JP2009197361A - Stretchable sheath-core conjugate yarn - Google Patents
Stretchable sheath-core conjugate yarn Download PDFInfo
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- JP2009197361A JP2009197361A JP2008040122A JP2008040122A JP2009197361A JP 2009197361 A JP2009197361 A JP 2009197361A JP 2008040122 A JP2008040122 A JP 2008040122A JP 2008040122 A JP2008040122 A JP 2008040122A JP 2009197361 A JP2009197361 A JP 2009197361A
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- 239000003063 flame retardant Substances 0.000 claims abstract description 34
- 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 claims abstract description 33
- 239000004744 fabric Substances 0.000 claims abstract description 25
- 229920000728 polyester Polymers 0.000 claims abstract description 14
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000002904 solvent Substances 0.000 claims abstract description 3
- 239000000835 fiber Substances 0.000 claims description 51
- 239000002131 composite material Substances 0.000 claims description 28
- -1 polyethylene terephthalate Polymers 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 14
- 229920006231 aramid fiber Polymers 0.000 claims description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 5
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 5
- 229920002972 Acrylic fiber Polymers 0.000 claims description 3
- 229920000742 Cotton Polymers 0.000 claims description 3
- 239000004693 Polybenzimidazole Substances 0.000 claims description 3
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- IISBACLAFKSPIT-UHFFFAOYSA-N Bisphenol A Natural products C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 2
- 239000004697 Polyetherimide Substances 0.000 claims description 2
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- 229920001230 polyarylate Polymers 0.000 claims description 2
- 229920006376 polybenzimidazole fiber Polymers 0.000 claims description 2
- 229920001601 polyetherimide Polymers 0.000 claims description 2
- 239000004800 polyvinyl chloride Substances 0.000 claims description 2
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- 210000002268 wool Anatomy 0.000 claims description 2
- 239000004698 Polyethylene Substances 0.000 claims 1
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- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 claims 1
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
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- 238000009991 scouring Methods 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 238000009941 weaving Methods 0.000 description 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- GSNUFIFRDBKVIE-UHFFFAOYSA-N DMF Natural products CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 1
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 229920000561 Twaron Polymers 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N cyclobenzothiazole Natural products C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000005802 health problem Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229920002480 polybenzimidazole Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 150000004060 quinone imines Chemical class 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000004762 twaron Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Multicomponent Fibers (AREA)
- Woven Fabrics (AREA)
Abstract
Description
本発明は、伸縮性が高く且つ耐熱性、風合い、外観的にも品位の優れた布帛を創出することのできる伸縮性複合仮撚糸および伸縮性複合糸に関する。 The present invention relates to a stretchable composite false-twist yarn and a stretchable composite yarn that can create a fabric having high stretchability and excellent in heat resistance, texture, and appearance.
従来、消防士が消火作業時に着用する耐熱性防護服としては、不燃性のアスベスト繊維やガラス繊維等からなる防護服が使われていたが、環境問題(健康問題)や作業容易性(動き易さ)などの観点から近年では、アラミド、ポリフェニレンスルフィド、ポリイミド、ポリベンズイミダゾールなどの難燃性の有機繊維が使用され、さらに火炎により活性する輻射熱を防止する目的から、これらの難燃性繊維からなる布帛に金属アルミニウムなどをコーティング法あるいは蒸着法により表面加工を施したものが多く使われている。又難燃糸や布帛に空気層を有する方法(特許文献1、特許文献2、特許文献3、特許文献4)により軽量化することが提案されている。確かに難燃性、耐熱性等は改善されるものの、糸ひいては布帛に伸縮性がないため作業性や着用感が悪いという問題があった。 Conventionally, as heat-resistant protective clothing worn by firefighters during firefighting work, protective clothing made of non-combustible asbestos fibers or glass fibers has been used, but environmental problems (health problems) and ease of work (easy to move) In recent years, flame retardant organic fibers such as aramid, polyphenylene sulfide, polyimide, and polybenzimidazole have been used. In addition, for the purpose of preventing radiant heat activated by flame, these flame retardant fibers are used. Many of these fabrics are surface-treated with metallic aluminum or the like by a coating method or a vapor deposition method. Further, it has been proposed to reduce the weight by a method (Patent Document 1, Patent Document 2, Patent Document 3, Patent Document 4) having an air layer on a flame retardant yarn or fabric. Although flame retardancy, heat resistance, etc. are certainly improved, there is a problem that workability and wearing feeling are poor because the yarn and thus the fabric is not stretchable.
難燃性を有し、伸縮性を有する布帛については特許文献5、特許文献6に開示されているように弾性糸を用いて伸縮性を付与し難燃剤を使用して難燃性を付与する布帛や衣服が開示されているが、耐熱性が低く又難燃性も十分なものではなかった。 About the cloth which has a flame retardance and has a stretching property, as disclosed in Patent Document 5 and Patent Document 6, the elastic yarn is used to impart the elasticity and the flame retardant is used to impart the flame resistance. Although fabrics and clothes have been disclosed, heat resistance is low and flame retardancy is not sufficient.
又耐熱性と難燃性を有し、伸縮性を有する糸や布帛については特許文献7、特許文献8に開示されているようにパラ系アラミド耐熱性捲縮糸を用いて伸縮性と難燃性、耐熱性を有する布帛や衣服が開示されているが、製織、精練、染色等布帛加工工程で捲縮糸の伸縮性が低下し布帛として十分な伸縮性が得られないという問題やコストが高くなるという問題点があった。 In addition, for yarns and fabrics having heat resistance and flame retardancy, as disclosed in Patent Literature 7 and Patent Literature 8, para-aramid heat resistant crimped yarn is used for elasticity and flame retardancy. Fabrics and clothes having heat resistance and heat resistance are disclosed, but there is a problem and cost that the stretchability of the crimped yarn is lowered in the fabric processing step such as weaving, scouring, and dyeing, and sufficient stretchability cannot be obtained as a fabric. There was a problem of becoming higher.
本発明は、上記従来技術の有する問題点を解決し、難燃性、耐熱性に優れた伸縮性芯鞘型複合糸及びそれからなる布帛に関するものである。 The present invention relates to a stretchable core-sheath composite yarn excellent in flame retardancy and heat resistance, and a fabric comprising the same, which solves the above-described problems of the prior art.
本発明らは上記目的を達成するために鋭意検討した結果、芯糸がポリエステルフィラメント糸、鞘糸が難燃性繊維糸からなる芯鞘型複合糸であって、芯糸がオルソクロロフェノール溶媒中、30℃で測定される固有粘度の差が0.1〜0.4dL/gの範囲にある2種のポリエステルがサイドバイサイド型に張合わされたコンジュゲート糸の延伸糸であることを特徴とする伸縮性芯鞘型複合糸、が提供される。 As a result of intensive studies to achieve the above object, the present inventors have found that a core-sheath-type composite yarn in which the core yarn is a polyester filament yarn and the sheath yarn is a flame-retardant fiber yarn, and the core yarn is in an orthochlorophenol solvent. Stretch characterized in that it is a drawn yarn of conjugate yarn in which two kinds of polyesters having a difference in intrinsic viscosity measured at 30 ° C. in the range of 0.1 to 0.4 dL / g are bonded to a side-by-side type. Core-sheath type composite yarn is provided.
その芯糸がイソフタル酸および/または、ビスフェノールA化合物を8〜15モル%共重合した高収縮性ポリエチレンテレフタレートと、[η]f(繊維固有粘度)が0.36〜0.47の低収縮性ポリエチレンテレフタレートとをサイドバイサイド型に複合した、伸度25〜45%のコンジュゲート糸の延伸糸からなり、鞘糸が全芳香族ポリアミド繊維、特にメタ系全芳香族ポリアミド繊維と座屈部を有するパラ系アラミド繊維が均一に混合されてなる紡績糸からなり、芯糸と部分的に混繊・交絡しながら交互反転状に巻き付いてなる芯鞘型複合糸(仮撚り加工糸)、更に好ましくは該鞘糸が芯糸をらせん状にかつ異なる方向に旋回してなるカバリングヤーンタイプの芯鞘型複合糸が提供される。 The core yarn is a highly shrinkable polyethylene terephthalate copolymerized with 8 to 15 mol% of isophthalic acid and / or a bisphenol A compound, and a low shrinkage of [η] f (fiber intrinsic viscosity) of 0.36 to 0.47. It consists of a drawn yarn of conjugate yarn with a degree of elongation of 25-45%, which is a side-by-side composite of polyethylene terephthalate, and the sheath yarn is a wholly aromatic polyamide fiber, especially a meta-type wholly aromatic polyamide fiber and a paraffin having a buckling part. Core-sheath type composite yarn (false twisted yarn) comprising a spun yarn in which a system aramid fiber is uniformly mixed and wound in an alternating inversion while partially mixed and entangled with the core yarn, more preferably A covering yarn type core-sheath type composite yarn in which a sheath yarn is formed by spirally turning a core yarn in different directions is provided.
本発明の難燃伸縮性芯鞘型複合糸を製織、精練、染色等布帛加工工程により布帛とすることにより、芯糸のポリエステルマルチフィラメント糸が熱工程で捲縮が発現し伸縮性を有する繊維糸となり布帛にストレッチ性を付与することが出来る。従来生じていた加工工程のテンションや熱工程で伸縮性の低下させることなく伸縮性を付与できるので難燃性、耐熱性、伸縮性を有するという布帛とすることができる。又鞘糸を紡績糸とすることで高耐熱高剛性難燃糸を用いても、ソフト性と高難燃耐熱性を両立させることができ伸縮性とあいまって有用な耐火防護衣料とすることができる。 By using the flame retardant stretch core-sheath composite yarn of the present invention as a fabric by a fabric processing step such as weaving, scouring, and dyeing, the polyester multifilament yarn of the core yarn is crimped in the heat step and has stretch properties. It becomes a thread and can impart stretch properties to the fabric. Since stretchability can be imparted without lowering stretchability by a tension in a conventional processing step or a heat step, a fabric having flame retardancy, heat resistance, and stretchability can be obtained. Also, by using a sheath yarn as a spun yarn, even if a high heat resistance and high rigidity flame retardant yarn is used, both softness and high flame resistance and heat resistance can be achieved, and combined with stretchability, it can be made a useful fireproof protective clothing. .
本発明に使用する難燃性繊維としては、アラミド繊維、ポリベンゾイミダゾール繊維、ポリイミド繊維、ポリ塩化ビニル繊維、ポリエーテルイミド繊維、ポリアリレート繊維、ポリパラフェニレンベンゾビスオキサゾール繊維、ノボロイト繊維、難燃アクリル繊維、ポリクラレート繊維、難燃ポリエステル繊維、難燃綿繊維、難燃ウール繊維、難燃レーヨン繊維からなる群から選ばれた少なくとも1種の繊維であり、これらの耐熱性繊維を一種以上組み合わせて、或いは一定量以上混在させ非耐熱性繊維を共に用いて耐熱性能が基準値を超えるようにして難燃耐熱性とすることが好ましい。 Examples of the flame retardant fiber used in the present invention include aramid fiber, polybenzimidazole fiber, polyimide fiber, polyvinyl chloride fiber, polyetherimide fiber, polyarylate fiber, polyparaphenylene benzobisoxazole fiber, noboroite fiber, flame retardant It is at least one fiber selected from the group consisting of acrylic fiber, polyclarate fiber, flame retardant polyester fiber, flame retardant cotton fiber, flame retardant wool fiber, flame retardant rayon fiber, and a combination of one or more of these heat resistant fibers, Alternatively, it is preferable to use a non-heat-resistant fiber together with a certain amount or more so that the heat-resistant performance exceeds the standard value to make it flame-retardant and heat-resistant.
難燃耐熱性の中でも優れたLOI(限界酸素指数)値を示し、なおかつ繊維そのものが白色で染色も可能なポリメタフェニレンイソフタルアミドは防護衣料を作成するにあたり非常に有用である。更にパラ系アラミド繊維、すなわちポリパラフェニレンテレフタルアミドやあるいはこれに第三成分を共重合した繊維を混合させることもが好ましく行われる。 Polymetaphenylene isophthalamide, which exhibits an excellent LOI (Limiting Oxygen Index) value among flame retardant heat resistance, and is capable of being dyed white and dyed, is very useful in preparing protective clothing. Furthermore, it is also preferable to mix para-aramid fibers, that is, polyparaphenylene terephthalamide or fibers obtained by copolymerizing a third component thereto.
ここで鞘糸としてはフィラメント糸及び紡績糸を用いることができるが中でも紡績糸とすることがアラミド繊維のような高剛性繊維を用いる場合布帛のソフト性、及びコストの調整又染色加工性の点で好ましい。 Here, filament yarn and spun yarn can be used as the sheath yarn. Among them, when using a highly rigid fiber such as an aramid fiber as the spun yarn, the softness of the fabric, the cost adjustment, and the dyeing processability Is preferable.
またポリパラフェニレンテレフタルアミドの染色性をより向上させるために、押しこみ式捲縮などの物理的手段により座屈部(キンクバンド部)が形成されたポリパラフェニレンテレフタルアミド(PPTA)繊維を用いることが好ましい。その際PPTAを濃硫酸に溶解し、その粘調な溶液を紡糸口金から押し出し、空気中または水中に紡出することによりフィラメント状にした後、水酸化ナトリウム水溶液で中和し、最終的には120〜500℃の乾燥・熱処理をして得られるが、乾燥・熱処理前のPPTA繊維は結晶サイズ(110面)が50Å未満であり、乾燥・熱処理後では50Å以上となる一般的なPPTA繊維であれば、より一層染色性が改善されなお良い。 Further, in order to further improve the dyeability of polyparaphenylene terephthalamide, polyparaphenylene terephthalamide (PPTA) fibers in which buckling portions (kink band portions) are formed by physical means such as push-in crimps are used. It is preferable. At that time, PPTA is dissolved in concentrated sulfuric acid, the viscous solution is extruded from a spinneret, and is made into a filament by spinning in air or water, and then neutralized with an aqueous sodium hydroxide solution. It is obtained by drying and heat treatment at 120 to 500 ° C., but the PPTA fiber before drying and heat treatment is a general PPTA fiber having a crystal size (110 face) of less than 50 mm, and becomes 50 mm or more after drying and heat treatment. If present, the dyeability is further improved.
また芯糸に供されるポリエステルコンジュゲート糸は、互いに固有粘度が異なる2種類の溶融紡糸されサイドバイサイド型に貼り合わされた繊維横断面を有する。2種類のポリエステルの固有粘度差は、0.1〜0.4dL/g、好ましくは0.15〜0.30dL/gである。固有粘度差が0.1dL/g未満の場合は、貼り合わせ成分間の熱収縮特に湿熱収縮差が不十分であり、コンジュゲート糸としての潜在捲縮性能が不十分となり、一方、固有粘度差が0.4dL/gを超えると安定した製糸が困難となる。 The polyester conjugate yarn used for the core yarn has a fiber cross section in which two types of melt-spun fibers having different intrinsic viscosities are bonded to each other in a side-by-side manner. The intrinsic viscosity difference between the two types of polyester is 0.1 to 0.4 dL / g, preferably 0.15 to 0.30 dL / g. When the intrinsic viscosity difference is less than 0.1 dL / g, the heat shrinkage between the bonded components, particularly the wet heat shrinkage difference, is insufficient, and the latent crimping performance as a conjugate yarn is insufficient. If it exceeds 0.4 dL / g, stable yarn production becomes difficult.
なおこれらのポリエステルは、本発明の目的を損なわない範囲で、酸化防止剤、紫外線吸収剤、熱安定剤、難燃剤、酸化チタン、着色剤、不活性微粒子などの任意の添加剤を含有していてもよい。 These polyesters contain optional additives such as antioxidants, ultraviolet absorbers, heat stabilizers, flame retardants, titanium oxides, colorants, and inert fine particles as long as the object of the present invention is not impaired. May be.
本発明の難燃耐熱性芯鞘複合糸は、鞘糸の難燃耐熱性繊維糸が芯糸の回りに捲き付きながら包みこんでいることが重要である。
このような構造の芯鞘構造を構成する方法として公知の仮撚り工程を通して混繊、交絡させることができるし、より好ましくは鞘糸が芯糸を旋回する構造の複合糸とする。鞘糸が芯糸を旋回する構造の複合糸の製造方法の一例として、カバーリングヤーン法が挙げられる。即ち、上記のポリエステルコンジュゲート糸を芯糸に用い、難燃耐熱性糸を鞘糸に用いて、公知の方法によりカバーリングヤーンを製造する。シングルカバリングでもダブルカバリングでも良い。難燃耐熱性を高める効果の点からダブルカバリングヤーンが好ましい。
In the flame-retardant heat-resistant core-sheath composite yarn of the present invention, it is important that the flame-retardant heat-resistant fiber yarn of the sheath yarn is wrapped around the core yarn.
As a method of constructing the core-sheath structure having such a structure, it can be mixed and entangled through a known false twisting process, and more preferably a composite yarn having a structure in which the sheath yarn turns the core yarn. An example of a method for producing a composite yarn having a structure in which a sheath yarn turns a core yarn is a covering yarn method. That is, a covering yarn is produced by a known method using the above polyester conjugate yarn as a core yarn and a flame-retardant heat-resistant yarn as a sheath yarn. Single or double covering may be used. A double covering yarn is preferable from the viewpoint of enhancing the flame resistance and heat resistance.
本発明の難燃耐熱性複合糸を用いて製編織、精練、染色、リラックス工程により布帛とする。この一連の工程において、特に湿熱加工において芯糸のポリエステルコンジュゲート糸の捲縮が発現することにより複合糸のひいては布帛の伸縮特性が得られる。 The flame-retardant heat-resistant composite yarn of the present invention is used to form a fabric by knitting, scouring, dyeing, and relaxing processes. In this series of steps, the crimp property of the polyester conjugate yarn of the core yarn is developed especially in wet heat processing, whereby the stretch property of the composite yarn and thus the fabric can be obtained.
本発明の難燃耐熱性複合糸の染色方法は、特殊な設備や特殊な方法を必要とせず、既存の合成繊維の染色設備を用いることができる。また染料としては、カチオン染料、分散染料、また更にはカチオン/分散混合染料の何れも用いることが出来るが、緻密な構造に浸透しやすく、また染着性は一般的にイオン結合であり染色後の堅牢性や色相安定性がよいカチオン染料が望ましい。 The dyeing method for the flame-retardant heat-resistant composite yarn of the present invention does not require special equipment or special methods, and can use existing synthetic fiber dyeing equipment. As the dye, any of a cationic dye, a disperse dye, and even a cation / dispersed mixed dye can be used. However, it easily penetrates into a dense structure, and the dyeing property is generally an ionic bond, and after dyeing. Cationic dyes with good fastness and hue stability are desirable.
そのカチオン染料とは水に可溶性で、塩基性を示す基を有する水溶性染料をいい、アクリル繊維、天然繊維或いはカチオン可染型ポリエステル繊維等の染色に多く用いられており、ジ及びトリアクリルメタン系、キノンイミン(アジン、オキサジン、チアジン)系、キサンテン系、メチン系(ポリメチン、アザメチン)、複素環アゾ系(チアゾールアゾ、トリアゾールアゾ、ベンゾチアゾールアゾ)、アントラキノン系などがある。また、最近では塩基性基を封鎖することにより水分散型にしたカチオン染料もあるが、両者とも用いることが出来る。 The cationic dye is a water-soluble dye that is soluble in water and has a basic group, and is often used for dyeing acrylic fibers, natural fibers, or cationic dyeable polyester fibers. Type, quinoneimine (azine, oxazine, thiazine) type, xanthene type, methine type (polymethine, azamethine), heterocyclic azo type (thiazole azo, triazole azo, benzothiazole azo), anthraquinone type, and the like. Recently, there is a cationic dye which is made water-dispersible by blocking a basic group, but both can be used.
染色温度は、115℃以上150℃以下が好ましく120℃以上がより好ましい。染色温度が115℃以下であると、染色性が不充分になる場合がある。また染色温度は高いほど染着性高まるものの、反面、染料の分解やアラミド繊維と他の素材を複合している場合には複合素材の劣化の問題も発生し始めるので、必ずしも高温にすればするほど良いわけではなく高くても140℃程度が好ましい。 The dyeing temperature is preferably 115 ° C or higher and 150 ° C or lower, more preferably 120 ° C or higher. If the dyeing temperature is 115 ° C. or lower, the dyeability may be insufficient. Also, the higher the dyeing temperature, the higher the dyeing property, but on the other hand, if the dye is decomposed or aramid fiber is combined with other materials, problems of deterioration of the composite material will begin to occur. About 140 ° C. is preferable even if it is not high.
またキャリヤーとしては、メタノール、エタノール、プロパノール、イソプロピルアルコール、ベンジルアルコール、アセトン、アセトフェノン、NMP、DMSO、DMF、エチレングリコール、アセトニトリル、プロピレンあるいはエチレングリコールフェニルエーテル、或いは市販キャリヤ、膨潤剤から選択された少なくとも1種以上用いて染色することを特徴とするが、染色環境に見合った(処理能力、作業環境など)環境負荷低減を考慮したキャリヤーを用いることが好ましい。 The carrier is at least selected from methanol, ethanol, propanol, isopropyl alcohol, benzyl alcohol, acetone, acetophenone, NMP, DMSO, DMF, ethylene glycol, acetonitrile, propylene or ethylene glycol phenyl ether, or a commercially available carrier and swelling agent. Although it is characterized by dyeing using 1 or more types, it is preferable to use the carrier which considered environmental load reduction suitable for the dyeing environment (processing capacity, work environment, etc.).
上述の布帛は常法により裁断、縫製し衣服とする。撥水や撥油などの防汚性を高めるために表面に皮膜を形成させたり、耐火性、熱防護性を高めるために上記布帛を用いた表地層と内層から構成して二枚重ね等することも好ましい。 The above-mentioned fabric is cut and sewn according to a conventional method. In order to improve antifouling properties such as water and oil repellency, a film is formed on the surface, and in order to improve fire resistance and thermal protection, it is composed of a surface layer and an inner layer using the above fabric, and two layers are laminated. preferable.
以下、実施例を挙げて、本発明の構成および効果を詳細に説明する。
尚、実施例/比較例で行った被染色物の評価方法は下記の方法に従って行った。
ストレッチ率および伸長回復率
5×20cmの試験片を自動記録装置付き引張り試験機を用いて初荷重20g、間隔10cmになるように試験片をつかみ、荷重−伸張曲線を描いた。このときの伸長距離をLとした。次いで直ちに元の位置まで戻し、残留伸びをRcmとした。
ストレッチ率=((L−10)/10)*100 (%)
伸長回復率 =((L−R)/L)*100 (%)
Hereinafter, an example is given and the composition and effect of the present invention are explained in detail.
In addition, the evaluation method of the to-be-dyed object performed by the Example / comparative example was performed according to the following method.
Using a tensile tester with an automatic recording device, a test piece having a stretch rate and an elongation recovery rate of 5 × 20 cm was grasped so as to have an initial load of 20 g and an interval of 10 cm, and a load-extension curve was drawn. The extension distance at this time was L. Then, immediately returned to the original position, the residual elongation was Rcm.
Stretch rate = ((L-10) / 10) * 100 (%)
Elongation recovery rate = ((LR) / L) * 100 (%)
[実施例1]
イソフタル酸を10モル%以上共重合した固有粘度0.64のポリエチレンテレフタレートと、固有粘度0.42のポリエチレンテレフタレートを重量比50/50をサイドバイサイドに貼り合わせたコンジュゲート糸を延伸熱処理して得た、50デニール/12フィラメント、伸度35%、沸水収縮率14%の延伸糸を用意した。
[Example 1]
Obtained by drawing and heat-treating a conjugate yarn in which polyethylene terephthalate having an intrinsic viscosity of 0.64 obtained by copolymerization of isophthalic acid at least 10 mol% and polyethylene terephthalate having an intrinsic viscosity of 0.42 are bonded side by side at a weight ratio of 50/50. , 50 denier / 12 filament, 35% elongation, 14% boiling water shrinkage was prepared.
得られた延伸糸を芯糸として、鞘糸にポリメタフェニレンイソフタルアミド(商標名:コーネックス、帝人テクノプロダクツ(株)製)からなる短繊維とポリパラフェニレンテレフタルアミド(商標名:テイジントワロン、帝人アラミド株製)からなる短繊維を90:10の割合で略均一に混合した耐熱性繊維を用いてなる紡績糸(綿番手40番)2本を用いて、ダブルカバリング法による下撚(Z)および上撚(S)して芯鞘複合糸を得た。 The obtained drawn yarn is used as a core yarn, and the sheath fiber is made of short fibers made of polymetaphenylene isophthalamide (trade name: Cornex, manufactured by Teijin Techno Products Co., Ltd.) and polyparaphenylene terephthalamide (trade name: Teijin Twaron, Twist yarn by double covering method (Z) using two spun yarns (cotton count No. 40) made of heat-resistant fibers in which short fibers made of Teijin Aramid Co., Ltd. are mixed almost uniformly at a ratio of 90:10 ) And upper twist (S) to obtain a core-sheath composite yarn.
得られた複合糸を、常法により製織して織物とし、精練−リラックス−セット(190℃で1分間処理)−染色−セットの仕上げ加工を施した。ここで、リラックス温度を普通より高めの120℃とし、強めの揉み効果を付与することによりコンジュゲート糸の捲縮がよく発現し、特にストレッチ性が発現した。経ストレッチ率20%、緯ストレッチ率23%と良好なストレッチ性を有し、またストレッチ回復率も経、緯ともに90%以上と良好であった。
また染色はキャリヤを供した染色液で下記の通り染色し、均一良染色製織物を得ることができた。
またこの得られた染色物製織物の耐熱性(LOI)は28であった。
The obtained composite yarn was woven by a conventional method to form a woven fabric, and subjected to a finishing process of scouring-relax-set (treated at 190 ° C. for 1 minute) -dye-set. Here, the relaxation temperature was set to 120 ° C., which is higher than usual, and a strong stagnation effect was imparted, whereby the crimp of the conjugate yarn was well expressed, and in particular, stretch properties were expressed. The stretch ratio was 20%, the weft stretch ratio was 23% and the stretchability was good, and the stretch recovery ratio was both 90% or more.
The dyeing was carried out with a dyeing solution provided with a carrier as follows to obtain a uniform and well-dyed fabric.
Further, the heat resistance (LOI) of the obtained dyed fabric was 28.
下記染浴で常温から2℃/分の速度で昇温し、135℃で60分間染色処理した。
・カチオン染料(Kayacryl Blue GSL−ED)6 %owf
・硝酸Na 25 g/l
・酢酸 0.5 cc/l
・ベンジルアルコール(キャリヤ) 70 g/l
浴比1:30
結果を表1に示す。
The temperature was increased from room temperature to 2 ° C./min in the following dye bath, and dyeing was performed at 135 ° C. for 60 minutes.
・ Cationic dye (Kayaacryl Blue GSL-ED) 6% owf
・ Nitric acid Na 25 g / l
・ Acetic acid 0.5 cc / l
・ Benzyl alcohol (carrier) 70 g / l
Bath ratio 1:30
The results are shown in Table 1.
[実施例2〜3、比較例1〜2]
コンジュゲートを構成するポリマー特性、あるいはカバーリング法を表1のように変更した以外は、実施例1と同様にした。また何れの染色製織物の難燃性(LOI)も28であった。
結果を表1に示す。
[Examples 2-3, Comparative Examples 1-2]
The same procedure as in Example 1 was conducted except that the polymer characteristics constituting the conjugate or the covering method were changed as shown in Table 1. Moreover, the flame retardancy (LOI) of any dyed fabric was 28.
The results are shown in Table 1.
消防士が消火作業時に着用する耐熱性防護服として難燃性、耐熱性を維持し作業性、着用性が大幅に改善されるので有用である。 It is useful as a heat-resistant protective clothing worn by firefighters during fire extinguishing work, because it maintains flame retardancy and heat resistance and greatly improves workability and wearability.
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102756502A (en) * | 2012-06-29 | 2012-10-31 | 昆山市周市镇吉盛服装厂 | High-elasticity fabric |
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KR101427225B1 (en) * | 2012-12-27 | 2014-09-19 | 주식회사 휴비스 | Conjugate Polyester Filaments with Excellent Cool Touch Effect and Stretchability and Process of Preparing Same |
WO2014199969A1 (en) * | 2013-06-11 | 2014-12-18 | 帝人株式会社 | Fabric and textile product |
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JP2016060968A (en) * | 2014-09-12 | 2016-04-25 | 東レ・デュポン株式会社 | Composite spun yarn comprising long and short fibers and woven or knitted fabric and protective material including the same |
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WO2018113766A1 (en) * | 2016-12-23 | 2018-06-28 | 东丽纤维研究所(中国)有限公司 | Filling body and use thereof |
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EP2666894B1 (en) * | 2012-05-21 | 2021-08-18 | IBENA Textilwerke GmbH | Fabric for the manufacture of personal protective equipment |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59216940A (en) * | 1983-05-25 | 1984-12-07 | 帝人株式会社 | Spun-like crimped processed yarn |
JP2003119631A (en) * | 2001-10-10 | 2003-04-23 | Du Pont Toray Co Ltd | Covered yarn and method for producing the same |
JP2004084103A (en) * | 2002-08-26 | 2004-03-18 | Teijin Ltd | Composite yarn |
-
2008
- 2008-02-21 JP JP2008040122A patent/JP2009197361A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59216940A (en) * | 1983-05-25 | 1984-12-07 | 帝人株式会社 | Spun-like crimped processed yarn |
JP2003119631A (en) * | 2001-10-10 | 2003-04-23 | Du Pont Toray Co Ltd | Covered yarn and method for producing the same |
JP2004084103A (en) * | 2002-08-26 | 2004-03-18 | Teijin Ltd | Composite yarn |
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TWI631249B (en) * | 2013-06-11 | 2018-08-01 | 帝人股份有限公司 | Cloth and fiber products |
JP2014240532A (en) * | 2013-06-11 | 2014-12-25 | 帝人株式会社 | Stretchable flame-retardant fabric and textile product |
US9580843B2 (en) | 2013-06-11 | 2017-02-28 | Teijin Limited | Cloth and textile product |
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