US3619337A - Dimensionally stable fabric having a suedelike texture - Google Patents
Dimensionally stable fabric having a suedelike texture Download PDFInfo
- Publication number
- US3619337A US3619337A US752739A US3619337DA US3619337A US 3619337 A US3619337 A US 3619337A US 752739 A US752739 A US 752739A US 3619337D A US3619337D A US 3619337DA US 3619337 A US3619337 A US 3619337A
- Authority
- US
- United States
- Prior art keywords
- fabric
- texture
- suedelike
- dimensionally stable
- fused
- 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.)
- Expired - Lifetime
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 98
- -1 alkylene glycol Chemical compound 0.000 claims abstract description 35
- 239000004952 Polyamide Substances 0.000 claims abstract description 23
- 229920002647 polyamide Polymers 0.000 claims abstract description 23
- 229920001410 Microfiber Polymers 0.000 claims abstract description 19
- 239000003658 microfiber Substances 0.000 claims abstract description 19
- 238000002844 melting Methods 0.000 claims abstract description 14
- 230000008018 melting Effects 0.000 claims abstract description 14
- 239000011159 matrix material Substances 0.000 claims abstract description 13
- 229920001059 synthetic polymer Polymers 0.000 claims abstract description 11
- 229920000728 polyester Polymers 0.000 claims description 28
- 229920002292 Nylon 6 Polymers 0.000 claims description 5
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 5
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 5
- 239000004793 Polystyrene Substances 0.000 claims description 3
- 229920002492 poly(sulfone) Polymers 0.000 claims description 3
- 239000004417 polycarbonate Substances 0.000 claims description 3
- 229920000515 polycarbonate Polymers 0.000 claims description 3
- 229920006324 polyoxymethylene Polymers 0.000 claims description 3
- 229920006389 polyphenyl polymer Polymers 0.000 claims description 3
- 229920002223 polystyrene Polymers 0.000 claims description 3
- 239000004800 polyvinyl chloride Substances 0.000 claims description 3
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 3
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 229920000306 polymethylpentene Polymers 0.000 claims 1
- 239000011116 polymethylpentene Substances 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 42
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract description 16
- 238000000034 method Methods 0.000 abstract description 8
- 230000001680 brushing effect Effects 0.000 abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract description 4
- 230000008569 process Effects 0.000 abstract description 4
- 230000004927 fusion Effects 0.000 description 15
- 239000000835 fiber Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 239000006185 dispersion Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000004902 Softening Agent Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-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
- 239000000155 melt Substances 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000002787 reinforcement Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- OOGKXQSCDZDEFV-UHFFFAOYSA-N 2-[(2-carboxyphenyl)diazenyl]benzoic acid Chemical compound OC(=O)C1=CC=CC=C1N=NC1=CC=CC=C1C(O)=O OOGKXQSCDZDEFV-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- BJLUCDZIWWSFIB-UHFFFAOYSA-N 5-tert-butylbenzene-1,3-dicarboxylic acid Chemical compound CC(C)(C)C1=CC(C(O)=O)=CC(C(O)=O)=C1 BJLUCDZIWWSFIB-UHFFFAOYSA-N 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241000790917 Dioxys <bee> Species 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000002979 fabric softener Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- LVPMIMZXDYBCDF-UHFFFAOYSA-N isocinchomeronic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)N=C1 LVPMIMZXDYBCDF-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 108700005457 microfibrillar Proteins 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- GJAWHXHKYYXBSV-UHFFFAOYSA-N pyridinedicarboxylic acid Natural products OC(=O)C1=CC=CN=C1C(O)=O GJAWHXHKYYXBSV-UHFFFAOYSA-N 0.000 description 1
- YHUVMHKAHWKQBI-UHFFFAOYSA-N quinoline-2,3-dicarboxylic acid Chemical compound C1=CC=C2N=C(C(O)=O)C(C(=O)O)=CC2=C1 YHUVMHKAHWKQBI-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06Q—DECORATING TEXTILES
- D06Q1/00—Decorating textiles
- D06Q1/08—Decorating textiles by fixation of mechanical effects, e.g. calendering, embossing or Chintz effects, using chemical means
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/20—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads
- D03D15/283—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads synthetic polymer-based, e.g. polyamide or polyester fibres
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/40—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the structure of the yarns or threads
- D03D15/47—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the structure of the yarns or threads multicomponent, e.g. blended yarns or threads
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- D03—WEAVING
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- D03D15/50—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads
- D03D15/587—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads adhesive; fusible
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- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
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- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/4334—Polyamides
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
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- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
- D04H1/43825—Composite fibres
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
- D04H1/43838—Ultrafine fibres, e.g. microfibres
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/144—Alcohols; Metal alcoholates
- D06M13/148—Polyalcohols, e.g. glycerol or glucose
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- D10B2331/02—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyamides
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- D—TEXTILES; PAPER
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- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
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- D10B2331/04—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyesters, e.g. polyethylene terephthalate [PET]
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- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
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- D10B2401/04—Heat-responsive characteristics
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- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2501/00—Wearing apparel
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/904—Artificial leather
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
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- Y10T428/2395—Nap type surface
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/23979—Particular backing structure or composition
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
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- Y10T428/31725—Of polyamide
- Y10T428/31736—Next to polyester
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/31743—Next to addition polymer from unsaturated monomer[s]
-
- 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
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
Definitions
- All0rney-R0y H. Massengill ABSTRACT A dimensionally stable fabric having a suedelike texture is produced by a process which comprises brushing or napping a fabric containing filaments comprising a polyamide matrix having microfibers of a higher melting synthetic polymer dispersed therein.
- a substantial number of the fila- DIMENSIONALLY STABLE FABRIC HAVING A SUEDELIKE TEXTURE BACKGROUND OF THE INVENTION This invention relates to dimensionally stable fabric having a suedelike texture. More particularly this invention relates to a process for producing a dimensionally stable fabric having a suedelike texture by treating a fused fabric comprised of a biconstituent fiber with an alkylene glycol.
- Fabrics having a suedelike texture are known in the prior art, however, the novel dimensionally stable fabric having a suedelike texture of the present invention which is comprised of a polyamide matrix having microfibers of a higher melting synthetic polymer dispersed therein is novel to the art and offers many useful advantages over prior art fabrics having a suedelike texture.
- the dimensionally stable fabric having a suedelike texture of the present invention is useful in many commercial fields such as apparel, home furnishings, and building materials.
- a few specific examples are wall paneling, wall paper, lamp shades, shoes, slippers and the like.
- An example of the versatility and value of the fabric of the present invention is in the production of a shoe upper.
- the dimensionally stable fabric having a suedelike texture can be molded into the shape ofa shoe upper thereby eliminating the need for resins and resin curing while at the same time retaining the suedelike texture for fashion effects.
- the dimensional stability of the fabric eliminates the need for backings or reinforcements such as polyurethane foam, however, such backings and reinforcements can be used for any additional desirable effects.
- a dimensionally stable fabric having a suedelike texture is produced by a process which comprises brushing or napping a fabric containing filaments comprising a polyamide matrix having microfibers of a higher melting synthetic polymer dispersed therein. A substantial number of the filaments of the base or ground of the napped fabric are then fused together at their crossover points to impart dimensional stability to the fabric and retain the original fabriclike appearance.
- the dimensionally stable fabric retaining its original fabriclike appearance is then contacted with an alkylene glycol having two to about l carbon atoms for a period of time sufficient to soften the dimensionally stable fabric thereby imparting a suedelike texture on the brushed or napped surface of the fabric without any substantial loss of dimensional stability in the fused fabric.
- the fabric treated in accordance with the present invention can be woven, nonwoven, or knitted from filaments or fibers prepared from dispersions of a higher melting synthetic polymer in a polyamide.
- Suitable higher melting synthetic polymers include, for example, polyesters, polysulfones, polyphenyl oxides, polycarbonates, polyacetals, crystalline polyvinyl chloride, polystyrene, certain polyolefins such as isotactic poly(3-methyl-l-butene) and isotactic poly (4- methyl-l-pentene) and the like.
- the fabric treated in accordance with the present invention can be woven, nonwoven, or knitted from filaments or fibers prepared from dispersions of polyester in polyamide such as disclosed in US. Pat. 3,369,057 to Twilley.
- dispersions of polyester in polyamide such as disclosed in US. Pat. 3,369,057 to Twilley.
- the proportion ofend groups of the polyamide, especially amine groups, which are reactive in the melt with the polyester should be restricted to not over 40 percent of the polyamide end groups.
- other dispersions of polyester in polyamide are satisfactory for purposes of this invention, including those disclosed in US. Pats. 3,378,055, 3,378,056, and 3,378,602; British Pat. l,097,068; Belgian Pat. 702,813; and Netherlands Pats.
- the polyester ingredient is dispersed as discrete microfibers throughout the polyamide which forms a continuous phase or matrix.
- the microfibers can be continuous or discontinuous throughout the matrix.
- the polyester microfibers have average diameter not above 1 micron and preferably not above 0.5 micron. In length the microfibers vary widely, but substantially all are elongated. On the average they are at least 5 times and usually at least 20 times longer than the average diameter, typically averaging in length about 250 times their average diameter.
- the microfibers lie predominantly in the direction of the filament axis.
- the dispersion of microfibers in the filament is substantially uniform, both lengthwise and across each filament. Typically at least 100 microfibers traverse each cross section of each filament.
- the microfibers will generally have essentially round cross section, although their diameter may vary along their length and they may taper toward their ends as a result of the shears imposed during drawing.
- the filaments or fibers of the fabrics treated in accordance with the preferred embodiment of this invention comprise, per 100 parts by weight total polyamide and polyester, about 50 to parts of the polyamide as the matrix and dispersed therein about 50 to 10 parts of the polyester.
- Suitable polyamides for use in the present invention include, for example, those prepared by condensation of hexamethylene diamine and adipic acid, known as nylon 6,6 or by polymerization of e-caprolactam, known as nylon 6.
- polyesters useful in the practice of this invention can be prepared in general by condensation reactions between dicarboxylic acids or their derivatives and compounds containing two hydroxyl groups, or materials possessing both an alcohol group and a carboxylic acid group or derivative thereof; or by the condensation-polymerization of lactones.
- Dicaroxylic acid derivatives which can be employed include esters, salts, anhydrides and acid halides.
- the monomeric species employed in the preparation of the polyesters are preferably not more highly functional than difunctional in their reactivity so as to produce essentially linear, noncrosslinked polymer structures.
- Suitable polyesters for use in the present invention include those polymers in which one of the recurring units in the polyester chain is the diacylaromatic radical from terephthalic acid, isophthalic acid, 5-t-butylisophthalic acid, a naphthalene dicarboxylic acid such as naphthalene 2,6 and 2,7 dicarboxylic acids, a diphenyl-dicarboxylic acid, a diphenyl ether dicarboxylic acid, a diphenyl alkylene dicarboxylic acid, a diphenyl sulfone dicarboxylic acid, an azo dibenzoic acid, a pyridine dicarboxylic acid, a quinoline dicarboxylic acid, and analogous aromatic species including the sulfonic acid analogues; diacyl radicals containing cyclopentane or cyclohexane rings between the acyl groups; and such radicals substituted in the ring, e.g. by
- the dioxy radical representing the other principal recurring unit in the polyester chain can be an open chain aliphatic such as ethylene glycol or ether thereof, for example, the diether, or can contain rings such as those which form part of the above noted diacyl radicals.
- the carboxy and/or the oxy chain members can be directly attached to a ring or removed by one or more carbon atoms therefrom, as in the 1,4 dioxymethyl cyclohexane radical.
- the fabric treated in accordance with the present invention can be a conventional knitted, woven or nonwoven fabric, however, it is preferred that the fabric be of such a construction which is designed for brushing or napping.
- the brushing or napping of the fabric can be carried out on conventional brushing or napping equipment.
- the fabric is brushed or napped on only one side, however. it may, in some cases, be desirable to brush or nap both sides of the fabric and it is within the scope of the present invention that both sides of the fabric can be brushed or napped ifdesired.
- a forced air oven with a nitrogen purge a static draft oven without nitrogen, heated match-die molds, a molding press (without pressure) or a steam autoclave.
- the method of heating is of little consequence, with the autoclave having only slight advantages in that there is less discoloration since lower fusion temperatures can be achieved thereby.
- the temperature and time will vary depending on the ratio of polymeric materials, article size, shape, desired rigidity, mode of heat application and other variables. In general, it is necessary to apply heat without excessive degradation of sufficient intensity and duration at least as high as the melting point of the nylon matrix until the fabric yarns have fused to each other yet still retain the yarn or fabric identity. if the fabric yarns are spun from staple fibers, the fibers forming the yarn will fuse together individually in addition to fusion at the cross points of the fabric. Fusion can be achieved without undesirable flow; it is this phenomenon which permits the present invention to provide unique dimensional stability and appearance to textile materials and, therefore, regulates the minimum and maximum heat-set conditions. Thus,'the fabric interstices are practically unaltered by the fusion as described herein since there is no polymer flow or migration, provided the dimensions of the fabric are maintained.
- the optimum fusion temperature for a nylon-polyester combination containing 30 parts by weight of polyethylene terephthalate microfibers dispersed in 70 parts by weight of nylon 6, is about 240 C. for efficient fusion, fiber integrity retention, coloration, and controllable hand and texture suitable for treatment.
- time for fusion is dependent on many factors, including the amount of polyester dispersed in the polyamide matrix, the filament or yarn size, fabric construction, that is, knit, weave, loose, tight, etc. and, of course, the ultimate texture desired in the fabric having a suede-like texture.
- time periods are determined by the mass to be heated and the type of heat source employed. For example, when employing an oven, durations as short as about 15-20 seconds at about 230 C. have been found effective for at least partial fusion when a softer fabric is desired. Fusion times of up to about minutes and longer at about 255 C. can be employed, however, the breaking strength of the fabric is reduced somewhat.
- the fused napped fabric prepared in accordance with the above procedure is then treated with an alkylene glycol having two to about 10 carbon atoms which can be substituted with nonreactive groups such as alkyl, for example, methyl, ethyl, and the like, and alkoxy, for example, methoxy, ethoxy, and the like.
- Suitable alkylene glycols include ethylene, propylene, butylene, diethylene and triethylene glycol and the like with ethylene glycol being preferred.
- the fused, napped fabric can be wound on tubes or similar packaging devices and immersed in the alkylene glycol or the fused, napped fabric can be continuously passed through the alkylene glycol.
- the alkylene glycol can be used in undiluted form or the alkylene glycol can be diluted with a nonreactive solvent such as water.
- concentration of alkylene glycol in water can range as low as about 40 weight percent or even lower depending upon the texture desired of the treated fabric.
- the alkylene glycol treatment of the fused napped fabric is conducted at a temperature ranging from about 20 to C. for a period of time sufficient to produce the desired suedelike texture on the fused napped fabric.
- the fused napped fabric is treated with heated undiluted alkylene glycol for about 10 to 120, preferably about 15 to 60, minutes.
- the weight of the glycol treating solution to the weight of the fused fabric can vary depending upon the treating conditions. For most treating conditions, the weight ofthe glycol solution is about 30 to 100 times the weight of the fused fabric treated, however, lower or higher ratios may be used for certain treating conditions.
- Rinsing is desirable to clear the fabric of any excess alkylene glycol left over from the alkylene glycol contacting stage.
- the dimensionally stable fused napped fabric having a suede-like texture can be dried at ordinary temperature, usually not more than 100 C.
- EXAMPLE 1 A synthetic multifilament yarn containing 30 parts by weight of polyethylene terephthalate microfibers dispersed in 70 parts by weight of nylon 6 was knitted into a two bar tricot fabric. The yarn contained twelve filaments and was drawn at a draw ratio of about 3.5x to a final denier of 40. The polyethylene terephthalate microfibers had an average diameter not above 1 micron and had an average length at least 20 times their average diameter. The microfibers lay predominantly in the direction of the filament axis. One side of the knitted fabric was then brushed or napped on conventional napping equipment. The napped fabric was then bonded by fusing it on a tenter frame at 30 percent overfeed for 10 seconds at about 244 C. in accordance with the method described in US.
- EXAMPLE 2 A sample of the fused fabric prepared in example 1 was placed in a watch glass containing heated ethylene glycol. The ethylene glycol was heated by placing the watch glass over a beaker of boiling water. The fused fabric was immersed in the heated ethylene glycol for about 30 minutes, removed, and dried in air at room temperature for about 24 hours. The ethylene glycol treatment produced a soft, suedelike texture on the napped side of the fabric which had a rough and sand paperlike texture prior to the ethylene glycol treatment.
- the softener solutions were prepared by dissolving 2.5 grams of each softener in L300 ml. of hot tap water. The fused fabric samples were placed in the respective softener solutions and agitated for 20 minutes.
- a control sample of fused fabric was also run under the above conditions using only hot tap water as the softener.
- the fused fabric samples were removed from their respective softener solutions and were evaluated for softness and suedelike texture prior to drying. None of the softeners evaluated produced a suedelike texture on the fused fabrics.
- the treatment with Achovel NC produced the greatest amount of softening but was not as effective a softener as ethylene glycol. in addition, the Achovei NC treated fabric lost its dimensional stability.
- the treatments with the other softeners did not affect the dimensional stability and were effective as softeners in the following order: Tanalube RF, Ceranine NCS, Avitone T, hot water.
- the treated fused fabric samples were then dried in air at room temperature for about 3 hours. There was no appreciable change in any of the fabric samples after drying.
- a dimensionally stable fabric having a suedelike texture which comprises a fused napped fabric containing filaments comprising a polyamide matrix having microfibers of a higher melting synthetic polymer dispersed therein, said napped fabric having been fused in such a manner to thereby retain its original fabriclike appearance and said fused napped fabric having been softened to thereby have said suedelike texture; said textile material having been heat-treated at a temperature in the range above the melting point of the matrix but below the melting point of the dispersed fibrils such that the multiconstituent filaments thereof are set and fusion bonded at least at their cross points without substantial polymer flow or migration so that the fabric interstices are maintained substantially unaltered; and said fused textile material being characterized by said dispersed fibrils being bonded together as determined by removing the polymeric material with a solvent to show the remaining dispersed fibrils have maintained a true fabric appearance, being cohesive and elastic.
- the higher melting synthetic polymer is selected from the group consisting of polyesters, polysulfones, polyphenyl oxides, polycarbonates, polyacetals, crystalline polyvinyl chloride, polystyrene, and polyolefms selected from the group consisting of isotactic poly(3-methyl-i-butene) and isotactic poly(4-methyl-l-pentene).
- said filaments comprising a polyamide matrix having polyester microfibers dispersed therein contain, per 100 parts by weight total polyamide and polyester, about 50 to parts of polyamide and dispersed therein about 50 to 10 parts of polyester.
Abstract
A dimensionally stable fabric having a suedelike texture is produced by a process which comprises brushing or napping a fabric containing filaments comprising a polyamide matrix having microfibers of a higher melting synthetic polymer dispersed therein. A substantial number of the filaments of the base or ground of the napped fabric are then fused together at their crossover points to impart dimensional stability to the fabric and retain the original fabriclike appearance. The dimensionally stable fabric retaining its original fabriclike appearance is then contacted with an alkylene glycol having two to about 10 carbon atoms for a period of time sufficient to soften the dimensionally stable fabric thereby imparting a suedelike texture on the brushed or napped surface of the fabric without any substantial loss of dimensional stability in the fused fabric.
Description
United States Patent 72] inventors Gene C. Weedon Richmond; Robert C. Wincklhoier, Richmond; George H. Collingwood, Hopewell, all of Va. [21] Appl. No. 752,739 [22] Filed Aug. 15, 1968 [45] Patented Nov. 9,1971 [73] Assignee Allied Chemical Corporation New York, N.Y.
[54] DIMENSIONALLY STABLE FABRIC HAVING A SUEDELIKE TEXTURE 6 Claims, No Drawings [52| US. Cl 161/64, [56/148,156/181,156/306,161/92,161/150, 161/176 [51 1 Int. Cl D03d27/00, D04h 11/00 [50] Field of Search 161/90-92,
[56] References Cited UNITED STATES PATENTS 3,034,194 5/1962 Priester et al 161/64 3,090,097 5/1963 Ruckstuhl 161/65 X 3,099,067 7/1963 Merriam et al. 28/82 3,348,983 10/1967 Sissons 161/81 X 3,369,057 2/1968 Twiliey 260/857 3,382,305 5/1968 Breen 264/171 FOREIGN PATENTS 1,035,908 7/1966 Great Britain Primary Examiner- William .L Van Balen Assistant Examiner-Roger L. May
All0rney-R0y H. Massengill ABSTRACT: A dimensionally stable fabric having a suedelike texture is produced by a process which comprises brushing or napping a fabric containing filaments comprising a polyamide matrix having microfibers of a higher melting synthetic polymer dispersed therein. A substantial number of the fila- DIMENSIONALLY STABLE FABRIC HAVING A SUEDELIKE TEXTURE BACKGROUND OF THE INVENTION This invention relates to dimensionally stable fabric having a suedelike texture. More particularly this invention relates to a process for producing a dimensionally stable fabric having a suedelike texture by treating a fused fabric comprised of a biconstituent fiber with an alkylene glycol.
Fabrics having a suedelike texture are known in the prior art, however, the novel dimensionally stable fabric having a suedelike texture of the present invention which is comprised of a polyamide matrix having microfibers of a higher melting synthetic polymer dispersed therein is novel to the art and offers many useful advantages over prior art fabrics having a suedelike texture.
The dimensionally stable fabric having a suedelike texture of the present invention is useful in many commercial fields such as apparel, home furnishings, and building materials. A few specific examples are wall paneling, wall paper, lamp shades, shoes, slippers and the like.
An example of the versatility and value of the fabric of the present invention is in the production of a shoe upper. The dimensionally stable fabric having a suedelike texture can be molded into the shape ofa shoe upper thereby eliminating the need for resins and resin curing while at the same time retaining the suedelike texture for fashion effects. The dimensional stability of the fabric eliminates the need for backings or reinforcements such as polyurethane foam, however, such backings and reinforcements can be used for any additional desirable effects.
SUMMARY OF THE INVENTION In accordance with the present invention, a dimensionally stable fabric having a suedelike texture is produced by a process which comprises brushing or napping a fabric containing filaments comprising a polyamide matrix having microfibers of a higher melting synthetic polymer dispersed therein. A substantial number of the filaments of the base or ground of the napped fabric are then fused together at their crossover points to impart dimensional stability to the fabric and retain the original fabriclike appearance. The dimensionally stable fabric retaining its original fabriclike appearance is then contacted with an alkylene glycol having two to about l carbon atoms for a period of time sufficient to soften the dimensionally stable fabric thereby imparting a suedelike texture on the brushed or napped surface of the fabric without any substantial loss of dimensional stability in the fused fabric.
The fabric treated in accordance with the present invention can be woven, nonwoven, or knitted from filaments or fibers prepared from dispersions of a higher melting synthetic polymer in a polyamide. Suitable higher melting synthetic polymers include, for example, polyesters, polysulfones, polyphenyl oxides, polycarbonates, polyacetals, crystalline polyvinyl chloride, polystyrene, certain polyolefins such as isotactic poly(3-methyl-l-butene) and isotactic poly (4- methyl-l-pentene) and the like. In a preferred embodiment, the fabric treated in accordance with the present invention can be woven, nonwoven, or knitted from filaments or fibers prepared from dispersions of polyester in polyamide such as disclosed in US. Pat. 3,369,057 to Twilley. As disclosed in Twilley, supra, the proportion ofend groups of the polyamide, especially amine groups, which are reactive in the melt with the polyester should be restricted to not over 40 percent of the polyamide end groups. In addition, other dispersions of polyester in polyamide are satisfactory for purposes of this invention, including those disclosed in US. Pats. 3,378,055, 3,378,056, and 3,378,602; British Pat. l,097,068; Belgian Pat. 702,813; and Netherlands Pats. 66,06838 and 66,l2628, and filaments or fibers can also be prepared from these dispersions by known melt spinning techniques. In the drawn filaments or fibers comprising the fabrics treated in accordance with the preferred embodiment of the present invention, the polyester ingredient is dispersed as discrete microfibers throughout the polyamide which forms a continuous phase or matrix. The microfibers can be continuous or discontinuous throughout the matrix. The polyester microfibers have average diameter not above 1 micron and preferably not above 0.5 micron. In length the microfibers vary widely, but substantially all are elongated. On the average they are at least 5 times and usually at least 20 times longer than the average diameter, typically averaging in length about 250 times their average diameter. In the drawn filaments, the microfibers lie predominantly in the direction of the filament axis. The dispersion of microfibers in the filament is substantially uniform, both lengthwise and across each filament. Typically at least 100 microfibers traverse each cross section of each filament. The microfibers will generally have essentially round cross section, although their diameter may vary along their length and they may taper toward their ends as a result of the shears imposed during drawing.
The filaments or fibers of the fabrics treated in accordance with the preferred embodiment of this invention comprise, per 100 parts by weight total polyamide and polyester, about 50 to parts of the polyamide as the matrix and dispersed therein about 50 to 10 parts of the polyester.
Suitable polyamides for use in the present invention include, for example, those prepared by condensation of hexamethylene diamine and adipic acid, known as nylon 6,6 or by polymerization of e-caprolactam, known as nylon 6.
The polyesters useful in the practice of this invention can be prepared in general by condensation reactions between dicarboxylic acids or their derivatives and compounds containing two hydroxyl groups, or materials possessing both an alcohol group and a carboxylic acid group or derivative thereof; or by the condensation-polymerization of lactones. Dicaroxylic acid derivatives which can be employed include esters, salts, anhydrides and acid halides. The monomeric species employed in the preparation of the polyesters are preferably not more highly functional than difunctional in their reactivity so as to produce essentially linear, noncrosslinked polymer structures.
Suitable polyesters for use in the present invention include those polymers in which one of the recurring units in the polyester chain is the diacylaromatic radical from terephthalic acid, isophthalic acid, 5-t-butylisophthalic acid, a naphthalene dicarboxylic acid such as naphthalene 2,6 and 2,7 dicarboxylic acids, a diphenyl-dicarboxylic acid, a diphenyl ether dicarboxylic acid, a diphenyl alkylene dicarboxylic acid, a diphenyl sulfone dicarboxylic acid, an azo dibenzoic acid, a pyridine dicarboxylic acid, a quinoline dicarboxylic acid, and analogous aromatic species including the sulfonic acid analogues; diacyl radicals containing cyclopentane or cyclohexane rings between the acyl groups; and such radicals substituted in the ring, e.g. by alkyl or halo substituents.
The dioxy radical representing the other principal recurring unit in the polyester chain can be an open chain aliphatic such as ethylene glycol or ether thereof, for example, the diether, or can contain rings such as those which form part of the above noted diacyl radicals. The carboxy and/or the oxy chain members can be directly attached to a ring or removed by one or more carbon atoms therefrom, as in the 1,4 dioxymethyl cyclohexane radical.
The fabric treated in accordance with the present invention can be a conventional knitted, woven or nonwoven fabric, however, it is preferred that the fabric be of such a construction which is designed for brushing or napping.
The brushing or napping of the fabric can be carried out on conventional brushing or napping equipment. Generally, the fabric is brushed or napped on only one side, however. it may, in some cases, be desirable to brush or nap both sides of the fabric and it is within the scope of the present invention that both sides of the fabric can be brushed or napped ifdesired.
Several systems are suitable for heat treating the napped fabric of the present invention, as for example, a forced air oven with a nitrogen purge, a static draft oven without nitrogen, heated match-die molds, a molding press (without pressure) or a steam autoclave. The method of heating is of little consequence, with the autoclave having only slight advantages in that there is less discoloration since lower fusion temperatures can be achieved thereby.
For any given fabric, the temperature and time will vary depending on the ratio of polymeric materials, article size, shape, desired rigidity, mode of heat application and other variables. In general, it is necessary to apply heat without excessive degradation of sufficient intensity and duration at least as high as the melting point of the nylon matrix until the fabric yarns have fused to each other yet still retain the yarn or fabric identity. if the fabric yarns are spun from staple fibers, the fibers forming the yarn will fuse together individually in addition to fusion at the cross points of the fabric. Fusion can be achieved without undesirable flow; it is this phenomenon which permits the present invention to provide unique dimensional stability and appearance to textile materials and, therefore, regulates the minimum and maximum heat-set conditions. Thus,'the fabric interstices are practically unaltered by the fusion as described herein since there is no polymer flow or migration, provided the dimensions of the fabric are maintained.
Thus, while no empirical or mathematical formula has been found for determining the minimum heat-setting conditions to fuse the filaments used in the present invention, appearance after heating, and in particular, after fusion and removal of the nylon. by formic acid has been found to be an important criterion.
The discovery has been made that an unusual fusion characteristic of this invention exists in the structure formed by the dispersed fibrils which unexpectedly are bonded together even though the melt temperature thereof has not been reached during the heat-set operation. The appearance of this fused microfibrillar dispersion can be evaluated as a reliable index of the degree of fusion.
The optimum fusion temperature for a nylon-polyester combination containing 30 parts by weight of polyethylene terephthalate microfibers dispersed in 70 parts by weight of nylon 6, is about 240 C. for efficient fusion, fiber integrity retention, coloration, and controllable hand and texture suitable for treatment. Naturally the time for fusion is dependent on many factors, including the amount of polyester dispersed in the polyamide matrix, the filament or yarn size, fabric construction, that is, knit, weave, loose, tight, etc. and, of course, the ultimate texture desired in the fabric having a suede-like texture. Thus, time periods are determined by the mass to be heated and the type of heat source employed. For example, when employing an oven, durations as short as about 15-20 seconds at about 230 C. have been found effective for at least partial fusion when a softer fabric is desired. Fusion times of up to about minutes and longer at about 255 C. can be employed, however, the breaking strength of the fabric is reduced somewhat.
To summarize, for 70 denier yarn, 10 to 300 seconds in a dry oven at 240 C. appears to be the optimum fusion condition where substantially complete fusion is obtained, as determined by removing the nylon with formic acid to determine if the remaining polyester has maintained a true fabric appearance, being cohesive and elastic.
The fused napped fabric prepared in accordance with the above procedure is then treated with an alkylene glycol having two to about 10 carbon atoms which can be substituted with nonreactive groups such as alkyl, for example, methyl, ethyl, and the like, and alkoxy, for example, methoxy, ethoxy, and the like. Suitable alkylene glycols include ethylene, propylene, butylene, diethylene and triethylene glycol and the like with ethylene glycol being preferred. The fused, napped fabric can be wound on tubes or similar packaging devices and immersed in the alkylene glycol or the fused, napped fabric can be continuously passed through the alkylene glycol. The alkylene glycol can be used in undiluted form or the alkylene glycol can be diluted with a nonreactive solvent such as water. The concentration of alkylene glycol in water can range as low as about 40 weight percent or even lower depending upon the texture desired of the treated fabric. The alkylene glycol treatment of the fused napped fabric is conducted at a temperature ranging from about 20 to C. for a period of time sufficient to produce the desired suedelike texture on the fused napped fabric. Generally speaking, the fused napped fabric is treated with heated undiluted alkylene glycol for about 10 to 120, preferably about 15 to 60, minutes. Longer or shorter treatment times can be used depending upon the treatment temperature, amount of alkylene glycol dilution, if any used, and degree of softness and pliability desired in the resulting suedelike material. The weight of the glycol treating solution to the weight of the fused fabric can vary depending upon the treating conditions. For most treating conditions, the weight ofthe glycol solution is about 30 to 100 times the weight of the fused fabric treated, however, lower or higher ratios may be used for certain treating conditions.
Rinsing is desirable to clear the fabric of any excess alkylene glycol left over from the alkylene glycol contacting stage. After rinsing, the dimensionally stable fused napped fabric having a suede-like texture can be dried at ordinary temperature, usually not more than 100 C.
PREFERRED EMBODIMENTS The following examples illustrate the practice and principles of this invention and mode of carrying out the invention.
EXAMPLE 1 A synthetic multifilament yarn containing 30 parts by weight of polyethylene terephthalate microfibers dispersed in 70 parts by weight of nylon 6 was knitted into a two bar tricot fabric. The yarn contained twelve filaments and was drawn at a draw ratio of about 3.5x to a final denier of 40. The polyethylene terephthalate microfibers had an average diameter not above 1 micron and had an average length at least 20 times their average diameter. The microfibers lay predominantly in the direction of the filament axis. One side of the knitted fabric was then brushed or napped on conventional napping equipment. The napped fabric was then bonded by fusing it on a tenter frame at 30 percent overfeed for 10 seconds at about 244 C. in accordance with the method described in US. application Ser. No. 727,327. filed May 7, 1968. The fused fabric was dimensionally stable and had a crisp, paperlike stiffness. The napped side of the fabric had a rough, sand paperlike texture and the unnapped side retained its original fabric appearance.
EXAMPLE 2 A sample of the fused fabric prepared in example 1 was placed in a watch glass containing heated ethylene glycol. The ethylene glycol was heated by placing the watch glass over a beaker of boiling water. The fused fabric was immersed in the heated ethylene glycol for about 30 minutes, removed, and dried in air at room temperature for about 24 hours. The ethylene glycol treatment produced a soft, suedelike texture on the napped side of the fabric which had a rough and sand paperlike texture prior to the ethylene glycol treatment.
Other commercial fabric softeners were evaluated on samples of the fused fabric prepared in example 1. The softeners evaluated were Achovel NC (a nonionic. antistatic textile softening agent), Avitone T (a chemical material based on hydrocarbon sodium sulfonates that is used principally as a softening agent), Ceranine HCS (a cationic fatty acid condensation product), and Tanalube RF (a sulfated fatty ester surfactant of the anionic type). The softener solutions were prepared by dissolving 2.5 grams of each softener in L300 ml. of hot tap water. The fused fabric samples were placed in the respective softener solutions and agitated for 20 minutes. A control sample of fused fabric was also run under the above conditions using only hot tap water as the softener. The fused fabric samples were removed from their respective softener solutions and were evaluated for softness and suedelike texture prior to drying. None of the softeners evaluated produced a suedelike texture on the fused fabrics. The treatment with Achovel NC produced the greatest amount of softening but was not as effective a softener as ethylene glycol. in addition, the Achovei NC treated fabric lost its dimensional stability. The treatments with the other softeners did not affect the dimensional stability and were effective as softeners in the following order: Tanalube RF, Ceranine NCS, Avitone T, hot water. The treated fused fabric samples were then dried in air at room temperature for about 3 hours. There was no appreciable change in any of the fabric samples after drying.
It is claimed:
1. A dimensionally stable fabric having a suedelike texture which comprises a fused napped fabric containing filaments comprising a polyamide matrix having microfibers of a higher melting synthetic polymer dispersed therein, said napped fabric having been fused in such a manner to thereby retain its original fabriclike appearance and said fused napped fabric having been softened to thereby have said suedelike texture; said textile material having been heat-treated at a temperature in the range above the melting point of the matrix but below the melting point of the dispersed fibrils such that the multiconstituent filaments thereof are set and fusion bonded at least at their cross points without substantial polymer flow or migration so that the fabric interstices are maintained substantially unaltered; and said fused textile material being characterized by said dispersed fibrils being bonded together as determined by removing the polymeric material with a solvent to show the remaining dispersed fibrils have maintained a true fabric appearance, being cohesive and elastic.
2. The fabric of claim 1 wherein the higher melting synthetic polymer is selected from the group consisting of polyesters, polysulfones, polyphenyl oxides, polycarbonates, polyacetals, crystalline polyvinyl chloride, polystyrene, and polyolefms selected from the group consisting of isotactic poly(3-methyl-i-butene) and isotactic poly(4-methyl-l-pentene).
3. The fabric of claim 2 wherein the higher melting synthetic polymer is a polyester.
4. The fabric of claim 3 wherein said filaments comprising a polyamide matrix having polyester microfibers dispersed therein contain, per 100 parts by weight total polyamide and polyester, about 50 to parts of polyamide and dispersed therein about 50 to 10 parts of polyester.
5. The fabric of claim 4 wherein said polyamide is nylon 6.
6. The fabric of claim 4 wherein said polyester is polyethylene terephthalate.
Claims (5)
- 2. The fabric of claim 1 wherein the higher melting synthetic polymer is selected from the group consisting of polyesters, polysulfones, polyphenyl oxides, polycarbonates, polyacetals, crystalline polyvinyl chloride, polystyrene, and polyolefins selected from the group consisting of isotactic poly(3-methyl-1-butene) and isotactic poly(4-methyl-1-pentene).
- 3. The fabric of claim 2 wherein the higher melting synthetic polymer is a polyester.
- 4. The fabric of claim 3 wherein said filaments comprising a polyamide matrix having polyester microfibers dispersed therein contain, per 100 parts by weight total polyamide and polyester, about 50 to 90 parts of polyamide and dispersed therein about 50 to 10 parts of polyester.
- 5. The fabric of claim 4 wherein said polyamide is nylon 6.
- 6. The fabric of claim 4 wherein said polyester is polyethylene terephthalate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US75273968A | 1968-08-15 | 1968-08-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3619337A true US3619337A (en) | 1971-11-09 |
Family
ID=25027614
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US752739A Expired - Lifetime US3619337A (en) | 1968-08-15 | 1968-08-15 | Dimensionally stable fabric having a suedelike texture |
Country Status (1)
Country | Link |
---|---|
US (1) | US3619337A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4151023A (en) * | 1975-09-05 | 1979-04-24 | Phillips Petroleum Company | Method for the production of a nonwoven fabric |
EP0018785A1 (en) * | 1979-05-04 | 1980-11-12 | Toray Industries, Inc. | A nap-raised fabric and a method for its manufacture |
US20110059288A1 (en) * | 2009-09-04 | 2011-03-10 | Shavel Jonathan G | Flannel sheeting fabric for use in home textiles |
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Publication number | Priority date | Publication date | Assignee | Title |
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US3034194A (en) * | 1957-11-04 | 1962-05-15 | Callaway Mills Co | Method for producing a tufted fabric having a deep fleecelike surface and the resulting product |
US3090097A (en) * | 1959-02-24 | 1963-05-21 | Terlinden & Company | Method of making synthetic velvetlike knitted fabric |
US3099067A (en) * | 1957-09-13 | 1963-07-30 | Union Carbide Corp | Plastic fibers |
GB1035908A (en) * | 1962-07-31 | 1966-07-13 | British Nylon Spinners Ltd | Improvements in or relating to methods and apparatus for the production of heterofilaments and heteroyarns |
US3348983A (en) * | 1963-11-07 | 1967-10-24 | Nippon Telegraph & Telephone | Process for producing square hysteresis magnetic alloys |
US3369057A (en) * | 1964-05-18 | 1968-02-13 | Allied Chem | Polyamide-polyester dispersions wherein the polyamide is less than 40% amine terminated |
US3382305A (en) * | 1954-10-29 | 1968-05-07 | Du Pont | Process for preparing oriented microfibers |
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- 1968-08-15 US US752739A patent/US3619337A/en not_active Expired - Lifetime
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3382305A (en) * | 1954-10-29 | 1968-05-07 | Du Pont | Process for preparing oriented microfibers |
US3099067A (en) * | 1957-09-13 | 1963-07-30 | Union Carbide Corp | Plastic fibers |
US3034194A (en) * | 1957-11-04 | 1962-05-15 | Callaway Mills Co | Method for producing a tufted fabric having a deep fleecelike surface and the resulting product |
US3090097A (en) * | 1959-02-24 | 1963-05-21 | Terlinden & Company | Method of making synthetic velvetlike knitted fabric |
GB1035908A (en) * | 1962-07-31 | 1966-07-13 | British Nylon Spinners Ltd | Improvements in or relating to methods and apparatus for the production of heterofilaments and heteroyarns |
US3348983A (en) * | 1963-11-07 | 1967-10-24 | Nippon Telegraph & Telephone | Process for producing square hysteresis magnetic alloys |
US3369057A (en) * | 1964-05-18 | 1968-02-13 | Allied Chem | Polyamide-polyester dispersions wherein the polyamide is less than 40% amine terminated |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4151023A (en) * | 1975-09-05 | 1979-04-24 | Phillips Petroleum Company | Method for the production of a nonwoven fabric |
EP0018785A1 (en) * | 1979-05-04 | 1980-11-12 | Toray Industries, Inc. | A nap-raised fabric and a method for its manufacture |
US20110059288A1 (en) * | 2009-09-04 | 2011-03-10 | Shavel Jonathan G | Flannel sheeting fabric for use in home textiles |
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