WO2014091376A1 - A dipping material for cord fabrics and a production method thereof - Google Patents

A dipping material for cord fabrics and a production method thereof Download PDF

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Publication number
WO2014091376A1
WO2014091376A1 PCT/IB2013/060693 IB2013060693W WO2014091376A1 WO 2014091376 A1 WO2014091376 A1 WO 2014091376A1 IB 2013060693 W IB2013060693 W IB 2013060693W WO 2014091376 A1 WO2014091376 A1 WO 2014091376A1
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WO
WIPO (PCT)
Prior art keywords
dipping solution
production method
epoxy
cord fabrics
composition
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Application number
PCT/IB2013/060693
Other languages
French (fr)
Inventor
Nacide Nurcin CEVAHIR
Ali Ersin Acar
Serkan BAS
Original Assignee
Kordsa Global Endustriyel Iplik Ve Kord Bezi Sanayi Ve Ticaret Anonim Sirketi
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Application filed by Kordsa Global Endustriyel Iplik Ve Kord Bezi Sanayi Ve Ticaret Anonim Sirketi filed Critical Kordsa Global Endustriyel Iplik Ve Kord Bezi Sanayi Ve Ticaret Anonim Sirketi
Priority to US14/441,121 priority Critical patent/US10294385B2/en
Priority to ES13818447.8T priority patent/ES2623132T3/en
Priority to EP13818447.8A priority patent/EP2931791B1/en
Priority to KR1020157015292A priority patent/KR20150095657A/en
Priority to BR112015013484A priority patent/BR112015013484A8/en
Priority to SI201330616A priority patent/SI2931791T1/en
Priority to LU92519A priority patent/LU92519B1/en
Priority to CN201380065132.6A priority patent/CN105121520B/en
Publication of WO2014091376A1 publication Critical patent/WO2014091376A1/en

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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
    • C08J5/06—Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/02—Copolymers with acrylonitrile
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/06—Copolymers with styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/06—Copolymers with styrene
    • C08L9/08—Latex
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D109/00—Coating compositions based on homopolymers or copolymers of conjugated diene hydrocarbons
    • C09D109/06—Copolymers with styrene
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D109/00—Coating compositions based on homopolymers or copolymers of conjugated diene hydrocarbons
    • C09D109/06—Copolymers with styrene
    • C09D109/08—Latex
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/395—Isocyanates
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/227—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated
    • D06M15/233—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated aromatic, e.g. styrene
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/356—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms
    • D06M15/3562—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms containing nitrogen
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/55—Epoxy resins
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/693—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural or synthetic rubber, or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2321/00—Characterised by the use of unspecified rubbers

Definitions

  • the present invention relates to a dipping solution for cord fabrics which enables the synthetic fiber and the rubber to be attached to each other by providing a phase between the said two structures, and which is environmental friendly, and a production method thereof.
  • the synthetic fibers have high strength and low elongation whereas the rubbers contrarily are polymeric materials which have high elongation and low strength.
  • the polar groups amide, hydroxyl and carbonyl groups present in the structure of the synthetic fibers are incompatible with the non-polar structures of the rubber. This incompatibility is eliminated with water-based Resorcinol- Formaldehyde-Latex (RFL) adhesive solutions which form a phase between the cord and the rubber and enable the rubber and the fiber to be attached to each other.
  • RTL Resorcinol- Formaldehyde-Latex
  • RFL Main function of RFL is to serve as adhesive attaching two incompatible structures by forming phase between fiber and rubber.
  • RF functional group within RFL is attached to the polar groups of fiber
  • Latex (L) group is attached to the fiber with vulcanization and the rubber-fiber composite structure is formed.
  • the vehicle tire application amongst the most significant product examples wherein the said composite structure is used.
  • the water based RFL adhesives are applied on cord fabric during "dipping" process which is the final step of cord fabric production. The strength of the bonds formed between the rubber and the cord is examined with adhesion tests. Adhesion is very important parameter in high tenacity cord reinforced rubber products. Because cord-rubber adhesion is a critical factor which affects the tire performance.
  • United States Patent document no US20120041113 an application known in the state of the art, discloses preparing a composition comprising epoxy, blocked isocyanate, epoxy curing agent and vinyl pyridine latex.
  • United States Patent document no US5118545 discloses the synthesis of an aramide with multiple double bonds. It is stated that the synthesized resin is applied on the aramide based cord fabric and the double bonds in aramide resin are vulcanized with the double bonds in rubber, and the amide groups provide physical adhesion to the aramide fiber.
  • United States Patent document no US4472463 another application known in the state of the art, discloses dipping non-adhesive activated PET fibers with two step process dipping.
  • the first step dipping comprises aromatic glycidyl ester epoxy and blocked isocyanate, while the second step dipping comprises two various latex.
  • the first latex is styrene-butadiene-vinyl pyridine copolymer, and the other one is acrylic acid-methyl methacrylate-styrene copolymer. It is stated that higher adhesion values are obtained in H-adhesion tests compared to RFL dipping solution.
  • United States Patent document no US20040249053 another application in the state of the art wherein an environmental friendly dipping material is disclosed.
  • the maleinized polybutadiene is reacted with polyethylene glycol and become water soluble.
  • the PET cords modified with epoxy are first dipped with this resin and then with styrene-butadiene-vinyl pyridine latex.
  • the stripping-adhesion strength of the rubber with PET cords dipped with this resin is lower than the fabrics with RFL.
  • RFL adhesive formulation has been used as adhesive material in all synthetic fiber reinforced materials for over half century because of its stable structural characteristics and low cost.
  • both resorcinol and formaldehyde are the hazardous chemicals which create a great risk for human and environmental health. Therefore, their use has to be limited.
  • feedbacks have come from international organizations and customers. It is known that the resorcinol causes itching and rash when it contacts the skin, irritates the eye and shows toxic properties in liver and cardiovascular systems.
  • Formaldehyde is riskier than resorcinol for human health and safety.
  • formaldehyde is classified as group 2A chemical (possible carcinogen in humans) by a group of scientists in International Agency for research on Cancer (IARC) of World Health Organization, and as group 1 (carcinogen for humans) for a group of scientists.
  • group 2A chemical possibly carcinogen in humans
  • group 1 carcinogen for humans
  • formaldehyde is included in list of chemicals causing leukemia by IARC. According to these, formaldehyde is suggested to be gene mutagen. Even low amounts of formaldehyde (lppm) cause eye, nose and throat irritation.
  • formaldehyde resins have advantage in terms of cost, both producers and consumers search for alternatives because of the reasons expressed above.
  • a further objective of the present invention is to provide a dipping solution for cord fabrics which is in white color and thus makes it possible to produce colorful cords.
  • Figure 1 is the view of the flowchart of the method.
  • Figure 2 is the view of the table wherein the strip adhesion values of 8 different inventive mixtures, the composition ratios of which are different, and Resorcinol- Formaldehyde-Latex (RFL) adhesive solutions are compared.
  • the production method for the dipping solution for cord fabrics (10) comprises the steps of:
  • first functional acrylic resin (polymer) material comprising carboxylic acid is added into the water (1).
  • the functionality of the resin comprising carboxylic acid, at least one of the monomers such as acrylic acid, methacrylic acid, itaconic acid, crotonic acid, cinnamic acid, maleic acid is used.
  • the amount of carboxylic acid within acrylic polymer is between 1- 50% by mole. In one embodiment of the invention this rate is kept between 1- 30%.
  • pH value of this composition comprising water and acrylic polymer is adjusted (2).
  • ammonium hydroxide is added to the composition until the pH value of the composition is 10-11.
  • epoxy is added into the composition (3).
  • the epoxy which is used is water soluble or water based dispersion.
  • At least one of the materials such as glycidyl based glycerol and sorbitol epoxy, phenol novalac epoxy, cresol novalac epoxy is used as epoxy.
  • Any epoxy which is water soluble or can be prepared in dispersion can be used in this invention.
  • polyisocyanate is added to the composition (4).
  • polyurethane prepolymer comprising water based blocked polyisocyanate or water based blocked isocyanate groups is used.
  • the molecular weight of the polyurethane prepolymer comprising water based blocked isocyanate groups is in the range of 1000-10000 g/mol, in one embodiment of the invention this value is between 1500-3000 g/mol.
  • latex is added (5).
  • latex there are butadiene- styrene- vinyl -pyridine monomers.
  • the solid amount inside the latex is between 35-45 % by weight.
  • the dipping solution is obtained by adding all materials mentioned in the previous steps into the water at room temperature and stirring it (6).
  • Different acrylic polymers, epoxies and polyisocyanates were used in different ratios and 8 compositions were prepared.
  • the related table is given in Figure 2, and strip adhesion values of these compositions are indexed according to strip adhesion value of Resorcinol-Formaldehyde-Latex (RFL) adhesive solution.
  • acrylic resin ratio of 1-7 % by weight, epoxy in ratio of 0.6-2.5 %, and polyisocyanate in ratio of 6-21 % are used.
  • the dipping solution prepared with the inventive production method for cord fabrics (10) can be used in dipping cords such as nylon 6.6, nylon 6, polyethylene terephthalate, polyethylene naphthalate, rayon, aramide, and it is not limited to these.
  • dipping cords such as nylon 6.6, nylon 6, polyethylene terephthalate, polyethylene naphthalate, rayon, aramide, and it is not limited to these.
  • the inventive dipping material is dipped with the inventive dipping material and dried at between 100- 150 °C and then cured at between 200-240 °C.
  • the dipped cords are pressed into the non-vulcanized (green) rubber composition in molds.
  • the said composite material is generally cured at 170 °C under pressure for about 20 minutes, and the final cord is obtained.
  • the amount of solid is determined as 15%, and pH is adjusted to 10-11 range by adding ammonium hydroxide (12).
  • the inventive dipping solution method was used in dipping 2 layered, 1400 dtex value, 396x396 twisted nylon 6.6 cords. The dipped cords were first dried for 60 seconds at 130°C, then cured for 60 seconds at 235 and 230 °C, respectively. Acrodur 950 and 3515 were used as acrylic functional polymer.
  • the said water based polymers comprise carboxylic acid, polybasic alcohol groups with 50% solid.
  • EX313 and EX614B were used as epoxy.
  • EX313 is a glycerol based glycidyl epoxy
  • EX614B is sorbitol based glycidyl epoxy resin. The said resins are 100% soluble in water.
  • Grilbond IL-6 or BN-27 was used as blocked polyisocyanate or polyurethane.
  • Grilbond IL-6 is water based caprolactam blocked 1,4-phenylene diisocyanate with 60% solid.
  • BN-27 is a water based polyurethane prepolymer comprising blocked isocyanates with 30% solid.
  • the solid amount of styrene-butadiene-vinyl-pyridine latex is 41%, and pH value is 10.5
  • the inventive dipping solution production method provides opportunities such as cost and time saving. Since the final product is white it is aesthetically appealing and also enables cord fabrics to be produced in various colors with pigment additives.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Textile Engineering (AREA)
  • Materials Engineering (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Manufacturing & Machinery (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

The present invention relates to a dipping solution for cord fabrics and a production method thereof comprising the steps of adding acrylic resin (polymer) into water (11), adjusting pH value (12), adding epoxy to the composition (13), adding polyisocyanate to the composition (14), adding latex to the composition (15), obtaining the dipping material (16); enabling the synthetic fiber and the rubber used in cord fabric reinforced rubber materials production to be attached to each other by providing an interface between two said materials; not as hazardous as RFL for human health and also being environmental friendly.

Description

A DIPPING MATERIAL FOR CORD FABRICS AND A PRODUCTION
METHOD THEREOF
Field of the Invention
The present invention relates to a dipping solution for cord fabrics which enables the synthetic fiber and the rubber to be attached to each other by providing a phase between the said two structures, and which is environmental friendly, and a production method thereof.
Background of the Invention
Since the chemical structures of synthetic fibers used in the cord fabric production and the rubber are considerably different from each other, the said materials are incompatible with each other in terms of their chemical and physical structures. The synthetic fibers have high strength and low elongation whereas the rubbers contrarily are polymeric materials which have high elongation and low strength. The polar groups (amide, hydroxyl and carbonyl groups) present in the structure of the synthetic fibers are incompatible with the non-polar structures of the rubber. This incompatibility is eliminated with water-based Resorcinol- Formaldehyde-Latex (RFL) adhesive solutions which form a phase between the cord and the rubber and enable the rubber and the fiber to be attached to each other.
Main function of RFL is to serve as adhesive attaching two incompatible structures by forming phase between fiber and rubber. RF functional group within RFL is attached to the polar groups of fiber, Latex (L) group is attached to the fiber with vulcanization and the rubber-fiber composite structure is formed. The vehicle tire application amongst the most significant product examples wherein the said composite structure is used. The water based RFL adhesives are applied on cord fabric during "dipping" process which is the final step of cord fabric production. The strength of the bonds formed between the rubber and the cord is examined with adhesion tests. Adhesion is very important parameter in high tenacity cord reinforced rubber products. Because cord-rubber adhesion is a critical factor which affects the tire performance.
Formaldehyde-free dipping solutions for rubber materials reinforced with cord have been reported in various studies.
United States Patent document no US20120041113, an application known in the state of the art, discloses preparing a composition comprising epoxy, blocked isocyanate, epoxy curing agent and vinyl pyridine latex.
International Patent document no WO9600749, another application known in the state of the art, discloses applying dipping solutions formulated with three functional epoxy resins, styrene-butadiene-vinyl pyridine and styrene-butadiene- aery lonitrile- acrylic acid latex to the polyethylene terephthalate (PET) material and adhesion strength with rubber.
United States Patent document no US5118545, another application known in the state of the art, discloses the synthesis of an aramide with multiple double bonds. It is stated that the synthesized resin is applied on the aramide based cord fabric and the double bonds in aramide resin are vulcanized with the double bonds in rubber, and the amide groups provide physical adhesion to the aramide fiber.
United States Patent document no US4472463, another application known in the state of the art, discloses dipping non-adhesive activated PET fibers with two step process dipping. The first step dipping comprises aromatic glycidyl ester epoxy and blocked isocyanate, while the second step dipping comprises two various latex. The first latex is styrene-butadiene-vinyl pyridine copolymer, and the other one is acrylic acid-methyl methacrylate-styrene copolymer. It is stated that higher adhesion values are obtained in H-adhesion tests compared to RFL dipping solution. United States Patent document no US20040249053, another application in the state of the art wherein an environmental friendly dipping material is disclosed. In that application, the maleinized polybutadiene is reacted with polyethylene glycol and become water soluble. The PET cords modified with epoxy are first dipped with this resin and then with styrene-butadiene-vinyl pyridine latex. However the stripping-adhesion strength of the rubber with PET cords dipped with this resin is lower than the fabrics with RFL.
RFL adhesive formulation has been used as adhesive material in all synthetic fiber reinforced materials for over half century because of its stable structural characteristics and low cost. However, both resorcinol and formaldehyde are the hazardous chemicals which create a great risk for human and environmental health. Therefore, their use has to be limited. Regarding this subject, feedbacks have come from international organizations and customers. It is known that the resorcinol causes itching and rash when it contacts the skin, irritates the eye and shows toxic properties in liver and cardiovascular systems.
Formaldehyde is riskier than resorcinol for human health and safety. In 2004, formaldehyde is classified as group 2A chemical (possible carcinogen in humans) by a group of scientists in International Agency for research on Cancer (IARC) of World Health Organization, and as group 1 (carcinogen for humans) for a group of scientists. In 2009, formaldehyde is included in list of chemicals causing leukemia by IARC. According to these, formaldehyde is suggested to be gene mutagen. Even low amounts of formaldehyde (lppm) cause eye, nose and throat irritation. Although formaldehyde resins have advantage in terms of cost, both producers and consumers search for alternatives because of the reasons expressed above.
Summary of the Invention
The objective of the present invention is to provide a dipping material for cord fabrics which comprises more environment friendly chemicals than formaldehyde and resorcinol. Another objective of the present invention is to provide production method for dipping solution of cord fabrics which takes shorter time than the method used in the state of the art.
A further objective of the present invention is to provide a dipping solution for cord fabrics which is in white color and thus makes it possible to produce colorful cords.
Detailed Description of the Invention
The dipping material for cord fabrics and a production method thereof developed to fulfill the objective of the present invention is illustrated in the accompanying figure, in which;
Figure 1 is the view of the flowchart of the method.
Figure 2 is the view of the table wherein the strip adhesion values of 8 different inventive mixtures, the composition ratios of which are different, and Resorcinol- Formaldehyde-Latex (RFL) adhesive solutions are compared.
The production method for the dipping solution for cord fabrics (10) comprises the steps of:
- adding acrylic resin (polymer) into water (11),
adjusting pH value (12),
adding epoxy to the composition (13),
adding polyisocyanate to the composition (14),
adding latex to the composition (15),
- obtaining the dipping material (16).
In the inventive production method for dipping material for cord fabrics (10), first functional acrylic resin (polymer) material comprising carboxylic acid is added into the water (1). The functionality of the resin comprising carboxylic acid, at least one of the monomers such as acrylic acid, methacrylic acid, itaconic acid, crotonic acid, cinnamic acid, maleic acid is used. In the preferred embodiment of the invention, the amount of carboxylic acid within acrylic polymer is between 1- 50% by mole. In one embodiment of the invention this rate is kept between 1- 30%.
Then, pH value of this composition comprising water and acrylic polymer is adjusted (2). In the preferred embodiment of the invention, ammonium hydroxide is added to the composition until the pH value of the composition is 10-11.
After pH is adjusted to the desired level, epoxy is added into the composition (3). In the preferred embodiment of the invention, the epoxy which is used is water soluble or water based dispersion. At least one of the materials such as glycidyl based glycerol and sorbitol epoxy, phenol novalac epoxy, cresol novalac epoxy is used as epoxy. However their use is not limited to these. Any epoxy which is water soluble or can be prepared in dispersion can be used in this invention.
Then polyisocyanate is added to the composition (4). In the preferred embodiment of the invention, polyurethane prepolymer comprising water based blocked polyisocyanate or water based blocked isocyanate groups is used. At least one of tetramethylene diisocyanaye, hexamethylene disocyanate (1,6- diisocyanatohexane), octamethylene diisocyanate, decamethylene diisocyanae, dodecamethylene diisocyanate, aromatic diisocyanates 2,4- or 2,6-tolylene diisocyanate, tetramethyilxyliene diisocyanate, p-xylene diisocyanate, 2,4'- or 4- 4'-diisocyanatediphenylmethane, 1,3- or 1,4-phenylene diisocyanate is used as polyisocyanate by itself or as it is added to the polymers. In the preferred embodiment of the invention, the molecular weight of the polyurethane prepolymer comprising water based blocked isocyanate groups is in the range of 1000-10000 g/mol, in one embodiment of the invention this value is between 1500-3000 g/mol. After adding polyisocyanate, latex is added (5). Within latex, there are butadiene- styrene- vinyl -pyridine monomers. In the preferred embodiment of the invention, the solid amount inside the latex is between 35-45 % by weight.
The dipping solution is obtained by adding all materials mentioned in the previous steps into the water at room temperature and stirring it (6). Different acrylic polymers, epoxies and polyisocyanates were used in different ratios and 8 compositions were prepared. The related table is given in Figure 2, and strip adhesion values of these compositions are indexed according to strip adhesion value of Resorcinol-Formaldehyde-Latex (RFL) adhesive solution.
In the preferred embodiment of the invention, acrylic resin ratio of 1-7 % by weight, epoxy in ratio of 0.6-2.5 %, and polyisocyanate in ratio of 6-21 % are used.
The dipping solution prepared with the inventive production method for cord fabrics (10) can be used in dipping cords such as nylon 6.6, nylon 6, polyethylene terephthalate, polyethylene naphthalate, rayon, aramide, and it is not limited to these. After the said cords are prepared in certain constructions (ply number and twist), it is dipped with the inventive dipping material and dried at between 100- 150 °C and then cured at between 200-240 °C. The dipped cords are pressed into the non-vulcanized (green) rubber composition in molds. The said composite material is generally cured at 170 °C under pressure for about 20 minutes, and the final cord is obtained.
In an exemplary embodiment of the composition, the amount of solid is determined as 15%, and pH is adjusted to 10-11 range by adding ammonium hydroxide (12). The inventive dipping solution method was used in dipping 2 layered, 1400 dtex value, 396x396 twisted nylon 6.6 cords. The dipped cords were first dried for 60 seconds at 130°C, then cured for 60 seconds at 235 and 230 °C, respectively. Acrodur 950 and 3515 were used as acrylic functional polymer. The said water based polymers comprise carboxylic acid, polybasic alcohol groups with 50% solid.
EX313 and EX614B were used as epoxy. EX313 is a glycerol based glycidyl epoxy, and EX614B is sorbitol based glycidyl epoxy resin. The said resins are 100% soluble in water.
Grilbond IL-6 or BN-27 was used as blocked polyisocyanate or polyurethane. Grilbond IL-6 is water based caprolactam blocked 1,4-phenylene diisocyanate with 60% solid. BN-27 is a water based polyurethane prepolymer comprising blocked isocyanates with 30% solid. The solid amount of styrene-butadiene-vinyl-pyridine latex is 41%, and pH value is 10.5
It is possible to obtain a dipping solution for rubber composites by using environmental friendly chemicals with the inventive dipping solution production method (10). Furthermore, the said method provides opportunities such as cost and time saving. Since the final product is white it is aesthetically appealing and also enables cord fabrics to be produced in various colors with pigment additives.
Within the framework of these basic concepts, it is possible to develop various embodiments of the inventive dipping material for cord fabrics and a production method thereof. The invention cannot be limited to the examples described herein and it is essentially as defined in the claims.

Claims

1. A production method of dipping solution for cord fabrics (10), which enables the synthetic fiber and the rubber to be attached to each other by providing an interface in between the said two structures and is also environmental friendly, characterized by the steps of
-adding acrylic resin (polymer) into water (11),
-adjusting pH value (12),
-adding epoxy to the composition (13),
-adding polyisocyanate to the composition (14),
-adding latex to the composition (15),
-obtaining the dipping material (16).
2. A production method for dipping solution for cord fabrics (10) according to claim 1, characterized by the step of adding acrylic resin (polymer) in to the water (11) wherein functional acrylic resin comprising carboxylic acid is used.
3. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of adding acrylic resin (polymer) into the water (11) wherein at least one of the monomers such as acrylic acid, methacrylic acid, itaconic acid, crotonic acid, cinnamic acid, maleic acid is used as carboxylic acid.
4. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of adding acrylic resin (polymer) into the water (11) wherein the carboxylic acid amount inside the acrylic polymer is in the range of 1-50% by mol.
5. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of adjusting pH level (12) wherein ammonium hydroxide is added until pH value is 10-11.
6. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of adding epoxy into the composition (13) wherein epoxy material is used as water soluble or water based dispersion.
7. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of adding epoxy to the composition (13) wherein at least one of epoxies such as glycidyl based glycerol and sorbitol epoxy, phenol novalac epoxy, cresol novalac epoxy or epoxy water dispersion of which is can be prepared is used the epoxy.
8. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of adding polyisocyanate into the composition (14) wherein polyurethane polymer comprising water based blocked polyisocyanate or water based blocked isocyanate groups is used.
9. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of adding polyisocyanate into the composition (14) wherein at least one of tetramethylene diisocyanaye, hexamethylene disocyanate (1,6- diisocyanatohexane), octamethylene diisocyanate, decamethylene diisocyanae, dodecamethylene diisocyanate, aromatic diisocyanates 2,4- or 2,6-tolylene diisocyanate, tetramethyilxyliene diisocyanate, p-xylene diisocyanate, 2,4'- or 4-4'-diisocyanatediphenylmethane, 1,3- or 1,4- phenylene diisocyanate is used as polyisocyanate by itself or as it is added to the polymers.
10. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of adding latex into the composition (15) wherein latex comprising butadiene, styrene, vinyl pyridine monomers is used.
11. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of obtaining dipping solution (16) wherein the final product is obtained by adding the materials used in the previous steps into the water and stirring at room temperature.
12. A production method for dipping solution for cord fabrics (10) according to any one of the preceding claims, characterized by the step of obtaining the dipping solution (16) wherein a dipping solution is acquired which comprises acrylic resin ratio of 1-7 % by weight, epoxy in ratio of 0.6-2.5 %, and polyisocyanate in ratio of 6-21 %.
13. A dipping solution for cord fabrics which is obtained with a method according to any one of the preceding claims.
14. Nylon 6.6, nylon 6, polyethylene teraphthalate, polyethylene naphthalate, rayon or aramide cord which is dipped with a dipping solution according to claim 13.
PCT/IB2013/060693 2012-12-13 2013-12-06 A dipping material for cord fabrics and a production method thereof WO2014091376A1 (en)

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US14/441,121 US10294385B2 (en) 2012-12-13 2013-12-06 Dipping material for cord fabrics and a production method thereof
ES13818447.8T ES2623132T3 (en) 2012-12-13 2013-12-06 An immersion material for lace fabrics and a production method thereof
EP13818447.8A EP2931791B1 (en) 2012-12-13 2013-12-06 A dipping material for cord fabrics and a production method thereof
KR1020157015292A KR20150095657A (en) 2012-12-13 2013-12-06 A dipping material for cord fabrics and a production method thereof
BR112015013484A BR112015013484A8 (en) 2012-12-13 2013-12-06 MATERIAL FOR IMMERSION OF CORDONEL CANVAS AND METHOD FOR THE PRODUCTION OF THE SAME
SI201330616A SI2931791T1 (en) 2012-12-13 2013-12-06 A dipping material for cord fabrics and a production method thereof
LU92519A LU92519B1 (en) 2012-12-13 2013-12-06 A dipping material for cord fabrics and a production method thereof
CN201380065132.6A CN105121520B (en) 2012-12-13 2013-12-06 Cord impregnated material and preparation method thereof

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TR2012/14628 2012-12-13
TR201214628 2012-12-13

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US20150259560A1 (en) 2015-09-17

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