JPH0547659B2 - - Google Patents
Info
- Publication number
- JPH0547659B2 JPH0547659B2 JP1201978A JP20197889A JPH0547659B2 JP H0547659 B2 JPH0547659 B2 JP H0547659B2 JP 1201978 A JP1201978 A JP 1201978A JP 20197889 A JP20197889 A JP 20197889A JP H0547659 B2 JPH0547659 B2 JP H0547659B2
- Authority
- JP
- Japan
- Prior art keywords
- treatment
- whiteness
- bleaching
- hydrogen peroxide
- minutes
- 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.)
- Expired - Lifetime
Links
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatment Of Fiber Materials (AREA)
Description
(産業上の利用分野)
本発明は、白度とソフト性を兼ね備え、しか
も、これの短時間処理を可能とした従来にない新
規な漂白法を提供するものである。
(従来の技術)
セルロース系繊維の漂白に関しては、亜塩素酸
ナトリウム、過酸化水素等による方法が一般的で
あるが、白度を高めようとすると風合いが硬くな
り、逆にソフト性を重視すると白度が低下する問
題がある。
かかる点に関しては、亜塩素酸ナトリウム漂白
と過酸化水素漂白を組み合せ、低温で処理する方
法もあるが白度アツプのために長時間かけて処理
せねばならず、風合いの面においてもなお満足で
きないものがある。
(発明が解決しようとする問題点)
本発明はかかる点、白度、風合いとも優れ、し
かもこれの短時間処理を可能としたものである。
(問題点を解決するための手段)
しかるに、本発明は、その漂白方法において、
濃度3〜8%owf、PH=3〜4の亜塩素酸ナトリ
ウム液浸漬後における被漂白物を90〜100℃で10
〜30分間スチーム処理する第1処理と、次いでこ
れを濃度3〜8%owf、PH=10〜12の過酸化水素
液に浸漬して、40〜70℃で1〜10分間スチーム処
理する第2処理を組み合わせて成ることに特徴を
有するセルロース系繊維のソフト漂白法に関す
る。但し、亜塩素酸ナトリウム液は25%、過酸化
水素液は35%の濃度のものを使用する。
本発明は、ソフト性に影響の大きい漂白時間を
できるだけ短くすること、しかもその時間比率に
おいて被漂白生地に対する脆化の程度が少ない亜
塩素酸ナトリウム液による漂白時間の割合を高
め、その温度も短時間で白度がでるよう常圧下で
の最高温度域としたこと、次いで過酸化水素によ
る処理においては漂白生地への必要以上の反応を
コントロールするため時間と温度を最小限とし、
漂白液の効率利用が図れるようにしたことに特徴
を有する。
(作用)
本発明方法の亜塩素酸ナトリウム漂白において
は、パツド、高温スチーム、短時間処理により浴
比が最小となり、付与した熱、薬剤の有効な利用
が図れ、浸漬法や液流法に比べ非常に短時間で高
い白度が得られる。また、被漂白生地と漂白液と
の接触を機械的に行なわないため被漂白生地を必
要以上に硬化させることがない。
かかる処理においては、その温度が90℃未満で
あると、30分間処理しても所定の白度を得ること
が困難であり、100℃を越えると密閉化された高
圧設備を要し、設備的にも操作的にも好ましくな
い。
また、かかる条件下における処理時間は、これ
が10分未満であるとその反応が不十分であり、所
定の白度を得ることが困難で、30分を越えると白
度が平衡に達し、生地が脆化して硬化する問題を
生ずるので好ましくない。
また、前記処理浴中にポリカルボン酸系化合物
等のキレート分散剤を入れると金属イオンによる
過激反応を抑制することができ、更にその効果を
助長できる。
一方、かかる処理後における過酸化水素漂白も
前工程と同様パツトスチーム、短時間法の利用で
あり、低温で行なうことによりアルカリによる綿
ワツクスの分解と過酸化水素自身による綿の脆化
を極力抑えるもので、残留色素除去と前工程の亜
塩素ナトリウムの残留分の中和に効果がある。
かかる処理においては、その温度が40℃未満で
あると、漂白反応が進みにくく、十分な白度が得
られない。また、70℃を越えると、白度は得られ
るものの温度の上昇につれ加速度的に生地の脆化
を招く。
また、かかる条件下における処理時間が1分未
満であると、反応が不十分に終り、薬剤の有効利
用がはかれない。また、10分を越えると白度の上
昇は僅かであるのに生地の脆化が優先的に進み問
題がある。
また、前記処理浴中にポリカルボン酸系化合物
等のキレート分散剤を入れると金属イオンによる
過激反応を抑制することができ、更にその効果を
助長することができる。
尚、両処理におけるスチーム処理とは、パツド
スチーム連続処理のことであり、従つてこれを連
続的に配置し、例えば、処理浴への浸漬、パデイ
ング、スチーム処理、湯洗、水洗等を連続的に行
なうことができるものである。
以下、実施例を挙げて説明する。
(Industrial Field of Application) The present invention provides a novel bleaching method that combines whiteness and softness and can be processed in a short time. (Conventional technology) For bleaching cellulose fibers, methods such as sodium chlorite and hydrogen peroxide are commonly used, but if you try to increase the whiteness, the texture becomes hard, whereas if you emphasize softness, the texture becomes hard. There is a problem that whiteness decreases. Regarding this point, there is a method of combining sodium chlorite bleaching and hydrogen peroxide bleaching and processing at low temperature, but it requires a long processing time to increase the whiteness, and the texture is still unsatisfactory. There is something. (Problems to be Solved by the Invention) The present invention is excellent in these points, in terms of whiteness and texture, and can be processed in a short time. (Means for solving the problem) However, in the bleaching method of the present invention,
After soaking in a sodium chlorite solution with a concentration of 3 to 8% owf and a pH of 3 to 4, the object to be bleached is heated to 90 to 100℃ for 10 minutes.
The first treatment involves steam treatment for ~30 minutes, and the second treatment involves immersing it in a hydrogen peroxide solution with a concentration of 3~8% OWF and pH=10~12 and steaming it at 40~70°C for 1~10 minutes. The present invention relates to a soft bleaching method for cellulosic fibers characterized by a combination of treatments. However, use a sodium chlorite solution with a concentration of 25% and a hydrogen peroxide solution with a concentration of 35%. The purpose of the present invention is to shorten the bleaching time as much as possible, which has a large effect on softness, increase the proportion of the bleaching time using a sodium chlorite solution, which has a low degree of embrittlement to the bleached fabric, and shorten the temperature. The maximum temperature range under normal pressure was chosen so that the whiteness could be achieved in a short amount of time.Then, in the treatment with hydrogen peroxide, the time and temperature were kept to a minimum in order to control unnecessary reactions to the bleached fabric.
The feature is that the bleaching solution can be used efficiently. (Function) In the sodium chlorite bleaching method of the present invention, the bath ratio is minimized by pad, high temperature steam, and short time treatment, and the applied heat and chemicals can be used effectively, compared to the immersion method and liquid flow method. High whiteness can be obtained in a very short time. Furthermore, since the fabric to be bleached is not brought into contact with the bleaching solution mechanically, the fabric to be bleached is not hardened more than necessary. In such treatment, if the temperature is less than 90°C, it is difficult to obtain the desired whiteness even after 30 minutes of treatment, and if the temperature exceeds 100°C, sealed high-pressure equipment is required, resulting in equipment problems. It is also undesirable in terms of operation. In addition, if the processing time under these conditions is less than 10 minutes, the reaction will be insufficient and it will be difficult to obtain the desired whiteness, and if the processing time exceeds 30 minutes, the whiteness will reach equilibrium and the dough will deteriorate. This is not preferable because it causes problems of embrittlement and hardening. Furthermore, if a chelate dispersant such as a polycarboxylic acid compound is added to the treatment bath, radical reactions caused by metal ions can be suppressed and the effect can be further enhanced. On the other hand, the hydrogen peroxide bleaching after this treatment also uses a short steam method, similar to the previous process, and is carried out at low temperatures to minimize the decomposition of the cotton wax by alkali and the embrittlement of the cotton by the hydrogen peroxide itself. It is effective in removing residual pigments and neutralizing residual sodium chlorite from the previous process. In such a treatment, if the temperature is less than 40°C, the bleaching reaction will be difficult to proceed and sufficient whiteness will not be obtained. Furthermore, if the temperature exceeds 70°C, whiteness may be obtained, but as the temperature rises, the fabric becomes brittle at an accelerated rate. Furthermore, if the treatment time under such conditions is less than 1 minute, the reaction will be insufficient and the drug will not be used effectively. Moreover, if the time exceeds 10 minutes, the fabric becomes brittle preferentially, which causes a problem, although the increase in whiteness is slight. Furthermore, if a chelate dispersant such as a polycarboxylic acid compound is added to the treatment bath, radical reactions caused by metal ions can be suppressed and the effect can be further enhanced. In addition, the steam treatment in both treatments refers to continuous padded steam treatment, and therefore, this is arranged continuously, for example, immersion in a treatment bath, padding, steam treatment, hot water washing, water washing, etc. It is something that can be done. Examples will be described below.
【表】【table】
【表】【table】
【表】【table】
【表】
尚、実施例1〜3における処理は以下により行
なつた。
使用生地:コツトンフライス生地
亜塩素酸ナトリウム漂白:亜塩素酸ナトリウム
液の濃度25%
浸漬時間5分
絞り率140%
過酸化水素漂白:過酸化水素液の濃度35%、
浸漬時間5分、絞り率140%
スチーム処理:パツドスチーム連続処理
かかる処理は連続的に行ない亜塩素酸ナトリウ
ム漂白、過酸化水素漂白の後にはそれぞれ湯洗工
程を設けた。また、比較例はバツチ式によりおの
おの浸漬処理したもので従来法である。
キレート分散剤は以下のとおりである。
A:ポリカルボン酸系 B:マグネシウム塩系
C:ホスホン酸系
(発明の効果)
以上のように処理した本発明方法による漂白物
は、以下の表1に示すように従来法である比較例
と比べほぼ同一の白度を得るとともに、優れたソ
フト性を有し、処理時間も大幅に短縮できた。
尚、各々の評価は以下によつて行なつた。
白度:CIELAB色空間よりL*−3b*として算
出(Macbeth 2020微小面積にて測色)
ソフト性:測定試料布をミシンで、から縫いし、
(針:ORGAN DB×1 11号)あいた穴の数
を次の式に代入してソフト性を評価する数値と
した。
但し、比較例のソフト性を100として算出した。
ソフト性=100/あいた穴の数×100
尚、ソフト性を評価する数値は、大きい方が良
いことを表している。[Table] The treatments in Examples 1 to 3 were carried out as follows. Fabric used: Cotton milling fabric Sodium chlorite bleaching: Sodium chlorite solution concentration 25%, soaking time 5 minutes, squeezing rate 140% Hydrogen peroxide bleaching: Hydrogen peroxide solution concentration 35%, soaking time 5 minutes, squeezing Rate: 140% Steam treatment: Padded steam continuous treatment This treatment was carried out continuously, and hot water washing steps were provided after sodium chlorite bleaching and hydrogen peroxide bleaching, respectively. In addition, in the comparative example, each sample was immersed in batches, which is a conventional method. The chelate dispersants are as follows. A: Polycarboxylic acid type B: Magnesium salt type C: Phosphonic acid type (Effects of the invention) The bleached products treated as described above according to the method of the present invention are different from the comparative example using the conventional method as shown in Table 1 below. In comparison, almost the same whiteness was obtained, excellent softness was obtained, and the processing time was significantly shortened. In addition, each evaluation was performed as follows. Whiteness: Calculated as L*-3b* from CIELAB color space (color measurement in Macbeth 2020 micro area) Softness: The measurement sample cloth was sewn from the sewing machine,
(Needle: ORGAN DB×1 No. 11) The number of holes made was substituted into the following formula to obtain a value for evaluating softness. However, the softness of the comparative example was calculated as 100. Softness = 100/Number of holes x 100 The larger the numerical value for evaluating softness, the better.
【表】
以上のように本発明方法によれば、白度、ソフ
ト性を兼ね備えた処理が可能であり、これにより
得られた漂白物は特に肌着用として好適である。[Table] As described above, according to the method of the present invention, it is possible to achieve both whiteness and softness, and the bleached product obtained thereby is particularly suitable for wearing under the skin.
Claims (1)
トリウム液に浸漬後、90〜100℃で10〜30分間ス
チーム処理する第1処理と、濃度3〜8%owf、
PH=10〜12の過酸化水素液に浸漬後、40〜70℃で
1〜10分間スチーム処理する第2処理を組み合せ
て成ることを特徴とするセルロース系繊維のソフ
ト漂白法。 (但し、亜塩素酸ナトリウム液は25%、過酸化水
素液は35%の濃度のものを使用する。)[Claims] 1. A first treatment of immersion in a sodium chlorite solution with a concentration of 3 to 8% owf and a pH of 3 to 4, followed by steam treatment at 90 to 100°C for 10 to 30 minutes; %owf,
A soft bleaching method for cellulose fibers, which comprises a second treatment of immersion in a hydrogen peroxide solution having a pH of 10 to 12 and then steam treatment at 40 to 70°C for 1 to 10 minutes. (However, use a sodium chlorite solution with a concentration of 25% and a hydrogen peroxide solution with a concentration of 35%.)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1201978A JPH0364574A (en) | 1989-08-02 | 1989-08-02 | Soft bleaching of cellulose-based fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1201978A JPH0364574A (en) | 1989-08-02 | 1989-08-02 | Soft bleaching of cellulose-based fiber |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0364574A JPH0364574A (en) | 1991-03-19 |
| JPH0547659B2 true JPH0547659B2 (en) | 1993-07-19 |
Family
ID=16449914
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1201978A Granted JPH0364574A (en) | 1989-08-02 | 1989-08-02 | Soft bleaching of cellulose-based fiber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0364574A (en) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62110967A (en) * | 1985-11-08 | 1987-05-22 | 日本カ−リツト株式会社 | How to bleach textiles |
-
1989
- 1989-08-02 JP JP1201978A patent/JPH0364574A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0364574A (en) | 1991-03-19 |
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