WO2006134966A1 - 人工皮革用基材およびその製造方法 - Google Patents
人工皮革用基材およびその製造方法 Download PDFInfo
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- WO2006134966A1 WO2006134966A1 PCT/JP2006/311925 JP2006311925W WO2006134966A1 WO 2006134966 A1 WO2006134966 A1 WO 2006134966A1 JP 2006311925 W JP2006311925 W JP 2006311925W WO 2006134966 A1 WO2006134966 A1 WO 2006134966A1
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- Prior art keywords
- fiber
- artificial leather
- base material
- nonwoven fabric
- thickness direction
- Prior art date
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Classifications
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- 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
-
- 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
- D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
- D06N3/0004—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate using ultra-fine two-component fibres, e.g. island/sea, or ultra-fine one component fibres (< 1 denier)
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- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/44—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling
- D04H1/46—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
- D04H1/74—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being orientated, e.g. in parallel (anisotropic fleeces)
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- 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
- D06N3/04—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 by reactions only involving carbon-to-carbon unsaturated bonds
- D06N3/06—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 by reactions only involving carbon-to-carbon unsaturated bonds with polyvinylchloride or its copolymerisation products
-
- 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
- D06N3/14—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 polyurethanes
-
- 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
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
- Y10T428/24438—Artificial wood or leather grain surface
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- 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.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2369—Coating or impregnation improves elasticity, bendability, resiliency, flexibility, or shape retention of the fabric
- Y10T442/2377—Improves elasticity
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- 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.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/608—Including strand or fiber material which is of specific structural definition
- Y10T442/614—Strand or fiber material specified as having microdimensions [i.e., microfiber]
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- 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.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
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- 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.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
- Y10T442/64—Islands-in-sea multicomponent strand or fiber material
Definitions
- the present invention relates to a base material for artificial leather in which a polymer elastic body is contained inside a nonwoven fabric composed of ultrafine fiber bundles.
- natural leather that has been crushed for apparel uses a synthetic leather with silver that has a soft texture and a soft texture that has no resilience, and has a fine crease, and a fine surface touch.
- the present invention relates to a base material for artificial leather that can be used for producing nubuck-like artificial leather having an elegant lighting effect.
- the conventional method for producing artificial leather including an ultrafine process is generally as follows: (1) a process of stapling ultrafine fiber-generating fibers composed of two types of polymers with different solubility; (2 ) Web using a card, cross wrapper, random weber, etc., (3) Entangling non-woven fabric by interlacing fibers by needle punch, etc., (4) Polymer elastic body represented by polyurethane (5) A step of removing one component in the ultrafine fiber-generating fiber to form an ultrafine fiber. There is also a method in which step (4) and step (5) are performed in the reverse order. By these methods, a flexible artificial leather made of ultrafine fibers can be obtained.
- ultra-fine long-fiber nonwoven fabric an ultra-fine fiber generating long fiber (hereinafter sometimes referred to as a composite long fiber) composed of two or more incompatible polymers is converted into a non-woven fabric, and then the ultra-fine fiber generating type A method in which long fibers are peeled and divided in the length direction at the interface of the polymer to make them ultrafine is mainly used.
- the resulting ultra-thin fiber non-woven fabric is mainly used for the production of silver-finished artificial leather, and to obtain an ultra-thin fiber non-woven fabric that can be applied to suede-like artificial leather. Was difficult.
- Patent Document 3 a silver-tone artificial leather using a long-fiber nonwoven fabric has been proposed (see, for example, Patent Document 3).
- Patent Document 3 long fibers are actively cut when they are entangled by a needle punch, and the cut ends of 5 to 100 pieces / mm 2 of fibers are present on the nonwoven fabric surface. It is described that the distortion that occurs characteristically in the entanglement process is eliminated.
- there are 5 to 70 fiber bundles per lcm width that is, the number of fibers oriented in the thickness direction by the needle punch is equal to Equivalent to 5 to 70 per lcm width).
- the total area occupied by the fiber bundle is 5 to 70% of the cross-sectional area in an arbitrary cross-section orthogonal to the thickness direction of the long-fiber nonwoven fabric.
- the proposed long fiber nonwoven fabric structure is used. In order to obtain the structure, it is necessary to cut a considerable number of long fibers. Therefore, the advantage of long fibers, that is, the contribution to the non-woven fabric strong physical properties due to the continuity of the fibers is remarkably reduced, and the characteristics of the long fibers cannot be fully utilized.
- Patent Document 1 Japanese Patent Publication No. 63-5518 (pages 2 to 4)
- Patent Document 2 Japanese Patent Laid-Open No. 185777 (2-3 pages)
- the object of the present invention is that various combinations of ultrafine fibers and polymer elastic bodies are possible, and it has a soft feeling without repulsion like a natural leather sheep and a texture with a waist, and a fine folded fold.
- a base material for artificial leather that can produce artificial leather with silver, suede-like or nubuck-like artificial leather with fine and powerful surface touch and elegant lighting effect, and a method for producing the same It is to provide.
- fiber bundles oriented in the thickness direction exist in the range of 75 to 300 per lcm width.
- the fiber bundles oriented in the thickness direction is present in the range of lmm 2 30 to 800 present per
- the present invention further includes a silver-tone artificial leather obtained by forming a coating layer on at least one surface of the aforementioned artificial leather substrate, and at least one surface of the aforementioned artificial leather substrate.
- the present invention relates to a suede-like artificial leather that is brushed.
- the present invention further provides (1) a step of using an ultrafine fiber-generating fiber capable of generating ultrafine fibers having an average single fineness of 0.5 decitex or less as a fiber web;
- a brush belt is disposed so that a brush tip is in contact with at least one surface of the fiber web, and the fiber web is needle punched while gripping the ultrafine fiber generating fiber protruding from the fiber web in the brush. And obtaining the entangled nonwoven fabric;
- the present invention relates to a method for producing a base material for artificial leather, comprising a step of converting the ultrafine fiber-generating fiber into a fiber bundle of ultrafine fibers having an average single fineness of 0.5 dtex or less.
- FIG. 1 is an electron micrograph (60 times) of an arbitrary cross section parallel to the thickness direction of a silver-tone artificial leather comprising the artificial leather substrate of the present invention. It shows how the fiber bundles in the nonwoven fabric are oriented in the thickness direction.
- FIG. 3 is a side view of an example of a velor needle device used in the present invention.
- the ultrafine fiber constituting the base material for artificial leather of the present invention is a composite fiber (ultrafine fiber generating fiber) composed of at least two types of spinnable polymers having different chemical or physical properties. It is a fiber obtained by extracting and removing at least one kind of polymer at an appropriate stage before or after impregnation with an elastic body.
- ultrafine fiber-generating fibers include composite fibers such as sea-island-type cross-section fibers, multi-layer laminate-type cross-section fibers, and radiation-type laminate-type cross-section fibers manufactured by a chip blend (mixed spinning) method, a composite spinning method, and the like.
- the sea-island cross-section fibers are preferred in terms of the uniformity of ultrafine fibers, with less fiber damage during needle punching.
- the island component polymer of the sea-island type cross-sectional fiber is not particularly limited, but is polyester such as polyethylene terephthalate (PET), polytrimethylene terephthalate (PTT), polybutylene terephthalate (PBT), polyester elastomer, etc.
- Resin nylon 6, nylon 66 Polyamide resins such as nylon 610, nylon 12, aromatic polyamide, polyamide elastomer, and the like, and fiber-forming polymers such as polyurethane resins and polyolefin resins are suitable.
- polyester resins such as PET, PTT, and cocoon are particularly preferable from the viewpoint of the feel of the final product and practical performance because they are easily heat-shrinkable.
- the melting point of the island component polymer is preferably 160 ° C. or more from the viewpoint of shape stability and practicality.
- a fiber-forming crystalline resin having a melting point of 180 to 2500C is more preferable.
- fusing point is mentioned later.
- the resin constituting the ultrafine fiber may contain colorants such as dyes and pigments, ultraviolet absorbers, heat stabilizers, deodorants, fungicides, and various stabilizers.
- the sea-component polymer of the sea-island type cross-sectional fiber is not particularly limited, but is different from the island-component polymer in solubility or decomposability and has a low affinity with the island component and melts under spinning conditions.
- Polymers having a viscosity less than that of the island component polymer or a surface tension less than that of the island component polymer are preferred.
- at least one kind selected from polymers such as polyethylene, polypropylene, polystyrene, ethylene propylene copolymer, ethylene vinyl acetate copolymer, styrene ethylene copolymer, styrene acrylic copolymer, and polybutyl alcohol resin.
- the polymer is used as a sea component polymer. It is possible to produce a base material for artificial leather without using chemicals, etc., and considering the spinning properties, needle punch characteristics, environmental pollution, ease of dissolution and removal of sea-island cross-section fibers, and the like, sea component polymers It is preferable to use a water-soluble thermoplastic polybutyl alcohol resin (PVA resin).
- PVA resin water-soluble thermoplastic polybutyl alcohol resin
- the viscosity average degree of polymerization of the PVA resin (hereinafter simply referred to as the degree of polymerization) is preferably from 200 to 500, more preferably from 230 to 470 force S, and even more preferably from 250 to 450.
- the degree of polymerization is 200 or more, it can be stably combined with an island component polymer having a moderately high melt viscosity.
- the degree of polymerization is 500 or less, the melt viscosity is not too high and discharge from the spinning nozzle is easy. Also, by using a so-called low polymerization degree PVA having a polymerization degree of 500 or less, dissolution in hot water can be accelerated.
- the saponification degree is S preferably from 90 to 99 ⁇ 99 mole 0/0 force of the PVA-based resin, 93-99.
- Ri 98 mole 0/0 Gayo Preferably, from 94 to 99.97 Monore 0/0 force S further preferably, from 96 to 99.96 Monore 0/0 force S particularly preferably Rere.
- the degree of saponification is 90 mol% or more, melt spinning can be carried out without gelling, and the biodegradability is also good. Furthermore, even when it is modified with a copolymerization monomer, which will be described later, it is possible to obtain a suitable composite fiber in which water solubility does not decrease. PVA with a saponification degree greater than 99.99 mol% is difficult to produce stably
- the PVA resin used in the present invention has biodegradability, and is decomposed into water and carbon dioxide when activated sludge treatment or soil is buried.
- the activated sludge process is preferred for the treatment of PVA-containing waste liquid obtained by dissolving and removing PVA resin.
- the waste liquid containing PVA is continuously treated with activated sludge, it is decomposed in 2 days to 1 month. Also, since the PVA resin has low combustion heat and a small load on the incinerator, the PVA-containing waste liquid can be dried to incinerate the VA resin.
- the melting point (Tm) of the PVA resin is 160 to 230 ° C force S, preferably 170 to 227 ° C force S, more preferably 175 to 224 ° C, and 180 to 220 ° C. Especially preferred.
- the melting point is 160 ° C. or higher, the crystallinity is sufficient, good fiber strength is obtained, the thermal stability is good, and fiberization is easy.
- melt spinning can be performed at a low temperature, and the difference between the spinning temperature and the decomposition temperature of the PVA resin can be increased, so that the composite fiber can be stably produced. it can.
- the melting point is measured by the method described later.
- the PVA-based resin can be obtained by canning a polymer mainly composed of a bull ester unit.
- the bull compound monomers for forming the bull ester unit include formic acid bull, acetic acid bull, propionate bull, valelic acid bull, strong purinate bull, lauric acid bull, vinyl stearate, benzoate bull, and bivalic acid. Examples thereof include bure and versatic acid bulle, and butyl acetate is preferred because the production of PVA resin is easy.
- the PVA-based resin is a modified PVA in which a copolymer unit is introduced even if it is a homopolymer.
- modified PVA is preferred from the viewpoint of melt spinnability, water solubility, and fiber properties.
- the comonomer include ⁇ -olefins having 4 or less carbon atoms such as ethylene, propylene, 1-butene, and isobutene, methylbinoleatenole, and ethinolevy from the viewpoints of copolymerizability, melt spinnability, and water solubility.
- the content of copolymerized units is preferably 1 to 20 mol% of all structural units in the modified PVA. 4 to 15 mol% is more preferred 6 to 13 mol% is more preferred.
- the copolymerized unit is an ethylene unit, the fiber properties are improved, and ethylene-modified PVA is particularly preferable.
- the ethylene unit content is 4 to 15 Monore 0/0 force S Preferably, 6: 13 mole 0/0 is more preferable.
- the PVA-based resin is produced by a known method such as a bulk polymerization method, a solution polymerization method, a suspension polymerization method, or an emulsion polymerization method.
- a bulk polymerization method or a solution polymerization method in which polymerization is performed without solvent or in a solvent such as alcohol is usually employed.
- the alcohol used as the solvent for the solution polymerization include lower alcohols such as methyl alcohol, ethyl alcohol, and propyl alcohol.
- the initiator include a, a′-azobisisobutyronitrile, 2,2′-azobis (2,4-dimethylvaleronitrile), benzoyl peroxide, and n-propyl peroxycarbonate.
- Known initiators such as zo initiators and peroxide initiators may be mentioned.
- the polymerization temperature is not particularly limited, but a range of 0 to 150 ° C is appropriate.
- the fiber web composed of the composite fiber containing the PVA-based resin removing component and the heat-shrinkable resin as the ultrafine fiber forming component is bulky, rough curing of the nonwoven fabric due to fiber damage hardly occurs during needle punching.
- the PVA resin is plasticized to some extent. If the composite fiber is shrunk by heat treatment in this state, the nonwoven fabric can be easily and stably densified.
- the densified non-woven fabric is impregnated with a water-based emulsion of a polymer elastic body at a low temperature so that the PVA resin does not dissolve in water, and then the PVA resin is dissolved and removed with water to make the composite fiber extremely fine.
- the ultrafine fiber generating fiber is a sea-island cross-section fiber
- the content of the sea component in the fiber is preferably 5 to 70% by mass, more preferably 10 to 60% by mass. More preferably, it is 15 to 50% by mass.
- the content ratio is 5% by mass or more, the spinning stability of the composite fiber is good, the amount of the removal component is sufficient, and a sufficient amount of voids are formed between the ultrafine fiber and the polymer elastic body. It is preferable because an artificial leather having good flexibility can be obtained.
- the content is 70% by mass or less, it is possible to avoid the disadvantage that a large amount of the elastic polymer is required to stabilize the form of the artificial leather because the amount of the removed component is too large.
- the amount of water added for plasticizing the PVA resin may not be significantly increased. Therefore, less heat is needed for drying and productivity is improved. Furthermore, there is no phenomenon that the shrinkage is insufficient or the shrinkage state is significantly different depending on the location, which is preferable in terms of quality stability.
- an ultrafine fiber-generating fiber obtained by spinning and drawing to a desired fineness is an arbitrary fiber after crimping. It may be cut into a long length and stapled, and the obtained staple may be formed into a fiber web using a card, a cross wrapper, a random weber or the like.
- a suction device such as an air jet nozzle is used to take up 1000 to 6000 m / min so as to obtain the desired fineness. After pulling and thinning with high-speed air at a speed corresponding to the speed, it is deposited on a collection surface such as a mobile net while opening. If necessary, a long fiber web can be obtained by subsequently pressing the long fibers partially to stabilize the form.
- a method for producing a long fiber web has a production advantage that a series of large equipment such as a raw cotton feeding device, a fiber opening device, and a card machine, which are essential for the short fiber web production method, is not required.
- the obtained long fiber nonwoven fabric and the base material for artificial leather using the same are composed of continuous fibers having high continuity
- the short fiber nonwoven fabric and the artificial material using the same which have been conventionally used in physical properties such as strength, are used.
- the basis weight of the long fiber web is preferably 20 to 500 g / m 2 from the viewpoints of handleability and quality stability.
- the fineness, fiber length, crimped state, and the like are limited to ranges suitable for devices such as a fiber opening device and a card machine. For example, the fineness is constrained to 2 dtex or more, and 3 to 6 dtex is generally adopted in consideration of stability.
- the restriction by the device is basically a fineness of about 0.5 dtex or more, and even if considering the handleability in the subsequent process, select a wide range of force from 1 to 10 dtex. be able to.
- the average single fineness of the ultrafine fiber-generating long fibers is preferably 1 to 5 dtex from the viewpoint of physical properties and texture of the obtained artificial leather substrate. Further, it is preferable to set the fineness, the cross-sectional shape, the content ratio of the removal component, etc. of the ultrafine fiber-generating fiber so as to obtain an ultrafine fiber having an average single fineness of 0.0003-0.5 dtex.
- a fiber web (preferably a fine fiber generation type) is obtained by superimposing a plurality of fiber webs, preferably long fiber webs obtained in this manner, as necessary, and entanglement treatment including needle punching described below.
- the fiber is entangled with each other while the fibers are oriented in the thickness direction without cutting the fiber as much as possible to obtain an entangled nonwoven fabric.
- the brush belt 4 is disposed so as to be in contact with one surface (raised surface) of the fiber web 3, and the force on the opposite surface (punching surface) is used as a needle punching machine.
- a method of punching a needle 5 having a large number of one or more barbs planted on the needle board 2 is adopted as at least a part of the needle punching process.
- the punching at least one perb of each needle is punched at such a depth that it penetrates the fiber web 3, and the fibers protruding from the fiber web are held in the brush of the brush belt 4.
- the brush belt 4 is formed by a brush longer than the protruding length of the fiber protruding in the form of an internal force loop on the endless belt.
- the tip of the brush is the fiber web.
- the fiber web 3 is arranged so as to move in the same direction while being in contact with the raised surface 3.
- the velor needle punching is adopted as a part of the needle punching not only by the formation of the loop-like raised layer 6 but the ultrafine fiber generating fiber inside the fiber web is highly efficient in the thickness direction. This is for orientation. Therefore, normal needle punching using a metal plate (hereinafter referred to as a bed plate) provided with a hole for penetrating the needle instead of the brush belt may be performed before or after the bellow needle punching, You can also apply the same velor needle punching to the side force of the looped raised surface.
- a bed plate provided with a hole for penetrating the needle instead of the brush belt
- nonwoven fabric in which fibers are intertwined by bringing the raised fibers back into the nonwoven fabric by subjecting the looped raised surface after velor needle punching to normal needle punching and further bellow needle punching.
- velor needle punching is performed on both sides, looped raised fibers generated by the first velor needle punching can be converted into fibers oriented in the thickness direction inside the nonwoven fabric by the next velor needle punching. Therefore, it is possible to obtain a nonwoven fabric with a higher degree of orientation in the thickness direction of fibers in the nonwoven fabric with higher efficiency.
- the shape of the needle suitably used in the velor needle punching can be selected from the intermediate force of a felt needle having a shape generally employed as long as needle breakage and fiber damage do not occur.
- the number of perbs is:! ⁇ 9 is preferred, and 3 perbs are used at the top of the triangular blade cross-section, and the tip force is the same distance to the crown needle. This is preferable because the fibers can be oriented in the thickness direction with less punching.
- the punching depth is such that the first perb reaches the depth of preferably 3 mm or more, more preferably 5 mm or more from the brush surface, that is, the tip of the brush. Is preferably adopted.
- Velor needle punching density determined by the number of needles per unit area of the needle board and the number of times the needles are pierced into the fiber web, that is, the need per unit area
- the number of stabs (P / cm 2 ) indicates the fineness of the fibers contained in the fiber web to be treated, the basis weight of the fiber web, the shape of the needle used, the physical properties, the apparent density, and the thickness of the target entangled nonwoven fabric. It is preferable to select from the range of 200 to 1000 P / cm 2 depending on the fiber orientation state in the direction.
- the velor needle punching density is within the above-mentioned range, it is easy to obtain the orientation state of the fiber described later, which is the object of the present invention, and the geometric pattern by a large number of fine holes formed by the pierced needle, that is, the needle This is preferable because marks are not easily generated. It is also preferable to select a needle shape in which this needle mark is difficult to form.
- the apparent density of the entangled nonwoven fabric obtained as described above is preferably 0.:! To 0.6 g / cm 3 .
- the entangled non-woven fabric is heat-treated by the method described below, and the entangled non-woven fabric is subjected to area shrinkage by utilizing the shrinkage ability of the fiber to obtain a dense fiber entangled structure that cannot be obtained only by the entanglement treatment. preferable.
- the apparent density is preferably in the above range.
- the apparent density is more preferably in the range of 0.:! To 0.4 g / cm 3 , and still more preferably in the range of 0.13 to 0.2 g / cm 3 .
- Each apparent density is calculated by calculating the mass per unit area by measuring the mass of the entangled nonwoven fabric cut into a certain area, and then calculating the mass per unit area. The thickness was measured with a load of 0.7 gf / cm 2 applied to the surface of the film, and the mass per unit area was divided by the thickness.
- the entangled nonwoven fabric after velor needle punching or after area shrinkage treatment is heat-shrinked with hot water or steam to be densified. It is also preferable to do.
- a sea-island composite fiber in which the sea component is the PVA resin is used as the ultrafine fiber generating fiber
- 5% by mass or more of water of the PVA resin is applied to the entangled nonwoven fabric, and the relative humidity
- a method of heat shrinking in an atmosphere of 75 to 95% is preferable. More preferably, it is carried out in an atmosphere with a relative humidity of 90 to 95% by applying water of 10% by mass or more of the PVA resin.
- the shrinkage treatment is preferably performed at an atmospheric temperature of 60 to 95 ° C. in terms of easy management on equipment and the ability to impart high shrinkage to ultrafine fiber-generating fibers.
- the amount of water applied is 5% by mass or more, the sea component (PVA resin) of the ultrafine fiber-generating fiber is sufficiently plasticized, and the island component sufficiently shrinks.
- the relative humidity is 75% or more, it is possible to prevent the applied water from quickly drying and hardening the sea component, and to obtain sufficient shrinkage.
- the upper limit value of water to be applied is not particularly limited, but in order to prevent the dissolved PVA resin from contaminating the process and to improve the drying efficiency, 50% by mass or less of the PVA resin is required. preferable.
- the amount of water referred to in the present invention is a value based on the amount of PVA-based resin in the entangled nonwoven fabric after being allowed to stand for 24 hours in a standard state (23 ° C, 65% RH). .
- Examples of the water application method include a method of spraying water on the entangled nonwoven fabric, a method of applying water vapor or mist-like water droplets to the entangled nonwoven fabric, and a method of applying water to the surface of the entangled nonwoven fabric.
- a method of applying water vapor or mist-like water droplets to the entangled nonwoven fabric is particularly preferred.
- the temperature of the water to be applied is preferably a temperature at which the PVA resin does not substantially dissolve.
- heat shrink treatment may be performed in an atmosphere with a relative humidity of 75% or more, or heat shrink treatment may be performed simultaneously with the application of water.
- the entangled nonwoven fabric was impregnated with a solution of a polymer elastic body such as polyurethane or an emulsion solution to coagulate the polymer elastic body. Thereafter, it is preferable to remove one component in the ultrafine fiber generating fiber such as the sea-island type composite fiber and convert it into an ultrafine fiber bundle to obtain a base material for artificial leather.
- Ultrafine fiber generation type After the fiber has been made ultrafine, an impregnation / solidification step of the polymer elastic body may be performed. In this case, since a site where the polymer elastic body and the ultrafine fiber are bonded is generated, there is an advantage that the shape stability of the base material for artificial leather can be improved with a very small amount of the polymer elastic body.
- the method of applying the water-based emulsion of the polymer elastic body is not particularly limited, and a conventionally known immersion is known. It can be applied by a dipping method, a spray method, a coating method or the like.
- a method of applying a water-based emulsion to a surface opposite to the densified surface of the entangled nonwoven fabric and allowing it to penetrate is preferable in order to obtain a surface that does not contain a polymer elastic body.
- the applied polymer elastic body is subjected to a hydrothermal treatment at 70 to 100 ° C or a steam treatment at 100 to 200 ° C, or a dry method in which heat treatment is performed in a drying apparatus at 50 to 200 ° C.
- it is solidified by a dry method.
- the polymer elastic body concentration in the aqueous emulsion solution is preferably 3 to 40% by mass.
- the amount of the polymer elastic body to be impregnated is preferably 1 to 40% by mass, more preferably 3 to 25% by mass in terms of solid content, with respect to the mass of the nonwoven fabric after the ultrafine treatment. It is. Within the above range, the ultrafine fibers (fiber bundles) are sufficiently fixed, bent creases, morphological stability and surface smoothness are good, the texture is cured, and the elastic properties of the polymer elastic body are The low resilience flexibility of natural leather that does not appear strongly is obtained.
- Examples of the polymer elastic body include poly salt cellulose, polyamide, polyester, polyester ether copolymer, polyacrylate copolymer, polyurethane, neoprene, styrene butadiene copolymer, silicone resin, polyamino acid, polyamino acid.
- Examples thereof include synthetic resins such as polyurethane copolymers, natural polymer resins, and mixtures thereof. If necessary, pigments, dyes, crosslinking agents, fillers, plasticizers, stabilizers, etc. may be added. Since a soft texture can be obtained, polyurethane or a mixture of this and other resins is preferably used.
- the removal component such as PVA resin is extracted and removed from the ultrafine fiber generating fiber with water to form a fiber bundle of ultrafine fibers.
- a dyeing machine such as a liquid flow dyeing machine or jigger, or a scouring power machine such as an open soaper is not limited to these.
- the water temperature of the extraction bath is preferably selected from the range of 80 to 95 ° C. and the extraction time of 5 to 120 minutes in consideration of the density of the nonwoven fabric and the component ratio of the ultrafine fiber generating fibers. It is preferable to extract and remove most or all of the removed components by immersing the nonwoven fabric impregnated with the polymer elastic body in an extraction bath and then repeating the operation of squeezing water several times.
- the average single fineness of the obtained ultrafine fibers is preferably 0.0003 to 0.5 dtex, more preferably 0.005 to 0.35 dtex, and more preferably 0.001 to 0.2 dtex. Masle. flat If the average fineness is 0.0003 dtex or more, the nonwoven fabric structure can be prevented from being crushed and unnecessarily increased in density, and a light and flexible base material for artificial leather can be obtained.
- the suede-like artificial leather obtained from the artificial leather base material has good color developability. It is preferable that the average single fineness is 0.5 dtex or less, since a base material for artificial leather having flexibility without rebound, and a silver-tone artificial leather excellent in surface smoothness and fineness of folded folds can be obtained. .
- the fineness of the fiber bundle of ultrafine fibers is usually 0.25 to 5 dtex, and one fiber bundle usually contains 4 to: 10,000 ultrafine fibers
- the apparent density of the base material for artificial leather obtained as described above is 0.35-0. From the point that it reproduces the fullness of natural leather and has flexibility. 65g / cm 3 force, 0.40 ⁇ 0.55g / cm 3 girls dress.
- fibers are highly oriented in the thickness direction by velor needle punching.
- velor needle punching By such fiber orientation, it is possible to obtain an effect that the nonwoven fabric is densified and filled with a polymer elastic body having a continuous warming force.
- the effect of velor needle punching is particularly remarkable when the long fiber nonwoven fabric is entangled.
- the orientation of the fibers obtained by needle punching in the thickness direction is maintained by the resistance due to crimp, but since long fibers are straight fibers with no crimp, Since resistance is low, it becomes difficult to maintain the orientation of the fiber in the thickness direction.
- the long fibers protruding from the surface of the nonwoven fabric by needle punching are efficiently held in the brush of the brush belt, it is possible to effectively maintain the orientation of the long fibers inside the nonwoven fabric in the thickness direction.
- coarse bent folds with less loose fibers are likely to appear in the long-fiber nonwoven fabric structure.
- the fiber bundle is highly oriented in the thickness direction, and the deformation of the front and back of the nonwoven fabric is united, so the effect of reducing the occurrence of coarse bending wrinkles becomes significant. Further, even when the content of the elastic polymer contained in the entangled nonwoven fabric is small, the effect of reducing the generation of coarse bent wrinkles is excellent.
- the above-mentioned effects obtained by the entanglement treatment by velor needle punching are as follows: This is achieved by a characteristic fiber orientation state satisfying the conditions (1) and (2). That is, in an arbitrary cross section parallel to the thickness direction of the nonwoven fabric forming the artificial leather base material, the fiber bundles oriented in the thickness direction are perpendicular to the thickness direction (parallel to the surface of the artificial leather base material). It exists in the range of 75 to 300, preferably 100 to 270, more preferably 120 to 250 per minute lcm (condition (1)). If condition (1) is satisfied, a leather-like artificial leather with a fine crease will be obtained. Is obtained. In addition, the softness and firmness without rebound of natural leather sheep are obtained.
- any section perpendicular to the thickness direction of the nonwoven fabric 30 to 800 pieces cross section lmm 2 per fiber bundles oriented in the thickness direction, is favored properly It exists in the range of 100 to 750, more preferably 150 to 700 (condition (2)). If condition (2) is satisfied, a silver-tone artificial leather with a fine crease will be obtained, and a fine surface touch will give an elegant lighting effect and a suede tone with an excellent nubuck feeling. Artificial leather is obtained. In addition, a natural leather sheep-like feeling of resilience, softness and a soft texture can be obtained.
- the nonwoven fabric structure satisfying the conditions (1) and (2) can be obtained by entanglement treatment by the above-described velor needle punching. It is impossible to obtain by only normal needle punching using a bed plate instead of a brush belt.
- velor needle punching as described above, the orientation of the fibers obtained by needle punching in the thickness direction can be efficiently maintained, so a needle that causes less fiber damage and fiber cutting is used.
- a mild condition such as a relatively small number of punches, an orientation state in the thickness direction far exceeding that of normal needle punching can be obtained. Therefore, the surface of the entangled nonwoven fabric has very little fiber cutting in the process of entanglement of the fiber web.
- the average number of cut portions of the ultrafine fiber-generating fiber is 5 pieces / mm 2 or less (including zero), and the strength and elongation of the resulting artificial leather substrate is improved.
- the number of cut portions is preferably 4 pieces / mm 2 or less.
- the number of the fiber bundle cut portions is 5 Zmm 2 or less, preferably 4 Zmm 2 or less (each including zero). A leather substrate is obtained.
- the base material for artificial leather thus obtained is coated with a resin for the surface coating layer under a desired condition by a known method, and further subjected to treatment such as embossing, softening treatment, and dyeing.
- treatment such as embossing, softening treatment, and dyeing.
- by smoothing the surface by heating and melting the surface it is possible to obtain an artificial leather with a silvery or semi-silvered tone.
- a suede or nubuck artificial leather by raising and fluffing the surface and further softening and dyeing if necessary.
- fluffing it is preferable to buff using force sandpaper or a cloth that can use a known method.
- these artificial leather combines the softness of natural leather-like resilience with a soft texture, a dense crease, and a draping property derived from long fibers for clothing, It is suitable as a material for products such as shoes, gloves, bags, baseball gloves, belts, balls or interiors such as sofas.
- FIG. 1 shows an electron micrograph of a cross section parallel to the thickness direction of the base material for artificial leather obtained in Example 1.
- FIG. 1 shows a fiber bundle in which reference numeral 1 is oriented in the thickness direction.
- FIG. 2 shows an electron micrograph of a cross section perpendicular to the thickness direction of the base material for artificial leather obtained in Example 1.
- the circular part indicated by reference numeral 1 shows the cross section of one fiber bundle oriented in the thickness direction.
- Samples (silver-tone artificial leather) were evaluated by the following criteria by five panelists.
- A Soft and non-repulsive texture.
- A There are 0 to 2 buckling rods.
- the saponification degree of the obtained ethylene-modified PVA was 98.4 mol%. Further, the modified PVA was incinerated and then dissolved in an acid, and the sodium content measured by an atomic absorption photometer was 0.03 parts by mass with respect to 100 parts by mass of the modified PVA. In addition, after removing unreacted vinyl acetate monomer after polymerization, methanol solution of polyacetic acid butyl obtained by adding to n-hexane was precipitated, and then reprecipitation purification was performed 3 times after dissolving in acetone. The product was dried under reduced pressure at ° C for 3 days to obtain purified polyacetic acid butyl. The polyacetate bur is dissolved in d6_DMS 0 and is used 80 using a 500 MHz proton NMR iEOL GX-500). When measured by C, the ethylene unit content was 10 mol%.
- the NaOHZ acetic acid unit was 0.5 (molar ratio). After the gelled product was pulverized and allowed to stand at 60 ° C for 5 hours to further proceed with saponification, methanol Soxhlet extraction was performed for 3 days, and then 80 Purified ethylene-modified PVA was obtained by drying under reduced pressure for 3 days at ° C.
- the average degree of polymerization of the purified modified PVA was 330 when measured according to a conventional JIS K6726.
- the 1,2-glycol bond content and the hydroxyl group content of the 3-hydroxyl group of the purified modified PVA were determined by a 5000 MHz proton NMR C EOL GX-500) apparatus, and found to be 1.50 mol% and 83%, respectively. .
- a cast film having a thickness of 10 / im was prepared using a 5% aqueous solution of the purified modified PVA.
- the film was dried under reduced pressure at 80 ° C. for 1 day, and the melting point was measured by the above-mentioned method. As a result, it was 206 ° C.
- the above water-soluble thermoplastic PVA (ethylene-modified PVA) is used as a sea component, polyethylene terephthalate with an isophthalic acid modification degree of 6 mol% is used as an island component, and the number of islands per ultrafine fiber generating fiber is 25.
- the die for melt compound spinning that becomes an island was also discharged at 260 ° C with a mass ratio of sea component / island component 30/70. Adjust the pressure of the ejector so that the spinning speed is 4500 m / min, collect the long fibers with a net, and create a long fiber web with a basis weight of 30 g / m 2 made of ultrafine fiber generating fiber with an average fineness of 2.0 dtex. Got.
- the nonwoven fabric was impregnated with water-based polyurethane emulsion ("Superflex E-4800" manufactured by Daiichi Pharmaceutical Co., Ltd.) by dipping, dried and cured at 150 ° C, and polymer A resin-containing non-woven fabric having an elastic body / ultrafine fiber generating fiber ratio of 6Z94 was obtained.
- the resin-containing non-woven fabric was immersed in hot water at 95 ° C. to dissolve and remove the PVA, thereby obtaining an ultra-fine fiber entangled non-woven fabric (artificial leather substrate).
- the single fineness of the ultrafine fibers was 0.1 decitex.
- Example 1 Twenty long fiber webs used in Example 1 were overlapped by cross-wrapping and sprayed with a needle breakage preventing oil. Next, using a crown needle with a distance of 3 mm from the needle tip to the pub, perform bellows needle punching for a total of 500 PZcm 2 from both sides at a needle depth of 10 mm, and then move the distance from the needle tip to the pub. Using a 1 mm pub needle of 3 mm, a needle punch of 1000 P / cm 2 was alternately carried out from both sides at a needle depth of 8 mm, to obtain a nonwoven fabric entangled with long fibers.
- the long fiber entangled nonwoven fabric was pressed with a hot roll to obtain a nonwoven fabric having a smooth surface with a basis weight of 670 gZm 2 and an apparent density of 0.45 g / cm 3 .
- Water based polyurethane emulsion on the nonwoven fabric Yon (“Superflex E-4800", manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) was impregnated by the dipping method, dried and cured at 150 ° C, and the polymer elastic body / ultrafine fiber generating fiber was 18 / 82 resin-containing non-woven fabrics were obtained.
- the resin-containing non-woven fabric was immersed in hot water at 95 ° C.
- an ultra-thin fiber entangled non-woven fabric artificial leather substrate.
- the single fineness of the ultrafine fibers was 0.08 dtex.
- the resulting silver-coated artificial leather had a soft texture with a soft feeling without repulsion and a dense fold.
- the surface of the base material for artificial leather obtained in Example 1 was brushed with sandpaper to obtain a suede-like artificial leather.
- the resulting suede-like artificial leather is a suede-like artificial leather that combines softness with a feeling of resilience and a soft texture, and has a fine and powerful surface touch and an elegant lighting effect.
- a silver-finished artificial leather was produced in the same manner as in Example 2 except that only needle punching 2 was performed.
- the resulting silver-tone artificial leather had a good texture, but it was crumpled and immediately lacked fullness.
- Table 1 shows the measurement results of Examples 1 and 2 and Comparative Example:!
- Thickness (mm) 1.3 4 1. 2 9 1. 4 1 1. 3 3 1. 2 3 Apparent density (g Z c rn 3 ) 0.4 4 9 0. 4 5 0. 5 1 0. 4 4 0 . 5 8 Artificial leather with silver
- the artificial leather base material of the present invention various combinations of ultrafine fibers and polymer elastic bodies are possible, and there is a soft and waist-like texture that does not have a repulsive feeling like a natural leather sheep.
- it is suitable for the production of artificial leather with silver that has a fine crease and a suede or nubuck artificial leather that has an unprecedented fine surface touch and an elegant lighting effect.
- the artificial leather obtained from the artificial leather base material of the present invention can be applied to leather products such as shoes, balls, furniture, vehicle seats, clothing, gloves, baseball gloves, bags, berets, and bags.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Dispersion Chemistry (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Nonwoven Fabrics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
Claims
Priority Applications (5)
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KR1020077029387A KR101242361B1 (ko) | 2005-06-17 | 2006-06-14 | 인공 피혁용 기재 및 그 제조 방법 |
EP06766694A EP1895044B1 (en) | 2005-06-17 | 2006-06-14 | Base material for artificial leathers and method of producing the same |
CN2006800216141A CN101198742B (zh) | 2005-06-17 | 2006-06-14 | 人造革用基材及其制造方法 |
US11/917,665 US8053060B2 (en) | 2005-06-17 | 2006-06-14 | Base material for artificial leathers and method of producing the same |
JP2007521322A JP4869228B2 (ja) | 2005-06-17 | 2006-06-14 | 人工皮革用基材およびその製造方法 |
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JP2005-178195 | 2005-06-17 | ||
JP2005178195 | 2005-06-17 |
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PCT/JP2006/311925 WO2006134966A1 (ja) | 2005-06-17 | 2006-06-14 | 人工皮革用基材およびその製造方法 |
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US (1) | US8053060B2 (ja) |
EP (1) | EP1895044B1 (ja) |
JP (1) | JP4869228B2 (ja) |
KR (1) | KR101242361B1 (ja) |
CN (1) | CN101198742B (ja) |
TW (1) | TWI422728B (ja) |
WO (1) | WO2006134966A1 (ja) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2011058108A (ja) * | 2009-09-08 | 2011-03-24 | Kuraray Co Ltd | 人工皮革用基材およびその製造方法 |
CN102758358A (zh) * | 2011-04-27 | 2012-10-31 | 三芳化学工业股份有限公司 | 含有复合纤维的人造皮革和其制造方法 |
JP2014005564A (ja) * | 2012-06-22 | 2014-01-16 | Kuraray Co Ltd | 銀付調人工皮革及びその製造方法 |
Families Citing this family (6)
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KR101523394B1 (ko) * | 2007-03-30 | 2015-05-27 | 가부시키가이샤 구라레 | 은 부조 피혁양 시트 및 그 제조 방법 |
KR101712209B1 (ko) * | 2008-06-25 | 2017-03-03 | 주식회사 쿠라레 | 인공 피혁용 기재 및 그 제조 방법 |
US20140230286A1 (en) * | 2013-02-20 | 2014-08-21 | Tracy Ann Paugh | Biodegradable shoe sole with fixed or detachable upper shoe components |
CN105683441B (zh) * | 2013-11-01 | 2018-10-26 | 可乐丽股份有限公司 | 牛巴戈状皮革片及其制造方法 |
CN109661491B (zh) * | 2016-09-14 | 2022-04-19 | 株式会社可乐丽 | 经过染色的人造革基材、立毛状人造革、带有树脂层的人造革、鞋、装饰用片及装饰成型体 |
CN117127408B (zh) * | 2023-09-05 | 2024-06-07 | 浙江聚康科技发展有限公司 | 一种化学机械抛光垫用复合材料及其制备方法和应用 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999011853A1 (fr) * | 1997-08-29 | 1999-03-11 | Teijin Limited | Tissu non tisse et similicuir |
JPH11181632A (ja) * | 1997-12-19 | 1999-07-06 | Kuraray Co Ltd | 極細ポリエステル繊維発生型繊維及びその製造方法 |
JP2000273769A (ja) * | 1999-03-25 | 2000-10-03 | Teijin Ltd | 長繊維不織布およびそれを含む人工皮革 |
JP2001192976A (ja) * | 2000-01-07 | 2001-07-17 | Kuraray Co Ltd | 人工皮革用基材およびその製造方法 |
JP2002317387A (ja) * | 2001-04-18 | 2002-10-31 | Kuraray Co Ltd | 銀付人工皮革及びその製造方法 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59199856A (ja) * | 1983-04-25 | 1984-11-13 | 東レ株式会社 | 不織シ−ト及びその製造方法 |
DE3444763A1 (de) | 1984-12-07 | 1986-06-12 | Oskar Dilo Maschinenfabrik Kg, 6930 Eberbach | Anlage zum herstellen strukturierter textiler velournadelfilzbahnen |
DE69424918T2 (de) * | 1993-10-29 | 2000-10-12 | Kuraray Co., Ltd | Rauhlederartiges Kunstleder |
US6716776B2 (en) * | 1999-05-13 | 2004-04-06 | Teijin Limited | Nonwoven fabric made from filaments and artificial leather containing it |
TW479086B (en) * | 1999-05-19 | 2002-03-11 | Teijin Ltd | Nonwoven fabric made from filaments and artificial leather containing it |
DE10162463B4 (de) | 2001-12-19 | 2006-08-10 | Techtex Gmbh Vliesstoffe | Verwendung eines durch Fadenmaschen oder Fasermaschen verfestigten Vliesstoffes als textilen Träger für Beschichtungen |
KR100534525B1 (ko) * | 2002-02-01 | 2005-12-07 | 주식회사 코오롱 | 저신장성 및 유연성이 우수한 인공피혁용 복합시트 |
TW200413122A (en) * | 2002-08-22 | 2004-08-01 | Teijin Cordley Ltd | Leather-like sheet and process for production thereof |
-
2006
- 2006-06-14 CN CN2006800216141A patent/CN101198742B/zh not_active Expired - Fee Related
- 2006-06-14 EP EP06766694A patent/EP1895044B1/en not_active Expired - Fee Related
- 2006-06-14 JP JP2007521322A patent/JP4869228B2/ja not_active Expired - Fee Related
- 2006-06-14 WO PCT/JP2006/311925 patent/WO2006134966A1/ja active Application Filing
- 2006-06-14 US US11/917,665 patent/US8053060B2/en not_active Expired - Fee Related
- 2006-06-14 KR KR1020077029387A patent/KR101242361B1/ko not_active IP Right Cessation
- 2006-06-15 TW TW95121337A patent/TWI422728B/zh not_active IP Right Cessation
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999011853A1 (fr) * | 1997-08-29 | 1999-03-11 | Teijin Limited | Tissu non tisse et similicuir |
JPH11181632A (ja) * | 1997-12-19 | 1999-07-06 | Kuraray Co Ltd | 極細ポリエステル繊維発生型繊維及びその製造方法 |
JP2000273769A (ja) * | 1999-03-25 | 2000-10-03 | Teijin Ltd | 長繊維不織布およびそれを含む人工皮革 |
JP2001192976A (ja) * | 2000-01-07 | 2001-07-17 | Kuraray Co Ltd | 人工皮革用基材およびその製造方法 |
JP2002317387A (ja) * | 2001-04-18 | 2002-10-31 | Kuraray Co Ltd | 銀付人工皮革及びその製造方法 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011058108A (ja) * | 2009-09-08 | 2011-03-24 | Kuraray Co Ltd | 人工皮革用基材およびその製造方法 |
CN102758358A (zh) * | 2011-04-27 | 2012-10-31 | 三芳化学工业股份有限公司 | 含有复合纤维的人造皮革和其制造方法 |
JP2014005564A (ja) * | 2012-06-22 | 2014-01-16 | Kuraray Co Ltd | 銀付調人工皮革及びその製造方法 |
Also Published As
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TWI422728B (zh) | 2014-01-11 |
US8053060B2 (en) | 2011-11-08 |
EP1895044A1 (en) | 2008-03-05 |
CN101198742A (zh) | 2008-06-11 |
EP1895044A4 (en) | 2010-03-24 |
CN101198742B (zh) | 2010-12-08 |
KR101242361B1 (ko) | 2013-03-14 |
TW200710305A (en) | 2007-03-16 |
EP1895044B1 (en) | 2011-11-30 |
JPWO2006134966A1 (ja) | 2009-01-08 |
US20090087618A1 (en) | 2009-04-02 |
JP4869228B2 (ja) | 2012-02-08 |
KR20080017370A (ko) | 2008-02-26 |
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