JPS5936155A - Ionic dye-dyeable polymer composition - Google Patents

Ionic dye-dyeable polymer composition

Info

Publication number
JPS5936155A
JPS5936155A JP14514582A JP14514582A JPS5936155A JP S5936155 A JPS5936155 A JP S5936155A JP 14514582 A JP14514582 A JP 14514582A JP 14514582 A JP14514582 A JP 14514582A JP S5936155 A JPS5936155 A JP S5936155A
Authority
JP
Japan
Prior art keywords
component
polyamide
polyester
polymer composition
acid
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
JP14514582A
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 JP14514582A priority Critical patent/JPS5936155A/en
Publication of JPS5936155A publication Critical patent/JPS5936155A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide titled composition of excellent heat resistance and formability, free from both coloring and decomposition, capable of forming acid dye-dyeable fiber, comprising each specific thermoplastic polyester and polyamide. CONSTITUTION:The objective composition comprising (A) a thermoplastic polyester (pref. consisting mainly of ethylene terephthalate unit) with a 5-alkali metal sulfoisophthalic acid component as a copolymerized one, and (B) a thermoplastic polyamide with an N,N'-bis(amino-n-propyl)piperazine as a component. The amount of said sulfoisophthalic acid component in the above polyester should be 0.5-7 (pref. 1-6)mol% based on the dibasic acid one. It is preferable that either or both of the polyester and polyamide would contain a polyalkylene oxide component as a copolymerized one.

Description

【発明の詳細な説明】 本発明は成形品、特に繊維に適したイオン性染料可染性
重合体組成物に関するものであり、詳しくは、5−アル
カリ金属スルホイソフタル酸成分を共重合成分とする熱
可塑性ポリエステル及びN、H’−ビス(アミノ−n−
デpビ/I/)ピペラジノな一成分とする熱可塑性ポリ
アミドとからなるイオン性染料可染性重合体組成物を要
旨とするものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an ionic dye-dyeable polymer composition suitable for molded articles, particularly fibers, and more specifically, a polymer composition containing a 5-alkali metal sulfoisophthalic acid component as a copolymer component. Thermoplastic polyester and N,H'-bis(amino-n-
The gist of the invention is an ionic dye-dyeable polymer composition comprising a thermoplastic polyamide having a piperazine as one component.

ポリエステル成形品、特にポリエステ/I/繊維を酸性
染料に対して可染性にしようとする試みは古くからあり
、アミノ基含有のエステル基形成性七ツマ−をポリエス
テルに共重合する方法、アミノ基含有化合物(主として
ポリマー)をポリエステルにブレンドする方法を中心に
検討されてきた。
Attempts have been made for a long time to make polyester molded products, especially polyester/I/fibers, dyeable with acid dyes. Studies have focused on methods of blending containing compounds (mainly polymers) into polyesters.

しかしながら、これらの方法で問題になるのは。However, there are problems with these methods.

導入すべきモノマーやポリマーの耐熱性の欠如。Lack of heat resistance of monomers and polymers to be introduced.

ポリエステルとの相互作用などのために重合時あるいは
成形時に着色・分解したり、混和性が十分でないために
成形性に欠けたりすることであり。
This may result in coloring or decomposition during polymerization or molding due to interaction with polyester, or lack of moldability due to insufficient miscibility.

成功した例がほとんどないのが実状である。The reality is that there are very few successful cases.

本発明者らはポリエステル成形品の酸性染料可染化にお
けるこのような欠点を改良すべく種々検討した結果、5
−アルカリ金属ヌルホイソフタル酸(以下SIPと略称
)成分を共重合成分とするボ1リエステル及びN、 N
’−ビス(アミノ−n−プロピル)ピペラジン(以下B
APPと略称)を−成分とするポリアミドとのブレンド
物は上述のような欠点のない組成物を与え、  SIP
成分による塩基性染料に対する可染化と相まつ°C9価
値のある製品を提供することを知り、冒頭に記載したご
とき本発明に至った。
The present inventors have conducted various studies to improve these drawbacks in dyeing polyester molded products with acid dyes, and have found that 5.
- A polyester containing an alkali metal nulphoisophthalic acid (hereinafter abbreviated as SIP) component as a copolymerization component, and N, N
'-bis(amino-n-propyl)piperazine (hereinafter referred to as B
Blends of APP (abbreviated as APP) with polyamides as a component give compositions without the above-mentioned drawbacks, and SIP
The present invention as described at the beginning was realized based on the knowledge that the combination of dyeability with basic dyes by ingredients can provide a product with a value of C9.

以下本発明について説明する。The present invention will be explained below.

本発明におけるSIP成分を共重合成分とするボリエメ
テ〜としてはポリエチレンテレフタレート。
In the present invention, polyethylene terephthalate is used as the polyethylene methane whose copolymerization component is the SIP component.

ポリブチレンテレフタレート、ポリエチレン−2,6−
ナフタレート、ポリ−1,4−シクロヘキシレンジメチ
レンテレフタレートなど及びこれらを主成分とするポリ
エステルに5−ナトリウム(又はカリウム)ヌルホイソ
フタル酸成分を共重合したものが用いられ、これらは通
常公知の方法で製造されるが、その汎用性からSIP成
分を共重合成分トするポリエチレンテレフタレートが最
適である。そしてポリエステル中のS工P成分の量をよ
二塩基酸成分1こ関して0.5〜7モル%、好ましくは
1〜6モル%であることが、ポリアミドとの混和性。
Polybutylene terephthalate, polyethylene-2,6-
Naphthalate, poly-1,4-cyclohexylene dimethylene terephthalate, etc., and polyesters containing these as main components are copolymerized with a 5-sodium (or potassium) nulphoisophthalic acid component, and these are usually carried out by known methods. However, due to its versatility, polyethylene terephthalate, which is copolymerized with the SIP component, is most suitable. The miscibility with polyamide is such that the amount of S-P component in the polyester is 0.5 to 7 mol%, preferably 1 to 6 mol%, based on one dibasic acid component.

塩基性染料に対する可染性の点から適当である。It is suitable from the viewpoint of dyeability with basic dyes.

また9本発明におけるBAPPを一成分とする熱可塑性
ポリアミドとは、アジピン酸、七ノ(シン酸。
9 In the present invention, the thermoplastic polyamide containing BAPP as one component includes adipic acid and hetano(cinic acid).

アゼライン酸、テレフタル酸、イソフタル酸、ブーフタ
ル酸などのジカルボン酸もしくはこれらのエステル又は
ハロリド、エチレンジアミン、テ1ラメチレンジアミン
、ヘキサメチレンジアミン、P−フェニレンジアミン、
pn−フェニレンジアミン。
Dicarboxylic acids such as azelaic acid, terephthalic acid, isophthalic acid, boophthalic acid or their esters or halides, ethylenediamine, tetramethylenediamine, hexamethylenediamine, P-phenylenediamine,
pn-phenylenediamine.

P−キシリレンジアミン、m−キシリレンジアミン、ビ
ス(4−アミノシロヘキシル)メタンナトのジアミン、
カブロックタム、ラウリルヲクタムなどのフクタム、ε
−アミノカプロン酸、ω−アミノラウリン酸などのアく
ノカルポン酸とBAPPとを適宜組み合わせることによ
って得られるポリアミドを意味し9通常公知の重縮合法
によつC得られる。この際、  BAPP成分はポリア
ミド中の6〜30重量%、好ましくは5〜25重爪%を
占めることがよい。
P-xylylene diamine, m-xylylene diamine, bis(4-aminosilohexyl)methanato diamine,
Fuctums such as cabroctum and lauryl octum, ε
- It means a polyamide obtained by appropriately combining an acinocarboxylic acid such as aminocaproic acid or ω-aminolauric acid with BAPP. 9C is obtained by a commonly known polycondensation method. In this case, the BAPP component preferably occupies 6 to 30% by weight, preferably 5 to 25% by weight, of the polyamide.

本発明の重合体組成物は公知の方法によって製造するこ
とができる。すなわち、ポリエステルとポリアミドとの
配合は成形以前の任意の段階で動的又は静的の溶融混合
機を用いて行えばよい。耐熱剤、1Tlit光剤、防炎
剤、帯電防止剤、つや消し剤などを使用目的に応じ゛C
添加し°Cもさしつかえない。そして要求される染色性
能、用途などによつ°〔異なるが9重合体組成物中のS
工P成分及びBAPP成分の量はスルホン酸アルカリ金
属塩基及び3級アミノ基の濃度がそれぞれろ0−10当
量/トン。
The polymer composition of the present invention can be produced by a known method. That is, blending of polyester and polyamide may be carried out using a dynamic or static melt mixer at any stage prior to molding. Depending on the purpose of use, heat resistant agents, 1Tlit light agents, flame retardants, antistatic agents, matting agents, etc.
Addition and temperature at °C are also acceptable. Depending on the required dyeing performance, usage, etc.
The amounts of the P component and the BAPP component are such that the concentration of the alkali metal sulfonate base and the tertiary amino group is 0-10 equivalent/ton, respectively.

50〜500当J’i/)ン稈度となるように調合する
ことが望ましい。
It is desirable to prepare the culm so that it has a culm degree of 50 to 500 equivalent J'i/).

また1本発明におけるポリエステル及びポリアミドのう
ちの一方又は両方がポリエチレンオキシド、ポリプロピ
レンオキシド、エチレンオキシドーグロピVンオキシド
のコポリマーなどのポリアルキレンオキシド成分を共重
合成分とする重合体である場合には2重合体組成物の染
色温度を下げる効果があり、有利な場合もある。
In addition, in the case where one or both of the polyester and polyamide in the present invention is a polymer containing a polyalkylene oxide component as a copolymerization component, such as a copolymer of polyethylene oxide, polypropylene oxide, or ethylene oxide, It has the effect of lowering the dyeing temperature of the combined composition, which may be advantageous.

本発明の重合体組成物は繊維をはじめ、フィルムその他
成形品として広く応用できる。また9本発明の組成物を
一成分とし他の#J!維形成形成性良好合体を他方の成
分とする複合糸2本発明の組成物からなる114mと他
の繊維との混繊品、混紡品。
The polymer composition of the present invention can be widely applied as fibers, films, and other molded products. In addition, 9 other #J! compositions of the present invention are used as one component. A blended fiber product or blended product of 114m made of the composition of the present invention and other fibers.

交編量、交織品などにも展CDできる。Exhibition CDs can also be used for mixed knitting and mixed woven products.

以下実施例によつ°C本発明をさらに具体的に説明する
。実施例中の部は重量部を示す。
EXAMPLES The present invention will be explained in more detail below using Examples. Parts in the examples indicate parts by weight.

実施例1 BAPP 15 部*  カブロックタム74部、アジ
ピン酸11部及び水15部を攪拌機付オートクレーブに
仕込み、温度を250℃に保つ°C9制圧期(6kV/
d ) 2時間、放圧期2時間、常圧期2時間の条件で
重縮合を行い、96優硫酸中、25Cでの固有粘度が1
.2のほぼ白色のポリアミドチップを得た。
Example 1 15 parts of BAPP * 74 parts of cabroctam, 11 parts of adipic acid, and 15 parts of water were charged into an autoclave equipped with a stirrer, and the temperature was kept at 250°C.
d) Polycondensation was carried out under the conditions of 2 hours, 2 hours of pressure release period, and 2 hours of normal pressure period, and the intrinsic viscosity at 25C in 96 superior sulfuric acid was 1.
.. Almost white polyamide chips of No. 2 were obtained.

このポリアミドチップ10部と3モル%の5IP(Wa
塩型)成分共重合ポリエチレンテレフタレート90部と
を混合し、エクストルーダー型溶融紡糸機を用い、28
0Cで、紡糸孔数36孔の紡出孔より吐出させ、 12
00 m/minの速度で巻取った。次いで、延伸温度
90℃、延伸倍率5.3倍、ヒートセット温度150℃
、延伸速JX 800 m/min (り条件で延伸し
て75d156f 、強度4.8f/d、伸度35%の
白色の延伸糸を得た。毛羽、切断などは発生せず製糸性
は良好であった・ この延伸糸を筒編して得た編地を精練後後。
10 parts of this polyamide chip and 3 mol% of 5IP (Wa
Salt type) component copolymerized polyethylene terephthalate (90 parts) was mixed with 90 parts of copolymerized polyethylene terephthalate, and using an extruder type melt spinning machine,
At 0C, the material is discharged from a spinning hole with a number of spinning holes of 36, and 12
It was wound up at a speed of 0.00 m/min. Next, the stretching temperature was 90°C, the stretching ratio was 5.3 times, and the heat setting temperature was 150°C.
The yarn was drawn at a drawing speed of 800 m/min (JX) to obtain a white drawn yarn of 75 d 156 f, strength 4.8 f/d, and elongation 35%. No fuzz or breakage occurred, and the yarn spinnability was good. After scouring the knitted fabric obtained by tubular knitting this drawn yarn.

Nylomine Blue AG (ICI社製酸性
染料)296owf。
Nylomine Blue AG (acid dye manufactured by ICI) 296owf.

浴比1/100. 120℃、1時間の条件で染色した
とこ・5.鮮明な青色の布となった。また、別の網地に
対して赤色塩基性染料洛中で120c、1時間の条件で
染色した場合にも鮮明な染色布が得られた。
Bath ratio 1/100. 5. Dyeing at 120°C for 1 hour. The cloth became a clear blue color. Furthermore, when another net fabric was dyed in red basic dye Raku at 120C for 1 hour, a clearly dyed fabric was obtained.

実施例2 ビスフェノ−A/Aに20倍モルのエチレンオキシドを
付加させ′C得た化合物を5重量優及びS工P(Na塩
型)成分を2.54/L/96共重合したポリエチレン
テレフタレート85部に、実施例1で得たポリアミド1
5部を混合し、実施例1と同様の操作を行って、はぼ白
色の延伸糸を得た。
Example 2 Polyethylene terephthalate 85 was obtained by adding 20 times the molar amount of ethylene oxide to bispheno-A/A and copolymerizing the compound obtained by 5% by weight and S-P (Na salt type) component at 2.54/L/96. Part of polyamide 1 obtained in Example 1
5 parts were mixed and the same operation as in Example 1 was performed to obtain a pale white drawn yarn.

この延伸糸を筒編して得た布は、酸性染料及び塩基性染
料に100℃の浴温で染まり得ることが確認された・ 特許出願人 ユニチカ株式会社
It has been confirmed that the fabric obtained by tube-knitting this drawn yarn can be dyed with acid dyes and basic dyes at a bath temperature of 100°C. Patent applicant: Unitika Co., Ltd.

Claims (1)

【特許請求の範囲】 (1)5−アルカリ金属スルホイソフタル酸成分を共重
合成分とする熱可塑性ポリエステル及びN、N’−ビス
(アミノ−n−プロピ/L/)ピペラジノを一成分とす
る熱可塑性ポリアミドとからなるイオン性染料可染性重
合体組成物。 12) %可塑性ポリエステルがエチレンテレフタレー
ト単位を主成分とするポリエステルである特許請求の範
囲第1項記載の重合体組成物。 (3)熱可塑性ポリエステル及び熱可塑性ポリアミドの
うちの一方又は両方がポリアルキレンオキシド成分を共
重合成分とする重合体である特許請求の範囲第1項記載
の重合体組成物。
[Claims] (1) A thermoplastic polyester containing a 5-alkali metal sulfoisophthalic acid component as a copolymerization component and a thermoplastic polyester containing N,N'-bis(amino-n-propy/L/)piperazino as a component. An ionic dye-dyeable polymer composition comprising a plastic polyamide. 12) The polymer composition according to claim 1, wherein the % plastic polyester is a polyester containing ethylene terephthalate units as a main component. (3) The polymer composition according to claim 1, wherein one or both of the thermoplastic polyester and the thermoplastic polyamide is a polymer having a polyalkylene oxide component as a copolymer component.
JP14514582A 1982-08-20 1982-08-20 Ionic dye-dyeable polymer composition Pending JPS5936155A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14514582A JPS5936155A (en) 1982-08-20 1982-08-20 Ionic dye-dyeable polymer composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14514582A JPS5936155A (en) 1982-08-20 1982-08-20 Ionic dye-dyeable polymer composition

Publications (1)

Publication Number Publication Date
JPS5936155A true JPS5936155A (en) 1984-02-28

Family

ID=15378454

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14514582A Pending JPS5936155A (en) 1982-08-20 1982-08-20 Ionic dye-dyeable polymer composition

Country Status (1)

Country Link
JP (1) JPS5936155A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6133382A (en) * 1995-08-31 2000-10-17 Prisma Fibers, Inc. Fiber-forming polyamide composition containing polyamide and a sulfonated polyester concentrate
US6433107B1 (en) * 1995-08-31 2002-08-13 Prisma Fibers, Inc. Fiber-forming polyamide with concentrate of polyamide and sulfonated aromatic acid

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6133382A (en) * 1995-08-31 2000-10-17 Prisma Fibers, Inc. Fiber-forming polyamide composition containing polyamide and a sulfonated polyester concentrate
US6334877B1 (en) * 1995-08-31 2002-01-01 Prisma Fibers, Inc. Carpet fibers from polyamide and sulfonated polyester concentrate
US6433107B1 (en) * 1995-08-31 2002-08-13 Prisma Fibers, Inc. Fiber-forming polyamide with concentrate of polyamide and sulfonated aromatic acid
US6589466B2 (en) * 1995-08-31 2003-07-08 Prisma Fibers Inc. Yarn by extruding polyamide fibers and sulfonated polyester concentrate
US6680018B2 (en) * 1995-08-31 2004-01-20 Prisma Fibers, Inc. Melt extrusion spinning polyamide fibers with sulfonated reagent and thermoplastic carrier

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