JPH03180574A - Finish processing of fiber structure - Google Patents

Finish processing of fiber structure

Info

Publication number
JPH03180574A
JPH03180574A JP31547389A JP31547389A JPH03180574A JP H03180574 A JPH03180574 A JP H03180574A JP 31547389 A JP31547389 A JP 31547389A JP 31547389 A JP31547389 A JP 31547389A JP H03180574 A JPH03180574 A JP H03180574A
Authority
JP
Japan
Prior art keywords
fiber structure
urethane resin
fiber
resin
stabilizer
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
JP31547389A
Other languages
Japanese (ja)
Inventor
Hideki Shiozaki
英樹 塩崎
Midori Kondo
みどり 近藤
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.)
KANAGAWA PREF GOV
Kanagawa Prefecture
Nissan Motor Co Ltd
Original Assignee
KANAGAWA PREF GOV
Kanagawa Prefecture
Nissan Motor 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 KANAGAWA PREF GOV, Kanagawa Prefecture, Nissan Motor Co Ltd filed Critical KANAGAWA PREF GOV
Priority to JP31547389A priority Critical patent/JPH03180574A/en
Publication of JPH03180574A publication Critical patent/JPH03180574A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To simultaneously impart durability, excellent color fastness to light and abrasion resistance to a fiber structure by immersing the fiber structure in a treating agent comprising an aqueous urethane resin and a stabilizer for the urethane resin and subsequently heating the treated fiber structure. CONSTITUTION:A fiber structure is immersed in an aqueous treating bath compounded with aqueous urethane resin of blocked polyisocyanate prepolymer type and with a stabilizer for the resin, such as 6-hexanemethylene-bis-(N- dimethylsemicarbazide) in an amount of >=10wt.% based on the resin, followed by heating the immersed fiber structure to form a stable coat on the fiber structure, thereby improving the aging deterioration, touch deterioration and color-fading inclination of the fiber structure and further improving the color fastness to light and abrasion resistance of the fiber substrate itself. The method provides a good result when applied to the dry cleaning process of high grade fiber products such as silk.

Description

【発明の詳細な説明】 (産業上の利用分野〉 本発明は繊維構造物に耐久性を付与する仕上加工方法、
特に耐光性と耐摩耗性−とを同時に付与する繊維構造物
の仕上加工方法に関する。
Detailed Description of the Invention (Industrial Application Field) The present invention provides a finishing method for imparting durability to a fiber structure;
In particular, the present invention relates to a finishing method for fiber structures that simultaneously imparts light resistance and abrasion resistance.

(従来の技術) 織布やニット布、レースのような繊維構造物は精練漂白
後、あるいは染色後の最終工程において仕上加工される
のが一般的であり、製品としての性能向上や、風合、感
性などの要求される製品特性に応じて多種多様な仕上剤
が利用されている。
(Prior art) Textile structures such as woven fabrics, knitted fabrics, and lace are generally finished in the final process after scouring and bleaching or dyeing, to improve product performance and texture. A wide variety of finishing agents are used depending on the required product characteristics, such as sensitivity.

最近では衣料分野において機能性と感性の特化加工への
追求が盛んになり、特に仕上加工におけるウレタン樹脂
による特化加工が注目されている。
Recently, the pursuit of specialized processing for functionality and sensibility has become active in the clothing field, and specialized finishing using urethane resin is attracting particular attention.

分子中に−NH−CO−結合を有するウレタン樹脂は一
般にポリイソアネートとポリオールとを主原料として重
付加反応で合成されるが、原料の組合せにより多種多様
の分子構造と物性を有するウレタン樹脂仕上げ剤が市販
されるようになった。繊維加工用としては主として水性
タイプのものが実用化されており、特に熱反応性のブロ
ック化インシアネートプレポリマータイプ(例えば第一
工業製薬■製、エラストロン〉が多く用いられている。
Urethane resins that have -NH-CO- bonds in their molecules are generally synthesized by polyaddition reaction using polyisoanate and polyol as main raw materials, but urethane resin finishing agents with a wide variety of molecular structures and physical properties can be produced depending on the combination of raw materials. It has become commercially available. For fiber processing, mainly aqueous types are in practical use, and in particular, heat-reactive blocked incyanate prepolymer types (for example, Elastron manufactured by Daiichi Kogyo Seiyaku ■) are often used.

このタイプのものは熱処理によってブロック剤を解離し
て繊維上で高分子被膜を形成すると共に、繊維内官能性
側鎖〈例えば水酸基〉とも化学反応し得るといわれる。
In this type, the blocking agent is dissociated by heat treatment to form a polymer film on the fiber, and it is said that it can also chemically react with functional side chains (eg, hydroxyl groups) within the fiber.

このタイプのウレタン樹脂は一般に柔軟で弾力のある風
合を繊維構造物に付与すると共に、耐摩耗性や防縮性を
顕著に向上することから高い評価を受けている。代表的
な例としては羊毛の防縮加工としてのシロランBAP加
工が著名であるが、最近ではセルロース系繊維の防しわ
加工〈特開昭64−77678号公報〉や絹紡織物のス
レ(毛羽立ち)発生防止加工(特開昭63−81579
号公報)に用いる試みも提案されている。
This type of urethane resin is generally highly evaluated because it imparts a soft and elastic feel to fibrous structures and significantly improves abrasion resistance and shrink-proofing properties. A typical example is Siloran BAP processing, which is a well-known anti-shrunk treatment for wool, but recently, wrinkle-proofing treatment for cellulose fibers (Japanese Patent Application Laid-open No. 77678/1984) and threading (fuzzing) on silk textiles have become more popular. Prevention processing (JP-A-63-81579
An attempt to use this method has also been proposed.

(発明が解決しようとする課題〉 ウレタン樹脂は前記の如く原料の組合せによって多種多
様な性能のものが製造されていて、多岐にわたる分野に
用途が伸びているが、その原料組成によって差異はある
にしても光、熱、酸素、水、NOxなどによる着色、劣
化、分解を起こしやすいと言われている。繊維の仕上加
工においては未だ経験の浅いこともあって、現状では防
縮、耐摩耗、風合改善等の加工効果のみが強調されてい
るが、日光による着色や劣化、長期間経過後の性能変化
などの故障事故がウレタン樹脂の弱点として起こり得る
と考えられる。
(Problem to be solved by the invention) As mentioned above, urethane resins are manufactured with a wide variety of performance depending on the combination of raw materials, and their applications are expanding in a wide variety of fields. However, it is said that it is susceptible to discoloration, deterioration, and decomposition due to light, heat, oxygen, water, NOx, etc.As there is still little experience in the finishing of textiles, at present there are no shrink-proof, abrasion-resistant, wind-resistant Although only the effects of processing such as improved chemical composition are emphasized, failure accidents such as coloring and deterioration due to sunlight and changes in performance after a long period of time are thought to be the weaknesses of urethane resin.

従って本発明の目的はウレタン樹脂による繊維加工にお
いて、防縮、防しわ、耐摩耗など一般物性の向上効果を
従来通りに充分に発揮しまた、繊維製品の風合を低下さ
せることなく、且つ日光や紫外線に対しても高い耐久性
を有するような仕上加工方法を提供することにある。
Therefore, the purpose of the present invention is to fully exhibit the effect of improving general physical properties such as shrink-proofing, wrinkle-proofing, and abrasion resistance in fiber processing using urethane resin, without deteriorating the texture of textile products, and without reducing sunlight and sunlight. An object of the present invention is to provide a finishing method that has high durability even against ultraviolet rays.

(課題を解決するため手段) ウレタン樹脂の底形などでは樹脂用安定剤として酸化防
止剤や紫外線吸収剤などが添加されるが、この種安定剤
の中で活性光線保護基をもつヒドラジン誘導体、例えば
1,6−ヘキサメチレン−ビス−(N、 N’−ジメチ
ルセミカルバジド)(商品名、 HN−130,日本ヒ
ドラジン■製)はウレタン樹脂だけでなく、種々の高分
子物に対しても持続性の長い劣化防止効果をもつこと、
最近では絹の黄変防止効果も認められている〈特開昭6
2−6976号公報)。
(Means for solving the problem) Antioxidants and ultraviolet absorbers are added as stabilizers for resins such as bottom-type urethane resins, but among these stabilizers, hydrazine derivatives with active ray-protecting groups, For example, 1,6-hexamethylene-bis-(N,N'-dimethylsemicarbazide) (trade name, HN-130, manufactured by Nippon Hydrazine ■) has long-lasting properties not only for urethane resins but also for various polymers. have a long deterioration prevention effect,
Recently, the effect of preventing yellowing of silk has also been recognized.
2-6976).

本発明者らはウレタン樹脂による繊維構造物の仕上加工
においてウレタン樹脂安定剤好ましくはHN−130を
ウレタン樹脂純分に対して10重量%以上、好ましくは
10〜20重量%添加する方法を採用することによって
、紫外線による繊維の着色、劣化を防止するだけでなく
、繊維上のウレタン被膜の光劣化の防止にも長期間に亘
り有効であることを見出した。
The present inventors have adopted a method in which a urethane resin stabilizer, preferably HN-130, is added in an amount of 10% by weight or more, preferably 10 to 20% by weight, based on the pure urethane resin in the finishing process of a fiber structure made of urethane resin. It has been found that this method is effective not only in preventing coloring and deterioration of fibers due to ultraviolet rays, but also in preventing photodeterioration of the urethane coating on the fibers over a long period of time.

第1図に、絹35匁付羽二重を068%イルガランブル
ーFBLで染色した後、ウレタン樹脂〔エラストロンM
F−9(30%溶液)  1150g/ Rとし、HN
−130の分量を変えて作製した処理浴に浸漬し、絞液
、乾燥した後、キセノン3 SUNによりキセノン先に
100時間照射し黄変度を測定した結果を示す。第1図
よりHN−130が10重量%以上で黄変度(Δb)が
改善されることが明らかである。
Figure 1 shows silk 35 momme Habutae dyed with 068% Irugalan Blue FBL, then urethane resin [Elastron M
F-9 (30% solution) 1150g/R, HN
-130 was immersed in treatment baths prepared with varying amounts, squeezed, dried, and then irradiated with xenon for 100 hours using Xenon 3 SUN to measure the degree of yellowing. It is clear from FIG. 1 that the degree of yellowing (Δb) is improved when HN-130 is contained in an amount of 10% by weight or more.

さらには、懲戒される被膜自体もllN−130の添加
によってより柔軟性を増すために、デリケートな触感が
重視される薄地布やニット布の仕上加工にこの方法を用
いれば、よりすぐれた感性をもつ製品が得られること、
まな外衣等の重衣料用織布に用いる場合にもウレタン樹
脂付着量を従来の限界量以上に増しても風合を損なう心
配がなく、それだけ耐摩耗性等の向上効果を高めること
が可能となった。
Furthermore, the coating itself becomes more flexible with the addition of LLN-130, so if this method is used for finishing thin fabrics and knit fabrics where delicate tactility is important, superior sensitivity can be achieved. that you can obtain a product with
Even when used in woven fabrics for heavy clothing such as outerwear, there is no fear that the texture will be impaired even if the amount of urethane resin adhered is increased beyond the conventional limit, and the effect of improving abrasion resistance etc. can be increased accordingly. became.

従って本発明の繊維構造物の仕上加工方法は、水性ウレ
タン樹脂とウレタン樹脂用安定剤とから成る処理浴を繊
維構造物に含浸し、熱処理、好ましくは60〜120℃
の温度で熱処理することを特徴とする。
Therefore, in the finishing method of a fibrous structure of the present invention, the fibrous structure is impregnated with a treatment bath consisting of an aqueous urethane resin and a stabilizer for urethane resin, and then heat-treated, preferably at 60 to 120°C.
It is characterized by heat treatment at a temperature of .

本発明に用いられるウレタン樹脂は繊維仕上加工である
ことから水溶性ブロックタイプのものが望ましく、現在
市販されている代表例としてはエラストロンMP−9(
第一工業製薬■製〉エラストロンBAP (第一工業製
薬■製)、シンタプレッ) BAP(バイエル社製)な
どを挙げることができる。また目的とする加工効果の要
求項目によっては、これに反応触媒、ベースレジン、ポ
リアミド、ポリアクリルなどを併用することもできる。
Since the urethane resin used in the present invention is fiber-finished, it is desirable to use a water-soluble block type resin, and a typical example currently on the market is Elastron MP-9 (
Examples include Elastron BAP (manufactured by Daiichi Kogyo Seiyaku ■), Syntapret BAP (manufactured by Bayer), and the like. Depending on the requirements for the desired processing effect, a reaction catalyst, base resin, polyamide, polyacrylic, etc. may also be used in combination.

本発明に用いるlN−130は水溶性であり、繊維やウ
レタン樹脂に化学結合することはないので、本発明加工
製品は水系洗濯によって耐光効果は損なわれる。したが
って水系洗濯の必要性が低い外衣やインテリア関係に特
に有用であり、また洗濯した場合には最終すすぎにHN
−130を添加すれば再び耐光性は発揮される。しかし
ながら、ドライクリーニングを適用することが最も推奨
され、特に絹のような水洗い不可のデリケートな高級品
に最も適した方法である。
Since IN-130 used in the present invention is water-soluble and does not chemically bond to fibers or urethane resins, the light resistance of the processed products of the present invention is impaired by aqueous washing. Therefore, it is particularly useful for outer clothing and interior items that require less water-based washing, and when washed, HN is used for the final rinse.
If -130 is added, the light resistance will be exhibited again. However, applying dry cleaning is the most recommended method, especially for delicate luxury items that cannot be washed with water, such as silk.

(実施例) 本発明を次の実施例により説明する。(Example) The invention is illustrated by the following examples.

実施例 1 経、緯糸ともに絹紡糸使いの平織物(60g/m2富士
絹)を次の処理浴(水溶液)に常温で3分間浸漬し、ロ
ールマングルで約85%に絞液、次いで100℃で3分
間熱処理し乾燥した。
Example 1 A plain woven fabric (60 g/m2 Fuji Silk) using spun silk for both the warp and weft was immersed in the following treatment bath (aqueous solution) at room temperature for 3 minutes, squeezed to about 85% with a roll mangle, and then heated at 100°C. It was heat-treated for 3 minutes and dried.

エラストロンMF−9(30%溶液)  150g/ 
RHN−1305g/ 1 この加工試料およびエラストロンMF−9のみの処理浴
で同様に処理した対照処理試料並びに未処理試料の性能
は表1に示す如くであった。ウレタン樹脂単独処理(対
照処理試料)は精紡織物の紡しわ性等を向上する効果が
あるが、紫外線照射によって著しく黄変、脆化を生じた
が、lN−130をウレタン樹脂に添加した実施例1の
本発明加工試料は耐光性が非常にすぐれていた。
Elastron MF-9 (30% solution) 150g/
RHN-1305g/1 The performance of this processed sample, a control sample treated in the same manner with a treatment bath containing only Elastron MF-9, and an untreated sample were as shown in Table 1. Treatment with urethane resin alone (control treated sample) had the effect of improving the wrinkling properties of spun fabrics, but it caused significant yellowing and embrittlement due to ultraviolet irradiation. The sample processed according to the invention in Example 1 had excellent light resistance.

実施例 2 0.8%イルガランブルーFBL (金属錯塩染料)に
よって染色した14匁付絹羽二重を次の処理浴に常置で
3分間浸漬し、約88%に絞液、100℃で3公開乾燥
した。
Example 2 A 14-momme silk habutae dyed with 0.8% Irugalan Blue FBL (metal complex dye) was immersed permanently in the following treatment bath for 3 minutes, squeezed to about 88%, and heated to 100°C for 3 minutes. Publicly dried.

エラストロンMF−9(30%溶液)  120g/ 
IHN−1306g/ n tlN−130を含まない浴による対照処理試料および
未処理試料との性能比較結果を表2に示す。
Elastron MF-9 (30% solution) 120g/
The performance comparison results with the control treated sample and the untreated sample with the bath without IHN-1306 g/ntlN-130 are shown in Table 2.

表2 本 剛軟度、ハートループ法 実施例2の加工箱はキセノン先に長時間照射してもほと
んど変退色を生ぜず、風合も変わらないことが明らかで
ある。これに対して、ウレタン樹脂単独加工箱は変退色
が著しいばかりでなく、風合もかなり悪化した。
Table 2 Bending resistance, Hartloop method It is clear that the processed box of Example 2 shows almost no discoloration or fading even if the xenon tip is irradiated for a long time, and the texture remains unchanged. On the other hand, the box treated solely with urethane resin not only showed significant discoloration and fading, but also had a considerably worse texture.

実施例 3 精練した20匁付相羽二重を次の処理浴に常温で3分間
浸漬し、85%に絞液、110℃で3分間乾燥した。
Example 3 Refined 20 momme Aba double was immersed in the following treatment bath at room temperature for 3 minutes, squeezed to 85% and dried at 110°C for 3 minutes.

エラストロン 1.I F −9120g/之スミテッ
クスレジン八へ−1(ポリアミド20%)60g/ (
! HN−1306g/ N HN−130を含まない対照処理試料および未処理試料
との性能比較試験結果を表3に示す。
Elastron 1. IF-9120g/Sumitex Resin Hachihe-1 (20% polyamide) 60g/(
! HN-1306g/NH Table 3 shows the performance comparison test results with a control treated sample that does not contain HN-130 and an untreated sample.

本 折目摩耗、JISL1004C(0,5ボンド荷重
〉実施例3の加工箱はキセノン光照射によっても高い耐
摩耗性を保持しており、耐黄変性もすぐでいることがわ
かる。
It can be seen that the processing box of Example 3 maintains high abrasion resistance even when irradiated with xenon light, and is quickly resistant to yellowing.

実施例 4 2%ミカシオンブルー2R(反応染料)で染色した羊毛
モスリンを次の処理浴に常温で5分間浸漬し、72%に
絞液、120℃で4分間乾燥した後、140℃で2分間
キュアリングした。
Example 4 A wool muslin dyed with 2% Mikasion Blue 2R (reactive dye) was immersed in the following treatment bath at room temperature for 5 minutes, squeezed to 72%, dried at 120°C for 4 minutes, and then treated at 140°C for 2 minutes. Cured for minutes.

エラストロンBAP (20%溶液)     80g
/ 1炭酸水素ナトリウム       3g/f亜硫
酸水素ナトリウム      8g#)IN−1306
g/ I HN−130を含まない対照処理試料および未処理試料
との比較試験結果を表4に示す。
Elastron BAP (20% solution) 80g
/ 1 Sodium hydrogen carbonate 3g/f Sodium hydrogen sulfite 8g #) IN-1306
The comparative test results with the control treated sample without g/I HN-130 and the untreated sample are shown in Table 4.

耐 フェルト収縮、アクセレロータ法;本2 抗ピリン
グ、  JISL1076F実施例4の加工試料と対照
処理試料とは同じような防縮・抗ピリング性を付与する
が、耐光性は実施例4の方がすぐれていることがわかる
Resistance to felt shrinkage, Accelerotor method; Book 2 Anti-pilling, JISL1076F Example 4 processed sample and control treated sample provide similar anti-shrinkage and anti-pilling properties, but Example 4 has better light resistance. I understand that.

実施例 5 1%ダイヤコツトンブラウンCB (直接染料)で染色
した木綿カナキン(40’ S)に次の処理浴を飽充し
く75%絞液)、100℃で3分間乾燥、160℃で3
分間キユアリングした。
Example 5 Cotton kanakin (40' S) dyed with 1% Diamond Brown CB (direct dye) was thoroughly soaked in the following treatment bath (75% squeezed solution), dried at 100°C for 3 minutes, and dried at 160°C for 3 minutes.
Cured for a minute.

エラストロンMF−9200g/ I!エラストロンキ
ャタリスト64 5g#2スミテックスレジンN5−1
8 1608/ j2(45%グリオキザール樹脂) HN−1308g/ I! ポリエチレン系柔軟剤    10g/ RHN−13
0を含有しない同様の対照処理試料及び未処理試料との
比較試験結果を表5に示す。
Elastron MF-9200g/I! Elastron Catalyst 64 5g #2 Sumitex Resin N5-1
8 1608/ j2 (45% glyoxal resin) HN-1308g/ I! Polyethylene softener 10g/RHN-13
Comparative test results are shown in Table 5 with a similar control treated sample that does not contain 0 and an untreated sample.

表5 木綿繊維と直接染料の組合せに対しても、実施例5の加
工試料の耐光性向上効果が顕著に認められる。
Table 5 The effect of improving the light resistance of the processed sample of Example 5 is also observed in the combination of cotton fiber and direct dye.

(発明の効果) 本発明はウレタン樹脂による従来の仕上加工にヒドラジ
ン系ウレタン樹脂安定剤を添加することにより、繊維上
に形成される樹脂被膜の安定性を向上させ、被膜の経時
的劣化、風合悪化、変退色傾向を改善すると共に、繊維
基質自体の耐光性をも向上することができる。しかもこ
の効果は車なる酸化防止剤や紫外線吸収剤を用いる場合
よりもはるかに持続性があり、また被膜自体の柔軟性も
増すという利点もある。
(Effects of the Invention) The present invention improves the stability of the resin coating formed on fibers by adding a hydrazine-based urethane resin stabilizer to the conventional finishing process using urethane resin, and prevents deterioration of the coating over time. It is possible to improve not only the deterioration of the composition and the tendency towards discoloration and fading, but also the light resistance of the fiber matrix itself. Furthermore, this effect is much more sustainable than when using antioxidants or ultraviolet absorbers, and it also has the advantage of increasing the flexibility of the film itself.

【図面の簡単な説明】 第1図は絹35匁付羽二重の試料を染色後ウレタン樹脂
とウレタン樹脂安定剤で仕上加工した場合の安定剤の分
量による黄変度の変化を示す曲線図である。
[Brief explanation of the drawing] Figure 1 is a curve diagram showing the change in yellowing degree depending on the amount of stabilizer when a sample of silk 35 momme Habutae is finished with urethane resin and urethane resin stabilizer after dyeing. It is.

Claims (1)

【特許請求の範囲】 1、水性ウレタン樹脂とウレタン樹脂用安定剤とから成
る処理浴を繊維構造物に含浸し、熱処理することを特徴
とする繊維構造物の仕上加工方法。 2、水性ウレタン樹脂がブロック化ポリイソシアネート
プレポリマータイプであることを特徴とする請求項1記
載の方法。 3、ウレタン樹脂用安定剤が1,6−ヘキサメチレン−
ビス−(N,N′−ジメチルセミカルバジド)であり、
ウレタン樹脂純分に対して安定剤を10重量%以上含有
することを特徴とする請求項1記載の方法。
[Scope of Claims] 1. A method for finishing a fibrous structure, which comprises impregnating the fibrous structure with a treatment bath consisting of an aqueous urethane resin and a stabilizer for urethane resin, and heat-treating the fibrous structure. 2. The method according to claim 1, wherein the aqueous urethane resin is of the blocked polyisocyanate prepolymer type. 3. Stabilizer for urethane resin is 1,6-hexamethylene-
bis-(N,N'-dimethylsemicarbazide),
The method according to claim 1, characterized in that the stabilizer is contained in an amount of 10% by weight or more based on the pure content of the urethane resin.
JP31547389A 1989-12-06 1989-12-06 Finish processing of fiber structure Pending JPH03180574A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31547389A JPH03180574A (en) 1989-12-06 1989-12-06 Finish processing of fiber structure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31547389A JPH03180574A (en) 1989-12-06 1989-12-06 Finish processing of fiber structure

Publications (1)

Publication Number Publication Date
JPH03180574A true JPH03180574A (en) 1991-08-06

Family

ID=18065782

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31547389A Pending JPH03180574A (en) 1989-12-06 1989-12-06 Finish processing of fiber structure

Country Status (1)

Country Link
JP (1) JPH03180574A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5771482A (en) * 1980-10-22 1982-05-04 Osamu Ogata Prevention of discoloration of colored staple fiber due to light and heat
JPS6356557A (en) * 1986-08-27 1988-03-11 Kao Corp Complex stabilizer for polyurethane resin

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5771482A (en) * 1980-10-22 1982-05-04 Osamu Ogata Prevention of discoloration of colored staple fiber due to light and heat
JPS6356557A (en) * 1986-08-27 1988-03-11 Kao Corp Complex stabilizer for polyurethane resin

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