EP0056907A1 - Verfahren zur Herstellung eines aufgerauhten wildlederartigen Textilgebildes - Google Patents
Verfahren zur Herstellung eines aufgerauhten wildlederartigen Textilgebildes Download PDFInfo
- Publication number
- EP0056907A1 EP0056907A1 EP81306092A EP81306092A EP0056907A1 EP 0056907 A1 EP0056907 A1 EP 0056907A1 EP 81306092 A EP81306092 A EP 81306092A EP 81306092 A EP81306092 A EP 81306092A EP 0056907 A1 EP0056907 A1 EP 0056907A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkali solution
- constituents
- fabric
- raised
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000004744 fabric Substances 0.000 title claims abstract description 83
- 238000000034 method Methods 0.000 title claims abstract description 32
- 238000002360 preparation method Methods 0.000 title claims description 9
- 239000003513 alkali Substances 0.000 claims abstract description 103
- 239000000470 constituent Substances 0.000 claims abstract description 85
- 239000000835 fiber Substances 0.000 claims abstract description 60
- 239000002131 composite material Substances 0.000 claims abstract description 52
- 229920000728 polyester Polymers 0.000 claims abstract description 33
- 229920001515 polyalkylene glycol Polymers 0.000 claims abstract description 11
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 10
- -1 polyethylene terephthalate Polymers 0.000 claims description 30
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 27
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 21
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 21
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 9
- 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 claims description 6
- WSQZNZLOZXSBHA-UHFFFAOYSA-N 3,8-dioxabicyclo[8.2.2]tetradeca-1(12),10,13-triene-2,9-dione Chemical group O=C1OCCCCOC(=O)C2=CC=C1C=C2 WSQZNZLOZXSBHA-UHFFFAOYSA-N 0.000 claims description 4
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 claims description 2
- 238000009987 spinning Methods 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 81
- 229920000642 polymer Polymers 0.000 description 17
- 239000002759 woven fabric Substances 0.000 description 17
- 230000004580 weight loss Effects 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 10
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 9
- 238000002074 melt spinning Methods 0.000 description 8
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000002202 Polyethylene glycol Substances 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 244000137852 Petrea volubilis Species 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 229910001651 emery Inorganic materials 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 3
- 238000009941 weaving Methods 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 229920006240 drawn fiber Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000009981 jet dyeing Methods 0.000 description 2
- 238000009940 knitting Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- QOSTVEDABRQTSU-UHFFFAOYSA-N 1,4-bis(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(NC)=CC=C2NC QOSTVEDABRQTSU-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- SXPWTBGAZSPLHA-UHFFFAOYSA-M cetalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SXPWTBGAZSPLHA-UHFFFAOYSA-M 0.000 description 1
- 229960000228 cetalkonium chloride Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940077386 sodium benzenesulfonate Drugs 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- MZSDGDXXBZSFTG-UHFFFAOYSA-M sodium;benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC=C1 MZSDGDXXBZSFTG-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/14—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyester as constituent
Definitions
- the present invention relates to a process for the preparation of suede-like raised fabrics having extra fine naps. More particularly, the present invention relates to a process for the preparation of suede-like raised fabrics from a polyester composite fiber which consists of constituents easily soluble in an alkali solution and constituents hardly soluble in an alkali solution.
- Polyester composite fibers having polyester constituents containing polyalkylene glycol and/or anionic surfactant as constituents easily soluble in an alkali solution have hitherto been publicly known (See Japanese Patent Application Publication Nos.47532/72, 47533/72 and 13169/73).
- a raised woven fabric is obtained according to the method in which a raised woven fabric is first woven of fibers of islands-in-sea type which consist of polyester (polyethylene terephthalate) copolymerized by 9 mole % 3,5-di(carbomethoxy)sodium benzenesulfonate as sea constituents and another polyester, which is not copolymerized by any other components, as island constituents, and this fabric is then treated continuously in the alkali bath containing alkali of 10 to 20 g/l at 90°C to dissolve the copolymerized polyester constituents to give a raised woven fabric having extra fine naps and consisting
- a raised woven fabric having extra fine naps and comprising polyester not copolymerized by other components was obtained by first weaving a fabric of fibers of islands-in-sea type which consist of a mixture of polyethylene glycol and polyethylene terephthalate as sea constituents and polyethylene terephthalate not copolymerized by any other components as island constituents, then treating this woven fabric with an alkali solution having concentration of 20 g/l of alkali at 98°C for 20 minutes and further with an alkali solution having concentration of 5 g/l at 90°C for 60 minutes, and finally raising the surface of the woven fabric.
- polyester yarns (75 denier/24 filaments), which consisted of constituents easily soluble in an alkali solution and was obtained by melt-spinning and drawing polyethylene terephthalate which contains 4% by weight of polyethylene glycol having molecular weight of 20,000 and 2% by weight of sodium lauryl sulfonate according to the ordinary method
- another polyester yarns (75 denier/24 filaments), which consisted of constituents hardly soluble in an alkali solution and was obtained by melt-spinning and drawing ordinary polyethylene terephthalate.
- the object of the present invention is to provide a process for the preparation of a suede-like raised fabric having extra fine naps, in which comparatively low alkali concentration and compar- tively short time can be accepted as conditions of treatment.
- the present invention is directed to a process for the preparation of a suede-like raised fabric having extra fine naps which comprises (1) producing a polyester composite fiber which consists of constituents easily soluble in an alkali solution and constituents hardly soluble in an alkali solution, said constituents easily soluble in an alkali solution containing 3 to 12% by weight of polyalkylene glycol and/or anionic surfactant and at least 70% by weight of ethylene terephthalate units and said constituents hardly soluble in an alkali solution containing not less than 80% by weight of ethylene terephthalate and/or butylene terephthalate units, (2) preparing a raised fabric by using said polyester composite fibers, and (3) dissolving said constituents easily soluble in an alkali solution from the polyester composite fibers in the raised fabric by treating the raised fabric in an aqueous alkali solution at a temperature of 110°C to 150°C.
- a polyester composite fiber in the present invention is a so-called islands-in-sea type composite fiber, segmental multilayer type composite fiber, etc. in which each of the constituents easily soluble in an alkali solution and each of the constituents hardly soluble in an alkali solution are arranged and distributed independently in the same fiber. And this constituent easily soluble in an alkali solution contains polyalkylene glycol and/or anion active agent equal to 3 to 12% of the whole constituent by weight and at least 70% by weight of the whole constituent consists of ethylene terephthalate units.
- polyalkylene glycol As concrete example of polyalkylene glycol to be used in the present invention, polyoxyethylene glycol, polypropylene glycol, polytetramethylene glycol, and a copolymer of propylene glycol and tetramethylene glycol may be mentioned but not to be limited to them.
- Said anionic surfactant is a surfactant which contains at least one of the alkaline metal salts of any of sulfonic acid, carboxylic acid, and phosphonic acid as a hydrophilic group and has a hydrophobic group of appropriate size in the same molecule. More concretely, such ones as those having the following chemical structures, for instance, may be mentioned but are not limited to them.
- M indicates an alkali metal salt.
- the substantially complete removal by solution of the constituent in the alkali treatment increases the percentage of weight loss of the constituents hardly soluble in an alkali solution.
- the quantity of polyalkylene glycol and/or anionic surfactant contained in the constituents easily soluble in an alkali solution is large, the spinnability and drawability of the polyester fiber are degraded. Therefore, it is desirable to keep the content of polyalkylene glycol and/or anionic surfactant in the range of 3 to 12% by weight, perferably in.the range of 4 to 6% by weight.
- Polyester to be used in the constituents easily soluble in an alkali solution should necessarily contain at least 70% by weight of ethylene terephthalate units to maintain adequate strength required for the meet-spinning, weaving, and knitting processes.
- the constituents easily soluble in an alkali solution may contain one or two kinds of publicly known third constituent such as isophthalic acid, adipic acid, cebacic acid, diethylene glycol, and 1,4-butanediol. Also well-known titanium oxide, antioxidant, etc. may be added thereto.
- an alkalin solution which consist of polyester containing 80% by weight or more ethylene terephthalate units and/or butylene terephthalate units, should not contain any component that will make the constituents more soluble in the alkali treatment than the constituents easily soluble in an alkali solution, but may contain such alkali-resistant polymers as polycarbonate, poly c-capramide, etc. and inactive titanium oxide.
- alkali-resistant polymers as polycarbonate, poly c-capramide, etc. and inactive titanium oxide.
- a polyester composite fiber of the present invention consists of two kinds of fiber forming polymer components, each of which has a different hydrosis rate, i.e. constituents easily soluble in an alkali solution and constituents hardly soluble in an alkali solution, and these two different polymer components are arranged and distributed independently from each other in the same fiber. More particularly, these polymer components are substantially arranged extending along the longitudinal axis of the fiber continuously and present themselves distributed independently from each other when the fiber is viewed cross-sectionally.
- the presence of two or more polymer components distributed independently from each other on the cross-sectional view of the composite fiber means that the polymer components are so distributed that, when one kind of the polymer component, or the constituents easily soluble in an alkali solution, is removed by solution in the alkali treatment of a composite fiber, extra fine filaments comprising other kind of the polymer component, or the constituents hardly soluble in an alkali solution, are formed plurally.
- an islands-in-sea type composite fiber, hollow type or solid type segmental multilayer composite fiber, and sandwich type composite fiber are desirably used in the present invention.
- the sea component should necessarily be the constituents easily soluble in an alkali solution. It is desirable to set the size of a composite fiber in the range of 1 to 10 denier so that the formed extra fine filament resulting from a single constituent hardly soluble in an alkali solution may be 0.01 to 0.5 denier, preferably 0.05 to 0.3 denier. From the viewpoint of spinnability, drawability, and workability for making extra fine filaments, a hollow type segmental multilayer composite fiber is especially desirable for use. In this case, it is preferable to keep the hollow ratio in the range of 1 to 30%.
- a fabric is next prepared by use of polyester composite fibers obtained in the procedure mentioned above.
- What is referred to as a fabric in the present invention means a nonwoven fabric, woven fabric, knitted fabric or a combination thereof.
- Nonwoven fabrics may include all those prepared according to any known methods.
- a raised fabric having extra fine naps of the present invention can be obtained by raising one or both surfaces of a nonwoven fabric with the use of such a raising machine as roller sander machine with sand paper or emery cloth.
- the woven fabric is woven of multifilament yarns or spun yarns, which are prepared from the composite yarns of the present invention, used as warps and/or wefts by use of an ordinary weaving machine.
- One or both surfaces of thus obtained woven fabric may be raised by using a conventional raising machine such as emery raising machine, teazel raising machine, wire raising machine, and roller sander machine with sand paper or emery cloth, to give a raised fabric of the present invention.
- a satin fabric which is composed of a multifilament yarn or spun yarn having a yarn size of 50 to 500 denier consisting of the composite fibers as the weft and a multifilament yarn, mixed filament yarn, spun yarn, or mixed spun yarn having a yarn size of 50 to 300 denier consisting of ordinary fibers as the warp.
- a double faced woven fabric having a satin structure on both surfaces.
- 3- to 5-shaft satin fabrics are especially desirable.
- a crimped textured yarn consisting of such polyester as polyethylene terephthalate or such polyamide as nylon 6 and nylon 66 is particularly preferable.
- the knitted fabric is prepared from a multi- filament yarn or a spun yarn consisting of the composite fibers of the present invention by using a conventional knitting machine.
- a warp knitted fabric it is preferable to use a multi- filament yarn or a spun yarn consisting of the composite fibers as the front yarn and a spun yarn or a mixed spun yarn consisting of the ordinary fibers as the back yarn.
- a circular knitted fabric it is preferable to use a multi- filament yarn or a spun yarn consisting of the composite fibers as yarns for the front portion and back portion or only for the front portion.
- One or both surfaces of the knitted fabric are raised as in the case of the woven fabric to obtain a raised fabric of the present invention.
- the raised fabric obtained in the above is then treated in an aqueous alkali solution under high temperature and high pressure to dissolve and remove the constituents easily soluble in an alkali solution in the polyester composite fibers woven into the raised fabric.
- Polyester yarns which consisted of constituents easily soluble in an alkali solution and was obtained by melt-spinning and drawing polyethylene terephthalate which contained 4% by weight of polyethylene glycol having molecular weight of 20,000 and 2% by weight of sodium lauryl sulfonate according to the ordinary method
- another polyester yarns 75 denier/24 filaments
- constituents hardly soluble in an alkali solution and was obtained by melt-spinning and drawing ordinary polyethylene terephthalate were treated in an aqueous solution of caustic soda in a bath ratio of 1:50 at 130°C.
- caustic soda As the alkalis to be used in the present invention, caustic soda, caustic potash, sodium carbonate, and potassium carbonate may be mentioned but not limited to them; however, caustic soda is most preferable from the functional as well as economical viewpoint. It is desirable to maintain the alkali concentration in the range of 3 g/£ to 30 g/i. When such a quanternary ammonium salt as lauryl dimethylbenzyl ammonium chloride, cetyl dimethylbenzyl ammonium chloride, etc. is used together with alkali, the hydrolysis of the polymer component is accelerated.
- a quanternary ammonium salt as lauryl dimethylbenzyl ammonium chloride, cetyl dimethylbenzyl ammonium chloride, etc.
- the temperature of the treatment by aqueous alkali solution proposed in the present invention at least 110°C is necessary. It is unadvisable to try the treatment at the temperature below 110°C since the alkali consumption and the percentage of weight loss of the constituents hardly soluble in an alkali solution increases. If the treatment temperature is too high, the constituents hardly soluble in an alkali solution become brittle. Therefore, it is advisable to keep the temperature at 150°C at the highest. The temperature, therefore, should preferably be kept in the range of 115 to 140°C. The use of an ordinary high temperature and pressure dyeing machine is advisable for this treatment.
- such a method as to first apply an aqueous alkali solution to the fabric with the use of pads and then treat the fabric with high pressure steam should be avoided.
- the aqueous alkali solution is hardly allowed to move about in the texture of fabric to exercise its function effectively. Accordingly, if the treatment conditions are made satisfactorily enough to remove the constituents easily soluble in an alkali solution, the weight loss of the constituents hardly soluble in an alkali solution would be very great. Therefore, the alkali treatment in the present invention must be carried out in an aqueous alkali solution and it is preferable for the treatment to be accompanied by stirring. It does not matter at all whether the fabric may be pushed out of the aqueous solution (exposed to the atmosphere) once in a while due.to the stirring:
- an elastic polymer to the suede-like raised fabric obtained according to the present invention is an especially preferable mode of treatment, because it remarkably improves the resiliency of the naps and crease resistance of the fabric.
- elastic polymers natural rubber and synthetic elastic polymers such as acrylonitrile-butadiene copolymer, polychloroprene, styrene-butadiene copolymer, polybutadiene, polyisoprene, ethylene-propylene copolymer, acrylate type copolymers, silicone, polyurethane, polyacrylate, polyvinyl chloride, polyvinyl acetate, ethylene-vinyl acetate copolymer, etc. can be used.
- Polyurethane is especially preferable among them all.
- the method which comprises applying an urethane prepolymer, in which a free isocyanate group is blocked, to the fabric and then heating the applied fabric to form polyurethane in the fabric is also preferably employed in the present invention.
- the elastic polymer is applied to the fabric in the form of a solution such as an organic solvent solution, aqueous solution or emulsion of the elastic polymer.
- a solution of the elastic polymer there are a method of impregnating the raised fabric with the solution, a method of coating the raised fabric with the solution and a method of spraying the raised fabric with the solution.
- the raised fabric may be sheared, brushed'or buffed.
- a suede-like raised fabric obtained according to the present invention has very soft, mellow hand and also has a lustrous and beautiful surface and an excellent writing effect similar to natural suede products.
- the fabric has the outstanding resiliency and crease resistance, too. Accordingly, the fabric has a wide variety of uses as clothings such as jackets, jumpers, blazers, skirts, trousers, shorts, slacks, dresses, suits, vests, coats and gloves, or bags, boots, chair covers, etc.
- An undrawn hollow composite fiber having a 3% hollow ratio and a total denier size of 205 denier and a single yarn denier size of 6.8 denier was obtained by composite melt spinning 70 parts of polyethylene terephthalate having the intrinsic viscosity of 0.64 determined at 25°C in orthochlorophenol (as constituents hardly soluble in an alkali solution) and 30 parts of mixed polyethylene terephthalate, having the intrinsic viscosity of 0.64 determined at 25°C in orthochlorophenol, prepared by adding 2 parts of sodium alkyl sulfonate having 15 carbon atoms and 2 parts of polyethylene glycol having molecular weight of about 15,000 to 96 parts of polyethylene terephthalate at the time of its polymerization (as constituents easily soluble in an alkali solution).
- the composite melt spinning was carried out at the discharge temperature of 285°C and withdrawing rate of 1100 m/min. in such a way as to form a composite fiber of hollow, segmental multilayer type, in which said two constituents were distributed alternately side by side in 32 segments arranged radially on a cross-sectional view of the fiber according to the method disclosed in U.S. Patent 4,109,038.
- This undrawn hollow composite fiber was drawn at a drawing ratio of 3.35 with a heating roller at 80°C, made to go through a slit heater kept at 210°C, and wound up to give a drawn fiber of total denier size of 61 denier, having 0.09-denier polyethylene terephthalate components (constituents hardly soluble in an alkalin solution) and 2.04-denier single yarns.
- Three composite fibers thus obtained were then folded into a multifilament yarn of 183 denier/90 filaments.
- a 4-shaft satin fabric having the density of 70 warp ends per inch and 50 filling picks per inch was made of the abovementioned weft yarn and warp yarn.
- the weight of the composite fiber was 56.7% of the whole fabric and the weight of the constituents easily soluble in an alkalin solution was 17%.
- the obtained fabric was made to relax in a hot bath at 98°C for 30 minutes, dried at 120°C for 3 minutes, and treated with an oil mainly consisting of a mineral oil. Thereafter, the fabric had its surface raised fifteen times at a running speed of 30 meters per minute by use of a wire raising machine equipped with a 33-gauge wire fillet. The raised fabric was then preheated at 170°C for 30 seconds with a heat setter of the pin tenter type.
- the raised fabric thus obtained was treated in an aqueous solution of caustic soda (concentration 8 g/£) at 130°C for 20 minutes by using a high pressure jet dyeing machine (Circular VII type: manufactured by Nichiban Seisakusho Co.). The temperature was raised to 100°C in 25 minutes, from 100°C to 130°C in 15 minutes and lowered from 130°C to 100°C in 10 minutes. After the fabric was washed thoroughly with water, the percentage of weight loss was determined to be 20.7% as a whole, from which the percentage of weight loss of the constituents hardly soluble in an alkali solution was calculated at 45% ( x 100). A suede-like raised fabric having extra fine naps (0.09 denier) was thus obtained.
- the pre-heat set raised fabric was dyed in a water dye bath containing 4% Duranol Brilliant Blue G (C.I.No.63305, trade name for a disperse dye manufactured by I.C.I.) (based on the weight of the fabric), 0.2 ml/l, density of acetic acid, and 1 g/k density of a dispersing agent mainly consisting of a condensation product of naphthalane- sulfonic acid and formamido at 130°C for 60 minutes, subjected to soaping in an aqueous solution of nonionic detergent at 80°C for 20 minutes, and dried at 120°C for 3 minutes.
- 4% Duranol Brilliant Blue G C.I.No.63305, trade name for a disperse dye manufactured by I.C.I.
- This example shows how an elastic polymer was applied to the raised fabric obtained in Example 1.
- An urethane pre-polymer having free isocyanate groups was prepared by allowing the following mixture (the mole ratio between isocyanate groups and active hydrogen atoms was 2.06) at 100 to 105°C for 1 hour in a stream of nitrogen gas.
- the mixture consisted of (1) 21 parts of a block-copolymerized polyether diol having a number average molecular weight of 2,400 which was obtained by reacting polypropylene glycol having a number average molecular weight of about 1,200 with ethylene oxide, (2) 56 parts of a polyester diol which was obtained by reacting adipic acid, 1,6-hexane diol and neopentyl glycol in a mole ratio of 10:7:4 respectively, (3) 3 parts of 1,6-hexane diol, and (4) 20 parts of hexamethylene diisocyanate.
- the contents of the isocyanate groups and oxyethylene groups in the resultant urethane pre- polymer were 5.02% and 10.2% respectively
- the resultant urethane pre-polymer was cooled to 40°C and diluted by adding 20 parts of dioxane. 65 parts of an aqueous solution of sodium bisulfate having a concentration of 25% by weight was further added to the diluted urethane prepolymer and mixed thoroughly at 40°C for 30 minutes. After that, 202 parts of water and a proper amount of hydrogen peroxide were added to the reaction system to obtain an aqueous solution of urethane pre-polymer (pH 3) having a concentration of about 30% by weight.
- the raised woven fabric obtained in Example 1 was immersed in an 8% aqueous solution (whose pH value was adjusted to 6.0 with sodium bicarbonate) of the abovementioned urethane pre-polymer and then squeezed to a pick-up ratio of 70% based on the weight of the fabric.
- the fabric was dried at 100°C for 3 minutes and heat-treated at 140°C for 30 seconds.
- the raised surface of the heat-treated raised woven fabric was then fuffed one time by use of a roller sander having 100-mesh sand paper and further brushed.
- the raised woven fabric thus obtained had a beautiful lustrous surface look and excellent resiliency and crease resistance similar to natural suede.
- Polyethylene terephthalate chip was prepared after the polymerization of polyethylene terephthalate was carried out according to the ordinary method with addition of 3 parts of polyoxyethylene glycol having molecular weight of 20,000 and 1.5 parts of sodium lauryl sulfonate before starting polymerization. Then a composite fiber of hollow, segmental multilayer type, in which two constituents, i.e.
- a satin tricot fabric of 36 gauge, back 01/21 and front 10/34 was prepared by using thus prepared 45-denier filament yarn as a front yarn and a polyethylene terephthalate filament yarn (30 denier/10 filaments) as a back yarn (the weight of the composite fiber was 77% of the whole fabric and the weight of the constituents easily soluble in an alkali solution was 23.1%).
- the obtained knitted fabric was relaxed in a hot water bath for 10 seconds, dried and raised 15 times with a wire raising machine.
- the raised knitted fabric was heat set at 170°C for 30 seconds on the pin tenter.
- the knitted fabric was then treated with an aqueous solution of caustic soda having the concentration of 7.5 g/l at 130°C for 30 minutes with the use of a jet dyeing machine (Uniace, made by Japan Dyeing Machine Co.), in which treatment the temperature of the solution was first raised to 130°C and then lowered after the treatment was over according to the same way as described in Example 1, and washed with water after having been cooled.
- the percentage of weight loss of the whole treated knitted fabric was 28.5%.
- the weight loss of the constituents hardly soluble in an alkali solution was 7.0%.
- the knitted fabric was further dyed, heat set, and brushed to give a suede-like fabric having densely raised extra fine naps with very soft_ hand on the surface.
- An undrawn hollow composite fiber having a 4% hollow ratio and a total denier size of 190 denier and a single yarn denier size of 6.3 denier was obtained by composite melt spinning 70 parts of polybutylene terephthalate having the intrinsic viscosity of 0.85 determined at 25°C in orthochlorophenol (as constituents hardly soluble in an alkali solution) and 30 parts of mixed polyethene terephthalate, having the intrinsic viscosity of 0.64 determined at 25°C in orthochlorophenol, prepared by adding 2 parts of sodium alkyl sulfonate having 15 carbon atoms and 2 parts of polyethylene glycol having molecular weight of about 15,000 to 96 parts of polyethylene terephthalate at the time of its polymerization (as constituents easily soluble in an alkali solution).
- the composite melt spinning was carried out at the discharge temperature of 286°C and withdrawing rate of 1200 m/min. in such a way as to form a composite fiber of hollow, segmental multilayer type, in which said two constituents were distributed alternately side by side in 32 segments arranged radially on a cross-sectional view of the fiber according to the method disclosed in U.S. Patent 4,109,038.
- This undrawn hollow composite fiber was drawn at a drawing ratio of 3.1 with a heating roller at 80°C, made to go through a slit heater kept at 210°C, and wound up to give a drawn fiber of total denier size of 61 denier, having 0.09-denier polyethylene terephthalate components (constituents hardly soluble in an alkali solution) and 2.04-denier single yarns.
- Three composite fibers thus obtained were then folded into a multi-filament yarn of 183 denier/90 filaments.
- a raised woven fabric was obtained according to the same method as described in Example 1, dyed and treated with an alkali solution to give a suede-like raised woven fabric having extra fine naps (0.09 denier) comprising polybutylene terephthalate.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP183728/80 | 1980-12-26 | ||
| JP55183728A JPS57112462A (en) | 1980-12-26 | 1980-12-26 | Production of suede like raised fabric |
| JP63407/81 | 1981-04-28 | ||
| JP6340781A JPS57193572A (en) | 1981-04-28 | 1981-04-28 | Treatment of polyester fabric |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0056907A1 true EP0056907A1 (de) | 1982-08-04 |
Family
ID=26404527
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP81306092A Ceased EP0056907A1 (de) | 1980-12-26 | 1981-12-23 | Verfahren zur Herstellung eines aufgerauhten wildlederartigen Textilgebildes |
Country Status (1)
| Country | Link |
|---|---|
| EP (1) | EP0056907A1 (de) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0436966A3 (en) * | 1990-01-09 | 1992-01-02 | Dai-Ichi Kogyo Seiyaku Co., Ltd. | Methods for manufacture of porous resin mouldings, ultrafine fibres and ultrafine fibre nonwoven fabrics |
| JP2015505917A (ja) * | 2012-09-21 | 2015-02-26 | クレンボン カンパニー リミテッド | カットループ組織を有する生地、その製造方法及びそれを用いた製品 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1306974A (en) * | 1970-07-16 | 1973-02-14 | Toray Industries | Synthetic fine filament bundle and island-in-a-sea- type composite filament usable for manufacturing the bundle and processes of manufacturing the same |
| JPS546965A (en) * | 1977-06-09 | 1979-01-19 | Kuraray Co | Production of separated fiber containing cloth |
| JPS5427058A (en) * | 1977-07-26 | 1979-03-01 | Kuraray Co | Production of separated fiber containing cloth |
-
1981
- 1981-12-23 EP EP81306092A patent/EP0056907A1/de not_active Ceased
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1306974A (en) * | 1970-07-16 | 1973-02-14 | Toray Industries | Synthetic fine filament bundle and island-in-a-sea- type composite filament usable for manufacturing the bundle and processes of manufacturing the same |
| JPS546965A (en) * | 1977-06-09 | 1979-01-19 | Kuraray Co | Production of separated fiber containing cloth |
| JPS5427058A (en) * | 1977-07-26 | 1979-03-01 | Kuraray Co | Production of separated fiber containing cloth |
Non-Patent Citations (4)
| Title |
|---|
| Derwent Japanese Patents Report, Vol. T, No.50, 16 January 1973 F, page 6, & JP-A-47 047532 (Toray) (30-11-1972) *the whole Abstract* * |
| Derwent Japanese Patents Report, Vol.T, No.50, 16 January 1973 F, page 6, & JP-A-47 047533 (Toray) (30-11-1972) *the whole Abstract* * |
| Japanese Patents Gazette, Section Ch; week B09, 11 Avril 1979 j5-F, page 5, No. 16535 & JP-A-54 006965 (Kuraray KK)(19-01-1979) *the whole Abstract* * |
| Japanese Patents Gazette, Section Ch; week B14, 16 May 1979, j5-F, page 8, No. 27086 & JP-A-54 027058 (Kuraray KK) (01-03-1979) *the whole Abstract* * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0436966A3 (en) * | 1990-01-09 | 1992-01-02 | Dai-Ichi Kogyo Seiyaku Co., Ltd. | Methods for manufacture of porous resin mouldings, ultrafine fibres and ultrafine fibre nonwoven fabrics |
| JP2015505917A (ja) * | 2012-09-21 | 2015-02-26 | クレンボン カンパニー リミテッド | カットループ組織を有する生地、その製造方法及びそれを用いた製品 |
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