a rubber matrix ( or elastomeric, both terms are synonymous) to form a reinforced rubber composite of the coated tanned steel reinforcing member;
  • the invention therefore applies to any type of rubber composite capable of being obtained by the method described above, comprising at least one rubber matrix, in particular of diene elastomer, bonded to the reinforcing element made of bronzed steel via an adhesive interphase based on the adhesive composition described above.
  • the diene elastomer of the composite is preferably chosen from the group consisting of polybutadienes (BR), natural rubber (NR), synthetic polyisoprenes (IR), butadiene-styrene copolymers (SBR) and isoprene copolymers.
  • BR polybutadienes
  • NR natural rubber
  • IR synthetic polyisoprenes
  • SBR butadiene-styrene copolymers
  • BIR butadiene
  • SBIR butadiene-styrene-isoprene copolymers
  • a preferred embodiment consists in using an "isoprene" elastomer, that is to say a homopolymer or a copolymer of isoprene, in other words a diene elastomer chosen from the group consisting of natural rubber (NR). , the synthetic polyisoprenes (IR), the various isoprene copolymers and the mixtures of these elastomers.
  • the isoprene elastomer is preferably natural rubber or synthetic polyisoprene of the cis-1,4 type.
  • the coated bronzed steel reinforcing element and the composite described above are advantageously used for reinforcing tires of all types of vehicles, in particular passenger vehicles or industrial vehicles such as heavy vehicles.
  • the single appended figure shows very schematically (without respecting a specific scale), a radial section of a tire according to the invention for a vehicle of the heavy vehicle type.
  • This tire 1 has a crown 2 reinforced by a crown reinforcement or belt 6, two sidewalls 3 and two beads 4, each of these beads 4 being reinforced with a rod 5.
  • the crown 2 is surmounted by a tread not shown in this schematic figure.
  • a carcass reinforcement 7 is wound around the two rods 5 in each bead 4, the upturn 8 of this armature 7 being for example disposed towards the outside of the tire 1 which is shown here mounted on its rim 9.
  • the carcass reinforcement 7 is in known manner constituted of at least one sheet reinforced by so-called "radial" cables, for example metallic, that is to say that these cables are arranged substantially parallel to each other and extend from a bead to the other so as to form an angle of between 80 ° and 90 ° with the median circumferential plane (plane perpendicular to the axis of rotation of the tire which is located midway between the two beads 4 and passes through the middle of the crown frame 6).
  • This tire 1 of the invention has for example the characteristic that at least one crown reinforcement 6 and / or its carcass reinforcement 7 comprises a coated bronzed steel reinforcing element or a composite according to the invention.
  • it is for example the rods 5 which could consist, in whole or in part, of a tanned steel reinforcing element coated according to the invention.
  • the invention relates to the objects previously described, namely the coated bronzed steel reinforcing element and the rubber composite such as pneumatic comprising it, both in the green state (before firing or vulcanization) and in the cooked state (after cooking).
  • the adhesive composition makes it possible for the tanned steel reinforcement elements to adhere to any rubber matrix, in particular non-acrylic rubber matrices, without using a halogenated polymer or a metal oxide (unlike EP2006341).
  • Each adhesive composition C-1.1 to C-1.7 is based on an aromatic aldehyde whose nucleus carries two aldehyde functions.
  • the aldehydes of compositions C-1.1 to C-1.6 are selected from the group consisting of 1,2-benzene-dicarboxaldehyde, 1,3-benzenedicarboxaldehyde, 1,4-benzenedicarboxaldehyde, 2-hydroxybenzene, and 1,3,5-tricarbaldehyde and mixtures thereof.
  • the aldehyde is selected from the group consisting of 1,2-benzene-dicarboxaldehyde, 1,3-benzene-dicarboxaldehyde and 1,4-benzene-dicarboxaldehyde.
  • the aldehyde of the composition C-1.7 is selected from the group consisting of furfuraldehyde, 2,5-furanedicarboxaldehyde and mixtures of these compounds.
  • the aldehyde is 2,5-furanedicarboxaldehyde.
  • compositions C-1.1 to C-1.7 comprise one or more aromatic ring (s), it being understood that:
  • adhesive compositions C-1.1 to C-1.7 are also based on natural rubber latex (NR), styrene-butadiene copolymer latex (SBR) and vynilpyridine-styrene-butadiene latex (VP-SBR).
  • NR natural rubber latex
  • SBR styrene-butadiene copolymer latex
  • VP-SBR vynilpyridine-styrene-butadiene latex
  • each composition C-1.1 to C-1.7 comprises a gelatin.
  • each wired reinforcement element tested has no intermediate layer of non-metallic adhesion.
  • the steel of the core is a standard steel comprising less than 0.5% by weight of chromium and less than 2% by weight of nickel.
  • the rubber composition of the rubber matrix is a conventional composition useful for calendering tire metal plies, based on natural rubber, carbon black and conventional additives.
  • the rubber composition comprises 100 phr of natural rubber, 70 phr of 300 series carbon black, 1.5 phr of N, 3-dimethylbutyl-N-phenyl-para-phenylenediamine, 1 phr of a salt. of cobalt, 0.9 phr of stearic acid, 6 phr of insoluble molecular sulfur, 0.8 phr of N-tertiarybutyl-2-benzothiazole sulfonamide and 7.5 phr of ZnO.
  • the copper-tin alloy coating layer of the wire reinforcing element was coated directly with each adhesive composition tested, and the coated steel reinforcing elements thus coated were dried in a drying oven at 180 ° C. 30 sec.
  • the adhesive composition was then cured by passing the coated tanned steel reinforcing elements in a treatment oven at 240 ° C for 30 seconds. Then the assembly was fused to a rubber matrix by vulcanization heat treatment to form composite specimens as described below.
  • the vulcanized rubber matrix is a rubber block consisting of two plates of dimensions 200 mm by 12.5 mm and 7 mm thick, applied one on the other before firing (the thickness of the resulting block is then 14 mm). It is during the manufacture of this block that the coated tanned steel reinforcement elements (15 sections in total) are trapped between the two rubber plates in the raw state, at equal distance and allowing them to pass from one side to the other. Another of these plates is an end of the coated tanned steel reinforcing element of sufficient length for subsequent traction. The block comprising the tanned coated steel reinforcement elements is then placed in a suitable mold and then baked under pressure.
  • the temperature and the cooking time are adapted to the targeted test conditions and left to the initiative of those skilled in the art; for example, in the present case, the firing of the block is carried out at 160 ° C for 20 min.
  • the test piece thus formed of the vulcanized block and the sections of coated bronzed steel reinforcing elements is placed in the jaws of a traction machine adapted to allow each section to be tested in isolation. at a given speed and temperature (for example, in the present case at 100 mm / min and 23 ° C).
  • the adhesion levels are characterized by measuring the pulling force (denoted F max ) to tear off the bronzed steel reinforcement elements coated with the test piece.
  • F max pulling force
  • the results of the tests carried out on the specimens are summarized in Table 1.
  • the reinforcing elements made of tanned steel coated with the adhesive compositions Cl. 1 to C-1.7 exhibit a particularly high and unexpected pull-up force F max for those skilled in the art, since it is greatly increased compared to a conventional RFL adhesive of the composition C-1 -0, and this without using any a matrix of specific rubber, halogenated polymer and metal oxide.
  • the adhesive composition may be free of formaldehyde, the use of which it is desirable to reduce or even eventually eliminate in the adhesive compositions, due to the recent evolution of European regulations on this type of compound.
  • formaldehyde is a compound derived from petroleum which we want as possible to get rid of for reasons of rarefaction.
  • the adhesive composition can be used and performed on reinforcing elements made of bronzed steel, which makes it possible to guarantee that the adhesion between the metal reinforcing elements and the rubber matrices is perennial, unlike reinforcing elements of brass steel.
  • the copper-tin alloy does not include zinc participating in the adhesion which could undergo a dezinsification over time.
  • the invention is not limited to the embodiments described above. It may also be envisaged to coat several wire reinforcing elements each comprising a steel core.
  • the wire reinforcing elements are assembled together and the copper-tin alloy coating layers coating the steel cores of the wire reinforcing elements by the adhesive composition are collectively coated.
  • the coating layer is coated individually. of copper-tin alloy coating the steel core of each wire reinforcement member with the adhesive composition and then assembling the wire reinforcing elements together.
  • coated bronzed steel reinforcing elements comprising a non-metallic adhesion interlayer directly coating the copper-tin alloy coating layers of the filamentary reinforcing elements, the layer of the adhesive coating then directly this intermediate layer of non-metallic adhesion.
  • Phloroglucinol from Alfa Aesar, 99% pure
  • Latex NR Trang Latex
  • Latex SBR (Encord-201" from Jubilant, diluted to 41% by weight)

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Ropes Or Cables (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
EP15704499.1A 2014-02-06 2015-02-05 Durch eine klebstoffzusammensetzung mit aromatischem aldehyd und polyphenol haftbar gemachtes verstärkungselement aus bronziertem metall Withdrawn EP3102646A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR1450903A FR3017071B1 (fr) 2014-02-06 2014-02-06 Element de renfort metallique bronze adherise par une composition adhesive a base d'aldehyde aromatique et de polyphenol
PCT/EP2015/052363 WO2015118044A1 (fr) 2014-02-06 2015-02-05 Elément de renfort métallique bronzé adhérisé par une composition adhésive à base d'aldéhyde aromatique et de polyphénol

Publications (1)

Publication Number Publication Date
EP3102646A1 true EP3102646A1 (de) 2016-12-14

Family

ID=50624772

Family Applications (1)

Application Number Title Priority Date Filing Date
EP15704499.1A Withdrawn EP3102646A1 (de) 2014-02-06 2015-02-05 Durch eine klebstoffzusammensetzung mit aromatischem aldehyd und polyphenol haftbar gemachtes verstärkungselement aus bronziertem metall

Country Status (6)

Country Link
US (1) US20170166011A1 (de)
EP (1) EP3102646A1 (de)
JP (1) JP2017506706A (de)
CN (1) CN105940074A (de)
FR (1) FR3017071B1 (de)
WO (1) WO2015118044A1 (de)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3017133B1 (fr) 2014-02-06 2016-03-11 Michelin & Cie Composite de caoutchouc renforce d'au moins un element de renfort en acier adherise par une composition adhesive a base d'aldehyde aromatique et de polyphenol
FR3049611A1 (fr) 2016-04-01 2017-10-06 Michelin & Cie Composition adhesive aqueuse comportant une resine thermodurcissable
FR3051474B1 (fr) * 2016-05-20 2018-05-18 Compagnie Generale Des Etablissements Michelin Composite et courroie de transmission de puissance
FR3051473A1 (fr) * 2016-05-20 2017-11-24 Michelin & Cie Composite et courroie de transmission de puissance
FR3054226A1 (fr) 2016-07-21 2018-01-26 Compagnie Generale Des Etablissements Michelin Composition de caoutchouc a haute rigidite
FR3054233A1 (fr) 2016-07-21 2018-01-26 Compagnie Generale Des Etablissements Michelin Composition de caoutchouc a haute rigidite
FR3071853A1 (fr) 2017-09-29 2019-04-05 Compagnie Generale Des Etablissements Michelin Procede d'electrodeposition d'une composition adhesive comportant un sel de phosphate et une resine thermodurcissable sur un element conducteur
FR3071839A1 (fr) 2017-09-29 2019-04-05 Compagnie Generale Des Etablissements Michelin Composite et courroie de transmission de puissance
JP2020535268A (ja) 2017-09-29 2020-12-03 コンパニー ゼネラール デ エタブリッスマン ミシュラン リン酸塩および熱硬化性樹脂を含む接着剤組成物
US20210321700A1 (en) * 2020-04-15 2021-10-21 Chris TREVINO Protective Glove

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2343551A (en) * 1938-07-02 1944-03-07 Us Rubber Co Adhesive composition
US3411980A (en) * 1965-03-26 1968-11-19 Goodyear Tire & Rubber In-situ resin adhesion of reinforcing element-to-rubber
JPS56244B2 (de) * 1973-02-02 1981-01-07
FR2711149A1 (fr) * 1993-10-15 1995-04-21 Michelin & Cie Fil en acier inoxydable pour carcasse d'enveloppe de pneumatique.
US5535612A (en) 1994-10-21 1996-07-16 The Goodyear Tire & Rubber Company Method and apparatus for drawing wire through a plurality of standard dies at the die positions
JP2000219938A (ja) 1999-01-28 2000-08-08 Nippon Steel Corp 高張力鋼線用線材およびその製造方法
AU2005325821A1 (en) * 2005-01-25 2006-08-03 Pirelli Tyre S.P.A. Pneumatic tyre with improved bead structure
JP4929807B2 (ja) 2006-04-13 2012-05-09 Nok株式会社 加硫接着剤組成物
FR2913355B1 (fr) 2007-03-08 2009-08-21 Michelin Soc Tech Procece de trefilage humide de fils d'acier destines au renforcement de bandages pneumatiques
BRPI0721685B1 (pt) * 2007-06-05 2019-05-28 Nv Bekaert Sa Pneu
US8247490B1 (en) * 2011-02-17 2012-08-21 Milliken & Company Adhesion composition and textile materials and articles treated therewith
EP2675839B1 (de) * 2011-02-17 2019-08-14 Milliken & Company Klebstoffzusammensetzung und textilmaterialien und damit behandelte gegenstände
FR2978771B1 (fr) * 2011-08-04 2013-09-27 Michelin Soc Tech Composition adhesive aqueuse a base de polyaldehyde et 2,2', 4,4'-tetrahydroxydiphenyl sulfide
FR2978770B1 (fr) * 2011-08-04 2013-09-27 Michelin Soc Tech Composition adhesive aqueuse a base de polyaldehyde et phloroglucinol
FR2978769B1 (fr) * 2011-08-04 2013-09-27 Michelin Soc Tech Composition adhesive aqueuse a base de polyaldehyde et de polyphenol
FR3017133B1 (fr) * 2014-02-06 2016-03-11 Michelin & Cie Composite de caoutchouc renforce d'au moins un element de renfort en acier adherise par une composition adhesive a base d'aldehyde aromatique et de polyphenol
FR3017070B1 (fr) * 2014-02-06 2017-08-25 Michelin & Cie Element de renfort en acier revetu par une composition adhesive a base d'aldehyde aromatique et de polyphenol

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
None *
See also references of WO2015118044A1 *

Also Published As

Publication number Publication date
FR3017071A1 (fr) 2015-08-07
FR3017071B1 (fr) 2016-01-29
WO2015118044A1 (fr) 2015-08-13
US20170166011A1 (en) 2017-06-15
JP2017506706A (ja) 2017-03-09
CN105940074A (zh) 2016-09-14

Similar Documents

Publication Publication Date Title
EP3102407B1 (de) Stahlbewehrungselement mit einer beschichtung aus einer klebstoffzusammensetzung mit aromatischem aldehyd und polyphenol
EP3102645B1 (de) Stahlbewehrungselement mit einer beschichtung aus einer klebstoffzusammensetzung mit aromatischem aldehyd und polyphenol
EP3102406B1 (de) Mit einer haftstoffzusammensetzung mit aromatischem aldehyd und polyphenol haftend gemachte kautschukzusammensetzung mit mindestens einem stahlverstärkungselement
WO2015118044A1 (fr) Elément de renfort métallique bronzé adhérisé par une composition adhésive à base d'aldéhyde aromatique et de polyphénol
EP3022241B1 (de) Wässrige klebstoffzusammensetzung mit einer basis aus aldehyd und polyphenol biologischen ursprungs
EP2739691B1 (de) Wässrige klebstoffzusammensetzung auf basis von polyaldehyd und 2,2 ', 4,4'-tetrahydroxydiphenylsulfid
EP2739693B1 (de) Wässrige klebstoffzusammensetzung auf der basis von polyaldehyd und polyphenol
EP2739692B1 (de) Wässrige klebstoffzusammensetzung auf der basis von polyaldehyd und phloroglucinol
EP3458503B1 (de) Komposit für kraftübertragung und kraftübertragungsriemen
WO2017168107A1 (fr) Composition adhesive aqueuse comportant une resine thermodurcissable et un latex
WO2014111440A2 (fr) Composition adhesive aqueuse a base de polyaldehyde et de polyphenol
EP2914444B1 (de) Mit einer styrol-butadien enthaltenden zusammensetzung in-situ gummiertes metallseil
EP3688104B1 (de) Elektrotauchlackierungsverfahren von einer wässrigenklebstoffzusammensetzung enthaltend ein phosphatsalz und ein wärmehärtbares harz auf einem leitfähigen element
EP3458504B1 (de) Komposit für kraftübertragung und kraftübertragungsriemen
FR3022265A1 (fr) Produit semi-fini comprenant un cable gomme in situ noye dans une composition de caoutchouc de calandrage

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20160906

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20170531

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: COMPAGNIE GENERALE DES ETABLISSEMENTS MICHELIN

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: COMPAGNIE GENERALE DES ETABLISSEMENTS MICHELIN

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20180712

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: COMPAGNIE GENERALE DES ETABLISSEMENTS MICHELIN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20181123