JP2873979B2 - Method for modifying hydrophilic surface of polyester fiber - Google Patents

Method for modifying hydrophilic surface of polyester fiber

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Publication number
JP2873979B2
JP2873979B2 JP1581691A JP1581691A JP2873979B2 JP 2873979 B2 JP2873979 B2 JP 2873979B2 JP 1581691 A JP1581691 A JP 1581691A JP 1581691 A JP1581691 A JP 1581691A JP 2873979 B2 JP2873979 B2 JP 2873979B2
Authority
JP
Japan
Prior art keywords
fiber
weight
polyester fiber
polyester
water
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.)
Expired - Fee Related
Application number
JP1581691A
Other languages
Japanese (ja)
Other versions
JPH04214466A (en
Inventor
泰史 山口
秋郎 田中
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.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon Co Ltd
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Filing date
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Application filed by Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP1581691A priority Critical patent/JP2873979B2/en
Publication of JPH04214466A publication Critical patent/JPH04214466A/en
Application granted granted Critical
Publication of JP2873979B2 publication Critical patent/JP2873979B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、吸水性、吸湿性、ソイ
ルレリーズ(SR)性及び制電性に優れ、かつ耐洗濯性
及び染色堅牢性に優れたポリエステル繊維の表面改質方
法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for modifying the surface of a polyester fiber which is excellent in water absorption, moisture absorption, soil release (SR) and antistatic properties, and is excellent in washing resistance and dyeing fastness.

【0002】[0002]

【従来の技術】ポリエステル繊維を親水化する方法とし
て、一殻に繊維表面に加工剤を付与する方法があるが、
吸水性は向上するが吸湿性は向上せず、又、その耐久性
能が悪く、更に堅牢度の低下が懸念され十分とは言い難
い。特昭63−196768号公報には、ケトン基含
有ポリエステル繊維にアクリル酸及びメタクリル酸をグ
ラフト重合し、更にカルボキシル基をアルカリ金属塩に
して親水化する方法が提案されている。
2. Description of the Related Art As a method for hydrophilizing polyester fibers, there is a method in which a processing agent is applied to the fiber surface in one shell.
Although water absorbency is improved, moisture absorbency is not improved, and its durability is poor, and furthermore, it is hard to say that it is sufficient because of the fear of a decrease in fastness. In Japanese Open Sho 63-196768 discloses, acrylic acid and methacrylic acid graft-polymerized to the ketone group-containing polyester fibers, have been proposed further methods of hydrophilizing in the alkali metal salt of carboxyl group.

【0003】しかしながら、この方法で得られた繊維
は、吸水性、吸湿性、制電性良好であり、かつ耐久性に
も優れるが、繊維の強力の低下を来たし、又染色堅牢度
の面に問題がある。
[0003] However, the fiber obtained by this method is excellent in water absorbency, moisture absorbency and antistatic properties and also excellent in durability, but has a reduced strength of the fiber and has a poor dyeing fastness. There's a problem.

【0004】[0004]

【発明が解決しようとする課題】本発明は、かかる従来
のポリエステル繊維の親水化加工の問題点を解決し、耐
久性に優れた吸水性、吸湿性、SR性及び制電性を有し
かつ堅牢度良好なポリエステル繊維の親水化表面改質方
法を提供しようとするものである。
SUMMARY OF THE INVENTION The present invention solves the problems of the conventional hydrophilic treatment of polyester fiber, and has excellent water-absorbing, hygroscopic, SR and antistatic properties. An object of the present invention is to provide a method for modifying a hydrophilic surface of a polyester fiber having good fastness.

【0005】[0005]

【課題を解決するための手段】本発明は、ポリエステル
繊維にカルボキシル基含有不飽和ビニルモノマー0.5
〜20重量%(対繊維)及びメラミン誘導体化合物1〜
20重量%(対繊維)を含む水溶液を付着させ熱処理し
た後、金属イオン吸着処理を施すことを特徴とする吸湿
性ポリエステル繊維の親水化表面改質方法にある。
SUMMARY OF THE INVENTION The present invention relates to a method for producing a carboxyl group-containing unsaturated vinyl monomer in a polyester fiber.
-20% by weight (based on fiber) and melamine derivative compound 1
A method for modifying a hydrophilic surface of a hygroscopic polyester fiber, comprising applying an aqueous solution containing 20% by weight (relative to the fiber), heat-treating the resultant, and then performing metal ion adsorption treatment.

【0006】更に本発明は、分子量2,000〜20
0,000のポリエチレングリコールを0.1〜5重量
%含有するポリエステル繊維を5〜30重量%のアルカ
リ減量を行った後上記の親水化表面改質方法を施すこと
を包含する。
Further, the present invention provides a method for producing a polymer having a molecular weight of
The method includes subjecting a polyester fiber containing 0.1 to 5% by weight of polyethylene glycol of 000 to a weight reduction of 5 to 30% by weight to an alkali, and then performing the above-mentioned hydrophilic surface modification method.

【0007】本発明で使用されるカルボキシル基含有不
飽和ビニルモノマーとしては、アクリル酸、メタクリル
酸、イタコン酸等が挙げられるが、これらに限定される
ものではない。またこれらビニルモノマーは2種以上の
混合物として使用できる。繊維へのカルボキシル基含有
不飽和ビニルモノマーの付着量は0.5〜20重量%
(対繊維)、カルボキシル基量としては、0.02mm
ol/g以上0.6mmol/g未満である。ビニルモ
ノマーの付着量が0.5重量%未満では充分な吸水性、
吸湿性、SR性及び制電性が得られず、また20重量%
を超えると繊維の風合いが硬化する。
The carboxyl group-containing unsaturated vinyl monomer used in the present invention includes, but is not limited to, acrylic acid, methacrylic acid, itaconic acid and the like. These vinyl monomers can be used as a mixture of two or more kinds. The amount of the carboxyl group-containing unsaturated vinyl monomer attached to the fiber is 0.5 to 20% by weight.
(To fiber), the amount of carboxyl group is 0.02 mm
ol / g or more and less than 0.6 mmol / g . If the adhesion amount of the vinyl monomer is less than 0.5% by weight, sufficient water absorption,
Hygroscopicity, SR property and antistatic property are not obtained, and 20% by weight
If it exceeds, the texture of the fiber hardens.

【0008】カルボキシル基含有不飽和ビニルモノマー
と併用されるメラミン誘導体化合物は、例えばトリメチ
ロール、ヘキサメチロール、トリブチロール化メラミン
等の化合物が挙げられ、繊維への付着量は1〜20重量
%(対繊維)である。付着量が1重量%未満では、繊維
表面に形成される被膜が弱く簡単に性能が低下してしま
うおそれがある。また付着量が20重量%を超えると被
膜は強固となるが、単繊維間の接着が発生し風合いが硬
化する。
The melamine derivative compound used in combination with the carboxyl group-containing unsaturated vinyl monomer includes, for example, compounds such as trimethylol, hexamethylol, and tributyrolated melamine. ). If the amount is less than 1% by weight, the film formed on the fiber surface may be weak and the performance may be easily reduced. On the other hand, if the amount exceeds 20% by weight, the film becomes strong, but the adhesion between the single fibers occurs and the texture hardens.

【0009】付着処理は、カルボキシル基含有不飽和ビ
ニルモノマー及びメラミン誘導体化合物を含む水溶液の
浴に浸漬する方法が好ましく用いられる。
For the adhesion treatment, a method of immersing in an aqueous solution bath containing a carboxyl group-containing unsaturated vinyl monomer and a melamine derivative compound is preferably used.

【0010】熱処理の方法は、乾熱方式、コールドバッ
チ方式、スチーミング方式、または浴中で熱処理と付着
処理を同時に行なう浴中処理方式が挙げられる。熱処理
の温度は何れの方法においても40℃以上で行なうこと
が望ましい。スチーミング方式の場合は90〜130℃
で5〜30分の飽和蒸熱処理、コールドバッチ方式では
40〜100℃で10〜120分の熱処理、乾熱方式の
場合は150〜200℃で1〜5分の処理が望しい。浴
中処理方式の場合は、40〜100℃で5〜60分の処
理が望ましい。また必要に応じて触媒等を添加すること
も可能である。
The method of heat treatment includes a dry heat method, a cold batch method, a steaming method, and a treatment method in a bath in which heat treatment and adhesion treatment are simultaneously performed in a bath. The heat treatment is preferably performed at a temperature of 40 ° C. or more in any method. 90-130 ° C for the steaming method
It is preferable to perform a saturated steam heat treatment at 5 to 30 minutes, a heat treatment at 40 to 100 ° C. for 10 to 120 minutes in the cold batch method, and a treatment at 150 to 200 ° C. for 1 to 5 minutes in the dry heat method. In the case of the in-bath treatment method, treatment at 40 to 100 ° C. for 5 to 60 minutes is desirable. It is also possible to add a catalyst or the like as needed.

【0011】次に、このように処理された繊維に金属イ
オンを吸着させる。本発明でいう金属イオンとは、ナト
リウム、カリウム等のアルカリ金属イオン、カルシウ
マグネシウム等のアルカリ土類金属イオン、亜鉛、
ニッケル、コバルト等の遷移金属イオン、その他アルミ
ニウム、チタン、ジルコニウム、銅、銀等のイオンを含
み、本発明の目的を妨げないものであれば何れの金属イ
オンも使用することが出来る。
Next, metal ions are adsorbed on the fiber thus treated. The metal ions referred to in the present invention include alkali metal ions such as sodium and potassium, and calcium ions.
Beam, alkaline earth metal ions, zinc and magnesium,
Any metal ion including transition metal ions such as nickel and cobalt, and ions of aluminum, titanium, zirconium, copper, silver and the like can be used as long as the object of the present invention is not hindered.

【0012】これ等の金属イオンは、水酸化化合物、炭
酸塩、ハロゲン化物、硝酸塩等の水溶性化合物を水に溶
解させることで容易に得られる。これ等の水溶液中に前
記の処理を施した繊維を浸漬し、必要に応じて50℃以
上に加熱して金属イオンを吸着させる。金属イオンの付
着量は、カルボキシル基含有不飽和ビニルモノマーのカ
ルボキシル基の付着モル量に相当する量結合させること
が好ましく、0.02mmol/g以上0.6mmol
/g未満とすることが望ましい。
These metal ions can be easily obtained by dissolving a water-soluble compound such as a hydroxide compound, a carbonate, a halide and a nitrate in water. The fibers treated as described above are immersed in these aqueous solutions, and if necessary, heated to 50 ° C. or higher to adsorb metal ions. The amount of the metal ion attached is preferably such that the amount corresponds to the amount of the carboxyl group attached to the carboxyl group-containing unsaturated vinyl monomer in an amount of 0.02 mmol / g to 0.6 mmol.
/ G is desirable.

【0013】本発明の親水化表面改質方法が適用できる
ポリエステル繊維は、通常のポリエチレンテレフタレー
主たる構成成分とする繊維である。繊維の形態は繊
維状、織物、編物、不織布状又はその加工品であっても
よい。これ等はまた、通常の染色を行なったものでもよ
い。染色が施されたポリエステル繊維に本発明の表面改
質処理を行っても、繊維表面にメラミン誘導体化合物を
中心とした親水性被膜が形成されるため繊維の強力低下
は殆んどなく、また染色堅牢度の低下もない。
[0013] Polyester fibers hydrophilic surface modification method can be applied to the present invention are fibers whose main component an ordinary polyethylene terephthalate. The form of the fiber may be fibrous, woven, knitted, non-woven, or a processed product thereof. These may also be those that have been subjected to normal dyeing. Even if the dyed polyester fiber is subjected to the surface modification treatment of the present invention, a hydrophilic coating mainly comprising a melamine derivative compound is formed on the fiber surface, so that the fiber strength hardly decreases, and There is no decrease in robustness.

【0014】本発明で使用されるポリエステル繊維は、
上記の如く通常のもので充分であるが、分子量2,00
0〜200,000のポリエチレングリコール0.1〜
5重量%含有するポリエステル繊維を5〜30重量%の
アルカリ減量を行なったものに、本発明の親水化表面改
質方法を施すと、一層制電性に優れたものとなる特徴を
有する。
The polyester fibers used in the present invention are:
As described above, the usual one is sufficient, but the molecular weight is 2,000.
0-200,000 polyethylene glycol 0.1-
When a polyester fiber containing 5% by weight is subjected to an alkali weight reduction of 5 to 30% by weight and the hydrophilic surface modification method of the present invention is applied to the polyester fiber, there is a feature that the antistatic property is further improved.

【0015】このポリエステル繊維は、分子量2,00
0〜200,000のポリエチレングリコールを0.1
〜5重量%含有する。ポリエチレングリコールの分子量
が2,000未満では繊維から脱落し易く、制電性の洗
濯耐久性が得られず、200,000を超えると制電性
及び溶融紡糸時に紡糸性の低下を来すので好ましくな
い。又、繊維中に含有されるポリエチレングリコールの
量が0.1重量%未満では制電性能が十分でなく、5重
量%を超えると、紡糸性の低下及び単繊維の強力低下を
招き易い。
This polyester fiber has a molecular weight of 2,000.
0.1 to 200,000 polyethylene glycol
-5% by weight. If the molecular weight of the polyethylene glycol is less than 2,000, it easily falls off from the fiber, and the antistatic washing durability is not obtained. If the molecular weight exceeds 200,000, the antistatic property and the spinnability at the time of melt spinning decrease, so that it is preferable. Absent. If the amount of polyethylene glycol contained in the fiber is less than 0.1% by weight, the antistatic performance is not sufficient, and if it exceeds 5% by weight, the spinnability and the strength of the single fiber are liable to be reduced.

【0016】アルカリ減量の方法は、上記繊維を水酸化
カリウム、水酸化ナトリウム等のアルカリ水溶液に浸漬
し浴中で処理する方法、又はアルカリ水溶液に浸漬後ニ
ップし、乾熱又は湿熱処理を行う方法等が挙げられる
が、繊維の形態を著しく損なう方法でなければ何れの方
法であってもよい。
The method for reducing the alkali is a method in which the fiber is immersed in an aqueous alkali solution such as potassium hydroxide or sodium hydroxide and treated in a bath, or a method in which the fiber is immersed in an aqueous alkali solution and then nipped and subjected to dry heat or wet heat treatment. Etc., but any method may be used as long as the method does not significantly impair the form of the fiber.

【0017】アルカリ減量率としては、5〜30重量%
が望ましい。減量率が5重量%未満では繊維表面に溝が
十分に生成されず、表面積の増大による性能の向上及び
溝の内部への被膜の形成が減少し、性能向上が期待でき
ない。減量率が30重量%を超えると繊維の強力が低下
する。
The alkali weight loss rate is 5 to 30% by weight.
Is desirable. When the weight loss rate is less than 5% by weight, grooves are not sufficiently formed on the fiber surface, and the performance is improved due to an increase in the surface area and the formation of a coating film inside the grooves is reduced, so that the performance cannot be expected to be improved. When the weight loss rate exceeds 30% by weight, the strength of the fiber decreases.

【0018】アルカリ減量処理したポリエチレングリコ
ール含有ポリエステル繊維は、次いで、前述の方法に従
ってカルボキシル基含有不飽和ビニルモノマー及びメラ
ミン誘導体化合物を含む水溶液を付着させ、熱処理後金
属イオン吸着処理を施してカルボキシル基をアルカリ金
属塩とすることにより一層高い性能が得られる。
The polyethylene fiber containing polyethylene glycol which has been subjected to alkali weight reduction is then adhered to an aqueous solution containing a carboxyl group-containing unsaturated vinyl monomer and a melamine derivative compound according to the method described above, and after heat treatment, is subjected to metal ion adsorption treatment to remove carboxyl groups. Even higher performance can be obtained by using an alkali metal salt.

【0019】ポリエステル繊維は、ポリエチレングリコ
ールを含有させることで、制電性が付与され、さらにア
ルカリ減量により繊維表面に、繊維軸方向に沿った無数
の溝及び繊維を構成するポリエステル分子のアルカリに
よる加水分解で生じたカルボキシル基及び水酸基等が導
入される。このため繊維の表面において樹脂の架橋反応
及びモノマーの重合反応で被膜が形成される際、より広
い表面積及び溝の内部まで被膜が形成される。さらに、
繊維表面のカルボキシル基、水酸基等の極性基により樹
脂被膜の接着性の向上、及びカルボキシル基と樹脂との
架橋反応等により、性能の向上、及び耐久性能の向上が
期待できる。
The polyester fiber is provided with antistatic properties by containing polyethylene glycol, and further has an infinite number of grooves along the fiber axis direction and an alkali hydrolyzed polyester molecule constituting the fiber on the fiber surface due to the reduction in alkali. Carboxyl groups and hydroxyl groups generated by the decomposition are introduced. Therefore, when a film is formed on the surface of the fiber by a crosslinking reaction of a resin and a polymerization reaction of a monomer, the film is formed to a larger surface area and to the inside of the groove. further,
The polar group such as a carboxyl group or a hydroxyl group on the fiber surface can be expected to improve the adhesiveness of the resin film and to improve the performance and the durability by the crosslinking reaction between the carboxyl group and the resin.

【0020】[0020]

【実施例】次に本発明を、実施例により説明する。実施
例中の評価項目の測定は、次の方法で行った。なお実施
例中の%は重量%を意味する。吸湿率;繊維を120℃
で絶乾後20℃×65%RHに24時間放置し、重量増
加より吸湿率を算出した。 吸湿率(%)=吸湿後重量−絶乾重量/絶乾重量×10
0 吸水長;バイレック法JIS−L−1096法 水滴消失;0.01mlの水滴を繊維上へ落し、水滴が完
全に消失するまでの時間(秒) 制電性;摩擦帯電圧法JIS−L1094B法に基づき
20℃×30%RHで対綿布で行った。
Next, the present invention will be described by way of examples. The measurement of the evaluation items in the examples was performed by the following method. In the examples,% means% by weight. Moisture absorption; fiber at 120 ° C
And left at 20 ° C. × 65% RH for 24 hours, and the moisture absorption was calculated from the increase in weight. Moisture absorption (%) = weight after moisture absorption-absolute dry weight / absolute dry weight × 10
0 Water absorption length; Vilec method JIS-L-1096 method Water drop disappearance; Time until 0.01 ml of water drop is dropped on fiber and water drop completely disappears (seconds) Antistatic property: Friction charge voltage method JIS-L1094B method At 20 ° C. × 30% RH with a cotton cloth.

【0021】[0021]

【実施例1】ポリエステル繊維75d/36fの繊維織
物を、トリメチロールメラミン6%、アクリル酸10
%、過硫酸アンモニウム0.5%、有機アミン系酸触媒
2%の水溶液中に浸漬し、ニップ(ピックアップ100
%)して常圧スチーム中で20分間熱処理を行なった。
その後水洗し、硫酸ニッケル1%の水溶液に浸漬し、沸
騰状態で20分間処理する。次いで充分水洗した後、乾
燥し、親水化ポリエステル繊維織物を得た。得られた織
物の吸水性、SR性を測定したところ表1に示すように
良好であり、堅牢度の低下もなく、洗濯耐久性も良好で
あった。堅牢度の評価は、Dianix Rubine FG-SE (三菱
化成(株)製分散染料)4%OWFを130℃×60分
で染色した試料で測定した。
EXAMPLE 1 A fiber woven fabric composed of 75d / 36f polyester fibers was prepared by adding 6% of trimethylolmelamine and 10% of acrylic acid.
%, 0.5% ammonium persulfate, and 2% organic amine-based acid catalyst,
%) And heat-treated in steam under normal pressure for 20 minutes.
Thereafter, it is washed with water, immersed in an aqueous solution of nickel sulfate 1%, and treated in a boiling state for 20 minutes. Next, after sufficiently washing with water, drying was performed to obtain a hydrophilic polyester fiber fabric. The water absorption and SR property of the obtained woven fabric were measured, and as shown in Table 1, the woven fabric was good, there was no decrease in fastness, and the washing durability was good. The evaluation of the fastness was performed on a sample dyed with 4% OWF of Dianix Rubine FG-SE (Disperse dye manufactured by Mitsubishi Kasei Corporation) at 130 ° C. for 60 minutes.

【0022】[0022]

【表1】 [Table 1]

【0023】[0023]

【実施例2】実施例1で使用した織物を、トリメチロー
ルメラミン及びアクリル酸を表2に示した量、過硫酸ア
ンモニウム0.5%、有機アミン系酸触媒2.0%の水
溶液中に、浸漬し、ニップし(ピックアップ100%)
し、常圧スチーム中で20分間処理を行なった。更に水
洗し、硫酸ニッケル1%水溶液に浸漬し、沸騰状態で2
0分間処理した。充分水洗した後乾燥し、親水化ポリエ
ステル繊維織物を得た。その結果を表2に示した。
Example 2 The woven fabric used in Example 1 was immersed in an aqueous solution of trimethylolmelamine and acrylic acid in the amounts shown in Table 2, 0.5% ammonium persulfate, and 2.0% organic amine-based acid catalyst. Then nip (pickup 100%)
Then, the treatment was performed in normal pressure steam for 20 minutes. Further wash with water, immerse in a 1% aqueous solution of nickel sulfate, and boil
Treated for 0 minutes. After sufficiently washing with water, drying was performed to obtain a hydrophilic polyester fiber fabric. The results are shown in Table 2.

【0024】[0024]

【表2】 [Table 2]

【0025】表2に於てAは加工上り、Bは洗濯10回
後の数値を示す。
In Table 2, A is the value after processing, and B is the value after 10 washes.

【0026】得られた織物の水滴消失、吸水長を測定し
たところ表2に示すように良好であり、洗濯耐久性も良
好であった。なお表2に比較例として主たる条件を変更
し、他の条件を同じにして処理した例を示したが、N
o.1及び7は水滴消失の洗濯耐久性が不良であり、N
o.6及び8は親水性は良好であったが樹脂による白化
が生じた。
The water loss and water absorption length of the obtained woven fabric were measured, and as shown in Table 2, the woven fabric was good and the washing durability was good. Table 2 shows an example in which the main condition was changed and the other conditions were the same as the comparative example.
o. Nos. 1 and 7 are poor in wash durability due to disappearance of water drops, and N
o. Samples Nos. 6 and 8 had good hydrophilicity, but were whitened by the resin.

【0027】[0027]

【実施例3】分子量20,000のポリエチレングリコ
ール(PEG)2.0%を含有したポリエステル繊維7
5d/25fの編地を水酸化ナトリウム20g/lの水
溶液中に浸漬し、沸騰処理して約10%減量させた。つ
いで、トリメチロールメラミン6%、アクリル酸10
%、過硫酸アンモニウム0.5%及び有機アミン系酸触
媒2%を含む水溶液中に浸漬し、ニップ(ピックアップ
100%)して常圧スチーム中で20分間熱処理を行な
った。その後水洗し、水酸ナトリウム1g/lの水溶液
中で40℃で10分間処理した。充分水洗した後乾燥し
て、吸湿性ポリエステル繊維編地を得た。得られた編地
の吸湿性、制電性を測定したところ表3に示すように良
好であり洗濯耐久性も良好であった。なお表3に比較例
として主たる条件を変更し、他の条件を同じにして処理
した例を示したが、何れも制電性、吸湿性及びそれらの
洗濯耐久性が不良であった。
Example 3 Polyester fiber 7 containing 2.0% of polyethylene glycol (PEG) having a molecular weight of 20,000
The knitted fabric of 5d / 25f was immersed in an aqueous solution of 20 g / l of sodium hydroxide and subjected to a boiling treatment to reduce the weight by about 10%. Then, trimethylol melamine 6%, acrylic acid 10
%, Ammonium persulfate 0.5%, and an organic amine-based acid catalyst 2% were immersed in an aqueous solution, nipped (pickup 100%), and heat-treated in normal-pressure steam for 20 minutes. Thereafter, it was washed with water and treated at 40 ° C. for 10 minutes in an aqueous solution of sodium hydroxide 1 g / l. After sufficiently washing with water, drying was performed to obtain a knitted fabric of hygroscopic polyester fiber. When the moisture absorption and antistatic property of the obtained knitted fabric were measured, it was good as shown in Table 3, and the washing durability was also good. Table 3 shows, as comparative examples, examples in which the main conditions were changed and the other conditions were the same, and the antistatic properties, the hygroscopicity, and the washing durability thereof were all poor.

【0028】[0028]

【表3】 [Table 3]

【0029】[0029]

【実施例4】分子量20,000のポリエチレングリコ
ールを3.2%含有したポリエステル繊維75d/24
fの編地を水酸化ナトリウムの水溶液中に浸漬し沸騰処
理して13.5%減量させた。次いで表4に示す組成の
浴中に浸漬後、実施例3と同様の熱処理、アルカリ処理
を行ないそれぞれの制電性、吸湿性を測定した。なお過
硫酸アンモニウム0.5%、有機アミン酸系触媒2%は
いずれも共通に添加した。その結果本発明による例は良
好な吸湿性、制電性を示した。
Example 4 Polyester fiber 75d / 24 containing 3.2% of polyethylene glycol having a molecular weight of 20,000
The knitted fabric of f was immersed in an aqueous solution of sodium hydroxide and subjected to boiling treatment to reduce the weight by 13.5%. Next, after immersion in a bath having the composition shown in Table 4, the same heat treatment and alkali treatment as in Example 3 were performed, and the antistatic property and hygroscopic property of each were measured. Note that 0.5% of ammonium persulfate and 2% of an organic amine acid catalyst were commonly added. As a result, the examples according to the present invention exhibited good hygroscopicity and antistatic properties.

【0030】[0030]

【表4】 [Table 4]

【0031】[0031]

【発明の効果】本発明によるポリエステル繊維は、吸水
性、吸湿性、ソイルレリーズ(SR)性が良好であり、
従来法にみられた単繊維の強力低下、染色性及び染色堅
牢度の低下が全くなく、更に洗濯耐久性にも優れてい
る。又、ポリエチレングリコールを含有するポリエステ
ル繊維をアルカリ減量を行なったものを使用することに
より、加えて制電性も著しく良好となり衣料分野、電子
工業用作業衣分野等へ広く適用しうる。
The polyester fiber according to the present invention has good water absorption, moisture absorption and soil release (SR) properties,
There is no decrease in single fiber strength, dyeability and dyeing fastness seen in the conventional method, and the washing durability is excellent. In addition, by using a polyester fiber containing polyethylene glycol which has been subjected to alkali weight reduction, in addition, the antistatic property is remarkably improved, and it can be widely applied to the field of clothing, the field of working clothes for the electronics industry, and the like.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI // D01F 6/92 307 D06M 5/02 F D06M 101:32 (58)調査した分野(Int.Cl.6,DB名) D06M 13/203,13/368 ──────────────────────────────────────────────────続 き Continuation of the front page (51) Int.Cl. 6 identification symbol FI // D01F 6/92 307 D06M 5/02 F D06M 101: 32 (58) Investigated field (Int.Cl. 6 , DB name) D06M 13 / 203,13 / 368

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ポリエステル繊維にカルボキシル基含有
不飽和ビニルモノマー0.5〜20重量%(対繊維)及
びメラミン誘導体化合物1〜20重量%(対繊維)を含
む水溶液を付着させ熱処理した後、金属イオン吸着処理
を施すことを特徴とするポリエステル繊維の親水化表面
改質方法。
An aqueous solution containing 0.5 to 20% by weight of carboxyl group-containing unsaturated vinyl monomer (based on fiber) and 1 to 20% by weight of melamine derivative compound (based on fiber) is applied to polyester fiber and heat-treated. A method for modifying the surface of a polyester fiber to be hydrophilic, comprising performing an ion adsorption treatment.
【請求項2】 分子量2,000〜200,000のポ
リエチレングリコールを0.1〜5重量%含有するポリ
エステル繊維を5〜30重量%のアルカリ減量を行なっ
た後、カルボキシル基含有不飽和ビニルモノマー0.5
〜20重量%(対繊維)及びメラミン誘導体化合物1〜
20重量%(対繊維)を含む水溶液を付着させ熱処理し
た後、金属イオン吸着処理を施すことを特徴とするポリ
エステル繊維の親水化表面改質方法。
2. A polyester fiber containing 0.1 to 5% by weight of polyethylene glycol having a molecular weight of 2,000 to 200,000 is subjected to an alkali weight reduction of 5 to 30% by weight. .5
-20% by weight (based on fiber) and melamine derivative compound 1
A method for modifying the surface of a polyester fiber to be hydrophilic, comprising applying an aqueous solution containing 20% by weight (to the fiber), heat-treating the resultant, and then performing metal ion adsorption treatment.
JP1581691A 1990-01-23 1991-01-16 Method for modifying hydrophilic surface of polyester fiber Expired - Fee Related JP2873979B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1581691A JP2873979B2 (en) 1990-01-23 1991-01-16 Method for modifying hydrophilic surface of polyester fiber

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2-12936 1990-01-23
JP1293690 1990-01-23
JP1581691A JP2873979B2 (en) 1990-01-23 1991-01-16 Method for modifying hydrophilic surface of polyester fiber

Publications (2)

Publication Number Publication Date
JPH04214466A JPH04214466A (en) 1992-08-05
JP2873979B2 true JP2873979B2 (en) 1999-03-24

Family

ID=26348633

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1581691A Expired - Fee Related JP2873979B2 (en) 1990-01-23 1991-01-16 Method for modifying hydrophilic surface of polyester fiber

Country Status (1)

Country Link
JP (1) JP2873979B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101070676B (en) * 2007-05-18 2013-03-20 广东德美精细化工股份有限公司 Fiber-material modifying method and dyeing process

Also Published As

Publication number Publication date
JPH04214466A (en) 1992-08-05

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