JPS6312192B2 - - Google Patents

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Publication number
JPS6312192B2
JPS6312192B2 JP60225305A JP22530585A JPS6312192B2 JP S6312192 B2 JPS6312192 B2 JP S6312192B2 JP 60225305 A JP60225305 A JP 60225305A JP 22530585 A JP22530585 A JP 22530585A JP S6312192 B2 JPS6312192 B2 JP S6312192B2
Authority
JP
Japan
Prior art keywords
scouring
temperature
carbon atoms
group
polyester fibers
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
Application number
JP60225305A
Other languages
Japanese (ja)
Other versions
JPS6285071A (en
Inventor
Mototsugu Tokunaga
Yukio Sato
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.)
DKS Co Ltd
Original Assignee
Dai Ichi Kogyo Seiyaku 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 Dai Ichi Kogyo Seiyaku Co Ltd filed Critical Dai Ichi Kogyo Seiyaku Co Ltd
Priority to JP60225305A priority Critical patent/JPS6285071A/en
Publication of JPS6285071A publication Critical patent/JPS6285071A/en
Publication of JPS6312192B2 publication Critical patent/JPS6312192B2/ja
Granted legal-status Critical Current

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  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はポリエステル系繊維の高温精練方法に
関する。 ポリエステル系繊維の精練は編物、または織物
においても、一般的には100℃以下において精練
されているが、染色性の向上、風合の改善のた
め、ポリエステル繊維の中でも、特に強撚糸織物
では、付加価値をあげるためシボ立、リラツクス
工程が必須であり、これらの目的のため100℃以
上で精練を行なうことが提案されている。この
際、通常の界面活性剤を用いて精練すると、工程
中において気泡が発生することにより、シボ立が
不充分であつたり、リラツクスが不満足であつた
り、又染色性が劣る原因となる。 また100℃以上になると高圧になるため、空気
抜きを実施するが、気泡性の高いものは急激な泡
立ちを示し、トラブルの原因となる等の欠点を有
している。 本発明者らは、100℃〜180℃の高温精練方法に
ついて、鋭意研究の結果、本発明に到達したもの
である。即ち、本発明はポリエステル系繊維を
100℃〜180℃の温度にて、 一般式 R―O―(EO)n(PO)mH [R:炭素数8〜36のアルキル基、炭素数6
〜30のアルキル基を有するアルキルア
リール基、 EO:オキシエチレン基、PO:オキシプロ
ピレン基 n:4〜50の整数 m:1〜50の整数 但し、 n≧m ] で示されるノニオン系界面活性剤を含有してなる
水系において、精練することを特徴とするポリエ
ステル系繊維の高温精練方法を提供するものであ
る。 一般的にはポリエステル強撚糸織物の場合、織
工程での織布性を良くするため、ケバぶせ効果の
高いポリアクリル酸系糊剤、平滑性のあるエステ
ル化油、シリコーン系オイル、鉱油、パラフイ
ン、集束性被覆性樹脂としてポリアクリル系水溶
性樹脂、ポリエステル系水溶性樹脂、ポリアマイ
ド系水溶性樹脂、ポリウレタン系水溶性樹脂等が
併用または単独使用されている。これらを効果的
に取り除くために、一般的にはアルカリ剤を併用
してアニオン系、両性系、ノニオン系の界面活性
剤を使用して100℃以下において精練されている。 しかし、強撚糸使いの加工糸織物では、充分撚
りを戻すために、100℃〜180℃での高温条件が必
要であり、パツケージ型の液流精練機が、省エネ
ルギーの面から低浴比で利用される場合が多くな
つている現状である。この場合には、界面活性剤
の起泡性のため、空気を、まき込んで空回り、流
量低下をきたすため、低起泡性界面活性剤が必要
不可欠である。またシボ立を充分に行なうために
は、低浴比下で機械的叩き効果が必要であり、こ
の面からも、起泡性の高い界面活性剤は効果的で
はない。 しかし、ポリエステル繊維織物には、前述した
水不溶性油剤および糊剤が含まれており、乳化力
の高い界面活性剤が必要である。 100℃〜180℃の温度において、低起泡性で、乳
化力の強い、かつ精練浴で分離しない、界面活性
剤に関して、検討の結果、前記一般式中、アルキ
ル基の炭素数が8より小さい場合、またはアルキ
ル基の炭素数が6より小さいアルキルアリール基
の場合には、浸透力が高いが、乳化力が低く、ア
ルキル基の炭素数が36より大きい場合、またはア
ルキル基の炭素数が30より大きいアルキルアリー
ル基の場合には、水溶性が悪く、分離する傾向が
見られた。プロピレンオキサイドの付加モル数が
エチレンオキサイド付加モル数より多い場合に
は、同様に水溶性が悪く分離傾向を示し、洗浄力
も悪かつた。 エチレンオキサイド付加モル数(n)とプロピ
レンオキサイド付加モル数(m)との合計はRの
分子量により異なり、一般的にはRが大きい程、
n+mの数が大きい程、良好な低泡性および洗浄
力を示した。 前記一般式で示される化合物が高温において優
れた性能を発揮する理由は明確でないが、低温側
での浸透力と高温側での油の乳化力のバランスに
あると推定される。 この理由は、より浸透力の高い、Rが炭素数8
より小さいアルキル基の場合、またはアルキル基
の炭素数が6より小さいアルキルアリール基の場
合には、併用される苛性ソーダの浸透力を補助す
るため、より低温側で、サイジング剤の急激な膨
張が生じ、不溶性樹脂および油剤がとりこまれる
ため、黒ずみや、染色性が悪くなる傾向が見られ
ることから判断して、前記一般式化合物によれ
ば、浸透力がある程度あり、徐々に解撚すること
により、油を乳化分散しながらシボ立をすること
が良いものと考えられる。 前記一般式で示される化合物は、曇点を有して
いることが良く知られているが、100℃以上に設
定された高温側でも、分離をしないために、より
曇点の高い一般的なアルキルポリエチレングリコ
ール、アルキルアーリルポリエチレングリコー
ル、両性界面活性剤、アニオン系界面活性剤が低
泡性を阻害しない程度において、配合しても何等
さしつかえない。 以下に本発明を実施例により具体的に説明す
る。 実施例 1 表―1に示した界面活性剤を用いて、温度130
℃における乳化性および起泡性について、試験し
た結果を表―1に示した。 尚、乳化性の試験は耐圧ガラス容器に油1g/
1、界面活性剤1g/1400c.c.を入れて、130℃に
加熱した後、乳化状態を観察した。 評価方法 ○ :白濁した安定した乳化状態を示し、全く
分離が認められない。 △ :白濁した安定した乳化状態を示すが、分
離、油滴が認められる。 × :全く乳化を示さないで、分離する。 実施例 2 表―2に示した種々の界面活性剤を用い、市販
高温高圧ロータリーワツシヤーFW―100型[福
伸工業(株)社製]を使用して、ポリエステル強
撚糸織物300Kg、界面活性剤2g/1および苛性
ソーダ(固)2g/1を用いて、浴比1:10に
て、ドラム回転15回転、昇温50℃より3℃/分に
おいて、130℃×30分後、冷却してシボ立および
精練性を試験した結果を表―2に示した。
The present invention relates to a method for high-temperature scouring of polyester fibers. Polyester fibers are generally scoured at temperatures below 100°C for knitted or woven fabrics, but in order to improve dyeability and texture, polyester fibers, especially highly twisted woven fabrics, are scoured at temperatures below 100°C. Graining and relaxing processes are essential to increase added value, and scouring at 100°C or higher has been proposed for these purposes. At this time, if a normal surfactant is used for scouring, air bubbles are generated during the process, resulting in insufficient graining, unsatisfactory relaxation, and poor dyeability. Moreover, when the temperature exceeds 100°C, the pressure becomes high, so air is removed, but highly foamy products exhibit rapid foaming, which can cause trouble. The present inventors have arrived at the present invention as a result of intensive research into a high temperature scouring method at 100°C to 180°C. That is, the present invention uses polyester fibers.
At a temperature of 100℃ to 180℃, general formula R-O-(EO)n(PO)mH [R: alkyl group with 8 to 36 carbon atoms, 6 carbon atoms]
Alkylaryl group having ~30 alkyl groups, EO: oxyethylene group, PO: oxypropylene group n: an integer of 4 to 50 m: an integer of 1 to 50, provided that n≧m] A nonionic surfactant represented by The present invention provides a method for high-temperature scouring of polyester fibers, which comprises scouring polyester fibers in an aqueous system containing the following. Generally speaking, in the case of polyester hard-twisted fabrics, in order to improve the weaving properties during the weaving process, polyacrylic acid glues with high fluffing effects, esterified oils with smoothness, silicone oils, mineral oils, paraffin oils, etc. are used. As the focusing coating resin, water-soluble polyacrylic resins, water-soluble polyester resins, water-soluble polyamide resins, water-soluble polyurethane resins, etc. are used in combination or alone. In order to effectively remove these substances, scouring is generally carried out at 100°C or lower using an anionic, amphoteric, or nonionic surfactant in combination with an alkaline agent. However, processed yarn fabrics using highly twisted yarns require high-temperature conditions of 100℃ to 180℃ to fully untwist them, and package-type liquid jet scouring machines are used at low bath ratios to save energy. Currently, this is becoming more and more common. In this case, a low foaming surfactant is indispensable because the foaming property of the surfactant causes air to be drawn in and cause the flow rate to decrease. In addition, in order to achieve sufficient texturing, a mechanical beating effect is required at a low bath ratio, and surfactants with high foaming properties are not effective in this respect as well. However, polyester fiber fabrics contain the aforementioned water-insoluble oil and sizing agent, and require a surfactant with high emulsifying power. As a result of investigation, we found that surfactants with low foaming properties, strong emulsifying power, and do not separate in a scouring bath at temperatures of 100°C to 180°C have a carbon number of less than 8 in the alkyl group in the general formula above. When the number of carbon atoms in the alkyl group is larger than 36, or when the number of carbon atoms in the alkyl group is larger than 30, the penetrating power is high, but the emulsifying power is low. Larger alkylaryl groups showed poor water solubility and a tendency to separate. When the number of moles of propylene oxide added was greater than the number of moles added of ethylene oxide, the water solubility was similarly poor and there was a tendency for separation, and the detergency was also poor. The total number of moles of ethylene oxide added (n) and the number of moles of propylene oxide added (m) varies depending on the molecular weight of R, and generally, the larger R is,
The larger the number of n+m, the better the low foaming property and detergency. The reason why the compound represented by the above general formula exhibits excellent performance at high temperatures is not clear, but it is presumed that it lies in the balance between the penetrating power at low temperatures and the emulsifying power of oil at high temperatures. The reason for this is that R has 8 carbon atoms, which has higher penetrating power.
In the case of a smaller alkyl group, or in the case of an alkylaryl group in which the alkyl group has fewer than 6 carbon atoms, rapid expansion of the sizing agent occurs at a lower temperature to assist the permeability of the caustic soda used in combination. Judging from the fact that insoluble resins and oil agents are taken in, there is a tendency for darkening and poor dyeing properties.According to the above general formula compound, there is a certain degree of penetrating power, and by gradual untwisting, It is thought that it is better to emulsify and disperse the oil while forming the grain. It is well known that the compound represented by the above general formula has a clouding point, but since it does not separate even at high temperatures set to 100°C or higher, the compound represented by the general formula has a higher clouding point. There is no problem in adding alkyl polyethylene glycol, alkylaryl polyethylene glycol, amphoteric surfactant, and anionic surfactant to the extent that they do not impair low foaming properties. The present invention will be specifically explained below using examples. Example 1 Using the surfactants shown in Table 1, a temperature of 130
Table 1 shows the results of tests regarding emulsifying and foaming properties at ℃. In addition, for the emulsifying test, 1 g of oil/
1. After adding 1 g/1400 c.c. of surfactant and heating to 130°C, the emulsified state was observed. Evaluation method ○: Shows a cloudy, stable emulsified state, with no separation observed at all. △: Shows a cloudy and stable emulsified state, but separation and oil droplets are observed. x: Separation occurs without emulsification at all. Example 2 Using various surfactants shown in Table 2 and a commercially available high temperature and high pressure rotary washer model FW-100 [manufactured by Fukushin Kogyo Co., Ltd.], 300 kg of polyester strongly twisted yarn fabric and surface active Using 2 g/1 of agent and 2 g/1 of caustic soda (solid) at a bath ratio of 1:10, the drum was rotated 15 times, the temperature was increased from 50°C to 3°C/min, and after 30 minutes at 130°C, it was cooled. Table 2 shows the results of tests on graininess and scouring properties.

【表】【table】

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】 1 ポリエステル系繊維を100℃〜180℃の温度に
て、 一般式 R―O―(EO)n(PO)mH [R:炭素数8〜36のアルキル基、炭素数6
〜30のアルキル基を有するアルキルア
リール基、 EO:オキシエチレン基、PO:オキシプロ
ピレン基 n:4〜50の整数 m:1〜50の整数 但し、 n≧m ] で示されるノニオン系界面活性剤を含有してなる
水系において精練することを特徴とするポリエス
テル系繊維の高温精練方法。
[Claims] 1 Polyester fibers are heated to a temperature of 100°C to 180°C to form a compound with the general formula R-O-(EO)n(PO)mH [R: alkyl group having 8 to 36 carbon atoms, 6 carbon atoms]
Alkylaryl group having ~30 alkyl groups, EO: oxyethylene group, PO: oxypropylene group n: an integer of 4 to 50 m: an integer of 1 to 50, provided that n≧m] A nonionic surfactant represented by A method for high-temperature scouring of polyester fibers, which comprises scouring in an aqueous system containing.
JP60225305A 1985-10-09 1985-10-09 High temperature mercerization of polyester fiber Granted JPS6285071A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60225305A JPS6285071A (en) 1985-10-09 1985-10-09 High temperature mercerization of polyester fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60225305A JPS6285071A (en) 1985-10-09 1985-10-09 High temperature mercerization of polyester fiber

Publications (2)

Publication Number Publication Date
JPS6285071A JPS6285071A (en) 1987-04-18
JPS6312192B2 true JPS6312192B2 (en) 1988-03-17

Family

ID=16827260

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60225305A Granted JPS6285071A (en) 1985-10-09 1985-10-09 High temperature mercerization of polyester fiber

Country Status (1)

Country Link
JP (1) JPS6285071A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0420936A (en) * 1990-05-16 1992-01-24 Tokuyama Soda Co Ltd Electrochromic display element

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH081633U (en) * 1992-03-25 1996-12-03 義一 角畠 Hanamochi plate
JPH0748044Y2 (en) * 1992-04-14 1995-11-08 株式会社三和企画 Gardening container
JPH081553U (en) * 1993-05-06 1996-11-05 進 平井 "External installation set of stanchions for flower pots"

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5317712A (en) * 1976-08-02 1978-02-18 Ibm Data recorder reproducer
JPS5450675A (en) * 1977-09-22 1979-04-20 Mitsubishi Chem Ind Scouring and detergent composition for fiber

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5317712A (en) * 1976-08-02 1978-02-18 Ibm Data recorder reproducer
JPS5450675A (en) * 1977-09-22 1979-04-20 Mitsubishi Chem Ind Scouring and detergent composition for fiber

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0420936A (en) * 1990-05-16 1992-01-24 Tokuyama Soda Co Ltd Electrochromic display element

Also Published As

Publication number Publication date
JPS6285071A (en) 1987-04-18

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