JPH05295657A - Production of fiber structure - Google Patents

Production of fiber structure

Info

Publication number
JPH05295657A
JPH05295657A JP9268492A JP9268492A JPH05295657A JP H05295657 A JPH05295657 A JP H05295657A JP 9268492 A JP9268492 A JP 9268492A JP 9268492 A JP9268492 A JP 9268492A JP H05295657 A JPH05295657 A JP H05295657A
Authority
JP
Japan
Prior art keywords
fiber structure
fiber
plasma treatment
temperature plasma
amino 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.)
Granted
Application number
JP9268492A
Other languages
Japanese (ja)
Other versions
JP3077370B2 (en
Inventor
Masao Seki
昌夫 関
Takashi Hashimoto
貴史 橋本
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP9268492A priority Critical patent/JP3077370B2/en
Publication of JPH05295657A publication Critical patent/JPH05295657A/en
Application granted granted Critical
Publication of JP3077370B2 publication Critical patent/JP3077370B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To provide hygroscopicity, dry touch handle and excellent adhesion to a fiber structure by applying an amino acid to the fiber structure and then subjecting the fiber structure to low-temperature plasma treatment. CONSTITUTION:An amino acid such as alanine, glycine, glutamic acid or aminoacetic acid is impregnated into a fiber structure such as woven and knitted fabric, tow, string or rope, each made of a synthetic fiber such as polyester, nylon or polyacryl, a semi-synthetic fiber or a regenerated fiber such as acetate or rayon, a natural fiber such as wool, cotton or silk or their blend. Then the treated fiber structure is subjected to low temperature plasma treatment using non-polymerizable gas such as argon or helium between a discharge electrode made of glass-coated metal and an earth electrode made of a metal under conditions capable of satisfying the formula W1=18.5T1+3.5 and the formula W2=9T2+3.5 [W1 and W2: electric power (W/cm<2>) per unit area of the discharge electrode; T1 and T2: vacuum degree (Torr)].

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、吸湿性、ドライタッチ
な風合い、接着性に優れた繊維構造物の製造方法に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a fiber structure excellent in hygroscopicity, dry-touch texture and adhesiveness.

【0002】[0002]

【従来の技術】近年、合成繊維、特にポリエステルの衣
料用分野で天然繊維の高吸湿性にかかわる着用時の快適
感を狙って吸湿性能を付与する試みが数多く提案されて
いる。たとえば、アクリル酸、メタクリル酸などを繊維
にグラフトしたり、第三成分を共重合またはブレンドし
たポリマーを使用したりすることが知られている。
2. Description of the Related Art In recent years, in the field of clothing made of synthetic fibers, especially polyester, many attempts have been proposed to impart a hygroscopic property to a comfortable feeling during wearing, which is related to the high hygroscopicity of natural fibers. For example, it is known to graft fibers of acrylic acid, methacrylic acid, etc., or to use a polymer obtained by copolymerizing or blending a third component.

【0003】しかしながら、前者の方法は、性能がばら
つき易く処理の再現性に乏しい上に、繊維の強力の大幅
な低下や染色堅牢度の低下をきたすという欠点を有する
ものであった。後者の方法は、製糸性の低下や物性およ
び堅牢度が低下する欠点を有していた。
However, the former method has the drawbacks that the performance tends to vary and the reproducibility of the treatment is poor, and the strength of the fiber is greatly reduced and the dyeing fastness is lowered. The latter method has a drawback that the yarn formability is deteriorated and the physical properties and fastness are deteriorated.

【0004】また、繊維表面の接着性を高める方法とし
て、低温プラズマが広く検討されている。かかる方法に
は、非重合性ガスプラズマで繊維表面に水酸基、アミノ
基、カルボキシル基などを形成する、いわゆる化学修飾
しプラズマ重合により繊維表面に重合物を堆積させた
り、プラズマ処理で繊維表面にラジカルを作り、ビニル
モノマーを接触させてグラフト重合する方法がある。
Further, low temperature plasma has been widely studied as a method for improving the adhesiveness of the fiber surface. Such methods include forming hydroxyl groups, amino groups, and carboxyl groups on the fiber surface with non-polymerizable gas plasma, so-called chemical modification and depositing a polymer on the fiber surface by plasma polymerization, or radicals on the fiber surface by plasma treatment. And a vinyl monomer is brought into contact therewith to perform graft polymerization.

【0005】前者の方法は、繊維表面の親水基が繊維ポ
リマーの内部に潜り込むことにより、経時的に表面機能
が変化するという重大な欠点を有する。一方、重合によ
る後者の方法は、重合の再現性に乏しく、処理装置が汚
染するなどの欠点があった。また、旧来から接着剤を塗
布する方法が行なわれているが、この方法は接着膜によ
る風合いの硬化という問題があった。
The former method has a serious drawback that the surface function changes with time due to the hydrophilic groups on the surface of the fiber penetrating inside the fiber polymer. On the other hand, the latter method by polymerization has drawbacks such as poor reproducibility of polymerization and contamination of the processing equipment. Also, a method of applying an adhesive has been conventionally used, but this method has a problem that the texture is hardened by an adhesive film.

【0006】[0006]

【発明が解決しようとする課題】本発明は、吸湿性とド
ライな表面タッチ風合いを持ち、しかも粗硬化や経時変
化がなく再現性に優れた接着性を有する繊維構造物を製
造する方法を提供せんとするものである。
DISCLOSURE OF THE INVENTION The present invention provides a method for producing a fibrous structure having hygroscopicity and dry surface touch texture, and having adhesiveness with excellent reproducibility without rough curing or aging. It is something to do.

【0007】[0007]

【課題を解決するための手段】本発明は、かかる目的を
達成するため、次のような構成を有する。すなわち、本
発明の繊維構造物の製造方法は、繊維構造物にアミノ酸
を付与した後、低温プラズマ処理することを特徴とする
ものである。
The present invention has the following constitution in order to achieve such an object. That is, the method for producing a fiber structure of the present invention is characterized by applying an amino acid to the fiber structure and then performing low-temperature plasma treatment.

【0008】[0008]

【作用】本発明は、繊維構造物、特にポリエステル系繊
維構造物にアミノ酸を付与した後、特定の条件でプラズ
マ処理すればアミノ酸が架橋重合し、繊維表面に強固に
固着し、それによって、吸湿性や風合い、さらには接着
性まで改善することを究明したものである。
According to the present invention, when an amino acid is added to a fiber structure, particularly a polyester fiber structure, and then plasma-treated under a specific condition, the amino acid undergoes cross-linking polymerization and firmly adheres to the fiber surface, thereby absorbing moisture. It has been clarified that the properties, texture and even adhesiveness are improved.

【0009】以下、本発明を詳細に説明する。The present invention will be described in detail below.

【0010】本発明でいう繊維構造物は、ポリエステ
ル、ナイロン、アクリル、アセテート、レーヨンなど合
成繊維および半合成繊維、羊毛、木綿、絹などの天然繊
維など、およびこれらの混用繊維が使用され、また、こ
れらの繊維は長繊維、短繊維のいずれをも使用すること
ができ、編物、不織布、トウ、ひも、ロープなどの構造
のものを使用することができる。
In the fiber structure of the present invention, synthetic fibers and semi-synthetic fibers such as polyester, nylon, acryl, acetate and rayon, natural fibers such as wool, cotton and silk, and mixed fibers thereof are used. As the fibers, both long fibers and short fibers can be used, and knitted fabrics, non-woven fabrics, tows, strings, ropes and the like can be used.

【0011】本発明のアミノ酸とは、分子中に酸性基と
塩基性基を持つもので、例えば、アラニン、グリシン、
Lグルタミン酸、εアミノ酸など、たとえば改訂2版化
学便覧基礎編I(日本化学会編集 丸善株式会社発行)
第326〜329頁に例示さされたものなどを使用する
ことができる。
The amino acid of the present invention has an acidic group and a basic group in the molecule, and includes, for example, alanine, glycine,
L-glutamic acid, ε-amino acid, etc., for example, revised 2nd edition, Chemical Handbook Basic Edition I
The materials exemplified on pages 326 to 329 can be used.

【0012】かかるアミノ酸を繊維構造物に付与する方
法は、アミノ酸の水溶液を用い、パディング法、浸漬
法、スプレー法などにより処理し、乾燥する方法が使用
することができる。
As a method of applying the amino acid to the fiber structure, a method of using an aqueous solution of the amino acid, treating it by a padding method, a dipping method, a spray method or the like and then drying it can be used.

【0013】本発明は、かかるアミノ酸を付与した後、
特定の条件範囲で低温プラズマ処理することにより、目
的とする前記効果が達成される。
The present invention, after adding such an amino acid,
By carrying out the low temperature plasma treatment within a specific condition range, the above-mentioned desired effects can be achieved.

【0014】本発明の低温プラズマとは、特定のガスを
封入した減圧容器内で、電極間に高電圧を印加すること
により発生するものであり、かかる放電は、火花放電、
コロナ放電、グロー放電など種々の形態のものがある
が、放電が均一で活性化作用に優れたグロー放電が特に
好ましい。
The low-temperature plasma of the present invention is generated by applying a high voltage between the electrodes in a decompression container filled with a specific gas, and such discharge is spark discharge,
Although there are various forms such as corona discharge and glow discharge, glow discharge, which has a uniform discharge and an excellent activation effect, is particularly preferable.

【0015】本発明の高電圧を印加する電源は、交流、
直流のどちらでも使用することができる。交流の中では
特に周波数が10〜10000KHz が放電の持続性、均
一性から好ましい。
The power supply for applying a high voltage of the present invention is an alternating current,
Either direct current can be used. Among alternating currents, a frequency of 10 to 10,000 KHz is particularly preferable in terms of sustainability and uniformity of discharge.

【0016】本発明の低温プラズマ処理における非重合
性ガスとしては、たとえば、アルゴン、ヘリウム、窒
素、酸素、空気、水素、水、一酸化炭素、二酸化炭素、
アンモニア、四フッ化メタンなど、およびこれらの混合
物を用いることができる。
As the non-polymerizable gas in the low temperature plasma treatment of the present invention, for example, argon, helium, nitrogen, oxygen, air, hydrogen, water, carbon monoxide, carbon dioxide,
Ammonia, methane tetrafluoride, etc., and mixtures thereof can be used.

【0017】本発明の低温プラズマ処理は、放電電力と
真空度の組み合わせの特定の範囲でおこなうのが好まし
い。
The low temperature plasma treatment of the present invention is preferably performed within a specific range of the combination of discharge power and vacuum degree.

【0018】すなわち、放電電力と真空度の関係式が、 W1 =18.5T1 +3.5と、 W2 =9T2 +3.5 [ここで W1 、W2 は、放電電極の単位面積当たりの
電力(W/cm2 )、T1 、T2 は、真空度(Torr)であ
る。]の2式で囲まれた電力と真空度を組み合わせて処
理する。この範囲を外れる条件は本発明の効果を達成し
にくい。本発明の放電電力は、好ましくは4〜21W/
cm2 であり、4W/cm2 より小さいと処理に長時間を要
するし、21W/cm2 を越えると放電が不安定になり、
処理ムラを発生することがあるので好ましくない。
That is, the relational expression between the discharge power and the degree of vacuum is as follows: W 1 = 18.5T 1 +3.5 and W 2 = 9T 2 +3.5 [where W 1 and W 2 are the unit area of the discharge electrode] The power per unit (W / cm 2 ), T 1 , and T 2 are the degree of vacuum (Torr). ] The electric power and the vacuum degree surrounded by the two equations are combined and processed. Conditions outside this range are difficult to achieve the effects of the present invention. The discharge power of the present invention is preferably 4 to 21 W /
cm 2, and to take a long time to 4W / cm 2 less than the process, and the discharge becomes unstable exceeds 21W / cm 2,
Processing irregularities may occur, which is not preferable.

【0019】本発明の低温プラズマ処理の真空度として
は、0.01〜0.5Torrがよく、0.01Torrより低
いと活性種の平均自由工程距離が小さく被処理物への到
達する確率が高くなるが、生成する活性種の絶対量が少
なくなり、それだけ処理時間が長くなるきらいがあり、
0.5Torrを越えると、活性種が電離していないガス分
子に遮られるためか処理時間が長かったり、必要以上の
放電電力を必要とするなど好ましくない。本発明は、非
重合性ガスの存在下で、かかる真空度と放電電力を組み
合わせて発生させたプラズマ雰囲気下で処理することに
より本発明の目的を達成することができる。
The vacuum degree of the low temperature plasma treatment of the present invention is preferably 0.01 to 0.5 Torr. When it is lower than 0.01 Torr, the average free process distance of the active species is small and the probability of reaching the object to be treated is high. However, there is a tendency that the absolute amount of active species generated will decrease and the processing time will increase accordingly,
If it exceeds 0.5 Torr, the active species may be blocked by the gas molecules that have not been ionized, and the treatment time may be long, or more discharge power may be required, which is not preferable. The present invention can achieve the object of the present invention by treating in the presence of a non-polymerizable gas in a plasma atmosphere generated by combining such a degree of vacuum and discharge power.

【0020】本発明の処理をおこなう装置としては、放
電電極として、銅、鉄、ステンレス、アルミニュウムな
どの金属製チューブをガラスで被覆したものを用い、ア
ース電極としては、ステンレス、アルミニュウムなどの
金属からなる板、ドラムを使用することがよい。かかる
電極の組み合わせにより、均一な放電が形成でき、本発
明の効果を効率よく達成することができる。本発明の電
極は、必要に応じて水などを循環させて冷却する。
In the apparatus for carrying out the process of the present invention, a discharge electrode is a metal tube made of copper, iron, stainless steel, aluminum or the like covered with glass, and a ground electrode is made of metal such as stainless steel or aluminum. It is better to use a different plate or drum. By combining such electrodes, uniform discharge can be formed, and the effect of the present invention can be efficiently achieved. The electrode of the present invention is cooled by circulating water or the like as necessary.

【0021】本発明のプラズマ処理により、アミノ酸が
重合し水に不溶性の高分子を形成し、しかも繊維表面に
強固に接着するので、吸湿、風合い、接着のいずれの機
能も改善することができる。
By the plasma treatment of the present invention, amino acids are polymerized to form a water-insoluble polymer and firmly adhere to the fiber surface, so that any function of moisture absorption, texture and adhesion can be improved.

【0022】[0022]

【実施例】以下、実施例により詳しく説明するが、本発
明は、これらに限定されるものではない。
EXAMPLES The present invention will be described in more detail below with reference to examples, but the present invention is not limited thereto.

【0023】実施例1〜11、比較例1〜4 経糸に75デニール36フィラメント、緯糸に100デ
ニール48フィラメントのポリエステル仮より加工糸
(東レ株式会社製)を使用した平織物を常法により精
練、ヒートセットした。該織物を次に示す条件で処理し
性能を評価した結果を表1に示す。
Examples 1 to 11 and Comparative Examples 1 to 4 Plain woven fabrics made of polyester temporary twisted yarn (manufactured by Toray Industries, Inc.) of 75 denier 36 filaments for warp and 100 denier 48 filaments for weft are scoured by a conventional method, Heat set. The results of evaluating the performance of the woven fabric treated under the following conditions are shown in Table 1.

【0024】(アミノ酸加工) A:アミノ酢酸150g/l 水溶液に浸漬した後、ウエッ
トピックアップが90%になるようにマングルで絞り1
00℃で乾燥した。 B:DL−α−アラニンをAと同様に処理した。 C:εアミノカプロン酸をAと同様に処理した。 (プラズマ処理) 処理装置:内部電極型 放電電極は外径8mmのアルミ管
を外径12mmのガラス管で被覆したもの アース電極は外径300mmのステンレス製ドラム 放電周波数:500KHz 放電電力:2〜30 KW/cm2 ガス及び流量:アルゴン 100cc/min 真空度:0.05〜1.0Torr ドラム回転速度:10cm/min なを、表中の重合効率は、アミノ酸のパディング・乾燥
後の付着重量を100とし、プラズマ処理後90℃の水
で20分間洗浄し乾燥した後の不溶成分の重量の割合を
求めた。また、吸湿率は、試料を100℃で4時間乾燥
した後の重量を100とし、20℃、65%RHの条件
で48時間処理した後の重量から、増加重量分の割合を
求めた。
(Amino acid processing) A: After dipping in 150 g / l of aminoacetic acid aqueous solution, squeeze with a mangle so that the wet pickup becomes 90% 1
It was dried at 00 ° C. B: DL-α-alanine was treated as in A. C: ε-aminocaproic acid was treated as in A. (Plasma treatment) Treatment device: Internal electrode type Discharge electrode is an aluminum tube with an outer diameter of 8 mm covered with a glass tube with an outer diameter of 12 mm. The ground electrode is a stainless steel drum with an outer diameter of 300 mm. Discharge frequency: 500 KHz Discharge power: 2-30 KW / cm 2 Gas and flow rate: Argon 100 cc / min Vacuum degree: 0.05 to 1.0 Torr Drum rotation speed: 10 cm / min The polymerization efficiency in the table is 100% of the weight of the amino acid after adhesion and drying. After the plasma treatment, the weight ratio of the insoluble component after washing with water at 90 ° C. for 20 minutes and drying was determined. As for the moisture absorption rate, the weight after the sample was dried at 100 ° C. for 4 hours was set to 100, and the ratio of the increased weight was calculated from the weight after the sample was treated at 20 ° C. and 65% RH for 48 hours.

【0025】比較例1、2、3はアミノ酸を付着させた
後、プラズマ処理をしないで90℃の水で20分間洗浄
したもので、比較例4はアミノ酸処理、プラズマ処理と
も行わない原布である。
Comparative Examples 1, 2 and 3 are prepared by adhering amino acids and then washed with water at 90 ° C. for 20 minutes without plasma treatment. Comparative Example 4 is a base cloth which is not subjected to amino acid treatment or plasma treatment. is there.

【0026】[0026]

【表1】 表1から、実施例1〜11のものは、アミノ酸が重合し
て水不溶化し、原布に対し3〜4倍の吸湿性を持ち、ま
た、織物の風合いは、サラサラしたタッチの優れたもの
であった。なお、実施例7は部分的に黄化しており均一
処理の点から、やや劣るものであった。
[Table 1] From Table 1, those of Examples 1 to 11 are those in which amino acids are polymerized to be insoluble in water and have 3 to 4 times the hygroscopicity with respect to the woven fabric, and the texture of the woven fabric is excellent in a smooth touch. Met. In addition, Example 7 was partially yellowed and slightly inferior in terms of uniform treatment.

【0027】実施例12、比較例5〜6 経糸及び緯糸に70デニール24フィラメントのナイロ
ン6(東レ株式会社製)を使用した平織物を常法により
精練、ヒートセットした。
Example 12, Comparative Examples 5 to 6 A plain weave fabric using nylon 6 of 70 denier 24 filaments (manufactured by Toray Industries, Inc.) as warp and weft was scoured and heat set by a conventional method.

【0028】実施例12:εアミノカプロン酸200g/
l 水溶液に浸漬し、ウエットピックアップが70%にな
るようにマングルで絞り、110℃で乾燥した。次い
で、実施例1と同様のプラズマ処理機で次ぎの条件でプ
ラズマ処理し、コーティング加工した。
Example 12: Epsilon aminocaproic acid 200 g /
l Immersed in an aqueous solution, squeezed with a mangle so that the wet pickup would be 70%, and dried at 110 ° C. Then, the same plasma treatment machine as in Example 1 was used to perform plasma treatment under the following conditions to perform coating.

【0029】(プラズマ処理) ガス、流量:空気 100cc/min 真空度:0.4Torr 放電電力:16W/cm2 処理速度:10cm/min (コーティング)ポリエステル系ポリウレタン樹脂(ク
リスボン8006-HV 三洋化成株式会社製)のジメチ
ルホルムアミド溶液をナイフコーターで塗布量25/ m
2 コーティングし、湿式法で凝固しコーティング加工し
た。該コーティング布帛の膜剥離強力はプラズマ処理し
てから12時間後にコ−ティングしたものは、840g/
cmであり、プラズマ処理してから120時間後にコーテ
ィングしたものは、850g/cmとプラズマ処理後の経時
変化のないものであった。
(Plasma treatment) Gas, flow rate: air 100 cc / min Vacuum degree: 0.4 Torr Discharge power: 16 W / cm 2 Treatment speed: 10 cm / min (Coating) Polyester polyurethane resin (Crisbon 8006-HV Sanyo Kasei Co., Ltd.) Product) dimethylformamide solution with a knife coater coating amount 25 / m
2 coating, coagulation by wet method and coating processing. The film peeling strength of the coated cloth was 840 g / m after being coated 12 hours after the plasma treatment.
The value was cm, and the coating after 120 hours from the plasma treatment was 850 g / cm, which did not change with time after the plasma treatment.

【0030】比較例5は、アミノ酸処理をしない以外は
実施例12と同様に処理した。プラズマ処理してから1
2時間後および120時間後にコーティングしたものの
膜剥離強力は、それぞれ720g/cm、610g/cmであり
プラズマ処理後の経時変化が認められた。
Comparative Example 5 was treated in the same manner as Example 12 except that the amino acid treatment was not performed. 1 after plasma treatment
The film peeling strengths of the coatings after 2 hours and 120 hours were 720 g / cm and 610 g / cm, respectively, and changes with time after the plasma treatment were observed.

【0031】比較例6は、アミノ酸処理、プラズマ処理
をせずに実施例12と同様にコーティング加工したもの
の膜剥離強力は、510g/cmであった。
In Comparative Example 6, the film peeling strength of the coating processed in the same manner as in Example 12 without amino acid treatment and plasma treatment was 510 g / cm.

【0032】以上から、実施例12のものは、比較例5
のものに比して、経時変化のない優れた接着性を有する
ことがわかる。
From the above, Comparative Example 5 was used in Example 12.
It can be seen that it has excellent adhesiveness with no change over time as compared with the above.

【0033】[0033]

【発明の効果】本発明によれば、経時変化のない高接着
性と吸湿性およびドライタッチな風合いを有する繊維構
造物を提供し得る。
Industrial Applicability According to the present invention, it is possible to provide a fibrous structure having a high adhesiveness which does not change with time, a hygroscopic property, and a dry-touch texture.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】繊維構造物にアミノ酸を付与した後、低温
プラズマ処理することを特徴とする繊維構造物の製造方
法。
1. A method for producing a fiber structure, which comprises applying an amino acid to the fiber structure and then performing a low temperature plasma treatment.
【請求項2】低温プラズマ処理が、非重合性ガスプラズ
マであり、次に示す(1)と(2)式で囲まれた範囲の
放電電力と真空度の組み合わせで処理する請求項1記載
の繊維構造物の製造方法。 W1 =18.5T1 +3.5 ・・・・(1) W2 =9T2 +3.5 ・・・・(2) ここでW1 、W2 は、放電電極の単位面積当たりの電力
(W/cm2 )、 T1 、T2 は、真空度(Torr)をあらわす。
2. The low-temperature plasma treatment is a non-polymerizable gas plasma, and the treatment is performed with a combination of discharge power and vacuum within a range surrounded by the following formulas (1) and (2). A method for manufacturing a fiber structure. W 1 = 18.5 T 1 +3.5 ··· (1) W 2 = 9T 2 +3.5 ··· (2) Here, W 1 and W 2 are electric power per unit area of the discharge electrode ( W / cm 2 ), T 1 and T 2 represent the degree of vacuum (Torr).
【請求項3】低温プラズマ処理が、放電電力が4〜21
W/cm2 、真空度が0.01〜0.5Torrである請求項
1記載の繊維構造物の製造方法。
3. The low temperature plasma treatment has a discharge power of 4 to 21.
The method for producing a fiber structure according to claim 1, wherein W / cm 2 and the degree of vacuum are 0.01 to 0.5 Torr.
【請求項4】低温プラズマ処理が、放電電極が金属をガ
ラスで被覆したものであり、アース電極が金属製である
請求項1記載の繊維構造物の製造方法。
4. The method for producing a fiber structure according to claim 1, wherein in the low temperature plasma treatment, the discharge electrode is a metal coated with glass and the ground electrode is made of metal.
JP9268492A 1992-04-13 1992-04-13 Manufacturing method of fiber structure Expired - Fee Related JP3077370B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9268492A JP3077370B2 (en) 1992-04-13 1992-04-13 Manufacturing method of fiber structure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9268492A JP3077370B2 (en) 1992-04-13 1992-04-13 Manufacturing method of fiber structure

Publications (2)

Publication Number Publication Date
JPH05295657A true JPH05295657A (en) 1993-11-09
JP3077370B2 JP3077370B2 (en) 2000-08-14

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Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102312375A (en) * 2010-07-01 2012-01-11 辽宁天泽产业集团纺织有限公司 Method for performing anhydrous greasy dirt prevention treatment on filter medium prepared from textile fibers
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CN105908263A (en) * 2016-06-21 2016-08-31 朱兰英 Method for preparing garlic bolt leaf fibers

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Publication number Priority date Publication date Assignee Title
CN102677474A (en) * 2012-06-06 2012-09-19 天津工业大学 Method for improving water and moisture absorbability of polyester fabric by using gamma-polyglutamic acid hydrogel
CN102926209A (en) * 2012-11-16 2013-02-13 天津工业大学 Method for finishing dacron by gamma-polyglutamic acid hydrogel

Cited By (4)

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Publication number Priority date Publication date Assignee Title
CN102312375A (en) * 2010-07-01 2012-01-11 辽宁天泽产业集团纺织有限公司 Method for performing anhydrous greasy dirt prevention treatment on filter medium prepared from textile fibers
CN105839417A (en) * 2016-06-21 2016-08-10 朱兰英 Garlic sprout leaf fiber
CN105908263A (en) * 2016-06-21 2016-08-31 朱兰英 Method for preparing garlic bolt leaf fibers
CN105839417B (en) * 2016-06-21 2018-10-30 朱兰英 A kind of garlic bolt leaf fibre

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