JPS59144616A - Antistatic conjugate fiber - Google Patents

Antistatic conjugate fiber

Info

Publication number
JPS59144616A
JPS59144616A JP1933083A JP1933083A JPS59144616A JP S59144616 A JPS59144616 A JP S59144616A JP 1933083 A JP1933083 A JP 1933083A JP 1933083 A JP1933083 A JP 1933083A JP S59144616 A JPS59144616 A JP S59144616A
Authority
JP
Japan
Prior art keywords
component
acid
antistatic
polyester
polyamide
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
Application number
JP1933083A
Other languages
Japanese (ja)
Inventor
Osami Shinonome
東雲 修身
Katsuyuki Toma
当麻 克行
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unitika Ltd
Original Assignee
Unitika Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Unitika Ltd filed Critical Unitika Ltd
Priority to JP1933083A priority Critical patent/JPS59144616A/en
Publication of JPS59144616A publication Critical patent/JPS59144616A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:An antistatic conjugate yarn that is obtained by coating a polyester, polyamide or polyesteramide copolymer containing a specific component with a thermoplastic polymer, thus showing good antistatic properties and high light resistance. CONSTITUTION:A polyester, polyamide or polyesteramide copolymer that is obtained by copolymerizing an alkali metal-sulfoisophthalic acid component such as 5-sodiosulfoisophthalic acid and a polyalkylene oxide component with dicarboxylic acid components such as adipic acid, diol components such as ehtylene glycol, diamine components such as ethylenediamine is used as the core or island component and another thermoplastic polymer such as polyethylene terephthalate is used as the sheath or sea component to give the objective antistatic conjugate yarn.

Description

【発明の詳細な説明】 本発明は制電性を有する複合繊維に関するものである。[Detailed description of the invention] The present invention relates to composite fibers having antistatic properties.

ポリアミt”、ポリエステルなとの合成繊維製品の静′
セ気障1!イを抑制するにはポリアルキレンオキシI・
系化合物の導入が有効なことは周知の通りである。傷に
ポリアルキレンオキシド成分とポリエステルあるいはポ
リアミド成分とからなるブロックポリマーを練り込む方
法は耐久性のある制電糸を((Iるのに最適であるとさ
れている。しかし、ごの方法では制電剤であるポリアル
キレンオキシド成分が繊維分子中に拘束されやすく、モ
ヒリティか低下し、冬期におりるような低湿度下では十
分な効果を発現し難いばかりでなく、繊維の耐光性を低
下さゼろという欠点がある。また、耐光性の問題を解消
すへくポリアルキレンオキシド成分を芯又は島成分とし
2通常のポリエステルやポリアミドをさや又は海成分と
する方法も提案されているか、この場合には繊維表面部
に制電剤か存在しないためか、肝要の制電効果が小さい
という問題がある。
Synthetic fiber products such as polyamide and polyester
Sensei disorder 1! To suppress polyalkyleneoxy I,
It is well known that the introduction of system compounds is effective. The method of kneading a block polymer consisting of a polyalkylene oxide component and a polyester or polyamide component into the wound is said to be optimal for applying durable antistatic thread. The polyalkylene oxide component, which is an electric agent, is easily bound in the fiber molecules, resulting in a decrease in mobility, which not only makes it difficult to achieve sufficient effects in low humidity conditions such as those experienced in winter, but also reduces the light resistance of the fiber. In addition, in order to solve the problem of light resistance, a method has been proposed in which a polyalkylene oxide component is used as a core or island component and ordinary polyester or polyamide is used as a sheath or sea component. There is a problem in that the important antistatic effect is small, probably because there is no antistatic agent on the fiber surface.

本発明者らは制電効果と耐光性にずくれた合成繊維を提
供すべく種々検討した結果、ポリアルキレンオキシド成
分とともに、アルカリメタルスルホイソフタル酸(SI
Pという)成分をポリエステル、ポリアミドもしくはポ
リエステルアミドに共重合したブロックコポリマーを芯
又は島成分とし1通審の静電気を帯びやすい重合体をさ
や又は海成分とする複合繊維が上記目的に適っているこ
とを知り9本発明に至った。
The present inventors conducted various studies to provide a synthetic fiber with excellent antistatic effect and light resistance. As a result, we found that, together with the polyalkylene oxide component, alkali metal sulfoisophthalic acid (SI)
A composite fiber whose core or island component is a block copolymer copolymerized with polyester, polyamide, or polyester amide (referred to as P) and whose sheath or sea component is a polymer that is easily charged with static electricity according to the first judgment is suitable for the above purpose. This led to the present invention.

ずなわら1本発明は、SIP成分とポリアルキレンオキ
シド成分とを共重合成分とするポリエステル、ポリアミ
ドもしくはポリエステルアミドからなる[A]成分と(
A)成分を被覆する熱可塑性重合体からなる(B)成分
とで構成された制電性複合繊維を要旨とするものである
Zunawara 1 The present invention consists of a component [A] consisting of polyester, polyamide or polyester amide containing a SIP component and a polyalkylene oxide component as copolymerized components;
The gist of the invention is an antistatic composite fiber composed of component (A) and component (B) made of a thermoplastic polymer covering component (A).

本発明において[A)成分のヘースとなるポリエステル
、ポリアミドもしくはポリエステルアミドは、アジピン
酸、セバシン酸、テレフタル酸。
In the present invention, the polyester, polyamide, or polyester amide serving as the haze of component [A] is adipic acid, sebacic acid, or terephthalic acid.

イソソタル酸、ナフタル酸などのジカルボン酸成分、エ
チレンクリコール、プロピレングリコール。
Dicarboxylic acid components such as isosomal acid and naphthalic acid, ethylene glycol, and propylene glycol.

1、  II−フ゛タンジオール、シj二チレングリコ
ール。
1. II-butanediol, diethylene glycol.

1.4−ソクロヘキザンジメタノール、キシリレングリ
ニノールなどのジオール成分、エチレンジアミン7 テ
トラメチレンジアミン、ヘキサメチレンツアミン、キソ
リレンンアミンなどのシアミン成分、ε−アミノカブ(
コン酸1 ω−アミノトチカン酸などのアミノ酸成分、
ε−カプロラクタム、ラウリルツクタムなどのラククム
成分を適宜組み合ね一層て重縮合して得られろポリマー
である。〔Δ〕酸成分ポリマーはこれらのポリマーの合
成時にS I l)成分とエステルもしくはアミド形成
性官能基を有するポリアルキレンオキシド化合物とを添
加することにより得られる。
1. Diol components such as 4-isochlorohexanedimethanol and xylylene glinol, ethylene diamine 7, cyamine components such as tetramethylene diamine, hexamethylene diamine, and xylylene amine, ε-aminocarb (
Amino acid components such as conic acid 1 ω-aminototicanic acid,
It is a polymer obtained by suitably combining lacum components such as ε-caprolactam and lauryl lactam and polycondensing them. [Δ] Acid component polymers can be obtained by adding the S I l) component and a polyalkylene oxide compound having an ester- or amide-forming functional group during the synthesis of these polymers.

SIP成分としては5−ナトリウムスルホイソフタル酸
、5−カリウムスルホイソフタル酸及びこれらのエステ
ルか好ましい。
Preferred SIP components include 5-sodium sulfoisophthalic acid, 5-potassium sulfoisophthalic acid, and esters thereof.

また、ポリアルキレンオキシド化合物としてはヒドロキ
シル基、カルホキシル基、アルコキシカルボニル基、ア
ミノ基等を1個以」二、好ましくは2(固有するポリエ
チレンオキシド、ポリプロピレンオキシト、コニチレン
オキシドーブ1コピレンオキシドコボリマ−などのポリ
アルキレンオキシドセグメントを有する化合物が用いら
れ2分子中にヒスフェノール残基を有するポリアルキレ
ンオキシド化合物は耐熱性が良好で好ましい。ポリアル
キレンオキシド化合物の分子量は400〜20,000
.好ましくは800〜10.000が適当である。
The polyalkylene oxide compound may contain one or more hydroxyl groups, carboxyl groups, alkoxycarbonyl groups, amino groups, etc. A polyalkylene oxide compound having a hisphenol residue in two molecules is preferable because it has good heat resistance.The molecular weight of the polyalkylene oxide compound is 400 to 20,000.
.. Preferably, 800 to 10,000 is appropriate.

[A)成分のポリマーにおいて、srp成分の導入量は
スルポン酸基の量が30〜500当量/トン、好ましく
は50〜300当M/トンとなる量が適当であり、ポリ
アルキレンオキシド成分の量は10〜70重量%、好ま
しくは20〜60重量%かj&当である。
In the polymer of component [A), the amount of the srp component introduced is such that the amount of sulfonic acid groups is 30 to 500 equivalents/ton, preferably 50 to 300 equivalents/ton, and the amount of the polyalkylene oxide component is is 10 to 70% by weight, preferably 20 to 60% by weight.

次に本発明における(B)成分の熱可塑性重合(木とし
ては+45リコニチレンテレフクレ−1・、ボリソ′チ
レンテレフタレ−1・、ポリーp−コニチレンオキシヘ
ンヅエ−1−など及びこれらを主成分とするポリエステ
ル、ナイロン6、ツーイロン12.ナイ【:Jン46.
ナイlコンロG、ナイl:Iン610なと及び、これら
を主成分とするポリアミド、ポリエステル。
Next, thermoplastic polymerization of component (B) in the present invention (for wood, +45 tylene terephthalene 1. Ingredients include polyester, nylon 6, two-iron 12.
Nyl Stove G, Nyl:In 610, and polyamides and polyesters containing these as main components.

ボリゾIlピレンなと及びこれらを主成分とするポリオ
レフィンか好適である。
Preferred are borisoIlpyrene and polyolefins containing these as main components.

本発明の繊維は(A)成分がCB)成分によって被覆さ
れた形状を自する複合繊維であり、芯さや型又&J海、
’A型の形状を有する。かかる形状の繊維は公知の方法
で得られる。そして制電性能、耐光性、製糸性、糸質物
性などを考応:すると〔△〕成分とCB)成分との割合
は断面積比て5:95〜50・50の範囲がよい。また
、 〔A〕酸成分CB)成分のうらいJ゛れか又は両方
に難燃剤、耐熱剤、つや消し剤1着色剤などを含んでい
てもよいことはもちろんである。CB)成分中に耐光性
に影響を与える成分を含有させることば望ましくないが
、少量であればポリアルキレンオキシド成分をCB)成
分に含有させて制電性を一層向上させるようにしてもよ
い。
The fiber of the present invention is a composite fiber having a shape in which the component (A) is covered with the component CB), and has a core, sheath, Katamata & Jkai,
'Has an A-shaped shape. Fibers having such a shape can be obtained by known methods. Taking into account antistatic performance, light resistance, yarn reeling properties, fiber properties, etc., the ratio of the [Δ] component to the CB) component is preferably in the range of 5:95 to 50.50 based on the cross-sectional area ratio. It goes without saying that either or both of the [A] acid component CB) component may contain a flame retardant, a heat resistant agent, a matting agent, a coloring agent, and the like. Although it is not desirable to include components that affect light resistance in component CB), a polyalkylene oxide component may be included in component CB) in a small amount to further improve antistatic properties.

以下実施例によって本発明をさらに具体的に説明する。The present invention will be explained in more detail below with reference to Examples.

実施例中の制電性の測定は2京大化研式lコータリース
タチソクテスターを用い5綿布を摩擦体として、20℃
、40%RHの雰囲気中で摩ljS帯電圧と半減期を求
める方法で行ったものである。(部は重量部を示す。) 実施例1 ヒス(β−ヒドロキシエチル)テレフタレート7os、
5−すl−リウムスルポイソフタル酸のビス(β−ヒド
ロキシエチル)エステル8部及びヒスフェノール八にエ
チレンオキシドをイ」加させて得た平均分子量2.00
0の化合物22部の混合物に三酸化アンチモン0.02
部を加え、 0.2 )ル。
The antistatic properties in the examples were measured using a 2-Kyoto University Kaken type l coater static tester using a cotton cloth as the friction body at 20°C.
, in an atmosphere of 40% RH using a method to determine the charging voltage and half-life of ljS. (Parts indicate parts by weight.) Example 1 His(β-hydroxyethyl) terephthalate 7os,
Average molecular weight: 2.00 obtained by adding ethylene oxide to 8 parts of bis(β-hydroxyethyl) ester of 5-sl-lium sulpoisophthalic acid and hisphenol 8
0.02 parts of antimony trioxide in a mixture of 22 parts of the compound of
0.2) l.

260’c、3時間の条件て重縮合して共重合ポリエス
ラール〔Δ1〕を得た。
Polycondensation was carried out at 260'c for 3 hours to obtain copolymerized polyesteral [Δ1].

(A+’l と通常のポリエチレンテレツクレート(0
,5小量%の酸化チタン粒子を含む)CB+)とを、(
A+)が芯を形成し、断面積比か10:90の芯さや型
複合糸となるように、エクス1−ルーグー型熔融紡糸機
を用い、 280 cで、紡糸孔数36孔の紡出孔より
吐出させ、  l 、 200n+/分の速度で巻き取
った。次いで延伸温度90°C2延伸倍率3.3倍で延
伸して、  75d/36f 、強度4.1g/d。
(A+'l and ordinary polyethylene telecrate (0
, CB+) containing 5 small % titanium oxide particles) and (
A+) forms the core and a core-sheath type composite yarn with a cross-sectional area ratio of 10:90 is obtained using an Ex1-Rougu type melt spinning machine, with a spinning hole of 36 holes at 280 c. The sample was discharged from the container and wound up at a speed of 1,200 n+/min. Next, it was stretched at a stretching temperature of 90° C. and a stretching ratio of 3.3 times to obtain a film of 75 d/36 f and a strength of 4.1 g/d.

伸度35%の延伸糸とした。糸切れなどの問題はほとん
と発生せず、製糸性は良好であった。
The drawn yarn had an elongation of 35%. There were almost no problems such as yarn breakage, and the yarn spinnability was good.

上記の延伸糸を50g/ mの密度で筒蝙後、精練し、
寿色分散染料を含む浴中で135°C130分間の条件
で染色した。iMられた染色布の摩擦帯電圧と半減期は
それぞれ1.000 V、及び10秒を示し。
The above drawn yarn was milled at a density of 50 g/m, and then refined.
Dyeing was carried out at 135°C for 130 minutes in a bath containing Suishoku disperse dye. The frictional charging voltage and half-life of the iM dyed fabric were 1.000 V and 10 seconds, respectively.

この性能はボームランドリーを30回くり返しても低下
しなかった。
This performance did not deteriorate even after Baum laundry was repeated 30 times.

実施例2 5−すl・リウムスルホイソフタル酸5部2両末端がア
ミノ基のポリエチレンオキシド (平均分子ffl 3
,000)  35部、ヘキサメチレンジアミン2部及
びカブロラククム52部とから通常の溶融重縮合法によ
り共重合ポリアミド〔A2〕を得た。
Example 2 5-sl-lium sulfoisophthalic acid 5 parts 2 polyethylene oxide with amino groups at both ends (average molecular ffl 3
, 000), 2 parts of hexamethylene diamine, and 52 parts of cabrolaccum to obtain copolyamide [A2] by a conventional melt polycondensation method.

〔A2〕と通常のナイロン6(0,3重量%の酸化チタ
ン粒子を含む)CB2)とから〔A2〕が芯を形成する
芯さや型複合糸を下記の条件で製糸した。
A core-sheath type composite yarn in which [A2] forms a core was spun from [A2] and ordinary nylon 6 (containing 0.3% by weight of titanium oxide particles) CB2) under the following conditions.

芯:さや断面積比      io’: 90紡糸温度
   265℃ 紡糸孔数   16孔 紡糸巻取速度      1,200 、m /分延伸
温度   30°C 延伸倍率   3.2倍 得られた延伸糸(70d/16f 、強度4.5 g/
 d 。
Core:pod cross-sectional area ratio io': 90 Spinning temperature 265°C Number of spinning holes 16 holes Spinning take-up speed 1,200, m/min Drawing temperature 30°C Stretching ratio 3.2 times Obtained drawn yarn (70d/16f , strength 4.5 g/
d.

伸度35%)を50g/n?の密度で筒編後、精練し、
青色酸性染料を含む浴中で98℃、40分間染色した。
50g/n? After knitting in a tube at a density of
Dyeing was carried out at 98° C. for 40 minutes in a bath containing blue acid dye.

染色布の摩擦帯電圧と半減期はそれぞれ800V及び6
秒を示した。
The frictional charging voltage and half-life of dyed cloth are 800V and 6, respectively.
Showed seconds.

比較例 実施例2て用いたポリエチレンオキシド化合物4or+
++、アジピン酸1.5部及びカブ+:r :フクタノ
、58.5部から得られたポリアミドを〔八2〕の代り
に用いて、実施例2と同様の操作を行ったか、染色布の
摩1が’H)電圧及び214減期はそれぞれ2,0OO
V 。
Comparative Example Polyethylene oxide compound 4or+ used in Example 2
++, 1.5 parts of adipic acid and turnip +:r: Using the polyamide obtained from Fukutano, 58.5 parts instead of [82], the same operation as in Example 2 was carried out, or The voltage and the 214 decay time are each 2,0OO
V.

70秒であった。It was 70 seconds.

特許出願人  ユニチカ株式会社Patent applicant: Unitika Co., Ltd.

Claims (1)

【特許請求の範囲】 +1+アル力リメタルスルボイソフタル酸成分とポリア
ルキレンオキシド成分とを共重合成分とするポリコニス
テル、ポリアミドもしくはポリエステルアミドからなる
〔Δ〕成分と(A)成分を被覆する熱可塑性重合体から
なる( T3 )成分とて構成された制電性複合繊維。
[Scope of Claims] A thermoplastic polymer that covers the [Δ] component and the (A) component, which is made of polyconister, polyamide, or polyester amide, which is a copolymerized component of a +1+ alkaline metal sulfoisophthalic acid component and a polyalkylene oxide component. An antistatic composite fiber composed of a (T3) component consisting of a combination.
JP1933083A 1983-02-07 1983-02-07 Antistatic conjugate fiber Pending JPS59144616A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1933083A JPS59144616A (en) 1983-02-07 1983-02-07 Antistatic conjugate fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1933083A JPS59144616A (en) 1983-02-07 1983-02-07 Antistatic conjugate fiber

Publications (1)

Publication Number Publication Date
JPS59144616A true JPS59144616A (en) 1984-08-18

Family

ID=11996394

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1933083A Pending JPS59144616A (en) 1983-02-07 1983-02-07 Antistatic conjugate fiber

Country Status (1)

Country Link
JP (1) JPS59144616A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01156573A (en) * 1987-12-10 1989-06-20 Kuraray Co Ltd Cloth excellent in feeling
JP2017057513A (en) * 2015-09-15 2017-03-23 東レ株式会社 Antistatic polyamide core-sheath composite fiber with excellent durability

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53111116A (en) * 1977-03-03 1978-09-28 Asahi Chem Ind Co Ltd Antistatic, sheath-core type conjugate fiber and its fiber mixing
JPS5747942A (en) * 1980-09-05 1982-03-19 Toray Industries Polyeter type anti-static composite blended fiber yarn
JPS57117619A (en) * 1981-01-13 1982-07-22 Unitika Ltd Preparation of modified synthetic fiber
JPS57176216A (en) * 1981-04-22 1982-10-29 Unitika Ltd Composite fiber having antistatic and water repellent property

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53111116A (en) * 1977-03-03 1978-09-28 Asahi Chem Ind Co Ltd Antistatic, sheath-core type conjugate fiber and its fiber mixing
JPS5747942A (en) * 1980-09-05 1982-03-19 Toray Industries Polyeter type anti-static composite blended fiber yarn
JPS57117619A (en) * 1981-01-13 1982-07-22 Unitika Ltd Preparation of modified synthetic fiber
JPS57176216A (en) * 1981-04-22 1982-10-29 Unitika Ltd Composite fiber having antistatic and water repellent property

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01156573A (en) * 1987-12-10 1989-06-20 Kuraray Co Ltd Cloth excellent in feeling
JP2017057513A (en) * 2015-09-15 2017-03-23 東レ株式会社 Antistatic polyamide core-sheath composite fiber with excellent durability

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