JPS62177208A - Production of composite fiber - Google Patents
Production of composite fiberInfo
- Publication number
- JPS62177208A JPS62177208A JP31258486A JP31258486A JPS62177208A JP S62177208 A JPS62177208 A JP S62177208A JP 31258486 A JP31258486 A JP 31258486A JP 31258486 A JP31258486 A JP 31258486A JP S62177208 A JPS62177208 A JP S62177208A
- Authority
- JP
- Japan
- Prior art keywords
- modifier
- polymer
- composite fiber
- streams
- stream
- 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.)
- Granted
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 24
- 239000002131 composite material Substances 0.000 title claims abstract description 19
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 229920000642 polymer Polymers 0.000 claims abstract description 44
- 239000003607 modifier Substances 0.000 claims abstract description 31
- 238000004898 kneading Methods 0.000 claims abstract description 13
- 229920000728 polyester Polymers 0.000 claims description 8
- 230000003068 static effect Effects 0.000 claims description 7
- 239000002216 antistatic agent Substances 0.000 claims description 4
- 239000004952 Polyamide Substances 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 239000012757 flame retardant agent Substances 0.000 claims 1
- 238000009987 spinning Methods 0.000 abstract description 18
- -1 polyethylene terephthalate Polymers 0.000 description 14
- 238000000034 method Methods 0.000 description 11
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 230000005611 electricity Effects 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 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
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 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
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229940011182 cobalt acetate Drugs 0.000 description 1
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000000051 modifying effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Multicomponent Fibers (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
Abstract
Description
【発明の詳細な説明】 本発明は複合繊維の製造法に関するものである。[Detailed description of the invention] The present invention relates to a method for manufacturing composite fibers.
従来、複合繊維の製造法に関しては、粘度の異なる同種
重合体、イオン化性基の含有量を異にする同種重合体、
単一重合体と共重合体、或いは異種の重合体等を並列型
又は芯鞘型に接合紡糸することが知られており、この為
接合すべき重合体を夫々別々に準備する必要があり、製
造する複合繊維の目的に応じてその銘柄を変更せねばな
らないので、装置も複雑となり、作業性も低下する。又
、1種の溶融重合体流を2個に分割し、その一方に加熱
器を設けて加熱劣化させることにより両者の夫々の重合
体の熱履歴を変えることにより両者の収縮性に差を与え
て潜在収縮性を有する繊維を製造することも提案されて
いる。しかしながら斯かる方法では、単に熱履歴のみを
変えるため、例えば熱収縮の差にしても当然ある限界を
越えるものではなく、しかも制電性、防燃性、吸湿性等
を付与し得るものではない。Conventionally, methods for producing composite fibers have been made using homogeneous polymers with different viscosities, homogeneous polymers with different contents of ionizable groups,
It is known to jointly spin a single polymer and a copolymer, or different types of polymers, etc. in a parallel type or core-sheath type, and for this reason, it is necessary to prepare each polymer to be joined separately, and the manufacturing process is slow. Since it is necessary to change the brand of composite fiber depending on the purpose of the composite fiber, the equipment becomes complicated and work efficiency decreases. In addition, by dividing one kind of molten polymer stream into two parts and installing a heater in one part to heat and deteriorate the flow, the thermal history of each of the two polymers can be changed, thereby creating a difference in the shrinkability of the two polymers. It has also been proposed to produce fibers with latent shrinkage. However, in such a method, only the thermal history is changed, so the difference in thermal contraction, for example, naturally does not exceed a certain limit, and furthermore, it is not possible to impart antistatic properties, flame retardance, moisture absorption properties, etc. .
本発明者等は一つのポリマー流より種々の特性を有する
複合繊維を製造すべく鋭意研究の結果本発明を完成した
ものである。The present inventors completed the present invention as a result of intensive research aimed at producing composite fibers having various properties from a single polymer stream.
本発明の目的は種々の特性を有する複合繊維を提供する
にある。他の目的は単一の装置を用いて種々の特性を有
する複合繊維を工業的容易且つ安価に製造する方法を提
供するにある。An object of the present invention is to provide composite fibers having various properties. Another object of the present invention is to provide a method for industrially easily and inexpensively producing composite fibers having various properties using a single device.
本発明方法は単一の溶融ポリマー流を二つ以上に分割し
、少なくともその一つに改質剤を注入し、次いで急速混
練及び定量計量した後、これらを接合することを特徴と
する。The method of the present invention is characterized in that a single molten polymer stream is divided into two or more parts, a modifier is injected into at least one of the parts, and after rapid kneading and quantitative metering, these parts are joined.
本発明に通用する溶融ポリマーはナイロン6゜ナイロン
66、ナイロン610.ナイロン1) 又はそれらの
共重合体であるポリアミド類、芳香族ジカルボン酸とグ
リコール類とを縮重合して得られるポリエチレンテレフ
タレートで代表されるポリエステル類、ポリエチレン及
びポリプロピレン等のポリオレフィン類、ポリウレタン
等が挙げられるが改質の必要性、その容易さ等の点で特
にポリエステル類が好ましい。Molten polymers applicable to the present invention include nylon 6°, nylon 66, nylon 610. Examples include polyamides which are nylon 1) or their copolymers, polyesters represented by polyethylene terephthalate obtained by condensation polymerization of aromatic dicarboxylic acids and glycols, polyolefins such as polyethylene and polypropylene, and polyurethanes. However, polyesters are particularly preferred in view of the necessity of modification and the ease of modification.
又本発明に通用される改質剤としては公知の改質剤、例
えば易染性向上剤、難燃性付与剤、吸湿性向上剤、制電
剤、易滑剤、原着剤、つや消削等が挙げられる。具体的
には、例えばポリエチレンオキサイド、ポリプロピレン
オキサイド、ポリエチレンオキサイド−ポリプロピレン
オキサイド共重合物、ポリエチレンオキサイド−ポリエ
ステルブロック共重合物、ポリエチレンオキサイド−ポ
リエステル混合物、カチオン可染性ポリエステル共重合
物、ポリヒドロキシエチルイソシンコメロン酸又はその
ポリエチレングリコールテレフタレート、ポリカプロラ
クトン、ポリブチレンゲリコールテレフタレート、ポリ
アミド、ポリスチロール、フェノール樹脂初期縮合物、
ポリエステル。Modifiers that can be used in the present invention include known modifiers, such as dyeability improvers, flame retardant imparters, hygroscopicity improvers, antistatic agents, lubricants, base dyes, matting agents, etc. etc. Specifically, for example, polyethylene oxide, polypropylene oxide, polyethylene oxide-polypropylene oxide copolymer, polyethylene oxide-polyester block copolymer, polyethylene oxide-polyester mixture, cationic dyeable polyester copolymer, polyhydroxyethyl isocinco Melonic acid or its polyethylene glycol terephthalate, polycaprolactone, polybutylene gelicol terephthalate, polyamide, polystyrene, phenolic resin initial condensate,
polyester.
ポリウレタン、ポリアクリロニトリル、ポリオレフィン
、ポリ塩化ビニール、ポリ塩化ビニリデン。Polyurethane, polyacrylonitrile, polyolefin, polyvinyl chloride, polyvinylidene chloride.
酸化チタン、弗化リチウム、弗化カルシウム、ステアリ
ン酸マグネシウム、酢酸コバルト、カーボンブラック、
顔料、染料、ポリジメチルシロキサン、ポリメチルフェ
ニルシロキサン、炭酸ガス。Titanium oxide, lithium fluoride, calcium fluoride, magnesium stearate, cobalt acetate, carbon black,
Pigments, dyes, polydimethylsiloxane, polymethylphenylsiloxane, carbon dioxide gas.
窒素ガス、フレオンガスなどがある。Examples include nitrogen gas and freon gas.
改質剤のポリマーに対する添加量は改質剤及びポリマー
の種類又は改質の目的等により異なるが通常0.5〜1
0重量%、好ましくは2〜8重量%程度である。The amount of modifier added to the polymer varies depending on the type of modifier and polymer, the purpose of modification, etc., but is usually 0.5 to 1.
It is about 0% by weight, preferably about 2 to 8% by weight.
本発明方法は溶融ポリマー流を二つ以上に分割し、少な
くともその一つに改質剤を注入した後急速混練するが、
急速混練は静止混練素子を有する混練器、例えばケニッ
クス社製の「スタティック・ミキサー」、特殊機化工社
の[ロスーISG−ミキサー」等が挙げられる。混線効
果を上げるため、通常改質剤を注入後急速混練器を通し
、更に計量ポンプ通過後急速混練器を通過せしめること
が好ましい。この場合、静止混練素子の数は少なくとも
12ケ、好ましくは20〜40ケ程度設置する。In the method of the present invention, a molten polymer stream is divided into two or more parts, a modifier is injected into at least one of the parts, and then rapidly kneaded.
For rapid kneading, kneaders having static kneading elements, such as "Static Mixer" manufactured by Kenix Co., Ltd. and "Rossu ISG-Mixer" manufactured by Tokushu Kikako Co., Ltd., can be used. In order to increase the cross-mixing effect, it is usually preferable to pass the modifier through a rapid kneader after injection, and further to pass through a rapid kneader after passing through a metering pump. In this case, the number of static kneading elements is at least 12, preferably about 20 to 40.
本発明は通常の紡糸装置にも利用できるが、特に直連重
・直紡の紡糸装置に適用すれば一つの装置より変化に富
む特質を有する複合繊維が得られる為有利である。Although the present invention can be applied to ordinary spinning equipment, it is especially advantageous to apply it to a straight-connection/straight-spinning type of spinning equipment, since composite fibers having a wide variety of characteristics can be obtained from a single equipment.
以下、本発明方法の一例を図面により説明する。An example of the method of the present invention will be explained below with reference to the drawings.
第1図は本発明方法の概略説明図であり、ポリマー流1
はポリマー流2及び3に分割された後、混練ブロックA
に於いてポリマー流2には改質剤4がポンプ5で計量さ
れ弁6を通して注入される。FIG. 1 is a schematic illustration of the method of the present invention, in which polymer stream 1
is divided into polymer streams 2 and 3, then kneading block A
A modifier 4 is metered into the polymer stream 2 by a pump 5 and injected through a valve 6.
会合したポリマーと改質剤は急速混練器7で混合された
後紡糸用ポンプ8で計量され、更に急速混練器9で均一
に混合され紡糸パック10に送られる。一方、混練ブロ
ックBでは改質剤4′を注入しないよう弁6′を閉止し
、ポリマー流3は改質することなく紡糸パックlOに至
り、そこで改質ポリマーと接合され、複合繊維1)とし
て紡出される。The associated polymer and modifier are mixed in a rapid kneader 7, metered by a spinning pump 8, further uniformly mixed in a rapid kneader 9, and sent to a spinning pack 10. On the other hand, in the kneading block B, the valve 6' is closed so that the modifier 4' is not injected, and the polymer stream 3 reaches the spinning pack 10 without being modified, where it is joined with the modified polymer to form the composite fiber 1). Spun.
尚、改質剤4と異なる改質剤4′を一方のポリマーに注
入したい場合には弁6″を開けば、2種類の改質剤を含
む複合繊維を製造することができる。Incidentally, when it is desired to inject a modifier 4' different from the modifier 4 into one of the polymers, by opening the valve 6'', a composite fiber containing two types of modifiers can be produced.
斯くして、本発明方法によれば任意の繊維形成性重合体
に易染性、難燃性、制電性、吸湿性などの改質特性のう
ち少くとも1つを賦与することが可能である。しかも、
紡出直前にて改質剤を溶融重合体に急速混練せしめるの
で、改質剤の熱劣化及び/又は改質剤と溶融重合体との
相互作用による繊維物性の低下がきわめて少ないという
利点がある。したがって、本発明は広範囲にわたる有機
又は無機化合物の改質剤も繊維形成性重合体の物性を損
うことなくこれに混合して紡出することが可能であり、
産業上極めて有用である。Thus, according to the method of the present invention, it is possible to impart at least one of the modifying properties such as easy dyeability, flame retardancy, antistatic property, and hygroscopicity to any fiber-forming polymer. be. Moreover,
Since the modifier is rapidly kneaded into the molten polymer immediately before spinning, there is an advantage that there is very little deterioration in fiber properties due to thermal deterioration of the modifier and/or interaction between the modifier and the molten polymer. . Therefore, in the present invention, a wide range of organic or inorganic compound modifiers can be mixed with the fiber-forming polymer and spun without impairing the physical properties of the fiber-forming polymer.
It is extremely useful in industry.
特に、近年差別化商品が要求されている時代に、同一装
置から簡単にしかも迅速に多品種の製品を製造可能であ
ることは設備、人員等コストから考えても極めて利用価
値の高い製造方法である。In particular, in an era where differentiated products are required in recent years, the ability to easily and quickly manufacture a wide variety of products from the same equipment is a manufacturing method with extremely high utility value, considering costs such as equipment and personnel. be.
以°下、実施例により本発明を具体的に説明する。Hereinafter, the present invention will be specifically explained with reference to Examples.
実施例1
ポリエチレンテレフタレートよりなるポリマー流1をポ
リマー流2及び3に分割し、各混線ブロックA及びBの
改質剤4,4′として染色性向上剤及び制電剤を夫々弁
6,6′よりポリマー流2.3に注入する。染色性向上
剤として数平均分子量2.000のポリエチレングリコ
ール又制電剤としてはエチレンテレフタレートオリゴマ
ーとポリエチレングリコール(数平均分子量2.000
)とよりなる数平均分子量15,000の低重合体を用
い、ポリエチレンテレフタレートに対し夫々5重量%添
加した。Example 1 A polymer stream 1 made of polyethylene terephthalate is divided into polymer streams 2 and 3, and a dyeability improver and an antistatic agent are applied as modifiers 4 and 4' of each crosstalk block A and B through valves 6 and 6', respectively. Inject into polymer stream 2.3. Polyethylene glycol with a number average molecular weight of 2.000 is used as a dyeability improver, and ethylene terephthalate oligomer and polyethylene glycol (with a number average molecular weight of 2.000) are used as antistatic agents.
) with a number average molecular weight of 15,000 were used, and 5% by weight of each was added to polyethylene terephthalate.
急速混練器7.7″、9.9″はそれぞれ素子数が20
.12ケであり均質混練されたポリマー流の温度はそれ
ぞれ285℃にコントロールした。これら混練ブロック
A、 Bからポリマーを1対1の割合で紡糸用バック1
0に導き、紡糸温度290℃、紡糸速度800+++/
分、ホール数500の円型ノズルを用い、吐出量大々2
65g /分で並列型に接合紡糸した。紡出時での虫、
糸切れは全くなく、未だ伸糸の繊度変動率は3.4%で
あった。この未延伸糸を70℃の温水中で38倍に延伸
し130℃で熱処理したものは繊度3.13d、強度4
.06g/d。Rapid kneader 7.7″ and 9.9″ each have 20 elements.
.. The temperature of each of the 12 homogeneously kneaded polymer streams was controlled at 285°C. Polymers from these kneading blocks A and B are added to the spinning bag 1 in a 1:1 ratio.
0, spinning temperature 290℃, spinning speed 800+++/
Using a circular nozzle with 500 holes, the discharge amount is approximately 2.
Joint spinning was carried out in parallel at 65 g/min. Insects during spinning,
There was no yarn breakage at all, and the fineness fluctuation rate of the yarn drawing was still 3.4%. This undrawn yarn was stretched 38 times in hot water at 70°C and heat treated at 130°C, with a fineness of 3.13d and a strength of 4.
.. 06g/d.
伸度47.2%であった。得られた複合繊維の染色吸尽
率、静電気発生量は夫々80.3%、+1.4KV(3
0℃/25%)であった。また、染色斑も全く見い出せ
なかった。The elongation was 47.2%. The dye exhaustion rate and static electricity generation amount of the obtained composite fiber were 80.3% and +1.4KV (3
0°C/25%). Further, no staining spots were found at all.
比較の為に改質剤を注入しない以外は前記と全く同様に
して得られた繊維について上記各物性値を求めたが、そ
れぞれ36.5%、 + 10.7KVテあった。For comparison, the above physical property values were determined for fibers obtained in exactly the same manner as above except that no modifier was injected, and they were 36.5% and +10.7 KV, respectively.
尚、染色吸尽率は次の条件で行なった。Incidentally, the dyeing exhaustion rate was measured under the following conditions.
染料: Miketon Po1yester Blu
e P、BL、 3% out浴比: 1:30(
キャリアーなし)温度; 97〜98℃(常圧沸騰)
時間: 60分
また、静電気発生量とは、雰囲気30℃、25%RHの
雰囲気においてアクリル板で一定条件の摩擦を与えた時
発生する電圧を集電式静電気で測定した値である。Dye: Miketon Polyester Blue
e P, BL, 3% out bath ratio: 1:30 (
(No carrier) Temperature: 97-98℃ (normal pressure boiling) Time: 60 minutes Also, the amount of static electricity generated is the voltage generated when constant friction is applied to an acrylic plate in an atmosphere of 30℃ and 25% RH. This is the value measured using current collecting static electricity.
実施例2
実施例1と同様の方法により、中空複合繊維を製造した
。混練ブロックAの改質剤として数平均分子量6,00
0のポリエチレングリコールをポリエチレンテレフタレ
ートに対して5重量%添加した。Example 2 Hollow composite fibers were produced in the same manner as in Example 1. Number average molecular weight 6,00 as a modifier for kneading block A
0 polyethylene glycol was added in an amount of 5% by weight based on polyethylene terephthalate.
混線ブロックBには、パルプ6を閉止し改質剤を添加し
なかった。これらポリマーを紡糸温度290℃、紡糸速
度780IIl/分、ホール数400の()型ノズルを
用い、吐出量大々390 g/分で並列型に接合紡糸し
た。In the crosstalk block B, the pulp 6 was closed and no modifier was added. These polymers were jointly spun in parallel at a spinning temperature of 290° C., a spinning speed of 780 IIl/min, and a ( ) type nozzle with 400 holes at a discharge rate of approximately 390 g/min.
紡糸時での虫、糸切れは全くなく、未延伸糸の繊維変動
率は2.5%であった。この未延伸糸を70℃の温水中
で3.7倍に延伸しその後170℃で熱処理したものは
繊度6.03.強度4.5?、伸度49.4%であった
。得られたものを76dmにカットしてカーディングし
たものは公知方法で製造された中空複合繊維のフトン綿
と嵩高性能に於て大差のないものであった。しかしなが
ら、白変においては本発明による方法が優れていた。There were no insects or yarn breakage during spinning, and the fiber fluctuation rate of the undrawn yarn was 2.5%. This undrawn yarn was stretched 3.7 times in hot water at 70°C and then heat-treated at 170°C, resulting in a fineness of 6.03. Strength 4.5? , the elongation was 49.4%. The obtained product was cut into 76 dm pieces and carded, and the bulk and performance were not significantly different from futon cotton, which is a hollow composite fiber produced by a known method. However, the method according to the present invention was superior in terms of white discoloration.
第1図は本発明の概略説明図である。 FIG. 1 is a schematic explanatory diagram of the present invention.
Claims (6)
くともその一つに改質剤を注入し、次いで急速混練及び
定量計量した後、これらを接合することを特徴とする複
合繊維の製造法。(1) A composite fiber characterized in that a single molten polymer flow is divided into two or more parts, a modifier is injected into at least one of them, and then these are joined after rapid kneading and quantitative metering. Manufacturing method.
ある特許請求の範囲第1項記載の製造法。(2) The manufacturing method according to claim 1, wherein the molten polymer is polyamide or polyester.
剤を注入する特許請求の範囲第1項記載の製造法。(3) The production method according to claim 1, wherein the molten polymer stream is divided into two parts and a modifier is injected into one of the parts.
上剤又は制電剤である特許請求の範囲第1項記載の製造
法。(4) The manufacturing method according to claim 1, wherein the modifier is a dyeability improver, a flame retardant agent, a hygroscopicity improver, or an antistatic agent.
る特許請求の範囲第1項記載の製造法。(5) The manufacturing method according to claim 1, wherein the rapid kneading uses a kneader having a static kneading element.
す特許請求の範囲第1項又は第3項記載の製造法。(6) The manufacturing method according to claim 1 or 3, wherein the bonding is of a parallel type or a core-sheath type in the cross section of the fibers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31258486A JPS62177208A (en) | 1986-12-27 | 1986-12-27 | Production of composite fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31258486A JPS62177208A (en) | 1986-12-27 | 1986-12-27 | Production of composite fiber |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8730779A Division JPS5615405A (en) | 1979-07-09 | 1979-07-09 | Production of conjugate fiber |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62177208A true JPS62177208A (en) | 1987-08-04 |
JPH024685B2 JPH024685B2 (en) | 1990-01-30 |
Family
ID=18030963
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP31258486A Granted JPS62177208A (en) | 1986-12-27 | 1986-12-27 | Production of composite fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62177208A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998009008A1 (en) * | 1996-08-30 | 1998-03-05 | Kimberly-Clark Worldwide, Inc. | Single extruder multiportion fiber |
-
1986
- 1986-12-27 JP JP31258486A patent/JPS62177208A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998009008A1 (en) * | 1996-08-30 | 1998-03-05 | Kimberly-Clark Worldwide, Inc. | Single extruder multiportion fiber |
US5762734A (en) * | 1996-08-30 | 1998-06-09 | Kimberly-Clark Worldwide, Inc. | Process of making fibers |
Also Published As
Publication number | Publication date |
---|---|
JPH024685B2 (en) | 1990-01-30 |
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