JPH08158264A - Method for processing cellulose-based textile fabric - Google Patents

Method for processing cellulose-based textile fabric

Info

Publication number
JPH08158264A
JPH08158264A JP6291245A JP29124594A JPH08158264A JP H08158264 A JPH08158264 A JP H08158264A JP 6291245 A JP6291245 A JP 6291245A JP 29124594 A JP29124594 A JP 29124594A JP H08158264 A JPH08158264 A JP H08158264A
Authority
JP
Japan
Prior art keywords
epoxy
modified
treatment
amino
modified organopolysiloxane
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
JP6291245A
Other languages
Japanese (ja)
Inventor
Mieko Inaoka
美恵子 稲岡
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 JP6291245A priority Critical patent/JPH08158264A/en
Publication of JPH08158264A publication Critical patent/JPH08158264A/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 provide a processing method intended to afford cellulose-based textile fabric with excellently soft and resilient tough feeling. CONSTITUTION: Cellulose-based textile fabric is impregnated with an one-bath treatment liquor comprising a water-based polyurethane resin, epoxy compound, epoxy-modified organopolysiloxane, amino-modified organopolysiloxane and metal salt-based acid catalyst, being dried and heat-treated, and then subjected to flex treatment with a batch-type dyeing machine. The polyurethane resin is pref. a polyurethane made from a polyether and aliphatic isocyanate, the epoxy compound is e.g. glycerol polyglycidyl ether, and the modified organosiloxane is e.g. an epoxy-modified or amino-modified silicone softener, each publicly known as a textile finisher. The flex treatment is pref. conducted simultaneously with dyeing operation.

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,セルロース系繊維布帛
に洗濯耐久性の優れたソフトで反撥性を有する風合を付
与する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 processing method for imparting a soft and repulsive texture having excellent washing durability to a cellulosic fiber cloth.

【0002】[0002]

【従来の技術】近年,衣料分野では,ソフトでありなが
ら反撥性のある風合が好まれるようになってきた。従来
より,このような風合は,布帛を精練,漂白,染色した
後の仕上げ加工工程で行われており,加工薬剤としてソ
フトな風合にするためにはシリコン系柔軟剤を用い,反
撥性を有した風合にするためにはウレタン樹脂を用い,
これら薬剤の単独処理液または混合処理液を布帛に含浸
し,熱処理を行うことにより,ソフトで反撥性のある風
合を布帛に付与している。
2. Description of the Related Art In recent years, in the garment field, a soft and repulsive texture has been favored. Traditionally, such a texture has been used in the finishing process after scouring, bleaching, and dyeing the fabric. A silicone softener is used as a processing agent to provide a soft texture. In order to create a texture with a urethane resin,
The cloth is impregnated with a single treatment solution or a mixed treatment solution of these chemicals, and a heat treatment is performed to give the cloth a soft and repulsive texture.

【0003】シリコン系柔軟剤のみを用いてセルロース
系繊維布帛上で皮膜を形成したものは,皮膜強度,耐水
性等は優れたものが多いが,シリコン皮膜とセルロース
との結合が弱いため,洗濯によりシリコン皮膜の脱離が
生じやすいという問題点がある。ウレタン樹脂のみを用
いてセルロース系繊維布帛に反応させたものは,セルロ
ースと架橋反応しているため,反撥性はよいが,ソフト
性に欠けるという問題がある。シリコン系柔軟剤とウレ
タン樹脂のみの混合処理液を用いたものは,加工上りは
ソフトで反撥性のある風合が得られるが,洗濯によりシ
リコン系柔軟剤が脱落し,風合が粗硬となるという問題
がある。また,最近では,ビーティングや高速移送によ
る風合加工機を用いてソフト感やボリューム感を出す加
工が行われているが,特殊な機械装置が必要であるのと
処理時間がかかるという問題がある。
[0003] Many of the ones in which a film is formed on a cellulosic fiber cloth using only a silicone softening agent have excellent film strength and water resistance, but since the bond between the silicon film and cellulose is weak, it is washed. Therefore, there is a problem that the silicon film is likely to be detached. A product obtained by reacting a cellulosic fiber cloth with only a urethane resin has a good resilience but lacks softness because it has a cross-linking reaction with cellulose. The one using the mixed treatment liquid of only the silicone type softener and urethane resin gives a soft and repulsive texture after processing, but the silicone type softener falls off by washing and the texture is rough and hard. There is a problem of becoming. In addition, recently, processing that gives a soft feeling and a volume feeling is performed using a texture processing machine by beating or high-speed transfer, but there is a problem that a special mechanical device is required and processing takes time. .

【0004】[0004]

【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,セルロース系繊維布帛に
洗濯耐久性の優れたソフトで反撥性を有する風合を付与
する加工方法を得ることを目的とするものである。
SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and is a processing method for imparting a soft and repulsive texture having excellent washing durability to a cellulosic fiber cloth. The purpose is to obtain.

【0005】[0005]

【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,次の構成によりなるものである。すなわ
ち,本発明は,水系ポリウレタン樹脂,エポキシ化合
物,エポキシ変性オルガノポリシロキサン,アミノ変性
オルガノポリシロキサンおよび金属塩系酸性触媒の混合
処理液をセルロース系繊維布帛に含浸し,乾燥,熱処理
を行い,しかる後にバッチ式染色機を用いて揉み処理を
行うことを特徴とするセルロース系繊維布帛の加工方法
を要旨とするものである。以下,本発明を詳細に説明す
る。
The present invention achieves the above object and has the following configuration. That is, in the present invention, a cellulosic fiber cloth is impregnated with a mixed treatment liquid of an aqueous polyurethane resin, an epoxy compound, an epoxy-modified organopolysiloxane, an amino-modified organopolysiloxane, and a metal salt-based acidic catalyst, followed by drying and heat treatment. A gist is a method of processing a cellulose fiber cloth, which is characterized in that a kneading treatment is performed later by using a batch type dyeing machine. Hereinafter, the present invention will be described in detail.

【0006】本発明では,セルロース系繊維布帛を加工
の対象として用いる。ここで用いるセルロース系繊維布
帛は,木綿,麻等の天然繊維,ビスコースレーヨン等の
再生繊維を主に用いた布帛であり,これらの天然繊維や
再生繊維の混用率が50%以上のものが好ましく,混用
率が50%以下であると,後述の混合処理剤とセルロー
スとの反応が少なくなるため,洗濯耐久性のあるソフト
で反撥性を有する風合をセルロース系繊維布帛に付与す
ることができなくなる。
In the present invention, a cellulosic fiber cloth is used as an object to be processed. The cellulosic fiber cloth used here is a cloth mainly using natural fibers such as cotton and hemp, and regenerated fibers such as viscose rayon, and those having a mixture ratio of these natural fibers and regenerated fibers of 50% or more. Preferably, when the mixing ratio is 50% or less, the reaction between the later-described mixing treatment agent and cellulose is reduced, so that a soft and repulsive texture with washing durability can be imparted to the cellulosic fiber cloth. become unable.

【0007】本発明では,まず上述のセルロース系繊維
布帛に水系ポリウレタン樹脂,エポキシ化合物,エポキ
シ変性オルガノポリシロキサン,アミノ変性オルガノポ
リシロキサンおよび金属塩系酸性触媒の混合処理液を含
浸し,乾燥,熱処理を行う。本発明で用いる水系ポリウ
レタン樹脂としては,長鎖のポリオールにポリエステル
型ポリウレタンとポリエーテル型ポリウレタンがあるう
ち,加水分解性の点からみてポリエーテル型ポリウレタ
ンを用いる方が望ましく,イソシアネート別では,芳香
族イソシアネート系ポリウレタンと脂肪族イソシアネー
ト系ポリウレタンのうち,耐光性の点から脂肪族イソシ
アネート系ポリウレタンを用いる方が望ましく,特に,
脂肪族エーテル型ポリウレタン樹脂を用いるの望まし
い。
In the present invention, first, the above-mentioned cellulosic fiber cloth is impregnated with a mixed treatment liquid of an aqueous polyurethane resin, an epoxy compound, an epoxy-modified organopolysiloxane, an amino-modified organopolysiloxane and a metal salt-based acidic catalyst, followed by drying and heat treatment. I do. As the water-based polyurethane resin used in the present invention, among the long-chain polyols, polyester type polyurethane and polyether type polyurethane, it is preferable to use the polyether type polyurethane from the viewpoint of hydrolysis property. Of the isocyanate-based polyurethane and the aliphatic isocyanate-based polyurethane, it is preferable to use the aliphatic isocyanate-based polyurethane from the viewpoint of light resistance.
It is desirable to use an aliphatic ether type polyurethane resin.

【0008】本発明で用いるエポキシ化合物としては,
同一分子内の末端にエポキシ基を2個以上有するエポキ
シ化合物を用い,具体的には,グリセロールポリグリシ
ジルエーテル,ソルビトールポリグリシジルエーテル等
を挙げることができる。本発明で用いるエポキシ変性オ
ルガノポリシロキサンは,下記式1で表され,セルロー
スと効果的に反応するために,同一分子内に少なくとも
2個以上エポキシ基が含まれていることが望ましい。
The epoxy compound used in the present invention includes
An epoxy compound having two or more epoxy groups at the end in the same molecule is used, and specific examples thereof include glycerol polyglycidyl ether and sorbitol polyglycidyl ether. The epoxy-modified organopolysiloxane used in the present invention is represented by the following formula 1, and preferably has at least two epoxy groups in the same molecule in order to effectively react with cellulose.

【0009】[0009]

【化1】 Embedded image

【0010】具体的には,繊維仕上げ加工剤として市販
されているエポキシ変性シリコン柔軟仕上げ剤を用いれ
ばよい。
Specifically, a commercially available epoxy modified silicone softening agent may be used as the fiber finishing agent.

【0011】本発明で用いるアミノ変性オルガノポリシ
ロキサンは,下記式2で表され,具体的には,繊維仕上
げ加工剤として市販されているアミノ変性シリコン柔軟
仕上げ剤を用いればよい。
The amino-modified organopolysiloxane used in the present invention is represented by the following formula 2, and specifically, an amino-modified silicone softening agent commercially available as a fiber finishing agent may be used.

【0012】[0012]

【化2】 Embedded image

【0013】上述の水系ポリウレタン樹脂,エポキシ化
合物,エポキシ変性オルガノポリシロキサンおよびアミ
ノ変性オルガノポリシロキサンの各樹脂の使用量は,目
的とする風合により異なるが,水系ポリウレタン樹脂は
20〜200g/リットル,エポキシ化合物は水系ポリ
ウレタン樹脂に対して10〜50重量%使用し,エポキ
シ変性オルガノポリシロキサンおよびアミノ変性オルガ
ノポリシロキサンは各々10〜30g/リットル程度使
用するとよい。
The amount of each of the above-mentioned water-based polyurethane resin, epoxy compound, epoxy-modified organopolysiloxane and amino-modified organopolysiloxane used varies depending on the desired texture, but the water-based polyurethane resin is 20 to 200 g / liter, The epoxy compound may be used in an amount of 10 to 50% by weight based on the water-based polyurethane resin, and the epoxy-modified organopolysiloxane and the amino-modified organopolysiloxane may each be used in an amount of about 10 to 30 g / liter.

【0014】本発明で用いる金属塩系酸性触媒として
は,亜鉛,マグネシウム,アルミニウム等の塩化物,硝
酸化物,硼弗化物等の塩類を挙げることができ,具体的
には,塩化亜鉛,塩化マグネシウム,塩化アルミニウ
ム,硝酸亜鉛,硼弗化亜鉛,硼弗化マグネシウム等を挙
げることができる。金属塩系酸性触媒の使用量は,上述
のエポキシ化合物とエポキシ変性オルガノポリシロキサ
ンに対して3〜10重量%が適量であるが,使用する触
媒の活性力により使用量は異なるので,必要により適宜
調節して用いるとよい。
Examples of the metal salt-based acidic catalyst used in the present invention include chlorides such as zinc, magnesium and aluminum, salts such as nitric oxide and borofluoride, and specifically, zinc chloride and magnesium chloride. , Aluminum chloride, zinc nitrate, zinc borofluoride, magnesium borofluoride and the like. The appropriate amount of the metal salt-based acidic catalyst used is 3 to 10% by weight based on the epoxy compound and the epoxy-modified organopolysiloxane, but the amount varies depending on the activity of the catalyst used. It is good to use it after adjusting.

【0015】本発明では,上述の樹脂を混合した混合処
理液をセルロース系繊維布帛に含浸するが,この含浸に
際しては,パッダー,マングル等の通常の樹脂加工装置
を用いて布帛を混合処理液に浸漬し,絞液率50〜12
0%にて絞液することにより布帛に処理液を含浸する。
In the present invention, the cellulosic fiber cloth is impregnated with the mixed treatment liquid obtained by mixing the above-mentioned resins. At the time of this impregnation, the cloth is treated with the mixed treatment liquid by using a normal resin processing device such as a padder or a mangle. Immersion, squeezing rate 50-12
The cloth is impregnated with the treatment liquid by squeezing the solution at 0%.

【0016】混合処理液の含浸後,布帛を乾燥し,14
0〜180℃にて2〜4分間の熱処理を行う。このよう
にして,洗濯耐久性のある皮膜をセルロース系繊維布帛
上に反応形成させる。
After impregnation with the mixed treatment liquid, the cloth is dried,
Heat treatment is performed at 0 to 180 ° C. for 2 to 4 minutes. In this way, a wash-durable coating is reactively formed on the cellulosic fiber fabric.

【0017】この後,バッチ式染色機を用いてセルロー
ス系繊維布帛の揉み処理を行う。ここで用いるバッチ式
染色機としては,ウインス染色機,ドラム染色機,パド
ル染色機,ジガー染色機,液流染色機,ビーム染色機,
気流染色機等を挙げることができ,物理的な揉み効果の
高い気流染色機を用いるのが望ましい。揉み処理条件
は,40〜80℃にて30〜60分間程度で十分であ
る。
Thereafter, the cellulosic fiber cloth is kneaded using a batch type dyeing machine. The batch-type dyeing machines used here include Wins dyeing machines, drum dyeing machines, paddle dyeing machines, jigger dyeing machines, jet dyeing machines, beam dyeing machines,
An airflow dyeing machine can be used, and it is desirable to use an airflow dyeing machine having a high physical rubbing effect. Rubbing treatment conditions of 40 to 80 ° C. for 30 to 60 minutes are sufficient.

【0018】この揉み処理に際しては,吸尽染色を同時
に行い,染色工程を揉み処理工程と兼ねて行うと,より
一層合理的である。このとき吸尽染色に用いる染料とし
ては直接染料,反応染料,塩基染料,バット染料,硫化
染料,ナフトール染料等を挙げることができるが,染色
堅牢度,汎用性の点から反応染料を用いるのが望まし
い。染色方法は,使用する染料によりそれぞれ異なる
が,その染料で一般に行われている通常の方法で行えば
よい。
In this kneading treatment, it is more rational to perform exhaustion dyeing at the same time and perform the dyeing process also as the kneading treatment process. At this time, the dyes used for exhaust dyeing include direct dyes, reactive dyes, basic dyes, vat dyes, sulfur dyes, naphthol dyes, etc., but reactive dyes are used from the viewpoint of dyeing fastness and versatility. desirable. The dyeing method differs depending on the dye used, but the dyeing method may be an ordinary method generally used for the dye.

【0019】以上のように,前工程で耐久性のある皮膜
をセルロース系繊維上に反応形成した後,後工程でバッ
チ染色機を用いて揉み処理を行うことにより,ソフトで
反撥性を有した風合をセルロース系繊維布帛に付与する
ことができる。本発明は,以上の構成よりなるものであ
る。
As described above, after the durable film was formed by reaction on the cellulosic fiber in the previous step, the kneading treatment was performed in the subsequent step using the batch dyeing machine to obtain a soft and repulsive property. The texture can be imparted to the cellulosic fiber cloth. The present invention has the above configuration.

【0020】[0020]

【作用】ポリウレタン樹脂,エポキシ化合物,エポキシ
変性オルガノポリシロキサン,アミノ変性オルガノポリ
シロキサン,金属塩系酸性触媒の混合処理液を用いるこ
となく,これらの樹脂を従来法によってそれぞれ別工程
で単独使用すると,個々の樹脂とセルロースとの結合が
弱いため,洗濯によりセルロース系繊維布帛上に形成さ
れた樹脂皮膜の脱離が生じてしまい,洗濯耐久性のある
加工を行うことができないが,本発明のごとくこれらの
樹脂を同浴で用いると,まずポリウレタン樹脂にエポキ
シ化合物が反応することになり,ウレタン樹脂皮膜の強
度,耐水性,耐熱性等を向上させて反撥性の優れた皮膜
を得ることができるとともに,エポキシ変性オルガノポ
リシロキサンに金属塩系酸性触媒が作用して,エポキシ
変性オルガノポリシロキサンのエポキシ基がセルロース
の水酸基と反応し,さらにアミノ変性オルガノポリシロ
キサンにアミノアマイドの塩類の併用によりセルロース
の水酸基との反応を向上させることができるようにな
り,その結果,ソフト性の耐久性を図ることができるよ
うになる。このように,セルロースと反応した耐久性の
ある皮膜をセルロース系繊維上に形成させた状態でバッ
チ式染色機を用いて物理的な揉み処理を行うと,布帛の
風合はより一層柔軟になり,本発明の目的とするソフト
で反撥性を有し,しかもその性能の洗濯耐久性を有する
加工布帛を得ることができるようになる。
[Function] Polyurethane resin, epoxy compound, epoxy-modified organopolysiloxane, amino-modified organopolysiloxane, without using a mixed treatment solution of a metal salt-based acidic catalyst, if these resins are individually used in different steps by the conventional method, Since the resin and the cellulose are weakly bonded to each other, the resin film formed on the cellulosic fiber cloth is detached due to the washing, so that the washing durable processing cannot be performed. When these resins are used in the same bath, the epoxy compound first reacts with the polyurethane resin, and the strength, water resistance, heat resistance, etc. of the urethane resin film can be improved and a film with excellent repulsion can be obtained. At the same time, the metal salt-based acidic catalyst acts on the epoxy-modified organopolysiloxane to form an epoxy-modified organopolysiloxane. The epoxy group of roxane reacts with the hydroxyl group of cellulose, and it becomes possible to improve the reaction with the hydroxyl group of cellulose by using the amino-modified organopolysiloxane together with the salt of amino amide. As a result, the durability of softness is improved. Will be able to In this way, the physical texture of the fabric becomes even more soft when the physical rubbing treatment is performed using a batch-type dyeing machine with a durable film that has reacted with cellulose formed on the cellulosic fiber. Therefore, it becomes possible to obtain a processed cloth which is the object of the present invention and which has softness and resilience and has the washing durability of its performance.

【0021】[0021]

【実施例】次に,本発明を実施例によってさらに具体的
に説明するが,実施例における布帛の性能の測定,評価
は,下記の方法で行った。 (1)ソフト性 加工上がり及び下記第(3)項による洗濯耐久性試験後
の布帛について,柔軟な風合を手触りによる感応テスト
により,相対的に次の3段階で評価した。 ○ 良 好 △ 普 通 × 不 良 (2)反撥性 加工上がり及び下記第(3)項による洗濯耐久性試験後
の布帛について,反撥性を手触りによる感応テストによ
り相対的に次の3段階で評価した。 ○ 良 好 △ 普 通 × 不 良 (3)洗濯耐久性試験 JIS L−0217(103法)により30回の洗濯
を行う。
EXAMPLES Next, the present invention will be described in more detail with reference to Examples. Measurement and evaluation of the performance of the fabrics in Examples were carried out by the following methods. (1) Softness With respect to the fabric after finishing the processing and after the washing durability test according to the item (3) below, the soft feeling was relatively evaluated in the following three stages by a touch-sensitive test. ○ Good △ Normal × Poor (2) Repulsion Repulsion of the fabric after processing and after the washing durability test according to item (3) below is relatively evaluated by the touch test by the following three grades. did. Good Good Fair Normal Poor (3) Washing durability test Wash 30 times according to JIS L-0217 (method 103).

【0022】実施例1 木綿100%の晒上がりの平織物(経糸18s/−,緯
糸18s/−;経糸密度110本/吋,緯糸密度55本
/吋)を用意し,これに下記処方1の処理液を含浸し,
マングルで絞液率80%にて圧搾絞液後,ピンテンター
にて100℃で2分間の乾燥を行い,続いて160℃で
3分間の熱処理を行った。
Example 1 A plain weave fabric made of 100% cotton (warp 18s /-, weft 18s /-; warp density 110 yarns / inch, weft density 55 yarns / inch) was prepared. Impregnated with treatment liquid,
After squeezing and squeezing with a mangle at a squeezing rate of 80%, it was dried with a pin tenter at 100 ° C. for 2 minutes, and then heat-treated at 160 ° C. for 3 minutes.

【0023】処方1 エバファノールN 100g/リットル (水溶性ウレタンポリマー,日華化学工業株式会社製) NKカタリストCS 5g/リットル (触媒,日華化学工業株式会社製) デナコールEX−314 10g/リットル (エポキシ化合物,ナガセ化成工業株式会社製) ポロンMF−18 50g/リットル (エポキシ変性ポリシロキサンエマルジョン,信越化学
工業株式会社製) 硼弗化亜鉛 6g/リットル ニッカシリコンAM−3000 50g/リットル (アミノ変性ポリシロキサンエマルジョン,日華化学工
業株式会社製)
Formulation 1 Evaphanol N 100 g / liter (water-soluble urethane polymer, Nichika Chemical Industry Co., Ltd.) NK Catalyst CS 5 g / liter (catalyst, Nika Chemical Industry Co., Ltd.) Denacol EX-314 10 g / liter (epoxy Compound, manufactured by Nagase Kasei Co., Ltd.) PORON MF-18 50 g / liter (epoxy-modified polysiloxane emulsion, manufactured by Shin-Etsu Chemical Co., Ltd.) Zinc borofluoride 6 g / liter Nikka Silicon AM-3000 50 g / liter (amino-modified polysiloxane) Emulsion, Nika Chemical Industry Co., Ltd.)

【0024】次に,液流染色機を用いて,下記処方2の
染色液により浴比1:20にて20℃から昇温速度0.5
℃/分で昇温し,80℃で60分間の吸尽染色兼揉み処
理を行い,本発明の加工織物を得た。
Then, using a jet dyeing machine, a dyeing solution of the following formulation 2 was used to raise the temperature from the temperature of 20 ° C. to 0.5 at a bath ratio of 1:20.
The temperature was raised at a rate of ° C / min and exhaust dyeing and kneading treatment was carried out at 80 ° C for 60 minutes to obtain a processed woven fabric of the present invention.

【0025】処方2 Kayacion Blue AB 3%owf (反応染料,日本化薬株式会社製) 無水芒硝 80g/リットル ソーダ灰 20g/リットルFormulation 2 Kayacion Blue AB 3% owf (reactive dye, manufactured by Nippon Kayaku Co., Ltd.) Anhydrous Glauber's salt 80 g / liter Soda ash 20 g / liter

【0026】本発明との比較のため,本実施例における
処方2の吸尽染色を処方1による処理より先に行い,そ
の後に処方1による処理を行うほかは,本実施例とまっ
たく同一の方法により比較用の加工織物(比較例1)を
得た。
For comparison with the present invention, exactly the same method as in the present embodiment except that the exhaust dyeing of the prescription 2 in this embodiment is performed before the treatment of the prescription 1 and then the treatment of the prescription 1 is performed. Thus, a processed woven fabric for comparison (Comparative Example 1) was obtained.

【0027】また本発明との比較のため,本実施例の処
方1からデナコールEX−314,ポロンMF−18,
硼弗化亜鉛,ニッカシリコンAM−3000を除くほか
は,本実施例とまったく同一の方法により比較用の加工
織物(比較例2)を得た。
For comparison with the present invention, Formulation 1 to Denacol EX-314, Polon MF-18,
A processed woven fabric for comparison (Comparative Example 2) was obtained by the same method as that of this Example except that zinc borofluoride and Nikka Silicon AM-3000 were removed.

【0028】さらに本発明との比較のため,本実施例の
処方1からエバファノールN,NKカタリストCS,デ
ナコールEX−314,硼弗化亜鉛を除くほかは,本実
施例とまったく同一の方法により比較用の加工織物(比
較例3)を得た。
Further, for comparison with the present invention, a comparison was made by the same method as in this example except that Evaphanol N, NK Catalyst CS, Denacol EX-314 and zinc borofluoride were excluded from Formulation 1 of this example. A processed woven fabric (Comparative Example 3) was obtained.

【0029】本発明および比較用の加工織物の性能を評
価し,その結果を合わせて表1に示した。
The performances of the present invention and the comparative woven fabric were evaluated, and the results are shown together in Table 1.

【0030】[0030]

【表1】 [Table 1]

【0031】表1より明らかなごとく,本発明方法によ
る加工織物は,ソフトで反撥性を有し,しかもその性能
の洗濯耐久性においても優れていることが分かる。
As is clear from Table 1, the processed woven fabric produced by the method of the present invention is soft and repellent, and is excellent in washing durability.

【0032】実施例2 レーヨン100%の晒上がりの綾織物(経糸30/−,
緯糸30/−;経糸密度140本/吋,緯糸密度70本
/吋)を用意し,これに下記処方3の処理液を含浸し,
マングルで絞液率90%にて圧搾絞液後,ビンテンター
にて100℃で2分間の乾燥を行った後,160℃で3
分間の熱処理を行った。
Example 2 Twill fabric with 100% rayon bleached (warp yarn 30 /-,
Weft thread 30 /-; warp density 140 threads / inch, weft density 70 threads / inch) are prepared and impregnated with the treatment liquid of the following prescription 3
After squeezing and squeezing with a mangle at a squeezing rate of 90%, it was dried with a bottle tenter at 100 ° C for 2 minutes and then at 160 ° C for 3 minutes.
Heat treatment was performed for 1 minute.

【0033】処方3 エバファノールN 30g/リットル (水溶性ウレタンポリマー,日華化学工業株式会社製) NKカタリストCS 1.5g/リットル (触媒,日華化学工業株式会社製) デナコールEX−314 3g/リットル (エポキシ化合物,ナガセ化成工業株式会社製) ポロンMF−18 30g/リットル (エポキシ変性ポリシロキサンエマルジョン,信越化学
工業株式会社製) 硼弗化亜鉛 4g/リットル (45%水溶液,試薬1級) ニッカシリコンAM−3000 30g/リットル (アミノ変性ポリシロキサンエマルジョン,日華化学工
業株式会社製)
Formulation 3 Evaphanol N 30 g / liter (water-soluble urethane polymer, Nichika Chemical Industry Co., Ltd.) NK Catalyst CS 1.5 g / liter (catalyst, Nika Chemical Industry Co., Ltd.) Denacol EX-314 3 g / liter (Epoxy compound, manufactured by Nagase Kasei Co., Ltd.) PORON MF-18 30 g / liter (Epoxy-modified polysiloxane emulsion, manufactured by Shin-Etsu Chemical Co., Ltd.) Zinc borofluoride 4 g / liter (45% aqueous solution, reagent first grade) Nikka Silicon AM-3000 30 g / liter (amino-modified polysiloxane emulsion, manufactured by Nika Chemical Industry Co., Ltd.)

【0034】次に,実施例1で用いた処方2の染色液に
より,液流染色機を用いて実施例1と同一条件で吸尽染
色兼揉み処理を行い,本発明の加工織物を得た。
Next, with the dyeing solution of formulation 2 used in Example 1, exhaust dyeing and kneading treatment was performed under the same conditions as in Example 1 using a jet dyeing machine to obtain a processed fabric of the present invention. .

【0035】本発明との比較のため,本実施例において
援用した実施例1の処方2による吸尽染色兼揉み処理を
先に行い,その後に処方3による処理を行うほかは,本
実施例とまったく同一の方法により比較用の加工織物
(比較例4)を得た。
For comparison with the present invention, except that the exhaust dyeing and kneading treatment according to the prescription 2 of the embodiment 1 incorporated in the present embodiment is performed first, and then the treatment according to the prescription 3 is performed, the same as the present embodiment. A processed woven fabric for comparison (Comparative Example 4) was obtained by the same method.

【0036】本発明および比較用の加工織物の性能を評
価し,その結果を合わせて表2に示した。
The performances of the inventive and comparative fabrics were evaluated and the results are summarized in Table 2.

【0037】[0037]

【表2】 [Table 2]

【0038】表2より明らかなごとく,本発明方法によ
る加工織物は,ソフトで反撥性を有し,しかもその性能
の洗濯耐久性においても優れていることが分かる。
As is clear from Table 2, the processed woven fabric produced by the method of the present invention is soft and repellent, and is excellent in washing durability.

【0039】[0039]

【発明の効果】本発明によれば,ソフトで反撥性を有
し,しかもその性能の洗濯耐久性の優れたセルロース系
繊維布帛を得ることができる。
EFFECTS OF THE INVENTION According to the present invention, it is possible to obtain a cellulosic fiber cloth which is soft and repellent and has excellent washing durability.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 水系ポリウレタン樹脂,エポキシ化合
物,エポキシ変性オルガノポリシロキサン,アミノ変性
オルガノポリシロキサンおよび金属塩系酸性触媒の混合
処理液をセルロース系繊維布帛に含浸し,乾燥,熱処理
を行い,しかる後にバッチ式染色機を用いて揉み処理を
行うことを特徴とするセルロース系繊維布帛の加工方
法。
1. A cellulosic fiber cloth is impregnated with a mixed treatment liquid of an aqueous polyurethane resin, an epoxy compound, an epoxy-modified organopolysiloxane, an amino-modified organopolysiloxane and a metal salt-based acidic catalyst, followed by drying and heat treatment. A method for processing a cellulosic fiber cloth, which comprises performing a rubbing treatment using a batch type dyeing machine.
JP6291245A 1994-11-25 1994-11-25 Method for processing cellulose-based textile fabric Pending JPH08158264A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6291245A JPH08158264A (en) 1994-11-25 1994-11-25 Method for processing cellulose-based textile fabric

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6291245A JPH08158264A (en) 1994-11-25 1994-11-25 Method for processing cellulose-based textile fabric

Publications (1)

Publication Number Publication Date
JPH08158264A true JPH08158264A (en) 1996-06-18

Family

ID=17766368

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6291245A Pending JPH08158264A (en) 1994-11-25 1994-11-25 Method for processing cellulose-based textile fabric

Country Status (1)

Country Link
JP (1) JPH08158264A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100821845B1 (en) * 2007-04-30 2008-04-14 주식회사 삼광염직 Shape retentioner for cellulose fiber and shape retentioning using thereof
US20130079475A1 (en) * 2008-03-17 2013-03-28 Henkel Corporation Adhesive compositions for use in die attach applications

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100821845B1 (en) * 2007-04-30 2008-04-14 주식회사 삼광염직 Shape retentioner for cellulose fiber and shape retentioning using thereof
US20130079475A1 (en) * 2008-03-17 2013-03-28 Henkel Corporation Adhesive compositions for use in die attach applications
US8835574B2 (en) * 2008-03-17 2014-09-16 Henkel IP Holding GmbH Adhesive compositions for use in die attach applications

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