WO2001004230A1 - Process for producing adhesive for fusion bonding, adhesive for fusion bonding obtained by the process, and adhesive fabric containing the adhesive for fusion bonding - Google Patents
Process for producing adhesive for fusion bonding, adhesive for fusion bonding obtained by the process, and adhesive fabric containing the adhesive for fusion bonding Download PDFInfo
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- WO2001004230A1 WO2001004230A1 PCT/JP2000/004613 JP0004613W WO0104230A1 WO 2001004230 A1 WO2001004230 A1 WO 2001004230A1 JP 0004613 W JP0004613 W JP 0004613W WO 0104230 A1 WO0104230 A1 WO 0104230A1
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- adhesive
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- thermoplastic resin
- heat
- production method
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- 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
- D06M17/00—Producing multi-layer textile fabrics
- D06M17/04—Producing multi-layer textile fabrics by applying synthetic resins as adhesives
- D06M17/08—Polyamides polyimides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/50—Mixing liquids with solids
- B01F23/51—Methods thereof
- B01F23/511—Methods thereof characterised by the composition of the liquids or solids
-
- 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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/21—Paper; Textile fabrics
-
- 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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/35—Heat-activated
-
- 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
- D06M15/507—Polyesters
-
- 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
- D06M15/59—Polyamides; Polyimides
-
- 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
- D06M17/00—Producing multi-layer textile fabrics
- D06M17/04—Producing multi-layer textile fabrics by applying synthetic resins as adhesives
-
- 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
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
- D06M23/14—Processes for the fixation or treatment of textile materials in three-dimensional [3D] forms
-
- 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
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
- D06M23/16—Processes for the non-uniform application of treating agents, e.g. one-sided treatment; Differential treatment
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/12—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
- D06N3/121—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyesters, polycarbonates, alkyds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/12—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
- D06N3/125—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyamides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F2101/00—Mixing characterised by the nature of the mixed materials or by the application field
- B01F2101/36—Mixing of ingredients for adhesives or glues; Mixing adhesives and gas
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/50—Mixing liquids with solids
- B01F23/56—Mixing liquids with solids by introducing solids in liquids, e.g. dispersing or dissolving
-
- 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
- C09J2400/263—Presence of textile or fabric in the substrate
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2205/00—Condition, form or state of the materials
- D06N2205/02—Dispersion
- D06N2205/023—Emulsion, aqueous dispersion, latex
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2209/00—Properties of the materials
- D06N2209/10—Properties of the materials having mechanical properties
- D06N2209/105—Resistant to abrasion, scratch
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2209/00—Properties of the materials
- D06N2209/12—Permeability or impermeability properties
- D06N2209/121—Permeability to gases, adsorption
- D06N2209/125—Non-permeable
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2209/00—Properties of the materials
- D06N2209/14—Properties of the materials having chemical properties
- D06N2209/143—Inert, i.e. inert to chemical degradation, corrosion resistant
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/30—Woven fabric [i.e., woven strand or strip material]
- Y10T442/3049—Including strand precoated with other than free metal or alloy
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/30—Woven fabric [i.e., woven strand or strip material]
- Y10T442/3065—Including strand which is of specific structural definition
- Y10T442/3073—Strand material is core-spun [not sheath-core bicomponent strand]
Definitions
- the present invention relates to a method for producing a heat-sealing adhesive, a heat-sealing adhesive obtained by the method, and an adhesive cloth using the heat-sealing adhesive.
- the present invention relates to a method for producing a heat sealing adhesive.
- the present invention also relates to the heat-sealing adhesive obtained by the method. Further, the present invention relates to an adhesive cloth obtained by heat-sealing the heat-sealing adhesive to the surface of a base cloth.
- thermoplastic resin Conventionally, by coating various base materials with thermoplastic resin and forming a coating film, various properties such as oil resistance, solvent resistance, chemical resistance, abrasion resistance, gas barrier property, adhesive property etc. has been performed. Above all, an adhesive cloth in which a woven or nonwoven fabric containing fibers is used as a base cloth and a thermoplastic resin is coated on the surface of the base cloth is mainly used as an adhesive interlining in the field of clothing.
- Japanese Patent Application Laid-Open No. 6-145413 proposes an adhesive core prepared as follows. That is, first, a fibrous nonwoven fabric as a base fabric is coated with a composition in which an acryl-based polymer emulsion such as an acrylate ester resin is added with a sili force and a silane force ringing agent, and dried. Next, a powder of a thermoplastic resin such as a polyamide resin, a polyester resin, a polyethylene resin, an ethylene-vinyl acetate resin, or a polyvinyl chloride resin is sprayed on the coating and melted to form an adhesive core. .
- a thermoplastic resin such as a polyamide resin, a polyester resin, a polyethylene resin, an ethylene-vinyl acetate resin, or a polyvinyl chloride resin is sprayed on the coating and melted to form an adhesive core.
- thermoplastic resin powder there are various methods for heating and fusing the thermoplastic resin powder to the surface of the base fabric, such as a skittle ring method, a powder dot method, a spray method, a paste dot method, and a double dot method.
- the scattering method which is used and divided according to the type of the base cloth, involves uniformly dispersing a thermoplastic resin powder on the surface of the base cloth in a “medium: pure” manner, and then heat-fusing the powder.
- a thermoplastic resin powder is first adhered to a gravure roll, and then 15 copies are applied to the surface of the base fabric, followed by aging and fusing.
- a paste in which a thermoplastic resin powder is dispersed in water is sprayed on the surface of the base fabric as it is, and then heated and dried and fused.
- the paste-dot method is a method in which a paste obtained by dispersing a thermoplastic resin powder in water is coated in a dot form on the surface of a substrate using a coating screen having pores, and then heated and dried and fused.
- the acrylic emulsion is coated in the form of dots on the surface of the base fabric using a coating screen having pores, and the thermoplastic resin is applied on the resulting dot-shaped acrylic coating.
- the method includes a step of spraying the resin powder, a step of removing excess thermoplastic resin powder, and a step of heating, drying and fusing the thermoplastic resin powder remaining on the base cloth.
- the thermoplastic resin powder heat-fused to the surface of the base fabric by these methods acts as an adhesive for heat-sealing, and when heated again during use, heat-fuses the base fabric to the surface material.
- the role of the adhesive cloth, especially the adhesive interlining, is to supplement the performance of the outer material, mainly to finish the clothes three-dimensionally, to make sewing easier, and at the same time not to lose its shape due to wearing, washing, dry cleaning, etc. Imparting morphological stability. Normally used for men's suits, women's suits, collars, cuffs, front body, etc.The required properties vary depending on the application, place of use, etc. In consideration of various conditions such as the method and the type of the base cloth, a suitable adhesive interlining is selected.
- Thermoplastic resin powder is a mechanical pulverization that mechanically pulverizes thermoplastic resins such as copolymerized boride resin, copolymerized polyester resin, ethylene-vinyl acetate copolymer resin, polyethylene resin and polyurethane resin at room temperature. It is prepared by pulverization by a method or a frozen pulverization method in which pulverization is performed under freezing.
- the base cloth In the powder dot method, the base cloth must be pre-heated to 180 to 250 ° C in order to improve powder separation when transferring the powder from the gravure roll to the base cloth. Depending on the type, there is a problem that preheating causes shrinkage and impairs the texture.
- the paste dot method a relatively small particle size resin powder having a particle size in the range of 5 to 80 ⁇ m is used in the form of a paste, so that the feeling is somewhat improved.
- the particle diameter is in the range of 5 to 80 ⁇
- the weight average particle diameter of the resin powder is usually 30 to It is about 50 ⁇ m, and the pores of the coating screen are likely to be clogged with M. Therefore, it is difficult to reduce the pore diameter of the screen to 200 m or less, and as a result, the dot interval is widened, which causes problems such as a decrease in adhesive strength and a deterioration in feeling.
- the base adhesive used in the spray method and paste dot method is manufactured by dispersing a thermoplastic resin powder in water, it is difficult to increase the resin concentration to 4% by weight or more. Therefore, there is also a problem that drying takes time and productivity is low.
- the double dot method has improved these disadvantages.
- a resin powder is sprayed on an acryl resin coating applied in a dot form, and the resin powder adhered only to the acryl resin coating portion is used as an adhesive for heat fusion. If excess powder resin is removed by suction after spraying, the resin powder should originally remain only on the acrylic resin application dot.However, in practice, the powder cannot be completely removed by suction but remains in areas other than the dots. There is also a problem that the retained powder causes a deterioration in the texture, and the adhesive strength is reduced due to separation between the acryl resin and the adhered resin powder. Disclosure of the invention
- An object of the present invention is to provide an adhesive interlining that does not impair the feel of clothes, retains form stability, and sufficiently satisfies drapeability even when applied to thin fabrics, particularly thin fabrics for women.
- Another object of the present invention is to provide a heat-sealing adhesive obtained by such a manufacturing method.
- Yet another object of the present invention is to provide an adhesive cloth in which such a heat-sealing adhesive is heat-sealed to the surface of a base cloth.
- a heat-sealing adhesive for heat-sealing a base fabric to a surface material, wherein the thermoplastic resin is heated to a temperature equal to or higher than a softening point of the resin.
- a method for producing a heat-sealing adhesive which comprises dispersing in a water-based medium.
- a heat-sealing adhesive which is an aqueous thermoplastic resin dispersion obtained by the above production method.
- thermoplastic resin used in the present invention is not particularly limited, and examples thereof include copolymerized polyamide resin, copolymerized polyester resin, ethylene monoacetate copolymer resin, polyethylene resin, and polyurethane resin. . These may be used alone or as a mixture.
- copolymerized boronamide resin can be used to keep the texture of thin fabrics good, and from the viewpoint of dry cleaning resistance and washing resistance.
- Copolymerized polyester resins, and mixtures thereof are preferably used.
- the copolymerizable made of Polyamide resins, Re such are not particularly limited but, for example, - [NH (CH 2) 5 C0] -, - [NH (CH 2) 6 NHC0 (CH 2) 4 C0] - ,-[NH (CH 2 ) fi NHC0 (CH 2 ) 8 C0]-,-NH (CII,), 0 C0]-,-[NH (CH 2 ),, CO]-
- Examples include those having at least two types of structural units. Specific examples include 6/6 copolymer nylon, 6/610 copolymer nylon, 6/111 copolymer nylon, 6Z12 copolymer nylon, 6Z66 / 6 10 copolymer nylon, 6Z66 / 11 copolymer nylon.
- 6/6 6Z11 copolymer nylon, 6Z66Z12 copolymer nylon and 6Z66Z11Z12 copolymer nylon are preferable, and especially 6Z66Z12 copolymer nylon.
- Polymerized nylon is more preferred.
- the copolymerized polyester resin is not particularly limited.
- the acid component (A) containing terephthalic acid and isophthalic acid and ethylene glycol, diethylene glycol, polyethylene glycol, 1,4_ Copolymerized polyester resins obtained by a polycondensation reaction with a diol component (B) containing butanediol or 1,6-hexanediol are exemplified.
- terephthalic acid isophthalic acid Z1,4-butanediol copolymerized polyester resin terephthalic acid Z isophthalic acid Zl, 6-hexanediole copolymerized polyester resin, terephthalic acid nonisophthalic acid z polyethylene glycol Polymerized polyester resin, terephthalic acid / isophthalic acid Z-ethylene glycol / 1,4-butanediol copolymerized polyester resin, terephthalic acid Z-isophthalic acid Z adipic acid Z1,4—butanediol copolymerized polyester resin, terephthalic acid Z-isophthalic acid Acid Z i, 4-butanediol Z diethylene dalicol copolymerized polyester resin and the like.
- terephthalic acid Z isophthalic acid Z1,4-butanediol copolymerized polyester resin terephthalic acid z isophthalic acid / ethylene glycol Zl, 4-butanediol copolymerized polyester resin, terephthalic acid Z isophthalic acid Z 1 , 4-butanediol z-diethylene glycol copolymer polyester resin is preferable, and terephthalic acid / isophthalic acid Z1,4-butanediol copolymer polyester resin is more preferable.
- the resin in order to disperse the thermoplastic resin in the aqueous medium, the resin is heated to a temperature equal to or higher than the softening point of the resin to be in a softened state, and then a shearing force is applied to the aqueous medium by stirring. .
- the thermoplastic resin previously heated to a temperature equal to or higher than the softening point may be added to the heated aqueous medium under stirring, or the thermoplastic resin may be added to the aqueous medium under stirring.
- the thermoplastic resin may be heated together with the aqueous medium to a temperature equal to or higher than its softening.
- thermoplastic resin is a polyethylene resin having no functional group at the end or an ethylene monoacetate copolymer resin
- a surfactant or a dispersant is added to the aqueous medium as needed to disperse the resin. Even if promoted Good.
- thermoplastic resin is a co-S-polyamide resin having a carboxyl group at the end or a copolyester resin, etc.
- a basic substance is used. May be added to the aqueous medium.
- surfactant examples include anionic surfactants (eg, rosinate, fatty acid salt, alkylbenzene sulfonate), cationic surfactants (eg, dodecyl trimethylammonium chloride), nonionic surfactants Agents (eg, ethylene oxide propylene oxide block copolymer, boroxy ethylene alkyl ether, glycerin fatty acid ester, polyoxy ethylene fatty acid ethanol amide '), amphoteric surfactant (eg, ⁇ -alkyl mono-, ⁇ -dimethylammonium betaine).
- anionic surfactants eg, rosinate, fatty acid salt, alkylbenzene sulfonate
- cationic surfactants eg, dodecyl trimethylammonium chloride
- nonionic surfactants Agents eg, ethylene oxide propylene oxide block copolymer, boroxy ethylene alkyl ether, glycerin fatty acid
- dispersant examples include polyacrylates, polystyrene sulfonates, polystyrene maleic anhydride, polymer dispersants such as polyvinyl alcohol, hydroxyethyl cellulose, alumina sol, silica sol, calcium phosphate and the like. Inorganic dispersants are exemplified.
- Examples of the basic substance include alkali metal hydroxides such as sodium hydroxide and hydroxylating power, ammonia, and amine compounds.
- alkali metal hydroxides such as sodium hydroxide and hydroxylating power are preferably used in view of the dispersing effect.
- the dispersion is performed at a temperature equal to or higher than the softening point of the thermoplastic resin in an aqueous medium, usually at 50 to 300 ° C, and preferably at 70 to 220 ° C. can get. If the temperature is lower than 500 ° C, the thermoplastic resin is not sufficiently softened in the aqueous medium, so that uniform dispersion cannot be achieved. ,.
- the amount of the aqueous medium used in the production method of the present invention is usually 30 to 150 parts by weight, preferably 100 to 500 parts by weight, based on 100 parts by weight of the thermoplastic resin. Parts by weight. If the amount of water used is less than 30 parts by weight, the thermoplastic resin cannot be sufficiently dispersed in water. Even if the amount of water exceeds 150 parts by weight, the obtained thermoplastic resin aqueous dispersion Concentration is low, which is not preferable for use.
- the weight-average particle size of the resin particles in the aqueous dispersion of the water-soluble resin can be arbitrarily adjusted.
- the weight average particle diameter of the resin particles in the thermoplastic resin aqueous dispersion is less than 0.1 ⁇ m, the particles are easily aggregated and gelled, so that it is difficult to obtain a high resin concentration.
- the weight average particle diameter of the resin particles in the aqueous thermoplastic resin dispersion exceeds 20 ⁇ m, the pores of the coating screen are easily clogged, and the adhesive strength of the base fabric is reduced. It is preferable because it may impair the texture.
- the adhesive for heat fusion of the present invention is usually used after adjusting the viscosity to 500 to 50 OO OmPa.sec by adding a viscosity modifier. If it is smaller than 500 mPa.sec, the amount of permeation into the base fabric is increased, the texture becomes hard, and the dot formation becomes insufficient. If it exceeds 500,000 mPa ⁇ sec, it becomes difficult to apply it to the base fabric.
- the compounding amount of the viscosity modifier is usually 0.01 to 5 parts by weight based on 100 parts by weight of the aqueous thermoplastic resin dispersion so as to fall within the above viscosity range.
- viscosity modifiers include polyacrylamide, sodium polyacrylate, carboxymethylcellulose, carboxyethylcellulose, hydroxyxetylsenorellose, polyacrylic acid ester, polyethylene oxide, and ethylene oxide propylene oxide.
- examples include natural or synthetic polymer-based thickeners such as oxide random copolymers. If necessary, a plasticizer, a dispersing aid, an antifoaming agent, a softening agent, a stabilizer and the like may be added.
- the obtained aqueous dispersion of thermoplastic resin may be adjusted to an arbitrary concentration by using an appropriate concentration means such as using a semipermeable membrane.
- the obtained aqueous dispersion of thermoplastic resin (whether or not concentrated) may be used as it is, or after solid-liquid separation by centrifugation or filtration, and then pulverized by drying means such as spray drying. You can do it.
- an adhesive cloth which is obtained by applying the heat-sealing adhesive to a surface of a base cloth and heat-sealing the base cloth.
- the adhesive cloth thus obtained is suitably used particularly as an adhesive interlining that does not impair the feel of the thin cloth.
- the base fabric used for the adhesive fabric of the present invention is not particularly limited, and a woven fabric or a nonwoven fabric containing various fibers is used.
- the fiber material include natural fibers such as cotton, hemp, silk, and wool, regenerated fibers such as rayon and cupra, acetate, and triacetate. And other synthetic fibers such as polyester, nylon, acrylic, urethane, polypropylene, polyethylene, and polychlorinated vinyl.
- the woven fabric include a woven fabric and a knitted fabric made of a fiber material.
- the nonwoven fabric include a web formed by entanglement of a fiber material by a chemical method, a mechanical method, or a combination thereof.
- the method for applying the heat-sealing adhesive to the base fabric is not particularly limited.
- the heat-sealing adhesive of the present invention is obtained as an aqueous dispersion, particularly preferable results are obtained when the heat-sealing adhesive is heat-sealed to the surface of the base fabric using the base-dot method.
- a heat-sealing adhesive is injected into a rotary screen having a large number of pores, extruded from the pores of the rotary screen onto a base cloth, and applied in a dot form. is there.
- the pore size of the rotary screen is usually about 200 m, but a screen of about 50 to 200 m can be used by using the heat-sealing adhesive of the present invention.
- the number of dots is usually 50 to 120 / cm 2 with respect to the base cloth, but the maximum is about 400 / cm 2 by using the adhesive for heat sealing of the present invention.
- the coating amount is usually 10 to 20 g Zm : 2 , but by using the adhesive for heat sealing of the present invention, depending on the type of the base cloth, even a cloth of 5 g Zm 2 or less is sufficient. Adhesive strength is obtained.
- the heat-sealing adhesive After applying the heat-sealing adhesive to the base cloth, if the base cloth is heated at a temperature of 80 to 150 ° C, the heat-sealing adhesive will dry and melt, and will be fused to the base cloth. Is obtained.
- the obtained adhesive cloth can be bonded to various types of outer fabrics, for example, as an adhesive interlining with an iron or a hot press machine, and when used for thin fabrics, especially thin fabrics for women, it is finished with a very good texture.
- the weight-average particle diameter of the obtained 6/6 6 Z12 copolymerized polyamide resin aqueous dispersion was measured with a laser-diffraction particle size distribution analyzer (SALD 2000, manufactured by Shimadzu Corporation). The diameter was 1.2 m.
- the weight average particle diameter of the obtained aqueous dispersion of terephthalic acid / 'isophthalic acid Z 1,4-butanediol copolymerized polyester resin was measured with a laser diffraction particle size distribution analyzer (S ALD 2000 manufactured by Shimadzu Corporation). As a result of measurement, the weight average particle size was 2.5 ⁇ .
- Example 4 Preparation of adhesive cloth
- Example 2 To 100 parts by weight of the aqueous dispersion of terephthalic acid Z isophthalic acid Zl, 4-butanediol copolymerized polyester resin obtained in Example 2 was added 0.2 parts by weight of sodium polyacrylate, and the viscosity was 2 OOOO m P a. Thus, a paste-like adhesive for heat fusion was obtained.
- Example 2 50 parts by weight of the aqueous 6Z66Z12 copolymer resin dispersion obtained in Example 1 and the copolymer of terephthalic acid Z isophthalic acid Z1,4-butanediol obtained in Example 2 0.2 parts by weight of sodium polyacrylate was added to a mixture of 50 parts by weight of the aqueous polyester resin dispersion to obtain a paste-like adhesive for thermal fusion having a viscosity of 2000 mPa ⁇ sec. .
- Copolymerized polyamide resin (softening point 130 ° C) is freeze-pulverized, and then classified with a standard sieve with an opening of 80 m to obtain a weight average particle diameter of 45 m.
- a copolymer resin powder was obtained. 64.8 parts by weight of water and 0.2 parts by weight of sodium polyacrylate were added to 35 parts by weight of the obtained 6-6 Z12 copolymerized copolymer resin powder, and the mixture was stirred to obtain a viscosity of 2,300.
- OmP a ⁇ sec paste-like adhesive for heat fusion was obtained.
- the obtained adhesive for heat fusion was coated on a screen with a pore diameter of 80 / zm using a non-woven nonwoven fabric with a coating weight of 25 g Zm 2 .
- the number of dots was 300 / cm.
- the coating amount was 5 g Z'm 2 , and it was applied in the form of dots. However, a part of the screen was clogged and could not be applied in the form of dots.
- copolymerized polyamide resin (softening point: 130 ° C) is frozen and pulverized, and then classified by a standard sieve with an opening of 80 ⁇ m to obtain a resin having a weight average particle diameter of 45 m. 12 copolymerized boriamid resin powder was obtained. 66.8 parts by weight of the obtained 666-Z12 copolymerized resin resin powder, 64.8 parts by weight of water and 0.2 part by weight of sodium polyacrylate were added and stirred, and the viscosity was 2300 OmPa ⁇ sec.
- the pasty heat wearing adhesive obtained to obtain a heat wearing adhesive using a screen with a pore size of 200 mu m, the surface of 3 ⁇ 42 of 5 gZm 2 nylon with nonwoven fabric I, having 1 to 50 dots No. cm 2 , application m 10 g Zm 2 , and applied in dot form. Then, it was dried and fused at 150 ° C. for 2 minutes to obtain an adhesive cloth.
- 1,4-butanediol copolymerized terephthalic acid / isophthalic acid polyester resin (softening point 90 ° C) is frozen and pulverized, and then classified with a standard sieve having an aperture of 80 m to obtain a weight; average particle size of 42 ⁇ m.
- terephthalic acid / isophthalic acid Z 1,4-butanediol ⁇ ⁇ ⁇ ⁇ ⁇ ⁇ polyester resin powder 3 obtained terephthalic acid / isophthalic acid / '1,4 -butanediol copolymerized polyester resin powder 3 5 parts by weight 64.8 parts by weight of water and 0.2 parts by weight of sodium polyacrylate were added and stirred to obtain a paste-like heat-sealing adhesive having a viscosity of 22000 mPa'sec.
- the obtained heat-sealing adhesive was applied to the surface of a polyester nonwoven fabric having a basis weight of 25 g / m 2 , with 300 dots Zcm 2 and a coating amount of 5 g. Zm 2 was applied in the form of dots, but the screen was partially clogged and could not be applied in the form of dots.
- Terephthalic acid / isophthalic acid Zl, 4-butanediol copolymerized polyester tree The moon (softening point 90 ° C) is freeze-pulverized and then classified with a standard sieve with openings of 80 ⁇ m to obtain a weight average particle size of 4
- a 2-m terephthalic acid-sophthalic acid / 1,4-butanediol-combined polyester resin powder was obtained.
- 64.8 parts by weight of water and 0.2 part by weight of sodium polyacrylate were added and stirred.
- a paste-like heat-sealing adhesive having a viscosity of 2300 mPa-sec was obtained.
- the sensory test was used to determine the following criteria.
- thermoplastic resin in the aqueous medium has a weight average particle diameter in the range of 0.1 to 20 m, It is evenly distributed. Therefore, when applying by the paste dot method, the adhesive can be applied to the surface of the base cloth with small dots and at high density without clogging the screen. As a result, when the obtained adhesive cloth is used as an adhesive interlining for thin cloth, especially for thin cowboys for women, the aesthetic functions required for clothes, the texture and drape necessary to obtain a beautiful silket are obtained. It can give excellent properties such as aesthetic formability, which does not impair the formability. On the other hand, in Comparative Examples 1 to 4, the heat-sealing adhesive could not be applied to the base fabric, or even if it could be applied, the texture was poor.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Details Of Garments (AREA)
- Adhesive Tapes (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/030,845 US6743741B1 (en) | 1999-07-12 | 2000-07-10 | Process for producing adhesive for fusion bonding, adhesive for fusion bonding obtained by the process, and adhesive fabric containing the adhesive for fusion bonding |
| EP00944387A EP1231247A4 (en) | 1999-07-12 | 2000-07-10 | METHOD FOR PRODUCING ADHESIVE FOR FUSION ASSEMBLY, ADHESIVE FOR FUSION ASSEMBLY OBTAINED BY THIS METHOD, AND ADHESIVE FABRIC CONTAINING SUCH ADHESIVE FOR FUSION ASSEMBLY |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19696999A JP2001019937A (ja) | 1999-07-12 | 1999-07-12 | 熱融着用接着剤および接着布 |
| JP11/196969 | 1999-07-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2001004230A1 true WO2001004230A1 (en) | 2001-01-18 |
Family
ID=16366670
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2000/004613 Ceased WO2001004230A1 (en) | 1999-07-12 | 2000-07-10 | Process for producing adhesive for fusion bonding, adhesive for fusion bonding obtained by the process, and adhesive fabric containing the adhesive for fusion bonding |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US6743741B1 (https=) |
| EP (1) | EP1231247A4 (https=) |
| JP (1) | JP2001019937A (https=) |
| WO (1) | WO2001004230A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108913079A (zh) * | 2018-05-14 | 2018-11-30 | 启东鑫天鼎热熔胶有限公司 | 一种耐低温聚酯热熔胶的配方及其制备方法 |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002226819A (ja) * | 2001-01-30 | 2002-08-14 | Dainippon Ink & Chem Inc | 接着剤用球形ポリエステル樹脂粒子分散液 |
| JP2005126562A (ja) * | 2003-10-23 | 2005-05-19 | Sumitomo Seika Chem Co Ltd | 熱融着用接着剤および接着布 |
| CN101956305A (zh) * | 2010-08-03 | 2011-01-26 | 陈国新 | 一种耐砂洗丝绸浆点衬的生产工艺 |
| JP5988771B2 (ja) * | 2012-08-27 | 2016-09-07 | 住友精化株式会社 | ポリアミド樹脂水性分散液の製造方法 |
| JP6226649B2 (ja) * | 2013-09-05 | 2017-11-08 | 住友精化株式会社 | 熱融着接着剤 |
| CN103767199A (zh) * | 2014-01-06 | 2014-05-07 | 浙江金三发粘合衬有限公司 | 一种耐洗丝绸浆点衬的制备工艺 |
| US10202722B2 (en) * | 2016-11-01 | 2019-02-12 | Larry E Mashburn | Method of applying a theromplastic polymer coating |
| US10689803B2 (en) | 2017-03-27 | 2020-06-23 | Textile Rubber And Chemical Company, Inc. | Aqueous polymer dispersion composition and method of adhering textile materials |
| US10815365B2 (en) | 2017-05-30 | 2020-10-27 | Textile Rubber and Chemical Company Inc. | Scatter coating process for synthetic turf and product |
| CN112118964A (zh) | 2018-10-03 | 2020-12-22 | 惠普发展公司,有限责任合伙企业 | 热转印 |
| US11351766B2 (en) | 2019-11-11 | 2022-06-07 | Textile Rubber And Chemical Company, Inc. | Process for applying film backing to synthetic turf and product |
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| JPS61119778A (ja) * | 1984-11-15 | 1986-06-06 | ダイセル化学工業株式会社 | 熱融着用水性分散液 |
| EP0328301A2 (en) * | 1988-02-03 | 1989-08-16 | Union Camp Corporation | Polyamide resin dispersions and method for the manufacture thereof |
| WO1992015634A1 (en) * | 1991-03-04 | 1992-09-17 | Union Camp Corporation | Stable polyamide resin dispersions and methods for the manufacture thereof |
| JPH078772A (ja) * | 1993-06-25 | 1995-01-13 | Nittetsu Mining Co Ltd | 水系分散液の製造装置 |
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| JPH10231402A (ja) * | 1997-02-20 | 1998-09-02 | Nippon Paper Ind Co Ltd | 水分散液及びその製造方法 |
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| JPH1180602A (ja) * | 1997-09-16 | 1999-03-26 | Dainippon Ink & Chem Inc | 粉体スラリー塗料の製造方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3082482B2 (ja) | 1992-11-02 | 2000-08-28 | 日本ゼオン株式会社 | ホットメルト樹脂浸透防止用組成物及び接着芯地 |
-
1999
- 1999-07-12 JP JP19696999A patent/JP2001019937A/ja active Pending
-
2000
- 2000-07-10 US US10/030,845 patent/US6743741B1/en not_active Expired - Fee Related
- 2000-07-10 WO PCT/JP2000/004613 patent/WO2001004230A1/ja not_active Ceased
- 2000-07-10 EP EP00944387A patent/EP1231247A4/en not_active Withdrawn
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| JPS61119778A (ja) * | 1984-11-15 | 1986-06-06 | ダイセル化学工業株式会社 | 熱融着用水性分散液 |
| EP0328301A2 (en) * | 1988-02-03 | 1989-08-16 | Union Camp Corporation | Polyamide resin dispersions and method for the manufacture thereof |
| WO1992015634A1 (en) * | 1991-03-04 | 1992-09-17 | Union Camp Corporation | Stable polyamide resin dispersions and methods for the manufacture thereof |
| JPH078772A (ja) * | 1993-06-25 | 1995-01-13 | Nittetsu Mining Co Ltd | 水系分散液の製造装置 |
| JPH08117578A (ja) * | 1994-10-20 | 1996-05-14 | Nittetsu Mining Co Ltd | 熱可塑性樹脂の水系乳化分散液の製造方法及び装置 |
| JPH10231464A (ja) * | 1997-02-18 | 1998-09-02 | Toagosei Co Ltd | 感熱粘着剤組成物および感熱粘着シート |
| JPH10231402A (ja) * | 1997-02-20 | 1998-09-02 | Nippon Paper Ind Co Ltd | 水分散液及びその製造方法 |
| JPH1180602A (ja) * | 1997-09-16 | 1999-03-26 | Dainippon Ink & Chem Inc | 粉体スラリー塗料の製造方法 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108913079A (zh) * | 2018-05-14 | 2018-11-30 | 启东鑫天鼎热熔胶有限公司 | 一种耐低温聚酯热熔胶的配方及其制备方法 |
| CN108913079B (zh) * | 2018-05-14 | 2020-12-22 | 启东鑫天鼎热熔胶有限公司 | 一种耐低温聚酯热熔胶的配方及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2001019937A (ja) | 2001-01-23 |
| EP1231247A1 (en) | 2002-08-14 |
| EP1231247A4 (en) | 2006-04-12 |
| US6743741B1 (en) | 2004-06-01 |
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