JP2000234218A - Polyamide conjugated fiber having excellent heat retaining property and feeling - Google Patents
Polyamide conjugated fiber having excellent heat retaining property and feelingInfo
- Publication number
- JP2000234218A JP2000234218A JP11034380A JP3438099A JP2000234218A JP 2000234218 A JP2000234218 A JP 2000234218A JP 11034380 A JP11034380 A JP 11034380A JP 3438099 A JP3438099 A JP 3438099A JP 2000234218 A JP2000234218 A JP 2000234218A
- Authority
- JP
- Japan
- Prior art keywords
- sheath
- fiber
- polyamide
- core
- alkali
- 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 75
- 239000004952 Polyamide Substances 0.000 title claims abstract description 46
- 229920002647 polyamide Polymers 0.000 title claims abstract description 46
- 239000003513 alkali Substances 0.000 claims abstract description 21
- 229920006122 polyamide resin Polymers 0.000 claims abstract description 4
- 239000002131 composite material Substances 0.000 claims description 15
- 239000004744 fabric Substances 0.000 abstract description 28
- 229920005992 thermoplastic resin Polymers 0.000 abstract description 14
- -1 polyethylene terephthalate Polymers 0.000 abstract description 12
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 8
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 8
- 229920000742 Cotton Polymers 0.000 abstract description 7
- 229920002292 Nylon 6 Polymers 0.000 abstract description 5
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 208000016261 weight loss Diseases 0.000 description 19
- 230000004580 weight loss Effects 0.000 description 10
- 239000013585 weight reducing agent Substances 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 238000009987 spinning Methods 0.000 description 5
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 238000002074 melt spinning Methods 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000007665 sagging Methods 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- 238000009941 weaving Methods 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000012510 hollow fiber Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- PBLZLIFKVPJDCO-UHFFFAOYSA-N 12-aminododecanoic acid Chemical compound NCCCCCCCCCCCC(O)=O PBLZLIFKVPJDCO-UHFFFAOYSA-N 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000009940 knitting Methods 0.000 description 2
- 150000003951 lactams Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 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 2
- 229920001778 nylon Polymers 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- CSPVUHYZUZZRGF-RNFRBKRXSA-N (4R,6R)-hydroxy-2,2,6-trimethylcyclohexanone Chemical compound C[C@@H]1C[C@@H](O)CC(C)(C)C1=O CSPVUHYZUZZRGF-RNFRBKRXSA-N 0.000 description 1
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- SQAPJTNHAUBTOP-UHFFFAOYSA-N 2,4-dimethyloctane-1,8-diamine Chemical compound NCC(C)CC(C)CCCCN SQAPJTNHAUBTOP-UHFFFAOYSA-N 0.000 description 1
- ZPXGNBIFHQKREO-UHFFFAOYSA-N 2-chloroterephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(Cl)=C1 ZPXGNBIFHQKREO-UHFFFAOYSA-N 0.000 description 1
- UFMBOFGKHIXOTA-UHFFFAOYSA-N 2-methylterephthalic acid Chemical compound CC1=CC(C(O)=O)=CC=C1C(O)=O UFMBOFGKHIXOTA-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- PMZBHPUNQNKBOA-UHFFFAOYSA-N 5-methylbenzene-1,3-dicarboxylic acid Chemical compound CC1=CC(C(O)=O)=CC(C(O)=O)=C1 PMZBHPUNQNKBOA-UHFFFAOYSA-N 0.000 description 1
- MBRGOFWKNLPACT-UHFFFAOYSA-N 5-methylnonane-1,9-diamine Chemical compound NCCCCC(C)CCCCN MBRGOFWKNLPACT-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- 229930185327 Actinol Natural products 0.000 description 1
- 101100116283 Arabidopsis thaliana DD11 gene Proteins 0.000 description 1
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229920000572 Nylon 6/12 Polymers 0.000 description 1
- 229920000007 Nylon MXD6 Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-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
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- XBZSBBLNHFMTEB-UHFFFAOYSA-N cyclohexane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCCC(C(O)=O)C1 XBZSBBLNHFMTEB-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000010036 direct spinning Methods 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- KLNPWTHGTVSSEU-UHFFFAOYSA-N undecane-1,11-diamine Chemical compound NCCCCCCCCCCCN KLNPWTHGTVSSEU-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
- Multicomponent Fibers (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ポリアミドからな
る中空部を有する複合繊維であって、製編織することに
よって、軽量で保温性に富み、優れた風合いを有する布
帛を得ることが可能なポリアミド複合繊維に関するもの
である。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a conjugate fiber having a hollow portion made of polyamide, which can be knitted and woven to obtain a lightweight, heat-insulating cloth having an excellent texture. It relates to a conjugate fiber.
【0002】[0002]
【従来の技術】ポリアミド繊維からなる布帛に軽量性や
保温性を付与するために、ポリアミド繊維の形態を中空
にしたり、高異形度にして繊維と繊維の間に空間を持た
せたり、さらには、高異形度中空繊維にする方法があ
る。しかしながら、このような繊維は、製糸性が劣った
り、布帛にするまでの加工で中空部の割れや繊維形態の
変形が生じるという問題がある。2. Description of the Related Art In order to impart lightness and heat retention to a fabric made of polyamide fiber, the form of the polyamide fiber is made hollow, a high degree of irregularity is provided to provide a space between the fibers, and There is a method of forming hollow fibers having a high degree of irregularity. However, such a fiber has a problem in that the fiber formability is poor, and the hollow portion is cracked and the fiber shape is deformed in the processing up to fabric.
【0003】この問題を解決するために、紡糸段階で
は、中空部を持たない複合繊維として製糸し、布帛にし
た後にアルカリ減量により中空部を形成させる繊維が提
案されている。例えば、特開平3-124857号公報、特開平
3-249266号公報、特開平4-245985号公報には、鞘部をポ
リアミド、芯部をポリエステルとした芯鞘複合繊維をア
ルカリ減量することによって得られた中空繊維や、芯部
と鞘部の間に空間がある繊維が提案されている。[0003] In order to solve this problem, there has been proposed a fiber which is formed into a conjugate fiber having no hollow portion in the spinning step, formed into a fabric, and then the hollow portion is formed by reducing the amount of alkali. For example, JP-A-3-124857,
JP-A-3-249266, JP-A-4-245985, the hollow fiber obtained by reducing the alkali-weight of the core-sheath conjugate fiber with polyamide sheath, polyester core, and the core and sheath. Fibers with spaces between them have been proposed.
【0004】これらの繊維では製糸性は改善されたが、
中空繊維の場合は、鞘部の割合が少ないと潰れが生じ、
また強度も低いのでこの繊維より得られる布帛はへたり
があり、保温性にも劣るものであった。一方、芯部と鞘
部の間に空間がある繊維も、芯部全てがポリエステルで
あるため、得られる布帛は、はりやこしには優れるが柔
軟性には乏しくなるという問題があった。また、芯部の
ポリエステルの一部を減量処理して空間を形成するもの
であるため、減量処理速度が遅く、コスト面でも問題が
あった。[0004] These fibers have improved yarn-making properties,
In the case of hollow fibers, crushing occurs when the ratio of the sheath is small,
Further, since the strength was low, the fabric obtained from this fiber had sagging and was inferior in heat retention. On the other hand, even for fibers having a space between the core and the sheath, the entire core is made of polyester, so that the resulting fabric has a problem in that it is excellent in abrasion and stiffness but poor in flexibility. In addition, since a part of the polyester in the core is subjected to weight reduction processing to form a space, the speed of weight reduction processing is slow, and there is also a problem in cost.
【0005】[0005]
【発明が解決しようとする課題】本発明は、上述の問題
点を解決し、中空率が高く、鞘部の割合が少なくても潰
れが生じにくく、製編織するとへたりがなく軽量で保温
性に富み、かつ、繊維表面に綿表面と同様な軽い撚りを
有し、綿様で柔軟性に優れる風合いを有する布帛を得る
ことができるポリアミド複合繊維を提供することを技術
的な課題とするものである。DISCLOSURE OF THE INVENTION The present invention solves the above-mentioned problems, has a high hollow ratio, is hard to be crushed even if the ratio of the sheath portion is small, and has no sagging when knitting and weaving. The technical object of the present invention is to provide a polyamide conjugate fiber which is rich in the fiber and has a light twist similar to that of the cotton surface on the fiber surface, and is capable of obtaining a cloth having a cotton-like and excellent texture. It is.
【0006】[0006]
【課題を解決するための手段】本発明者らは、このよう
な課題を解決するために検討した結果、本発明に到達し
た。すなわち、本発明は、ポリアミドからなる芯鞘複合
繊維であって、芯部は中空部と島状部とからなり、繊維
断面における鞘部の面積割合が5〜55%、中空部の面
積割合が20%以上、島状部の割合割合が10%以上で
あることを特徴とする保温性と優れた風合いを有するポ
リアミド複合繊維を要旨とするものである。Means for Solving the Problems The present inventors have studied to solve such problems, and as a result, have reached the present invention. That is, the present invention relates to a core-sheath composite fiber made of polyamide, in which the core portion is composed of a hollow portion and an island portion, and the area ratio of the sheath portion in the fiber cross section is 5 to 55%, and the area ratio of the hollow portion is 5%. The gist of the present invention is a polyamide composite fiber having a heat retaining property and an excellent texture, characterized in that the proportion of the island-shaped portion is at least 20% and the proportion of the island-shaped portion is at least 10%.
【0007】[0007]
【発明の実施の形態】以下、本発明を詳細に説明する。
本発明のポリアミド複合繊維は、芯鞘複合繊維であっ
て、芯部は中空部と島状部とからなり、鞘部と島状部は
ポリアミドからなるものである。本発明におけるポリア
ミドとは、アミノカルボン酸、ラクタムあるいはジアミ
ンとジカルボン酸から形成されるアミド結合(-CONH-)
を有する重合体または共重合体である。このようなポリ
アミドを形成するモノマーの例を挙げると、次のような
ものがある。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail.
The polyamide conjugate fiber of the present invention is a core-sheath conjugate fiber, in which the core portion is composed of a hollow portion and an island portion, and the sheath portion and the island portion are composed of polyamide. The polyamide in the present invention is an amide bond (-CONH-) formed from an aminocarboxylic acid, a lactam or a diamine and a dicarboxylic acid.
Is a polymer or a copolymer having The following are examples of monomers for forming such a polyamide.
【0008】アミノカルボン酸としては、6-アミノカプ
ロン酸、11- アミノウンデカン酸、12- アミノドデカン
酸等が挙げられる。ラクタムとしては、ε- カプロラク
タム、ω- ラウロラクタム等が挙げられる。ジアミンと
しては、テトラメチレンジアミン、ヘキサメチレンジア
ミン、ウンデカメチレンジアミン、ドデカメチレンジア
ミン、2, 2, 2-トリメチルヘキサメチレンジアミン、2,
4, 4-トリメチルヘキサメチレンジアミン、5-メチルノ
ナメチレンジアミン、2,4- ジメチルオクタメチレンジ
アミン、メタキシレンジアミン等が挙げられる。Examples of the aminocarboxylic acid include 6-aminocaproic acid, 11-aminoundecanoic acid, 12-aminododecanoic acid and the like. Examples of the lactam include ε-caprolactam and ω-laurolactam. As the diamine, tetramethylene diamine, hexamethylene diamine, undecamethylene diamine, dodecamethylene diamine, 2,2,2-trimethylhexamethylene diamine, 2,
Examples thereof include 4,4-trimethylhexamethylenediamine, 5-methylnonamethylenediamine, 2,4-dimethyloctamethylenediamine, and metaxylenediamine.
【0009】ジカルボン酸としては、アジピン酸、セバ
シン酸、テレフタル酸、イソフタル酸、ナフタレンジカ
ルボン酸、2-クロロテレフタル酸、2-メチルテレフタル
酸、5-メチルイソフタル酸、5-ナトリウムスルホイソフ
タル酸、ヘキサヒドロテレフタル酸、ヘキサヒドロイソ
フタル酸、ジグリコール酸等が挙げられる。The dicarboxylic acids include adipic acid, sebacic acid, terephthalic acid, isophthalic acid, naphthalenedicarboxylic acid, 2-chloroterephthalic acid, 2-methylterephthalic acid, 5-methylisophthalic acid, 5-sodium sulfoisophthalic acid, Hydroterephthalic acid, hexahydroisophthalic acid, diglycolic acid and the like can be mentioned.
【0010】具体的には、ナイロン6 、ナイロン46、ナ
イロン66、ナイロン610 、ナイロン612 、ナイロン116
、ナイロン11、ナイロン12、ナイロンMXD6等が好
ましく、中でも、ナイロン6 がコストや製糸性の面から
特に好ましい。[0010] Specifically, nylon 6, nylon 46, nylon 66, nylon 610, nylon 612, nylon 116
, Nylon 11, Nylon 12, Nylon MXD6, etc. are preferred, and Nylon 6 is particularly preferred in view of cost and spinnability.
【0011】なお、これらのポリアミドには、本来の特
性を損なわない程度において他の共重合成分、静電防止
剤、可塑剤、顔料、着色剤、難燃剤、強化剤、潤滑剤、
帯電防止剤、酸化防止剤、紫外線吸収剤、光安定剤等が
添加されていてもよい。These polyamides have other copolymer components, an antistatic agent, a plasticizer, a pigment, a colorant, a flame retardant, a reinforcing agent, a lubricant, and the like, to the extent that the original properties are not impaired.
An antistatic agent, an antioxidant, an ultraviolet absorber, a light stabilizer and the like may be added.
【0012】ポリアミドの重合度は一般衣料用に用いら
れる範囲であればよく、ナイロン6の場合には、相対粘
度が2.0 〜3.5 のものが好ましい。相対粘度がこの範囲
よりも大きくても小さくても紡糸性が急激に低下するの
で好ましくない。The degree of polymerization of the polyamide may be within the range used for general clothing, and in the case of nylon 6, the relative viscosity is preferably 2.0 to 3.5. It is not preferable that the relative viscosity is larger or smaller than this range because the spinnability rapidly decreases.
【0013】また、鞘部と芯部の島状部を構成するポリ
アミドは同種のものとすることが好ましいが、異種のも
のでもよい。It is preferable that the polyamide constituting the sheath and the core island is of the same type, but they may be of different types.
【0014】次に、本発明のポリアミド複合繊維の形状
を図面を用いて説明する。図1(A)〜(D)は本発明
のポリアミド複合繊維の断面形状を示す断面模式図であ
る。本発明のポリアミド複合繊維は、繊維断面における
鞘部1の面積割合が5〜55%、好ましくは10〜45
%であり、中空部2の面積割合が20%以上、島状部3
の割合が10%以上である。Next, the shape of the polyamide composite fiber of the present invention will be described with reference to the drawings. 1 (A) to 1 (D) are schematic cross-sectional views showing the cross-sectional shape of the polyamide composite fiber of the present invention. In the polyamide composite fiber of the present invention, the area ratio of the sheath 1 in the fiber cross section is 5 to 55%, preferably 10 to 45%.
%, The area ratio of the hollow portion 2 is 20% or more, and the island-shaped portion 3
Is 10% or more.
【0015】本発明のポリアミド複合繊維は、このよう
な構成を有し、芯部と島状部ともにポリアミドであるこ
とによって、鞘部の割合を少なく、中空部の割合を高く
しても、芯部の島状部によって強度が保持され、繊維の
潰れが生じず、保温性に優れる。そして、製編織する
と、繊維表面に綿表面と同様の軽い撚りが発生し、綿様
で柔軟性に優れた風合いの布帛が得られる。The polyamide conjugate fiber of the present invention has such a structure, and since both the core and the island-like portion are made of polyamide, even if the ratio of the sheath portion is small and the ratio of the hollow portion is high, The strength is maintained by the island-like portions, the fibers are not crushed, and the heat retention is excellent. Then, when weaving and weaving, a light twist similar to the cotton surface is generated on the fiber surface, and a cotton-like fabric having excellent texture is obtained.
【0016】鞘部の割合が5%未満であると、鞘部が薄
くなりすぎ、鞘部が破れやすくなるとともに、繊維表面
がフィブリル化しやすくなる。一方、55%を超える
と、鞘部が厚くなり、上記のような綿表面と同様の軽い
撚りが発生しなくなり、風合いに劣るものとなる。な
お、芯部の島状部が鞘部に実質的に結合している場合、
鞘部にはこの島状部も含むものとする。When the ratio of the sheath portion is less than 5%, the sheath portion becomes too thin, the sheath portion is easily broken, and the fiber surface is easily fibrillated. On the other hand, if it exceeds 55%, the sheath becomes thick, and the same light twisting as on the cotton surface as described above does not occur, resulting in poor texture. In addition, when the island-shaped portion of the core is substantially connected to the sheath,
The sheath portion also includes this island-shaped portion.
【0017】次に、中空部の面積割合が20%未満であ
ると、得られる布帛は保温性に劣るものとなり、島状部
の割合が10%未満であると、繊維の強度が保持でき
ず、潰れが生じて、得られる布帛はへたりのあるものと
なる。Next, if the area ratio of the hollow portion is less than 20%, the obtained fabric is inferior in heat retention, and if the ratio of the island portion is less than 10%, the fiber strength cannot be maintained. Then, the fabric is crushed, and the resulting fabric has sagging.
【0018】芯部の島状部は1つ〔図1(C)や
(D)〕であっても、複数〔図1(A)や(B)〕であ
ってもよく、島状部が存在する位置はどの位置でもよ
い。そして、鞘部と芯部の繊維横断面における形状は、
円形断面をはじめ、扁平、六葉、三角断面等の異形でも
よい。中でも、円形断面は綿表面のような撚りがかかり
やすいので好ましい。The core may have a single island (FIGS. 1C and 1D) or a plurality of islands (FIGS. 1A and 1B). The existing position may be any position. And the shape of the sheath and the core in the fiber cross section is
In addition to a circular cross section, a deformed shape such as a flat, six-lobe, or triangular cross section may be used. Above all, a circular cross section is preferable because it is easy to twist like a cotton surface.
【0019】本発明のポリアミド複合繊維は、上記のよ
うな芯鞘構造の形態とするには、直接紡糸口金より溶融
紡糸を行って製造してもよいが、延伸時に繊維の変形や
中空割れが生じることなく、操業性よく製造を行うに
は、芯部をポリアミドを5〜80重量%含有するアルカ
リ易溶性熱可塑性樹脂とし、布帛にした後にアルカリ減
量処理することによって、芯部のアルカリ易溶性熱可塑
性樹脂を溶出させて、本発明のポリアミド複合繊維とす
ることが好ましい。The polyamide conjugate fiber of the present invention may be produced by melt-spinning directly from a spinneret in order to obtain the above-described core-sheath structure. In order to produce the core with good operability without causing the alkali, the core is made of an alkali-soluble thermoplastic resin containing 5 to 80% by weight of a polyamide. It is preferable to elute the thermoplastic resin to obtain the polyamide composite fiber of the present invention.
【0020】この場合、芯鞘複合繊維の芯部に用いるポ
リアミドを含有するアルカリ易溶性熱可塑性樹脂として
は、ポリアミドとブレンドして溶融紡糸可能で、しかも
アルカリ減量ができれば特に限定するものではないが、
エステル結合(-COO-)を有する重合体又は共重合体が好
適である。エステル結合を有する重合体または共重合体
としては、ポリエチレンテレフタレート、ポリプロピレ
ンテレフタレート、ポリブチレンテレフタレート、ポリ
エチレンナフタレート等が挙げられる。中でも、ポリエ
チレンテレフタレートはコスト面で好ましい。In this case, the alkali-soluble thermoplastic resin containing polyamide used for the core of the core-sheath composite fiber is not particularly limited as long as it can be melt-spinned by blending with polyamide and can reduce the alkali. ,
A polymer or a copolymer having an ester bond (—COO—) is preferred. Examples of the polymer or copolymer having an ester bond include polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate. Among them, polyethylene terephthalate is preferred in terms of cost.
【0021】そして、エステル結合を有する共重合体の
共重合成分としてはイソフタル酸、無水フタル酸、5-ナ
トリウムスルホイソフタル酸、ナフタレンジカルボン
酸、ジエチレングリコール、プロピレングリコール、1
、4-シクロヘキサンジメタノール、ペンタエリスリト
ール、4-ヒドロキシ安息香酸、ε- カプロラクタム、ア
ジピン酸、セバシン酸、1 、4-ブタンジオール、1 、6-
ヘキサンジオール、ポリエチレングリコール等が挙げら
れる。これらの共重合成分は必要に応じて添加すればよ
いが、中でも、5-ナトリウムスルホイソフタル酸とポリ
エチレングリコールは、添加するとアルカリ減量しやす
くなるので特に好ましい。The copolymer component of the copolymer having an ester bond includes isophthalic acid, phthalic anhydride, 5-sodium sulfoisophthalic acid, naphthalenedicarboxylic acid, diethylene glycol, propylene glycol,
, 4-cyclohexanedimethanol, pentaerythritol, 4-hydroxybenzoic acid, ε-caprolactam, adipic acid, sebacic acid, 1,4-butanediol, 1,6-
Hexanediol, polyethylene glycol and the like can be mentioned. These copolymerization components may be added as needed, and among them, 5-sodium sulfoisophthalic acid and polyethylene glycol are particularly preferable because addition thereof facilitates alkali reduction.
【0022】アルカリ易溶性熱可塑性樹脂としてポリエ
チレンテレフタレートを用いる場合、ポリエチレンテレ
フタレートの相対粘度は1.0 〜1.6 であることが好まし
い。相対粘度がこの範囲よりも大きいと、紡糸応力が高
く、配向結晶化をコントロールしにくくなり、また、相
対粘度がこの範囲よりも小さいと、ポリアミドとの粘度
差が大きくなりすぎて好ましくない。When polyethylene terephthalate is used as the alkali-soluble thermoplastic resin, the polyethylene terephthalate preferably has a relative viscosity of 1.0 to 1.6. If the relative viscosity is larger than this range, spinning stress is high and it is difficult to control oriented crystallization. On the other hand, if the relative viscosity is smaller than this range, the viscosity difference from polyamide becomes too large, which is not preferable.
【0023】また、アルカリ易溶性熱可塑性樹脂にも、
ポリアミド樹脂と同様に、本来の特性を損なわない程度
において他の共重合成分や各種の添加剤が添加されてい
てもよい。なお、艶消剤等として酸化チタンが含まれて
いると、アルカリ減量時に酸化チタンが中空部の内壁に
付着し、光沢斑を生じる傾向にあるので、芯部となるポ
リアミド樹脂とアルカリ易溶性熱可塑性樹脂ともに酸化
チタンを実質的に含まないようにすることが好ましい。In addition, the alkali-soluble thermoplastic resin also includes
Like the polyamide resin, other copolymer components and various additives may be added to the extent that the original properties are not impaired. If titanium oxide is contained as a matting agent, etc., when the alkali is reduced, the titanium oxide tends to adhere to the inner wall of the hollow portion and cause spots of gloss. It is preferable that both of the plastic resins do not substantially contain titanium oxide.
【0024】アルカリ易溶性熱可塑性樹脂中にはポリア
ミドが5〜80重量%含まれていることが好ましい。す
なわち、アルカリ減量処理後はポリアミドが島状部を形
成するので、ポリアミドの量が80重量%よりも多い
と、繊維断面における中空部を20%以上とすることが
困難となり、一方、5重量%未満であると、繊維断面に
おける島状部を10%以上とすることが困難となる。It is preferable that the alkali-soluble thermoplastic resin contains polyamide in an amount of 5 to 80% by weight. That is, since the polyamide forms an island portion after the alkali weight reduction treatment, if the amount of the polyamide is more than 80% by weight, it becomes difficult to make the hollow portion in the fiber cross section 20% or more, while 5% by weight. If it is less than 10%, it is difficult to make the island-shaped portion in the fiber cross section 10% or more.
【0025】ポリアミドをアルカリ易溶性熱可塑性樹脂
に均一に分散させる方法としては、紡糸時に混練するこ
とが好ましい。例えば、エクストルーダーでのライン中
にスタティックミキサーを用いて混練する方法やポリア
ミドとアルカリ易溶性熱可塑性樹脂のマスターチップを
作るのが好ましい。As a method for uniformly dispersing the polyamide in the alkali-soluble thermoplastic resin, it is preferable to knead the polyamide during spinning. For example, it is preferable to use a kneading method using a static mixer in a line in an extruder or to prepare a master chip of a polyamide and an alkali-soluble thermoplastic resin.
【0026】図1に示した繊維は、上記のようにアルカ
リ減量処理を施すことによって得られたものであるが、
(A)は、島状部(ポリアミド)が不定型で複数存在す
る例、(B)は、島状部がある程度凝集し、一部が鞘部
に付着している例、(C)、(D)は、(A)や(B)
のような複数の島状部の凝集がさらに進み、1つの島状
部を形成した場合の例である。The fiber shown in FIG. 1 is obtained by performing the alkali reduction treatment as described above.
(A) is an example in which a plurality of island-shaped portions (polyamide) are irregular and present, (B) is an example in which the island-shaped portions are aggregated to some extent and a part of them is attached to the sheath, (C), ( D) is (A) or (B)
This is an example in which aggregation of a plurality of islands further progresses to form one island.
【0027】次に、本発明のポリアミド複合繊維の製造
方法について説明する。はじめから中空部が形成された
本発明のポリアミド複合繊維を紡糸して製造する場合、
アルカリ易溶性熱可塑性樹脂を芯部に含み、アルカリ減
量処理によって中空部が形成される芯鞘型複合繊維を製
造する場合ともに、公知の複合紡糸装置を用いて溶融紡
糸を行う。Next, a method for producing the polyamide composite fiber of the present invention will be described. When spinning and manufacturing the polyamide composite fiber of the present invention having a hollow portion formed from the beginning,
When producing a core-in-sheath composite fiber in which a core portion contains an alkali-soluble thermoplastic resin and a hollow portion is formed by alkali reduction treatment, melt spinning is performed using a known composite spinning apparatus.
【0028】溶融紡糸した糸条はガラス転移以下に冷却
し、400 〜5000m/分の速度で引き取り糸条を得る。加
熱筒の有無及び温度や長さ、冷却風の温度、吹き付け
量、引き取り速度、吐出量、口金の孔数は適宜調整す
る。The melt-spun yarn is cooled to a temperature lower than the glass transition temperature, and a drawn yarn is obtained at a speed of 400 to 5000 m / min. The presence or absence and the temperature and length of the heating cylinder, the temperature of the cooling air, the blowing amount, the take-up speed, the discharge amount, and the number of holes in the base are appropriately adjusted.
【0029】得られた糸条は延伸するが、延伸は糸条を
一旦捲き取ってから延伸する2工程法、及び捲き取るこ
となく連続して延伸する直接紡糸延伸法のいずれの方法
によってもよい。また、冷延伸、熱延伸いずれの方法で
あってもかまわない。熱延伸における加熱装置としては
熱ロール、ヒートプレート、スチームジェット装置等が
挙げられ、これらは適宜併用すればよい。延伸された糸
条には必要に応じて熱処理や弛緩処理が行われる。The obtained yarn is stretched, and the stretching may be performed by any of a two-step method in which the yarn is once wound and then stretched, and a direct spinning and stretching method in which the yarn is continuously stretched without winding. . In addition, any of cold stretching and hot stretching may be used. Examples of the heating device in the thermal stretching include a hot roll, a heat plate, a steam jet device, and the like, and these may be appropriately used in combination. The drawn yarn is subjected to a heat treatment or a relaxation treatment as necessary.
【0030】アルカリ易溶性熱可塑性樹脂を芯部に含む
複合繊維の場合、本発明のポリアミド複合繊維とするに
は、布帛にした段階でアルカリ易溶性熱可塑性樹脂をア
ルカリ減量処理し、溶出除去することが好ましいが、減
量処理方法も特に限定されるものではなく、薬剤として
は苛性アルカリ(濃度10〜100g/l、温度80〜120 ℃程
度)で、例えば苛性ソーダや苛性カリ等が用いられる。
その処理条件は、鞘部の厚さ、ポリアミドやアルカリ易
溶性熱可塑性樹脂の種類、繊維の配向結晶化の程度等に
よって適宜調整する。In the case of the conjugate fiber containing the alkali-soluble thermoplastic resin in the core portion, in order to obtain the polyamide conjugate fiber of the present invention, the alkali-soluble thermoplastic resin is subjected to alkali weight reduction treatment and eluted and removed at the stage of forming the fabric. It is preferable, but the method of weight reduction is not particularly limited, and caustic alkali (concentration: 10 to 100 g / l, temperature: about 80 to 120 ° C.), for example, caustic soda or caustic potash is used.
The treatment conditions are appropriately adjusted depending on the thickness of the sheath, the kind of polyamide or the alkali-soluble thermoplastic resin, the degree of oriented crystallization of the fiber, and the like.
【0031】[0031]
【実施例】次に、本発明を実施例によって具体的に説明
する。なお、特性値の測定は次のとおりである。 (a) ポリアミドの相対粘度 96%硫酸を溶媒とし、濃度 1.0g/dlの溶液を温度25℃で
測定した。 (b) ポリエステルの相対粘度 フェノールとテトラクロロエタンとの等重量混合物を溶
媒とし、濃度 0.5g/dl、温度20℃で測定した。 (c) 強伸度 JIS L-1013 7.5.1 に記載された方法に従って測定し
た。 (d) アルカリ減量率(%) 以下の式で算出した。 〔(減量前の重量−減量後の重量)/減量前の重量〕×
100 (e) 繊維表面形状(撚りと鞘破れの有無) 電子顕微鏡にて繊維表面を3000倍の倍率で観察し、綿表
面と同様な軽い撚りと鞘部の鞘破れの有無を調べた。 (f) 鞘部、中空部、島状部の割合 繊維断面を光学顕微鏡または電子顕微鏡にて撮影後、写
真よりそれぞれの面積を測定し、全断面積に対する割合
を求めた。 (g) 布帛の目付 アルカリ減量処理後の布帛を25cm×25cmの試験片にし、
平衡水分率以下になるように十分に乾燥、20℃、65%RH
の室内に24時間放置して、水分平衡になった後、その試
験片の重量を測定し、得られた試験片の重量を1m2 あ
たりに換算し、布帛5枚の平均値を目付とした。 (h) 布帛の風合い アルカリ減量処理後の布帛を触感により、綿様の風合い
と柔軟性を判断した。これらの両性質に優れているもの
を良、劣っているものを悪とした。 (i) 保温性(CLO 値) アルカリ減量処理後の布帛を用い、20℃、65%RHの環境
下に調湿させた後、40℃±0.1 ℃に設定されたSm2 の
熱板上に設置し、1分経過後の安定した状態で、熱板か
ら布帛を通して環境下に放出される熱損失量を、熱板面
積Sm2 及び消費電力EWから次式によって算出する。
なお、この時、熱板から対流による放熱を防止するた
め、熱板周辺は上部に開閉口のある樹脂製ケースで覆っ
て無風状態とした。 CLO値=(1/0.155)×( 20×S/E)Next, the present invention will be described specifically with reference to examples. The measurement of the characteristic values is as follows. (a) Relative viscosity of polyamide A solution having a concentration of 1.0 g / dl was measured at a temperature of 25 ° C. using 96% sulfuric acid as a solvent. (b) Relative viscosity of polyester The measurement was carried out at a concentration of 0.5 g / dl and a temperature of 20 ° C. using an equal weight mixture of phenol and tetrachloroethane as a solvent. (c) Strong elongation Measured according to the method described in JIS L-1013 7.5.1. (d) Alkali weight loss rate (%) It was calculated by the following equation. [(Weight before weight loss-weight after weight loss) / weight before weight loss] x
100 (e) Fiber surface shape (presence or absence of twist and sheath breakage) The fiber surface was observed with an electron microscope at a magnification of 3000 times, and light twist similar to the cotton surface and the presence or absence of sheath breakage in the sheath portion were examined. (f) Ratio of sheath portion, hollow portion and island portion After the fiber cross section was photographed with an optical microscope or an electron microscope, the area of each was measured from the photograph, and the ratio to the total cross sectional area was determined. (g) The basis weight of the fabric The fabric after the alkali weight reduction treatment was converted into a 25 cm x 25 cm test piece,
Dry enough to be below the equilibrium moisture content, 20 ℃, 65% RH
After being left in the room for 24 hours to achieve water equilibrium, the weight of the test piece was measured, the weight of the obtained test piece was converted to per 1 m 2, and the average value of five cloths was used as the basis weight. . (h) Texture of Fabric The fabric after the alkali weight loss treatment was judged to have a cotton-like texture and flexibility by touch. Those excellent in both of these properties were evaluated as good, and those inferior were evaluated as bad. (i) Insulation (CLO value) Using a fabric after the alkali weight reduction treatment, humidify the environment in an environment of 20 ° C and 65% RH, and place it on a Sm 2 hot plate set at 40 ° C ± 0.1 ° C. The heat loss amount released from the hot plate to the environment through the fabric in a stable state after a lapse of one minute from the hot plate is calculated from the hot plate area Sm 2 and the power consumption EW by the following formula.
At this time, in order to prevent heat radiation due to convection from the hot plate, the surroundings of the hot plate were covered with a resin case having an opening / closing opening at an upper portion to prevent a wind. CLO value = (1 / 0.155) x (20 x S / E)
【0032】実施例1 相対粘度2.5 のナイロン6(ユニチカ製、以下N6と略
す) と、5-ナトリウムスルホイソフタル酸2.0 モル%、
ポリエチレングリコール12.0モル%を共重合したポリエ
チレンテレフタレート(ユニチカ製、以下ASと略す。ア
ルカリ易溶性熱可塑性樹脂)を用い、通常の複合溶融紡
糸装置を使用して、鞘部にN6、芯部にASにN6を30重量%
含有させた混合樹脂を配し、孔径0.35mmの円形孔を24個
有する紡糸口金を用い、鞘部の割合が16重量%となるよ
うにして285 ℃で溶融紡糸した。そして、口金から紡出
された糸条を、300 ℃に加熱した加熱筒(5cm)内を
通過させ、温度18℃の冷却風(速度0.8 m/秒)を吹き
付けて固化させてから、油剤を付与し、4300m/分の速
度で捲き取り、高配向未延伸糸を得た。得られた未延伸
糸を延伸倍率1.297 になるように延伸し、680 m/分の
速度で引き取り、70デニール/24フィラメントの繊維を
得た。得られた繊維の強度、伸度を測定した結果を表1
に示す。次に、得られた繊維を筒編みして、2g/lのアク
チノールで精練した後、40g/lの苛性ソーダで30分、100
℃でアルカリ減量処理を行い、本発明のポリアミド複
合繊維からなる布帛を得た。Example 1 Nylon 6 having a relative viscosity of 2.5 (manufactured by Unitika, hereinafter abbreviated as N6), 2.0 mol% of 5-sodium sulfoisophthalic acid,
Using polyethylene terephthalate (manufactured by Unitika, hereinafter abbreviated as AS; alkali-soluble thermoplastic resin) obtained by copolymerizing 12.0 mol% of polyethylene glycol, N6 is used for the sheath portion and AS is used for the core portion using an ordinary composite melt spinning apparatus. 30% by weight of N6
The mixed resin contained therein was arranged, and melt-spun at 285 ° C. using a spinneret having 24 circular holes having a hole diameter of 0.35 mm so that the ratio of the sheath was 16% by weight. Then, the yarn spun from the die is passed through a heating cylinder (5 cm) heated to 300 ° C., and solidified by blowing cooling air (speed: 0.8 m / sec) at a temperature of 18 ° C. This was wound up at a speed of 4300 m / min to obtain a highly oriented undrawn yarn. The obtained undrawn yarn was drawn so as to have a draw ratio of 1.297, and was drawn at a speed of 680 m / min to obtain a fiber of 70 denier / 24 filaments. Table 1 shows the results of measuring the strength and elongation of the obtained fibers.
Shown in Next, the obtained fiber was knitted in a tube, scoured with 2 g / l of actinol, and then mixed with 40 g / l of caustic soda for 30 minutes, 100
An alkali weight reduction treatment was performed at ℃ to obtain a fabric comprising the polyamide composite fiber of the present invention.
【0033】実施例2〜7、比較例1〜4 溶融紡糸時の鞘部の割合、芯部のポリマー中のN6の割合
を表1に示すように種々変更した以外は、実施例1と同
様に行った。Examples 2 to 7 and Comparative Examples 1 to 4 The same as Example 1 except that the ratio of the sheath during melt spinning and the ratio of N6 in the polymer of the core were changed as shown in Table 1. I went to.
【0034】実施例8〜9 芯部のASのかわりに、相対粘度1.38のポリエチレンテレ
フタレート(以下PETと略す) (実施例8)、ポリプロ
ピレンテレフタレート(以下PPT と略す)(実施例9)
を用いた以外は実施例1と同様に行った。Examples 8 to 9 Instead of the core AS, polyethylene terephthalate (hereinafter abbreviated as PET) having a relative viscosity of 1.38 (Example 8), polypropylene terephthalate (hereinafter abbreviated as PPT) (Example 9)
Was performed in the same manner as in Example 1 except that was used.
【0035】実施例1〜9、比較例1〜4におけるアル
カリ減量率、アルカリ減量処理後の布帛の目付、風合
い、保温性、さらに、アルカリ減量処理後の布帛より取
り出した繊維についての繊維表面形状(撚りと鞘破れの
有無)、鞘部、島状部、中空部の割合を測定、評価した
結果を表1に示す。In Examples 1 to 9 and Comparative Examples 1 to 4, the alkali weight loss rate, the basis weight, texture, and heat retention of the fabric after the alkali weight loss treatment, and the fiber surface shape of the fiber taken out from the fabric after the alkali weight loss treatment Table 1 shows the results of measuring (evaluating the presence or absence of twisting and tearing of the sheath), the ratio of the sheath portion, the island-shaped portion, and the hollow portion and evaluating them.
【0036】[0036]
【表1】 [Table 1]
【0037】表1から明らかなように、実施例1〜9で
は、芯部がナイロンとアルカリ易溶性ポリエステルであ
るために、アルカリ減量した際、迅速に減量することが
できた。そして、減量後の繊維は表面に鞘割れがなく、
撚りが見られ、軽量でしかも風合いもよく、CLO値も
良好な値を示し、保温性に優れていた。一方、比較例1
では、芯部が全て5-ナトリウムスルホイソフタル酸とポ
リエチレングリコールを共重合したポリエステルであっ
たために、減量速度が遅く、しかも減量処理後の繊維
は、島状部の割合が少なすぎ、また、鞘破れが発生して
いたため、得られた布帛は風合いに劣っていた。比較例
2の繊維は、中空部の割合が少なすぎたため、繊維表面
に撚りもみられず、得られた布帛は保温性、風合いとも
に劣っていた。比較例3では、鞘部の割合が少なすぎた
ため、鞘破れが発生し、得られた布帛は風合いの悪いも
のであった。比較例4の繊維は、鞘部の割合が多すぎた
ため、繊維表面に撚りもみられず、得られた布帛は風合
いに劣っていた。As is clear from Table 1, in Examples 1 to 9, since the core was made of nylon and an alkali-soluble polyester, when the alkali was reduced, the weight could be reduced quickly. And the fiber after weight loss has no sheath crack on the surface,
Twist was observed, light weight, good texture, good CLO value, and excellent heat retention. On the other hand, Comparative Example 1
In the above, since the core portion was all polyester obtained by copolymerizing 5-sodium sulfoisophthalic acid and polyethylene glycol, the rate of weight loss was slow, and the fiber after the weight loss treatment had too little island-shaped portion, Since the fabric was torn, the obtained fabric was inferior in texture. Since the fiber of Comparative Example 2 had too little hollow portion, no twist was observed on the fiber surface, and the obtained fabric was inferior in both heat retention and texture. In Comparative Example 3, since the ratio of the sheath portion was too small, the sheath was broken, and the obtained fabric had poor texture. Since the fiber of Comparative Example 4 had too much sheath portion, no twist was observed on the fiber surface, and the obtained fabric was inferior in texture.
【0038】[0038]
【発明の効果】本発明の繊維は、中空率が高く、鞘部の
割合が少なくても潰れが生じにくく、へたりがなく軽量
で保温性に富んでおり、かつ、綿表面と同様な軽い撚り
を有しているので、製編織すれば保温性、柔軟性等の風
合いに優れる布帛を得ることが可能である。The fiber of the present invention has a high hollow ratio, is hard to be crushed even if the ratio of the sheath portion is small, has no sagging, is lightweight, has excellent heat retention, and is as light as the cotton surface. Since it has a twist, it is possible to obtain a fabric excellent in texture such as heat retention and flexibility by knitting and weaving.
【図1】(A)〜(D)は、本発明のポリアミド複合繊
維の実施態様を示す断面模式図である。FIGS. 1A to 1D are schematic cross-sectional views showing an embodiment of a polyamide conjugate fiber of the present invention.
1 鞘部 2 中空部 3 島状部 1 sheath part 2 hollow part 3 island part
フロントページの続き (72)発明者 樽石 一秋 京都府宇治市宇治小桜23 ユニチカ株式会 社中央研究所内 Fターム(参考) 4L031 AA20 AB06 AB10 BA11 CA01 DA00 DA01 4L041 AA08 AA18 AA20 BA04 BA05 BA16 BA17 BA24 BA42 BC04 BC20 BD14 CA06 CA08 CA16 CA21 DD01 DD11 DD14 DD18 EE08 EE15 EE20 4L045 AA05 BA03 BA18 BA20 BA24 BA49 BA51 BA60 CA25 CB09 CB13 DA15 DA23 DA42 DA48 DC03 Continued on the front page (72) Inventor Kazuaki Taruishi 23 Uji Kozakura, Uji City, Kyoto Prefecture Unitika F. term in Central Research Laboratory 4L031 AA20 AB06 AB10 BA11 CA01 DA00 DA01 4L041 AA08 AA18 AA20 BA04 BA05 BA16 BA17 BA24 BA42 BC04 BC20 BD14 CA06 CA08 CA16 CA21 DD01 DD11 DD14 DD18 EE08 EE15 EE20 4L045 AA05 BA03 BA18 BA20 BA24 BA49 BA51 BA60 CA25 CB09 CB13 DA15 DA23 DA42 DA48 DC03
Claims (2)
て、芯部は中空部と島状部とからなり、繊維断面におけ
る鞘部の面積割合が5〜55%、中空部の面積割合が2
0%以上、島状部の面積割合が10%以上であることを
特徴とする保温性と優れた風合いを有するポリアミド複
合繊維。1. A core-sheath conjugate fiber comprising a polyamide, wherein a core portion comprises a hollow portion and an island-like portion, and the area ratio of the sheath portion in the fiber cross section is 5 to 55%, and the area ratio of the hollow portion is 2%.
A polyamide composite fiber having heat retention and excellent texture, characterized in that the area ratio of the island-shaped portion is 0% or more and 0% or more.
するアルカリ易溶性熱可塑性樹脂、鞘部はポリアミド樹
脂からなる芯鞘複合繊維をアルカリ減量処理することに
よって得られた請求項1記載の保温性と優れた風合いを
有するポリアミド複合繊維。2. The core according to claim 1, wherein the core is obtained by subjecting a core-sheath conjugate fiber made of a polyamide resin to alkali reduction treatment, and the sheath is obtained by subjecting the core-sheath composite fiber made of a polyamide resin to 5-80% by weight of polyamide. Polyamide conjugate fiber with heat retention and excellent texture.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11034380A JP2000234218A (en) | 1999-02-12 | 1999-02-12 | Polyamide conjugated fiber having excellent heat retaining property and feeling |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11034380A JP2000234218A (en) | 1999-02-12 | 1999-02-12 | Polyamide conjugated fiber having excellent heat retaining property and feeling |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2000234218A true JP2000234218A (en) | 2000-08-29 |
Family
ID=12412575
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11034380A Pending JP2000234218A (en) | 1999-02-12 | 1999-02-12 | Polyamide conjugated fiber having excellent heat retaining property and feeling |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2000234218A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6907207B2 (en) * | 2001-08-22 | 2005-06-14 | T & M Corporation | Sealing material for rotary body, usage of the same, and developing apparatus |
| JP2009221627A (en) * | 2008-03-17 | 2009-10-01 | Kuraray Co Ltd | Core-sheath type hollow conjugate fiber having acoustic property |
| JP2010121265A (en) * | 2010-02-02 | 2010-06-03 | Japan Vilene Co Ltd | Fiber with porous surface and fiber sheet |
| CN103451772A (en) * | 2013-08-01 | 2013-12-18 | 安徽朗润新材料科技有限公司 | Antibacterial polyester and nylon composite conductive filament |
| CN110257952A (en) * | 2019-06-27 | 2019-09-20 | 苏州峰佳达化纤纺织有限公司 | A kind of preparation method of high-strength ventilative polyamide composite filaments |
| JPWO2019188525A1 (en) * | 2018-03-26 | 2021-04-01 | 日本ゼオン株式会社 | Acrylic rubber, acrylic rubber composition, acrylic rubber crosslinked product, sealing material, and hose material |
-
1999
- 1999-02-12 JP JP11034380A patent/JP2000234218A/en active Pending
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6907207B2 (en) * | 2001-08-22 | 2005-06-14 | T & M Corporation | Sealing material for rotary body, usage of the same, and developing apparatus |
| JP2009221627A (en) * | 2008-03-17 | 2009-10-01 | Kuraray Co Ltd | Core-sheath type hollow conjugate fiber having acoustic property |
| JP2010121265A (en) * | 2010-02-02 | 2010-06-03 | Japan Vilene Co Ltd | Fiber with porous surface and fiber sheet |
| CN103451772A (en) * | 2013-08-01 | 2013-12-18 | 安徽朗润新材料科技有限公司 | Antibacterial polyester and nylon composite conductive filament |
| JPWO2019188525A1 (en) * | 2018-03-26 | 2021-04-01 | 日本ゼオン株式会社 | Acrylic rubber, acrylic rubber composition, acrylic rubber crosslinked product, sealing material, and hose material |
| JP7276322B2 (en) | 2018-03-26 | 2023-05-18 | 日本ゼオン株式会社 | Acrylic rubber, acrylic rubber composition, cross-linked acrylic rubber, sealing material, and hose material |
| CN110257952A (en) * | 2019-06-27 | 2019-09-20 | 苏州峰佳达化纤纺织有限公司 | A kind of preparation method of high-strength ventilative polyamide composite filaments |
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