JPH0559664A - Method for resin finishing of fiber product - Google Patents

Method for resin finishing of fiber product

Info

Publication number
JPH0559664A
JPH0559664A JP3250387A JP25038791A JPH0559664A JP H0559664 A JPH0559664 A JP H0559664A JP 3250387 A JP3250387 A JP 3250387A JP 25038791 A JP25038791 A JP 25038791A JP H0559664 A JPH0559664 A JP H0559664A
Authority
JP
Japan
Prior art keywords
formaldehyde
fiber product
polyhydric alcohol
fiber
product
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
JP3250387A
Other languages
Japanese (ja)
Inventor
Takumi Minagawa
卓己 皆川
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.)
Toyobo Co Ltd
Original Assignee
Toyobo Co 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 Toyobo Co Ltd filed Critical Toyobo Co Ltd
Priority to JP3250387A priority Critical patent/JPH0559664A/en
Publication of JPH0559664A publication Critical patent/JPH0559664A/en
Pending legal-status Critical Current

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  • Treatment Of Fiber Materials (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

PURPOSE:To enable a resin finishing method of fiber product of providing the fiber product with flexibility, high wrinkle preventing ability and shrink preventing ability without lowering strength in subjecting a cellulosic fiber product to resin finishing with formaldehyde vapor by using a polyhydric alcohol having a specific boiling point. CONSTITUTION:A cellulosic fiber-containing fiber product is immersed, for example in an aqueous solution of a polyhydric alcohol having >=150 deg.C boiling point (preferably ethylene glycol or polyethylene glycol having 90-5,000 molecular weight), uniformly dried, the cloth is exposed to formaldehyde vapor, then provided with a catalyst such as sulfur dioxide gas, heat-treated, and crosslinking bond of cellulose molecules with formaldehyde is caused and the amount of the remaining formaldehyde is suppressed to a low content to provide the cellulosic fiber-containing fiber product with excellent wrinkle preventing properties and shrink preventing properties without reducing strength.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はセルロース系繊維を含有
する繊維製品に防しわ性、防縮性、永久プレスを付与す
る樹脂加工方法に関するものであり、さらに詳しくはホ
ルムアルデヒド蒸気にさらし、触媒の存在下で熱処理す
る繊維製品の改善された樹脂加工方法に関するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin processing method for imparting wrinkle resistance, shrink resistance, and permanent pressing to a fiber product containing a cellulosic fiber, and more specifically, it is exposed to formaldehyde vapor and the presence of a catalyst. The present invention relates to an improved resin processing method for a textile product which is heat-treated below.

【0002】[0002]

【従来の技術】綿または綿混紡のようなセルロース繊維
含有製品をホルムアルデヒドで処理してセルロース分子
の永久的交叉結合を起こさせることにより、永久的防し
わ性、防縮性、プレスを付与するための方法が数多く提
案されている。しかしながらこれらの方法では、ホルム
アルデヒドによる交叉結合反応の制御が困難であるため
に再現性に欠ける傾向があった。すなわち、改質が十分
でなければ防しわ性、防縮性等が満足せず、改質が進み
すぎると風合いが硬くなったり、強力低下が著しくなる
場合があった。また、これらの方法では残留ホルムアル
デヒドを低減するために執拗なソーピングを要した。こ
の問題を解決するため、ホルムアルデヒド処理前にセル
ロース繊維含有製品の水分率を調整したり、処理中に水
蒸気を導入したりして、ホルムアルデヒド−セルロース
の反応時におけるセルロース物質中に存在する水分を制
御しようとする方法がある。これらの方法ではセルロー
ス繊維を膨潤した状態でホルムアルデヒドによる交叉結
合をし得るので、強力低下の少ない改質が可能となる
が、しかしながら、セルロース繊維中の正確な水分制御
が困難であり、かえって、水分率の違いが改質バラツキ
に影響するという問題があった。また、度重なるソーピ
ングは加工工程の複雑化、コストアップにつながるとい
う問題があり、特に縫製製品状の加工においては、ソー
ピングの簡便化が望まれている。
BACKGROUND OF THE INVENTION For the purpose of imparting permanent wrinkle resistance, shrink resistance, and pressing by treating a cellulosic fiber-containing product such as cotton or cotton blend with formaldehyde to cause permanent cross-linking of cellulose molecules. Many methods have been proposed. However, these methods tend to lack reproducibility because it is difficult to control the cross-linking reaction with formaldehyde. That is, if the modification is not sufficient, wrinkle resistance, shrinkage resistance, etc. are not satisfied, and if the modification proceeds too much, the texture may become hard and the strength may be significantly reduced. In addition, these methods required persistent soaping to reduce the residual formaldehyde. In order to solve this problem, the moisture content of the cellulose fiber-containing product is adjusted before the formaldehyde treatment, or steam is introduced during the treatment to control the moisture present in the cellulosic material during the formaldehyde-cellulose reaction. There is a way to try. These methods allow cross-linking with formaldehyde in a state where the cellulose fibers are swollen, so that modification with less decrease in strength is possible, however, it is difficult to accurately control water content in the cellulose fibers, and rather water content There is a problem that the difference in the rate affects the variation in reforming. Further, repeated soaping has a problem in that the processing steps become complicated and the cost increases, and in particular, in the processing of sewn products, simplification of soaping is desired.

【0003】[0003]

【発明が解決しようとする課題】本発明はこのような現
状に鑑みて行われたもので、ホルムアルデヒドの蒸気処
理において、セルロース繊維含有製品に高度の防しわ
性、防縮性、永久的プレスおよび優れた洗濯後の外観
(W&W性)を強力低下が少なく、柔軟な風合いを付与
し、しかも残留ホルムアルデヒドを低く抑えることを目
的とする。
SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and in the steam treatment of formaldehyde, cellulose fiber-containing products have a high degree of wrinkle resistance, shrink resistance, permanent press and excellent properties. The purpose of the present invention is to reduce the strength (w & w property) after washing, to give a soft texture, and to keep the residual formaldehyde low.

【0004】[0004]

【課題を解決するための手段】本発明は上記目的を達成
するもので、次の構成よりなるものである。すなわち本
発明は、セルロース系繊維を含有する繊維製品をホルム
アルデヒド蒸気にさらし、触媒の存在下で熱処理するに
際し、沸点が150℃以上の多価アルコールを併用する
ことを特徴とする繊維製品の樹脂加工方法を要旨とする
ものである。以下、本発明について詳細に説明する。
The present invention achieves the above object and has the following structure. That is, the present invention is a resin processing of a fiber product, characterized in that when a fiber product containing a cellulosic fiber is exposed to formaldehyde vapor and heat-treated in the presence of a catalyst, a polyhydric alcohol having a boiling point of 150 ° C. or higher is used in combination. The method is the gist. Hereinafter, the present invention will be described in detail.

【0005】本発明でいうセルロース系繊維とは、綿、
麻等の天然セルロース繊維、レーヨン、ポリノジック等
の再生セルロース繊維を意味し、繊維製品とは、綿、
糸、織物、編物、不織布および縫製品等を意味し、これ
らの繊維製品は、セルロース系繊維単独であっても、合
成繊維等の他の繊維との混用製品であってもよい。
The cellulosic fibers referred to in the present invention are cotton,
Natural cellulosic fibers such as hemp, regenerated cellulosic fibers such as rayon and polynosic, and fiber products include cotton,
It means a thread, a woven fabric, a knitted fabric, a non-woven fabric, a sewn product and the like, and these fiber products may be cellulosic fibers alone or a mixed product with other fibers such as synthetic fibers.

【0006】本発明に用いる多価アルコールは、沸点が
150℃以上であり、例えば、グリセリン、エチレング
リコール、ジエチレングリコール、ポリエチレングリコ
ールや、ポリプロピレングリコール類であり、その他エ
チレンオキシ基およびプロピレンオキシ基を有するアル
キレングリコール等である。本発明で用いられる多価ア
ルコールは分子量が60〜6000の範囲にあるものが
特に好ましい。さらに好ましくは分子量が90〜500
0である。
The polyhydric alcohol used in the present invention has a boiling point of 150 ° C. or higher, and is, for example, glycerin, ethylene glycol, diethylene glycol, polyethylene glycol or polypropylene glycol, and other alkylene having an ethyleneoxy group and a propyleneoxy group. Such as glycol. The polyhydric alcohol used in the present invention preferably has a molecular weight in the range of 60 to 6000. More preferably, the molecular weight is 90 to 500.
It is 0.

【0007】本発明に用いる多価アルコールの付与量
は、被処理繊維重量に対して通常0.1〜10重量%で
あり、この場合、0.1重量%未満では本発明による効
果が低く、また、10重量%を越えてもそれに見合う効
果が得られないのみならず、感触的にも好ましくなくな
るので望ましくない。これらの多価アルコールはそれぞ
れ単独使用かまたは2種以上組み合わせて使用してもよ
い。
The amount of the polyhydric alcohol used in the present invention is usually 0.1 to 10% by weight based on the weight of the fiber to be treated. In this case, if the amount is less than 0.1% by weight, the effect of the present invention is low. Further, even if it exceeds 10% by weight, not only the effect corresponding thereto is not obtained, but also it is not preferable in terms of feel, which is not desirable. These polyhydric alcohols may be used alone or in combination of two or more.

【0008】本発明において、多価アルコールを被処理
製品に付与する方法としては、多価アルコールがセルロ
ース繊維に均一に付着すればいかなる方法でも適用で
き、付与する時期も染色された被処理製品がホルムアル
デヒド蒸気にさらされる以前であればいつでもよい。従
って、織編物状態で、多価アルコールの水溶液を必要量
の多価アルコールが付着するように通常のパッド・ドラ
イ法等で付与し、その後そのままホルムアルデヒド蒸気
処理するか、生地裁断、縫製した後にホルムアルデヒド
蒸気処理してもよい。あるいは、生地裁断、縫製した製
品に多価アルコールの水溶液を、必要量の多価アルコー
ルが付着するようにスプレーし、ホルムアルデヒド蒸気
処理してもよい。また、この多価アルコールを付与する
際に、通常の繊維加工用の柔軟剤、可縫製向上剤等(ポ
リシロキサン、ポリエチレンエマルジョン等)を同時も
しくはその前に付与してもよい。
In the present invention, the polyhydric alcohol may be applied to the product to be treated by any method as long as the polyhydric alcohol is uniformly attached to the cellulose fibers. Any time before exposure to formaldehyde vapor. Therefore, in the woven or knitted state, an aqueous solution of polyhydric alcohol is applied by a normal pad-dry method or the like so that a necessary amount of polyhydric alcohol adheres, and then formaldehyde vapor treatment is performed as it is, or after fabric cutting and sewing, formaldehyde is formed. It may be steamed. Alternatively, the product obtained by cutting and sewing the cloth may be sprayed with an aqueous solution of a polyhydric alcohol so that a necessary amount of the polyhydric alcohol may adhere to the product and subjected to formaldehyde vapor treatment. Further, when applying the polyhydric alcohol, a softening agent for fiber processing, a sewability improving agent and the like (polysiloxane, polyethylene emulsion, etc.) may be applied at the same time or before the application.

【0009】本発明におけるホルムアルデヒド蒸気処理
は通常の方法を採用でき、使用する触媒も通常の触媒を
使用することができ、特に制限されるものではない。例
えば、多価アルコールが必要量付与された被処理製品
を、ホルムアルデヒド蒸気処理に好ましいとされる水分
率(製品中のセルロース繊維重量に対して4〜20%)
に調整し、ホルムアルデヒド蒸気にさらした後、亜硫酸
ガス、塩化水素ガス等の触媒を付与し、50〜160℃
で熱処理する方法である。また、触媒の付与をホルムア
ルデヒド蒸気にさらす前に行う方法でもよい。
The formaldehyde vapor treatment in the present invention can be carried out by a usual method, and the catalyst used can also be a usual catalyst and is not particularly limited. For example, a product to which a required amount of polyhydric alcohol has been added has a moisture content (4 to 20% based on the weight of cellulose fiber in the product) that is considered preferable for formaldehyde vapor treatment.
After adjusting to, and exposing to formaldehyde vapor, apply a catalyst such as sulfurous acid gas and hydrogen chloride gas, and the temperature is 50 to 160 ° C.
It is a method of heat treatment in. Alternatively, a method of applying the catalyst before exposing it to formaldehyde vapor may be used.

【0010】本発明の繊維製品の樹脂加工方法によれ
ば、多価アルコールがセルロース繊維内に浸透した状態
で、ホルムアルデヒドによるセルロース分子の交叉結合
を起こさせるため、セルロース系繊維含有製品に高度の
防しわ性、防縮性、永久的プレスおよび優れた洗濯後の
外観(W&W性)を、強力低下が少なく、柔軟な風合い
で与え、かつ残留ホルムアルデヒドを低く抑えることが
できる。また、防しわ性において、特に湿潤時の防しわ
性の向上効果が著しく、洗濯後の外観においても、従来
の綿100%では達成が非常に困難であった3.5を容
易に達成することができる。
According to the resin processing method for a fiber product of the present invention, the cross-linking of cellulose molecules by formaldehyde is caused in a state where the polyhydric alcohol penetrates into the cellulose fiber, so that the product containing a cellulose fiber is highly protected. Wrinkle resistance, shrink resistance, permanent press and excellent appearance after washing (W & W property) can be imparted with a low softening strength, a soft texture, and a low residual formaldehyde. In addition, in terms of wrinkle resistance, the effect of improving wrinkle resistance particularly when wet is remarkable, and even in the appearance after washing, it is easy to achieve 3.5, which was very difficult to achieve with conventional 100% cotton. You can

【0011】[0011]

【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、実施例における各種性能の測定は次の方
法で行った。 (イ)防しわ性 JIS L−1096 B法(モンサント法)に準拠 (ロ)引裂強度 JIS L−1096 D法(ペンジュラム法)に準拠 (ハ)破裂強度 JIS L−1018 A法(ミューレン形法)に準拠 (ニ)洗濯外観 JIS L−1096 A法(かくはん形洗濯機を用い
る方法)・ライン乾燥に準拠 (ホ)遊離ホルムアルデヒド量 JIS L−1041 アセチルアセトン法に準拠
EXAMPLES The present invention will be described in more detail below with reference to examples, but various performances in the examples were measured by the following methods. (A) Wrinkle resistance Compliant with JIS L-1096 B method (Monsanto method) (b) Tear strength Compliant with JIS L-1096 D method (Pendulum method) (c) Bursting strength JIS L-1018 A method (Mullen type method) ) (D) Appearance of washing JIS L-1096 A method (method using a stirring type washing machine) ・ Conforming to line drying (e) Amount of free formaldehyde JIS L-1041 Conforming to acetylacetone method

【0012】実施例1 精練漂白後、溶液濃度0.4%のHakkolBRK
(昭和化学社製蛍光染料)で染色した40番手綿糸使い
の綿ブロード布を溶液濃度5%のポリエチレングリコー
ル(平均分子量1000)水溶液に浸漬し、ついでマン
グルで均一に絞った。このときの絞り率は70%であっ
た。ついで105℃で2分間乾燥し、環境下(25℃、
65%RH)で調湿した。その後、布を反応器に入れ、
パラホルムアルデヒドから発生したホルムアルデヒド蒸
気に4分間さらした。さらしている間の反応器の温度は
45℃であった。続いて反応器に亜硫酸ガスを流入して
布をさらし、その後、反応器の温度を150℃に上昇さ
せキュアリングした。ついで反応器にスチームを流入
し、布を2分間さらした。
Example 1 After scouring and bleaching, Hakkol BRK having a solution concentration of 0.4%
A cotton broad cloth using a # 40 cotton thread dyed with (Showa Kagaku Co., Ltd. fluorescent dye) was immersed in an aqueous solution of polyethylene glycol (average molecular weight 1000) having a solution concentration of 5%, and then uniformly squeezed with a mangle. The draw ratio at this time was 70%. Then, it is dried at 105 ° C for 2 minutes, and then in an environment (25 ° C,
The humidity was adjusted to 65% RH). Then put the cloth in the reactor,
It was exposed to formaldehyde vapor generated from paraformaldehyde for 4 minutes. The temperature of the reactor during the exposure was 45 ° C. Subsequently, sulfurous acid gas was introduced into the reactor to expose the cloth, and then the temperature of the reactor was raised to 150 ° C. for curing. Steam was then poured into the reactor and the fabric was exposed for 2 minutes.

【0013】比較例1 実施例1でポリエチレングリコール水溶液浸漬をしない
以外はまったく同様に処理して比較例1とした。
Comparative Example 1 Comparative Example 1 was carried out in the same manner as in Example 1 except that the polyethylene glycol aqueous solution was not immersed.

【0014】実施例2 実施例1でポリエチレングリコール水溶液に柔軟剤とし
てPOLON MF−7(信越化学社製)を3%添加し
た以外はまったく同様に処理して実施例2とした。
Example 2 Example 2 was carried out in the same manner as in Example 1 except that 3% of POLON MF-7 (manufactured by Shin-Etsu Chemical Co., Ltd.) as a softening agent was added to the polyethylene glycol aqueous solution.

【0015】実施例3 精練漂白後、溶液濃度1%のSumifix Supr
a Blue BRF(住友化学社製反応性染料)で染
色した60番手綿糸使いの綿天竺編地を溶液濃度2%の
ポリアルキレングリコール(エチレンオキシ基:プロピ
レンオキシ基=30:70(重量比)、分子量約370
0)水溶液に浸漬し、次いでマングルで均一に絞った。
このときの絞り率は95%であった。ついで105℃で
3分間乾燥し、環境下(25℃、65%RH)で調湿し
た。その後、布を反応器に入れ、パラホルムアルデヒド
から発生したホルムアルデヒド蒸気に6分間さらした。
さらしている間の反応器の温度は55℃であった。続い
て反応器に亜硫酸ガスを流入して布をさらし、その後、
反応器の温度を150℃に上昇させキュアリングした。
ついで反応器にスチームを流入し、布を2分間さらし
た。
Example 3 Sumifix Supr having a solution concentration of 1% after scouring and bleaching
a Blue BRF (a reactive dye manufactured by Sumitomo Chemical Co., Ltd.) is used to fabricate a cotton cloth using a 60th cotton yarn and a polyalkylene glycol (ethyleneoxy group: propyleneoxy group = 30: 70 (weight ratio)) having a solution concentration of 2%. Molecular weight about 370
0) Immersed in an aqueous solution, and then squeezed uniformly with a mangle.
The draw ratio at this time was 95%. Then, it was dried at 105 ° C. for 3 minutes and conditioned under the environment (25 ° C., 65% RH). The cloth was then placed in the reactor and exposed to formaldehyde vapor generated from paraformaldehyde for 6 minutes.
The temperature of the reactor during exposure was 55 ° C. Sulfurous acid gas is then introduced into the reactor to expose the cloth, and then
The temperature of the reactor was raised to 150 ° C. for curing.
Steam was then poured into the reactor and the fabric was exposed for 2 minutes.

【0016】比較例2 実施例3でポリアルキレングリコール水溶液浸漬をしな
い以外はまったく同様に処理して比較例2とした。
Comparative Example 2 Comparative Example 2 was carried out in the same manner as in Example 3 except that the polyalkylene glycol aqueous solution was not immersed.

【0017】実施例4 実施例3でポリアルキレングリコール水溶液に可縫製向
上剤としてメイカテックスHP−600(明成化学社
製)を0.3%添加した以外はまったく同様に処理して
実施例4とした。得られた加工品の各種物性値の測定結
果を表1に示す。
Example 4 The same treatment as in Example 4 was carried out except that 0.3% of Mecatex HP-600 (manufactured by Meisei Chemical Co., Ltd.) was added to the polyalkylene glycol aqueous solution as a sewing aid in Example 3. did. Table 1 shows the measurement results of various physical properties of the obtained processed product.

【0018】[0018]

【表1】 [Table 1]

【0019】[0019]

【発明の効果】本発明の樹脂加工方法によれば、機械的
強度低下が少なく、高度な防しわ性、防縮性、柔軟性、
さらに優れた洗濯後の外観(W&W性)を有し、残留ホ
ルムアルデヒドが少ない繊維製品を得ることができる。
Industrial Applicability According to the resin processing method of the present invention, there is little reduction in mechanical strength, and high degree of wrinkle resistance, shrink resistance, flexibility,
Further, it is possible to obtain a textile product having an excellent appearance (W & W property) after washing and having less residual formaldehyde.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 // D06M 101:06 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification number Office reference number FI technical display location // D06M 101: 06

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 セルロース系繊維を含有する繊維製品を
ホルムアルデヒド蒸気にさらし、触媒の存在下で熱処理
するに際し、沸点が150℃以上の多価アルコールを併
用することを特徴とする繊維製品の樹脂加工方法。
1. A resin processing of a fiber product, which comprises using a polyhydric alcohol having a boiling point of 150 ° C. or more when exposing a fiber product containing a cellulosic fiber to formaldehyde vapor and heat treating the same in the presence of a catalyst. Method.
JP3250387A 1991-09-02 1991-09-02 Method for resin finishing of fiber product Pending JPH0559664A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3250387A JPH0559664A (en) 1991-09-02 1991-09-02 Method for resin finishing of fiber product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3250387A JPH0559664A (en) 1991-09-02 1991-09-02 Method for resin finishing of fiber product

Publications (1)

Publication Number Publication Date
JPH0559664A true JPH0559664A (en) 1993-03-09

Family

ID=17207165

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3250387A Pending JPH0559664A (en) 1991-09-02 1991-09-02 Method for resin finishing of fiber product

Country Status (1)

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JP (1) JPH0559664A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08120556A (en) * 1994-08-29 1996-05-14 Uizu:Kk Shape stable processing of sewed product
WO2001057304A2 (en) * 2000-02-07 2001-08-09 The Procter & Gamble Company Enhanced fabric comprising substrates and process to provide same
WO2001057305A3 (en) * 2000-02-07 2001-12-06 Procter & Gamble Enhanced fabric comprising substrates and process to provide same
KR100464781B1 (en) * 1998-03-26 2005-04-06 주식회사 새 한 Form stability processing method of cellulose fiber containing spandex

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08120556A (en) * 1994-08-29 1996-05-14 Uizu:Kk Shape stable processing of sewed product
KR100464781B1 (en) * 1998-03-26 2005-04-06 주식회사 새 한 Form stability processing method of cellulose fiber containing spandex
WO2001057304A2 (en) * 2000-02-07 2001-08-09 The Procter & Gamble Company Enhanced fabric comprising substrates and process to provide same
WO2001057305A3 (en) * 2000-02-07 2001-12-06 Procter & Gamble Enhanced fabric comprising substrates and process to provide same
WO2001057304A3 (en) * 2000-02-07 2001-12-20 Procter & Gamble Enhanced fabric comprising substrates and process to provide same
US6544296B2 (en) 2000-02-07 2003-04-08 The Proctor & Gamble Company Enhanced fabric comprising substrates and process to provide same
JP2003521593A (en) * 2000-02-07 2003-07-15 ザ、プロクター、エンド、ギャンブル、カンパニー SUBSTRATE COMPRISING IMPROVED FABRIC AND METHOD OF PROVIDING THE SAME
US6953485B2 (en) 2000-02-07 2005-10-11 Strike Investments, Llc Enhanced fabric comprising substrates and process to provide same

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