JPS59144677A - Anti-stain raw fiber - Google Patents

Anti-stain raw fiber

Info

Publication number
JPS59144677A
JPS59144677A JP1932983A JP1932983A JPS59144677A JP S59144677 A JPS59144677 A JP S59144677A JP 1932983 A JP1932983 A JP 1932983A JP 1932983 A JP1932983 A JP 1932983A JP S59144677 A JPS59144677 A JP S59144677A
Authority
JP
Japan
Prior art keywords
weight
fluorine
fibers
fiber
group
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
JP1932983A
Other languages
Japanese (ja)
Inventor
東雲 修身
志朗 村上
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 JP1932983A priority Critical patent/JPS59144677A/en
Publication of JPS59144677A publication Critical patent/JPS59144677A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は防汚性原着繊維に関するものであり。[Detailed description of the invention] The present invention relates to stain-resistant spun-dyed fibers.

詳しくは、有彩色に原液着色された重合体からなる繊維
であって、その表面が含フツ素化合物で被覆されている
ことを特徴とする防汚性原着繊維を要旨とするものであ
る。
Specifically, the subject matter is a stain-resistant, source-dyed fiber comprising a polymer dyed in a chromatic solution, the surface of which is coated with a fluorine-containing compound.

含フツ素化合物で被覆処理した繊維製品は撥水性、撥油
性、防水性、耐ドライフィル性などの性能を有すること
から、スポーツ、インテリア、雨゛具の分野で広く展開
されている。従来、この被覆処理は繊維製品の染色後に
行う方法が採用されてきたが、最近では工程の簡略化・
コストダウンの目的で、原糸製造段階で含フツ素化合物
を付着させる方法が注目されている。しかしながら、こ
のような方法で得られる繊維の問題点として、繊維が撥
水性となるために染色し稚くなり、特に3鮮明な有彩色
に染色することが困難になるとともに。
Textile products coated with fluorine-containing compounds have properties such as water repellency, oil repellency, waterproofness, and dry fill resistance, and are therefore widely used in the fields of sports, interior design, and rain gear. Traditionally, this coating treatment was carried out after textile products were dyed, but recently the process has been simplified and
For the purpose of cost reduction, a method of attaching a fluorine-containing compound at the yarn manufacturing stage is attracting attention. However, the problem with the fibers obtained by this method is that because the fibers become water repellent, they become fragile when dyed, and it is difficult to dye them in particularly vivid chromatic colors.

通常の繊維に比し染色に要するエネルギーが大となった
り、染色斑が生じたりすることがある。
The energy required for dyeing may be greater than that of ordinary fibers, and staining may occur.

この問題を解決しようとしたのが本発明であり。The present invention attempts to solve this problem.

原液着色糸が後染め糸に比し耐光堅牢度において優れて
いることから、防汚性と耐光性とが要求される自動車関
係(例えばシート)中心としてその需要は大きく本発明
の価値は大きい。
Since solution-colored yarns are superior in light fastness to piece-dyed yarns, they are in great demand mainly in the automobile industry (for example, seats), which require stain resistance and light resistance, and the value of the present invention is great.

本発明の繊維はポリエチレンテレフタレ−1・。The fiber of the present invention is polyethylene terephthalate-1.

ポリブ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1ナイロン6、ナイロン46、ナイロ
ン66、ナイロン61帆ポリメタフエニレンイソフタラ
ミド、ポリパラフェニレンテレフタラミドなど及びこれ
らを特徴とする特許アミド、ポリエチレン、ポリプロピ
レンなど及びこれらを主成分とするポリオレフィン、ポ
リアクリロニトリルを主成分とするポリマー、ポリビニ
ルアルコール(又はそのアセタール化物)、ポリ塩化ビ
ニル、ポリ塩化ビニリデン、レーヨン、アセテートなど
の合成繊維、再生繊維及び半合成繊維のうち、有彩色に
原液着色されたものである。
Polybutylene terephthalate, etc., polyesters containing these as main components, nylon 6, nylon 46, nylon 66, nylon 61, polymethaphenylene isophthalamide, polyparaphenylene terephthalamide, etc., and patented amides and polyethylenes characterized by these. , polypropylene, etc. and polyolefins based on these, polymers based on polyacrylonitrile, polyvinyl alcohol (or its acetal), polyvinyl chloride, polyvinylidene chloride, rayon, acetate, and other synthetic fibers, recycled fibers, and semi-synthetic fibers. Among synthetic fibers, these are colored with undiluted chromatic colors.

着色剤としては、公知の任意のものが用いられるが、ポ
リマーの種類によって、また色調の鮮明さ。
Any known colorant can be used, but it depends on the type of polymer and the sharpness of the color tone.

ポリマーへの分散性、耐溶媒性、耐移行性1耐熱性、耐
候性、耐薬品性、電気特性、毒性などに注意して選択さ
れる。
Dispersibility in polymers, solvent resistance, migration resistance, heat resistance, weather resistance, chemical resistance, electrical properties, toxicity, etc. are selected with consideration.

なお1本発明の繊維を構成する重合体としては。In addition, one example of the polymer constituting the fiber of the present invention is as follows.

その汎用性、物理的・化学的性質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特に
好ましい。
Polyethylene terephthalate or a polyester containing polyethylene terephthalate as a main component is particularly preferred because of its versatility and physical and chemical properties.

次に本発明において、含フン素化合物とは通常防汚剤と
して用いられるものを意味するが1代表的なものをあげ
ると次のようなものがある。
Next, in the present invention, the fluorine-containing compound refers to a compound commonly used as an antifouling agent, and the following are typical examples.

(al下記一般式(1)〜(3)で表される含フッ素上
ツマ−を単独重合もしくは共重合したポリマー又はこれ
らのモノマーと他のフッ素原子を含有しない七ツマ−と
を共重合したポリマー。
(al) Polymers obtained by homopolymerizing or copolymerizing fluorine-containing monomers represented by the following general formulas (1) to (3), or polymers obtained by copolymerizing these monomers with other fluorine-containing monomers. .

I CH2= CC00Rf           fil
RI   R3 Ch = CC00Rt NOa SRf      
 (21RI   R3 Cl1クーCC0OR* N0CRf        
(31(ここでR1は水素原子又はメチル基、R2は炭
素原子数1〜10のアルキレン基、シクロアルキレン基
、了り−レン基又はアラルキレン基、 R3は水素原子
又は炭素原子数1〜10のアルキレン基1 シクロアル
キル基、アリール基又はアラルキル基、Rfはその炭素
原子上の水素原子の一部又は全部をフッ素原子で置換し
た炭素原子数7〜30のフルオロアルキル基を示す。ま
た、R1゜R3の炭素原子上の水素原子は一部又は全部
がフッ素もしくは塩素原子で置換されていてもよい。)
tb+f記一般式(4)で表される含フツ素ウレタン化
合物。
I CH2= CC00Rf fil
RI R3 Ch = CC00Rt NOa SRf
(21RI R3 Cl1cu CC0OR* N0CRf
(31 (Here, R1 is a hydrogen atom or a methyl group, R2 is an alkylene group having 1 to 10 carbon atoms, a cycloalkylene group, an aralkylene group, or an aralkylene group, and R3 is a hydrogen atom or a methyl group having 1 to 10 carbon atoms. Alkylene group 1 Cycloalkyl group, aryl group or aralkyl group, Rf represents a fluoroalkyl group having 7 to 30 carbon atoms in which some or all of the hydrogen atoms on the carbon atoms are substituted with fluorine atoms.Also, R1° Part or all of the hydrogen atoms on the carbon atoms of R3 may be substituted with fluorine or chlorine atoms.)
tb+f A fluorine-containing urethane compound represented by the general formula (4).

Rf 0CON+(−R4−N)ICOORf    
  (41(’R4ば炭素原子数2〜20のアルキレン
基、シクロアルキレン基、アリーレン基又はアラルキレ
ン基、Rfは既述の基を示す。) (C1下記一般式(5)で表される繰り返し単位を有す
る含フツ素ポリエステル。
Rf 0CON+(-R4-N)ICOORf
(41 ('R4 represents an alkylene group having 2 to 20 carbon atoms, a cycloalkylene group, an arylene group, or an aralkylene group, and Rf represents the group described above.) (C1 Repeating unit represented by the following general formula (5) A fluorine-containing polyester having

Rf ■ 一0OC−R4−COO−R5−(51(Rsは炭素原
子数2〜10の3価の炭化水素基。
Rf 10OC-R4-COO-R5-(51 (Rs is a trivalent hydrocarbon group having 2 to 10 carbon atoms).

R4,Rfは既述の基を示す。) 本発明の繊維は、その表面が含量・ノ素化合物の皮膜で
被覆されていることが特徴であり、紡糸孔から吐出後、
製編織前の任意の工程で皮膜形成が行われる。この場合
、公知の方法が適用されるが特に好ましいのは未延伸繊
維糸条に含量・ノ素化合物を含有する液を適量付着させ
た後、該糸条の延伸と該含フツ素化合物の熱固着処理を
同時又は別別に行う方法であり(熱固着処理は製編織後
でもよい。)未延伸繊維糸条から直接に含量・ノ素化合
物で被覆された繊維が得られる効果の他、皮膜と繊維と
の密着性が優れているという利点もある。
R4 and Rf represent the groups described above. ) The fiber of the present invention is characterized in that its surface is coated with a film of a chemical compound, and after being discharged from the spinning hole,
Film formation is performed at an arbitrary step before weaving. In this case, known methods can be applied, but it is particularly preferable to apply an appropriate amount of a liquid containing the nitrogen compound to the undrawn fiber yarn, and then draw the yarn and heat the fluorine-containing compound. This method performs fixation treatment simultaneously or separately (thermal fixation treatment may be performed after knitting and weaving).In addition to the effect of obtaining fibers coated with a high content of nitrogen compounds directly from undrawn fiber threads, it also has the effect of forming a film and Another advantage is that it has excellent adhesion to fibers.

そして繊維上に形成される含量・ソ素化合物の皮膜はそ
のフッ素含量が15重量%以上、好ましくは20重量%
以上であることがよく、皮膜の量は繊維に対して0.0
5重量%以上となるようにすることが好ましい。
The fluorine content of the fluorine compound film formed on the fiber is 15% by weight or more, preferably 20% by weight.
The amount of film is often 0.0 or more with respect to the fiber.
It is preferable that the amount is 5% by weight or more.

本発明の繊維は防汚用途ばかりでなく、いわゆる通気透
湿防水布帛への展開も可能である(この場合には細繊度
の糸を使用することが好ましい。)。
The fibers of the present invention can be used not only for antifouling purposes, but also for use in so-called breathable, moisture-permeable, and waterproof fabrics (in this case, it is preferable to use fine-grained yarns).

なお2本発明は染色不要な防汚性繊維を提供することを
主たる目的とするものであるが、場合によっては例えば
他の未着色繊維との混紡品、混繊品、混編品の形で染色
してもよいことばもちろんである。また、繊維中にH燃
剤、帯電防止剤などを含有させてもよいことは言うまで
もない。
2. Although the main purpose of the present invention is to provide stain-resistant fibers that do not require dyeing, it may be possible to provide stain-resistant fibers in the form of blends, blends, or knits with other uncolored fibers. Of course, the words may be dyed. It goes without saying that the fibers may also contain an H fuel agent, an antistatic agent, and the like.

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 2−バーフルオ口オクチルエチルアクリレート70重量
%、塩化ビニル25重量%、2−クロロエチルビニルエ
ーテル3重量%、2−ヒドロキシエチルアクリレート2
重量%からなる共重合体の水性乳化液(濃度30重量%
)6重量部、オレイルステアレー1−2重量部、ポリエ
チレンオキシド(分子量1’ooO)  2重量部、モ
ノラウリルホスフェートのカリウム塩0.1重量部及び
水90重量部からなる分散液を調製した。
Example 2 - 70% by weight of barfluoroctyl ethyl acrylate, 25% by weight of vinyl chloride, 3% by weight of 2-chloroethyl vinyl ether, 2-hydroxyethyl acrylate 2
Aqueous emulsion of copolymer consisting of % by weight (concentration 30% by weight)
), 1-2 parts by weight of oleyl stearate, 2 parts by weight of polyethylene oxide (molecular weight 1'ooO), 0.1 parts by weight of potassium salt of monolauryl phosphate, and 90 parts by weight of water.

この分散液を、紺青を0.5重量%分散させたポリエチ
レンテレフタレートを熔融紡糸する際に。
This dispersion was used when melt spinning polyethylene terephthalate in which 0.5% by weight of Prussian blue was dispersed.

紡糸口金から走下する三葉状断面の糸条に対して20重
量%付着させて800m /分の速度で巻き取った。
20% by weight of the yarn was attached to the trilobal cross-section yarn running down from the spinneret, and the yarn was wound at a speed of 800 m/min.

次いで、この未延伸糸を延伸温度90°C2延伸倍率3
.5倍、延伸速度1,500m/分で延伸し、引き続き
 270℃のエアジェツトで熱加工して1300d/6
8f、強度4.1g/d、伸度38%の糸条を得た。
Next, this undrawn yarn was stretched at a stretching temperature of 90°C and a stretching ratio of 3.
.. Stretched 5 times at a stretching speed of 1,500 m/min, then heat-treated with an air jet at 270°C to 1300 d/6.
A yarn with a diameter of 8 f, a strength of 4.1 g/d, and an elongation of 38% was obtained.

ごの糸条を2ブライで撚糸し、常法によりタフティング
1で、目付800 g/ mfのレヘルループカーペッ
トとした。得られた青色カーベントについて、水洗、乾
燥後、撥水性及び撥油性を調べたとごろ9次の結果が得
られた。
The yarns were twisted with 2 briers and tufted with 1 tuft in a conventional manner to form a leher loop carpet with a basis weight of 800 g/mf. After washing and drying the obtained blue carpet, water repellency and oil repellency were examined, and the following results were obtained.

(111a 水4a :イソブロビルアルコール、/水
の体積比20/ 80の混合液の1滴(約0.3m’l
)をカーペット上に置いたが、5分経過後も液は浸透し
なかった。
(111a Water 4a: 1 drop of a mixture of isobrobyl alcohol and water at a volume ratio of 20/80 (approximately 0.3 ml)
) was placed on the carpet, but the liquid did not penetrate even after 5 minutes.

(2)撥油性: AATC−TM118法で測定したと
ころ、撥油性は6級を示した。
(2) Oil repellency: When measured by the AATC-TM118 method, the oil repellency showed grade 6.

特許出願人 ユニ子力株式会社Patent applicant: Unikorikiki Co., Ltd.

Claims (2)

【特許請求の範囲】[Claims] (1)有彩色に原液着色された重合体からなる繊維であ
っ乙その表面が含フツ素化合物で被覆されていることを
特徴とする防汚性原着繊維。
(1) An antifouling, source-dyed fiber characterized by being a fiber made of a chromatic solution-colored polymer, the surface of which is coated with a fluorine-containing compound.
(2)重合体が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である特許請求の範囲第1項
記載の繊維。
(2) The fiber according to claim 1, wherein the polymer is polyethylene terephthalate or a polyester containing polyethylene terephthalate as a main component.
JP1932983A 1983-02-07 1983-02-07 Anti-stain raw fiber Pending JPS59144677A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1932983A JPS59144677A (en) 1983-02-07 1983-02-07 Anti-stain raw fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1932983A JPS59144677A (en) 1983-02-07 1983-02-07 Anti-stain raw fiber

Publications (1)

Publication Number Publication Date
JPS59144677A true JPS59144677A (en) 1984-08-18

Family

ID=11996366

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1932983A Pending JPS59144677A (en) 1983-02-07 1983-02-07 Anti-stain raw fiber

Country Status (1)

Country Link
JP (1) JPS59144677A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01306647A (en) * 1988-06-03 1989-12-11 Toray Ind Inc Pile cloth

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01306647A (en) * 1988-06-03 1989-12-11 Toray Ind Inc Pile cloth

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