JPS5936721A - Conjugate yarn dyeable with acid dye - Google Patents
Conjugate yarn dyeable with acid dyeInfo
- Publication number
- JPS5936721A JPS5936721A JP14739882A JP14739882A JPS5936721A JP S5936721 A JPS5936721 A JP S5936721A JP 14739882 A JP14739882 A JP 14739882A JP 14739882 A JP14739882 A JP 14739882A JP S5936721 A JPS5936721 A JP S5936721A
- Authority
- JP
- Japan
- Prior art keywords
- component
- polyester
- yarn
- polyamide
- 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
Links
- 239000000980 acid dye Substances 0.000 title description 5
- 229920000728 polyester Polymers 0.000 claims abstract description 21
- 239000004952 Polyamide Substances 0.000 claims abstract description 12
- 229920002647 polyamide Polymers 0.000 claims abstract description 12
- 239000000835 fiber Substances 0.000 claims description 12
- 239000002131 composite material Substances 0.000 claims description 10
- 238000007334 copolymerization reaction Methods 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- -1 polyethylene terephthalate Polymers 0.000 abstract description 9
- XUSNPFGLKGCWGN-UHFFFAOYSA-N 3-[4-(3-aminopropyl)piperazin-1-yl]propan-1-amine Chemical compound NCCCN1CCN(CCCN)CC1 XUSNPFGLKGCWGN-UHFFFAOYSA-N 0.000 abstract description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 6
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 6
- 239000000203 mixture Substances 0.000 abstract description 5
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract description 4
- 238000002074 melt spinning Methods 0.000 abstract description 2
- 229920001577 copolymer Polymers 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000000034 method Methods 0.000 description 6
- 238000004043 dyeing Methods 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- 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
- YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000012510 hollow fiber Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Multicomponent Fibers (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は酸性染料可染性複合m 411に関するもので
あり、詳しくは、11.V−ビス(アミノ−n−プロピ
/L/)ビペヲジンを共重合成分とするポリアミド(A
)又は(んとポリエステIv+INとの混合物からなる
成分CI)とポリエステルからなる成分〔■〕とから形
成されたlrj合IR維であって、 (1)、 (
II)のうち一方の成分が他の成分によって複数の領域
に分割されてIRt m表面部に露出又は突出するよう
に回転対称にna餘された断面形状を有する酸性染料可
染性複合繊維を要旨とするものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to acid dye dyeable composite m 411, and in detail, 11. Polyamide (A
) or (component CI consisting of a mixture of polyester Iv+IN) and a component [■] consisting of polyester, (1), (
An acid dye-dyeable conjugate fiber having a rotationally symmetrical cross-sectional shape in which one component of II) is divided into a plurality of regions by another component and exposed or protrudes from the IRtm surface area. That is.
ポリエステiv M’l JI#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をポリエステルにブレンド
する方法を中心に横1されてきた。Attempts to make polyester iv M'l JI# dyeable with acid dyes have been made for a long time, including a method of copolymerizing polyester with an ester group-forming monomer containing amino groups, and a method of copolymerizing polyester with an amino group-containing compound. A lot of research has focused on methods for blending with polyester.
しかし、なから、これらの方法で問題になるのは導入す
べきアミノ基含有化合物の耐熱性の欠如、ポリエステル
との相互作用なとのために重合時あるいは成形時に着色
・分解が起こったり、ポリエステルの載JIB形成能が
低下したりすることである。However, problems with these methods include the lack of heat resistance of the amino group-containing compound to be introduced and the interaction with the polyester, which may cause coloration and decomposition during polymerization or molding, and the polyester This may result in a decrease in the ability to form JIBs.
本発明者らはポリエステ/I/m雑の酸性染料可染化に
おけるこのような問題を解決すべく種々検討した結果、
ti、を丁′−ビス(アミノ−n−プロピ/I/)ビベ
フジン(以下BAPPと略称)を共重合成分とするポリ
アミド又は該ポリアミドとポリエステルとの混合物から
なる成分とポリニスデルからなる成分とを特定の形状と
なるように複合させることが撞めて有効であることを知
り、冒頭に記載した如き本発明に到達したものである。The present inventors have conducted various studies to solve these problems in dyeing polyester/I/m miscellaneous materials with acid dyes.
Specify a component consisting of a polyamide containing ti'-bis(amino-n-propy/I/) bibefudin (hereinafter abbreviated as BAPP) as a copolymerization component or a mixture of the polyamide and polyester, and a component consisting of polynisdel. The present invention as described at the beginning was achieved by finding that it is extremely effective to combine the materials so as to have the shape of the following.
以下本発明について説明する。The present invention will be explained below.
本発明において13APPを共重合成分とするポリアミ
ド(A)とは、アジピン酸、セバシン酸、アゼフィン酸
、テレフタル酸、イソフタル酸、ナフタル酸などのジカ
ルボン酸もしくはこれらのエヌテ/I/又はハロリド、
エチレンジアミン、テトツメチレンジアミン、ヘキサメ
チレンジアミン、P−フェニレンジアミン、m−フェニ
レンジアミン、P−キシリレンジアミン、ピペラジン、
ビス(4−7ミノシクロヘキシA/)メタンなどのジア
ミン。In the present invention, the polyamide (A) containing 13APP as a copolymerization component refers to dicarboxylic acids such as adipic acid, sebacic acid, azefinic acid, terephthalic acid, isophthalic acid, and naphthalic acid, or their NTE/I/or halide,
Ethylenediamine, tetotsumethylenediamine, hexamethylenediamine, P-phenylenediamine, m-phenylenediamine, P-xylylenediamine, piperazine,
Diamines such as bis(4-7minocyclohexyA/)methane.
カブロヲクタム、フウリルラクタムなどのツクタム ε
−アミノカプロン酸、 (tl−アミノツウリン酸な
どの1ミノカルボン酸とBAPPとを適宜組み合わせる
ことによって得られる共重合ポリアミドを意味し9通常
公知の重縮合法によって得られる。Tsucutams such as cabrooctum and furyllactam ε
-Aminocaproic acid (means a copolyamide obtained by appropriately combining a monocarboxylic acid such as tl-aminotouric acid and BAPP) 9 Usually obtained by a known polycondensation method.
この際、 BAPP成分はポリアミド中の5〜30重
r1%、好ましくは5〜25重fIl:%を占めること
力ζよい。また、本発明において01及び成分〔「〕の
ポリエステルとしては、゛ポリエチレンテレフタレート
、ポリブチレンプレフタレート、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、ポリーP−エチレンオキシベン
ゾエートなど及びこれらを主成分とするa t−tp形
成性良好な熱可塑性ポリエステルが好ましく用いられる
が、その汎用性からポリエチレンテレフタレート又はこ
れを主成分とするポリエステルが最適である。また、5
−アルカリ金属(すトリウム又はカリウム)スルホイソ
フタル酸成分を共重合成分とするポリエチレンプレフタ
レートは共重合ポリアミド(A)との混和性、密着性が
停れていること、霞維を塩基性染料に対しても可染性に
することなどから好適なポリエステルであり、ポリアル
キレンオキシドを共重合成分とするポリエステル・は染
色温度を低くできる効果が大きく、特にTB)として好
ましいポリニスデルの−っである。なお、(同と成分〔
「〕に用いられるポリエステルとは同一でも異なってい
てもよいことはもちろんである。In this case, it is preferable that the BAPP component occupies 5 to 30% by weight, preferably 5 to 25% by weight, of the polyamide. In addition, in the present invention, polyesters of 01 and component [''] include polyethylene terephthalate, polybutylene prephthalate, polyethylene-2,6
-Naphthalate, poly-1,4-cyclohexylene dimethylene terephthalate, poly-P-ethyleneoxybenzoate, etc., and thermoplastic polyesters having good a-t-tp formation properties are preferably used, but due to their versatility. Polyethylene terephthalate or polyester containing polyethylene terephthalate as the main component is most suitable. Also, 5
-Polyethylene prephthalate containing an alkali metal (storium or potassium) sulfoisophthalic acid component as a copolymerization component has poor miscibility and adhesion with the copolyamide (A), and the use of haze fibers as basic dyes. Polyesters containing polyalkylene oxide as a copolymerization component have a great effect of lowering the dyeing temperature, and polynisder is particularly preferred as TB). In addition, (same and ingredients)
It goes without saying that the polyester used in [ ] may be the same or different.
本発明の複合繊維は、共重合ポリアミド(N又は(Nと
ポリエステル(Blとの混合物からなる成分(I)とポ
リエステルからなる成分〔「〕とからなり。The composite fiber of the present invention is composed of a component (I) consisting of a copolymerized polyamide (N or a mixture of (N and polyester (Bl)) and a component (I) consisting of a polyester.
(II、 (II)のうちの一方の成分が他の成分に
よって複数の領域に分割されてJII!維表血部に露出
又は突出するように回転対称に配置された形状を有する
ことを特徴とするものであり、このような複合形態とす
ることによって本発明の目的のPR維が製糸性よ< i
i!造できるのである。そして複合amを形成する各成
分の量的関係は、11!合m、維中のBAPP成分の量
が0.5〜5M景形(3級アミノ基量で約50〜500
当景7トン)となり、成分(I)、’ (II)が重量
比で10:90〜7o:3oとなるようにすることが好
ましい。(II) One component of (II) is divided into a plurality of regions by the other component and is arranged rotationally symmetrically so as to be exposed or protrude from the JII! fiber surface blood area. By forming such a composite form, the PR fibers of the present invention have improved spinnability.
i! It can be built. And the quantitative relationship of each component forming the composite am is 11! In total, the amount of BAPP component in the fiber is 0.5 to 5M (the amount of tertiary amino group is about 50 to 500
It is preferable that the weight ratio of components (I) and '(II) be 10:90 to 7:3o.
第1〜5図は本発明の複合繊維の具体例を模式的に示し
た断面図である。(1)、 〔[)のうち一方の成分
(影点を付した部分)が枚数の領域に分割されてi a
t:表面部に露出又は突出して回転対称に配置され“C
いる。このような断面をもつ複合糸は公知の溶r1に複
合紡糸装置、延伸装置を用いて製糸されるが9分割個数
は2〜12個、好ましくは3〜8個がよく、第3図に示
すような中空糸の場合にはその中空度は70%以下が好
ましく、また第4図に示すような形状の場合にはその突
出度は60%以下であることが好ましい。 、
なお9本発明において成分(I)と〔「〕との親和性(
@画性)が乏しい場合、延伸工程や仮撚工程で剥障割糾
する可能性があるが、これを積極的に利用して風鱈光沢
などを改良することにも利用できる。また1本発明の繊
維につや消し剤、耐熱剤、1l11光剤、帯電防止剤、
防炎剤9着色剤などを含有させCもよいことはもちろん
である。1 to 5 are cross-sectional views schematically showing specific examples of the composite fiber of the present invention. (1), [[] One component (the shaded part) is divided into the number of regions i a
t: “C” exposed or protruding from the surface and arranged rotationally symmetrically.
There is. Composite yarn with such a cross section is spun using a known melt r1, composite spinning device, and drawing device, and the number of 9-split yarns is preferably 2 to 12, preferably 3 to 8, as shown in Figure 3. In the case of such hollow fibers, the degree of hollowness is preferably 70% or less, and in the case of the shape shown in FIG. 4, the degree of protrusion is preferably 60% or less. 9 In the present invention, the affinity between component (I) and [''] (
If the material has poor image quality, there is a possibility that it will peel off during the stretching or false-twisting process, but this can also be actively used to improve the luster of the cod. In addition, the fiber of the present invention may include a matting agent, a heat resistant agent, a 1l11 light agent, an antistatic agent,
It goes without saying that C may also be used as a flame retardant by containing a coloring agent and the like.
以下実施例によつ゛C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1
BAPP 10部、カブロックタム83部、アジピン酸
7.3部及び水15部を攪拌機つきオートクレーブに仕
込み、温度を250℃に係って、制圧期(6kq/d
) 2時間、放圧期2時冊、常圧期2時間の条件で重縮
合を行い、96%硫酸中9.25℃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 10 parts of BAPP, 83 parts of cabrotam, 7.3 parts of adipic acid, and 15 parts of water were charged into an autoclave equipped with a stirrer, and the temperature was set at 250°C.
) 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 9.25°C in 96% sulfuric acid was 1.
Almost white polyamide chips of No. 2 were obtained.
このポリアミドチップを脱モノマー処理後乾燥したもの
と、5−ナトリウムスルホイソフタル酸成分を2.0モ
/I/96共重合したポリエチレンテレフタレートチッ
プとを1通常のエクヌトルーダー型溶融紡糸機を用い、
第1図の断面形状で、前者が影点部で9m維の18重飛
%占めるように、溶融jR度285 Cの条件で0.3
1111*X36孔の吐出孔より紡出し、糸条を1,2
00 m/minで巻き取った。次いで延伸温度80c
、延伸倍率5.1倍で延伸しC75d156f 、強度
4.59/d、伸度66g6の延伸糸を得た。毛羽、糸
切れなどは発生ぜず紡糸、延伸性は良好であった。This polyamide chip was dried after demonomer treatment, and polyethylene terephthalate chips obtained by copolymerizing 2.0 mo/I/96 of 5-sodium sulfoisophthalic acid component were mixed using a normal Ecnuttruder type melt spinning machine.
In the cross-sectional shape shown in Fig. 1, the former was 0.3% under the condition of melting jR degree 285C so that the former accounted for 18% of the 9m fiber in the shaded area.
Spun from the discharge hole of 1111*X36 holes, 1 or 2 yarns
It was wound up at a speed of 0.00 m/min. Then the stretching temperature was 80c.
The yarn was drawn at a draw ratio of 5.1 times to obtain a drawn yarn having a C75d156f, a strength of 4.59/d, and an elongation of 66g6. No fuzz or yarn breakage occurred, and the spinning and drawing properties were good.
この延伸糸をtf6網して得た網地を精練後。After scouring the net fabric obtained by applying a tf6 net to this drawn yarn.
Hylomine Blue AG (ICI社製酸性
染料) 3 % owf 、浴比1/100で、98c
、1時間染色したところ、鮮明な青色の布となった。ま
た、別の絹地に対して赤色塩基性染料を含む浴中で12
0℃、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。Hylomine Blue AG (acid dye manufactured by ICI) 3% owf, bath ratio 1/100, 98c
After dyeing for 1 hour, the fabric became a bright blue color. In addition, for another silk fabric, 12
Even when dyeing was carried out at 0° C. for 1 hour, a clearly dyed cloth was obtained.
実施例2
ビスフェノ−1しAに20倍モルのエチレンオキシドを
イ1加させ゛〔11)だ化合物を5重量%共重合したポ
リエチt/ンテレフ′タレートチツブ70部と実施例1
のポリアミドヅッブ30部との/n Mjl混合物と、
jin常のポリエチレンテレフタレートとを第2図の
断面形状(等fft、爪)となるように実施例1とほぼ
同様な条件で紡糸・延伸し、 75d/36f 、強
度4、5 Q/d @ 伸度55%の延伸糸を得た。硬
糸性は良好であった。Example 2 Example 1 and 70 parts of polyethylene t/nterephthalate obtained by copolymerizing 5% by weight of a compound obtained by adding 20 times the mole of ethylene oxide to bispheno-1 and A [11].
/n Mjl mixture with 30 parts of polyamide tubing;
General polyethylene terephthalate was spun and drawn under almost the same conditions as in Example 1 so as to have the cross-sectional shape shown in Fig. 2 (equal fft, claw), and the result was 75d/36f, strength 4.5 Q/d @ elongation. A drawn yarn with a degree of strength of 55% was obtained. Hard thread properties were good.
この延伸糸を筒編・精練し、実施例1と同じ条ヂ1でσ
匈性染料で染色[7たところ、鮮明な青色の布となった
。This drawn yarn was tube-knitted and refined, and the same thread 1 as in Example 1 was used to obtain σ
After dyeing with a dyestuff, the cloth became a clear blue color.
第1・−5図は木イ1明の複合繊維のIL/i面形状の
具体例を1<人的に示したものである。
特許出願人 ユニチカ株式会社
第1図
第3[2]
」5日
52図
」+口Figures 1 and 5 are human illustrations of specific examples of the IL/i surface shape of the composite fiber made of wood. Patent applicant: Unitika Co., Ltd. Figure 1, Figure 3 [2] "5th Figure 52" + Mouth
Claims (1)
ペフジンを共重合成分とするポリアミド(N又は(A)
とポリエステA/(B)とのilR合物からなる成分(
I)とポリエステルからなる成分〔「〕とから形成され
た複合寅維であって、 (I)、 ([)のうちの
一方の成分が他の成分によって複数の領域に分割され°
C概維表面部に露出又は突出するように回転対称に配置
された断面形状を有する酸性染料可染性複合数組。[Scope of Claims] +1) Polyamide (N or (A)) containing H,N'-bis(amino-11-propyl)bipefudin as a copolymerization component
A component consisting of an ilR compound of and polyester A/(B) (
A composite fiber formed from a component (I) and a polyester component [''], in which one of the components (I) and ([) is divided into a plurality of regions by the other component.
C Several pairs of acid dye-dyeable composites having cross-sectional shapes arranged rotationally symmetrically so as to be exposed or protrude from the surface of the fibers.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14739882A JPS5936721A (en) | 1982-08-24 | 1982-08-24 | Conjugate yarn dyeable with acid dye |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14739882A JPS5936721A (en) | 1982-08-24 | 1982-08-24 | Conjugate yarn dyeable with acid dye |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5936721A true JPS5936721A (en) | 1984-02-29 |
Family
ID=15429373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14739882A Pending JPS5936721A (en) | 1982-08-24 | 1982-08-24 | Conjugate yarn dyeable with acid dye |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5936721A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62141077U (en) * | 1986-02-28 | 1987-09-05 |
-
1982
- 1982-08-24 JP JP14739882A patent/JPS5936721A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62141077U (en) * | 1986-02-28 | 1987-09-05 |
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