EP3784719A1 - Haftverbessernde zusammensetzung für textilmaterial und zugehöriges verstärkendes textilmaterial - Google Patents

Haftverbessernde zusammensetzung für textilmaterial und zugehöriges verstärkendes textilmaterial

Info

Publication number
EP3784719A1
EP3784719A1 EP19720124.7A EP19720124A EP3784719A1 EP 3784719 A1 EP3784719 A1 EP 3784719A1 EP 19720124 A EP19720124 A EP 19720124A EP 3784719 A1 EP3784719 A1 EP 3784719A1
Authority
EP
European Patent Office
Prior art keywords
latex
composition
methoxybenzaldehyde
aldehyde
rubber
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.)
Pending
Application number
EP19720124.7A
Other languages
English (en)
French (fr)
Inventor
Maëlle GOBIN
Léo POUPART
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.)
Porcher Industries SA
Original Assignee
Porcher Industries SA
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 Porcher Industries SA filed Critical Porcher Industries SA
Publication of EP3784719A1 publication Critical patent/EP3784719A1/de
Pending legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J197/00—Adhesives based on lignin-containing materials
    • C09J197/005—Lignin
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J197/00—Adhesives based on lignin-containing materials
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J109/00—Adhesives based on homopolymers or copolymers of conjugated diene hydrocarbons
    • C09J109/06—Copolymers with styrene
    • C09J109/08—Latex
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
    • C08H6/00—Macromolecular compounds derived from lignin, e.g. tannins, humic acids
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02—Non-macromolecular additives
    • C09J11/06—Non-macromolecular additives organic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/08—Macromolecular additives
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J111/00—Adhesives based on homopolymers or copolymers of chloroprene
    • C09J111/02—Latex
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J121/00—Adhesives based on unspecified rubbers
    • C09J121/02—Latex
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/358—Applications of adhesives in processes or use of adhesives in the form of films or foils for garments and textiles
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2400/00—Presence of inorganic and organic materials
    • C09J2400/20—Presence of organic materials
    • C09J2400/26—Presence of textile or fabric
    • C09J2400/266—Presence of textile or fabric in the pretreated surface to be joined
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2409/00—Presence of diene rubber
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2411/00—Presence of chloroprene
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2421/00—Presence of unspecified rubber
    • C09J2421/008—Presence of unspecified rubber in the pretreated surface to be joined
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2461/00—Presence of condensation polymers of aldehydes or ketones
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2497/00—Presence of lignin

Definitions

  • the present invention relates to an adhesive or adhesive composition for textile, in particular a composition for adhering a textile to a rubber.
  • the invention particularly relates to applications in the field of belts, pipes, tires, air springs (airspring) and, more generally, any part or article made of rubber, or comprising a part made of rubber, in which the rubber comprises a reinforcement.
  • the invention is therefore also related to textile reinforcements coated with this adhesive, and the parts or articles incorporating them both in surface and in depth.
  • the textile reinforcement must primarily ensure the dimensional stability of the belt. For this, it is requested reinforcement specific mechanical properties in various environments. To ensure the required properties, and in particular to avoid a risk of delamination, the reinforcement must adhere to the rubber of the belt.
  • the reinforcement may be in contact with a rubber or several different rubbers. To allow good compatibility with the rubber, the reinforcement is usually treated with an adhesive. More complex properties may also be required for reinforcement. For example the edge of the reinforcement being cut and exposed to the side of the belt, it should not fray, while being easy to cut. To ensure these other properties, other types of treatments can be made to the wire.
  • the chemical treatments are primarily aimed at adhering a given reinforcement to the different rubbers that it can meet.
  • the treatments are as varied as there are types of reinforcements [glass, aramid, polyamide (PA), polyethylene terephthalate (PET), etc.] and families of rubbers.
  • the core of the treatment for adhering a reinforcing textile to rubber is called resorcinol-formaldehyde-latex or RFL. It is a system mixing a latex (colloidal elastomer aqueous dispersion or of polymer) and thermosetting resins of the phenoplast or aminoplast type. This system is historical, it was largely developed in the 70s and remains the preferred treatment. Despite many attempts to replace, it has never been possible to offer a global solution to achieve its performance. It is completely optimized to obtain the maximum of static adhesion, that is to say out of dynamic stress.
  • the heat treatment has an impact on the chemical properties (adhesion) but also mechanical in the case of synthetic reinforcements. It impacts withdrawal characteristics, among others.
  • the treatment in the furnaces results from the consensus between the maintenance of the mechanical properties and the crosslinking of the adhesive.
  • the new treatment must therefore be able to adapt to the current treatment conditions, in order to guarantee the mechanical properties.
  • an adhesive allowing for a lower temperature treatment will potentially bring new and interesting properties in certain applications, and will have a favorable energy aspect.
  • any change in a formulation does not call into question the functionality of the different treatments, both chemical and thermal (or physical, more generally) usually used for this or that application.
  • RFL treatment has become the treatment of choice to allow adhesion between textile and rubber.
  • the phenomena involved in the adhesion are involved during the vulcanization of the rubber part, while the RFL treatment itself can be deposited on the textile several months before. This is why the term “adhesion” treatment is often used, the term “adhesion” being rather reserved for the adhesion state.
  • latex is a colloidal aqueous dispersions of elastomers or polymers, generally similar in nature to the rubber to be bonded. On the other hand, these latices do not have real mechanical properties in themselves.
  • a thermosetting (thermosetting) resin is added to maintain the system.
  • RF resin based on resorcinol and formaldehyde. Via its polarity, it allows a good adhesion to the textile. It forms a mesh in which the latex is trapped, which stiffens the system. This mesh remains sufficiently flexible to allow the diffusion of the elastomer chains in the matrix and then create good adhesion to the rubber (entanglement, molecular interactions and possibly co-curing during vulcanization).
  • the RFL contains formalin and resorcinol, which are now suspected carcinogens. It would be interesting to find an alternative to formalin and resorcinol or RFL as a whole.
  • the complex properties of the RFL both in terms of its implementation and in the end-use properties of the end products incorporating it, which have been recalled above, make the exercise of finding an alternative solution a real challenge. It would be even more interesting to find such a solution that is more than an alternative, but that allows an increase in performance. It is to meet these challenges that the inventors have set themselves.
  • the aim of the invention is therefore to provide novel bonding solutions which make it possible in particular to replace RFLs in their known applications, with performance levels close to or even higher, and this with acceptable components in the context of sustainable development and in favorable economic conditions.
  • Lignosulphonates are offered as a natural adhesive and as a short fiber binder for making mats (nonwovens) in combination with lignosulfonate hardeners, or as adhesives in wood-based multilayer products. They have never been proposed in compositions that are alternative to RFL and there is no indication that lignosulphonates may prove to be suitable for developing bonding formulas for bonding with rubbers, with sufficient mechanical performance.
  • the subject of the invention is therefore an adhesive or textile adhesive composition
  • an adhesive or textile adhesive composition comprising (or based on, consisting essentially of or consisting of) a lignosulfonate salt, an aldehyde hardener of this salt, and a polymer latex, in particular elastomer.
  • the adhesive composition may be a suitable bonding composition for adhering textiles to a rubber or like material.
  • the invention also relates to the use of an adhesive composition according to the invention, for imparting adhesion properties to a reinforcing textile, vis-à-vis a rubber or a similar material.
  • the invention also relates to a reinforcing textile, especially a yarn, cord or textile structure, at least partially coated and / or impregnated with an adhesive composition according to the invention.
  • the invention also relates to an article or piece made of rubber (or similar material) or comprising a rubber part (or similar material), in which the rubber comprises at least one reinforcement fabric according to the invention, at the surface and / or integrated inside the rubber or rubber matrix.
  • the invention therefore firstly relates to an adhesive or textile adhesive composition
  • an adhesive or textile adhesive composition comprising (or based on, consisting essentially of or consisting of) a lignosulfonate salt, an aldehyde hardener of this salt, and a latex of elastomer.
  • reaction product is meant of course the product of the reaction between the lignosulfonate and the aldehyde, which does not include any additives that could enter the final composition.
  • composition can in particular be obtained by a method, also object of the invention, according to which the three ingredients are mixed with stirring, and, preferably, the composition is cured.
  • the lignosulfonate salt can be solubilized in water before mixing the solution obtained with the latex and with the aldehyde.
  • This solubilization can be facilitated by working in a basic medium, by adding a sodium and / or ammonia type agent.
  • the lignosulphonate salt solution and the latex are first mixed, then only the aldehyde is then added.
  • the lignosulfonate salt in water with stirring and in the presence of the agent to be at basic pH is stirred until solubilization, preferably total, then added, with stirring, the latex, before incorporate, still stirring, the hardener (preferably it is previously dissolved or dispersed in water, eg with vigorous stirring).
  • the method makes it possible to obtain a composition that can be left to mature (for example several hours, for example from about 2 to about 48 hours, for example between about 15 and about 25 ° C.) allowing the reaction product to form.
  • the composition in particular after maturing, can be used as a ready-to-use or customizable adhesive composition.
  • an aqueous solution of lignosulfonate and aldehyde hardener can be mixed before stirring an aqueous latex dispersion.
  • the pH of the solution of lignosulfonate or lignosulfonate and hardener is adjusted to be basic, for example by addition of sodium hydroxide and / or ammonia, before incorporation of the latex.
  • the composition can then be left to mature under the same conditions as above.
  • the composition in particular after maturing, can be used as a ready-to-use or customizable adhesive composition.
  • the bonding composition comprises a reaction product between hardener and lignosulfonate.
  • This composition may especially be characterized by the absence or a reduced rate of hardener in the free state.
  • the ripening conditions are suitable for obtaining an adhesion composition that can be used in accordance with the invention. In particular, these conditions must not cause caking or excessive hardening of the composition which would render it unsuitable for its application on the media for which it is intended. It has been defined here a ripening of especially several hours, for example from about 2 to about 48 hours, for example at a temperature between about 15 and about 25 ° C. However, it may be possible to deviate from these conditions according to the ingredients used as the adhesive composition remains suitable for its use as described below, for example in terms of viscosity.
  • the latex is preferably a basic aqueous dispersion of the polymer (s) and / or elastomer (s). It is also possible to work according to the invention at neutral pH. The working pH values may in particular be those mentioned below with respect to the pH of the composition.
  • elastomer is meant, in particular, a polymer or copolymer chain whose glass transition temperature (T v ) is less than about 25 ° C. The elastomers are present in the rubber to be adhered and in the latex of the bonding composition.
  • An “elastomer latex” is an aqueous colloidal elastomer dispersion.
  • rubber or “elastomeric material” is meant here the vulcanized or crosslinked product prepared from elastomer or elastomeric gum, synthetic or natural, of one or more types, of filler ( s) reinforcing (s) (carbon blacks, silica, kaolins ...), plasticizer (s), vulcanizing agent (s) (sulfur, peroxide, metal oxides and necessary accelerators), possible other usual additives for the application in question (for example to facilitate the implementation, for protection against oxygen, ozone, heat, flame, UV).
  • the invention is as much concerned with synthetic rubbers as with natural rubber. Rubbers, formulated based on elastomers, are materials whose T v obtained is then lower than the working temperature of the part.
  • Lignosulphonates are by-products of wood processing, including the treatment of wood for the manufacture of paper pulp using the so-called "acid sulphite baking process". This process, which employs a bisulfite, makes it possible, depending on the nature of the counterion employed, to obtain the corresponding lignosulfonate salts. These lignosulfonates can also be from a die intended to produce them from wood.
  • the lignosulfonate salt may be a salt of sodium, potassium, magnesium, ammonium or calcium.
  • lignosulphonates prepared by the bisulphite process from maritime pine, for example from the Austin (France), are used.
  • the adhesion compositions do not include formaldehyde or formaldehyde.
  • the adhesion compositions do not include resorcinol.
  • the adhesion compositions do not include formaldehyde or formaldehyde or resorcinol.
  • the aldehyde hardener has at least 2 carbon atoms and carries at least one aldehyde group (-CHO).
  • the carbon atom of CHO is included in the number of carbons of the hardening compound.
  • the aldehydes may in particular be water-soluble or, if they are not, they may be dispersible in water, for example under adequate agitation.
  • the hardener may be a monoaldehyde (only 1 -CHO group), a dialdehyde (2 -CHO groups), a trialdehyde (3 -CHO groups), or a polyaldehyde in the form of a polymer carrying non-enolized aldehyde units.
  • Monoaldehyde compound containing an aldehyde group placed at the end of a hydrocarbon chain, such that the maximum length of the main carbon chain is less than or equal to 20 carbon atoms.
  • the structure of the chain can be either linear, branched or cyclic.
  • Fully saturated hydrocarbon chain having one or more branches only of hydrocarbon nature ⁇ More specifically, the maximum length of the main chain is C8, especially C3 to C8,
  • substituent groups may be methyl radicals, ethyl, propyl, butyl, pentyl, hexyl
  • the substituent groups of the linear chain may be saturated hydrocarbon rings, unsaturated, or aromatic, which may be themselves subles, specifically: cyclopentyl, cyclohexyl, cyclooctyl, cyclohexenyl, phenyl,
  • the maximum length of the main chain is C8, especially C3 to C8,
  • the substituent group may be methyl radicals, ethyl, propyl, butyl, pentyl, hexyl
  • the substituent groups of the linear chain may be saturated hydrocarbon rings, unsaturated, or aromatic, more specifically: cyclopentyl, cyclohexyl, cyclooctyl, cyclohexenyl, phenyl.
  • cinnamaldehyde More specifically selected from the following compounds: cinnamaldehyde, a-hexylcinnamaldehyde, ⁇ -amylcinnamaldehyde, phenylcinnamaldehyde,
  • the substituent groups of the linear chain may be aromatic rings having themselves a substituent on the aromatic ring.
  • a fully saturated hydrocarbon chain having one or more branches comprising a heteroatom having one or more branches comprising a heteroatom.
  • the maximum length of the main chain is C8, especially C3 to C8
  • hydrocarbon chain having one or more unsaturations and having one or more branches comprising a heteromate.
  • the maximum length of the main chain is C8, in particular C3 to C8,
  • Methoxycinnamaldehyde 3,5-Dimethoxy-4-hydroxycinnamaldehyde (Sinapinaldehyde), 4-Acetoxy-3-methoxycinnamaldehyde, 4-Hydroxy-3-methoxycinnamaldehyde
  • Cyclic aldehyde compounds compounds of the carbaldehyde family, that is to say compounds for which the aldehyde group is directly attached to a ring.
  • the ring is defined as being a monocycle comprising at most 8 carbon atoms, especially from 3 to 8 carbon atoms. More specifically, the cycle can be of nature:
  • the cycle can be in particular cyclopropane, cyclopentane, cyclohexane, cycloheptane, cyclooctane, and
  • cyclopentanal cyclopropanal, cyclohexanal, cycloheptanal, cyclooctanal • Or, with hydrocarbon and / or hetero atomic substituents on the ring
  • the substituents may be of a halogenated nature, more particularly chlorine, bromine, iodine and more specifically chosen from the following compounds: Chloro-4-chlorobenzaldehyde; 3-chlorobenzaldehyde; 2-chlorobenzaldehyde; 2,4-dichlorobenzaldehyde; 2,5-dichlorobenzaldehyde; 2,6-dichlorobenzaldehyde; 3,5-dichlorobenzaldehyde; 2,3,6-trichlorobenzaldehyde; 2-bromobenzaldehyde; 3-bromobenzaldehyde ; 4-bromobenzaldehyde; 3,4-dibromobenzaldehyde; 3,5-dibromobenzaldehyde; 2,5-dibromobenzaldehyde; 2-iodobenzaldehyde, 3-iodobenzaldehyde; 4-iodobenzaldeh
  • substituents may be of the alkyl (C1-C8), more particularly methyl, ethyl, propyl, butyl, phenyl,
  • 2-methylbenzaldehyde 3-methylbenzaldehyde
  • 4-methylbenzaldehyde isomers such as tolualdehyde
  • 2,4-dimethylbenzaldehyde isomers such as tolualdehyde
  • substituents may be ether in nature, more particularly methoxy, ethoxy, phenoxy and benzyloxy
  • Isomers of anisaldehyde 2-methoxybenzaldehyde; 3- methoxybenzaldehyde and 4-methoxybenzaldehyde; isomers of veratraldehyde: 2,3-dimethoxybenzaldehyde; 2,4-dimethoxybenzaldehyde; 2,5-dimethoxybenzaldehyde; 2,6-dimethoxybenzaldehyde; 3,4-dimethoxybenzaldehyde; 3,5-dimethoxybenzaldehyde; 2- ethoxybenzaldehyde; 3-ethoxybenzaldehyde
  • substituents may be hydroxyl in nature. o Still more specifically selected from the following compounds: 2-hydroxybenzaldehyde (salicylaldehyde); 3-hydroxybenzaldehyde;
  • aromatic ring has several substituents, these may be of a different nature, chosen from the families described above.
  • Dialdehyde compound containing 2 aldehyde groups such as:
  • the aldehyde groups are placed at the end of a hydrocarbon chain, such that the maximum length of the main carbon chain is less than or equal to 20 carbon atoms.
  • the chain may be substituted by linear, branched or cyclic C1-C8 alkyl, halogen, hydroxyl, ether or ester groups.
  • the carbon chain carrying the aldehyde group may be a ring. • More specifically: terephthaldehyde; o-Phthalaldehyde, m-Phthalaldehyde
  • the carbon chains can be linked together by heteroatoms (ether linkages), without the total number of carbon atoms of the structure formed being greater than 20 atoms.
  • Trialdehyde compound containing 3 aldehyde groups chosen from the compounds:
  • Polyaldehyde compounds formed of a polymer chain containing non-enolized aldehyde units such as
  • the aldehyde unit is present on the monomer (homopolymer) and is not engaged in the polymerization reaction
  • the aldehyde unit is present on at least one of the monomers (co-polymer) and is not engaged in the polymerization reaction
  • the aldehyde unit is obtained by post-polymerization reaction such that
  • the aldehydes having no hydrogen atom alpha to the CO are preferably chosen in that they are non-enolizable. It should be noted that these non-enolizable aldehydes can then carry out, under basic conditions, a Canizarro reaction and possibly lead to the presence of a carboxylic acid reaction intermediate.
  • Preferred examples of these non-enolizable aromatic aldehydes include:
  • hydroxybenzaldehyde (and isomers of position: 3-hydroxybenzaldehyde, 4-hydroxybenzaldehyde, salycylaldehyde); p-anisaldehyde (and isomer o-); p-tolualdehyde (and ortho isomer);
  • veratraldehyde for the poly-substituted: veratraldehyde, syringaldehyde, cuminaldehyde, vanillin, ethylvaniline, 2,4-dihydroxybenzaldehyde, 3,4-dihydroxybenzaldehyde; 3-hydroxy-4-methoxybenzaldehyde.
  • the aldehyde hardener may especially be an aldehyde selected from the group consisting of acetaldehyde; priopionaldéhyde; butyraldehyde; pentanal (valeraldehyde); hexanal; heptanal; octanal; nonanal; decanal; undecanal; dodecanal; tridecanal; tetradecanal (myristaldehyde); 2-butenal (crotonaldehyde); 3-butenal; 2-hexenal; 3- hexenal; 2-heptenal; 3-heptenal; 5-heptenal; 2-octenal; 2,4-pentadienal; 2,4-hexadienal; 2,4-heptadienal; 3,5-heptadienal; 2,4-octadienal; isobutyraldehyde; isovaleraldehyde; 2- methylbutyraldehyde
  • the hardener may especially be chosen from: benzaldehyde, 4-hydroxybenzaldehyde, 3-hydroxybenzaldehyde, 2-methylbutyraldehyde, salicylaldehyde, 7-hydroxy-3,7-dimethyloctanal, cyclohexanecarboxaldehyde, 3-chlorobenzaldehyde, 4-ethylbenzaldehyde, trans-2- hexenal, and mixtures thereof.
  • the latex may advantageously be a carboxylated acrylonitrile / butadiene copolymer latex (XNBR), a hydrogenated acrylonitrile / butadiene latex (HNBR), a chlorosulfonated polyethylene latex (CSM), a styrene-butadiene-vinylpyridine copolymer latex (VPSBR) , a styrene / butadiene copolymer latex (SBR), an acrylonitrile / butadiene copolymer latex (NBR), a polybutadiene latex (BR), a chlorobutadiene latex (CR), a natural rubber latex (NR), a latex polyurethane, or a mixture of at least two of them.
  • the solids content by weight of the composition may be in particular between about 2 and about 38%, in particular between about 4 and about 30%, more particularly between about 7 and about 25%.
  • composition according to the invention may in particular comprise from about 40 to about 95%, preferably from about 55 to about 90% or from about 40 to about 60, 70, 80 or 90% by weight of elastomer relative to to the composition.
  • composition is given in dry matter.
  • the hardener / salt weight ratio of lignosulfonate may be in particular between about 0.1 and about 3, more particularly between about 0.15 and about 2.5, typically between about 0.4 and about 1.6. Lower or higher values may be possible depending on the chosen lignosulfonate hardeners and salt pairs and this parameter is determinable by those skilled in the art on the basis of this description.
  • the mass ratio [hardener + lignosulfonate salt] The latex may be in particular between about 0.05 and about 0.6, more particularly between about 0.15 and about 0.5. Lower or higher values may be possible depending on the compounds chosen in combination and this parameter is determinable by those skilled in the art on the basis of this description.
  • the composition has a neutral or basic pH, in particular a pH of between about 7 and about 13, in particular between about 9 and about 13.
  • the composition may comprise for this purpose an additive that makes it possible to adjust the pH, for example soda.
  • the composition comprises water of the elastomer latex. Water may be added, in order to make the applicable composition sufficiently fluid for a conventional application, for example by impregnation.
  • the composition may also comprise additives at a content in particular between 0 or 0.1 and about 50% by dry weight.
  • the composition may especially comprise an adhesion promoter (for example epoxy, silane, blocked isocyanate), a surfactant, a dispersant, an antifoaming agent, a wax (for example microcrystalline hydrocarbon wax in emulsion), a filler (for example carbon black, silica), a dye, a metal oxide (eg ZnO), an elastomeric crosslinking agent, an anti-UV agent, an anti-ozone agent, a heat-protective agent.
  • adhesion promoter for example epoxy, silane, blocked isocyanate
  • a surfactant for example epoxy, silane, blocked isocyanate
  • a dispersant for example an antifoaming agent
  • a wax for example microcrystalline hydrocarbon wax in emulsion
  • a filler for example carbon black, silica
  • a dye for example carbon black, silica
  • the viscosity of the bonding composition measured at 23 ° C. using a Brookfield viscometer as detailed in the Examples section, may in particular be from about 1 to about 5, for example from about 1.5 to about 4.5, Cp or mPa.s. This viscosity can easily be adjusted by adjusting the water content, in particular.
  • composition according to the invention can be applied to any textile.
  • textile is intended to mean: monofilament continuous yarn, multifilament continuous yarn, staple fiber or yarn, any assembly of monofilament and / or multifilament continuous yarns or cut yarn, in particular a wick, a cord formed of such son by conventional twisting techniques and a "textile structure" formed of the assembly of yarns, twisted or cabled, especially in the form of fabric, grid, etc.
  • textile according to the invention does not cover nonwovens or short fiber mats.
  • the textiles of the invention, having been treated with the composition according to the invention are designated by the expression "reinforcing textiles".
  • the textile may be organic or inorganic in nature.
  • glass especially glass E or high modulus glass
  • basalt carbon
  • aramid metal or para
  • polyvinyl alcohols cellulose
  • HDPE high density polyethylenes
  • PET polyesters
  • PA polyamides
  • PA polyamides
  • PA polyamides
  • the subject of the invention is also a process for applying, or the use of, an adhesion composition according to the invention for imparting adhesion properties to such a textile, in particular with respect to an elastomeric material.
  • This use can be declined in terms of a method of adhesion of a textile according to the invention.
  • This use or this method comprises applying said composition to the textile (yarn, cord, textile structure), then drying it.
  • This application can be carried out by the methods used in industry, for coating, in particular by impregnation, as described infra.
  • the choice of the latex, therefore of the constituent elastomer is advantageously towards a similar formula to the nature of the constituent elastomer of the rubber to be treated, as is customary.
  • the invention also relates to a reinforcing textile coated and / or impregnated with an adhesive composition according to the invention. It also relates to the textile treatment process for producing the reinforcing textile, by application of the adhesive composition on said textile.
  • the invention particularly relates to a yarn coated and / or impregnated with a composition of adhesion according to the invention.
  • the yarn may be twisted before or after application of the composition, and solidification thereof.
  • the yarn can be impregnated to heart, if necessary by dishing the yarn (spacing of the filaments by means known to those skilled in the art) before coating it with the composition.
  • This yarn may in particular comprise or be coated with the hardened adhesion composition (dried and / or crosslinked).
  • the invention also relates to a cord coated and / or impregnated with a composition of adhesion according to the invention.
  • This cord may in particular comprise, or be coated with, the hardened adhesion composition (dried and / or crosslinked).
  • the cord may be formed of at least two non-coated yarns of the adhesive composition, typically each yarn is twisted, then the yarns are cabled (assembled together and twisted in the opposite direction to the twist of the elementary yarns), and then the cord is coated of the adhesive composition, which is cured after application.
  • the cord may also be formed of the assembly of at least two yarns coated with the adhesive composition, generally each yarn is twisted after solidification of the composition, and then the yarns are cabled (assembled together and twisted in the opposite direction of the twist elementary sons); it can then be provided a coating of the cord with other treatments ("overcoat” or “topcoat”), and drying.
  • the invention also relates to a textile structure formed by the son assembly by known techniques such as weaving or by gluing or welding in the case of grids. These textile structures are coated or impregnated with the composition of the invention, and the invention covers these textile structures coated with the cured adhesive composition.
  • adhesion compositions can be applied to textiles within the meaning of the invention by the methods used for RFL. First of all impregnation, dipping or dipping.
  • the subject of the invention is also an article or piece made of rubber (or comprising a rubber part), comprising at least one reinforcing textile, especially a thread, cabled and / or textile structure, according to the invention.
  • This reinforcing fabric may especially be applied to the surface of the article or piece and / or integrated inside the article or piece.
  • rubber is a vulcanizable formulation based on natural or synthetic elastomers, such as vulcanized (crosslinked) natural rubber (NR or polyisoprene), or vulcanized (crosslinked) synthetic rubber.
  • elastomers such as vulcanized (crosslinked) natural rubber (NR or polyisoprene), or vulcanized (crosslinked) synthetic rubber.
  • a rubber may also be a vulcanizable formulation based on blends or blends of such elastomeric gums.
  • the rubber may also be a formulation based on elastomeric thermoplastics (so-called “physically crosslinked” elastomers such as, for example, SBS, styrene-butadiene-styrene block).
  • elastomeric thermoplastics so-called "physically crosslinked" elastomers such as, for example, SBS, styrene-butadiene-styrene block).
  • the subject of the invention is in particular an article or piece of elastomer or rubber comprising, embedded in its mass of elastomer or rubber, an adhesive reinforcing textile according to the invention, for example one or more son, individual or cabled or assembled in textile structures, or more than one of these categories.
  • bonded is meant in particular that the reinforcing textile comprises or is coated with the cured adhesive composition (dried and / or crosslinked).
  • the invention also relates to an article or piece of elastomer or rubber comprising, bonded to at least one surface of this elastomeric material or rubber, an adhered textile structure according to the invention.
  • the invention further relates to an article or piece of elastomer or rubber comprising, embedded in its elastomer or rubber mass, one or more son, individual or cabled or assembled in textile structures, or more of these categories, and comprising in in addition, bonded to at least one surface of this elastomeric material or rubber, a textile structure according to the invention, these reinforcing fabrics being adhered according to the invention.
  • articles one can cite, without being exhaustive, the following articles, which can incorporate at least one bonded reinforcing textile according to the invention, in particular wire, cabled or textile structure treated by the adhesive composition of the invention, applied on the surface of the article to which it adheres and / or integrated within the elastomeric material of the article:
  • the belts may comprise yarns or cords embedded in the mass of elastomer or rubber. They may also comprise, instead of or in addition to the yarns and cords, a textile structure, in particular a fabric, adhering on the surface, for example on the back in the transmission belt, and on the back and notch for the belt. distribution
  • hoses Flexible or rigid hoses, especially brake hoses (comprising a braided textile structure, single or double braid), hoses, industrial hoses (comprising a gimped or spiral textile structure, that is to say fabricated by wrapping or spiraling) , including pipes for oil and gas, hoses (knitted textile structure).
  • brake hoses comprising a braided textile structure, single or double braid
  • industrial hoses comprising a gimped or spiral textile structure, that is to say fabricated by wrapping or spiraling
  • the braiding, spiraling, knitting is generally performed during the implementation of the pipe by extrusion.
  • transmission belt based on EPDM or CR
  • synchronous belts based on HNBR and CR
  • Pipes based on SBR, or EPDM, or NBR / PVC blend, or epichlorydrin, or butyl
  • Airspring CR-based
  • kinetic discs based on CR or NR
  • Tires thick part comprising several mixtures, based on NR, BR or SBR
  • the invention has the advantage of integrating into the recovery of non-food renewable raw material. It allows the valorization of lignin, currently a waste of the wood and paper industry. This compound is perfectly harmless, low cost, high performance. Its use does not compete with the food market, it is not subject to regulation on chemicals. It is an agro-resource. Examples:
  • the dry extract (or mass concentration) of the preparations is defined as the percentage of residual dry matter after evaporation of the volatile materials (water, solvent) according to a defined drying mode.
  • the sample is placed in a pre-weighed aluminum cup containing a fiberglass filter without binder, with a surface density of 52 g / cm 2 and a threshold of 1.6 ⁇ m.
  • the assembly is then subjected to a temperature of 120 ° C until total stabilization of the mass. The result is expressed in%.
  • the viscosity of the preparation is measured at 23 ° C. using a Brookfield viscometer. Unless otherwise stated, the measurement is carried out using an Ultra Low Viscosity Adaptator (ULA) module and a No. 1 mobile (low viscosity system) at a speed of 60 rpm (revolutions per minute).
  • ULA Ultra Low Viscosity Adaptator
  • the pH of the aqueous preparations is measured using a METLER 340 pH meter, calibrated for measurements in basic medium using buffer solutions. A glass electrode and a KOI 3M electrolyte are used.
  • the water used for the preparation of the preparations is water of osmotic quality, of residual conductivity lower than 70pS / cm.
  • Example 1-1 Preparation of an adhesive based on benzaldehyde, 4-hydroxybenzaldehyde or 3-hydroxybenzaldehyde
  • 82 g of sodium lignosulphonate (Arbo N18, Tembec) are dissolved with stirring in 1184 g of water.
  • 2.5 g of a 10% by weight sodium hydroxide solution are then added to the solution, which is kept stirring for 10 minutes to allow complete solubilization.
  • This solution is added with stirring to 983 g of a styrene-butadiene-vinylpyridine copolymer latex (VPSBR). The whole is kept stirred (150 rpm) during the hardener preparation phase.
  • VPSBR styrene-butadiene-vinylpyridine copolymer latex
  • compositions containing benzaldehyde 3 compositions containing 4-hydroxybenzaldehyde and 3 compositions containing 3-hydroxybenzaldehyde, by varying the following parameters:
  • hardener / lignosulfonate salt mass ratio from 24% to 54.8%
  • % by weight of dry latex in the composition from 80 to 84.5%.
  • Example 1-2 Preparation of an adhesive based on benzaldehyde or 4-
  • a second embodiment of the invention 55 g of sodium lignosulphonate are introduced into a vessel and 844 g of water are gradually added. The solution is stirred at 200 rpm. 23 g of a 10% by weight sodium hydroxide solution and 1 15 g of 20% by weight ammonia are then successively added with stirring to the preparation. The mixture is stirred at 200 rpm for 10 minutes.
  • the basic solution of sodium lignosulfonate is added with stirring to a latex preparation of a styrene-butadiene copolymer (wet latex SBR; 942 g) and water (179 g) previously homogenized.
  • a latex preparation of a styrene-butadiene copolymer (wet latex SBR; 942 g) and water (179 g) previously homogenized.
  • the preparation has a pH of 10.5, a solids content of 19.7% and a viscosity of 4.4 mPa.s.
  • Mass ratio hardener / lignosulfonate salt from 88% to 102%.
  • % by weight of dry latex in the composition from 78% to 82%.
  • Example 1-3 Another method for preparing a benzaldehyde, 4-hydroxybenzaldehyde or 3-hydroxybenzaldehyde adhesive, in the presence of several bases
  • a basic solution of sodium lignosulfonate is prepared by dissolving 30 g of sodium lignosulfonate with stirring in 968 g of water and adding 30 g of a 10% by weight sodium hydroxide solution. The preparation is stirred at 200 rpm for 10 minutes to allow complete solubilization.
  • a basic latex dispersion is prepared by introducing 167 g of water into a vessel, which is then stirred at 200 rpm. 1050 g of a styrene-butadiene copolymer latex (SBR), then 26 g of a solution of ammonia at 20% by mass are then introduced successively. The basic lignosulfonate solution is then added with stirring to the latex dispersion.
  • SBR styrene-butadiene copolymer latex
  • the preparation has a pH of 9.8, a solids content of 19.8% and a viscosity of 3.5 mPa.s.
  • Mass ratio hardener / lignosulfonate salt from 105% to 241%
  • % by weight of dry latex in the composition from 68% to 86%.
  • Example 1-4 Method of Preparation of a Diluted and Additive-Based Adhesive Based on Benzaldehyde
  • a basic sodium lignosulfonate solution is prepared by stirring dissolution of 33 g of sodium lignosulfonate in 1059 g of water and addition of 32 g of a 10% by weight sodium hydroxide solution. The preparation is stirred at 200 rpm for 10 minutes to allow complete solubilization.
  • a basic latex dispersion is prepared by introducing 155 g of water into a vessel, which is then stirred at 200 rpm. 1050g of copolymer latex styrene-butadiene (SBR), then 26 g of a solution of ammonia at 20% by weight are then introduced successively. The basic lignosulfonate solution is then added with stirring to the latex dispersion.
  • SBR copolymer latex styrene-butadiene
  • the preparation has a pH of 1.15, a solids content of 6.9% and a viscosity of 1.6 mPas.
  • Example 1-5 "One-Pot" Preparation Method of an Adhesive Based on Potassium Lipnosulfonate and Different Hardeners
  • the preparation has a pH of 10.8, a solids content of 20.2% and a viscosity of 2.2 mPa.s.
  • Ratio hardener / lignosulfonate salt from 13% to 64%
  • % by weight of dry latex in the composition from 64% to 79%.
  • compositions were made. 1-6: "one-pot" preparation method of a highly additive adhesive and with different hardeners.
  • the preparation has a pH of 1.1, a solids content of 14.1% and a viscosity of 2.2 mPa.s.
  • Ratio hardener / lignosulfonate salt from 13% to 64%
  • % by weight of dry latex in the composition from 48% to 59%
  • the definitions and methods of measurement or control described in this part apply generally to the application unless otherwise indicated.
  • the mechanical characteristics of treated textiles such as tensile tensile strength (tensile strengh), elongation at break ("elongation at break”), shrinkage, temperature shrinkage, shrinkage ("shrinkage”) contraction "), shrinkage force, linear weight, Dip pick-up, stiffness, etc., are measured according to the standards in force in the textile industry. The inventors endeavored to verify that the new treatments did not entail any modification of these properties, compared to the standard RFL.
  • the adhesive preparations of the invention are subject to an evaluation of their adhesion performance.
  • the textile After coating the textile, it is deposited in a matrix of uncured rubber, so that the surface of the textile in contact with the rubber remains clean of any pollution.
  • the matrix containing the textile is then vulcanized by compression, according to conditions of temperature, time and pressure specific to each rubber.
  • the textile + vulcanized matrix assembly forms an adhesion test tube.
  • Adhesion specimens can take many forms, described in various international standards, such as the ISO 36: 2017 standard.
  • the test pieces, and by extension the test conducted to determine adhesion, are commonly known to those skilled in the art under such names as Test-T ("pull-out test", ASTM D2229-04), Test-H (according to standard NF ISO 4647 or ASTM D4776-04), peeling (peel-test) ...
  • Test-T pulse-out test
  • ASTM D2229-04 Test-H (according to standard NF ISO 4647 or ASTM D4776-04), peeling (peel-test) ...
  • the test is then carried out by solicitation of the specimen until destruction of the interfacial contact zone, tearing of the textile, or tearing of the rubber matrix.
  • the adhesion is then evaluated according to criteria such as the appearance of the textile at break, the maximum adhesion force, the average tear force, possibly reduced to the thickness of the test piece.
  • the textile impregnation process is carried out by soaking ("dipping") in tanks containing the adhesive preparations.
  • a schematic of such a process is illustrated in Gomes A., Nabih N., Kramer T, Adhesion Activation of Tire Texts by Resorcinol Formaldehyde Free Coatings, Rubber World, March 2016.
  • the reel (s) of untreated yarns, cords and cords can be positioned on a creel at the line entry.
  • An accumulator system may optionally be used.
  • the son, ropes and cables can undergo either a direct dipping in a tray, or impregnation by a lick roller, for the application of the adhesive composition. After soaking or impregnation, the excess wet preparation is preferably removed for example by pressing (padding), suction or by foams. This is followed by drying and / or crosslinking of the adhesive composition.
  • the coated impregnated textile can thus pass through an oven to allow the drying and crosslinking of the adhesive composition.
  • the textile can again undergo an impregnation step, then passing through an oven, these steps can be repeated, including up to a total of 4 impregnations (2, 3 or 4).
  • the wires, cords or cords can be received on winders.
  • a combing system composed of comb and / or "pigtails" can be used at the outlet of the creel. It allows maximum opening of the multifilament yarn, to promote a strong impregnation.
  • the yarn is then twisted in line.
  • the wiring is preferably performed on an already treated wire. Additional treatments can be performed on the cords thus formed.
  • the speeds can range from 1 m / min to 150 m / min, the furnace temperatures from 30 ° C. to 350 ° C., more specifically from 100 to 300 ° C., and even more specifically from 140 to 220 ° C. vs.
  • Mechanical tension can also be applied to the textile.
  • the textiles were treated with the adhesion compositions object of the invention under conditions identical to those applied during a treatment with an RFL.
  • the inventors have endeavored to present a solution that can be used as a reinforcement, braided, spiraled, gimped or knitted in a brake pipe. For this, a 95 Z twist was applied to a polyethylene terephthalate (PET) yarn of 1 100 dtex title.
  • PET polyethylene terephthalate
  • the yarn obtained was treated by impregnation in the adhesive object of the invention, and then by heat-setting in an oven.
  • the adhesives used in this example have a solids concentration of 20%.
  • the various son impregnated with the adhesive were evaluated in adhesion on 2 rubber mixtures conventionally used in the brake pipes.
  • the first is a peroxide accelerated EPDM blend of 90 Shore A hardness.
  • the second is an EPDM blend of hardness 90 Shore A vulcanized with sulfur.
  • the test pieces were made by compression molding.
  • the PET yarn treated with the various adhesives of each of Examples 1-1, I-2 and I-3 showed satisfactory levels of adhesion over the RFL impregnated control yarn.
  • the values obtained are presented in Table I, and expressed in% of adhesion relative to the adhesion obtained with the control RFL yarn.
  • Adhesion (in% vs. adhesion of the treated PET thread + EPDM treated PET thread + EPDM control RFL) peroxide Sulfur
  • the inventors have endeavored to present a solution that can be used as a reinforcement in assemblies such as transmission belts or conveyor belts.
  • Such reinforcements require a first treatment to limit fraying when exposed on the wafer.
  • a wired PA 4-6 470 / 5x3 dtex construction (100/125) was built in successive stages of twisting and wiring.
  • the cord obtained was treated by a first impregnation in a solution of methylene diphenyl diisocyanate in toluene, then subjected to drying and heat setting in an oven.
  • the cord was then impregnated in a tray containing the adhesive of the invention, at a mass concentration of dry matter of 20%, in place of the RFL treatment usually applied.
  • the different son impregnated with the various adhesives obtained were evaluated in adhesion on 2 rubber mixtures that could be used for the manufacture of belts.
  • the first is a peroxide accelerated EPDM blend.
  • the second is a CR vulcanized metal oxide blend.
  • the test pieces were made by compression molding.
  • the Polyamide 4-6 cord treated with the various adhesives of Examples 1-1, I-2 and I-3 showed satisfactory levels of adhesion to EPDM compared to the RFL impregnated control yarn.
  • Polyamide yarn 4-6 treated with the various adhesives of Example I-5 showed satisfactory levels of adhesion to the CR mixture.
  • the adhesion levels obtained, as well as the observation of failure facings, show that the adhesives evaluated are compatible with the first treatment applied to the textile.
  • adhesion values obtained are presented in Table II, and expressed in% of adhesion relative to the adhesion obtained with the control RFL yarn.
  • the inventors have endeavored to present an invention that can be used as a reinforcement in profiles and joints, such as window or door seals.
  • Such reinforcements are made from glass wire containing a size with which the adhesive composition must be compatible.
  • the glass cord E treated with the various adhesives of Examples I-2, I-3 and I-4 showed satisfactory levels of adhesion to EPDM compared to the RFL impregnated control yarn.
  • the adhesion levels obtained, as well as the observation of failure facings, show that the adhesives evaluated are compatible with the size of the glass.
  • the adhesion values obtained are presented in Table III, and expressed in% adhesion relative to the adhesion obtained with the control RFL yarn.
  • Table III adhesions obtained for a treated glass for profiles.
  • the inventors have endeavored to present an invention that can be used as a radial reinforcement in tires.
  • Such reinforcements consist of a p-aramid yarn requiring prior treatment, called activation, to enable it to obtain the required adhesion levels.
  • a 1680 / 1x3 dtex (240/240) p-aramid cable was built in successive stages of twisting, then wiring.
  • the cord obtained was treated by a first impregnation in an aqueous preparation called "activation" based on polyepoxides, then subjected to drying and heat setting in an oven.
  • the cord was then impregnated in a tray containing the adhesive of the invention, at a mass concentration of dry matter of 7 to 20%, instead of the RFL treatment usually applied.
  • the cords thus treated showed a visual appearance of remarkable uniformity, testifying to a good compatibility between the adhesive treatment according to the invention and the preactivation treatment.
  • the different son impregnated with the various adhesives obtained were evaluated in adhesion on a rubber mixture based on a cut of SBR and NR that can be used in "heavyweight” tires.
  • the p-aramid cords treated with the adhesives of Examples 1-1 to I-4 showed satisfactory levels of adhesion to the rubber compared to the RFL impregnated control yarn.
  • the p-aramid cords treated with the adhesives of Examples I-2 and I-3 showed levels of adhesion with respect to the level of adhesion usually required for this type of applications, but which remain remarkable, d greater than 15 N / mm.
  • the observation of fracture facies confirms these levels by the presence of residual rubber on the textile.
  • Table IV adhesions obtained for a tire treated aramid.
  • the aluminum cups used have a diameter of 43 mm and a depth of 12 mm.
  • the glass transition temperature is measured by differential scanning calorimetry using METTLER TOLEDO DSC 3+ STAR 6 SYSTEM equipment.
  • the measured glass transition temperature is the temperature at the midpoint of the glass transition.
  • the sample is placed in the DSC equipment under nitrogen flow at 80 ml per minute. It is then fired at 25 to 190 ° C (20 ° C per minute), then cooled from 190 ° C to 25 ° C (20 ° C per minute), held at 25 ° C for 5 minutes, then a second rise of 25 ° C to 300 ° C (20 ° C per minute) during which the glass transition of the cooked product is measured.
  • Example 111-1-1 (Comparative): Preparation of a Formula Comprising a Lionosulfonate Salt in the Presence of Soda and in the Absence of Aldehyde Hardener
  • a few grams of the composition are introduced into an aluminum cup which is placed under a hood at room temperature for 24 hours, then in an oven at 105 ° C. for 15 minutes and then mounted in an oven at 180 ° C. and stabilized for 5 minutes at 180 ° C. ° C, to obtain a cooked product.
  • This fired product is then placed in the DSC equipment to measure the glass transition temperature as explained above.
  • the measured glass transition temperature is 155 ° C with an accuracy of +/- 1 ° C.
  • Example 111-1-2 (Comparative): Preparation of a Formula Comprising a Liqnosulfonate Salt in the Presence of Ammonia and in the Absence of Aldehyde Hardener.
  • compositions A few grams of the composition are introduced into an aluminum cup which is placed under a hood at room temperature for 24 hours, then in a drying oven. 105 ° C for 15 minutes and then rise of the oven at 180 ° C and stabilization for 5 minutes at 180 ° C, to obtain a cooked product.
  • This fired product is then placed in the DSC equipment to measure the glass transition temperature as explained above.
  • the measured glass transition temperature is 160 ° C with an accuracy of +/- 1 ° C.
  • Example 111-1 -3 Preparation of a Formula Comprising a Liqnosulfonate Salt in the Presence of Soda and in the Presence of Aldehyde Hardener
  • a few grams of the composition are introduced into an aluminum cup which is placed under a hood at room temperature for 24 hours, then in an oven at 105 ° C. for 15 minutes and then mounted in an oven at 180 ° C. and stabilized for 5 minutes at 180 ° C. ° C, to obtain a cooked product.
  • This fired product is then placed in the DSC equipment to measure the glass transition temperature as explained above.
  • compositions containing benzaldehyde 2 compositions containing trans-2-hexenal, 2 compositions containing 2-methylbutyraldehyde, 2 compositions containing salicylaldehyde, 2 compositions containing 7-hydroxy-3,7 -dimethyl-octanal, 2 compositions containing cyclohexanecarboxaldehyde, 2 compositions containing 3-chlorobenzaldehyde and 2 compositions containing 4-ethylbenzaldehyde, by varying the hardener / lignosulfonate salt weight ratio from 50% to 150%.
  • Example 111-1-4 Preparation of a Formula Comprising a Liqnosulfonate Salt in the Presence of Ammonia and in the Presence of Aldehyde Hardener
  • a few grams of the composition are introduced into an aluminum cup which is placed under a hood at room temperature for 24 hours, then in an oven at 105 ° C. for 15 minutes and then mounted in an oven at 180 ° C. and stabilized for 5 minutes at 180 ° C. ° C, to obtain a cooked product.
  • This fired product is then placed in the DSC equipment to measure the glass transition temperature as explained above.
  • compositions containing benzaldehyde 2 compositions containing trans-2-hexenal, 2 compositions containing 2-methylbutyraldehyde, 2 compositions containing salicylaldehyde, 2 compositions containing 7-hydroxy-3,7-dimethylocananal, 2 compositions containing cyclohexanecarboxaldehyde, 2 compositions containing chlorobenzaldehyde and 2 compositions containing 4-ethylbenzaldehyde, by varying the hardener / lignosulfonate salt mass ratio from 50% to 150%.
  • These fired products have glass transition temperatures higher than the glass transition temperature of the cooked control product of Example III-1-2. This increase in the glass transition temperature compared to the control shows that the aldehyde has hardened the lignosulfonate salt.
  • Example 111-2-1 Preparation of a Styrene-Butadiene-Vinylpyridine Copolymer Latex Adhesive (VPSBR)
  • Example 1 -3 127.1 g of water and 37.5 g of the composition of Example 1 -3 are added with stirring to 85.4 g of a styrene-butadiene-vinylpyridine copolymer latex comprising 35.0 g of dry VPSBR and 50.4 g of water. The agitation is maintained for a few minutes until total homogenization. After 12 hours of ripening, 250 g of a preparation that can be used for the textile treatment have been obtained. The preparation has a pH of 9.7, a solids content of 16.5% and a viscosity of 2.7 cP.
  • compositions of Example 1-3 and Example 1-4 contain benzaldehyde, 4 compositions contain trans-2-hexenal, 4 compositions contain 2-methylbutyraldehyde, 4 compositions contain salicylaldehyde, 4 compositions contain 7-hydroxy-3,7-dimethylocanal, 4 compositions contain cyclohexanecarboxaldehyde, 4 compositions contain chlorobenzaldehyde and 4 compositions contain 4-ethylbenzaldehyde, and vary the following parameters:
  • % by weight of dry latex in the composition approximately 70%
  • Mass ratio hardener / lignosulfonate salt from 50 to 150%
  • compositions were made and have the following characteristics: pH 7.8 to 10.4
  • Example III-2-2 Preparation of a chloroprene (CR) latex adhesive
  • Example 1 -3 153.2 g of water and 37.5 g of the composition of Example 1 -3 are added with stirring to 59.3 g of a chloroprene latex comprising 35.0 g of dry CR and 24.3 g of water. Stirring is maintained for a few minutes until complete homogenization. After 12 hours of ripening, 250 g of a preparation that can be used for the textile treatment have been obtained. The preparation has a pH of 10, a solids content of 17.4% and a viscosity of 2.1 cP.
  • compositions of Example 1-3 and Example 1-4 contain benzaldehyde, 4 compositions contain trans-2-hexenal, 4 compositions contain 2-methylbutyraldehyde, 4 compositions contain salicylaldehyde, 4 compositions contain 7-hydroxy-3,7-dimethylocanal, 4 compositions contain cyclohexanecarboxaldehyde, 4 compositions contain chlorobenzaldehyde and 4 compositions contain 4-ethylbenzaldehyde, and vary the following parameters:
  • % by weight of dry latex in the composition approximately 70%
  • Mass ratio hardener / lignosulfonate salt from 50 to 150%
  • Example III-2-3 Preparation of a Styrene-Butadiene Copolymer (SBR) Latex Adhesive
  • Example 1 -3 127.1 g of water and 37.5 g of the composition of Example 1 -3 are added with stirring to 85.4 g of a styrene-butadiene copolymer latex comprising 35.0 g of dry SBR and 50.4 g of water. Stirring is maintained for a few minutes until complete homogenization. After 12 hours of ripening, 250 g of a preparation that can be used for the textile treatment have been obtained. The preparation has a pH of 9.1, a solids content of 16.7% and a viscosity of 2.1 cP.
  • compositions of Example 1-3 and Example 1-4 contain benzaldehyde, 4 compositions contain trans-2-hexenal, 4 compositions contain 2-methylbutyraldehyde, 4 compositions contain salicylaldehyde, 4 compositions contain 7-hydroxy-3,7-dimethylocanal, 4 compositions contain cyclohexanecarboxaldehyde, 4 compositions contain chlorobenzaldehyde and 4 compositions contain 4-ethylbenzaldehyde, and vary the following parameters:
  • % by weight of dry latex in the composition approximately 70%
  • Mass ratio hardener / lignosulfonate salt from 50 to 150%
  • compositions were made and have the following characteristics: pH 7.7 to 10.2
  • Example 1 -3 138.0 g of water and 37.5 g of the composition of Example 1 -3 are added with stirring to 74.5 g of a butadiene-acrylonitrile copolymer latex comprising 35.0 g of dry NBR and 39.5 g of water. Stirring is maintained for a few minutes until complete homogenization. After 12 hours of ripening, 250 g of a preparation that can be used for the textile treatment have been obtained. The preparation has a pH of 9.7, a solids content of 17.5% and a viscosity of 2.6 cP.
  • compositions contain benzaldehyde
  • 4 compositions contain trans-2-hexenal
  • 4 compositions contain 2-methylbutyraldehyde
  • 4 compositions contain salicylaldehyde
  • 4 compositions contain 7-hydroxy-3,7-dimethyloctanal
  • 4 compositions contain cyclohexanecarboxaldehyde
  • 4 compositions contain chlorobenzaldehyde
  • 4 compositions contain 4-ethylbenzaldehyde, and vary the following parameters:
  • % by weight of dry latex in the composition approximately 70%
  • Mass ratio hardener / lignosulfonate salt from 50 to 150%
  • compositions were made and have the following characteristics: pH 7.8 to 10.1

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  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
EP19720124.7A 2018-04-26 2019-04-26 Haftverbessernde zusammensetzung für textilmaterial und zugehöriges verstärkendes textilmaterial Pending EP3784719A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR1853655A FR3080627B1 (fr) 2018-04-26 2018-04-26 Composition d'adherisage pour textile et textile de renfort y relatif
PCT/EP2019/060810 WO2019207141A1 (fr) 2018-04-26 2019-04-26 Composition d'adhérisage pour textile et textile de renfort y relatif

Publications (1)

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EP3784719A1 true EP3784719A1 (de) 2021-03-03

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US (1) US20210115310A1 (de)
EP (1) EP3784719A1 (de)
JP (1) JP7393346B2 (de)
KR (1) KR102673091B1 (de)
CN (1) CN112135862B (de)
CA (1) CA3098599A1 (de)
FR (1) FR3080627B1 (de)
MX (1) MX2020011345A (de)
WO (1) WO2019207141A1 (de)

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Publication number Priority date Publication date Assignee Title
CN118215764A (zh) * 2021-11-25 2024-06-18 东丽株式会社 橡胶/纤维用粘接处理剂和使用了该橡胶/纤维用粘接处理剂的橡胶增强用合成纤维帘线

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Publication number Priority date Publication date Assignee Title
US3884862A (en) * 1970-05-15 1975-05-20 Du Pont Adhesive composition and method of making same
US4026744A (en) * 1975-01-22 1977-05-31 The General Tire & Rubber Company Glass cord adhesives comprising vinyl pyridine terpolymer/lignin sulfonate-resorcinol-formaldehyde reaction product; method of use and composite article
US4016119A (en) * 1975-01-22 1977-04-05 The General Tire & Rubber Company Lignin sulfonate for glass cord adhesives
US4204982A (en) * 1977-10-17 1980-05-27 The General Tire & Rubber Company Lignin amine carboxylated conjugated diene tire cord adhesives
US4524093A (en) * 1984-04-30 1985-06-18 The B. F. Goodrich Company Fabric coating composition with low formaldehyde evolution
SG47174A1 (en) * 1995-09-18 1998-03-20 Ibm Cross-linked biobased materials and fabricating methods thereof
US7252735B2 (en) * 2002-05-13 2007-08-07 State Of Oregon Acting By And Through The Oregon State Board Of Higher Education On Behalf Of Oregon State University Formaldehyde-free lignocellulosic adhesives and composites made from the adhesives
JP2012121938A (ja) * 2010-12-06 2012-06-28 Hitachi Chemical Co Ltd 熱剥離性粘着フィルム
US20120309246A1 (en) * 2011-06-03 2012-12-06 Alexander Tseitlin Curable biopolymer nanoparticle latex binder for mineral, natural organic, or synthetic fiber products and non-woven mats
FR2978770B1 (fr) * 2011-08-04 2013-09-27 Michelin Soc Tech Composition adhesive aqueuse a base de polyaldehyde et phloroglucinol
GB201120137D0 (en) * 2011-11-22 2012-01-04 Dynea Oy Modified binder compositions
US9157016B2 (en) * 2012-10-01 2015-10-13 Georgia-Pacific Chemicals Llc Modified polyphenol binder compositions and methods for making and using same
FR3008707B1 (fr) * 2013-07-16 2017-11-10 Michelin & Cie Composition adhesive aqueuse a base d'aldehyde biosource et de polyphenol
EP3131943A4 (de) * 2014-03-12 2018-02-14 Hexion Research Belgium SA Polymere, verbundstoffe und verfahren zur herstellung von polymeren und verbundstoffen
WO2015147165A1 (ja) * 2014-03-28 2015-10-01 住友ベークライト株式会社 フェノール変性リグニン樹脂及びその製造方法、並びに、樹脂組成物、ゴム組成物、及び硬化物
FI126754B (en) * 2015-11-25 2017-05-15 Teknologian Tutkimuskeskus Vtt Oy Functionalization of cellulose with lignin for the production of high added value products
CN109196161A (zh) * 2016-06-30 2019-01-11 长濑化成株式会社 有机纤维用粘接剂以及有机纤维的处理方法

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MX2020011345A (es) 2021-01-29
KR20210005185A (ko) 2021-01-13
KR102673091B1 (ko) 2024-06-05
CN112135862B (zh) 2022-06-03
US20210115310A1 (en) 2021-04-22
JP2021522386A (ja) 2021-08-30
FR3080627A1 (fr) 2019-11-01
BR112020021786A2 (pt) 2021-02-23
FR3080627B1 (fr) 2021-02-26
CN112135862A (zh) 2020-12-25
WO2019207141A1 (fr) 2019-10-31
JP7393346B2 (ja) 2023-12-06
CA3098599A1 (fr) 2019-10-31

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