JPS6081369A - Processing of silk cloth - Google Patents

Processing of silk cloth

Info

Publication number
JPS6081369A
JPS6081369A JP18759483A JP18759483A JPS6081369A JP S6081369 A JPS6081369 A JP S6081369A JP 18759483 A JP18759483 A JP 18759483A JP 18759483 A JP18759483 A JP 18759483A JP S6081369 A JPS6081369 A JP S6081369A
Authority
JP
Japan
Prior art keywords
parts
processing
habutae
silk
dry
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.)
Granted
Application number
JP18759483A
Other languages
Japanese (ja)
Other versions
JPH0219229B2 (en
Inventor
池良 清
義文 石川
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.)
IKEIZUMI ORIMONO KK
ISHIKAWA KIGIYOU KK
Original Assignee
IKEIZUMI ORIMONO KK
ISHIKAWA KIGIYOU KK
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 IKEIZUMI ORIMONO KK, ISHIKAWA KIGIYOU KK filed Critical IKEIZUMI ORIMONO KK
Priority to JP18759483A priority Critical patent/JPS6081369A/en
Publication of JPS6081369A publication Critical patent/JPS6081369A/en
Publication of JPH0219229B2 publication Critical patent/JPH0219229B2/ja
Granted legal-status Critical Current

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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】 本発明は絹織物の品質を改善するだめの加工方法に関す
るものであり、’l”l−に、温和な条件下で多価アル
コール系エポキシ化合物を絹織物に反応させる事にょシ
、絹織物の実用的性能を向上せしめる事を目的としてい
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a processing method for improving the quality of silk fabrics, which involves reacting polyhydric alcohol-based epoxy compounds with silk fabrics under mild conditions. In particular, the purpose is to improve the practical performance of silk fabrics.

絹織物を洋装材料として用いる場合、優雅な光沢や、し
なやかな風合により、他種繊糾によっては得られない特
徴によって、より高級な完成品を製造する事が期待てき
るが、その反面、絹織物には実用的性能にいさプか欠け
るところがあり、特に、l−わになり易い事、型くずれ
し易い事、日光により変色脆化し易い事、摩擦によシ毛
羽立ちが生じ易い事等々の重大な欠点があΣ事を否定で
きない。
When silk fabric is used as a material for Western clothing, it is expected that it will produce a higher quality finished product due to its elegant luster and supple texture, characteristics that cannot be obtained by kneading other types of fibers. Silk fabrics have some shortcomings in their practical performance, and in particular, they tend to wrinkle easily, lose their shape easily, become discolored and brittle when exposed to sunlight, and tend to become fluffy due to friction. It cannot be denied that there are some drawbacks.

この様な欠点を除去するため、これ1で種々の化学的処
理方法が研究されて来だが、成功した例は少く、またこ
れらの欠点の一部が除去できた場合でも、そのだめの処
理によって絹織物本来の長所が失われてしまっだシ、或
は商業的に実用化が困難であると云う例が多かった。
In order to remove these defects, various chemical treatment methods have been studied, but there have been few successful cases, and even if some of these defects can be removed, the treatment may be insufficient. In many cases, the original advantages of silk fabrics have been lost, or it has been difficult to put them into practical use commercially.

実用可能のものとしては、エポキシ化合物を使用するも
のが、なんとかこの目的の為に有効であると考えられる
が、その様な場合でも、例えばアルカリ触媒を用いる方
式(特公昭38−25198参照)では、苛性ソーダと
か炭酸ソーダとかを触媒として高温で処理するため、絹
織物の脆化及び変色がともない実用には供し得ないもの
であった。
As a practical method, one using an epoxy compound is considered to be effective for this purpose, but even in such a case, for example, a method using an alkali catalyst (see Japanese Patent Publication No. 38-25198) However, since the treatment is carried out at high temperatures using caustic soda or soda carbonate as a catalyst, the silk fabric becomes brittle and discolored, making it impossible to put it to practical use.

また、中性塩触媒を使用する方法(特公昭52−381
61参照)に於ては、絹織物の脆化・変色と云う問題は
少いが、有機溶媒中で処理すると云う方式であるだめ、
大量の加工、特に織物の形での大量の加工処理には不適
当であると云わざるを得す、い1だに実用化はされてい
ガい。
In addition, a method using a neutral salt catalyst (Japanese Patent Publication No. 52-381
61), there are few problems of embrittlement and discoloration of silk fabrics, but since the process is carried out in an organic solvent,
It must be said that it is unsuitable for large-scale processing, especially large-scale processing in the form of textiles, and it has not yet been put to practical use.

本発明はこの様な状況を考慮し、エポキシ化合物の適用
方法を再検討し、大量の織物を加工処理する方法を得た
。すなわち本発明に於テハ、エポキシ化合物とモノカル
ボン酸アルカリ金属塩との水溶液を絹織物に飽充しノζ
後、湿熱処理する事によって、パンチ式でも連続式でも
、絹本来の光沢や風合を失う事なく、実用的性能を向上
せしめイ1する一jJ3を見出した。
The present invention took this situation into consideration, reconsidered the method of applying epoxy compounds, and obtained a method for processing large quantities of textiles. That is, in the present invention, a silk fabric is filled with an aqueous solution of an epoxy compound and an alkali metal salt of a monocarboxylic acid.
Afterwards, we have discovered that by applying moist heat treatment, the practical performance can be improved without losing the original luster and texture of silk, whether it is a punch type or a continuous type.

本発明に於て、触媒となるモノカルボン酸のアルカリ金
属塩としては、酢酸、ゾロピオン酸、酪酸等のナトリウ
ム、カリウム或はリチウム塩が適当であり、これらの−
を選び、エポキシ化合物の2〜20チ、望ましくUS〜
10%使用するのが最も望′ましい。これらの触媒は容
易に水に溶けて弱アルカリ性を示し、しかも水溶液中で
エポキシ化合物と共存しても、常温ではそれと反応しに
〈<、80度C以上の高温下で水分が存在してはじめて
エポキシ化合物の反応を促進する。従って、処理溶液中
でエポキシ化合物が消耗する事が少く、加工効果は湿熱
処理の条件によってコントロールできると云う利点があ
る。
In the present invention, suitable alkali metal salts of monocarboxylic acids serving as catalysts include sodium, potassium or lithium salts of acetic acid, zolopionic acid, butyric acid, etc.
and 2 to 20 inches of epoxy compound, preferably US~
Most preferably, 10% is used. These catalysts easily dissolve in water and exhibit weak alkalinity, and even if they coexist with epoxy compounds in an aqueous solution, they do not react with the epoxy compounds at room temperature. Accelerates the reaction of epoxy compounds. Therefore, there is an advantage that the epoxy compound is less consumed in the processing solution and the processing effect can be controlled by the conditions of the wet heat treatment.

また本発明に使用するエポキシ化合物としてハ、多価ア
ルコール系のエポキシ化合物が有用であり、その中でも
水に対する溶解度の高いエチレングリコールのグリシジ
ルエーテルが最も有用であシ、処理すべき絹の重量に対
して15〜28係程度使用した場合に最良の結果が得ら
れる。
In addition, as the epoxy compound used in the present invention, polyhydric alcohol-based epoxy compounds are useful, and among them, glycidyl ether of ethylene glycol, which has a high solubility in water, is the most useful. The best results are obtained when using about 15 to 28 coefficients.

処理溶液を絹に飽充し絞液率を50〜1DOヴ望ましく
は70〜90%として脱液した後、60〜70度Cの低
温で予備乾燥し、次に飽和蒸気中で10〜60分間熱処
理する事によって、絹の性能改善が達成される。熱処理
の温度は100度C最高で110度C−i!でが適当で
あり、それ以」二の高温を使用すると処理時間は短縮で
きるものの、絹の変色が生じるため望1しくない。
After filling the silk with the treatment solution and removing the liquid at a squeezing rate of 50 to 1 DOV, preferably 70 to 90%, it is pre-dried at a low temperature of 60 to 70 degrees Celsius, and then dried in saturated steam for 10 to 60 minutes. Through heat treatment, improved performance of silk is achieved. The heat treatment temperature is 100 degrees C and the maximum is 110 degrees C-i! However, using a higher temperature than that is suitable, and although the processing time can be shortened, it is not desirable because it causes discoloration of the silk.

性能改善による特に顕著な実用的性能の向上は、しわ回
復性、耐光性、劇アルカリ性、染色性に於て明瞭であシ
、それらの性能向上によって、より価値の高い洋装製品
を創出するだめの累月が得られる事が明がである。
Particularly remarkable improvements in practical performance due to improved performance are evident in wrinkle recovery properties, light resistance, strong alkali resistance, and dyeability, and improvements in these properties will lead to the creation of more valuable Western clothing products. It is clear that you can get the full moon.

次に具体的実施例にょシ本発[JJによるいくつかの処
理例を説明する。一 実施例1゜ 14匁付羽二重を精練し、こtしを エビオールE 100 150部 グロビオン酸ナトリウム 15部 水 1 0DD音1s から成る処理溶液に浸漬し、マングルにより約85%に
絞液し、60度Cで軽く予備乾燥する。
Next, some examples of processing by JJ will be described as specific examples. Example 1: Scour Habutae with 14 momme weight, dipped in a treatment solution consisting of 100 parts of Ebiol E, 150 parts of sodium globionate, 15 parts of water, 1 s of water, and squeezed to about 85% with a mangle. and lightly pre-dry at 60 degrees C.

洗、乾燥し、軽くアイロン仕上げをする。Wash, dry and lightly iron.

これによって得られた加工済品の性能は次の通りであっ
た。下表に於て未加工品と対比させてその数値を示す。
The performance of the processed product thus obtained was as follows. The table below shows the numerical values in comparison with unprocessed products.

試料14匁付羽二重 本発明加工 未加工品重量増加 
(%) 12.8 − (a)シわ回復角 乾 291 20B(a) “ 湿
 286 205 (b)引裂強度 <g ) 1280 1400(C)
剛軟度 (皿) 77 78 (d)次亜液溶解度 38 10n 日光黄変度(三日間) + 十十十++表中のa−dの
符号は次の内容を示す。
Sample 14 Habutae with momme Processed according to the invention Increased weight of unprocessed product
(%) 12.8 - (a) Wrinkle recovery angle Dry 291 20B (a) Wet 286 205 (b) Tear strength <g) 1280 1400 (C)
Bending resistance (dish) 77 78 (d) Hypochlorite solubility 38 10n Sunlight yellowing (3 days) + 110++ The symbols a to d in the table indicate the following contents.

a・−センサンド法(経十緯) b−°エルメントルフ法 C・・ハートループ法 d・−JIS LID 30 (以下各表とも同じ) 実施例2゜ 14匁付羽二重を精練し、これを エピオール G−100(グリセリン系) 150部プ
ロピオン酸ナトリウム 15部 水 10[10部 から成る処理溶液に浸偵し、マングルにより約85φに
絞液し、60度Cで軽くFイ111j乾燥する。
a. - Sensand method (longitude and latitude) b - ° Elmentorff method C.. Hartloop method d. - JIS LID 30 (same for each table below) Example 2 14 Momme Habutae was refined and Epiol G-100 (glycerin type) 150 parts Sodium propionate 15 parts Water 10 [10 parts] Sprinkle the solution into a treatment solution, squeeze the solution to about 85φ with a mangle, and lightly dry at 60 degrees Celsius.

次にこの羽二重を100度Cで15分間熱処理し、80
度Cの6%石鹸液で処理した後、水洗、乾燥し、軽くア
イロン什」二げをする。
Next, this habutae was heat-treated at 100 degrees C for 15 minutes, and
After treating with a 6% soap solution of degree C, wash with water, dry, and lightly iron.

これによって得られた加工済品の性能は次の通りであっ
た。下表に於て未加工品と対比させてその数値を示す。
The performance of the processed product thus obtained was as follows. The table below shows the numerical values in comparison with unprocessed products.

試料14匁付羽二重 本発明力[計重 体力1江品重量
増加(%) 121 − (a)シわ回復角 乾 280 208(a) “ 湿
 271 205 (b)引裂強度 (g) 1290 1400(c)剛
軟度 (mm) 76 78 (d) 次亜液溶解度 65100 日光黄変度(三日間)+ −1−++++14匁付羽二
重を精練し、これを エボライl−70P(プロピレングリコール系) 15
0部プロピオン酸カリウム 15部 水 i ooo部 から成る処理溶液に浸漬し、マングルにより約85%に
絞液し、60度Cで軽く予備乾燥する。
Sample 14 Habutae with momme Invention strength [Weighing Physical strength 1 Weight increase (%) 121 - (a) Wrinkle recovery angle Dry 280 208 (a) Wet 271 205 (b) Tear strength (g) 1290 1400 (c) Bending resistance (mm) 76 78 (d) Hypochlorite solubility 65100 Sunlight yellowing (3 days) + -1-+++14 Habutae with a momme is refined and mixed with Evolai l-70P (propylene glycol type) 15
It is immersed in a treatment solution consisting of 0 parts potassium propionate, 15 parts water, i ooo parts, squeezed to about 85% with a mangle, and lightly pre-dried at 60 degrees Celsius.

次にこの羽二重を100度Cで15分間熱処理し、80
度Cの6%石鹸液で処理した後、水洗、乾燥し、軽くア
イロン仕上げをする。
Next, this habutae was heat-treated at 100 degrees C for 15 minutes, and
After treating with 6% soap solution at degree C, wash with water, dry and lightly iron.

これによって得られた加工済品の性能は次の通りであっ
た。下表に於て未加工品と対比させてその数値を示す。
The performance of the processed product thus obtained was as follows. The table below shows the numerical values in comparison with unprocessed products.

試料14匁付羽二重 本発明加工品 未加工品重量増加
(%) 12.0 − (a)シわ回復角 乾 284 208(a) ” 湿
 274 205 (1))引裂強度(g ) 1272 1400(C)
 剛軟度(mm) 76 7B (d) 次亜液溶解度 38 10(]日光黄変度(三
日間) −1−十+十−1−+実施例4゜ 14匁付羽二重を精練し、これを エピオール E−1[]0 (エチレングリコール系)
150部プロピオン酸カリウム 15部 水 1ooo部 から成る処理溶液に浸漬し、マングルにより約85係に
絞液し、60度Cで軽く予備’+IL燥する。
Sample 14 Habutae with momme Processed product according to the invention Weight increase in unprocessed product (%) 12.0 - (a) Wrinkle recovery angle Dry 284 208 (a) "Wet 274 205 (1)) Tear strength (g) 1272 1400(C)
Bending resistance (mm) 76 7B (d) Hypochlorite solubility 38 10 (] Sunlight yellowing (3 days) -1-10+10-1-+Example 4゜14 Momme Habutae scouring , this is called Epiol E-1[]0 (ethylene glycol type)
It is immersed in a treatment solution consisting of 150 parts potassium propionate, 15 parts water, and 100 parts, squeezed with a mangle to about 85 parts, and lightly pre-dried at 60 degrees Celsius.

次にこの羽二重を100度Cで15分間熱処理し、80
度Cの3係石鹸液で処理した後、水洗、乾燥し、軽くア
イロン仕上けをする。
Next, this habutae was heat-treated at 100 degrees C for 15 minutes, and
After treating with a grade C soap solution, wash with water, dry, and lightly iron.

これによって得られた加工済品の性能は次の通りであっ
た。下表に於て未加工品と対比させてその数値を示す。
The performance of the processed product thus obtained was as follows. The table below shows the numerical values in comparison with unprocessed products.

試料14匁付羽二重 本発明加工品 未加工品重量増加
(チ) 12.8 − (a)シわ回復角 乾 290 208(a)シわ回復
角 湿 287 2[15Φ)引裂強度 (g ) 1
283 1400(C) 剛軟度 (mm ) 77 
78(d) 次亜液溶解度 39 100 日光黄変度(三日間) 十+++++ 実施例5゜ 14匁細別二重を精練し、これを エピオール G−100(グリセリン系) 150部プ
ロピオン酸カリウム 15部 水 1000部 から成る処理溶液に浸漬し、 マングルにより約85係
に絞液し、60度Cで軽く予備乾燥する。
Sample 14 Habutae with momme Processed product of the present invention Weight increase of unprocessed product (chi) 12.8 - (a) Wrinkle recovery angle Dry 290 208 (a) Wrinkle recovery angle Wet 287 2 [15Φ) Tear strength (g ) 1
283 1400(C) Bending resistance (mm) 77
78(d) Solubility of hypochlorite 39 100 Sunlight yellowing (3 days) 10++++++ Example 5 A 14 monme finely divided double layer was refined, and this was mixed with Epiol G-100 (glycerin type) 150 parts Potassium propionate 15 parts It is immersed in a treatment solution consisting of 1000 parts of water, squeezed with a mangle to about 85 parts, and lightly pre-dried at 60 degrees Celsius.

次にこの羽二重を100度Cで15分間熱処理し、80
度Cの6係石鹸液で処理した後、水洗、乾燥し、軽くア
イロン仕上げをする。
Next, this habutae was heat-treated at 100 degrees C for 15 minutes, and
After treating with a grade C 6 soap solution, wash with water, dry, and lightly iron.

これによって得られた加工済品の性能は次の通りであっ
た。下表に於て未加工品と対比させてその数値を示す。
The performance of the processed product thus obtained was as follows. The table below shows the numerical values in comparison with unprocessed products.

試料14匁付羽二重 本発明加工品 未加工品重量増加
(φ) 12.1 − (a)シわ回復角 乾 281 208(a)〃 湿 
270 205 (b) 引裂強度 (g ) 1288 +400(C
) 剛軟度 (nn++) 75 78(d) 次亜液
溶解度 37 100 日光黄変度(三日間)十++十丹 以上から明かな如く本発明方法により得られた製品は、
しわ回復性、耐光性及び耐アルカリ性に優れており、引
裂強度柔軟性ともに損われていない。
Sample 14 Habutae with momme Processed product of the present invention Weight increase of unprocessed product (φ) 12.1 - (a) Wrinkle recovery angle Dry 281 208 (a)〃 Wet
270 205 (b) Tear strength (g) 1288 +400 (C
) Bending resistance (nn++) 75 78 (d) Hypochlorite solubility 37 100 Sunlight yellowing (3 days) 10++ 10+ It is clear that the product obtained by the method of the present invention has a
It has excellent wrinkle recovery properties, light resistance, and alkali resistance, with no loss in tear strength and flexibility.

又、エチレングリコール系エポキシ化合物以外の、グリ
セリン系エポキシ化合物、プロピレン系エボギシ化合物
を使用した場合にも同様の良好な結果が得られた。
Similar good results were also obtained when using glycerin-based epoxy compounds and propylene-based epoxy compounds other than ethylene glycol-based epoxy compounds.

特許出願人 池泉織物株式会社patent applicant Ikeizumi Textile Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 絹織物を多価アルコール系エポキシ化合物とモノカルボ
ン酸のアルカリ金属塩との水溶液に浸漬し、脱液した後
、湿熱処理する小を特徴とする絹織物の加工方法。
A method for processing silk fabric, characterized by immersing silk fabric in an aqueous solution of a polyhydric alcohol-based epoxy compound and an alkali metal salt of a monocarboxylic acid, removing the liquid, and then subjecting the fabric to moist heat treatment.
JP18759483A 1983-10-06 1983-10-06 Processing of silk cloth Granted JPS6081369A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18759483A JPS6081369A (en) 1983-10-06 1983-10-06 Processing of silk cloth

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18759483A JPS6081369A (en) 1983-10-06 1983-10-06 Processing of silk cloth

Publications (2)

Publication Number Publication Date
JPS6081369A true JPS6081369A (en) 1985-05-09
JPH0219229B2 JPH0219229B2 (en) 1990-05-01

Family

ID=16208837

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18759483A Granted JPS6081369A (en) 1983-10-06 1983-10-06 Processing of silk cloth

Country Status (1)

Country Link
JP (1) JPS6081369A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2614634A1 (en) * 1987-04-28 1988-11-04 Kanebo Ltd SILK FIBERS HAVING GOOD RESISTANCE TO ABRASION AND GOOD RESISTANCE TO LIGHT AND METHODS FOR THEIR PREPARATION
JPH0284547A (en) * 1988-06-08 1990-03-26 Tasuku Matsumoto Finishing of silk fabric
US5250077A (en) * 1987-04-28 1993-10-05 Kanebo Co., Ltd. Silk fiber having good abrasion resistance and good light resistance and methods for the preparation thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5253015A (en) * 1975-10-22 1977-04-28 Kanagawa Prefecture Sericin fixing treatment for silk or sericinn containing fiber

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5253015A (en) * 1975-10-22 1977-04-28 Kanagawa Prefecture Sericin fixing treatment for silk or sericinn containing fiber

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2614634A1 (en) * 1987-04-28 1988-11-04 Kanebo Ltd SILK FIBERS HAVING GOOD RESISTANCE TO ABRASION AND GOOD RESISTANCE TO LIGHT AND METHODS FOR THEIR PREPARATION
DE3814450A1 (en) * 1987-04-28 1988-11-17 Kanebo Co SILK FIBER WITH HIGH ABRASION RESISTANCE AND GOOD LIGHT FASTNESS AND METHOD FOR THE PRODUCTION THEREOF
US4929248A (en) * 1987-04-28 1990-05-29 Kanebo Co., Ltd. Silk fiber having good abrasion resistance and good light resistance and methods for the preparation thereof
US5250077A (en) * 1987-04-28 1993-10-05 Kanebo Co., Ltd. Silk fiber having good abrasion resistance and good light resistance and methods for the preparation thereof
JPH0284547A (en) * 1988-06-08 1990-03-26 Tasuku Matsumoto Finishing of silk fabric

Also Published As

Publication number Publication date
JPH0219229B2 (en) 1990-05-01

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