JPS6285079A - Modification treatment of silk - Google Patents
Modification treatment of silkInfo
- Publication number
- JPS6285079A JPS6285079A JP22554885A JP22554885A JPS6285079A JP S6285079 A JPS6285079 A JP S6285079A JP 22554885 A JP22554885 A JP 22554885A JP 22554885 A JP22554885 A JP 22554885A JP S6285079 A JPS6285079 A JP S6285079A
- Authority
- JP
- Japan
- Prior art keywords
- silk
- silk thread
- aqueous solution
- alkali metal
- formula
- 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
Links
- 238000012986 modification Methods 0.000 title description 3
- 230000004048 modification Effects 0.000 title description 3
- 238000000034 method Methods 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000004593 Epoxy Substances 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 9
- 150000005846 sugar alcohols Polymers 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 159000000011 group IA salts Chemical class 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000012545 processing Methods 0.000 description 4
- 238000004383 yellowing Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 230000037303 wrinkles Effects 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- VSRMIIBCXRHPCC-UHFFFAOYSA-N 2-[2-[2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxy]ethoxy]ethoxymethyl]oxirane Chemical compound C1OC1COCCOCCOCCOCCOCC1CO1 VSRMIIBCXRHPCC-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 244000241257 Cucumis melo Species 0.000 description 1
- 235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
- 241000134884 Ericales Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 240000000249 Morus alba Species 0.000 description 1
- 235000008708 Morus alba Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 150000001218 Thorium Chemical class 0.000 description 1
- FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 238000012993 chemical processing Methods 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- KSCFJBIXMNOVSH-UHFFFAOYSA-N dyphylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1N(CC(O)CO)C=N2 KSCFJBIXMNOVSH-UHFFFAOYSA-N 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010998 test 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)
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】
3、発明の31 !illな説明
[産業上の利用分野1
本発明は絹の改質処理方法、特に絹繊維に防皺性、防縮
性、防変色性等を付与して品質を向上さUる絹糸の改質
処Jり!方法に130−Jる。[Detailed description of the invention] 3. 31 of the invention! [Industrial Field of Application 1] The present invention relates to a method for modifying silk, particularly a method for modifying silk thread that improves quality by imparting wrinkle resistance, shrink resistance, color resistance, etc. to silk fibers. Jri! 130-J on method.
Nil連技術とその問題点1
絹楳頻を実In衣料としてみる場合に、しわになり易い
こと、型くずれし易いこと、日光により黄変し易いこと
等の欠点をイiしていることは否定できない。この様な
絹の欠点を除去するため、これよで秤々の化学的処理法
が研究されてきたが、これら欠点の一部が改潜できた場
合でも、そのための処理によって絹本来の長所が損われ
てしまったり、あるいは工業的に採用づるのが困難であ
ることが多い。Nil-related technology and its problems 1 When looking at silk fabric as actual clothing, it is denied that it has disadvantages such as being easily wrinkled, easily losing its shape, and easily yellowing due to sunlight. Can not. In order to remove these defects of silk, a wide variety of chemical processing methods have been researched, but even if some of these defects can be removed, the treatment will not remove the inherent advantages of silk. They are often damaged or difficult to employ industrially.
例えば天川化の可能性があるらのとしてエポキシ化合物
による加工方法が知られているが、この場合であってら
、例えば特公昭38−25198月公報で提案されたア
ルカリ触媒を用いる方式ではアルカリ性条f’l”Fで
110〜160℃の高渇加熱処J■1を施す必要がある
ために、絹繊維は脆化・黄変するという欠点がある。ま
た、特公昭52−3813号公報で提案された中性塩触
媒を使用する方式では絹m雑の脆化という問題はほとん
ど生じないが有機溶媒中に浸漬し、溶媒の蒸発を防ぐよ
うに工夫した容4内で2〜6時間処]!!りるという方
式であるため、工業的規模の処理、特に織物の加工処理
には不適当であるとともに薬剤費が非常に高くなるとい
うn点を有していノご。For example, a processing method using an epoxy compound is known that has the possibility of Amakawa formation, but in this case, for example, the method using an alkali catalyst proposed in Japanese Patent Publication No. 38-25198, Silk fibers have the disadvantage of becoming brittle and yellowing due to the need to undergo high-temperature heat treatment J■1 at 110 to 160°C at 'l'F. In the method using a neutral salt catalyst, the problem of embrittlement of the silk material hardly occurs; !!Since it is a method called "Ruru", it is not suitable for industrial-scale processing, especially textile processing, and has the n points of being very expensive in terms of chemical costs.
[発明の目的]
本発明はこのような情況に鑑みてエポキシ化合物の適用
方法を研究した結果得られたものであり、上記欠点を解
馬し得る安価で簡単な絹の改質処理方法を提供すること
を目的とJる。[Objective of the Invention] The present invention was obtained as a result of research into methods of applying epoxy compounds in view of the above circumstances, and provides an inexpensive and simple method for modifying silk that can overcome the above-mentioned drawbacks. J Ru with the purpose of doing.
[発明の概要]
上記目的を達成するための本発明の概要は絹糸に、次の
一般式、
(式中、n −1〜9 、 R=H,CI+3 テアル
)で表わされる多価アルコール系エポキシ化合物と、ア
ルカリ金属水酸化物またはアルカリ金属のアルカリ性塩
とを含む水溶液を含浸し、前記水溶液を絹糸に30〜3
00%の割合で残留させた状態で室温に放置することに
あり、絹本来の長所を損わず、脆化や黄変す生じないよ
うに処理できるらのである。[Summary of the Invention] The outline of the present invention for achieving the above object is to add a polyhydric alcohol-based epoxy compound represented by the following general formula, (in the formula, n -1 to 9, R=H, CI+3 theal) to silk thread. A silk thread is impregnated with an aqueous solution containing a compound and an alkali metal hydroxide or an alkaline salt of an alkali metal.
By leaving silk at room temperature with 0.00% remaining, it is possible to process the silk without losing its inherent advantages and without causing brittleness or yellowing.
[発明の実施例1
本発明は絹糸に、次の一般式、
(式中、ロー 1〜9 、 R= H、CI3Tアル)
で表わされる多価アルコール系エポキシ化合物と、アル
カリ金属水酸化物またはアルカリ金属のアルカリ性塩と
を含む水溶液を含浸し、前記水溶液を絹糸に30〜30
0%の割合で95留させた状態で室温に放1uする乙の
である。[Embodiment 1 of the Invention The present invention provides silk thread with the following general formula, (wherein, R = H, CI3T al)
A silk thread is impregnated with an aqueous solution containing a polyhydric alcohol-based epoxy compound represented by
This is done by leaving 1 u of water at room temperature with 95% distillate at a ratio of 0%.
前記多価アルコール系エポキシ化合物として、水に対す
る溶解度の高いポリエチレングリコールあるいはポリプ
ロピレングリコール(重合度9以下)のジグリシジルエ
ーテルが最も有用であり、これらの一つを選び、処理す
べき絹の重浩に対して5〜20%程瓜用いることが好ま
しい。なお、前記多価アルコール系エポキシ化合物が水
に完全に溶解しない場合には低級アルコールのような溶
媒を可及的少量添加してもよい。また、本発明の実施例
において、反応触媒となるアルカリ金属水酸化物として
は水酸化プトリウムまたは水酸化カリウムが好ましく、
また、アルカリ金属のアルカリ性塩としては、■炭酸、
炭酸、レスキ炭のりトリウム塩またはカリウム塩が好ま
しく、これらの一つを選びlyi記エポキシ化合物重聞
に対して5〜50%、好ましくは10〜25%使用Jる
のが望ましい。また、本5を明の実施例において、処理
水溶液を絹繊維に含浸さU、保有水分率を30〜300
%、好ましくは75〜150%とした後、水分が蒸発し
ないように密封した状態ですくイ蒙くとも8時間以上好
ましくは12〜2011.S間室温に置くことによって
絹の改質が達成される。但し、室温が30℃以上になる
と絹は脆化する危険があるので、夏季にはこの点を注意
−4る必要がある。As the polyhydric alcohol-based epoxy compound, the diglycidyl ether of polyethylene glycol or polypropylene glycol (polymerization degree of 9 or less), which has a high solubility in water, is most useful. It is preferable to use about 5 to 20% of melon. In addition, when the polyhydric alcohol-based epoxy compound is not completely dissolved in water, a solvent such as a lower alcohol may be added in the smallest possible amount. In the examples of the present invention, the alkali metal hydroxide serving as the reaction catalyst is preferably puttrium hydroxide or potassium hydroxide.
In addition, as alkaline salts of alkali metals, ■ carbonic acid,
Carbonic acid, carbonate, thorium salt or potassium salt is preferred, and it is desirable to select one of these and use it in an amount of 5 to 50%, preferably 10 to 25%, based on the weight of the epoxy compound. In addition, in the example of Book 5, silk fibers were impregnated with the treated aqueous solution, and the retained moisture content was 30 to 300.
%, preferably 75 to 150%, and then cooled in a sealed state to prevent moisture from evaporating for at least 8 hours or more, preferably 12 to 2011%. Modification of the silk is achieved by keeping it at room temperature for a period of time. However, there is a risk that silk will become brittle if the room temperature exceeds 30°C, so care must be taken in the summer.
この改質による顕箸な大川的性能の向上は、皺回復性、
耐摩耗性、 1IiJ薬品性、耐光性、染色性等に於い
て良好であり、これらの性能向上によって、より価1/
jの高い絹製品が1SIられる。This modification has significantly improved the performance of chopsticks, including wrinkle recovery and
It has good abrasion resistance, 1IiJ chemical resistance, light resistance, dyeability, etc., and by improving these properties, it has even higher value.
Silk products with high j are valued at 1 SI.
次に具体的実施例によって本発明による処理例を説明す
る。Next, processing examples according to the present invention will be explained using specific examples.
実施例1
精練ずみの14万付羽二重を次の、
テトラエチレングリコールジグリシジルエーテル
120部セス4二1央酸ノ1〜
リウム 50部水
880 i!i11
から成る水溶液処理浴に通過ざV、マングルによって8
5%に絞液した。次にこの羽二重をビニル袋に密封し、
至!(20℃)で16時間放置し、よ(水洗した。ざら
に3%石鹸浴中80℃でソーピングし、水洗。Example 1 Refined 140,000 Habutae was treated with the following tetraethylene glycol diglycidyl ether.
120 parts Seth 421 central acid No 1~
Rium 50 parts water
880 i! i11
Passing through an aqueous treatment bath consisting of V, by mangle 8
The liquid was squeezed to 5%. Next, seal this habutae in a plastic bag,
To! Leave at (20°C) for 16 hours, then wash with water. Soap in a 3% soap bath at 80°C and wash with water.
乾燥した。Dry.
これによって1qられた加工羽二重の性能は次のとおり
であった。The performance of the processed habutae obtained by 1q was as follows.
人1
JIS L−1096B
(1)〔ンサンt−法(経→鈎)
(2)ハートル−プr去
(3)’JIS L−1030(次亜WLFIQ)I
−リウム)
(4)日光に5助1n照則し肉眼fl定表1の結果にみ
るように未加工絹に対比してみると、皺回復性(乾、湿
)、耐薬品性。Person 1 JIS L-1096B (1) [Nsan t-method (kei → hook) (2) Hartle-puri r (3)' JIS L-1030 (Jia WLFIQ) I
-Rium) (4) Compared to unprocessed silk, wrinkle recovery (dry and wet) and chemical resistance are shown in table 1 under the naked eye under sunlight.
h4光性が八しく向上していることが認められる。It is recognized that the h4 optical properties are significantly improved.
実浦例2
精練ずみの14万付羽二重を次の、
プロピレンゲリコールジグリシジルエーテル100部
水酸化カリウム 4部水
900部から成る水溶液の処1ル浴中に通過ざU、マン
グルによって85%に脱液した。次にこの羽二重をビニ
ル袋に密封し、室温(20℃)で18局間故Ia掛、水
洗、ソーピング、水洗。Saneura Example 2 140,000 yen of refined Habutae was mixed with the following: 100 parts of propylene gellicol diglycidyl ether 100 parts of potassium hydroxide 4 parts of water
An aqueous solution of 900 parts was passed through a bath and drained to 85% by means of a mangle. Next, this habutae was sealed in a plastic bag, and washed with water, soaped, and washed with water at room temperature (20°C) for 18 times.
乾燥した。これによって得られた羽二小の性能(ユ次の
通りであった。Dry. The performance of Hajisho obtained through this process was as follows.
表2 試験方法は表1に同じ 表2に示すように、*@復性、 M4桑品性。Table 2 The test method is the same as in Table 1. As shown in Table 2, *@resistance, M4 mulberry quality.
耐光性の向上が著しい。Significant improvement in light resistance.
実施例3
精練ずみの諸撚絹糸(27+I / I X3.600
1500−r/+n)を次の、
エチレングリコールジグリシジルエーテル150部
炭酸ナトリウム 50部水
850部からなる水溶液の処理浴に3分間浸し、水分率
120%になるように遠心脱水した。Example 3 Scoured plied silk yarn (27+I/I X3.600
1500-r/+n) to the following: 150 parts ethylene glycol diglycidyl ether 50 parts sodium carbonate
The sample was immersed in a treatment bath containing 850 parts of an aqueous solution for 3 minutes, and centrifugally dehydrated to a moisture content of 120%.
これをビニル袋に入れて室温(22℃)で16時間装い
てから水洗し、ソーピング、水洗。Put this in a plastic bag and leave it at room temperature (22℃) for 16 hours, then wash with water, soap, and rinse with water.
乾燥した。この加工絹糸および未加工絹糸を4%青色染
料(ラニルブリリアレ1〜ブルー〇)と5%酢酸アンモ
ニウムとの浴で30分間95℃で浸染した。Dry. The processed and unprocessed silk threads were dyed in a bath of 4% blue dye (Ranil Brilliare 1 to Blue 0) and 5% ammonium acetate for 30 minutes at 95°C.
これによって得られた加工絹糸の性能は次の通りであっ
た。The properties of the processed silk thread thus obtained were as follows.
表3
(1) 600mm波長の反射率から求めた(2)JI
S L−0849
(3)糸摩擦試験器(荷重209)
(4)テンシロン
表3の成績にみるように、本発明加工によって絹はより
濃色に染まり、染色堅牢度も向上していることがわかる
。まI;強度J3よび耐摩耗性も向上した。Table 3 (1) (2) JI determined from reflectance at 600 mm wavelength
SL-0849 (3) Thread friction tester (load 209) (4) As shown in the results in Tensilon Table 3, the processing of the present invention dyes silk a deeper color and improves the color fastness. Recognize. Also, strength J3 and abrasion resistance were improved.
〔発明の効果]
本発明は絹糸に、次の一般式、
(式中、「1−1〜9.R−H,CHsである)で表わ
される多価アルコール系エポキシ化合物と、アルカリ金
属水酸化物またはアルカリ金属のアルカリ性塩とを含む
水溶液を含浸し、前記水溶液を絹糸に30〜300%の
υ1合で残留させた状態でS!温に放置するように構成
されるから、加熱を要しない温和な条件下で多価アルコ
ール系エポキシ化合物を絹分子に化学反応さけることが
可能となり、安価で簡便な処理方法によって絹本来の長
所を保ちつつ脆化・黄変等を防止でき商品価値の高い絹
製品を提供でき、その効果は大きい。[Effects of the Invention] The present invention provides silk thread with a polyhydric alcohol-based epoxy compound represented by the following general formula (in the formula, "1-1 to 9.R-H, CHs") and an alkali metal hydroxide. The structure is such that the silk thread is impregnated with an aqueous solution containing an alkaline salt of a substance or an alkali metal, and is left at S! temperature with the aqueous solution remaining in the silk thread at a ratio of 30 to 300%, so no heating is required. It is now possible to chemically react polyhydric alcohol-based epoxy compounds to silk molecules under mild conditions, and this inexpensive and simple processing method prevents embrittlement, yellowing, etc. while preserving silk's original advantages, resulting in high commercial value. We can provide silk products, and the effect is great.
Claims (2)
される多価アルコール系エポキシ化 合物と、アルカリ金属水酸化物またはアル カリ金属のアルカリ性塩とを含む水溶液を 含浸し、前記水溶液を絹糸に30〜300 %の割合で残留させた状態で放置すること を特徴とする絹糸の改質処理方法。(1) Silk thread has a polyhydric alcohol-based epoxy compound represented by the following general formula, ▲mathematical formula, chemical formula, table, etc.▼ (in the formula, n = 1 to 9, R = H, CH_3), A method for modifying silk thread, which comprises impregnating the silk thread with an aqueous solution containing an alkali metal hydroxide or an alkaline salt of an alkali metal, and leaving the silk thread in a state where the aqueous solution remains in the silk thread at a ratio of 30 to 300%.
請求の範囲第1項記載の絹糸の改質 処理方法。(2) The method for modifying silk thread according to claim 1, which comprises leaving the silk thread at room temperature.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22554885A JPS6285079A (en) | 1985-10-08 | 1985-10-08 | Modification treatment of silk |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22554885A JPS6285079A (en) | 1985-10-08 | 1985-10-08 | Modification treatment of silk |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6285079A true JPS6285079A (en) | 1987-04-18 |
| JPH0121265B2 JPH0121265B2 (en) | 1989-04-20 |
Family
ID=16831017
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22554885A Granted JPS6285079A (en) | 1985-10-08 | 1985-10-08 | Modification treatment of silk |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6285079A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6420379A (en) * | 1987-07-14 | 1989-01-24 | Minoru Ban | Chemical modification of silk fiber product |
| JPS6420380A (en) * | 1987-07-14 | 1989-01-24 | Minoru Ban | Chemical processing of silk knitted 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 |
| CN110055754A (en) * | 2019-05-07 | 2019-07-26 | 四川丝玛帛科技有限公司 | Softness lubrication graft modification silk and preparation method thereof and fat liquor |
| US12472572B2 (en) | 2020-08-21 | 2025-11-18 | Aesculap Ag | Method for producing a surgical instrument for grasping and/or holding and/or guiding a needle |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS523813A (en) * | 1975-06-24 | 1977-01-12 | Asahi Fancy Plywood Co | Method of producing warppfree floor material |
| JPS5238131A (en) * | 1975-09-20 | 1977-03-24 | Sawafuji Electric Co Ltd | Power source device for vehicles |
| JPS5253015A (en) * | 1975-10-22 | 1977-04-28 | Kanagawa Prefecture | Sericin fixing treatment for silk or sericinn containing fiber |
-
1985
- 1985-10-08 JP JP22554885A patent/JPS6285079A/en active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS523813A (en) * | 1975-06-24 | 1977-01-12 | Asahi Fancy Plywood Co | Method of producing warppfree floor material |
| JPS5238131A (en) * | 1975-09-20 | 1977-03-24 | Sawafuji Electric Co Ltd | Power source device for vehicles |
| JPS5253015A (en) * | 1975-10-22 | 1977-04-28 | Kanagawa Prefecture | Sericin fixing treatment for silk or sericinn containing fiber |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| JPS6420379A (en) * | 1987-07-14 | 1989-01-24 | Minoru Ban | Chemical modification of silk fiber product |
| JPS6420380A (en) * | 1987-07-14 | 1989-01-24 | Minoru Ban | Chemical processing of silk knitted fabric |
| CN110055754A (en) * | 2019-05-07 | 2019-07-26 | 四川丝玛帛科技有限公司 | Softness lubrication graft modification silk and preparation method thereof and fat liquor |
| US12472572B2 (en) | 2020-08-21 | 2025-11-18 | Aesculap Ag | Method for producing a surgical instrument for grasping and/or holding and/or guiding a needle |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0121265B2 (en) | 1989-04-20 |
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