JPS6197473A - Antistaining synthetic fiber - Google Patents
Antistaining synthetic fiberInfo
- Publication number
- JPS6197473A JPS6197473A JP59212221A JP21222184A JPS6197473A JP S6197473 A JPS6197473 A JP S6197473A JP 59212221 A JP59212221 A JP 59212221A JP 21222184 A JP21222184 A JP 21222184A JP S6197473 A JPS6197473 A JP S6197473A
- Authority
- JP
- Japan
- Prior art keywords
- fluorine
- antifouling
- fiber
- synthetic fiber
- weight
- 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
Landscapes
- Artificial Filaments (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
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】
(産業上の利用分野)
本発明は、良好な光沢を有し、工程通過性の優れた防汚
性合成繊維に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to an antifouling synthetic fiber having good gloss and excellent processability.
(従来の技術)
繊維製品、特にスポーツ着、雨衣、カーペットなどに撥
水性、撥油性、耐液体汚染性、耐乾燥汚染性などの防汚
性能を付与する方法として、その表面をフッ素系防汚剤
で処理する方法が一般的に採用されている。その処理方
法としては、従来。(Prior technology) As a method of imparting stain-proofing properties such as water repellency, oil repellency, liquid stain resistance, and dry stain resistance to textile products, especially sportswear, raincoats, carpets, etc., the surface thereof is treated with fluorine-based stain resistance. A method of treatment with a chemical agent is generally adopted. Conventional methods are used to process it.
製品に後処理加工する方法が中心であり、工程が複雑化
し、操業性の低下、コストアンプにつながる欠点がある
。このため、近年、繊維形成直後の繊維糸条にフッ素化
合物を固着させる方法が提案され、一部はすでに実用化
の段階に至っている。This method mainly involves post-processing the product, which has the disadvantage of complicating the process, reducing operability, and increasing costs. For this reason, in recent years, methods have been proposed for fixing fluorine compounds to fiber threads immediately after fiber formation, and some of these methods have already reached the stage of practical application.
しかしながら、この種の防汚性繊維は、一般に二酸化チ
タンのような艶消剤を含まない光沢を有する繊維であり
、摩擦抵抗が大きく、工程通過性が悪いという問題があ
った。すなわち、原糸製造工程あるいは加工工程でピン
、ローラ、ガイド等と接触するとき、トラブルを起こし
易い。However, this type of antifouling fiber is generally a glossy fiber that does not contain a matting agent such as titanium dioxide, and has the problem of high frictional resistance and poor processability. That is, troubles are likely to occur when it comes into contact with pins, rollers, guides, etc. during the yarn manufacturing process or processing process.
(発明が解決しようとする問題点) 題とするものである。(Problem that the invention attempts to solve) This is the subject.
(問題点を解決するための手段)
本発明は上記課題を解決するもので、その要旨は平均粒
子径0.1〜3μのシリカ粒子を含有した重合体からな
り、その表面がフッ素系防汚剤を含有した皮膜で被覆さ
れていることを特徴とする防汚性合成繊維にある。(Means for Solving the Problems) The present invention solves the above problems, and its gist is that the present invention is made of a polymer containing silica particles with an average particle diameter of 0.1 to 3μ, and the surface thereof is fluorine-based antifouling. A stain-resistant synthetic fiber characterized by being coated with a film containing an agent.
本発明において繊維を形成する重合体はポリエチレンテ
レフタレ〜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。In the present invention, the polymer forming the fibers is polyethylene terephthalate ~1-. Polybutylene terephthalate, etc., and polyesters containing these as main components.
ナイロン6、ナイロン66など及びこれらを主成分とす
るポリアミド、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のごとき溶融紡糸
可能な重合体の他、湿式紡糸。In addition to melt-spinning polymers such as nylon 6, nylon 66, polyamides containing these as main components, polyethylene, polypropylene, etc., and polyolefins containing these as main components, wet spinning.
乾式紡糸あるいはエマルジョン紡糸可能な繊維形成重合
体である。It is a fiber-forming polymer that can be dry-spun or emulsion-spun.
次に、本発明において、繊維表面を被覆するフ素系防’
IT3剤としては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-based protective film that coats the fiber surface is
Typical IT3 drugs include the following.
(a)下記一般式(1)〜(3)で表される含フツ素モ
ノマー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モノマーと
を共重合したポリマー。(a) A polymer obtained by homopolymerizing or copolymerizing fluorine-containing monomers represented by the following general formulas (1) to (3), or a polymer obtained by copolymerizing these monomers and other monomers not containing fluorine atoms.
CI+2= CC00Rf (11
R+ R3
co2= CCOOR2NSO□I?f (2)
RI R3
「
ClI2 = CCOOR2NC0Rf (3
)(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、ア
リーレン基又はアラルキレン基。CI+2=CC00Rf (11
R+ R3 co2= CCOOR2NSO□I? f (2)
RI R3 "ClI2 = CCOOR2NC0Rf (3
) (Here, R1 is a hydrogen atom or a methyl group, and R2 is an alkylene group having 1 to 10 carbon atoms, a cycloalkylene group, an arylene group, or an aralkylene group.
R3は水素原子又は炭素原子数1〜10のアルキル基、
シクロアルキル基、アリール基又はアラルキル基、 R
fはその炭素原子上の水素原子の一部又は全部をフン素
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。R3 is a hydrogen atom or an alkyl group having 1 to 10 carbon atoms,
Cycloalkyl group, aryl group or aralkyl group, R
f 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.
R2,R3の炭素原子上の水素原子の一部又は全部がフ
ッ素もしくは塩素原子で置換されていてもよい。)
(bl下記一般式(4)で表される含フツ素ウレタン化
合物。Some or all of the hydrogen atoms on the carbon atoms of R2 and R3 may be substituted with fluorine or chlorine atoms. ) (bl A fluorine-containing urethane compound represented by the following general formula (4).
Rf 0OCNII−R4−N11COOI?f
f41(R,lは炭素原子数2〜20の2価の有機
基で。Rf 0OCNII-R4-N11COOI? f
f41 (R and l are divalent organic groups having 2 to 20 carbon atoms.
−O−、−SO□−2〜coo−、−co−。-O-, -SO□-2~coo-, -co-.
−N(R3)−などの結合を含んでもよい。It may also contain a bond such as -N(R3)-.
R,、Rfは既述の基を示す。)
(C)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。R, and Rf represent the groups described above. ) (C) A fluorine-containing polyester having a repeating unit represented by the following general formula (5).
Rf
00CRa Coo Rs (51(R
5は炭素原子数2〜lOの3価の炭化水素基。Rf 00CRa Coo Rs (51(R
5 is a trivalent hydrocarbon group having 2 to 10 carbon atoms.
R,、Rfは既述の基を示す。)
本発明において、繊維を形成する重合体中に含有させる
シリカ粒子は、その平均粒子径が0.1〜3μのもので
あることが必要であり、特に0.2〜2μのものが好ま
しい。平均粒子径が0.18未満では滑りをよくする効
果が乏しく13μを超えると繊維の物性及び製糸性を低
下させる。シリカ粒子の配合量は重合体に対して0.0
2〜2重量%、特に0.05〜1.5重量%が好ましい
。R, and Rf represent the groups described above. ) In the present invention, the silica particles contained in the polymer forming the fibers must have an average particle diameter of 0.1 to 3 μm, and preferably 0.2 to 2 μm. When the average particle diameter is less than 0.18, the effect of improving slippage is poor, and when it exceeds 13μ, the physical properties of the fiber and the spinning properties are deteriorated. The blending amount of silica particles is 0.0 with respect to the polymer.
2 to 2% by weight, especially 0.05 to 1.5% by weight are preferred.
本発明の繊維は公知の方法を応用して製造することがで
きる。すなわち、紡糸以前の任意の工程でシリカ粒子(
シリカゾルでもよい)を繊維形成用重合体に配合し、紡
糸孔から吐出後の任意の工程でフッ素系防汚剤液で処理
して皮膜形成を行う方法である。特に好ましいのは未延
伸繊維糸条にフッ素系防汚剤を含有する液を適量付着さ
せた移譲糸条の延伸とフッ素系防汚剤の熱固着処理を同
時又は別々に行う方法であり(熱固着処理は製編織後で
もよい。)、繊維形成工程で直接に防汚性繊維が得られ
る効果の他、フッ素系防汚剤の皮膜と繊維との密着性が
優れているという利点もある。The fiber of the present invention can be manufactured by applying a known method. In other words, silica particles (
This method involves blending a fiber-forming polymer (which may also be silica sol) into a fiber-forming polymer, and treating it with a fluorine-based antifouling agent liquid at an arbitrary step after it is discharged from a spinning hole to form a film. Particularly preferred is a method in which an appropriate amount of a liquid containing a fluorine-based antifouling agent is attached to an undrawn fiber yarn, and then drawing of the transferred yarn and heat fixing treatment of the fluorine-based antifouling agent are carried out simultaneously or separately (heat treatment). (The fixing treatment may be carried out after knitting and weaving.) In addition to the effect that antifouling fibers can be obtained directly in the fiber forming process, there is also the advantage that the adhesion between the fluorinated antifouling agent film and the fibers is excellent.
また、繊維の染色性を向上させるために防汚剤と湿潤剤
(含フッ素系のものが好ましい)を併用することも可能
であり、防汚性能を阻害することなく染色性を良好にで
きる点で好ましい。In addition, it is also possible to use an antifouling agent and a wetting agent (preferably a fluorine-containing agent) together to improve the dyeability of the fibers, which can improve the dyeability without impairing the antifouling performance. It is preferable.
フッ素防汚剤の量は、繊維に対して0.05〜0.5重
量%、特に0.1〜0.3重量%とするのが、シリ力粒
子配合による効果を阻害することなく、防汚性を44L
テできる点で好ましい。The amount of the fluorine antifouling agent should be 0.05 to 0.5% by weight, especially 0.1 to 0.3% by weight based on the fiber, without impairing the effect of the silicate particles. 44L of dirtiness
This is preferable because it allows you to
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。(この場合には単糸
繊度の小さい糸を使用することが好ましい。)また、繊
維内部や表面にテ1(燃剤、帯電防止剤2柔軟化剤など
を導入してもよいことば言うまでもない。特に繊維内部
にもフッ素化合物を導入すると繊維と防汚剤皮膜との密
着性が向」ニして好ましい。The fibers of the present invention can be used not only for antifouling purposes, but also for so-called breathable and moisture-permeable waterproof fabrics. (In this case, it is preferable to use a yarn with a small single filament fineness.) It goes without saying that it is also possible to introduce a fuel, an antistatic agent, a softening agent, etc. into the interior or surface of the fiber. It is preferable to introduce a fluorine compound into the inside of the fibers as this improves the adhesion between the fibers and the antifouling film.
(実施例)
以下、実施例によって本発明をさらに具体的に説明する
が、18水性及び18油性は次の方法で評価したもので
ある。(Example) Hereinafter, the present invention will be explained in more detail with reference to Examples, and 18 water-based and 18 oil-based were evaluated by the following method.
(]) jQ 水性: 体積比30/70のイソプロピ
ルアルコール/水混合液の1滴(約0.3m1)を試験
布−1−に静かに置き、5分後に浸み込まない場合を良
好とした。(]) jQ Aqueous: One drop (approximately 0.3 ml) of isopropyl alcohol/water mixture with a volume ratio of 30/70 was gently placed on the test cloth -1-, and the case where it did not soak in after 5 minutes was considered good. .
(2)撥油性: AATC(’ニーT門118法に拠っ
た。(2) Oil repellency: Based on AATC ('Nie T Gate 118 method).
実施例及び比較例
ε−カプロラクタム85重量部、水15重量部及び第1
表に示したシリカ粒子を攪拌機付オートクレーブに仕込
み、温度を250°Cに保って、制圧期(6kg/cJ
) 2時間、放圧器2時間、常圧期2時間の条件で重縮
合を行い、96%硫酸中。Examples and Comparative Examples 85 parts by weight of ε-caprolactam, 15 parts by weight of water and
The silica particles shown in the table were charged into an autoclave equipped with a stirrer, and the temperature was maintained at 250°C.
) Polycondensation was carried out under the conditions of 2 hours in a pressure relief vessel and 2 hours in a normal pressure period in 96% sulfuric acid.
25°Cで測定した固有粘度が約1.2のナイロン6チ
ップを得た。Nylon 6 chips with an intrinsic viscosity of about 1.2 measured at 25°C were obtained.
このナイロン6チップをエクスI・ルーグー型溶融紡糸
機に供給して270°C紡糸した。その際。The nylon 6 chips were fed to an Ex-I-Rougu type melt spinning machine and spun at 270°C. that time.
紡糸口金から走下する36フイラメントの糸条に対して
、2−パーフルオロ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31Tif1%、2−ヒドロキシエチルアクリ
レ−1・2重量%からなる共重合体4重量部及びフッ素
系湿潤剤
(C8F、70CNll (CHz)J (C)13
)3) C1゜1重量部を鉱物油系油剤液95重量部に
分散させた液を繊維に対して7重量%付着させて400
0m/minで引取り、90°Cの熱ローラで1.1倍
に延伸した後巻き取った。For the yarn of 36 filaments running down from the spinneret, 70% by weight of 2-perfluorooctylethyl acrylate, 25% by weight of vinyl chloride, 1% of 2-chloroethyl vinyl ether 31Tif, 1.2% of 2-hydroxyethyl acrylate. 4 parts by weight of a copolymer consisting of
) 3) 7% by weight of a solution prepared by dispersing 1 part by weight of C1° in 95 parts by weight of a mineral oil-based oil solution was applied to the fibers to form a 400%
The film was taken up at 0 m/min, stretched to 1.1 times with a heated roller at 90°C, and then wound up.
得られた延伸糸について、春日電気社製毛羽発見器で毛
羽数を測定した。The number of fluffs of the obtained drawn yarn was measured using a fluff detector manufactured by Kasuga Electric Co., Ltd.
また、延伸糸を経110本/2.54cm、緯100木
/2.54cmの密度でタフタに製織し、酸性染料を含
む染浴中で、98℃で1時間染色した。得られた布を1
05℃、1時間の条件で乾燥後、撥水、t8油性を測定
した。測定結果を第1表に示す。Further, the drawn yarn was woven into taffeta at a density of 110 warps/2.54 cm and weft 100 threads/2.54 cm, and dyed at 98° C. for 1 hour in a dye bath containing an acid dye. 1 of the obtained cloth
After drying at 05°C for 1 hour, water repellency and T8 oiliness were measured. The measurement results are shown in Table 1.
なお、上記の染色布はいずれも良好な光沢を有していた
。Note that all of the above dyed fabrics had good gloss.
第 1 表
(発明の効果)
以上のように、本発明によれば良好な光沢を有し、工程
通過性の優れた防汚性合成繊維が提供される。Table 1 (Effects of the Invention) As described above, according to the present invention, a stain-resistant synthetic fiber having good gloss and excellent process passability is provided.
Claims (3)
重合体からなり、その表面がフッ素系防汚剤を含有した
皮膜で被覆されていることを特徴とする防汚性合成繊維
。(1) An antifouling synthetic fiber made of a polymer containing silica particles with an average particle diameter of 0.1 to 3 μm, the surface of which is coated with a film containing a fluorine antifouling agent.
%である特許請求の範囲第1項記載の防汚性合成繊維。(2) The antifouling synthetic fiber according to claim 1, wherein the content of silica particles is 0.02 to 2% by weight of the polymer.
量%である特許請求の範囲第1項記載の防汚性合成繊維
。(3) The antifouling synthetic fiber according to claim 1, wherein the amount of the fluorine antifouling agent is 0.05 to 0.5% by weight of the fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59212221A JPS6197473A (en) | 1984-10-09 | 1984-10-09 | Antistaining synthetic fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59212221A JPS6197473A (en) | 1984-10-09 | 1984-10-09 | Antistaining synthetic fiber |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6197473A true JPS6197473A (en) | 1986-05-15 |
Family
ID=16618947
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59212221A Pending JPS6197473A (en) | 1984-10-09 | 1984-10-09 | Antistaining synthetic fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6197473A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7655609B2 (en) | 2005-12-12 | 2010-02-02 | Milliken & Company | Soil release agent |
JP2019052411A (en) * | 2017-09-11 | 2019-04-04 | 展頌股▲ふん▼有限公司 | Deodorized nylon 6 fiber and method for producing the same |
-
1984
- 1984-10-09 JP JP59212221A patent/JPS6197473A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7655609B2 (en) | 2005-12-12 | 2010-02-02 | Milliken & Company | Soil release agent |
JP2019052411A (en) * | 2017-09-11 | 2019-04-04 | 展頌股▲ふん▼有限公司 | Deodorized nylon 6 fiber and method for producing the same |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5025052A (en) | Fluorochemical oxazolidinones | |
CA1323370C (en) | Fluorochemical oxazolidinones | |
US3639154A (en) | Process for manufacturing fibrous structure having excellent recovery from extension by treatment with polyorganosiloxane and a polyethylene glycol or derivative thereof | |
AU2274397A (en) | Carpet yarn having high soil resistance | |
JPS5994621A (en) | Production of antistaining fiber | |
JPS6197473A (en) | Antistaining synthetic fiber | |
US3963437A (en) | Flame retardant process for cellulosic material including cyanamide, phosphonic acid, antimony oxide and polymeric halogen-containing material | |
US6426025B1 (en) | Process for extruding fibers | |
JPH07500884A (en) | Antifouling monofilament for paper machine filters, its manufacturing method and its uses | |
Redston et al. | Chemicals used as spin-finishes for man-made fibers | |
JPS60173166A (en) | Polyamide fabric | |
US2874023A (en) | Static-resistant hydrophobic resin composition, shaped article thereof and method formaking the latter | |
JPS5930919A (en) | Water repellency, oil repellency, and antifouling treatment of synthetic yarn | |
AU742193B2 (en) | Process for extruding fibers | |
JPS60224874A (en) | Anti-staining synthetic fiber | |
JPS61245370A (en) | Antistaining synthetic fiber | |
JPS60126374A (en) | Anti-staining synthetic fiber | |
JPS6359482A (en) | Production of antistaining synthetic fiber | |
US3371052A (en) | Polyepoxide compositions for rendering synthetic fibers free and undiscolored and process of utilizing same | |
JPH01148877A (en) | Production of antistaining synthetic fiber | |
JPS636114A (en) | Production of stainproof synthetic yarn | |
JPS5966570A (en) | Production of modified polyester fiber | |
JPS6155215A (en) | Antistatic polyester fiber | |
JPH0144837B2 (en) | ||
US2872424A (en) | Fiber-forming composition comprising cellulose acetate and acrylonitrile copolymer and fiber consisting essentially of same |