JPS5844794B2 - Polyamide Keisen Innosenshiyokukenroudozoshinho - Google Patents

Polyamide Keisen Innosenshiyokukenroudozoshinho

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Publication number
JPS5844794B2
JPS5844794B2 JP50027348A JP2734875A JPS5844794B2 JP S5844794 B2 JPS5844794 B2 JP S5844794B2 JP 50027348 A JP50027348 A JP 50027348A JP 2734875 A JP2734875 A JP 2734875A JP S5844794 B2 JPS5844794 B2 JP S5844794B2
Authority
JP
Japan
Prior art keywords
tannic acid
treatment
polyamide
innosenshiyokukenroudozoshinho
keisen
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
JP50027348A
Other languages
Japanese (ja)
Other versions
JPS51102185A (en
Inventor
純之 下広
昭雄 村田
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.)
Sumitomo Pharma Co Ltd
Original Assignee
Dainippon Pharmaceutical 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 Dainippon Pharmaceutical Co Ltd filed Critical Dainippon Pharmaceutical Co Ltd
Priority to JP50027348A priority Critical patent/JPS5844794B2/en
Publication of JPS51102185A publication Critical patent/JPS51102185A/ja
Publication of JPS5844794B2 publication Critical patent/JPS5844794B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明はポリアミド系合成繊維染色物をタンニン酸処理
し、ついで第一錫化合物で処理するかまたは第一錫化合
物を配合したタンニン酸で処理することにより染色堅牢
度を増進させる方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention improves dye fastness by treating a dyed polyamide synthetic fiber with tannic acid and then with a stannous compound or with tannic acid containing a stannous compound. Concerning how to improve.

一般にポリアミド系繊維はアニオン性の染料などで染色
されるが、このま\では染色堅牢度がきわめて弱いため
に種々の固着剤を用いて堅牢度を高める種々の方法が行
なわれている。
Generally, polyamide fibers are dyed with anionic dyes, but the color fastness of these fibers is extremely low, so various methods are being used to increase the fastness using various fixing agents.

たとえば、タンニン酸およ、び適量のアンチモン化合物
を主成分とするものを用いて一浴で処理する方法、タン
ニン酸処理しついで吐酒石処理するいわゆる二浴法が現
在まで知られている。
For example, a single bath treatment using tannic acid and an appropriate amount of an antimony compound as main components, and a so-called two-bath treatment in which tannic acid treatment and tartarstone treatment are known up to now.

それらの内でも、タンニン酸と吐酒石を用いる二浴処理
法が固着性能および酬スチームセット性にすぐれている
点で実用価値が最も高い。
Among these, the two-bath treatment method using tannic acid and tartarite has the highest practical value in that it has excellent fixing performance and steam setting properties.

タンニン酸−吐酒石の二浴法がすぐれた効果を示すのは
、繊維内で難溶性のタンニン酸−アンチモン化合物の巨
大分子を形成し、染料吸着部位に対する固着剤分子のカ
バリング作用を有するためと考えられる。
The reason why the tannic acid-tartarite two-bath method is so effective is that it forms macromolecules of poorly soluble tannic acid-antimony compounds within the fibers, which have a covering effect on the dye adsorption site with the fixing agent molecules. it is conceivable that.

しかしながら、吐酒石中のアンチモンは環境汚染の点に
おいて好ましくなく、本発明者等はそれに代替しうる種
々金属イオンについて研究を重ねた結果、吐酒石よりも
効果のすぐれた金属塩を発見し本発明を完成するに至っ
た。
However, antimony in tartarite is undesirable in terms of environmental pollution, and as a result of repeated research on various metal ions that could be substituted for it, the present inventors discovered a metal salt that is more effective than tartarite. The present invention has now been completed.

従来、タンニン酸処理に対しての金属イオンとして、ア
ルミニウム化合物(特公昭44−17595号、特公昭
43−20968号)、ビスマス化合物0持公昭41−
14628号)、銅化合物(%公昭33−6690号)
などが知られているが、これらも固着効果や環境汚染な
どの点でそれぞれ短所があり実用に供されていない。
Conventionally, as metal ions for tannic acid treatment, aluminum compounds (Japanese Patent Publication No. 17595/1972, Japanese Patent Publication No. 20968/1973), bismuth compounds 0, etc.
14628), copper compounds (% Kosho 33-6690)
Although these are known, they have disadvantages in terms of sticking effect, environmental pollution, etc., and are not put to practical use.

本発明は各種金属化合物の中でも第一錫化合物をタンニ
ン酸処理後もしくはタンニン酸の中に配合し処理する方
法であり、吐酒石使用の場合に比しよりすぐれた効果を
有する。
The present invention is a method in which a stannous compound among various metal compounds is treated with tannic acid or mixed into tannic acid, and has better effects than the case of using tartarite.

本発明に使用する第一錫化合物は水溶性の金属塩なら何
でもよく、たとえば酢酸第一錫、蓚酸第一錫、塩化第一
錫、硫酸第一錫等があげられる。
The stannous compound used in the present invention may be any water-soluble metal salt, such as stannous acetate, stannous oxalate, stannous chloride, stannous sulfate, and the like.

その使用量としてはタンニン酸使用量に対して金属イオ
ンとして0.03〜0.6%(w/w)好ましくは0.
06〜0.25%(w/w )である。
The amount used is 0.03 to 0.6% (w/w), preferably 0.03% (w/w) as metal ions, based on the amount of tannic acid used.
06-0.25% (w/w).

次に本発明の実施例をあげて具体的に説明する。Next, the present invention will be specifically explained by giving examples.

実施例 I 表に示した5種の酸性染料で染色したナイロン6ウーリ
ー加工糸をタンニン酸3%o、w−f、および酢酸1%
o、w、f、を含有せる染浴に浴比30:1(染液30
m1に対して被処理系1g)にて浸漬し、攪拌下徐々に
80℃まで昇温した後、80℃にて30分間処理した。
Example I Nylon 6 woolly textured yarn dyed with the five acid dyes shown in the table was treated with 3% o, w-f tannic acid, and 1% acetic acid.
o, w, f, bath ratio 30:1 (dye liquor 30:1)
1 g of the treated system), the temperature was gradually raised to 80° C. with stirring, and then treated at 80° C. for 30 minutes.

処理終了後、処理系は十分に水洗し、その後塩化第−錫
1%o、w、f、および酢酸1%o、w、f。
After completion of the treatment, the treatment system was thoroughly washed with water, and then treated with 1% o, w, f of stannous chloride and 1% o, w, f of acetic acid.

を含有せる染浴に浴比30:lにて浸漬し、攪拌下栓々
に70℃まで昇温した後、70℃にて20分間処理した
The sample was immersed in a dyebath containing 30:l at a bath ratio of 30:1, heated to 70°C with a stirring stopper, and then treated at 70°C for 20 minutes.

その後処理系を乾燥し、120℃にて60秒間の湿熱セ
ットを施してから、染色堅牢度試験を以下の方法により
観察した。
Thereafter, the treatment system was dried and subjected to a moist heat setting at 120° C. for 60 seconds, and then a color fastness test was observed by the following method.

1)洗濯堅牢度試験 J I 5−L−0844−A−
2号用)熱湯堅牢度試験 J I 5−L−0845−
2号用)汗堅牢度試験 J I 5−L−0846−
A法■)水堅牢度試験 J I 5−L−0846−
A法染色堅牢度試験の結果を表に示す。
1) Washing fastness test J I 5-L-0844-A-
For No. 2) Hot water fastness test J I 5-L-0845-
2) Sweat fastness test J I 5-L-0846-
Method A ■) Water fastness test J I 5-L-0846-
The results of the method A color fastness test are shown in the table.

なお、表中における染色堅牢度の欄の数値は染色物から
脱落した染料で汚染された添付布の汚れをJIS−L−
0805に規定されるグレースケールで測定した場合の
目盛である。
In addition, the values in the color fastness column in the table are based on JIS-L-
This is a scale when measured using the gray scale specified in 0805.

目盛5の場合汚れが最も少なく(染色堅牢度が最高)、
目盛lの場合汚れが最もひどい(染色堅牢度が最底)こ
とを意味している。
For scale 5, there is the least amount of staining (the highest color fastness),
A scale of 1 means that staining is the worst (color fastness is at the bottom).

実施例 2 実施例1と同様に染色したウーリー加工糸をタンニン酸
に対し、酢酸錫を4%(w/w )配合し、さらに50
%酢酸水溶液を加え、タンニン酸含有量40%とした液
剤5%O,Wef、および酢酸1%0.w、f、を含有
せる染浴に浴比30:lにて浸漬(7攪拌下栓々に80
℃まで昇温した後、80℃にて30分間処理した。
Example 2 Woolly processed yarn dyed in the same manner as in Example 1 was mixed with 4% (w/w) tin acetate in tannic acid, and further mixed with 50% tin acetate (w/w).
% acetic acid aqueous solution was added to make the tannic acid content 40%. Immersion in a dye bath containing w, f, at a bath ratio of 30:l (7:80:1 in a stirring stopper)
After raising the temperature to .degree. C., it was treated at 80.degree. C. for 30 minutes.

処理後、水洗・乾燥し以下実施例1と同様の方法に従っ
て染色堅牢度を観察した。
After the treatment, it was washed with water and dried, and the color fastness was observed in the same manner as in Example 1.

比較例 l 実施例Iと同様に染色したウーリー加工糸をタンニン酸
3%o、w、f、および酢酸1%o、w、f。
Comparative Example l Woolly textured yarn dyed as in Example I was treated with tannic acid 3% O, W, F and acetic acid 1% O, W, F.

を含有せる染浴に浴比30:1にて浸漬し、攪拌下栓々
に80℃まで昇温し、その後80’Cにて30分間処理
した。
The sample was immersed in a dye bath containing 30:1 at a bath ratio of 30:1, heated to 80° C. under stirring, and then treated at 80° C. for 30 minutes.

その後、処理系を十分に水洗し、水洗後吐酒石1.5%
o、w、f、および酢酸1%o、w、f、を含有せる染
浴に浴比30:lにて浸漬し、攪拌下徐徐に70℃まで
昇温し、その後70’Cにて20分間処理した。
After that, the treatment system was thoroughly washed with water, and after washing, 1.5% tartarite was added.
It was immersed in a dye bath containing o, w, f and acetic acid 1% o, w, f at a bath ratio of 30:l, and the temperature was gradually raised to 70°C with stirring, and then at 70'C for 20 Processed for minutes.

処理後、水洗・乾燥し以下実施例1と同様の方法に従っ
て染色堅牢度を観察した。
After the treatment, it was washed with water and dried, and the color fastness was observed in the same manner as in Example 1.

比較例 2 実施例1と同様に染色したウーリー加工糸をタンニン酸
に対し、吐酒石を7%(w/w)配合しさらに50%酢
酸水溶液を加え、タンニン酸含有量40%とした溶液5
%o、w、仁、および酢酸1%o、w、f、fi有せる
染浴(ど浴比30:1にて浸漬し、攪拌下栓々に80℃
まで昇温し、その後80℃にて30分間処理した。
Comparative Example 2 A solution of woolly processed yarn dyed in the same manner as in Example 1 was mixed with 7% (w/w) tartar to tannic acid, and a 50% acetic acid aqueous solution was added to make the tannic acid content 40%. 5
% o, w, kerosene, and acetic acid 1% o, w, f, fi (immersed in a dye bath with a bath ratio of 30:1, and heated under stirring at 80°C
The temperature was then raised to 80° C. for 30 minutes.

処理後、水洗・乾燥し以下実施例■の方法に従って染色
堅牢度を観察した。
After the treatment, it was washed with water and dried, and the color fastness was observed according to the method described in Example 2 below.

Claims (1)

【特許請求の範囲】[Claims] 1 ポリアミド系繊維染色物をタンニン酸処理し、つい
で第一錫化合物で処理するかまたは第一錫化合物を配合
したタンニン酸で処理することを特徴とするポリアミド
系繊維染色物の染色堅牢度増進法。
1. A method for improving the color fastness of dyed polyamide fibers, which comprises treating the dyed polyamide fibers with tannic acid and then with a stannous compound or with tannic acid containing a stannous compound. .
JP50027348A 1975-03-05 1975-03-05 Polyamide Keisen Innosenshiyokukenroudozoshinho Expired JPS5844794B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50027348A JPS5844794B2 (en) 1975-03-05 1975-03-05 Polyamide Keisen Innosenshiyokukenroudozoshinho

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50027348A JPS5844794B2 (en) 1975-03-05 1975-03-05 Polyamide Keisen Innosenshiyokukenroudozoshinho

Publications (2)

Publication Number Publication Date
JPS51102185A JPS51102185A (en) 1976-09-09
JPS5844794B2 true JPS5844794B2 (en) 1983-10-05

Family

ID=12218524

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50027348A Expired JPS5844794B2 (en) 1975-03-05 1975-03-05 Polyamide Keisen Innosenshiyokukenroudozoshinho

Country Status (1)

Country Link
JP (1) JPS5844794B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57143584A (en) * 1981-02-26 1982-09-04 Seiren Co Ltd Dyeing of polyamide type synthetic fiber knitted fabric
JPS6075691A (en) * 1983-10-01 1985-04-30 株式会社森本染工所 Silk dyeing method
JPS61102492A (en) * 1984-10-23 1986-05-21 ユニチカ株式会社 Enhancement of dye fastness

Also Published As

Publication number Publication date
JPS51102185A (en) 1976-09-09

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