JPS6325110B2 - - Google Patents
Info
- Publication number
- JPS6325110B2 JPS6325110B2 JP23250084A JP23250084A JPS6325110B2 JP S6325110 B2 JPS6325110 B2 JP S6325110B2 JP 23250084 A JP23250084 A JP 23250084A JP 23250084 A JP23250084 A JP 23250084A JP S6325110 B2 JPS6325110 B2 JP S6325110B2
- Authority
- JP
- Japan
- Prior art keywords
- silk
- fabric
- minutes
- methylol
- salt
- 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
Links
- 239000004744 fabric Substances 0.000 claims description 12
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 claims description 7
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 5
- 239000000243 solution Substances 0.000 claims description 4
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 238000003672 processing method Methods 0.000 claims description 3
- 239000011347 resin Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- 150000003606 tin compounds Chemical class 0.000 claims description 3
- 230000000694 effects Effects 0.000 description 7
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 238000012545 processing Methods 0.000 description 5
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 4
- 238000011160 research Methods 0.000 description 4
- 230000037303 wrinkles Effects 0.000 description 4
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000007809 chemical reaction catalyst Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- -1 stannic chloride Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
〔産業上の利用分野〕
本発明は絹織物に防燃性、防汚性、帯電防止
性、防しわ性、嵩高性などの性質を簡易に付与せ
しめる絹織物の樹脂加工方法に関する。
〔従来の技術〕
近時、絹の需要増進をはかるために、従来の和
装中心の用途だけでなく、洋装分野にも絹を大い
に利用しようとする研究が勢力的に行われている
が、洋装の場合には和装よりも活動的になること
や、長繊維特有の繊細でしなやかな風合が場合に
よつてはかえつて欠点になることなど、和装にと
らわれた感覚や技術では洋装分野に進出すること
は容易でなく、成功した例は極めて少いのがこれ
までの現状である。
〔発明が解決しようとする問題点〕
本発明者は和装的な技術で作られた絹織物でも
樹脂加工によつてこれを洋装に適した性能に改良
する研究を積み重ねた結果、ここに成功をみたも
のである。すなわち、N―メチロールアクリルア
ミド又はN―メチロールメタクリルアミドを主成
分とし、これに次式で表わされるスズ加合物を助
剤ならびに反応触媒として用いる加工を施すこと
によつて、絹織物に不足ないしは欠けている種々
の性能を大幅に改善できることを見出したのであ
る。
一般式
M2SnCl6 (但し、MはK又はNH4である)。
〔問題点を解決するための手段〕
N―メチロールアクリルアミドはセルロース系
繊維の加工剤として広く知られているが、これを
絹繊維に適用した場合には、木綿加工用の縮合反
応触媒では触媒効果が弱く、N―メチロール基の
反応が余り進まず、思わしい改質効果は得られな
い。しかし塩化第2スズをこれに併用すれば反応
はかなり促進されて、相当の効果を挙げることが
できるといわれる。しかし塩化第2スズ自体が水
溶液中で強酸性を示すために、熱処理の段階で絹
繊維を著しく損傷する欠点があり、またこの強酸
性をある程度中和してしまうと、水溶液中でスズ
化合物が加水分解を生じ、反応効果が失われてし
まう欠点があり、この加工法は成功しなかつた
(繊維工業試験所研究報告、79号、P17(1966)。
本発明に用いるピンク塩は塩化第2スズに比較
して酸性が弱いにもかかわらず、水溶液中での安
定性が高く、且つN―メチロール基の熱時縮合反
応促進効果が大きい。さらに、処理後の未反応薬
剤の除去を目的とする洗浄工程度においてピンク
塩は塩化第2スズと同様に水に不溶性のスズ塩と
なつて絹繊維内に永久固着されるので、N―メチ
ロールアクリルアミド又はN―メチロールメタク
リルアミド単独の加工では達し得ない高い性能改
善、たとえば防しわ性、嵩高性を得ることができ
る上に、スズ塩の寄与による防燃性や防汚性、帯
電防止性を得ることもできる。
本発明に用いるピンク塩は塩化第2スズの濃厚
水溶液に塩化カリウムあるいは塩化アンモニウム
を混合することによつて容易に生成する(日本蚕
糸学雑誌、36巻、P362(1967))。
したがつて予めSnCl4水溶液とMCl水溶液とを
混合しておいて、その所定量をN―メチロールア
クリルアミド又はN―メチロールメタクリルアミ
ド溶液に注入して処理浴を調合するが、スズ
(Sn)使用量としては処理浴1当り20〜200g
の範囲内がよく、これよりも多量に用いても改質
効果はもはや上昇することは期待できず、かえつ
て絹を変色、損傷する危険がある。また20g/
以下の少量では縮合反応は充分に進まず、スズ塩
の繊維内固着量も少なすぎて高い改質効果は得ら
れない。
N―メチロールアクリルアミドあるいはN―メ
チロールメタクリルアミドも余り多量に用いる
と、絹繊維の風合や光沢を損うので、処理浴1
当り250〜50gの範囲に抑える必要があり、絹織
物の種類によつて加減する必要がある。
かくして絹織物を処理浴に常温で5〜10分間浸
漬、2本ロールマングルで絞液率70―100%に脱
液し、60〜70℃の低温で3〜5分間予備乾燥し、
さらに120℃以下の温度で2〜10分間乾熱処理あ
るいは湿熱処理し、最後に水洗、必要ならばソー
ピング処理を行い、仕上げ乾燥する。
〔実施例〕
以下本発明の実施例について説明する。
実施例 1
12匁付絹羽二重(精練済み)を150g/N―
メチロールメタクリルアミドと75g/ヘキサク
ロルスズ酸アンモニウムとから成る処理浴に常温
で5分間浸漬、2本ロールマングルで絞液率90%
に脱液し、65℃で5分間予備乾燥した後、105℃
で5分間乾熱キユアリングした。この加工織物を
軽く水洗してから3g/石鹸液で50℃、20分間
ソーピング、水洗、乾燥した。この加工織物の性
能試験結果を表1に示す。
[Industrial Field of Application] The present invention relates to a resin processing method for silk fabrics that easily imparts properties such as flame retardancy, stain resistance, antistatic properties, wrinkle resistance, and bulkiness to silk fabrics. [Conventional technology] In recent years, in order to increase the demand for silk, research has been actively conducted to utilize silk not only for traditional Japanese clothing, but also for Western clothing. In some cases, it is more active than in Japanese clothing, and in some cases, the delicate and supple texture unique to long fibers can become a drawback. It is not easy to do so, and there have been very few successful cases to date. [Problem to be solved by the invention] The present inventor has conducted research on how to improve the performance of silk fabrics made using Japanese-style techniques through resin processing to make them suitable for Western-style clothing, and has succeeded here. This is what I saw. That is, by processing N-methylol acrylamide or N-methylol methacrylamide as a main component and using a tin compound represented by the following formula as an auxiliary agent and a reaction catalyst, defects or defects can be eliminated in silk fabrics. They discovered that various performance characteristics can be significantly improved. General formula M 2 SnCl 6 (where M is K or NH 4 ). [Means for solving the problem] N-methylolacrylamide is widely known as a processing agent for cellulose fibers, but when applied to silk fibers, it has no catalytic effect as a condensation reaction catalyst for cotton processing. is weak, the reaction of the N-methylol group does not proceed much, and the desired modification effect cannot be obtained. However, it is said that if stannic chloride is used in combination with this, the reaction can be considerably accelerated and a considerable effect can be achieved. However, since stannic chloride itself is strongly acidic in an aqueous solution, it has the disadvantage of significantly damaging silk fibers during heat treatment.Additionally, if this strong acidity is neutralized to some extent, the tin compound in an aqueous solution This processing method was not successful because it had the disadvantage of causing hydrolysis and losing the reaction effect (Textile Industry Research Institute Research Report, No. 79, P17 (1966). The pink salt used in the present invention is a dichloride salt. Although it is weakly acidic compared to tin, it has high stability in aqueous solutions and has a large effect of accelerating the thermal condensation reaction of N-methylol groups.Furthermore, it is used for the purpose of removing unreacted drugs after treatment. During the washing process, pink salt, like stannic chloride, becomes a water-insoluble tin salt and is permanently fixed within the silk fibers, so it cannot be achieved by processing with N-methylol acrylamide or N-methylol methacrylamide alone. Not only can high performance improvements such as wrinkle resistance and bulkiness be obtained, but also flame retardancy, stain resistance, and antistatic properties can be obtained due to the contribution of the tin salt.The pink salt used in the present invention is a chlorinated salt. It is easily produced by mixing potassium chloride or ammonium chloride with a concentrated aqueous solution of stannic (Japan Seriological Journal, Vol. 36, P362 (1967)). Therefore, a treatment bath is prepared by mixing an aqueous SnCl 4 solution and an aqueous MCl solution in advance and pouring a predetermined amount of the mixture into an N-methylol acrylamide or N-methylol methacrylamide solution, but the amount of tin (Sn) used is 20-200g per treatment bath
It is preferable that the amount is within the range of 1, and even if it is used in an amount larger than this, the modification effect cannot be expected to increase any more, and there is a risk of discoloring and damaging the silk. Also 20g/
If the amount is below, the condensation reaction will not proceed sufficiently, and the amount of tin salt fixed in the fibers will be too small, making it impossible to obtain a high modification effect. If too much N-methylol acrylamide or N-methylol methacrylamide is used, it will impair the texture and luster of silk fibers, so treatment bath 1
It is necessary to keep the amount within the range of 250 to 50 g per serving, and it is necessary to adjust the amount depending on the type of silk fabric. In this way, the silk fabric is immersed in the treatment bath for 5 to 10 minutes at room temperature, deliquified with a two-roll mangle to a squeezing rate of 70 to 100%, and pre-dried for 3 to 5 minutes at a low temperature of 60 to 70°C.
It is then subjected to dry heat treatment or wet heat treatment at a temperature of 120°C or less for 2 to 10 minutes, and finally washed with water, soaped if necessary, and finished dried. [Examples] Examples of the present invention will be described below. Example 1 150g/N- of 12 momme silk habutae (scoured)
Immersed in a treatment bath consisting of methylolmethacrylamide and 75g/ammonium hexachlorostannate at room temperature for 5 minutes, squeezing rate 90% with a two-roll mangle.
After deliquing and pre-drying at 65℃ for 5 minutes, drying at 105℃
Dry heat curing was performed for 5 minutes. This processed fabric was lightly washed with water, then soaped with 3 g/soap solution at 50°C for 20 minutes, washed with water, and dried. Table 1 shows the performance test results of this processed fabric.
【表】
表―1のデータから、この加工絹は約5%のス
ズ塩と約10%のメチロールメタクリルアミド縮合
体とを有することがうかがわれ、絹の強伸度性能
をほとんど損うことなく、防しわ性、防汚性、防
燃性、帯電防止性を向上していることがわかる。
実施例 2
12匁付絹羽二重(精練済み)をN―メチロール
アクリルアミド180gとヘキサクロルスズ酸カリ
ウム100g/とから成る処理浴で常温で5分間
浸漬、90%に絞液し、65℃で7分間予備乾燥し、
105℃で7.5分間乾熱キユアした。実施例1と同様
に洗浄し、乾燥した後の試験結果を表―2に示
す。[Table] From the data in Table 1, it can be seen that this processed silk has about 5% tin salt and about 10% methylolmethacrylamide condensate, which almost impairs the strength and elongation performance of the silk. It can be seen that wrinkle resistance, stain resistance, flame resistance, and antistatic properties are improved. Example 2 12 Momme silk habutae (refined) was immersed in a treatment bath consisting of 180 g of N-methylol acrylamide and 100 g of potassium hexachlorstannate at room temperature for 5 minutes, squeezed to 90%, and heated to 65°C. Pre-dry for 7 minutes,
Dry heat curing was performed at 105°C for 7.5 minutes. The test results after washing and drying in the same manner as in Example 1 are shown in Table 2.
本発明は上記実施例で明らかなように絹の強伸
度性能をほとんど損うことなく、防しわ性、防汚
性、防燃性、帯電防止性を向上するものである。
As is clear from the above examples, the present invention improves the wrinkle resistance, stain resistance, flame resistance, and antistatic properties of silk without substantially impairing its strength and elongation performance.
Claims (1)
はN―メチロールメタクリルアミドと次の一般式
で表わされるスズ化合物(ピンク塩) 一般式 M2SnCl6 (但しMはKまたはNH4) とからなる水溶液に浸漬した後、過剰の溶液を除
去して80℃以上の温度で熱処理することを特徴と
する絹織物の樹脂加工方法。[Scope of Claims] 1 Silk fabric is made of N-methylol acrylamide or N-methylol methacrylamide and a tin compound (pink salt) represented by the following general formula M 2 SnCl 6 (where M is K or NH 4 ) and A resin processing method for silk fabric, which comprises immersing the fabric in an aqueous solution consisting of the above, removing excess solution, and heat-treating the fabric at a temperature of 80°C or higher.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23250084A JPS61113883A (en) | 1984-11-06 | 1984-11-06 | Resin processing of silk fabric |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23250084A JPS61113883A (en) | 1984-11-06 | 1984-11-06 | Resin processing of silk fabric |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61113883A JPS61113883A (en) | 1986-05-31 |
| JPS6325110B2 true JPS6325110B2 (en) | 1988-05-24 |
Family
ID=16940297
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP23250084A Granted JPS61113883A (en) | 1984-11-06 | 1984-11-06 | Resin processing of silk fabric |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61113883A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02100582U (en) * | 1989-01-31 | 1990-08-10 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06123070A (en) * | 1992-08-31 | 1994-05-06 | Kanebo Ltd | Antistatic processing method for silk yarn structure |
-
1984
- 1984-11-06 JP JP23250084A patent/JPS61113883A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02100582U (en) * | 1989-01-31 | 1990-08-10 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61113883A (en) | 1986-05-31 |
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