JPS58180688A - Enhancement of chlorine fastness of dyed article - Google Patents
Enhancement of chlorine fastness of dyed articleInfo
- Publication number
- JPS58180688A JPS58180688A JP57062780A JP6278082A JPS58180688A JP S58180688 A JPS58180688 A JP S58180688A JP 57062780 A JP57062780 A JP 57062780A JP 6278082 A JP6278082 A JP 6278082A JP S58180688 A JPS58180688 A JP S58180688A
- Authority
- JP
- Japan
- Prior art keywords
- dyed
- reactive
- dyes
- fastness
- cellulose
- 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
Links
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は直接染料または反応性染料を用いてセルロース
系繊維を染色した染色物の塩素水堅牢度を向上させる方
法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for improving the fastness to chlorine water of dyed cellulose fibers using direct dyes or reactive dyes.
セルロース系繊維は主に直接染料、反応性染料により染
色されているが、その塩素水堅牢度は必らずしも良好と
はいえなかった。このような塩素水堅牢度の問題は水道
水で染色物を洗濯する際に多く発生する。Cellulose fibers are mainly dyed with direct dyes and reactive dyes, but their fastness to chlorine water has not always been good. Such problems with chlorine water fastness often occur when dyed items are washed with tap water.
これは殺菌を目的として、水道水に添加される塩素が、
染色物の脱色剤として作用するためであり、染色物は変
色もしくは脱色され、特に長時間その水道水にさらされ
た場合には作用した塩素の総量は非常に多くなり、その
影響は一層顕著となる。This is because chlorine, which is added to tap water for sterilization purposes,
This is because it acts as a decolorizing agent for dyed products, and the dyed products become discolored or bleached, and especially when exposed to tap water for a long time, the total amount of chlorine that acts becomes very large, and the effect becomes even more pronounced. Become.
このような染色物の塩素水堅牢度の向上策として、染料
の構造自体を改良することもなされてはいるが、特定の
色についてはなお未解決である。また特殊なフィックス
剤等の併用が考えられているが却って日光堅牢度の低下
や加工変せるすぐれた方法の開発が強く要望されている
。As a measure to improve the fastness to chlorine water of such dyed products, efforts have been made to improve the structure of the dye itself, but the problem with specific colors remains unsolved. Although the use of special fixing agents and the like has been considered, there is a strong demand for the development of superior methods that can reduce the fastness to sunlight and change processing.
本発明者等はこのような事情に鑑み鋭意研究の結果、直
接染料、反応性染料を用いたセルロース繊維染色物を、
繊維素反応型樹脂と尿素及び触媒を含む処理浴で樹脂加
工することにより卓越した塩素水堅牢度の染色物が得ら
れることを見い出し、本発明に至った。In view of these circumstances, the inventors of the present invention have conducted extensive research and have developed dyed cellulose fibers using direct dyes and reactive dyes.
It has been discovered that a dyed product with excellent chlorine water fastness can be obtained by resin processing with a treatment bath containing a cellulose-reactive resin, urea, and a catalyst, and the present invention has been achieved.
すなわち、本発明は、直接染料または反応性染料を用い
て染色されたセルロース系繊維染色物を、繊維素反応型
樹脂、尿素および触媒を含む処理浴で樹脂加工すること
を特徴とするセルロース系繊維染色物の塩素水堅牢度向
上法である。That is, the present invention provides a cellulose-based fiber, which is characterized in that a dyed cellulose-based fiber dyed using a direct dye or a reactive dye is subjected to resin processing in a processing bath containing a cellulose-reactive resin, urea, and a catalyst. This is a method for improving the fastness of dyed products to chlorine water.
本発明において、直接染料、反応性染料とは、それ自体
セルロース繊維用染料として知られているものであり、
すべてのものが使用できる。In the present invention, direct dyes and reactive dyes are known per se as dyes for cellulose fibers,
Everything can be used.
セルロース系繊維としては、木綿、麻、再生セルロース
およびこれらと合成繊維との混紡、交織、交編交撚物が
あげられる。Examples of cellulosic fibers include cotton, hemp, regenerated cellulose, and blends, weaves, and knits and twists of these and synthetic fibers.
直接染料、反応性染料、あるいはそれらの両方を使用し
てセルロース系繊維の染色物を得るには、それ自体公知
の方法で染色することにより行われろ。この場合、他の
染料、たとえば疎水性染料と反応性染料とで染色された
合成繊維とセルロース系繊維との混合繊維の染色物であ
ってもよい。Dyeings of cellulosic fibers using direct dyes, reactive dyes, or both can be obtained by dyeing in a manner known per se. In this case, the dyed product may be a mixed fiber of synthetic fibers and cellulose fibers dyed with other dyes, such as hydrophobic dyes and reactive dyes.
lil維素反応型樹脂とは、通常セルロース繊維等の樹
脂加工に使用されるものであって、たとえば次のものが
あげられる。lil fiber-reactive resins are those normally used for resin processing of cellulose fibers, etc., and include, for example, the following.
メチロールエチレン尿素
メチロールトリアゾン
メチロールウロン
メチロールプロピレン尿素
メチロールグリオキザールウレイン
メチロールグリオキザーJ3レイン
メチロールカーバメート
その使用量は目的とする防し、わ、防縮効果により異な
るが、通常処理浴に対して8−20重重量部範囲で使用
される。Methylol ethylene urea methylol triazone methylol uron methylol propylene urea methylol glyoxal urein methylol glyoxal J3 rhein methylol carbamate The amount used varies depending on the desired anti-shrinkage effect, but is usually 8-20% of the treatment bath. Used in heavy parts range.
触媒としては、前記のような繊維素反応型樹脂の硬化促
進のため使用されるもので、たとえば塩化マグネシウム
、ホウ弗化亜鉛、硝酸亜鉛、およびその有機酸混合物等
があげられ、これらは目的に芯じて適当量が添加される
。Catalysts are used to accelerate the curing of cellulose-reactive resins such as those mentioned above, and examples include magnesium chloride, zinc borofluoride, zinc nitrate, and organic acid mixtures thereof. An appropriate amount is added depending on the core.
本発明で使用される尿素の添加量は、処理浴に対して0
.06−5重量部の範囲であり、より好ましくは0.0
5−2重量部である。The amount of urea used in the present invention is 0 to the treatment bath.
.. 06-5 parts by weight, more preferably 0.0
It is 5-2 parts by weight.
本発明の処理浴には、その他薬剤として一般的に用いら
れる添加剤、たとえばソフナー、4毫水剤、フィックス
剤などを適宜添加することができる
本発明方法は具体的には、直接染料または反応性染料を
用いて染色されたセルロース系繊維染色物を、繊維素反
応型置@8−20重量4、尿素0.05−5重量部およ
び適当量の触媒を含有する処理浴を調製し、ついでこれ
を均一にzfジソグし、マングル等で均一に絞液した後
、80−110℃で予備乾燥を行ない、さらに18〇−
160℃で2−5分間キユアリング処理を行うことによ
り実施することができる。In the treatment bath of the present invention, other additives commonly used as chemicals, such as softeners, liquid additives, fixing agents, etc., may be appropriately added. A cellulosic fiber dyed product dyed using a synthetic dye is prepared in a treatment bath containing a cellulose reaction type @ 8-20 parts by weight, 0.05-5 parts by weight of urea and an appropriate amount of catalyst, and then After uniformly zf disogging this and squeezing the liquid uniformly with a mangle, pre-drying at 80-110°C, and further drying at 180-110°C.
This can be carried out by performing a curing treatment at 160°C for 2-5 minutes.
このようにして得られた樹脂加工製品の塩素水堅牢度は
従来法に比べてきわめてすぐれている。The fastness to chlorine water of the resin-processed product obtained in this way is extremely superior to that obtained by conventional methods.
以上、参考例、実施例により本発明を更に詳しく説明す
る。文中、部、鴫は重量部、重量部を表わす。The present invention will be described in more detail with reference to Reference Examples and Examples. In the text, parts and parts represent parts by weight.
参考例(染色物の調製) 実施例で使用した染色物の調製は下記の条件で行った。Reference example (preparation of dyed products) The dyed products used in the Examples were prepared under the following conditions.
◎使用した染料
スミフィックス ブランクB
(C0■、リアクティブ ブラック5)スミフィックス
イエローGR8
(C,■、リアクティブ イエロー116)スミフィッ
クス レッドB
(C0■、リアクティブ レッド22)スミライト ス
プラレッド4BL
(C1■、ダイレクト レッド79)
スミライトスプラバイオレットBL
(C0■、ダイレクト バイオレット66)(庄)スミ
フィックス゛住友化学社製反応性染料ス 2 ライ ト
二同直接染料
C,X、 :カラーインデックス◎染色条件
(11反応染料
染 料 24 (0,W、f)埜硝 50 ?
/l
ソーダー灰 2 0 f/を
浴 比 1 : 20
染色温度、時間50℃×60分間、のち洗浄する。◎Dye used Sumifix Blank B (C0■, Reactive Black 5) Sumifix Yellow GR8 (C, ■, Reactive Yellow 116) Sumifix Red B (C0■, Reactive Red 22) Sumifix Spra Red 4BL (C1 ■, Direct Red 79) Sumilite Spraviolet BL (C0■, Direct Violet 66) (Sho) Sumifix (manufactured by Sumitomo Chemical Co., Ltd.) Reactive dyes 2 Light 2 Direct dyes C, X, : Color index ◎ Dyeing conditions (11 Reactive dye dye 24 (0, W, f) Nosato 50 ?
/l soda ash 20 f/l in a bath ratio of 1:20 at a dyeing temperature of 50°C for 60 minutes and then washed.
(2〕直接染料 染料 1%(olw、f、) ?硝 59/を 浴 比 l : 80 染色、湿度時間90℃X60分間、のち洗浄する。(2) Direct dye Dye 1% (OLW, F,) ? Glass 59/ Bath ratio l: 80 Dyeing and humidity at 90°C for 60 minutes, then washed.
(8)被染織物
未シルケット綿メリヤス
実施例1
参考例で得られた各染色物を、下記の処理浴に含浸し、
マングルで絞液した後、80℃で2分間予備乾燥を行い
、ついで150℃で8分間キュアリジグを行った。(8) Dyed fabric unmercerized cotton knitted fabric Example 1 Each dyed product obtained in the reference example was impregnated in the following treatment bath,
After squeezing the liquid with a mangle, preliminary drying was performed at 80°C for 2 minutes, and then a curing jig was performed at 150°C for 8 minutes.
処理浴組成
1)
スミア・ノクス レジン N5−18 10 [
スミア・クス アクセレーター x−so” a
m尿 素 0.
2部スミテックス ソフナーL 79
合 計 lOO部(注+
l) 繊維素反応型グリオキザール系樹脂(住友化学
社製品)
2) 塩化マグネシウム系触媒
(住友化学社製品)
得られた樹脂加工布について塩素水堅牢度(I80法:
有効塩素20 im、室m(20C±2℃)×4時間〕
の試験を行ったところ!!!1の結果が得られた。Treatment bath composition 1) Smear Nox Resin N5-18 10 [
Sumia Kus Accelerator x-so” a
mUrea 0.
Part 2 Sumitex Softener L 79
Total 100 parts (Note +
l) Cellulose-reactive glyoxal resin (product of Sumitomo Chemical Co., Ltd.) 2) Magnesium chloride catalyst (product of Sumitomo Chemical Co., Ltd.) The fastness to chlorine water (I80 method:
Available chlorine 20 im, room m (20C±2℃) x 4 hours]
We just conducted a test! ! ! A result of 1 was obtained.
実施例2
下記処理浴を調製した後、実施例1と同様に樹脂加工を
行った。得られた樹脂加工布について塩素水堅牢度の試
験を行ったところ、表1の結果が得られた。Example 2 After preparing the following treatment bath, resin processing was performed in the same manner as in Example 1. When the resulting resin-treated cloth was tested for fastness to chlorine water, the results shown in Table 1 were obtained.
処理浴組成 水 残量 合計 lOO部Treatment bath composition Water remaining amount Total lOO part
Claims (1)
ス系繊維染色物を繊維素反応型樹脂、尿素および触媒を
含む処理浴で樹脂加工することを特徴とするセルロース
系繊維染色物の塩素水堅牢度向上法。Chlorine water fastness of dyed cellulose fibers, which is characterized by processing dyed cellulose fibers dyed with direct dyes or reactive dyes in a treatment bath containing a cellulose-reactive resin, urea, and a catalyst. Improvement method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57062780A JPS58180688A (en) | 1982-04-14 | 1982-04-14 | Enhancement of chlorine fastness of dyed article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57062780A JPS58180688A (en) | 1982-04-14 | 1982-04-14 | Enhancement of chlorine fastness of dyed article |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS58180688A true JPS58180688A (en) | 1983-10-22 |
Family
ID=13210214
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57062780A Pending JPS58180688A (en) | 1982-04-14 | 1982-04-14 | Enhancement of chlorine fastness of dyed article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58180688A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62104984A (en) * | 1985-10-29 | 1987-05-15 | 東海染工株式会社 | Enhancement of dyeing fastness of cellulosic fiber-containing structure to chlorine treatment water |
JPS62104985A (en) * | 1985-10-29 | 1987-05-15 | 東海染工株式会社 | Enhancement of dyeing fastness of cellulosic fiber-containing structure to chlorine treatment water |
JPS62104983A (en) * | 1985-10-29 | 1987-05-15 | 東海染工株式会社 | Enhancement of dyeing fastness of cellulosic fiber-containing structure to chlorine treatment water |
-
1982
- 1982-04-14 JP JP57062780A patent/JPS58180688A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62104984A (en) * | 1985-10-29 | 1987-05-15 | 東海染工株式会社 | Enhancement of dyeing fastness of cellulosic fiber-containing structure to chlorine treatment water |
JPS62104985A (en) * | 1985-10-29 | 1987-05-15 | 東海染工株式会社 | Enhancement of dyeing fastness of cellulosic fiber-containing structure to chlorine treatment water |
JPS62104983A (en) * | 1985-10-29 | 1987-05-15 | 東海染工株式会社 | Enhancement of dyeing fastness of cellulosic fiber-containing structure to chlorine treatment water |
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