WO1996027036A1 - Fil continu en polyester, son procede de production, articles tisses et tricotes a partir dudit fil continu, et procede de production desdits articles - Google Patents
Fil continu en polyester, son procede de production, articles tisses et tricotes a partir dudit fil continu, et procede de production desdits articles Download PDFInfo
- Publication number
- WO1996027036A1 WO1996027036A1 PCT/JP1996/000466 JP9600466W WO9627036A1 WO 1996027036 A1 WO1996027036 A1 WO 1996027036A1 JP 9600466 W JP9600466 W JP 9600466W WO 9627036 A1 WO9627036 A1 WO 9627036A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- polyester
- core
- filament
- discharge hole
- fin
- Prior art date
Links
- 229920000728 polyester Polymers 0.000 title claims abstract description 112
- 239000004744 fabric Substances 0.000 title claims abstract description 55
- 238000004519 manufacturing process Methods 0.000 title claims description 26
- 238000000034 method Methods 0.000 title description 24
- 230000008569 process Effects 0.000 title description 5
- 239000013585 weight reducing agent Substances 0.000 claims abstract description 21
- 239000000835 fiber Substances 0.000 claims description 33
- 208000016261 weight loss Diseases 0.000 claims description 28
- 150000001875 compounds Chemical class 0.000 claims description 25
- 238000000926 separation method Methods 0.000 claims description 24
- 229920000642 polymer Polymers 0.000 claims description 21
- 238000009987 spinning Methods 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 238000009835 boiling Methods 0.000 claims description 9
- 238000002074 melt spinning Methods 0.000 claims description 9
- 239000002344 surface layer Substances 0.000 claims description 7
- 238000009940 knitting Methods 0.000 claims description 6
- 238000007599 discharging Methods 0.000 claims description 5
- 238000009941 weaving Methods 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims 2
- 230000008018 melting Effects 0.000 claims 2
- 239000003513 alkali Substances 0.000 abstract description 17
- 206010016322 Feeling abnormal Diseases 0.000 abstract description 8
- 238000002474 experimental method Methods 0.000 description 22
- -1 polyethylene terephthalate Polymers 0.000 description 12
- 230000000694 effects Effects 0.000 description 11
- 230000009467 reduction Effects 0.000 description 11
- 239000004698 Polyethylene Substances 0.000 description 9
- 229920001223 polyethylene glycol Polymers 0.000 description 9
- 230000004580 weight loss Effects 0.000 description 8
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 7
- 239000004926 polymethyl methacrylate Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000009998 heat setting Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 238000011946 reduction process Methods 0.000 description 4
- 230000008961 swelling Effects 0.000 description 4
- 239000011800 void material Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- MIZLGWKEZAPEFJ-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical group FC=C(F)F MIZLGWKEZAPEFJ-UHFFFAOYSA-N 0.000 description 1
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920005593 poly(benzyl methacrylate) Polymers 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
- 229920000212 poly(isobutyl acrylate) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 230000037351 starvation Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/22—Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
- D02G3/24—Bulked yarns or threads, e.g. formed from staple fibre components with different relaxation characteristics
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/253—Formation of filaments, threads, or the like with a non-circular cross section; Spinnerette packs therefor
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/62—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/38—Oxides or hydroxides of elements of Groups 1 or 11 of the Periodic Table
-
- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2929—Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
-
- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
-
- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
- Y10T428/2969—Polyamide, polyimide or polyester
-
- 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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2973—Particular cross section
Definitions
- Polyester filament yarn Method for producing the same, woven or knitted material, and method for producing the same
- the present invention relates to a special polyester filament yarn, a method for producing the same, a woven / knitted material containing the same, and a method for producing the same. More specifically, a polyester filament yarn in which a part of a core and a fin portion are separated by an alkali weight reduction treatment to form large voids in the filament, a method for producing the same, and a method for producing such a filament.
- TECHNICAL FIELD The present invention relates to a woven or knitted fabric having a bulky and soft feel and a method for producing the same. Background technology
- Polyester filament yarns especially polyethylene terephthalate multifilament yarns, are widely used as clothing materials.However, due to their dense fiber structure, they have a hard feel, Poor ⁇ Has disadvantages.
- Japanese Patent Publication No. 1-12487 and Japanese Patent Publication No. 1-169922 have a wing part separated from a part of the body, and A bulky filament characterized by a free protruding fibrous end formed by breaking a part of the part and a cleavable filament from which the filament can be produced are disclosed.
- the cleavable filament is formed by discharging a polymer from a single discharge hole, a part of the body and the wing are completely integrated, and separation at the boundary between the two is not possible. Extremely difficult. Therefore, as a means for separating and breaking the wing part, a physical means such as a fluid nozzle treatment using a high-pressure compressed air flow, which causes a large energy movement, had to be adopted. Moreover, more than half of the wings separated by physical means as described above are broken. Since it is cut or fibrillated to form free-protruding fiber ends, its appearance is like a spun yarn characterized by fluff, and has the disadvantage of lacking uniformity when woven or knitted .
- Japanese Patent Publication No. 2-38699 discloses a substantially continuous main body portion and a roughened edge which splits from the main body portion and forms a part of a free-projecting fiber end.
- a yarn comprising a synthetic fiber element having a wing portion and having a free end of 10 to 150 per 1 cm of the yarn length is disclosed.
- This yarn is, like the above-mentioned filament, a spun yarn characterized by fluff, and has a wing portion having a rough edge, that is, a fibril-shaped free end. Had the disadvantage of lacking.
- An object of the present invention is to solve the above-mentioned problems of the prior art, to provide a polyester filament yarn in which a core part and a fiz portion are separated and a large void is formed inside, and such a polyester filament yarn. Offers an industrially advantageous method of producing filament yarn.
- Another object of the present invention is to provide a woven or knitted fabric composed of the polyester filament yarn as described above, having a bulky and soft feel and having a uniform appearance.
- the present inventors have conducted intensive studies to achieve the above object, and as a result, have a core part and a plurality of fin parts radially protruding from the core part along the length direction of the core part.
- the core part and the fin part are discharged from separate discharge holes and then joined to adjust the fin part orientation to the core part orientation.
- the fin is predominantly separated by the weight reduction treatment, and as a result, a film having desired characteristics is obtained.
- the present inventors have found that when the above-mentioned polyester is mixed with a compound capable of micro-phase separation with polyester, the effect of separating the fin portion is further promoted, and the present invention has been achieved.
- a core portion and a plurality of fin portions radially protruding from the core portion along the length direction of the core portion, and the following (1) to Polyester filler which simultaneously satisfies the requirement of the formula (3) is subjected to alkali weight reduction treatment, and is characterized in that at least a part of the fin portion is separated from the core portion.
- Laminate yarn is provided.
- SA is the cross-sectional area of a part of the core
- DA is the diameter of the cross-section of the core when the cross-section is a perfect circle
- SB, LB and WB are These indicate the cross-sectional area, maximum length and maximum width of the fin, respectively.
- the polyester polymer melt-discharged through the slit-shaped discharge hole for forming the part is joined in a molten state, cooled and solidified to form a part of the core and a part of the core along the length direction of the part of the core.
- the filament is subjected to a weight reduction process.
- a method for producing the above-mentioned polyester filament yarn is provided.
- polyester woven or knitted fabric containing the above-described polyester filament yarn.
- the polyester polymer melt-discharged through the discharge hole for forming a part of the core is provided with a plurality of radially arranged multi-layers around the discharge hole.
- the polyester polymer melt-discharged through the slit discharge holes for forming the fin portion is joined in a molten state, cooled and solidified to form a core portion and a core portion along the length direction of the core portion.
- a polyester filament consisting of a plurality of fins protruding radially from a part and simultaneously satisfying the requirements of the following equations (1) to (3) is obtained.
- SA is the cross-sectional area of a part of the core
- DA is the diameter of the part when the cross-section of the core is a perfect circle, and the diameter of its circumscribed circle if it is not a perfect circle.
- FIG. 1 is a partially enlarged view of an example of the polyester filament yarn of the present invention viewed from the side, where 4 is a filament yarn, 1 is a part of a core, and 2 and 3 project radially from a part of the core. This indicates that most of the fins are separated from the core.
- FIG. 2A is a plan view showing an example of a discharge hole of a die for producing the filament yarn of the present invention
- FIG. 2B is a plan view showing a modified form of the die of FIG. 2A
- 5 is a plan view.
- Reference numeral 6 denotes a central discharge hole forming a part of the core, and reference numeral 6 denotes a slit-like discharge hole forming a fin portion.
- FIG. 3 is a plan view showing a cross section of the filament discharged from the discharge hole of FIG. 2B.
- BEST MODE FOR CARRYING OUT THE INVENTION In the polyester filament yarn 4 of the present invention illustrated in FIG. 1, the fin portion joined to the core part 1 along the length direction of the core part 1 and projected radially from the core part 1 2 and 3 (shown in cross-section in Fig. 3) are separated from part 1 of the core by alkali reduction treatment, and become independent filaments.
- the fin portion is separated from the core part 1 continuously over the entire length of the filament as shown in the fin portion 2 in FIG. 1, and the fin portion is like an independent filament. It is preferable to be able to behave. However, it is not necessary that all the fins are separated over the entire length of the filament, and there may be a portion that is connected to a part of the core, such as the fin 3. In order to obtain a knitted fabric having good bulkiness, it is preferable that the separation ratio S of the fin portion described later is 30% or more.
- a filament having a cross section as shown in FIG. 3 is used for forming a kerf portion formed by discharging through a die having discharge holes 5 and 6 ′ as shown in FIG. 2B.
- the slit-shaped discharge hole 6 ′ has a smaller cross-sectional area than the circular discharge hole 5 for partially forming the core.
- the fin portion has a higher orientation than the core portion, shrinkage is unlikely to occur when heated in the alkali weight loss treatment, dyeing of woven or knitted fabric, or the finishing process, and a difference in shrinkage from the core portion becomes apparent. Yarn differences and loops are formed, and bulkiness and soft feeling are further improved.
- the fin portion separated from a part of the core it is preferable that generation of free protruding fiber ends (fluff) due to cutting of the fin portion is suppressed as much as possible.
- the generation of the free-protruding weave ends is suppressed as much as possible, as described in the aforementioned Japanese Patent Publication No. 11-24887, in which fuzz is applied to the yarn.
- fuzz is applied to the yarn.
- physical means such as high pressure air blowing nozzles.
- No free protruding fiber ends are formed.It is acceptable that a small percentage of free protruding fiber ends formed accidentally during the spinning or weaving process.
- the method for producing the polyester filament yarn of the present invention will be described in detail.
- the polyester polymer used in the present invention a polyester polymer in which 85 mol% or more, preferably 90 mol% or more of the repeating units are composed of ethylene terephthalate units is preferably used.
- the filament yarn of the present invention is composed of a single polyester polymer, which does not include a conjugate fiber composed of two or more types of polyester polymers. May be composed of two or more polyester polymers.
- the viscosity of the polyester used is not particularly limited, and those having an intrinsic viscosity of 0.5 to 1.1 usually used for melt spinning can be arbitrarily used.
- a small amount of a delustering agent or other various inorganic substances may be added to the above-mentioned polyester as long as the object of the present invention is not impaired.
- a compound having a compatibility parameter of 0.1 to 2.0 represented by the following formula is added to the above polyester in an amount of 0.5 to 5.0% by weight based on the total weight of the polyester, and the mixture is mixed.
- the separation between the fin portion and a part of the core is promoted, and a greater bulkiness and a feeling improving effect can be obtained.
- Va is the molar volume of the polyester (cmSZmol)
- R is the gas constant (JZm01K)
- T is the absolute Temperatures ( ⁇ )
- 5a and (5b) represent the solubility parameters (J i 'cm 3 ') of the polyester and the compound, respectively.
- the difference is less than 0.1, the polyester and the above compound are compatible with each other, and it becomes difficult to separate the fin portion due to the decrease in alkali.
- the value is more than 2.0, the polyester and the above compound are completely phase-separated and the polymer becomes viscous, so that the spinning condition is deteriorated.
- the above-mentioned compounds cause aggregation, and the effect of improving bulkiness is not sufficiently exhibited.
- Specific examples of the above compounds include polyethylene, polypropylene, polyisobutylene, polystyrene, polytetrafluoroethylene, polychlorotetraethylene, polychlorinated trifluoroethylene, polyvinylpropionate, and polybutafluorobutylacrylate.
- a conventionally known method for example, a method of melt-kneading a polyester and the above compound and then forming a pellet, and a method of injecting the above compound into the molten polyester in a melt spinning step.
- a method of blending with a static mixer can be used arbitrarily.
- a plurality of the above-mentioned polyester polymers are arranged radially at intervals around the circular discharge hole 5 for forming a part of the core and the circular discharge hole 5 as shown in FIG. 2A.
- (2 A: 4) A slit with a slit-shaped discharge hole 6 for forming the fin portion was melt-discharged and the discharge material from discharge hole 5 and the discharge material from discharge hole 6 were joined in a molten state. After cooling and solidification, as shown in Fig. 3, a core part with a circular cross section and a radial part from the core part along the length direction of the core part A polyester filament having a protruding fin portion is obtained.
- the spun filament may be subjected to stretching or heat treatment as necessary.
- the number of fin portions is one or seven or more, the voids in the filament formed by the alkali weight reduction treatment become small, and it becomes difficult to provide sufficient bulkiness.
- each fin portion protrudes radially isotropically with a part of the core as a center, but the present invention is not limited to this.
- the dimensions of the circular discharge hole 5 for partially forming the core and the slit-shaped discharge hole 6 for forming the fin portion are not particularly limited, but the cross-sectional area and diameter of a part of the core, and the dimensions of each of the cores.
- the cross-sectional area, maximum length and maximum width of the core portion is required.
- the diameter is D'A (when the cross-sectional shape of the discharge hole 5 is not a perfect circle, D'A is the diameter of the circumcircle of the discharge hole 5.), and the maximum length of the slit opening discharge hole 6 for forming the fin portion And the maximum width are L'B and W'B, respectively, and the shortest distance between discharge holes 5 and 6 on the discharge surface is AB, and D'A, JB, WB and J ) To (iii) are preferably satisfied at the same time.
- the spinning core may be deteriorated or the abrasion of the base may be accelerated.
- the slit-shaped discharge holes for forming the fin portions do not necessarily have to be a uniform rectangle, and as shown in FIG. The width may change continuously.
- the filaments obtained by the above method have the cross-sectional area and diameter of the core as SA and DA, and the cross-sectional area, maximum length and maximum width of each fin, respectively.
- SA and DA the cross-sectional area and diameter of the core
- LB and WB the cross-sectional area, maximum length and maximum width of each fin
- L BZD A that is, when a fin portion whose maximum length is less than 0.6 times the diameter of a part of the core exists, the bulkiness of the filament decreases, and —
- 3.0 and L BZD A that is, if there is a fin portion whose maximum size exceeds 3.0 times the diameter of a part of the core, the fin portion is bent, You can only get a rough and hard feel.
- WBZD A> 14 that is, when there is a fin portion whose maximum width is larger than 1 Z4, which is a direct part of the core, it is difficult to disassemble the fin portion by reducing the amount of force. .
- the denier of the fin portion is preferably 0.8 de or less, more preferably 0.6 de or less. If the denier in the fin portion is excessive, the fine fins cannot be obtained due to the divided fin portion, and if the fin portion has a large area, the drivability due to the division is inferior.
- the fineness of the core is preferably 1 de or more and 4 de or less. If the fineness of the core exceeds 4 de, a sufficient soft feeling cannot be obtained even if the fin portion and the core portion are divided, and the texture of the woven or knitted fabric becomes hard. Further, when the fineness is less than 1 de, even if it has a sharp multi-lobal cross section, the filling action of each other increases, and a large void cannot be obtained effectively.
- Separation of the fins by means of the weight reduction is effective in minimizing the formation of free protruding fiber ends (fluff) due to cutting of the fins and a part of the core.
- the free protruding fiber ends In addition to being formed in a large amount, the fin portion is cleaved in a fibril shape, so that when it is formed into a woven or knitted fabric, it has a spun yarn-like appearance, and the uniformity of the woven or knitted fabric is impaired.
- the above-mentioned reduction treatment may be performed in any state of filament, yarn or woven or knitted fabric. However, it is desirable to carry out the process in the state of a woven or knitted fabric.
- C As alkali treatment conditions, ordinary polyester fiber treatment conditions can be employed as they are. Specifically, an aqueous solution such as sodium hydroxide, hydroxylated lime, sodium carbonate, or carbonated lime is used, and the concentration is 10 to 1001, and the temperature is Once again 4 0 ⁇ 1 8 0 e C, the treatment time may be suitably set in a range of 2 minutes to 2 hours.
- the polyester filament is mixed and entangled with the filaments or with other filaments to form a multifilament, then formed into a woven or knitted fabric, and then subjected to a weight reduction treatment.
- a conventionally known method such as drawing, laying and air entanglement can be arbitrarily adopted.
- 30% by weight or more of the polyester filament (A) and 70% by weight or less of the filament (B) having a boiling water shrinkage rate of 5% or more larger than that of the filament A are mixed by, for example, an air entanglement nozzle. It is particularly preferable that the fibers are woven into a multifilament yarn, then into a woven or knitted fabric, and then subjected to a weight reduction treatment.
- the mixed fiber ratio of the multi-aperture cross section filament A in the mixed fiber multifilament yarn is preferably 30% or more. If it is less than 30%, the soft feeling / draving property is insufficient.
- the filament B mixed with the multi-lobal cross-section filament A has a shrinkage ratio of the boiling water larger than that of the filament A by 5% or more.
- the shrinkage of the woven or knitted fabric causes Filament A to be located mainly on the surface of the yarn.
- the filament B group is mainly located at the center of the yarn, and a yarn with a good feeling can be obtained.
- the filament B preferably has a shrinkage factor of 10% or more in order to impart a crimp structure to the mixed yarn and give the entire woven and knitted fabric a swelling and an elegant texture. . If the content is less than 10%, both the quality and the swelling are insufficient, resulting in a feeling of poor lightness. However, if the shrinkage is too high, the feeling is hardened, so it is preferable to keep the shrinkage at most 50%.
- the shrinkage of boiling water of Filament A is preferably less than 10%. That is, if the filament A becomes a sheath component of the mixed fiber and the fin is divided by the weight reduction treatment, voids are effectively provided on the yarn surface, and the degree of freedom between the yarns is reduced. It becomes woven and knitted with high softness and drape. As a result, the surface of the woven or The woven and knitted fabric is covered by the fins and has a more mellow texture.
- the multilobal cross-section filament A used for the production of the mixed fiber multifilament yarn has self-extensibility. More specifically, it is preferable that the dry heat shrinkage at 160 is 16% or more and less than 0%, and that the woven or knitted fabric has a self-extensibility that is exhibited when subjected to a heat setting treatment.
- the filament A is undesirably lifted up on the surface of the woven or knitted fabric, causing an irritation.
- the texture of the woven or knitted fabric becomes hard, so it is preferably 8 de or less, more preferably l de or more and 7 de or less.
- the cross-sectional shape and denier mix of Filament B are not particularly limited, and it is possible to produce a woven or knitted fabric having its own characteristics. For example, it may be any of round, flat, polygonal, hollow, or multi-portal as in filament A.
- the multifilament multifilament yarn is divided into multi-lobal cross-sectional filaments A for the first time in the alkali weight reduction process.
- the multi-lobal cross section yarn is subjected to a Taslan or air jet treatment at a pressure of pneumatic pressure of 10 to 40 kg Z cm 'to generate split fibers or fluff, giving a soft feeling and a feeling of spanning.
- a woven or knitted fabric is created using a yarn obtained by previously dividing a multi-opening and single-valve cross-sectional filament according to a method known from As a result, the effect of enlarging the space between the ketsui is not obtained. Therefore, according to this method, the swelling and the soft draining property, which is the object of the present invention, cannot be obtained, and problems arise in handling, weaving and knitting due to the fluff floating on the yarn surface. It will be.
- Typical production methods include the following three methods.
- Filament A and Filament B take the undrawn yarns of Filament A and Filament B at an optional spinning speed, and after continuous or once winding, draw them separately at an arbitrary magnification.
- Filament A and Filament B are mixed.
- Filaments A and B can be flat yarns (non-crimped yarns) or latent or actual crimped yarns.
- the filaments A and B are entangled under low tension through an interlace nozzle, a false twist nozzle or a Taslan nozzle.
- the single fiber is turned by the air flow, and the protruding fins repeatedly collide violently, so that the stress concentrates on the fin joint.
- This makes it easier for the alkali to diffuse and penetrate into the joint where the bond is weakened, and the division is easier to proceed.
- a strong fiber-mixing treatment such that the fin portion is divided results in a reduction in the effect of expanding the voids by the fin portion and causes a problem in weaving and knitting.
- a compressed air pressure of 5 kg Z cm 2 or more and 2.5 kg Z cm 2 or less is adopted.
- the second is a method in which melt-spinning is performed from separate or identical spinnerets forming undrawn yarns of filaments A and B, then taken up, continuously or once wound up, then aligned and simultaneously drawn and set. It is.
- Filament A and B may be mixed before drawing or after heat setting.
- filaments A and B are spun from the same spinneret, it is desirable that filament B is designed to have a high draft.
- the third method is to add self-extensibility to filament A.
- melt spinning At the time of melt spinning, it is drawn in a semi-stretched state with a spinning speed of about 2,000 to 4,000 OmZ, then continuously or once wound, stretched at an arbitrary magnification, and further relaxed. Heat treatment produces self-extending filament A. Next, self-extending filament A and filament B are mixed.
- a woven or knitted fabric is produced using the multifilament multifilament yarn thus produced, and through a shrinkage development step, ie, a relaxation step, when a difference in boiling water shrinkage is given to filaments A and B, a high shrinkage property is obtained.
- Filament B expresses the crimp structure, It is possible to obtain a bulkiness in which a higher-order structure is developed.
- the filament A is a self-extended yarn, by performing a heat treatment of 160 or more in a later heat setting step, the filament A is elongated, and the woven or knitted fabric is further entangled. Increase.
- the polyester filament yarn of the present invention is preferably formed into a multifilament yarn, then formed into a woven or knitted fabric, and then subjected to alkali reduction treatment to divide the fin portion.
- the degree of division of the fin due to the reduction of the total force is made higher than that of the center of the multifilament yarn.
- the treatment liquid permeates into the surface layer of the multifilament yarn constituting the woven or knitted fabric, and then penetrates into the center of the multifilament yarn. Therefore, there is a difference in the degree of division of the fin.
- the preferred range of the weight ratio for obtaining the desired woven or knitted fabric in the initial weight reduction process is 10 to 40% by weight. If the content is less than 10% by weight, the fin portion is not sufficiently divided and has a firm texture. Conversely, if the content exceeds 40%, the fin portion is divided at the center of the aggregated yarn similarly to the surface layer. Fins are completely eluted, etc. Tension, waist and bulkiness are lost, and the feel becomes thin and the quality deteriorates.
- the separation rate S of the fin part due to the alkali reduction treatment is 30% or more, and the separation rate S of the fin part of the filament located on the surface layer of the multifilament yarn is located at the center of the multifilament yarn. It is preferable that the separation rate S of the fin portion of the filament is larger than the separation rate S.
- the fin separation ratio S is a value defined by the following equation.
- the filaments located on the surface layer of the multifilament yarn are the total number of multilobal filaments described above. Of the multifilament yarn It means that the distance from the virtual circumscribed circle of the multifilament yarn is short to 30%. In addition, the filament located at the center of the multifilament yarn refers to a filament within a range of 30% from a short distance from the center of the virtual circumscribed circle as described above.
- a cross-sectional view of the filament before weight loss was taken at a magnification of 3,000, and the cross-sectional area (SS) and diameter (DA) of the core and the cross-sectional area of the fin (S ⁇ ) ), Maximum length and maximum width (WB) were determined.
- Melt spinning was carried out for 8 hours continuously, ⁇ when no yarn breakage occurred, ⁇ when single yarn breakage (fuzz) occurred, and ⁇ when breakage occurred.
- the number of separated fins was determined from photographic observations of the filaments that had been subjected to the force reduction treatment at a magnification of 1,000, and the surface of the multi-filament and the fin at the center were determined by the following formula.
- the separation rate S (%) was calculated.
- the bulkiness, softness and drapability of the woven or knitted fabric were comprehensively evaluated on a five-point scale from ⁇ (extremely good) to E (poor).
- solubility parameters (5a, (b) of the polyester and the compound that phase-separated from the polyester into the micro-mouth were determined, and calculated by the following formula.
- Va is the molar volume of the polyester (cm: / mo1)
- R is the gas constant UZmo1K
- T is the absolute temperature.
- K ⁇ a and 5b represent the solubility parameter (J-Zcm; '') of the polyester and the compound, respectively.
- Polyethylene terephthalate containing 0.055% by weight of titanium oxide as an antiquent and having an intrinsic viscosity of 0.64 was placed in a discharge hole with a contour as shown in Fig. 2B (Experiment Nos. 5, 8 to 16).
- the mixture was discharged at 275 ° C from the spinneret equipped with 24 sets, cooled while being joined in the horizontal blowing cylinder while joining the discharged core part and the fin part, and wound up at a speed of 1,000 OmZ.
- the dimensions of the circular discharge hole for forming the core part and the slit-shaped discharge hole for forming the fin portion, the number of slit-shaped discharge holes for forming the fin portion, and the discharge amount of the polymer, etc. was variously changed.
- the number of slit-shaped discharge holes for forming the fin portion is two (Experiment Nos. 2 and 3)
- the ones arranged at 180 ° and 90 ° with the circular discharge hole as the center are used.
- the number of slit discharge holes is 3 to 8 (Experiment No. 4 to 6, 8 to 16)
- the slit discharge holes are isotropically radially centered on the circular discharge hole. Was used.
- the wound filament group was subjected to stretching heat treatment at a magnification of 2.55 times using a stretching machine equipped with a hot roller at a temperature of 90 ° C and a slit heater at a temperature of 150 ° C.
- a multifilament yarn of 54 denier and 24 filaments was obtained.
- the obtained multifilament yarn is formed into a 20-gauge tubular knitted fabric, and the tubular knitted fabric is boiled for 20 minutes in an aqueous solution of sodium hydroxide having a concentration of 40 gZ1 to reduce the total strength.
- a stretching machine equipped with a hot roller at a temperature of 90 ° C and a slit heater at a temperature of 150 ° C.
- a multifilament yarn of 54 denier and 24 filaments was obtained.
- the obtained multifilament yarn is formed into a 20-gauge tubular knitted fabric, and the tubular knitted fabric is boiled for 20 minutes in an aqueous solution of sodium hydroxide having a concentration of
- Table 1 shows the cross-sectional shape and spinning condition of each filament
- Table 2 shows the separation rate of the fin portion and the feeling of the tubular knitted fabric after weight reduction.
- the cross-sectional area (SA) and diameter (DA) of the core, the cross-sectional area (SB :), the maximum length (LB) and the maximum width (WB) of the fin are
- SA cross-sectional area
- DA diameter
- SB maximum length
- WB maximum width
- Experiment No. 5 the same procedure as in Experiment No. 5 was repeated except that a compound that phase-separated into polyester and microsphere was added and mixed, and that the spinning of polyester, the production of multifilament yarn, and the knitting of tubular knitted fabric were performed. Each characteristic was evaluated.
- Table 3 shows the value and amount of the compatibility parameter of the compound added and the spinning condition of each filament, and the separation rate of the fin after alkali reduction treatment and the feeling of the tubular knitted fabric. See Table 4.
- PE polyethylene
- Table 5 shows the shrinkage ratios and mixing ratios of the multifilament A and multifilament B obtained in Experiment Nos. 30 to 32.
- Table 6 shows the hand feeling.
- Table 7 shows the fin separation rate and the texture of the tubular knitted fabric after the weight loss treatment. Table 7 Separation rate of fin (%)
- the polyester multifilament yarn of the present invention has a core part and a fin part separated from each other, a large void is formed inside, and the yarn is bulky.
- the woven or knitted fabric made of such a multifilament yarn has a bulky and soft feel and has an even appearance.
- a multi-opening, single-valve cross-section filament yarn composed of a part of the core and a plurality of fins radially protruding from the core has a remarkable effect of expanding the gap between the single fibers by the tension of the fin.
- this multi-opening filament cross section filament is subjected to weight reduction and the core is partly separated from the fin, the space that had been expanded by the fin before the weight reduction processing became a large fiber. This creates a gap between them.
- the separation of the fin is more remarkable than that in the center, and the cross section of the fin is generally smaller in width and longer than part of the core.
- a soft feeling and good drapability are exhibited.
- fiber voids are mainly provided by the effect of expanding and expanding the fin portion, and bulkiness, tension, and waist are developed.
- the orientation of the fin portion is higher than that of a part of the core, and the bonding strength of the bonding surface is low.
- the fin portion can be easily separated while being pressed down, and a woven fabric having a uniform appearance can be obtained. Therefore, the woven or knitted fabric obtained from the polyester filament yarn of the present invention is suitable for clothing.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Artificial Filaments (AREA)
- Woven Fabrics (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE69614790T DE69614790T2 (de) | 1995-02-28 | 1996-02-28 | Polyester-filomentgarn, verfahren zu seiner herstellung, daraus hergestellte gewebte oder gestrickte erzeugnisse und verfahren zur herstellung derselben |
JP08526153A JP3076372B2 (ja) | 1995-02-28 | 1996-02-28 | ポリエステルフィラメント糸、その製造方法ならびにその織編物およびその製造方法 |
US08/727,432 US5733656A (en) | 1995-02-28 | 1996-02-28 | Polyester filament yarn and process for producing same, and fabric thereof and process for producing same |
EP96904272A EP0758027B1 (en) | 1995-02-28 | 1996-02-28 | Polyester filament yarn, process for the production thereof, woven and knitted fabrics thereof, and process for the production thereof |
KR1019960706050A KR970702941A (ko) | 1995-02-28 | 1996-10-28 | 폴리에스테르 필라멘트사, 그 제조방법과 그 직편물 및 그 제조방법(polyester filament yarn, process for the production thereof, woven and knitted fabrics thereof, and proces for the production thereof) |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3977995 | 1995-02-28 | ||
JP7/39779 | 1995-02-28 | ||
JP4186695 | 1995-03-01 | ||
JP7/41866 | 1995-03-01 |
Publications (1)
Publication Number | Publication Date |
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WO1996027036A1 true WO1996027036A1 (fr) | 1996-09-06 |
Family
ID=26379166
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1996/000466 WO1996027036A1 (fr) | 1995-02-28 | 1996-02-28 | Fil continu en polyester, son procede de production, articles tisses et tricotes a partir dudit fil continu, et procede de production desdits articles |
Country Status (7)
Country | Link |
---|---|
US (1) | US5733656A (ja) |
EP (1) | EP0758027B1 (ja) |
JP (1) | JP3076372B2 (ja) |
KR (1) | KR970702941A (ja) |
DE (1) | DE69614790T2 (ja) |
TW (1) | TW293852B (ja) |
WO (1) | WO1996027036A1 (ja) |
Families Citing this family (8)
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JP3588967B2 (ja) * | 1997-04-03 | 2004-11-17 | チッソ株式会社 | 分割型複合繊維 |
US7014510B2 (en) * | 2001-10-04 | 2006-03-21 | Guide Corporation | Wedge base sealed lamp socket |
AU2003292819A1 (en) * | 2003-01-14 | 2004-08-10 | Teijin Fibers Limited | Polyester fibers having deformed section |
JPWO2005071149A1 (ja) * | 2004-01-08 | 2007-07-26 | 帝人ファイバー株式会社 | ポリエステル異収縮混繊糸およびその製造方法 |
US7560159B2 (en) * | 2004-02-23 | 2009-07-14 | Teijin Fibers Limited | Synthetic staple fibers for an air-laid nonwoven fabric |
KR20100128311A (ko) * | 2008-02-28 | 2010-12-07 | 엠엠티 텍스타일즈 리미티드 | 직물 |
WO2010117908A1 (en) * | 2009-04-06 | 2010-10-14 | University Of Virginia Patent Foundation | Anisotropic reinforcement and related method thereof |
US11060212B2 (en) * | 2016-10-04 | 2021-07-13 | Nike, Inc. | Textiles and garments formed using yarns space-treated with functional finishes |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61207638A (ja) * | 1985-03-11 | 1986-09-16 | カネボウ株式会社 | 不透明性に優れた織物 |
JPS62243848A (ja) * | 1986-04-14 | 1987-10-24 | 東レ株式会社 | 高吸水性織編物 |
JPS63295709A (ja) * | 1987-05-27 | 1988-12-02 | Mitsubishi Rayon Co Ltd | 溶融紡糸口金 |
JPH0233368A (ja) * | 1988-07-22 | 1990-02-02 | Toyobo Co Ltd | 極細不織布の製造方法及びメルトブローノズル |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB652948A (en) * | 1948-08-13 | 1951-05-02 | John D Arcy Henry Hall | Improvements in textile materials |
CA1116363A (en) * | 1977-01-26 | 1982-01-19 | Bobby M. Phillips | Fracturable textile filaments for producing yarns having free protruding ends and process |
US4364998A (en) * | 1981-07-20 | 1982-12-21 | E. I. Du Pont De Nemours And Company | Spunlike yarns |
US4381333A (en) * | 1981-10-02 | 1983-04-26 | Beggs James M Administrator Of | High temperature glass thermal control structure and coating |
WO1987005641A1 (en) * | 1986-03-12 | 1987-09-24 | Burlington Industries, Inc. | Production of polyester fabrics resembling wool |
US5059482A (en) * | 1988-09-13 | 1991-10-22 | Kuraray Company, Ltd. | Composite fiber and process for producing the same |
DE69316700T2 (de) * | 1992-10-13 | 1998-08-27 | Kuraray Co | Faser mit verjüngtem Ende und daraus hergestellte Florware |
-
1996
- 1996-02-28 WO PCT/JP1996/000466 patent/WO1996027036A1/ja active IP Right Grant
- 1996-02-28 US US08/727,432 patent/US5733656A/en not_active Expired - Lifetime
- 1996-02-28 DE DE69614790T patent/DE69614790T2/de not_active Expired - Lifetime
- 1996-02-28 JP JP08526153A patent/JP3076372B2/ja not_active Expired - Fee Related
- 1996-02-28 EP EP96904272A patent/EP0758027B1/en not_active Expired - Lifetime
- 1996-03-21 TW TW085103400A patent/TW293852B/zh not_active IP Right Cessation
- 1996-10-28 KR KR1019960706050A patent/KR970702941A/ko active IP Right Grant
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61207638A (ja) * | 1985-03-11 | 1986-09-16 | カネボウ株式会社 | 不透明性に優れた織物 |
JPS62243848A (ja) * | 1986-04-14 | 1987-10-24 | 東レ株式会社 | 高吸水性織編物 |
JPS63295709A (ja) * | 1987-05-27 | 1988-12-02 | Mitsubishi Rayon Co Ltd | 溶融紡糸口金 |
JPH0233368A (ja) * | 1988-07-22 | 1990-02-02 | Toyobo Co Ltd | 極細不織布の製造方法及びメルトブローノズル |
Non-Patent Citations (1)
Title |
---|
See also references of EP0758027A4 * |
Also Published As
Publication number | Publication date |
---|---|
JP3076372B2 (ja) | 2000-08-14 |
DE69614790D1 (de) | 2001-10-04 |
KR970702941A (ko) | 1997-06-10 |
EP0758027B1 (en) | 2001-08-29 |
EP0758027A4 (en) | 1999-01-07 |
EP0758027A1 (en) | 1997-02-12 |
DE69614790T2 (de) | 2002-05-23 |
US5733656A (en) | 1998-03-31 |
TW293852B (ja) | 1996-12-21 |
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