JPS59144617A - Antistatic conjugate fiber - Google Patents

Antistatic conjugate fiber

Info

Publication number
JPS59144617A
JPS59144617A JP1933183A JP1933183A JPS59144617A JP S59144617 A JPS59144617 A JP S59144617A JP 1933183 A JP1933183 A JP 1933183A JP 1933183 A JP1933183 A JP 1933183A JP S59144617 A JPS59144617 A JP S59144617A
Authority
JP
Japan
Prior art keywords
component
antistatic
polyalkylene oxide
amino
copolyamide
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
JP1933183A
Other languages
Japanese (ja)
Inventor
Osami Shinonome
東雲 修身
Katsumi Nakagawa
克己 中川
Takashi Ikeda
隆 池田
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 JP1933183A priority Critical patent/JPS59144617A/en
Publication of JPS59144617A publication Critical patent/JPS59144617A/en
Pending legal-status Critical Current

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  • Multicomponent Fibers (AREA)

Abstract

PURPOSE:An antistatic conjugate yarn that is formed by coating a copolyamide containing a specific compound as a copolymer component with a thermoplastic polymer, thus showing high antistatic properties and light resistance. CONSTITUTION:A copolyamide, which is obtained by adding a polyalkylene oxide bearing amide-forming functional groups such as amino groups and N, N'- bis(amino-n-propyl)piperazine, preferably in amounts of 10-70wt% and 1- 20wt%, respectively, when polycondensation reaction is carried out in an appropriate combination between dicarboxylic acid components such as adipic acid, diamines such as ethylenediamine or lactams such as caprolactam, is used as the core or island component. In the meantime, a thermoplastic polymer such as polyethylene terephthalate is used as the sheath of sea component to produce the objective antistatic conjugate yarn.

Description

【発明の詳細な説明】 、 本発明は制電性を右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 a composite fiber that exhibits antistatic properties.

ポリアミド、ポリエステルなどの合成化841 III
、! l’1111の静電気障害を抑制するにはポリア
ルキレンオキシド系化合物の導入が有効なことは周知の
通りで沙〕る。特にポリアルキレンオキシド成分とポリ
コースチルあるいはポリアミド成分とからなるブし2ツ
クポリマーを練り込む方法ば耐久性のある制電糸を摺る
のに最適であるとされている。しかし、この方法では制
電剤であるポリアルキレンオキシド成分か繊維分子中に
拘束されやすく、モビリティが低下し、冬期におりるよ
うな低湿度Fでは十分な効果を発現し難いばかりでな(
、繊維の耐光性を低下させるという欠点がある。また、
耐光性の問題を解消ずべくポリアルキレンオキシド成分
を芯又は島成分とし1適音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が、この
場合には繊維表面部に制電剤が存在しないためか、肝要
の制電効果か小さいという問題がある。
Synthesis of polyamide, polyester, etc. 841 III
,! It is well known that the introduction of a polyalkylene oxide compound is effective in suppressing the electrostatic damage caused by l'1111. In particular, a method of kneading a block polymer consisting of a polyalkylene oxide component and a polycoastyl or polyamide component is said to be optimal for producing durable antistatic yarn. However, with this method, the polyalkylene oxide component, which is an antistatic agent, tends to be bound in the fiber molecules, resulting in reduced mobility, and it is difficult to achieve sufficient effects at low humidity levels such as those experienced in winter.
, which has the disadvantage of reducing the light resistance of the fiber. Also,
In order to solve the problem of light resistance, a method has also been proposed in which a polyalkylene oxide component is used as a core or island component and a suitable polyester or polyamide is used as a sheath or sea component. The problem is that the essential antistatic effect is small, perhaps because no agent is present.

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、  N、N’−ビス(アミノ−n−ブにJ
ピル)ピペラジン(1)八■〕Pといつ’)成分を共重
合した共重合ボエアミトを芯又は島成分とし2通當の静
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1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, and found that, together with the polyalkylene oxide component, N,N'-bis(amino-n-butyl
Pill) Piperazine (1) 8■〕P and ``) components are copolymerized to form a core or island component of copolymerized boa mite, and a polymer that is easily charged with static electricity is a sheath or sea component for the above purpose. This led to the present invention.

すなわち5本発明は、アミド形成性官能基を自−3−る
ポリアルキレンオキシ1−系化合物とI鼎1)Pとを共
重合成分とする共重合ポリアミドからなる( A ’)
成分と〔Δ〕成分を被覆するメリ賓1J塑性重合体から
なる〔■3〕成分とて構成された制電性複合繊維を“小
計とするものである。
That is, the present invention consists of a copolymerized polyamide containing a polyalkyleneoxy 1-based compound having an amide-forming functional group and I(1)P as copolymerization components (A')
The antistatic conjugate fiber constituted by component [■3] consisting of Merihin 1J plastic polymer covering the component and [Δ] component is considered as the "subtotal".

本発明におりるポリアルキレンオキシド系化合物として
はアミノ尽、カルボキシル基、アル」キシカルボニル基
等のアミl−形成性官能基をl (IIJ以」二、好ま
しくは2(固自゛するポリエチレンオキシド。
The polyalkylene oxide compound according to the present invention has an amyl-forming functional group such as an amino group, a carboxyl group, or an alkoxycarbonyl group. .

ポリプロピレンオキシド じノピレン刊ギシトコボリマーなどのポリアルギレンオ
キシトセグメントを有する化合物か用いられ。
Compounds having polyalgylene oxyto segments, such as polypropylene oxide dinopylene polypropylene polymers, are used.

分子中にヒスフェノール残基を合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。
A polyalkylene oxide compound having a hisphenol residue in its molecule is preferred because it has good heat resistance.

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 molecular weight of the polyalkylene oxide compound is 400-20
,000, preferably 800 to 10,000.

本発明における〔△〕成分の共重合ポリアミドは,上述
のポリアルキレンオキシド化合物とI鼎11 pとを共
重合成父とーJるポリアミドであるが。
The copolyamide of the [△] component in the present invention is a polyamide obtained by copolymerizing the above-mentioned polyalkylene oxide compound and I-J.

、二のようなポリ)′ミドは公知の方法でi4Jられる
, 2 are i4J-converted using known methods.

ずなわら7エチレンシアミン、テ1−ラメチレンシアミ
ン,ヘキザノナし・ンシアミン,ハ・キザヒト【フキシ
リ1/ンシアミン,1ニス(4−アミノツクl’J ”
Zunawara 7 ethylenecyamine, 1-ramethylenecyamine, hexanonacyamine, hakizahito
.

キシル)メタン、キシリレンソアミン、フェーレンジア
ミンなどのシアミン成分,アジピン酸,セバシン酸,テ
レフタル酸,イソフタル酸,ナフタルf(i’Jのソカ
ルボン酸成分,εーアミノカプロン酸,ω−アミノドデ
カン酸なとのアミノ酸成分。
xyl) methane, xylylensoamine, cyamine components such as phelene diamine, adipic acid, sebacic acid, terephthalic acid, isophthalic acid, naphthalic acid (socarboxylic acid component of i'J, ε-aminocaproic acid, ω-aminododecanoic acid) Amino acid components of Nato.

カブ1:Jラクタム、ラウリルラクタムなとのラクタム
成分を適宜組み合わせて重縮合する際に,ポリアルキレ
ンオキシド化合物とII A 11 Pとを添加するこ
とによって得られる。そして、共重合ポリアミド中のポ
リアルキレンオキシド成分及びI(^IIP成分の量は
それぞれ10〜70市量%及び1〜20市量%稈度であ
ることか1良好な制電効果の発現とい・う点で好ましい
Turnip 1: Obtained by adding a polyalkylene oxide compound and II A 11 P during polycondensation of an appropriate combination of lactam components such as J lactam and lauryl lactam. The amount of polyalkylene oxide component and I(^IIP component) in the copolyamide should be 10 to 70% by market weight and 1 to 20% by market weight, respectively. It is preferable in this respect.

次に本発明における〔B〕成分の熱可塑性重合体として
はポリエヂレンテレソタレー1−、ポリブチレンチレフ
タレ− ト,ポリーpーエチレンオキシヘンゾエートな
ど及びこれらを主成分とするポリコースチル、ナイIJ
ン[i 、 ナイ1,1ン12,ナイ11ン46、−ノ
ーイ1Jン66,ナイ15ノン610など及びこれらを
主成分とー」るポリアミド、ポリエナレン,ボリブtコ
ビレンなと及びこれらを主成分とするポリオレフィンが
好適である。
Next, as the thermoplastic polymer of the component [B] in the present invention, polyethylene terethothalate 1-, polybutylene ethylene terephthalate, poly p-ethylene oxyhenzoate, etc., and polycoastyl and nylon containing these as main components are used. I.J.
Polyamides containing these as main components, polyenalene, bolybt-cobylene, etc., and polyamides containing these as main components; Polyolefins having the following properties are suitable.

本発明の繊維はCA.)成分が〔I3〕成分によ−。The fiber of the present invention has a CA. ) component is due to [I3] component.

て被覆された形状を有する複合繊維であり,芯さや型又
は11σ島型の形状を有する。かかる形状の繊維は公知
の方法で得られる。そして制′市性能,耐光性5製糸性
.糸質物性などを,ち′応、すると〔△〕成分と〔)3
部成分との割合は断面積比で5:95〜5(1:50の
範囲かよい。また、 〔Δ〕成分,[:B)成分のうら
いずれか又は両刀につ:「燃剤,銅熱剤。
It is a composite fiber coated with a core-sheath type or an 11σ island type. Fibers having such a shape can be obtained by known methods. Also, control performance, light resistance, 5 yarn reeling properties. If we change the filamentous properties, etc., we get [△] component and [)3
The cross-sectional area ratio between the two components is 5:95 to 5 (may be in the range of 1:50. Also, either or both of the [Δ] component and [:B) component: "Fuel agent, Copper heating agent. .

−)や消し剤.着色剤などを含んでい′c 、b 、に
いことはもちろんである。〔13部成分中に耐光性に影
響をIJえる成分を含有さーUることは望ましくないが
-) Matting agent. It goes without saying that it contains colorants and the like. [Although it is not desirable to include components that may affect light resistance in the 13-part component.

少量であればポリアルキレンオキシド成分を〔I3〕成
分に金白さ一層て制電性を−「−向」ニさせるようにし
ーCもよい。
If the amount is small, the polyalkylene oxide component may be added to the [I3] component to make it more golden-white and give it antistatic properties in the - direction.

ツI・実施例によって本発明をさら(こ具体的に説明す
る。実施例中の制電性の測定は,京大化研弐ロータリー
スタチックテスターを用い,綿布を摩擦体として,20
°C,/10%R I−1の雰囲気中で摩擦帯電圧と半
減期を求める方法で行ったものである。
The present invention will be further explained in detail with reference to Examples. In the Examples, the antistatic property was measured using a rotary static tester of Kyoto University Kaken 2, using a cotton cloth as a friction body.
The measurement was carried out using a method to determine the frictional charging voltage and half-life in an atmosphere of °C, /10% R I-1.

(部は重量部を示す、1) 実施例 両末端にアミノ基を有するポリエチレンオキシド(平均
分子量4.000 ) 35部, BAI’P5部,ア
ジピン酸3.5部及びカプロラクタム56,5部とから
通常の溶融重縮合法により共重合ポリアミドを得た。
(Parts indicate parts by weight, 1) Example: 35 parts of polyethylene oxide having amino groups at both ends (average molecular weight 4.000), 5 parts of BAI'P, 3.5 parts of adipic acid, and 56.5 parts of caprolactam. A copolyamide was obtained by a conventional melt polycondensation method.

ごの共重合ポリアミドと通常のポリエチレンテレフタレ
ート( 0.5重量%の酸化チタン粒子を含む)とを、
共重合ポリアミl−か芯を形成し,断面積比が1(]:
90の芯さや型複合糸となるよう番、二,エクストルー
ダー型溶融紡糸機を用い, 280 ’cで。
Copolymerized polyamide and ordinary polyethylene terephthalate (containing 0.5% by weight of titanium oxide particles),
A copolymerized polyamide core is formed, and the cross-sectional area ratio is 1 (]:
90 core/sheath type composite yarn was prepared using an extruder type melt spinning machine at 280'c.

紡糸孔@36孔の紡出孔より吐出させ.  1 、 2
(lom/分の速度で巻き取った。次いで延伸温度90
°C,延伸倍率3.3倍で延伸し一C.  15d/3
Gf 、強度4.1g/d,伸度35%の延伸糸とした
。糸切れなどの問題はほとんど発生せず,製糸性は良好
であった。
It is discharged from the spinning hole with 36 holes. 1, 2
(It was wound up at a speed of lom/min. Then, the stretching temperature was 90 m/min.
℃, stretching at a stretching ratio of 3.3 times. 15d/3
The drawn yarn had a Gf of 4.1 g/d, a strength of 4.1 g/d, and an elongation of 35%. There were almost no problems such as yarn breakage, and the yarn spinnability was good.

−に記の延伸糸を5部g/=の密度で筒編後、精練し、
  I’j色分散染料を含む浴中で135’C、30分
間の条件で染色した。得られた染色布の1¥1察帯電圧
と゛1′減期はそれぞれt、ooo v及び10秒を示
し、この性能はボームランドリーを30回くり返しても
低下しなかつ六−0 比較例 共重合ポリアミドとして、実施例で用いたポリエチレン
オキソド化合物7IO部、アジピン酸1.5部及びカシ
1jラクタム 58.5部からf4%られた共重合ポリ
アミドを用しゾで3実施例と同様の操作を行ったか、染
色布の1ダ擦帯電圧及び半減期はそれぞれ2.000 
V及び70秒であった。
- After tube knitting the drawn yarn described in 5 parts g/= density, scouring it,
Dyeing was carried out at 135'C for 30 minutes in a bath containing I'j color disperse dye. The resulting dyed fabric had a 1 yen static charge voltage and a 1' life of t, ooo v, and 10 seconds, respectively, and this performance did not deteriorate even after Baume laundry was repeated 30 times. As the polyamide, a copolyamide prepared by f4% from 7IO parts of the polyethylene oxide compound used in the example, 1.5 parts of adipic acid, and 58.5 parts of the oak 1j lactam was used, and the same operation as in Example 3 was carried out. The voltage and half-life of dyed cloth are 2.000 and 2.000, respectively.
V and 70 seconds.

特許出j頭人  ユニチカ株式会社Patent author: Unitika Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] (1)アミド形成性官能基を杓するポリアルキレンオキ
シド系化合物とN、N’−ビス、(アミノ−rl−ゾし
ノピル)ピペラジンとを共重合成分とする共重合ポリア
ミドからなる〔AJ成分と(A)成分を被覆する熱FI
IT塑性重合体から4yる〔I3〕成分とで構成された
制電性複合繊維。
(1) Consisting of a copolymerized polyamide containing a polyalkylene oxide compound containing an amide-forming functional group and N,N'-bis, (amino-rl-zoshinopyl)piperazine as copolymerization components [AJ component and (A) Thermal FI covering the components
An antistatic composite fiber composed of an IT plastic polymer and a 4y [I3] component.
JP1933183A 1983-02-07 1983-02-07 Antistatic conjugate fiber Pending JPS59144617A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1933183A JPS59144617A (en) 1983-02-07 1983-02-07 Antistatic conjugate fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1933183A JPS59144617A (en) 1983-02-07 1983-02-07 Antistatic conjugate fiber

Publications (1)

Publication Number Publication Date
JPS59144617A true JPS59144617A (en) 1984-08-18

Family

ID=11996420

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1933183A Pending JPS59144617A (en) 1983-02-07 1983-02-07 Antistatic conjugate fiber

Country Status (1)

Country Link
JP (1) JPS59144617A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7548298B2 (en) 2005-10-13 2009-06-16 Seiko Epson Corporation Liquid crystal panel, method for producing liquid crystal panel, and electronic apparatus
US11078331B2 (en) 2018-04-06 2021-08-03 Workers First LLC Acid neutralizing polymer materal and method of making same
US11952463B2 (en) 2018-04-06 2024-04-09 Workers First LLC Acid neutralizing polymer powder

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7548298B2 (en) 2005-10-13 2009-06-16 Seiko Epson Corporation Liquid crystal panel, method for producing liquid crystal panel, and electronic apparatus
US11078331B2 (en) 2018-04-06 2021-08-03 Workers First LLC Acid neutralizing polymer materal and method of making same
US11952463B2 (en) 2018-04-06 2024-04-09 Workers First LLC Acid neutralizing polymer powder

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