JPH11222727A - Hygroscopic conjugate fiber of uneven thickness - Google Patents
Hygroscopic conjugate fiber of uneven thicknessInfo
- Publication number
- JPH11222727A JPH11222727A JP2893998A JP2893998A JPH11222727A JP H11222727 A JPH11222727 A JP H11222727A JP 2893998 A JP2893998 A JP 2893998A JP 2893998 A JP2893998 A JP 2893998A JP H11222727 A JPH11222727 A JP H11222727A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- core
- acid
- moisture absorption
- component
- 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.)
- Pending
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 55
- 238000010521 absorption reaction Methods 0.000 claims abstract description 22
- 150000001875 compounds Chemical class 0.000 claims abstract description 13
- 229920000642 polymer Polymers 0.000 claims abstract description 13
- 229920006146 polyetheresteramide block copolymer Polymers 0.000 claims abstract description 10
- 239000002131 composite material Substances 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 4
- 238000003795 desorption Methods 0.000 claims description 2
- 239000000470 constituent Substances 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract description 4
- 229920000570 polyether Polymers 0.000 abstract description 4
- 150000002148 esters Chemical class 0.000 abstract description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 33
- 229920000728 polyester Polymers 0.000 description 31
- 239000000306 component Substances 0.000 description 24
- -1 alkylene terephthalate Chemical compound 0.000 description 20
- 229920002994 synthetic fiber Polymers 0.000 description 13
- 239000012209 synthetic fiber Substances 0.000 description 13
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 12
- 239000012510 hollow fiber Substances 0.000 description 9
- 239000002202 Polyethylene glycol Substances 0.000 description 8
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 8
- 239000004744 fabric Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 229920001223 polyethylene glycol Polymers 0.000 description 8
- 239000008358 core component Substances 0.000 description 7
- 238000004043 dyeing Methods 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 150000001991 dicarboxylic acids Chemical class 0.000 description 4
- 230000001771 impaired effect Effects 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229920002302 Nylon 6,6 Polymers 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000001361 adipic acid Substances 0.000 description 3
- 235000011037 adipic acid Nutrition 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 229920002164 Polyalkylene glycol copolymer Polymers 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 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 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 150000003951 lactams Chemical class 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 2
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 2
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 description 1
- RYRZSXJVEILFRR-UHFFFAOYSA-N 2,3-dimethylterephthalic acid Chemical compound CC1=C(C)C(C(O)=O)=CC=C1C(O)=O RYRZSXJVEILFRR-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- QUBNFZFTFXTLKH-UHFFFAOYSA-N 2-aminododecanoic acid Chemical compound CCCCCCCCCCC(N)C(O)=O QUBNFZFTFXTLKH-UHFFFAOYSA-N 0.000 description 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 229920000572 Nylon 6/12 Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- QFNNDGVVMCZKEY-UHFFFAOYSA-N azacyclododecan-2-one Chemical compound O=C1CCCCCCCCCCN1 QFNNDGVVMCZKEY-UHFFFAOYSA-N 0.000 description 1
- CJYXCQLOZNIMFP-UHFFFAOYSA-N azocan-2-one Chemical compound O=C1CCCCCCN1 CJYXCQLOZNIMFP-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000012661 block copolymerization Methods 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002433 hydrophilic molecules Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- ONCZDRURRATYFI-QTCHDTBASA-N methyl (2z)-2-methoxyimino-2-[2-[[(e)-1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]acetate Chemical compound CO\N=C(/C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-QTCHDTBASA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000765 poly(2-oxazolines) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Multicomponent Fibers (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は太細を有する吸湿性
繊維に関するものであり、更に詳しくは中衣、スポーツ
衣料などの衣料用素材に特に好適に使用することができ
るものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thick and thin hygroscopic fiber, and more particularly to a material which can be particularly suitably used as a material for clothing such as middle garments and sports clothing.
【0002】[0002]
【従来の技術】ポリエステルやポリアミドに代表される
熱可塑性合成繊維は機械的強度、耐薬品性、耐熱性など
に優れるため、衣料用途や産業用途などを主体に広く使
用されている。しかしながら、これらの合成繊維は極め
て吸湿性が低いため、インナー、中衣、スポーツ衣料な
どのように直接的に肌に触れてあるいは肌側に近い状態
で着用される分野に使用する場合には、肌からの発汗に
よるムレやベタツキなどを生じ、快適性の点で天然繊維
よりも劣り、前記衣料用途への進出は限定されているの
が実状である。この欠点を解消するため、たとえば特開
昭51−67465号公報、実開昭59−165485
号公報、あるいは特開昭60−215835号公報に記
載されているように、平衡水分率(吸湿率)の高い繊維
との各種の混繊、合撚、引揃えなどにより布帛として吸
湿快適性を得んとする試みが提案されている。これらの
方法を用いることで確かに快適性は向上するものの、そ
の効果は十分とはいえず、逆にその他の合成繊維特性に
おいて合成繊維を染色する際に一般的に使用される分散
染料によって汚染を生じたり、同色性に劣ったり、合成
繊維本来の物理的特性が失われるという問題点があっ
た。2. Description of the Related Art Thermoplastic synthetic fibers typified by polyester and polyamide are excellent in mechanical strength, chemical resistance, heat resistance and the like, and are therefore widely used mainly for apparel use and industrial use. However, since these synthetic fibers have extremely low hygroscopicity, when used in the field where they are worn directly on the skin or near the skin side, such as innerwear, inner garments, and sports clothing, In reality, sweating from the skin causes stuffiness and stickiness, and is inferior to natural fibers in terms of comfort. In order to solve this drawback, for example, Japanese Patent Laid-Open Publication No. Sho 51-67465, Japanese Utility Model Laid-Open Publication No. Sho 59-165485.
As described in Japanese Unexamined Patent Application Publication No. 60-215835 or Japanese Patent Application Laid-Open No. Sho 60-215835, various kinds of fibers with high equilibrium moisture content (moisture absorption), ply twisting, and drawing are used to improve the moisture absorption comfort. Attempts to achieve it have been proposed. Although these methods do improve comfort, they are not as effective, and conversely, are contaminated by disperse dyes commonly used when dyeing synthetic fibers in other synthetic fiber properties. There is a problem in that the synthetic fiber has poor physical properties and the same physical properties are lost.
【0003】また、ポリエステル繊維にアクリル酸やメ
タアクリル酸をグラフト重合すること、更にグラフト重
合後にそれらのカルボキシル基をアルカリ金属で置換す
ることにより吸湿性を付与する方法が知られているが、
ポリエステルがグラフト重合しにくい素材であること、
および染色堅牢性や耐光性、繊維物理特性、風合いなど
の低下を潜在的に有していることから、実用化には到っ
ていない。[0003] Further, there is known a method of graft-polymerizing acrylic acid or methacrylic acid to polyester fibers, and further imparting hygroscopicity by replacing their carboxyl groups with alkali metals after the graft polymerization.
That the polyester is difficult to graft polymerize,
It has not yet been put to practical use because it has potential deterioration in color fastness, light fastness, fiber physical properties, texture, and the like.
【0004】後加工段階で吸湿性を付与する方法では染
色時あるいは得られた布帛特性の点で種々の問題がある
ことから、繊維を製造する段階で吸湿性を付与しかつ前
記問題点を解消するため、常湿度下で吸湿率が10%以
上の吸湿性樹脂を芯部とし、それを鞘部であるポリエス
テルで覆った芯鞘型複合繊維が特開平2−99612号
公報で提案されている。しかしながら、この方法では染
色などの熱水処理時に芯部の吸湿・吸水率が高いが故、
芯部と鞘部との水膨潤差により鞘部に歪みがかかって繊
維表面にひび割れが生じ、高次工程でのトラブルを生じ
やすい等の欠点がある。[0004] The method of imparting hygroscopicity in the post-processing stage has various problems at the time of dyeing or in terms of the properties of the obtained fabric. For this purpose, Japanese Patent Laid-Open Publication No. 2-99612 proposes a core-sheath type composite fiber in which a hygroscopic resin having a moisture absorption of 10% or more at normal humidity is used as a core, and the core is covered with polyester as a sheath. . However, this method has high moisture absorption and water absorption of the core during hot water treatment such as dyeing,
There is a drawback in that the sheath portion is distorted due to the difference in water swelling between the core portion and the sheath portion, causing cracks on the fiber surface and causing troubles in higher-order processes.
【0005】また、特開昭51−136924号公報に
は親水性ポリエステルを芯成分、非親水性ポリエステル
を鞘成分とする芯鞘型複合ステープルについて提案され
ている。親水性ポリエステルとしてポリアルキレングリ
コール共重合体単独あるいは少量のポリアルキレングリ
コール共重合体に少量のスルホン酸や酸性リン酸エステ
ル誘導体を配合したものを用いるものであり、ステープ
ルとして繊維両端面を増加させ吸水性を向上させようと
いう提案である。しかしながら、本願発明者の検討では
該ステープルで吸水性を向上させることはできるが、吸
湿性の向上は困難であることがわかった。Japanese Patent Laid-Open Publication No. Sho 51-136924 proposes a core-sheath composite staple comprising a hydrophilic polyester as a core component and a non-hydrophilic polyester as a sheath component. As the hydrophilic polyester, a polyalkylene glycol copolymer alone or a mixture of a small amount of a polyalkylene glycol copolymer and a small amount of a sulfonic acid or acidic phosphate derivative is used.As a staple, both ends of the fiber are increased to absorb water. It is a proposal to improve the performance. However, the present inventors have found that although the staple can improve the water absorption, it is difficult to improve the moisture absorption.
【0006】また、特開昭53−111116号公報に
特定のポリエーテルエステルを芯成分とした芯鞘型の制
電性複合繊維が提案されている。しかし、該繊維の効果
は制電性であり、ポリエーテル成分を単独共重合したポ
リエステルを芯成分として用いているため、繊維物性が
経時的に変化するという問題がある。また該ポリエーテ
ルエステルの着色が激しく、得られる最終製品の品位が
損なわれるといった問題点がある。Japanese Patent Application Laid-Open No. Sho 53-111116 proposes a core-sheath type antistatic composite fiber containing a specific polyetherester as a core component. However, the effect of the fibers is antistatic, and there is a problem that the physical properties of the fibers change with time because a polyester obtained by homopolymerizing a polyether component is used as a core component. In addition, there is a problem that the polyetherester is strongly colored and the quality of the obtained final product is impaired.
【0007】また、特開昭62−267352公報には
特定のポリアルキレングリコールを50〜70重量%配
合してなるポリエステル組成物が開示されている。この
組成物を単独で繊維化した場合、繊維物性が低く、また
耐水性に劣るため衣料用および産業用での使用は困難で
ある。Japanese Patent Application Laid-Open No. 62-267352 discloses a polyester composition containing 50 to 70% by weight of a specific polyalkylene glycol. When this composition is fiberized alone, it is difficult to use it for clothing and industrial purposes due to low fiber properties and poor water resistance.
【0008】さらに、特開平6−123012号公報に
は芯鞘型吸湿性ポリエステル繊維が開示されている。こ
れはアルキレンテレフタレート、アルキレンスルホイソ
フタレート、およびポリオキシアルキレングリコールよ
りなる共重合体にブロックポリエーテルエステルをブレ
ンドして芯ポリマとして用いたものであるが、該特許記
載の内容では十分な吸湿性が得ることは難しく、満足す
るレベルではない。Further, Japanese Patent Application Laid-Open No. 6-123012 discloses a core-sheath type hygroscopic polyester fiber. This is a copolymer of an alkylene terephthalate, an alkylene sulfoisophthalate, and a polyoxyalkylene glycol blended with a block polyetherester and used as a core polymer, but the content described in the patent does not show sufficient hygroscopicity. It's hard to get, not a satisfactory level.
【0009】また、本願発明者は特開平8−81831
号公報で親水性化合物を共重合した吸湿性に優れた共重
合ポリエステルならびに該共重合ポリエステルを用いた
吸湿性に優れた繊維を発明するに至った。しかしなが
ら、該繊維は展開用途を拡げるためにはドライ感を向上
させる必要があることが判明した。一方、特開平9−1
11538号公報には染色性を異とする2種のポリエス
テルを用いた太細繊維に関する技術が開示されている
が、該公報の主目的は異なる色相および異なる濃度の多
色表現を可能にするものであって、吸湿性に関する記載
は全くされていない。以上のことを鑑み、鋭意検討した
結果、吸湿性繊維を太細化することにより、接触冷感と
タッチ感の相乗効果によってドライ感が発現することが
わかり、特に中空部を有する芯鞘複合糸に関して効果的
であることが判明し本発明に至った。The inventor of the present application has disclosed in Japanese Patent Laid-Open No. 8-81831.
Japanese Patent Application Laid-Open Publication No. H11-157, invented a polyester having excellent hygroscopicity obtained by copolymerizing a hydrophilic compound and a fiber having excellent hygroscopicity using the copolymerized polyester. However, it has been found that it is necessary to improve the dry feeling of the fiber in order to expand its use for development. On the other hand, Japanese Patent Laid-Open No. 9-1
Japanese Patent No. 11538 discloses a technique relating to a thin fiber using two kinds of polyesters having different dyeing properties. The main purpose of the publication is to enable multicolor expression with different hues and different densities. However, there is no description about hygroscopicity. In view of the above, as a result of intensive studies, it has been found that by making the hygroscopic fiber thinner, a dry feeling is exhibited due to a synergistic effect of a contact cooling feeling and a touch feeling, and in particular, a core-sheath composite yarn having a hollow portion. Was found to be effective for the present invention, and the present invention was achieved.
【0010】[0010]
【発明が解決しようとする課題】本発明の目的は、前記
従来技術の問題点を克服し、商品価値の高い、太細を有
する吸湿性合成繊維を提供することにある。SUMMARY OF THE INVENTION It is an object of the present invention to provide a thick and thin hygroscopic synthetic fiber which has a high commercial value and overcomes the problems of the prior art.
【0011】[0011]
【課題を解決するための手段】前記した本発明の目的
は、親水性成分および繊維形成性重合体を構成成分とし
た複合繊維であり、かつ吸放湿パラメーター(△MR)
が1.0%以上であり、該繊維の長さ方向の太さムラが
ウースタノーマルU%が5〜20%であることを特徴と
する太細を有する芯鞘型吸湿性合成繊維によって達成す
ることができる。SUMMARY OF THE INVENTION An object of the present invention is to provide a conjugate fiber comprising a hydrophilic component and a fiber-forming polymer as components, and a moisture absorption / desorption parameter (ΔMR).
Is 1.0% or more, and the thickness unevenness in the longitudinal direction of the fiber is achieved by a core-sheath type hygroscopic synthetic fiber having a fine and thin Uster Normal U% of 5 to 20%. can do.
【0012】[0012]
【発明の実施の形態】親水性成分は本発明の目的である
繊維に吸湿性を付与する成分であり、ベースとなる繊維
形成重合体よりも高い吸湿性を有することが必須であ
る。親水性成分としては繊維形成性重合体よりも高い吸
湿性を有する化合物であれば特に限定しないが、繊維に
高い吸湿性を付与するため、親水成分の吸湿特性(△M
R)は8%以上が好ましい。また安定した吸湿特性を発
現するためには△MRを15%以上とすることがさらに
好ましい。代表的な化合物として、ポリエーテルエステ
ル系化合物、ポリエーテルエステルアミド系化合物、ポ
リオキシアルキレン化合物、ポリオキサゾリン類、ポリ
アクリルアミドとその誘導体、ポリスルホエチルメタク
リレート、ポリ(メタ)アクリレート、ポリ(メタ)ア
クリル酸およびその塩、ポリヒドロキシエチル(メタ)
アクリレート、ポリビニルアルコール、およびポリビニ
ルピロリドンなどがあげられる。その中でもポリエーテ
ルエステル系化合物、ポリエーテルエステルアミド系化
合物が好ましい。BEST MODE FOR CARRYING OUT THE INVENTION A hydrophilic component is a component for imparting hygroscopicity to fibers, which is the object of the present invention, and it is essential that the hydrophilic component has higher hygroscopicity than a fiber-forming polymer as a base. The hydrophilic component is not particularly limited as long as it is a compound having higher hygroscopicity than the fiber-forming polymer. However, in order to impart high hygroscopicity to the fiber, the hydrophilic component (△ M
R) is preferably at least 8%. Further, in order to exhibit stable moisture absorption characteristics, it is more preferable that ΔMR is 15% or more. Representative compounds include polyetherester compounds, polyetheresteramide compounds, polyoxyalkylene compounds, polyoxazolines, polyacrylamide and its derivatives, polysulfoethyl methacrylate, poly (meth) acrylate, and poly (meth) acryl. Acid and its salt, polyhydroxyethyl (meth)
Examples include acrylate, polyvinyl alcohol, and polyvinylpyrrolidone. Among them, polyetherester compounds and polyetheresteramide compounds are preferred.
【0013】具体的にポリエーテルエステル化合物と
は、同一分子鎖内にエーテル結合とエステル結合を有す
る共重合体である。より具体的にはジカルボン酸とジオ
ールとのポリエステル成分とポリオキシアルキレングリ
コールからなるポリエーテル成分の共重合体である。ポ
リエステルの酸成分としてテレフタル酸、イソフタル
酸、ナフタレン−2、6−ジカルボン酸等の芳香族ジカ
ルボン酸、アジピン酸、セバシン酸等の脂肪族ジカルボ
ン酸等があげられる。またグリコール成分としてエチレ
ングリコール、プロピレングリコール、テトラメチレン
グリコール、ジエチレングリコール、ネオペンチルグリ
コール等があげられる。また、本発明の効果を損なわな
い範囲でトリメリット酸、ピロメリット酸等の多官能カ
ルボン酸、グリセリン、トリメチロールプロパン、ペン
タエリストール如きポリオールを用いても良い。ポリオ
キシアルキレングリコールとしては、ポリエチレングリ
コール、ポリ(1,2−および1,3−プロピレンオキ
シド)グリコール、ポリテトラメチレンオキシドグリコ
ール、ポリヘキサメチレンオキシドグリコール、エチレ
ンオキシドとプロピレンオキシドまたはテトラヒドロフ
ランとのランダムまたはブロック共重合等があげられ、
特にポリエチレングリコールが好ましい。Specifically, a polyetherester compound is a copolymer having an ether bond and an ester bond in the same molecular chain. More specifically, it is a copolymer of a polyester component of a dicarboxylic acid and a diol and a polyether component composed of a polyoxyalkylene glycol. Examples of the acid component of the polyester include aromatic dicarboxylic acids such as terephthalic acid, isophthalic acid, and naphthalene-2,6-dicarboxylic acid, and aliphatic dicarboxylic acids such as adipic acid and sebacic acid. Examples of the glycol component include ethylene glycol, propylene glycol, tetramethylene glycol, diethylene glycol, neopentyl glycol and the like. Polyfunctional carboxylic acids such as trimellitic acid and pyromellitic acid, and polyols such as glycerin, trimethylolpropane, and pentaeristol may be used as long as the effects of the present invention are not impaired. Examples of the polyoxyalkylene glycol include polyethylene glycol, poly (1,2- and 1,3-propylene oxide) glycol, polytetramethylene oxide glycol, polyhexamethylene oxide glycol, and a random or block copolymer of ethylene oxide and propylene oxide or tetrahydrofuran. Polymerization, etc.,
Particularly, polyethylene glycol is preferred.
【0014】また、ポリエーテルエステルアミド化合物
とは、同一分子鎖内にエーテル結合、エステル結合およ
びアミド結合を持つブロック共重合体である。より具体
的にはラクタム、アミノカルボン酸、ジアミンとジカル
ボン酸の塩から選ばれた1種もしくは2種以上のポリア
ミド形成性成分およびジカルボン酸とポリ(アルキレン
オキシド)グリコールからなるポリエーテルエステルを
重縮合反応させて得られるブロック共重合ポリマであ
る。本発明のポリエーテルエステルアミドのポリアミド
形成性成分としては、カプロラクタム、エナントラクタ
ム、ドデカラクタム、ウンデカラクタム等のラクタム
類、アミノカプロン酸、11−アミノウンデカン酸、1
2−アミノドデカン酸等などのω−アミノカルボン酸、
ナイロン66、ナイロン610、ナイロン612等の前
駆体であるジアミン−ジカルボン酸のナイロン塩類があ
り、これらを1種または2種以上混合して用いることが
できる。好ましいポリアミド形成性成分はε−カプロラ
クタム、ナイロン66塩である。[0014] The polyetheresteramide compound is a block copolymer having an ether bond, an ester bond and an amide bond in the same molecular chain. More specifically, polycondensation of one or more polyamide-forming components selected from lactams, aminocarboxylic acids, salts of diamines and dicarboxylic acids, and polyether esters of dicarboxylic acids and poly (alkylene oxide) glycols. It is a block copolymer obtained by the reaction. The polyamide-forming component of the polyetheresteramide of the present invention includes lactams such as caprolactam, enantholactam, dodecalactam and undecalactam, aminocaproic acid, 11-aminoundecanoic acid,
Ω-aminocarboxylic acids such as 2-aminododecanoic acid,
There are nylon salts of diamine-dicarboxylic acid which are precursors of nylon 66, nylon 610, nylon 612 and the like, and these can be used alone or in combination of two or more. Preferred polyamide-forming components are ε-caprolactam, a nylon 66 salt.
【0015】一方ポリエーテルエステルアミドのソフト
セグメントを構成するポリエーテルエステル成分として
は、炭素数4〜20のジカルボン酸とポリ(アルキレン
オキシド)グリコールとからなる。炭素数4〜20のジ
カルボン酸としてはコハク酸、グルタル酸、アジピン
酸、ピメリン酸、スベリン酸、セバシン酸、ドデカジ
酸、等の脂肪族ジカルボン酸、テレフタル酸、イソフタ
ル酸、2,6−ナフタレンジカルボン酸等の芳香族ジカ
ルボン酸、1,4−シクロヘキサンジカルボン酸等の脂
環式ジカルボン酸を挙げることができ、1種または2種
以上混合して用いることができる。好ましいジカルボン
酸はアジピン酸、セバシン酸、ドデカジ酸、テレフタル
酸、イソフタル酸である。ポリオキシアルキレングリコ
ールとしては、ポリエチレングリコール、ポリ(1,2
−および1,3−プロピレンオキシド)グリコール、ポ
リテトラメチレンオキシドグリコール、ポリヘキサメチ
レンオキシドグリコール、エチレンオキシドとプロピレ
ンオキシドまたはテトラヒドロフランとのランダムまた
はブロック共重合等があげられ、特にポリエチレングリ
コールが好ましい。On the other hand, the polyetherester component constituting the soft segment of the polyetheresteramide comprises a dicarboxylic acid having 4 to 20 carbon atoms and poly (alkylene oxide) glycol. Examples of the dicarboxylic acids having 4 to 20 carbon atoms include aliphatic dicarboxylic acids such as succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, sebacic acid, dodecadic acid, terephthalic acid, isophthalic acid, and 2,6-naphthalenedicarboxylic acid. Examples thereof include aromatic dicarboxylic acids such as acids, and alicyclic dicarboxylic acids such as 1,4-cyclohexanedicarboxylic acid, and one or more kinds thereof can be used in combination. Preferred dicarboxylic acids are adipic acid, sebacic acid, dodecadic acid, terephthalic acid, isophthalic acid. Examples of the polyoxyalkylene glycol include polyethylene glycol and poly (1,2).
-And 1,3-propylene oxide) glycol, polytetramethylene oxide glycol, polyhexamethylene oxide glycol, random or block copolymerization of ethylene oxide with propylene oxide or tetrahydrofuran, etc., with polyethylene glycol being particularly preferred.
【0016】本発明に於いて、快適性を得るためには繊
維として△MR=1.0%以上有すること必須である。
芯鞘型複合繊維の場合、芯部の親水性成分の複合比率
(重量%)は芯/鞘=5/95〜90/10とすること
が好ましい。さらに好ましくは7/93〜50/50、
特に好ましくは10/90〜30/70である。複合比
率は染色用途および染色なしの用途で任意に選ぶことが
できる。芯部の複合比率の下限は十分な吸湿性を付与す
る目的から設定され、複合繊維比率の上限は紡糸性の低
下や繊維物性の低下を防止する観点から設定される。In the present invention, in order to obtain comfort, it is essential that the fiber has ΔMR = 1.0% or more.
In the case of the core-sheath type composite fiber, it is preferable that the composite ratio (% by weight) of the hydrophilic component in the core part is core / sheath = 5/95 to 90/10. More preferably, 7/93 to 50/50,
Particularly preferably, it is 10/90 to 30/70. The composite ratio can be arbitrarily selected for dyeing use and non-dyeing use. The lower limit of the composite ratio of the core is set for the purpose of imparting sufficient hygroscopicity, and the upper limit of the composite fiber ratio is set from the viewpoint of preventing a decrease in spinnability and a decrease in fiber properties.
【0017】また親水性成分には、本発明の目的を損な
わない範囲で酸化チタン、カーボンブラック等の顔料、
アルキルベンゼンスルホン酸塩等の界面活性剤、従来公
知の抗酸化剤、着色防止剤、耐光剤、帯電防止剤等が添
加されても勿論良い。The hydrophilic component includes pigments such as titanium oxide and carbon black as long as the object of the present invention is not impaired.
Of course, a surfactant such as an alkylbenzene sulfonate, a conventionally known antioxidant, a coloring inhibitor, a light stabilizer, an antistatic agent, and the like may be added.
【0018】本発明において繊維形成性重合体に複合す
る主成分は、前記した共重合ポリエステルであるが、そ
の効果を損なわない範囲でポリオレフィン、ポリアミ
ド、ポリエステル、ポリカーボネート等を含んでいても
よい。また本発明において繊維形成性重合体としてポリ
エチレン、ポリプロピレン等のポリオレフィン、ナイロ
ン6、ナイロン66等のポリアミド、ポリエチレンテレ
フタレート、ポリブチレンテレフタレート等のポリエス
テルが挙げられるがこれらに限定されるものではない。
好ましくは衣料用合成繊維として最も汎用性の高い、ポ
リエチレンテレフタレートを主体とするポリエステルで
ある。In the present invention, the main component to be composited with the fiber-forming polymer is the above-mentioned copolymerized polyester, but may contain a polyolefin, polyamide, polyester, polycarbonate or the like as long as the effect is not impaired. In the present invention, examples of the fiber-forming polymer include polyolefins such as polyethylene and polypropylene; polyamides such as nylon 6 and nylon 66; and polyesters such as polyethylene terephthalate and polybutylene terephthalate, but are not limited thereto.
Preferably, it is a polyester mainly composed of polyethylene terephthalate, which is the most versatile synthetic fiber for clothing.
【0019】また繊維形成性重合体には、酸化チタン、
カーボンブラック等の顔料のほか従来公知の抗酸化剤、
着色防止剤、耐光剤、帯電防止剤等が添加されても勿論
良い。 本発明においてU%を5〜20%とすること
で、該繊維を用いた布帛は、染色による濃淡コントラス
トが小さく自然な斑感を有し、かつ布帛表面にも微少な
凹凸感を有することによって視覚的、触覚的にドライ感
素材が得られるものである。ウースタノーマルU%は好
ましくは6〜15%である。The fiber-forming polymer includes titanium oxide,
Other known antioxidants other than pigments such as carbon black,
Needless to say, a coloring prevention agent, a light resistance agent, an antistatic agent and the like may be added. In the present invention, by setting the U% to 5 to 20%, the fabric using the fiber has a small contrast of shading due to dyeing, has a natural spot feeling, and has a fine unevenness feeling on the surface of the fabric. A material with a dry feeling can be obtained visually and tactilely. Worst normal U% is preferably 6 to 15%.
【0020】合成繊維の形態として、芯鞘型複合繊維、
芯鞘型複合中空繊維があげられるが、ドライ感向上の効
果の点から芯鞘型複合中空繊維が好ましい。As the form of the synthetic fiber, a core-sheath type composite fiber,
A core-sheath type composite hollow fiber may be mentioned, but a core-sheath type composite hollow fiber is preferred from the viewpoint of improving the dry feeling.
【0021】本発明において複合繊維の製法としては従
来公知の方法で製造することができ、以下に芯鞘型複合
中空繊維の製造法を示す。In the present invention, the composite fiber can be produced by a conventionally known method, and a method for producing a core-sheath type composite hollow fiber will be described below.
【0022】芯鞘複合中空繊維の場合、ポリエステル
(鞘部)と親水性成分(芯部)をそれぞれ別々に溶融
し、紡糸パックに導き口金装置内で芯鞘複合流を形成
し、吐出孔から紡出する。紡出したフィラメント糸を所
定の速度で引取った後、一旦パッケージに巻上げ、得ら
れた未延伸糸を延伸機にて延伸する。繊維に太細を付与
するためには、特定条件で得られた未延伸糸を不均一延
伸する必要がある。具体的に例示すると紡速3000m
/分で得られた未延伸糸を延伸倍率1.4倍、熱ピン温
度80℃に設定し低倍率延伸することで得ることができ
る。In the case of the core-sheath composite hollow fiber, the polyester (sheath) and the hydrophilic component (core) are separately melted, guided to a spinning pack, and formed into a core-sheath composite flow in a spinneret. Spin. After taking out the spun filament yarn at a predetermined speed, it is once wound up in a package, and the obtained undrawn yarn is drawn by a drawing machine. In order to impart a fineness to the fiber, it is necessary to non-uniformly stretch the undrawn yarn obtained under specific conditions. To be specific, spinning speed is 3000m
Per minute, the undrawn yarn can be obtained by setting the draw ratio to 1.4 times and setting the hot pin temperature to 80 ° C., and then drawing at a low draw ratio.
【0023】本発明の合成繊維の複合形態は、同心円状
でも偏心円状でも多島状でも良く、繊維断面形状は丸ば
かりでなく、三角、偏平、多葉型などの異形断面でも良
い。また、該繊維の糸状形態はフィラメントであり、常
法によって得ることができる。布帛形態としては、織
物、編物、不織布など目的に応じて適宜選択できる。The composite form of the synthetic fiber of the present invention may be concentric, eccentric or multi-island, and the cross section of the fiber may be not only round but also irregular cross section such as triangular, flat or multi-lobed. The filamentous form of the fiber is a filament, which can be obtained by a conventional method. The fabric form can be appropriately selected depending on the purpose, such as a woven fabric, a knitted fabric, or a nonwoven fabric.
【0024】[0024]
【実施例】以下本発明を実施例により、さらに詳細に説
明する。なお、実施例中の各特性値は次の方法によって
求めた。 A.ポリエステルの極限粘度 [η] オルトクロロフェノール溶液とし、25℃で求めた。 B.ポリマおよび繊維の吸湿率差 △MR 吸湿率はポリマの場合、チップを約2mm角の立方体上
に裁断し、また繊維の場合は原糸をカセ取りし、絶乾時
の試料重量を約1gとし20℃×65%RHあるいは3
0℃×90%RHの雰囲気下、恒温恒湿器(タバイ製P
R−2G)中に24時間放置後の重量との重量変化か
ら、次式で求めた。 吸湿率(%)=(吸湿後の重量 − 絶乾時の重量)/
絶乾時の重量 ×100 上記測定した20℃×65%RHおよび30℃×90%
RHの条件での吸湿率(それぞれMR1およびMR2と
する)から、吸湿率差△MR(%)=MR2−MR1を
求める。ここで吸湿率差△MRは衣服着用時の衣服内の
湿気を外気に放出することにより快適性を得るためのド
ライビングフォースであり、軽〜中作業あるいは軽〜中
運動を行った際の30℃×90%RHに代表される衣服
内温度と20℃×65%RHに代表される外気温湿度と
の吸湿率差である。The present invention will be described in more detail with reference to the following examples. In addition, each characteristic value in an Example was calculated | required by the following method. A. Intrinsic viscosity of polyester [η] An orthochlorophenol solution was determined at 25 ° C. B. Difference in moisture absorption between polymer and fiber △ MR For moisture absorption, in the case of a polymer, a chip is cut into a cube of about 2 mm square, and in the case of a fiber, the original yarn is cut off, and the sample weight when completely dried is about 1 g. 20 ° C x 65% RH or 3
In an atmosphere of 0 ° C x 90% RH, a thermo-hygrostat (Tavai P
R-2G) was determined by the following equation from the weight change from the weight after standing for 24 hours in R-2G). Moisture absorption (%) = (weight after moisture absorption-weight when absolutely dry) /
Weight at absolute dryness × 100 20 ° C × 65% RH and 30 ° C × 90% measured above
From the moisture absorption rate under the condition of RH (referred to as MR1 and MR2, respectively), a moisture absorption rate difference ΔMR (%) = MR2-MR1 is obtained. Here, the difference in moisture absorption ΔMR is a driving force for obtaining comfort by releasing moisture in the clothes when the clothes are worn to the outside air, and is 30 ° C. when light to medium work or light to medium exercise is performed. The difference in moisture absorption between the temperature inside the clothes represented by × 90% RH and the outside temperature and humidity represented by 20 ° C. × 65% RH.
【0025】本発明では吸湿性評価の尺度としてこの△
MRをパラメーターとして用いるが、△MRは大きけれ
ば大きいほど吸湿性が高く着用時の快適性が良好である
ことに対応する。実用上として着用快適性を得るために
は繊維として1%以上が好ましい。In the present invention, this △ is used as a scale for evaluating hygroscopicity.
MR is used as a parameter, and the larger the ΔMR, the higher the hygroscopicity and the better the comfort when worn. In practical use, the fiber is preferably 1% or more to obtain wearing comfort.
【0026】C.強度、伸度 東洋ボールドウィン社製テンシロン引張り試験機を用い
て試長20cm、引張り速度10cm/分の条件で応力−歪み曲
線から値を求めた。C. Strength and elongation Using a Tensilon tensile tester manufactured by Toyo Baldwin Co., values were obtained from a stress-strain curve under the conditions of a test length of 20 cm and a tensile speed of 10 cm / min.
【0027】D.ウースタノーマルU% 繊維の長さ方向の太さムラは、USTER TESTER MONITOR C
で測定した。糸速度8m/分、チャート速度25cm/min、
TWIST S1.5、YARN TENTION 1.5、EVALUTION TIME 1
分、測定モードはノーマルで平均偏差U%を測定する。
測定値は試料の任意の3ヶ所を測定し、その平均値を用
いる。D. Uster Normal U% Fiber unevenness in the length direction is USTER TESTER MONITOR C
Was measured. Yarn speed 8m / min, chart speed 25cm / min,
TWIST S1.5, YARN TENTION 1.5, EVALUTION TIME 1
In the measurement mode, the average deviation U% is measured normally.
The measured value is measured at any three points of the sample, and the average value is used.
【0028】E.ドライ感 布帛のドライ感については5人のパネラーによる官能評
価によって判定した。5人全てがドライ感を感じた場合
◎、3〜4人の場合○、2人以下の場合×とした。E. Dry feeling The dry feeling of the fabric was determined by sensory evaluation by five panelists. When all five felt dry, ◎ when 3 to 4 ○, × when 2 or less.
【0029】F.中空率 芯鞘中空繊維の中空率は、繊維軸の横断面方向の写真を
撮影し、この写真を用い、面積比率によって求めた。F. Hollow Ratio The hollow ratio of the core-sheath hollow fiber was determined by taking a photograph of the fiber shaft in the transverse cross-sectional direction and using this photograph to determine the area ratio.
【0030】実施例1 親水性成分の共重合ポリエステルとして、ジメチルテレ
フタル酸194部、エチレングリコール124部、およ
びテトラブチルチタネート0.1部を加え、140〜2
30℃でメタノールを留出しつつエステル交換反応を行
った後、リン酸トリメチル0.08部のエチレングリコ
ール溶液および分子量4000のポリエチレングリコー
ル288部、抗酸化剤としてIrganox 1010(チバガイ
ギー社製)0.2部、消泡剤としてシリコン0.2部、
およびテトラブチルチタネート0.1部を加え、1.0
mmHgの減圧下250℃の条件下4時間重合を行い共
重合ポリエステルを得た。またこの共重合体に共重合さ
れたポリエチレングリコールの割合は60wt%であっ
た。得られた共重合ポリエステルの吸湿率△MRは28
%であった。Example 1 As copolymerized polyester of a hydrophilic component, 194 parts of dimethyl terephthalic acid, 124 parts of ethylene glycol, and 0.1 part of tetrabutyl titanate were added.
After transesterification while distilling off methanol at 30 ° C., an ethylene glycol solution of 0.08 part of trimethyl phosphate, 288 parts of polyethylene glycol having a molecular weight of 4000, and Irganox 1010 (manufactured by Ciba Geigy) 0.2 as an antioxidant were used. Parts, 0.2 parts of silicone as defoamer,
And 0.1 part of tetrabutyl titanate,
Polymerization was performed at 250 ° C. for 4 hours under reduced pressure of mmHg to obtain a copolymerized polyester. The proportion of polyethylene glycol copolymerized with this copolymer was 60% by weight. The obtained copolymerized polyester has a moisture absorption ΔMR of 28.
%Met.
【0031】該共重合ポリエステルを芯成分とし、極限
粘度0.70のポリエチレンテレフタレートを鞘成分と
して別々に溶融し、芯鞘複合中空口金から芯/鞘比率
(重量比)=15/85になるように吐出して紡糸速度
3000m/分で未延伸糸を得、次いで延伸倍率1.4
倍、熱ピン温度80℃に設定し低倍率延伸することによ
り75デニール24フィラメントの太細を有する芯鞘複
合中空繊維を得た。該繊維のU%は10%であった。ま
た該繊維の中空率は4%であった。この繊維を筒編みと
し、精練後の筒編地の吸湿特性を測定したところ△R=
2.8%であった。また染色布帛のドライ感は良好であ
り5人全てがドライ感があると感じた。The copolymerized polyester is used as a core component, and polyethylene terephthalate having an intrinsic viscosity of 0.70 is separately melted as a sheath component so that a core / sheath ratio (weight ratio) = 15/85 from a core / sheath composite hollow die. To obtain an undrawn yarn at a spinning speed of 3000 m / min, and then a draw ratio of 1.4.
The core / sheath composite hollow fiber having a thickness of 75 denier and 24 filaments was obtained by setting the hot pin temperature to 80 ° C. and drawing at a low magnification. The U% of the fiber was 10%. The hollow ratio of the fiber was 4%. This fiber was made into a tubular knit, and the moisture absorption characteristics of the tubular knitted fabric after scouring were measured.
2.8%. The dry feeling of the dyed fabric was good, and all five felt that there was a dry feeling.
【0032】実施例2〜4、比較例1、2 実施例1において延伸倍率を変更し繊維のU%を変えた
以外は同様に繊維化を行った。得られた繊維特性を表1
にまとめた。比較例2においてU%ムラを20以上にし
てしまうと未延伸部が多く残り、満足のいくレベルの原
糸を得ることができなかった。Examples 2 to 4 and Comparative Examples 1 and 2 Fiberization was carried out in the same manner as in Example 1 except that the draw ratio was changed and U% of the fiber was changed. Table 1 shows the obtained fiber properties.
Summarized in In Comparative Example 2, when the U% unevenness was set to 20 or more, many undrawn portions remained, and a satisfactory level of the original yarn could not be obtained.
【0033】[0033]
【表1】 実施例5〜9、比較例3、4 実施例1で得られた共重合ポリエステルを芯成分とし複
合比率を変更した以外は、実施例1と同様に75デニー
ル24フィラメントの芯太細を有する鞘複合中空繊維を
得た。繊維特性を表2にまとめたが、芯比率を上げると
ともに、ΔMRは向上するが、強伸度の低下が認められ
るようになり、比較例4では製糸できなくなる。また比
較例3においては満足する吸湿特性が得られなかった。[Table 1] Examples 5 to 9, Comparative Examples 3 and 4 A sheath having a core thickness of 75 denier and 24 filaments in the same manner as in Example 1 except that the copolymerized polyester obtained in Example 1 was used as a core component and the composite ratio was changed. A composite hollow fiber was obtained. The fiber properties are summarized in Table 2. As the core ratio is increased, ΔMR is improved, but a decrease in strong elongation is observed. In Comparative Example 3, satisfactory moisture absorption properties were not obtained.
【0034】[0034]
【表2】 実施例10〜12、比較例5 実施例1において共重合ポリエステル中のポリエチレン
グリコールの共重合量を変更する以外は同様な方法で共
重合ポリエステルを得た。該共重合ポリエステルを芯成
分とし、実施例1と同様な方法で75デニール24フィ
ラメントの芯鞘複合中空繊維を得た。繊維特性を表3に
まとめた。[Table 2] Examples 10 to 12 and Comparative Example 5 Copolymerized polyesters were obtained in the same manner as in Example 1 except that the copolymerization amount of polyethylene glycol in the copolymerized polyester was changed. Using this copolymerized polyester as the core component, a core-sheath composite hollow fiber of 75 denier and 24 filaments was obtained in the same manner as in Example 1. The fiber properties are summarized in Table 3.
【0035】[0035]
【表3】 実施例13 ポリエーテルエステルアミドを合成するにあたり、ε−
カプロラクタム340部、テレフタル酸18部、数平均
分子量が1000のポリエチレングリコール100部、
抗酸化剤としてIR1330 0.1部、耐光剤として
2−(2’−ヒドロキシ−5’−メチルフェニル)ベン
ゾトリアゾール4.4部およびトリメチルフォスフェー
ト0.01部とともに重合反応容器に仕込み、窒素気流
下に240℃で1時間加熱攪拌後、3酸化アンチモン
0,1部を添加し、昇温減圧プログラム下250℃、
0.5mmHg以下の条件で4時間重合反応を行うこと
により、N6成分の割合が45重量%であるポリエーテ
ルエステルアミドブロック共重合体を得た。またポリマ
の△MRは10.5%であった。[Table 3] Example 13 In synthesizing a polyetheresteramide, ε-
340 parts of caprolactam, 18 parts of terephthalic acid, 100 parts of polyethylene glycol having a number average molecular weight of 1000,
0.113 parts of IR1330 as an antioxidant, 4.4 parts of 2- (2'-hydroxy-5'-methylphenyl) benzotriazole and 0.01 part of trimethylphosphate as a light stabilizer were charged into a polymerization reaction vessel, and a nitrogen stream was supplied. After heating and stirring at 240 ° C. for 1 hour, 0.1 part of antimony trioxide was added, and 250 ° C.
The polymerization reaction was performed for 4 hours under the condition of 0.5 mmHg or less to obtain a polyetheresteramide block copolymer having a N6 component ratio of 45% by weight. The ΔMR of the polymer was 10.5%.
【0036】このポリエーテルエステルアミドを芯成分
とした以外は実施例1と同様な方法により75デニール
24フィラメントの太細を有する芯鞘複合中空繊維を得
た。Except that this polyetheresteramide was used as the core component, a thick core-sheath composite hollow fiber having 75 denier and 24 filaments was obtained in the same manner as in Example 1.
【表4】 実施例14 実施例1において、複合中空口金のかわりに同心円芯鞘
複合口金を用いた以外は同様な方法により太細を有する
芯鞘複合繊維を得た。結果を表5にまとめた。[Table 4] Example 14 A thick core-sheath composite fiber was obtained in the same manner as in Example 1, except that a concentric core-sheath composite mouthpiece was used instead of the composite hollow mouthpiece. The results are summarized in Table 5.
【0037】[0037]
【表5】 [Table 5]
【0038】[0038]
【発明の効果】本発明によって得られた共重合ポリエス
テルは非常に高い吸湿特性を有しており、またそれを用
いた合成繊維は、着用快適性を得るのに十分な吸湿性を
有し、かつドライタッチな風合いと高い染色堅牢性や耐
光性を有している。本発明の合成繊維は、下着、シャツ
・ブラウス類、中衣、スポーツウェア、スラックス類、
外衣、裏地、さらには、シーツ、フトンカバー等の寝装
用に適しており、極めて実用性の高いものである。The copolymerized polyester obtained according to the present invention has a very high hygroscopic property, and a synthetic fiber using the same has a sufficient hygroscopic property to obtain comfortable wearing. In addition, it has a dry touch texture, high color fastness and light fastness. The synthetic fibers of the present invention include underwear, shirts and blouses, middle garments, sportswear, slacks,
It is suitable for bedding such as outer garments, linings, sheets, futon covers and the like, and is extremely practical.
【図1】本発明による合成繊維の横断面の例示図FIG. 1 is an exemplary view of a cross section of a synthetic fiber according to the present invention.
1:共重合ポリエステル 2:繊維形成性ポリエステル 3:中空部 1: copolymerized polyester 2: fiber-forming polyester 3: hollow part
Claims (5)
成分とした複合繊維であり、かつ吸放湿パラメーター
(△MR)が1.0%以上であり、該繊維軸の長さ方向
の太さムラがウースタノーマルU%が5〜20%である
ことを特徴とする太細を有する吸湿性複合繊維。1. A conjugate fiber comprising a hydrophilic component and a fiber-forming polymer as constituent components, and having a moisture absorption / desorption parameter (ΔMR) of 1.0% or more, and a lengthwise direction of the fiber axis. A thick and thin hygroscopic conjugate fiber, wherein the unevenness in thickness is 5 to 20% in Uster Normal U%.
物を用いることを特徴とする請求項1記載の太細を有す
る吸湿性複合繊維。2. The thick and thin hygroscopic conjugate fiber according to claim 1, wherein a compound having a ΔMR of 8% or more is used as the hydrophilic component.
ミド系化合物および/またはポリエーテルエステル系化
合物のいずれかを用いることを特徴とする請求項1また
は2記載の太細を有する吸湿性複合繊維。3. The thick and thin hygroscopic composite fiber according to claim 1, wherein one of a polyetheresteramide compound and a polyetherester compound is used as the hydrophilic component.
〜90重量%であることを特徴とする請求項1〜3のい
ずれか1項記載の太細を有する吸湿性複合繊維。4. A composition comprising a hydrophilic component as one component and a composite ratio of 5
The thick and thin hygroscopic conjugate fiber according to any one of claims 1 to 3, wherein the amount is from 90 to 90% by weight.
徴とする請求項1〜4のいずれか1項記載の太細を有す
る吸湿性複合繊維。5. The thick and thin hygroscopic conjugate fiber according to any one of claims 1 to 4, wherein the conjugate fiber structure has a hollow portion.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2893998A JPH11222727A (en) | 1998-02-10 | 1998-02-10 | Hygroscopic conjugate fiber of uneven thickness |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2893998A JPH11222727A (en) | 1998-02-10 | 1998-02-10 | Hygroscopic conjugate fiber of uneven thickness |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH11222727A true JPH11222727A (en) | 1999-08-17 |
Family
ID=12262388
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2893998A Pending JPH11222727A (en) | 1998-02-10 | 1998-02-10 | Hygroscopic conjugate fiber of uneven thickness |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH11222727A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004204364A (en) * | 2002-12-24 | 2004-07-22 | Toray Ind Inc | Core-sheath type polyester fiber excellent in hygroscopicity, method for producing the same, and hygroscopic cloth |
-
1998
- 1998-02-10 JP JP2893998A patent/JPH11222727A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004204364A (en) * | 2002-12-24 | 2004-07-22 | Toray Ind Inc | Core-sheath type polyester fiber excellent in hygroscopicity, method for producing the same, and hygroscopic cloth |
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