JPH0768657B2 - Polyester stretchable dyed fiber structure and method for producing the same - Google Patents
Polyester stretchable dyed fiber structure and method for producing the sameInfo
- Publication number
- JPH0768657B2 JPH0768657B2 JP1323996A JP32399689A JPH0768657B2 JP H0768657 B2 JPH0768657 B2 JP H0768657B2 JP 1323996 A JP1323996 A JP 1323996A JP 32399689 A JP32399689 A JP 32399689A JP H0768657 B2 JPH0768657 B2 JP H0768657B2
- Authority
- JP
- Japan
- Prior art keywords
- polyester
- fiber
- cationic dye
- dyeable
- dyeing
- 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
- 239000000835 fiber Substances 0.000 title claims description 72
- 229920000728 polyester Polymers 0.000 title claims description 69
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 125000002091 cationic group Chemical group 0.000 claims description 51
- 238000004043 dyeing Methods 0.000 claims description 46
- 210000004177 elastic tissue Anatomy 0.000 claims description 45
- -1 polyethylene terephthalate Polymers 0.000 claims description 37
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 29
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 20
- 229920000570 polyether Polymers 0.000 claims description 20
- 229920001400 block copolymer Polymers 0.000 claims description 19
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 18
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 12
- 150000003871 sulfonates Chemical class 0.000 claims description 11
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 10
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 8
- 125000000524 functional group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 238000007334 copolymerization reaction Methods 0.000 claims description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 150000002989 phenols Chemical class 0.000 claims description 4
- FCDMUZZVRLCTLQ-UHFFFAOYSA-N 4-[1,1-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butyl]-2-tert-butyl-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(C=1C(=CC(O)=C(C=1)C(C)(C)C)C)(CCC)C1=CC(C(C)(C)C)=C(O)C=C1C FCDMUZZVRLCTLQ-UHFFFAOYSA-N 0.000 claims description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- 239000007983 Tris buffer Substances 0.000 claims description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 3
- 125000006289 hydroxybenzyl group Chemical group 0.000 claims 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims 1
- 239000000975 dye Substances 0.000 description 30
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 21
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 12
- 239000000460 chlorine Substances 0.000 description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 10
- 229910052801 chlorine Inorganic materials 0.000 description 10
- 239000000986 disperse dye Substances 0.000 description 10
- 230000006866 deterioration Effects 0.000 description 8
- 229920002635 polyurethane Polymers 0.000 description 8
- 239000004814 polyurethane Substances 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000012964 benzotriazole Substances 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 229920001778 nylon Polymers 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 239000010446 mirabilite Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910001873 dinitrogen Inorganic materials 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 206010022998 Irritability Diseases 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000000980 acid dye Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000007796 conventional method Methods 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
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- GJDRKHHGPHLVNI-UHFFFAOYSA-N 2,6-ditert-butyl-4-(diethoxyphosphorylmethyl)phenol Chemical compound CCOP(=O)(OCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 GJDRKHHGPHLVNI-UHFFFAOYSA-N 0.000 description 1
- XDZMPRGFOOFSBL-UHFFFAOYSA-N 2-ethoxybenzoic acid Chemical compound CCOC1=CC=CC=C1C(O)=O XDZMPRGFOOFSBL-UHFFFAOYSA-N 0.000 description 1
- HXIQYSLFEXIOAV-UHFFFAOYSA-N 2-tert-butyl-4-(5-tert-butyl-4-hydroxy-2-methylphenyl)sulfanyl-5-methylphenol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1SC1=CC(C(C)(C)C)=C(O)C=C1C HXIQYSLFEXIOAV-UHFFFAOYSA-N 0.000 description 1
- YRUPCSWZCGCUJC-UHFFFAOYSA-M 3,5-bis(2-hydroxyethoxycarbonyl)benzenesulfonate;tetraphenylphosphanium Chemical compound OCCOC(=O)C1=CC(C(=O)OCCO)=CC(S([O-])(=O)=O)=C1.C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 YRUPCSWZCGCUJC-UHFFFAOYSA-M 0.000 description 1
- PXQRVOCHISUSCC-UHFFFAOYSA-M 3-(2-hydroxyethoxycarbonyl)benzenesulfonate;tetrabutylphosphanium Chemical compound OCCOC(=O)C1=CC=CC(S([O-])(=O)=O)=C1.CCCC[P+](CCCC)(CCCC)CCCC PXQRVOCHISUSCC-UHFFFAOYSA-M 0.000 description 1
- KIINLFFTVAGQMM-UHFFFAOYSA-M 3-(2-hydroxyethoxycarbonyl)benzenesulfonate;tetraphenylphosphanium Chemical compound OCCOC(=O)C1=CC=CC(S([O-])(=O)=O)=C1.C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 KIINLFFTVAGQMM-UHFFFAOYSA-M 0.000 description 1
- JYQJLVPMTBJMTI-UHFFFAOYSA-M 4-(2-hydroxyethoxy)benzenesulfonate;tetrabutylphosphanium Chemical compound OCCOC1=CC=C(S([O-])(=O)=O)C=C1.CCCC[P+](CCCC)(CCCC)CCCC JYQJLVPMTBJMTI-UHFFFAOYSA-M 0.000 description 1
- WGLLPLKFAISNLZ-UHFFFAOYSA-K 4-sulfonatonaphthalene-2,6-dicarboxylate tetrabutylphosphanium Chemical compound CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC.[O-]C(=O)c1ccc2cc(cc(c2c1)S([O-])(=O)=O)C([O-])=O WGLLPLKFAISNLZ-UHFFFAOYSA-K 0.000 description 1
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 1
- QCSIRLGSMWDFMF-UHFFFAOYSA-K 5-sulfonatobenzene-1,3-dicarboxylate tetrabutylphosphanium Chemical compound [O-]C(=O)c1cc(cc(c1)S([O-])(=O)=O)C([O-])=O.CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC QCSIRLGSMWDFMF-UHFFFAOYSA-K 0.000 description 1
- BWLOPTUNEMCWSZ-UHFFFAOYSA-K 5-sulfonatobenzene-1,3-dicarboxylate tetraphenylphosphanium Chemical compound [O-]C(=O)c1cc(cc(c1)S([O-])(=O)=O)C([O-])=O.c1ccc(cc1)[P+](c1ccccc1)(c1ccccc1)c1ccccc1.c1ccc(cc1)[P+](c1ccccc1)(c1ccccc1)c1ccccc1.c1ccc(cc1)[P+](c1ccccc1)(c1ccccc1)c1ccccc1 BWLOPTUNEMCWSZ-UHFFFAOYSA-K 0.000 description 1
- FQVMIQKRLZHUDJ-UHFFFAOYSA-K 5-sulfonatobenzene-1,3-dicarboxylate tributyl(ethyl)phosphanium Chemical compound CCCC[P+](CC)(CCCC)CCCC.CCCC[P+](CC)(CCCC)CCCC.CCCC[P+](CC)(CCCC)CCCC.[O-]C(=O)c1cc(cc(c1)S([O-])(=O)=O)C([O-])=O FQVMIQKRLZHUDJ-UHFFFAOYSA-K 0.000 description 1
- DALNSBKXJGCIGM-UHFFFAOYSA-K 5-sulfonatobenzene-1,3-dicarboxylate tributyl(phenyl)phosphanium Chemical compound [O-]C(=O)c1cc(cc(c1)S([O-])(=O)=O)C([O-])=O.CCCC[P+](CCCC)(CCCC)c1ccccc1.CCCC[P+](CCCC)(CCCC)c1ccccc1.CCCC[P+](CCCC)(CCCC)c1ccccc1 DALNSBKXJGCIGM-UHFFFAOYSA-K 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- MAAPEMRACZBJAD-UHFFFAOYSA-K benzyl(tributyl)phosphanium 5-sulfonatobenzene-1,3-dicarboxylate Chemical compound [O-]C(=O)c1cc(cc(c1)S([O-])(=O)=O)C([O-])=O.CCCC[P+](CCCC)(CCCC)Cc1ccccc1.CCCC[P+](CCCC)(CCCC)Cc1ccccc1.CCCC[P+](CCCC)(CCCC)Cc1ccccc1 MAAPEMRACZBJAD-UHFFFAOYSA-K 0.000 description 1
- BUDPGRUUAXTNRB-UHFFFAOYSA-K benzyl(triphenyl)phosphanium 5-sulfonatobenzene-1,3-dicarboxylate Chemical compound [O-]C(=O)c1cc(cc(c1)S([O-])(=O)=O)C([O-])=O.C(c1ccccc1)[P+](c1ccccc1)(c1ccccc1)c1ccccc1.C(c1ccccc1)[P+](c1ccccc1)(c1ccccc1)c1ccccc1.C(c1ccccc1)[P+](c1ccccc1)(c1ccccc1)c1ccccc1 BUDPGRUUAXTNRB-UHFFFAOYSA-K 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- OCWYEMOEOGEQAN-UHFFFAOYSA-N bumetrizole Chemical compound CC(C)(C)C1=CC(C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O OCWYEMOEOGEQAN-UHFFFAOYSA-N 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- JHPRWPIHJBDGSI-UHFFFAOYSA-K butyl(triphenyl)phosphanium 5-sulfonatobenzene-1,3-dicarboxylate Chemical compound [O-]C(=O)c1cc(cc(c1)S([O-])(=O)=O)C([O-])=O.CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1 JHPRWPIHJBDGSI-UHFFFAOYSA-K 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- GVBWZHALHMDKQL-UHFFFAOYSA-K ethyl(triphenyl)phosphanium 5-sulfonatobenzene-1,3-dicarboxylate Chemical compound [O-]C(=O)c1cc(cc(c1)S([O-])(=O)=O)C([O-])=O.CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1 GVBWZHALHMDKQL-UHFFFAOYSA-K 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- MSBWDNNCBOLXGS-UHFFFAOYSA-L manganese(2+);diacetate;hydrate Chemical compound O.[Mn+2].CC([O-])=O.CC([O-])=O MSBWDNNCBOLXGS-UHFFFAOYSA-L 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
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 238000001782 photodegradation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Coloring (AREA)
- Artificial Filaments (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Woven Fabrics (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、ポリエステル系伸縮性染色繊維構造物および
その製造方法に関し、さらに詳しくは、外観が優れ、鮮
明で優れた染色堅牢度を有するポリエステル系伸縮性染
色繊維構造物およびその製造方法に関する。TECHNICAL FIELD The present invention relates to a polyester-based stretchable dyed fiber structure and a method for producing the same, and more specifically, a polyester having an excellent appearance, vividness and excellent dyeing fastness. Stretchable dyed fiber structure and a method for producing the same.
従来、弾性繊維としては、ポリウレタン系のものが多く
使用されているが、ポリウレタン系弾性繊維は、弾性回
復の点では優れた特性を示す反面、耐熱水性が劣り、ナ
イロン繊維との混用で酸性染料を中心にして、ボイル温
度付近で染色が行われている。Conventionally, polyurethane-based elastic fibers are often used as the elastic fibers, but the polyurethane-based elastic fibers have excellent properties in terms of elastic recovery, but have poor hot water resistance and are acidic dyes when mixed with nylon fibers. Is dyed around the boil temperature.
一方、弾性繊維として、ポリエーテル・ポリエステルブ
ロック共重合体弾性繊維も用いられるようになってきて
おり、ポリエチレンテレフタレート系ポリエステル繊維
と混用して、分散染料で染色する方法が提案されている
(特公昭61−49433号公報)。On the other hand, as the elastic fiber, a polyether / polyester block copolymer elastic fiber has come to be used, and a method of mixing it with a polyethylene terephthalate polyester fiber and dyeing with a disperse dye has been proposed (Japanese Patent Publication No. 61-49433).
しかしながら、ポリウレタン系弾性繊維とナイロン繊維
との混用においては、ナイロン繊維が寸法安定性に劣
り、満足な風合いが得られにくいという問題があり、さ
らにはスポーツ衣料の一部用途では、鮮明性の不足が指
摘されてきた。However, when the polyurethane elastic fiber and nylon fiber are mixed, there is a problem that the nylon fiber is inferior in dimensional stability and it is difficult to obtain a satisfactory texture. Furthermore, in some applications of sports clothing, lack of sharpness is insufficient. Has been pointed out.
また、ポリウレタン系弾性繊維とナイロン繊維とを組合
せたものを酸性染料で染色する場合と、染料のナイロン
に対する染着量が多く、逆にポリウレタン系弾性繊維に
対する染着量が少ないため、染色された布帛を伸長させ
た際に著しく審美性を損なうという欠点を有していた。Further, when a combination of polyurethane elastic fiber and nylon fiber is dyed with an acid dye, and when the dye has a large amount of dyeing on nylon, and conversely the amount of dyeing on polyurethane elastic fiber is small, it is dyed. It has a drawback that the aesthetic property is significantly impaired when the fabric is stretched.
他方、ポリエーテル・ポリエステルブロック共重合体弾
性繊維は、ポリウレタン系弾性繊維に比較して耐湿熱性
が良好で、ポリエステル繊維との混用で高温高圧染色が
可能である。On the other hand, the polyether / polyester block copolymer elastic fibers have better wet heat resistance than polyurethane elastic fibers, and can be mixed with polyester fibers for high temperature / high pressure dyeing.
しかし、このタイプの弾性繊維は、イオン性の染着座席
を持っていないのでイオン性染料では染色されず、通常
分散染料で染色がなされる。However, since this type of elastic fiber does not have an ionic dyeing seat, it is not dyed with an ionic dye, but is usually dyed with a disperse dye.
かかるタイプの弾性繊維とポリエステル系繊維を混用し
た繊維構造物を分散染料によって染色した場合、弾性繊
維は分散染料に対し易染性で、例えば60〜100℃の温度
領域で染着し、しかもポリエステル系繊維よりも染着度
が大きく、染めあがった繊維構造物の湿潤堅牢度が劣
り、実用に耐えうる染色濃度は、分散染料のタイプある
いは該繊維構造物の混用比率にもよるが、0.2重量%程
度までであり、極淡色程度の染色は可能であるが、中色
ないし濃色の染色は不可能であるという問題がある。When a fiber structure in which an elastic fiber of this type and a polyester fiber are mixed is dyed with a disperse dye, the elastic fiber is easily dyeable to the disperse dye, for example, dyes in a temperature range of 60 to 100 ° C., and is polyester. The degree of dyeing is larger than that of the system fiber, the wet fastness of the dyed fiber structure is inferior, and the dyeing concentration that can be practically used depends on the type of the disperse dye or the mixing ratio of the fiber structure, but is 0.2% by weight. %, And it is possible to dye extremely light colors, but there is a problem that it is impossible to dye medium to dark colors.
また、このタイプの弾性繊維は、一般にポリウレタン系
弾性繊維と同様に、光劣化、酸化劣化が大きく、長時間
にわたって光を照射したり、塩素水中に浸漬すると、伸
縮特性が劣化し、スキーパンツのような耐光性が要求さ
れる分野、あるいは水着のような耐塩素性が要求される
分野では、長時間の使用が困難であるという問題があ
る。In addition, this type of elastic fiber generally has large photodegradation and oxidative deterioration similarly to polyurethane-based elastic fiber, and when it is irradiated with light for a long time or immersed in chlorine water, its elastic property deteriorates, and ski pants There is a problem that it is difficult to use for a long time in such a field requiring light resistance or in a field requiring chlorine resistance such as a swimsuit.
従って、本発明の目的は、かかる従来技術の問題点を解
消し、審美性、鮮明性、染色堅牢度に優れ、さらには耐
光劣化性、耐塩素劣化性にも優れた伸縮性染色繊維構造
物およびその製造方法を提供することにある。Therefore, the object of the present invention is to solve the problems of the prior art, stretchable dyed fiber structure excellent in aesthetics, sharpness, dyeing fastness, and further excellent in light resistance and chlorine resistance. And to provide a manufacturing method thereof.
本発明は、カチオン染料可染ポリエチレンテレフタレー
ト系ポリエステル繊維とカチオン染料可染ポリエーテル
・ポリエステルブロック共重合体弾性繊維とを混用した
繊維構造物を、カチオン染料で染色してなるポリエステ
ル系伸縮性染色繊維構造物であって、該カチオン染料可
染ポリエチレンテレフタレート系ポリエステル繊維の見
掛染着度Laと、該カチオン染料可染ポリエーテル・ポリ
エステルブロック共重合体弾性繊維の見掛け染着度Lbと
が、下記式(I)を満足していることを特徴とするポリ
エステル系伸縮性染色繊維構造物である。The present invention is a polyester-based stretchable dyed fiber obtained by dyeing a fiber structure obtained by mixing a cationic dye-dyeable polyethylene terephthalate-based polyester fiber and a cationic dye-dyeable polyether / polyester block copolymer elastic fiber with a cationic dye. In the structure, the apparent dyeing degree La of the cationic dye-dyeable polyethylene terephthalate-based polyester fiber and the apparent dyeing degree Lb of the cationic dye-dyeable polyether / polyester block copolymer elastic fiber are as follows: A polyester stretchable dyed fiber structure characterized by satisfying the formula (I).
|La−Lb|≦35 ・・・・・(I) (式中、LaはCIE測色系で測色したカチオン染料可染ポ
リエチレンテレフタレート系ポリエステル繊維のL値
を、Lbは同じくCIE測色系で測色したカチオン染料可染
ポリエーテル・ポリエステルブロック共重合体弾性繊維
のL値を表す。) さらに、本発明は、カチオン染料可染ポリエチレンテレ
フタレート系ポリエステル繊維とカチオン染料可染ポリ
エーテル・ポリエステルブロック共重合体弾性繊維とを
混用した繊維構造物を、2−(3−t−ブチル−5−メ
チル−2−ヒドロキシフェニル)−5−クロロベンゾト
リアゾールおよび/または2−(3,5−ジ−t−ブチル
−2−ヒドロキシフェニル)−5−クロロベンゾトリア
ゾールならびにヒンダードフェノール系化合物を該繊維
構造物に対し各々0.1〜4重量%(owf)添加したカチオ
ン染料染浴で染色することを特徴とするポリエステル系
伸縮性染色繊維構造物の製造方法である。| La−Lb | ≦ 35 (I) (In the formula, La is the L value of the polyethylene terephthalate polyester fiber dyeable with a cationic dye, which is measured by the CIE colorimetric system, and Lb is the CIE colorimetric system. The L value of the cationic dye-dyeable polyether / polyester block copolymer elastic fiber is measured by.) Furthermore, the present invention is a cationic dye-dyeable polyethylene terephthalate-based polyester fiber and a cationic dye-dyeable polyether / polyester block. A fiber structure containing a mixture of a copolymer elastic fiber and a 2- (3-t-butyl-5-methyl-2-hydroxyphenyl) -5-chlorobenzotriazole and / or 2- (3,5-di- The t-butyl-2-hydroxyphenyl) -5-chlorobenzotriazole and the hindered phenol compound are each contained in the fiber structure in an amount of 0.1 to 4% by weight (owf). A method for producing a polyester-based stretchable dyed fiber structure, characterized by staining with the added cationic dye dyebath.
本発明において用いられる弾性繊維は、ポリエーテル・
ポリエステルブロック共重合体弾性繊維であり、特にテ
レフタル酸を主とするジカルボン酸および/またはその
エステル形成性誘導体(A成分)、 下記一般式(II)および/または(III)で表されるス
ルホン酸塩類(B成分)、 (式中、Z1芳香族基または脂肪族基を、A1はエステル形
成性官能基を、A2はA1と同一もしくは異なるエステル形
成性官能基または水素原子を、R1、R2、R3、およびR4は
アルキル基およびアリール基よりなる群から選ばれる同
一または異なる基を、nは正の整数を表す。) (式中、Z2は芳香族基または脂肪族基を、A3はエステル
形成性官能基を、A4はA3と同一もしくは異なるエステル
形成性官能基または水素原子を、Xは金属原子を、nは
正の整数を表す。) 1,4−ブタンジオールを主とするグリコールおよび/ま
たはそのエステル形成性誘導体(C成分)、および 平均分子量が約400〜6,000のポリオキシアルキレングリ
コール(D成分) を構成成分としたブロック共重合体であることが好まし
い。The elastic fiber used in the present invention is polyether.
Polyester block copolymer elastic fiber, particularly dicarboxylic acid mainly containing terephthalic acid and / or its ester-forming derivative (component A), sulfonic acid represented by the following general formula (II) and / or (III) Salts (B component), (In the formula, Z 1 aromatic group or aliphatic group, A 1 is an ester-forming functional group, A 2 is the same or different from A 1 an ester-forming functional group or a hydrogen atom, R 1 , R 2 , R 3 and R 4 represent the same or different groups selected from the group consisting of alkyl groups and aryl groups, and n represents a positive integer.) (In the formula, Z 2 is an aromatic group or an aliphatic group, A 3 is an ester-forming functional group, A 4 is an ester-forming functional group which is the same as or different from A 3 , or a hydrogen atom, and X is a metal atom. , N represents a positive integer.) Glycol mainly containing 1,4-butanediol and / or its ester-forming derivative (C component), and polyoxyalkylene glycol having an average molecular weight of about 400 to 6,000 (D component). It is preferable that the block copolymer is a block copolymer containing
テレフタル酸を主とするジカルボン酸および/またはそ
のエステル形成性誘導体(A成分)としては、テレフタ
ル酸の他に、例えばイソフタル酸、ナフタレンジカルボ
ン酸、ジフェニルジカルボン酸、ジフェノキシエタンジ
カルボン酸、β−ヒドロキシエトキシ安息香酸、p−オ
キシ安息香酸、アジピン酸、セバシン酸、1,4−シクロ
ヘキサンジカルボン酸の如き芳香族、脂肪族、脂環族の
二官能性カルボン酸およびそれらの炭素数1〜4の低級
ジアルキルエステル、フェニルエステルなどを挙げるこ
とができる。Examples of the dicarboxylic acid mainly containing terephthalic acid and / or its ester-forming derivative (component A) include, in addition to terephthalic acid, for example, isophthalic acid, naphthalenedicarboxylic acid, diphenyldicarboxylic acid, diphenoxyethanedicarboxylic acid, β-hydroxyl. Aromatic, aliphatic or alicyclic bifunctional carboxylic acids such as ethoxybenzoic acid, p-oxybenzoic acid, adipic acid, sebacic acid and 1,4-cyclohexanedicarboxylic acid and their lower ones having 1 to 4 carbon atoms. Examples thereof include dialkyl ester and phenyl ester.
スルホン酸塩類(B成分)としては、具体的には、3,5
−ジカルボキシベンゼンスルホン酸テトラブチルホスホ
ニウム塩、3,5−ジカルボキシベンゼンスルホン酸エチ
ルトリブチルホスホニウム塩、3,5−ジカルボキシベン
ゼンスルホン酸ベンジルトリブチルホスホニウム塩、3,
5−ジカルボキシベンゼンスルホン酸フェニルトリブチ
ルホスホニウム塩、3,5−ジカルボキシベンゼンスルホ
ン酸テトラフェニルホスホニウム塩、3,5−ジカルボキ
シベンゼンスルホン酸エチルトリフェニルホスホニウム
塩、3,5−ジカルボキシベンゼンスルホン酸ブチルトリ
フェニルホスホニウム塩、3,5−ジカルボキシベンゼン
スルホン酸ベンジルトリフェニルホスホニウム塩、3,5
−ジ(β−ヒドロキシエトキシカルボニル)ベンゼンス
ルホン酸テトラフェニルホスホニウム塩、3−(β−ヒ
ドロキシエトキシカルボニル)ベンゼンスルホン酸テト
ラブチルホスホニウム塩、3−(β−ヒドロキシエトキ
シカルボニル)ベンゼンスルホン酸テトラフェニルホス
ホニウム塩、4−ヒドロキシエトキシベンゼンスルホン
酸テトラブチルホスホニウム塩、2,6−ジカルボキシナ
フタレン−4−スルホン酸テトラブチルホスホニウム
塩、α−テトラブチルホスホニウムスルホコハク酸、ジ
メチルイソフタレート−S−スルホン酸ナトリウムなと
を挙げることができる。前記スルホン酸塩類は、1種の
みを単独で用いても2種以上併用してもよい。Specific examples of the sulfonates (B component) include 3,5
-Dicarboxybenzenesulfonic acid tetrabutylphosphonium salt, 3,5-dicarboxybenzenesulfonic acid ethyltributylphosphonium salt, 3,5-dicarboxybenzenesulfonic acid benzyltributylphosphonium salt, 3,
5-Dicarboxybenzenesulfonic acid phenyltributylphosphonium salt, 3,5-dicarboxybenzenesulfonic acid tetraphenylphosphonium salt, 3,5-dicarboxybenzenesulfonic acid ethyl triphenylphosphonium salt, 3,5-dicarboxybenzenesulfonic acid Butyltriphenylphosphonium salt, 3,5-dicarboxybenzenesulfonic acid benzyltriphenylphosphonium salt, 3,5
-Di (β-hydroxyethoxycarbonyl) benzenesulfonic acid tetraphenylphosphonium salt, 3- (β-hydroxyethoxycarbonyl) benzenesulfonic acid tetrabutylphosphonium salt, 3- (β-hydroxyethoxycarbonyl) benzenesulfonic acid tetraphenylphosphonium salt , 4-hydroxyethoxybenzenesulfonic acid tetrabutylphosphonium salt, 2,6-dicarboxynaphthalene-4-sulfonic acid tetrabutylphosphonium salt, α-tetrabutylphosphonium sulfosuccinic acid, dimethylisophthalate-S-sulfonic acid sodium salt, etc. Can be mentioned. The sulfonates may be used alone or in combination of two or more.
1,4−ブタンジオールを主とするグリコールおよび/ま
たはそのエステル形成性誘導体(C成分)の具体例とし
ては、1,4−ブタンジオールの他に、エチレングリコー
ル、1,3−プロパンジオール、トリエチレングリコー
ル、1,4−シクロヘキサンジメタノールおよびそれらの
エステルを挙げることができる。Specific examples of the glycol mainly containing 1,4-butanediol and / or its ester-forming derivative (component C) include 1,4-butanediol, ethylene glycol, 1,3-propanediol, and triglyceride. Mention may be made of ethylene glycol, 1,4-cyclohexanedimethanol and their esters.
平均分子量が約400〜6,000のポリオキシアルキレングリ
コール(D成分)としては、ポリエチレングリコール、
ポリプロピレングリコール、ポリテトラメチレングリコ
ールおよびこれらの共重合体なとが挙げられる。Polyoxyalkylene glycol (D component) having an average molecular weight of about 400 to 6,000 includes polyethylene glycol,
Examples thereof include polypropylene glycol, polytetramethylene glycol and copolymers thereof.
この場合、スルホン酸塩類(B成分)の共重合量は、共
重合体全体に対して0.2〜10モル%であることが必要で
ある。B成分の共重合量が0.2モル%未満の場合は、カ
チオン染料による染着度が低くなり、目的とする良好な
審美性が得られない。一方、B成分が10モル%を越える
場合は、乾熱処理、湿熱処理時に弾性特性が低下するた
め好ましくない。In this case, the copolymerization amount of the sulfonates (component B) needs to be 0.2 to 10 mol% with respect to the entire copolymer. When the copolymerization amount of the component B is less than 0.2 mol%, the degree of dyeing with the cationic dye is low and the desired good aesthetic properties cannot be obtained. On the other hand, if the content of the component B exceeds 10 mol%, the elastic properties are deteriorated during dry heat treatment and wet heat treatment, which is not preferable.
本発明で用いられるカチオン染料可染ポリエチレンテレ
フタレート系ポリエステル繊維は、前記一般式(II)お
よび/または(III)で表されるスルホン酸塩類(B成
分)を1〜5モル%共重合させたものであることが好ま
しい。The cationic dye-dyeable polyethylene terephthalate-based polyester fiber used in the present invention is obtained by copolymerizing 1 to 5 mol% of the sulfonates (component B) represented by the general formula (II) and / or (III). Is preferred.
スルホン酸塩類(B成分)の共重合量が1モル%未満で
あると、カチオン染料の染着度が低くなり、実用性がな
い。逆に、5モル%を越えると、カチオン染料染色物の
視感による染着濃度は飽和状態になるとともに、染色処
理により該繊維の強度劣化が起こり、繊維構造物の物性
低下があり好ましくない。If the copolymerization amount of the sulfonates (component B) is less than 1 mol%, the degree of dyeing of the cationic dye will be low, which is not practical. On the other hand, if it exceeds 5 mol%, the dyeing density of the cationic dye dyeing product becomes saturated and the strength of the fiber is deteriorated by the dyeing treatment, resulting in deterioration of the physical properties of the fiber structure, which is not preferable.
スルホン酸塩類の具体的化合物としては、前記(B)成
分として使用される化合物類を同一または異なって使用
でき、これらは1種のみを単独で用いても2種以上併用
してもよい。As specific compounds of the sulfonates, the compounds used as the component (B) may be the same or different, and these may be used alone or in combination of two or more.
本発明における繊維構造物は、不織布、織編物などの任
意の形態のものを含み、カチオン染料可染ポリエチレン
テレフタレート系ポリエステル繊維とカチオン染料可染
ポリエーテル・ポリエステルブロック共重合体弾性繊維
とを混用することにより形成されている。混用の方法と
しては、例えば弾性繊維をポリエステル繊維で被覆した
糸条を用いて、この糸条単独またはポリエステル繊維糸
条とともに織編物とすることができる。The fibrous structure in the present invention includes non-woven fabrics, woven and knitted fabrics and the like in any form, and uses a mixture of cationic dye-dyeable polyethylene terephthalate-based polyester fibers and cationic dye-dyeable polyether / polyester block copolymer elastic fibers. It is formed by As a mixing method, for example, a yarn in which elastic fibers are coated with polyester fibers is used, and the yarn alone or a polyester fiber yarn can be formed into a woven or knitted fabric.
弾性繊維をポリエステル繊維で被覆する方法としては、
中空スピンドルを利用した撚糸によりカバリングする方
法、引き揃え糸を合撚し、両繊維の伸度差により被覆す
る方法、精紡機を利用し、コアスパンによる方法などが
ある。さらに、弾性繊維を裸糸で使用し、ポリエステル
繊維糸条と交編織してもよい。As a method of coating the elastic fiber with the polyester fiber,
There are a method of covering with a twisted yarn using a hollow spindle, a method of twisting and aligning drawn yarns and covering with a difference in elongation of both fibers, and a method using a spinning machine and a core span. Further, the elastic fiber may be used as a bare thread and may be interwoven with the polyester fiber thread.
弾性繊維が裸糸で使用されるのは、編物の場合が多く、
経編物、丸編物のいずれでも使用することができる。The elastic fibers used in the bare thread are often knitted,
Either a warp knit or a circular knit can be used.
カチオン染料可染ポリエチレンテレフタレート系ポリエ
ステル繊維とカチオン染料可染ポリエーテル・ポリエス
テルブロック共重合体弾性繊維とを混用してなる繊維構
造物を、カチオン染料で染色するには通常の方法が採用
される。すなわち、染色温度は、80〜135℃の範囲内、
好ましくは100〜130℃が適当であり、さらには弾性繊
維、ポリエステル繊維の強度劣化を防止するために芒硝
を2〜3g/程度染浴に添加することが望ましい。淡色
に染色した場合の染色後の洗浄は省略可能であるが、濃
色染色後の洗浄方法はカチオン染料を洗浄するための通
常の方法が用いられる。特に好ましくは酢酸および/ま
たはアルキルアリスルホン酸塩のホルマリン縮合物の水
溶液で、60〜90℃の温度で洗浄するのが好ましい。A usual method is used for dyeing a fiber structure obtained by mixing a cationic dye-dyeable polyethylene terephthalate-based polyester fiber and a cationic dye-dyeable polyether / polyester block copolymer elastic fiber with a cationic dye. That is, the dyeing temperature is within the range of 80 to 135 ° C,
The temperature is preferably 100 to 130 ° C., and it is desirable to add Glauber's salt to the dyeing bath in an amount of about 2 to 3 g / in order to prevent the strength deterioration of the elastic fiber and the polyester fiber. Washing after dyeing in a light color can be omitted, but as a washing method after dark dyeing, a usual method for washing a cationic dye is used. It is particularly preferable to wash with an aqueous solution of a formalin condensate of acetic acid and / or alkylarisulfonate at a temperature of 60 to 90 ° C.
かくして染色されたポリエステル系伸縮性染色繊維構造
物において、カチオン染料可染ポリエチレンテレフタレ
ート系ポリエステル繊維の見掛け染着どLaとカチオン染
料可染ポリエーテル・ポリエステルブロック共重合体弾
性繊維の見掛け染着度Lbとが、 |La−Lb|≦35 なる関係を満足していることが必要である。ここで、見
掛け染着度La、Lbは、それぞれCIE測色系で測色したL
値であり、数値が低いほど濃色に染色していることを示
す。In the polyester stretchable dyed fiber structure dyed in this way, the apparent dyeing La of the cationic dye dyeable polyethylene terephthalate polyester fiber and the cationic dye dyeable polyether / polyester block copolymer elastic fiber apparent dyeing degree Lb And must satisfy the relationship | La−Lb | ≦ 35. Here, the apparent dyeing degrees La and Lb are L measured by the CIE colorimetric system, respectively.
It is a value, and the lower the value is, the darker the color is.
この関係を満足させるには、両繊維におけるスルホン酸
塩類の共重合量を適宜調節すればよい。|La−Lb|が35を
超えると染色繊維構造物を伸張した際にいらつきが生
じ、審美性が悪化する。In order to satisfy this relationship, the copolymerization amount of sulfonates in both fibers may be adjusted appropriately. When | La−Lb | exceeds 35, irritability occurs when the dyed fiber structure is stretched, resulting in poor aesthetics.
このようにしてカチオン染料で染色された繊維構造物
は、弾性繊維とポリエステル繊維の両方がイオン結合に
よってカチオン染料と結合しており、カチオン染料は酸
性染料、分散染料よりも鮮明なものが多いなどの理由か
ら、鮮明で染色湿潤堅牢性に優れたものとなり、しかも
弾性繊維とポリエステル繊維の見掛け染着度が特定範囲
内に規制されているため、外観、審美性に優れたものと
なる。In the fiber structure dyed with the cationic dye in this way, both the elastic fiber and the polyester fiber are bonded to the cationic dye by an ionic bond, and the cationic dye is often clearer than the acid dye and the disperse dye. For this reason, it is clear and has excellent dyeing wet fastness, and since the apparent dyeing degree of the elastic fiber and the polyester fiber is regulated within a specific range, the appearance and aesthetics are excellent.
さらに、本発明においては、カチオン染料可染ポリエチ
レンテレフタレート系ポリエステル繊維とカチオン染料
可染ポリエーテル・ポリエステルブロック共重合体弾性
繊維とを混用した繊維構造物をカチオン染料で染色する
に際し、2−(3−t−ブチル−5−メチル−2−ヒド
ロキシフェニル)−5−クロロベンゾトリアゾールおよ
び/または2−(3,5−ジ−t−ブチル−2−ヒドロキ
シフェニル)−5−クロロベンゾトリアゾールならびに
ヒンダードフェノール系化合物を該繊維構造物に対し各
々0.1〜4重量%(owf)添加した染浴で染色することに
より、弾性繊維の光劣化、塩素劣化を防止することがで
きる。Further, in the present invention, when dyeing a fiber structure in which a cationic dye-dyeable polyethylene terephthalate-based polyester fiber and a cationic dye-dyeable polyether / polyester block copolymer elastic fiber are mixed with a cationic dye, 2- (3) -T-Butyl-5-methyl-2-hydroxyphenyl) -5-chlorobenzotriazole and / or 2- (3,5-di-t-butyl-2-hydroxyphenyl) -5-chlorobenzotriazole and hindered Dyeing with a dye bath in which 0.1 to 4% by weight (owf) of the phenolic compound is added to the fiber structure can prevent the elastic fiber from being deteriorated by light and chlorine.
ここで用いられるヒンダードフェノール系化合物として
は、例えばオクタデシル−3−(3,5−ジ−t−ブチル
−4−ヒドロキシフェニル)プロピオネート、4,4′−
チオビス(3−メチル−6−t−ブチルフェノール)、
2,2′−メチレンビス−(4−メチル−6−t−ブチル
フェノール)、N,N′−ヘキサメチレンビス(3,5−ジ−
t−ブチル−4−ヒドロキシ−ヒドロシンナマイド)、
3,5−ジ−t−ブチル−4−ヒドロキシ−ベンジルホス
ホネート−ジエチルエステル、1,3,5−トリメチル−2,
4,6−トリス−(3,5−ジ−t−ブチル−4−ヒドロキシ
ベンジル)ベンゼン、トリス(2−メチル−4−ヒドロ
キシ−5−t−ブチルフェニル)ブタン、トリス(3,5
−ジ−t−ブチル−4−ヒドロキシベンジル)イソシア
ヌレイトなどがあげられるが、特に好ましくは、1,3,5
−トリメチル−2,4,6−トリス−(3,5−ジ−t−ブチル
−4−ヒドロキシベンジル)ベンゼン、トリス(2−メ
チル−4−ヒドロキシ−5−t−ブチルフェニル)ブタ
ン、トリス(3,5−ジ−t−ブチル−4−ヒドロキシベ
ンジル)イソシアヌレイトが挙げられる。Examples of the hindered phenol compound used here include octadecyl-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate and 4,4′-
Thiobis (3-methyl-6-t-butylphenol),
2,2'-methylenebis- (4-methyl-6-t-butylphenol), N, N'-hexamethylenebis (3,5-di-
t-butyl-4-hydroxy-hydrocinnamide),
3,5-di-t-butyl-4-hydroxy-benzylphosphonate-diethyl ester, 1,3,5-trimethyl-2,
4,6-Tris- (3,5-di-t-butyl-4-hydroxybenzyl) benzene, tris (2-methyl-4-hydroxy-5-t-butylphenyl) butane, tris (3,5
-Di-t-butyl-4-hydroxybenzyl) isocyanurate and the like, and particularly preferably 1,3,5
-Trimethyl-2,4,6-tris- (3,5-di-t-butyl-4-hydroxybenzyl) benzene, tris (2-methyl-4-hydroxy-5-t-butylphenyl) butane, tris ( 3,5-di-t-butyl-4-hydroxybenzyl) isocyanurate.
このように、特定のベンゾトリアゾール系化合物とヒン
ダードフェノール系化合物とを併用することにより、耐
光劣化性のみならず、耐塩素劣化性も大幅に改善され、
長期間にわたって弾性繊維の伸縮性が維持される。As described above, by using the specific benzotriazole-based compound and the hindered phenol-based compound in combination, not only the light deterioration resistance but also the chlorine resistance deterioration is significantly improved,
The elasticity of the elastic fiber is maintained for a long period of time.
本発明は、従来のポリウレタン系弾性繊維の耐熱性を改
良したポリエーテル・ポリエステルブロック共重合体弾
性繊維をカチオン染料可染タイプに改良したものと、カ
チオン染料可染ポリエチレンテレフタレート系ポリエス
テル繊維とを混用した繊維構造物をカチオン染料で染色
し、両繊維の見掛け染着濃度を特定の範囲に制御するこ
とにより、審美性、鮮明性はもとより、染色湿潤堅牢度
にも優れた伸縮性染色繊維構造物を得るものである。The present invention is a mixture of a polyether / polyester block copolymer elastic fiber improved in heat resistance of a conventional polyurethane elastic fiber into a cationic dye dyeable type and a cationic dye dyeable polyethylene terephthalate polyester fiber. Stretch-dyed fiber structure that is excellent not only in aesthetics and sharpness but also in dyeing wet fastness by dyeing the formed fiber structure with a cationic dye and controlling the apparent dyeing density of both fibers within a specific range. Is what you get.
また、この染色に際し、染浴に特定のベンゾトリアゾー
ル系化合物とヒンダードフェノール系化合物とを併用添
加することにより、耐光劣化性はもとより耐塩素劣化性
も大幅に改良される。Further, in this dyeing, by adding a specific benzotriazole-based compound and a hindered phenol-based compound together to the dyeing bath, not only the light resistance but also the chlorine resistance is significantly improved.
以下、実施例により本発明をさらに詳細に説明する。 Hereinafter, the present invention will be described in more detail with reference to Examples.
なお、実施例中の部は、重量基準を示す。In addition, the part in an Example shows a weight standard.
また、以下の実施例および比較例において、L値は、マ
クベス TYPE 2020(米国モルボーゲン社製)でD65光
源で測色したものであり、湿潤堅牢度は、AATCC II-A法
により測定したものである。In the following Examples and Comparative Examples, the L value was measured by Macbeth TYPE 2020 (Morbogen Company, USA) with a D65 light source, and the wet fastness was measured by the AATCC II-A method. is there.
さらに、審美性は、100%伸長時のいらつき程度を視感
判断したものである。Furthermore, the aesthetics is a visual judgment of the degree of irritability at 100% elongation.
さらに、耐光劣化性は、染色織物を30%伸長させた状態
で63℃で120時間フェード照射したのち、30倍実体顕微
鏡視野(径6mm円)中の弾性繊維の切断箇所が0個の場
合を○印、1〜4の場合を△印、5個以上の場合を×印
とした。Furthermore, the resistance to light deterioration was measured when the dyed fabric was faded at 63 ° C for 120 hours in a stretched state of 30%, and the number of elastic fiber cuts in the 30x stereoscopic microscope field (diameter 6 mm circle) was 0. The ∘ mark, the 1 to 4 cases were the Δ mark, and the cases of 5 or more were the X mark.
さらに、耐塩素劣化性は、染色織物を30%伸長させた状
態で次亜塩素酸ゾーダに有効塩素を300ppmに調整した塩
素水中で24℃で96時間浸漬したのち、30倍実体顕微鏡視
野(径6mm円)中の弾性繊維の切断箇所が0個の場合を
○印、1〜4の場合を△印、5個以上の場合を×印とし
た。In addition, the chlorine deterioration resistance is 30% stereoscopic field of view after dipping for 96 hours at 24 ° C in chlorine water with effective chlorine adjusted to 300ppm in hypochlorous acid soda with the dyed fabric stretched 30%. The number of cut points of the elastic fiber in 6 mm circle) is 0, the case of 1 to 4 is Δ, the case of 5 or more is x.
実施例1〜4および比較例1〜4 ジメチルテレフタレート167.3部、テトラメチレングリ
コール105部、数平均分子量2,000のポリテトラメチレン
グリコール275部、テトラブチルチタネート0.2部を反応
機に仕込み、内温190℃でエステル交換反応を行った。
理論量の約70重量%のメタノールが留出した時点で第1
表に示すスルホン酸塩類を添加し内温200〜240℃に昇温
し、弱真空下で60分、次いで高真空下で200分反応させ
た。Examples 1 to 4 and Comparative Examples 1 to 4 167.3 parts of dimethyl terephthalate, 105 parts of tetramethylene glycol, 275 parts of polytetramethylene glycol having a number average molecular weight of 2,000, and 0.2 parts of tetrabutyl titanate were charged in a reactor at an internal temperature of 190 ° C. A transesterification reaction was performed.
When about 70% by weight of theoretical amount of methanol was distilled, the first
The sulfonates shown in the table were added, the internal temperature was raised to 200 to 240 ° C., and the reaction was performed under a weak vacuum for 60 minutes and then under a high vacuum for 200 minutes.
生成したカチオン染料可染ポリエーテル・ポリエステル
ブロック共重合体をペレット化したのち、該ペレットを
乾燥後250℃で溶融し、6ホールのノズルを持つキャッ
プで押し出し、40デニール/6フィラメントの弾性糸を得
た。The produced cationic dye-dyeable polyether / polyester block copolymer is pelletized, the pellets are dried and then melted at 250 ° C., and extruded with a cap having a 6-hole nozzle to obtain 40 denier / 6 filament elastic yarn. Obtained.
一方、ジメチルテレフタレート100部、エチレングリコ
ール60部、酢酸マンガン水塩0.03部(ジメチルテレフタ
レートに対して0.024部)、ジメチルテレフタレートに
対して第1表のスルホン酸塩類をエステル交換缶に仕込
み、チッソガス雰囲気下3時間かけて、140℃から220℃
まで昇温して生成するメタノールを系外に留去しながら
エステル交換反応させた。On the other hand, 100 parts of dimethyl terephthalate, 60 parts of ethylene glycol, 0.03 part of manganese acetate hydrate (0.024 part to dimethyl terephthalate) and sulfonates of Table 1 were charged to dimethyl terephthalate in an ester exchange can under a nitrogen gas atmosphere. 140 ° C to 220 ° C over 3 hours
The transesterification reaction was carried out while evaporating the methanol produced by heating to the outside of the system.
続いて得られた生成物に、安定剤として正リン酸の56%
水溶液0.03部(ジメチルテレフタレートに対して0.033
モル%)を添加し、同時に過剰のエチレングリコール昇
温追い出しを開始した。10分後に重縮合触媒として三酸
化アンチモン0.04部(ジメチルテレフタレートに対して
0.027モル%)を添加した。内温が240℃に達した時点で
エチレングリコールの追い出しを完了し、反応生成物を
重合缶に移した。次いで、昇温しながら内温が260℃に
達するまで常圧反応させたのち、1時間かけて760mmHg
から1mmHgまで減圧し、同時に1時間30分かけて内温を2
80℃まで昇温した。1mmHg以下の減圧下、重合温度280℃
でさらに2時間重合した時点でチッソガスで真空を破っ
て重合反応を終了し、チッソガス加圧下に280℃でポリ
マーの移送を行った。The product obtained subsequently contained 56% of orthophosphoric acid as a stabilizer.
Aqueous solution 0.03 parts (0.033 parts for dimethyl terephthalate)
(Mol%) was added, and at the same time, excessive temperature rise of ethylene glycol was started. After 10 minutes, 0.04 part of antimony trioxide as a polycondensation catalyst (based on dimethyl terephthalate)
0.027 mol%) was added. When the internal temperature reached 240 ° C, the purging of ethylene glycol was completed, and the reaction product was transferred to the polymerization vessel. Then, the temperature was raised and the reaction was carried out at atmospheric pressure until the internal temperature reached 260 ° C, then 760 mmHg for 1 hour.
To 1 mmHg and reduce the internal temperature to 2 at the same time over 1 hour and 30 minutes.
The temperature was raised to 80 ° C. Polymerization temperature 280 ℃ under reduced pressure of 1mmHg or less
When the polymerization was continued for 2 hours, the vacuum was broken with nitrogen gas to terminate the polymerization reaction, and the polymer was transferred at 280 ° C. under the pressure of nitrogen gas.
このポリマーを290℃で溶融紡出し、紡出糸の延伸後の
単糸繊度が約3デニール、破断伸度が30%になるように
吐出量を調整し、1,000m/分で引き取った。次いで、破
断伸度が30%になる延伸倍率で予熱温度80℃で延伸し、
130℃で熱セットして、150デニール/72フィラメントの
ポリエステル繊維を得た。This polymer was melt-spun at 290 ° C., the discharge amount was adjusted so that the single yarn fineness of the spun yarn after stretching was about 3 denier, and the breaking elongation was 30%, and the polymer was collected at 1,000 m / min. Then, stretched at a preheating temperature of 80 ° C. at a stretch ratio at which the breaking elongation is 30%,
Heat setting was performed at 130 ° C. to obtain a polyester fiber having 150 denier / 72 filaments.
芯糸に前記弾性糸を、鞘糸に前記ポリエステル繊維を用
いて、ジングルカバーした糸を使用して経密度240本、
緯密度200本の平織組織に織成した。The elastic yarn as the core yarn, using the polyester fiber as the sheath yarn, the warp density 240 using the jingle-covered yarn,
A plain weave with a weft density of 200 was woven.
該織物を常法により精錬、リラックスプレセットを実施
し、下記条件にてカチオン染料で染色を実施したのち、
酢酸0.2g/で80℃、15分の洗浄を行った。After refining the fabric by a conventional method, performing a relax preset, after dyeing with a cationic dye under the following conditions,
Washing was carried out with acetic acid 0.2 g / 80 ° C. for 15 minutes.
カチオン染料:Cathilon Back CD-BLH(保土谷化学(株)
製);7%owf 酢酸;0.3g/ 無水芒硝;3g/ 浴比;1:30 温度;130℃ 時間;45分 なお、比較例3および4は、下記条件にて分散染料で染
色したのち、ハイドロサルファイト2g/と水酸化ナト
リウム2g/で80℃、20分の還元洗浄を実施した。Cationic dye: Cathilon Back CD-BLH (Hodogaya Chemical Co., Ltd.)
Manufactured); 7% owf acetic acid; 0.3 g / anhydrous mirabilite; 3 g / bath ratio; 1:30 temperature; 130 ° C. time; 45 minutes In Comparative Examples 3 and 4, after dyeing with a disperse dye under the following conditions, Reductive washing with hydrosulfite (2 g /) and sodium hydroxide (2 g /) at 80 ° C. for 20 minutes was performed.
分散染料:Dianix Black HG-FS(三菱化成(株)製);12%
owf 酢酸;0.2g/ 無水芒硝;3g/ 浴比;1:30 温度;135℃ 時間;45分 結果を第1表に示す。Disperse dye: Dianix Black HG-FS (manufactured by Mitsubishi Kasei); 12%
owf acetic acid; 0.2 g / anhydrous Glauber's salt; 3 g / bath ratio; 1:30 temperature; 135 ° C time; 45 minutes The results are shown in Table 1.
実施例5〜8および比較例5〜8 実施例1において、弾性糸ポリマー成分およびポリエス
テル繊維ポリマー成分のスルホン酸塩およびその共重合
量を第2表に示すように変更し、その他の条件は実施例
1と同様にして平織を織成した。 Examples 5-8 and Comparative Examples 5-8 In Example 1, the sulfonates of the elastic yarn polymer component and the polyester fiber polymer component and their copolymerization amounts were changed as shown in Table 2, and other conditions were changed. A plain weave was woven in the same manner as in Example 1.
この織物に、常法により精錬、リラックスプレセットを
施し、下記条件にて染色を実施したのち、酢酸0.2g/
で80℃にて15分間洗浄した。This woven fabric is subjected to refining and relaxing preset by a conventional method, and dyeing is performed under the following conditions, and then 0.2 g of acetic acid /
It was washed at 80 ° C for 15 minutes.
なお、染浴へのベンゾトリアゾール系化合物および/ヒ
ンダードフェノール系化合物の添加は、第2表に示すよ
うに変更した。The addition of the benzotriazole compound and / or the hindered phenol compound to the dye bath was changed as shown in Table 2.
カチオン染料:Aizen Cathilon Blue CD-BLH(保土ヶ谷
化学(株)製);2.0%owf 酢酸;0.3g/ 無水芒硝;3g/ ベンゾトリアゾール系化合物;2%owf ヒンダードフェノール系化合物;2%owf 浴比;1:30 温度;130℃ 時間;45分 ただし、比較例7および8は、下記条件で分散染料によ
り染色し、染浴へのベンゾトリアゾール系化合物および
/またはヒンダードフェノール系化合物の添加は、第2
表に示す通りであった。Cationic dye: Aizen Cathilon Blue CD-BLH (manufactured by Hodogaya Chemical Co., Ltd.); 2.0% owf acetic acid; 0.3 g / anhydrous mirabilite; 3 g / benzotriazole compound; 2% owf hindered phenolic compound; 2% owf bath ratio 1:30 temperature; 130 ° C. time; 45 minutes However, Comparative Examples 7 and 8 were dyed with a disperse dye under the following conditions, and the addition of a benzotriazole compound and / or a hindered phenol compound to the dye bath was Second
It was as shown in the table.
分散染料:Dianix Red UN-SE(三菱化成(株)製);1%owf 酢酸;0.2g/ 無水芒硝;3g/ ベンゾトリアゾール系化合物;2%owf ヒンダードフェノール系化合物;2%owf 浴比;1:30 温度;130℃ 時間;45分 結果を第2表に示す。Disperse dye: Dianix Red UN-SE (manufactured by Mitsubishi Kasei Co., Ltd.); 1% owf acetic acid; 0.2 g / anhydrous sodium sulfate; 3 g / benzotriazole compound; 2% owf hindered phenolic compound; 2% owf bath ratio; 1:30 Temperature; 130 ℃ Time; 45 minutes The results are shown in Table 2.
〔発明の効果〕 本発明によれば、外観、審美性、鮮明性、染色湿潤堅牢
度に優れたポリエステル系伸縮性染色繊維構造物が得ら
れ、さらには、光劣化、塩素劣化の少ないポリエステル
系伸縮性染色繊維構造物を提供することができる。 [Effects of the Invention] According to the present invention, a polyester stretchable dyed fiber structure excellent in appearance, aesthetics, sharpness, and dyeing wet fastness can be obtained, and further, a polyester-based stretched dye-resistant fiber structure with less deterioration by light and chlorine. A stretchable dyed fiber structure can be provided.
フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 D02G 3/32 D03D 15/08 D06P 3/52 (56)参考文献 特開 昭48−10346(JP,A) 特開 昭56−118911(JP,A) 特開 昭63−75133(JP,A) 特開 昭56−20675(JP,A) 特開 昭56−96966(JP,A)Continuation of the front page (51) Int.Cl. 6 Identification number Office reference number FI Technical display location D02G 3/32 D03D 15/08 D06P 3/52 (56) Reference JP-A-48-10346 (JP, A) JP-A-56-118911 (JP, A) JP-A-63-75133 (JP, A) JP-A-56-20675 (JP, A) JP-A-56-96966 (JP, A)
Claims (7)
ート系ポリエステル繊維とカチオン染料可染ポリエーテ
ル・ポリエステルブロック共重合体弾性繊維とを混用し
た繊維構造物を、カチオン染料で染色してなるポリエス
テル系伸縮性染色繊維構造物であって、該カチオン染料
可染ポリエチレンテレフタレート系ポリエステル繊維の
見掛染着度Laと該カチオン染料可染ポリエーテル・ポリ
エステルブロック共重合体弾性繊維の見掛け染着度Lbと
が、下記式(I)を満足していることを特徴とするポリ
エステル系伸縮性染色繊維構造物。 |La−Lb|≦35 ・・・・・(I) (式中、LaはCIE測色系で測色したカチオン染料可染ポ
リエチレンテレフタレート系ポリエステル繊維のL値
を、Lbは同じくCIE測色系で測色したカチオン染料可染
ポリエーテル・ポリエステルブロック共重合体弾性繊維
のL値を表す。)1. A polyester-based stretchable dyeing obtained by dyeing a fiber structure containing a mixture of a cationic dye-dyeable polyethylene terephthalate polyester fiber and a cationic dye-dyeable polyether / polyester block copolymer elastic fiber with a cationic dye. A fiber structure, wherein the apparent dyeing degree La of the cationic dye-dyeable polyethylene terephthalate-based polyester fiber and the apparent dyeing degree Lb of the cationic dye-dyeable polyether / polyester block copolymer elastic fiber are as follows: A polyester stretchable dyed fiber structure characterized by satisfying the formula (I). | La−Lb | ≦ 35 (I) (In the formula, La is the L value of the polyethylene terephthalate polyester fiber dyeable with a cationic dye, which is measured by the CIE colorimetric system, and Lb is the CIE colorimetric system. It represents the L value of the cationic dye dyeable polyether / polyester block copolymer elastic fiber measured by.
テルブロック共重合体弾性繊維が、テレフタル酸を主と
するジカルボン酸および/またはそのエステル形成性誘
導体(A成分)、 下記一般式(II)および/または(III)で表されるス
ルホン酸塩類(B成分)、 (式中、Z1は芳香族基または脂肪族基を、A1はエステル
形成性官能基を、A2はA1と同一もしくは異なるエステル
形成性官能基または水素原子を、R1、R2、R3、およびR4
はアルキル基およびアリール基よりなる群から選ばれる
同一または異なる基を、nは正の整数を表す。) (式中、Z2は芳香族基または脂肪族基を、A3はエステル
形成性官能基を、A4はA3と同一もしくは異なるエステル
形成性官能基または水素原子を、Xは金属原子を、nは
正の整数を表す。) 1,4−ブタンジオールを主とするクリコールおよび/ま
たはそのエステル形成性誘導体(C成分)、および 平均分子量が約400〜6,000のポリオキシアルキレングリ
コール(D成分) を構成成分とし、共重合体全体に対する該スルホン酸塩
類(B成分)の共重合量が0.2〜10モル%である請求項
1記載のポリエステル系伸縮性染色繊維構造物。2. A cationic dye-dyeable polyether / polyester block copolymer elastic fiber comprising a dicarboxylic acid mainly containing terephthalic acid and / or an ester-forming derivative thereof (component A), the following general formula (II) and / or Alternatively, a sulfonate represented by (III) (component B), (In the formula, Z 1 is an aromatic group or an aliphatic group, A 1 is an ester-forming functional group, A 2 is the same or different from A 1 an ester-forming functional group or a hydrogen atom, R 1 , R 2 , R 3 , and R 4
Are the same or different groups selected from the group consisting of alkyl groups and aryl groups, and n represents a positive integer. ) (In the formula, Z 2 is an aromatic group or an aliphatic group, A 3 is an ester-forming functional group, A 4 is an ester-forming functional group which is the same as or different from A 3 , or a hydrogen atom, and X is a metal atom. , N represents a positive integer.) Clycol mainly containing 1,4-butanediol and / or its ester-forming derivative (C component), and polyoxyalkylene glycol having an average molecular weight of about 400 to 6,000 (D component). The polyester-based stretchable dyed fiber structure according to claim 1, wherein the copolymerization amount of the sulfonates (component B) is 0.2 to 10 mol% with respect to the entire copolymer.
ート系ポリエステル繊維が、請求項2記載のスルホン酸
塩類を含む共重合体からなり、該共重合体全体に対する
該スルホン酸塩類の共重合量が、1〜5モル%である請
求項1記載のポリエステル系伸縮性染色繊維構造物。3. A polyethylene terephthalate-based polyester fiber dyeable with a cationic dye comprises a copolymer containing the sulfonate according to claim 2, and the copolymerization amount of the sulfonate with respect to the entire copolymer is 1 to The polyester stretchable dyed fiber structure according to claim 1, which is 5 mol%.
ート系ポリエステル繊維とカチオン染料可染ポリエーテ
ル・ポリエステルブロック共重合体弾性繊維とを混用し
た繊維構造物を、2−(3−t−ブチル−5−メチル−
2−ヒドロキシフェニル)−5−クロロベンゾトリアゾ
ールおよび/または2−(3,5−ジ−t−ブチル−2−
ヒドロキシフェニル)−5−クロロベンゾトリアゾール
ならびにヒンダードフェノール系化合物を該繊維構造物
に対し各々0.1〜4重量%(owf)添加したカチオン染料
染浴で染色することを特徴とするポリエステル系伸縮性
染色繊維構造物の製造方法。4. A fiber structure comprising a mixture of a cationic dye-dyeable polyethylene terephthalate-based polyester fiber and a cationic dye-dyeable polyether / polyester block copolymer elastic fiber is prepared from 2- (3-t-butyl-5-methyl). −
2-hydroxyphenyl) -5-chlorobenzotriazole and / or 2- (3,5-di-t-butyl-2-
Polyester stretchable dyeing characterized by dyeing with a cationic dye dyeing bath in which 0.1 to 4% by weight (owf) of the hydroxyphenyl) -5-chlorobenzotriazole and the hindered phenolic compound are added to the fiber structure. A method for manufacturing a fiber structure.
テル共重合体弾性繊維が、請求項2記載のカチオン染料
可染ポリエーテル・ポリエステル共重合体弾性繊維であ
る請求項4記載のポリエステル系伸縮性染色繊維構造物
の製造方法。5. The polyester-based stretchable dyeing according to claim 4, wherein the cationic dye-dyeable polyether / polyester copolymer elastic fiber is the cationic dye-dyeable polyether / polyester copolymer elastic fiber. A method for manufacturing a fiber structure.
ート系ポリエステル繊維が、請求項3記載のカチオン染
料可染ポリエチレンテレフタレート系ポリエステル繊維
である請求項4記載のポリエステル系伸縮性染色繊維構
造物の製造方法。6. The method for producing a polyester-based stretchable dyed fiber structure according to claim 4, wherein the cationic dye-dyeable polyethylene terephthalate-based polyester fiber is the cationic dye-dyeable polyethylene terephthalate-based polyester fiber.
−トリメチル−2,4,6−トリス(3,5−t−ブチル−4−
ヒドロキシベンジル)ベンゼン、トリス−(2−メチル
−4−ヒドロキシ−5−t−ブチルフェニル)ブタンお
よびトリス−(3,5−ジ−t−ブチル−4−ヒドロキシ
ベンジル)イソシアヌレートからなる群より選ばれた一
種以上の化合物である請求項4記載のポリエステル系伸
縮性染色繊維構造物の製造方法。7. A hindered phenol compound is 1,3,5.
-Trimethyl-2,4,6-tris (3,5-t-butyl-4-
Selected from the group consisting of hydroxybenzyl) benzene, tris- (2-methyl-4-hydroxy-5-t-butylphenyl) butane and tris- (3,5-di-t-butyl-4-hydroxybenzyl) isocyanurate. The method for producing a polyester stretchable dyed fiber structure according to claim 4, wherein the polyester-based stretchable dyed fiber structure is one or more compounds.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1323996A JPH0768657B2 (en) | 1989-12-15 | 1989-12-15 | Polyester stretchable dyed fiber structure and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1323996A JPH0768657B2 (en) | 1989-12-15 | 1989-12-15 | Polyester stretchable dyed fiber structure and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03185133A JPH03185133A (en) | 1991-08-13 |
JPH0768657B2 true JPH0768657B2 (en) | 1995-07-26 |
Family
ID=18160961
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1323996A Expired - Lifetime JPH0768657B2 (en) | 1989-12-15 | 1989-12-15 | Polyester stretchable dyed fiber structure and method for producing the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0768657B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1130485C (en) * | 1996-11-12 | 2003-12-10 | 帝人株式会社 | Dyed filament yarn having clear hue |
CN1103792C (en) * | 1998-08-21 | 2003-03-26 | 南亚塑胶工业股份有限公司 | Thermoplastic block copolyetheresters with improved light resistance |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5620675A (en) * | 1979-07-27 | 1981-02-26 | Matsui Shikiso Kagaku Kogyosho | Treatment of hydrophobic fibers |
JPS56118911A (en) * | 1980-02-21 | 1981-09-18 | Toray Ind Inc | Preparation of latently shrinkable elastic fiber and elastic fabric |
JPS5858476B2 (en) * | 1980-11-25 | 1983-12-26 | 三洋化成工業株式会社 | Dyeing aid for polyester fibers |
JPS6375133A (en) * | 1987-06-04 | 1988-04-05 | 東レ株式会社 | Polyester profile crimped processed yarn dyed uniformly |
-
1989
- 1989-12-15 JP JP1323996A patent/JPH0768657B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH03185133A (en) | 1991-08-13 |
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