JPS584885A - Composition and method for improving the fastness of dyed products - Google Patents
Composition and method for improving the fastness of dyed productsInfo
- Publication number
- JPS584885A JPS584885A JP56102501A JP10250181A JPS584885A JP S584885 A JPS584885 A JP S584885A JP 56102501 A JP56102501 A JP 56102501A JP 10250181 A JP10250181 A JP 10250181A JP S584885 A JPS584885 A JP S584885A
- Authority
- JP
- Japan
- Prior art keywords
- fastness
- tannin
- improving
- fixing agent
- dyed
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims description 16
- 238000000034 method Methods 0.000 title claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 22
- 229920001461 hydrolysable tannin Polymers 0.000 claims description 19
- 239000000985 reactive dye Substances 0.000 claims description 19
- 229920000742 Cotton Polymers 0.000 claims description 17
- 229920006317 cationic polymer Polymers 0.000 claims description 12
- 239000004753 textile Substances 0.000 claims description 4
- 238000011282 treatment Methods 0.000 description 18
- 229920001864 tannin Polymers 0.000 description 16
- 239000001648 tannin Substances 0.000 description 16
- 235000018553 tannin Nutrition 0.000 description 16
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 14
- 239000000460 chlorine Substances 0.000 description 14
- 229910052801 chlorine Inorganic materials 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000000047 product Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 239000004744 fabric Substances 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 229920000768 polyamine Polymers 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 238000005903 acid hydrolysis reaction Methods 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 230000003301 hydrolyzing effect Effects 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 239000000834 fixative Substances 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- AFWAHDXCIBPFNW-UHFFFAOYSA-J sodium;antimony(3+);2,3-dihydroxybutanedioate Chemical compound [Na+].[Sb+3].[O-]C(=O)C(O)C(O)C([O-])=O.[O-]C(=O)C(O)C(O)C([O-])=O AFWAHDXCIBPFNW-UHFFFAOYSA-J 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- FAPDDOBMIUGHIN-UHFFFAOYSA-K antimony trichloride Chemical compound Cl[Sb](Cl)Cl FAPDDOBMIUGHIN-UHFFFAOYSA-K 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- -1 etc. Substances 0.000 description 1
- DUYAAUVXQSMXQP-UHFFFAOYSA-N ethanethioic S-acid Chemical compound CC(S)=O DUYAAUVXQSMXQP-UHFFFAOYSA-N 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229960004337 hydroquinone Drugs 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Landscapes
- Coloring (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】
本発明は反応性染料で染色された綿繊維製品の染色堅牢
度増進に用いる組成物及び該繊維の染色堅牢一度増進方
法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a composition for improving the color fastness of cotton textiles dyed with reactive dyes and a method for once improving the color fastness of said fibers.
反応性染料は色相が鮮明なこと及び湿潤堅牢度が良好な
ことにより、近年その使用量が着実に増加している。The amount of reactive dyes used has steadily increased in recent years due to their vivid hues and good wet fastness.
反応性染料には、酸加水分解堅牢度力;経時的に低9下
するという欠点がある。染色後、酸等の影響により繊維
と反応性染料との強固な共有結合75;カ日水分解を受
け、染料が脱落することによる。これに対しては従来か
ら、染色後カチオン性ポ1)マー系固着剤で処理するこ
とが行なわれ、力・なりの効果をおさめている。Reactive dyes have the disadvantage that their fastness to acid hydrolysis decreases over time. After dyeing, a strong covalent bond 75 between the fiber and the reactive dye is formed due to the influence of acid, etc.; this is due to water decomposition and the dye falling off. Conventionally, this has been treated with a cationic polymer-based fixing agent after dyeing, which has suppressed the effect of strength and bending.
しかし力から、反応性染料の最も重大な欠、へは塩素堅
牢度が弱いことである。即ち、反応性染料で染色した綿
繊維製品は、水道水中等の微量活性塩素の作用により染
料が酸化され、退色したり変色したりする場合が非常に
多い。However, the most serious drawback of reactive dyes is their poor chlorine fastness. That is, in cotton fiber products dyed with reactive dyes, the dyes are oxidized by the action of trace amounts of active chlorine in tap water, and the colors often fade or change.
上記した固着剤による処理では、塩素堅牢度は、改善さ
れず、むしろ無処理に比して大きくイ氏下する場合がほ
とんどでちる。In the treatment with the above-mentioned fixing agent, the chlorine fastness is not improved, and in fact, in most cases, it is significantly lower than that without treatment.
塩素堅牢度の問題を解決するために、従来、繊維製品を
樹脂類と抗酸化作用を有する物質で処理する方法(特開
昭50−53693、同50−58373、同50−5
8374、同50−4’8395)等が提案されている
が、高熱処理等を必要とし省エネルギー面からも好まし
くない。In order to solve the problem of chlorine fastness, conventional methods have been proposed in which textile products are treated with resins and substances that have an antioxidant effect (JP-A-50-53693, JP-A-50-58373, JP-A-50-5).
8374, 50-4'8395), etc., but they require high heat treatment and are not preferable from an energy saving perspective.
本発明者等は、上述のような問題点を解決するため種々
の抗酸化剤に着目し、研究を行なったところ、少なくと
も次の2点が塩素堅牢度を増進するのに必要であること
を見出した。In order to solve the above-mentioned problems, the present inventors focused on various antioxidants and conducted research, and found that at least the following two points are necessary to improve chlorine fastness. I found it.
■塩素堅牢度を増進させるだめの化合物の酸化還元電位
が、反応性染料の電位よりも低く、かつその化合物の酸
化される速度が反応性染料のそれより速いこと。(2) The redox potential of the compound that increases chlorine fastness is lower than the potential of the reactive dye, and the rate of oxidation of the compound is faster than that of the reactive dye.
■核化合物の繊維に対する吸着量が犬であり、かつンー
ピング工程等で容易に繊維から脱落しないこと。■The amount of nuclear compound adsorbed to the fibers is small, and it does not easily fall off from the fibers during the looping process.
■の条件を満たす化合物として、レゾルシン、ハイドロ
キノン、没食子酸、ピロガロール、五倍子タンニン、タ
ラタンニン、没食子タンニンなどの多価フェノール類が
あげられるが、これらは■の条件を満足しない。そこで
■の条件を得るために該繊維と上記の多価フェノール類
とを、カチオン性ポリマー系固着剤によって結合せしめ
ることを試み−Iこ。Compounds that satisfy the condition (2) include polyhydric phenols such as resorcinol, hydroquinone, gallic acid, pyrogallol, pentad tannin, cod tannin, and gallic tannin, but these do not satisfy the condition (2). Therefore, in order to obtain the condition (2), an attempt was made to bond the fibers and the above-mentioned polyhydric phenols using a cationic polymer adhesive.
その結果、レゾルシン、ハイドロキノン等はほとんど染
色物に結合せしめることができないのに対し、五倍子タ
ンニン、タラタンニン、没食子タンニンなどの加水分解
型タンニンはよく結合せ;、7め得ることがわかった。As a result, it was found that resorcinol, hydroquinone, etc. could hardly be bound to the dyed material, whereas hydrolyzable tannins such as pentad tannin, cod tannin, and gallic tannin could be bound well.
以上の知見をもとに、本発明者等は更に研究を進め本発
明を完成した。Based on the above knowledge, the present inventors conducted further research and completed the present invention.
本発明においては、従来のごとくカチオン性ポリマー系
固着剤によって酸加水分解堅牢度を改善すると共に、該
固着剤によって加水分解型タンニンを染色物に固定せし
め、塩素堅牢度を増進することに成功した。In the present invention, in addition to improving acid hydrolytic fastness using a cationic polymer-based fixing agent as in the past, the fixing agent fixes hydrolyzable tannins to the dyed material, thereby successfully improving chlorine fastness. .
本発明の一つは、カチオン性ポリマー系固着剤と加水分
解型タンニンを混和してなる、反応性染料で染色された
綿繊維製品の染色堅牢度増進に用いる組成物である。One aspect of the present invention is a composition for improving the color fastness of cotton textile products dyed with reactive dyes, which is a mixture of a cationic polymeric fixing agent and a hydrolyzable tannin.
本発明の他の一つは、反応性染料で染色された綿繊維製
品をカチオン性ポリマー系固着剤で処理する際に加水分
解型タンニンを併用することよシなる染色堅牢度増進方
法である。Another aspect of the present invention is a method for improving color fastness, which involves using a hydrolyzable tannin in combination when treating a cotton fiber product dyed with a reactive dye with a cationic polymer fixing agent.
本発明の綿繊維製品とは、糸、編織物、不織布等又は綿
繊維と他繊維との混紡、混繊、交編織品等を意味する。The cotton fiber products of the present invention refer to yarns, knitted fabrics, non-woven fabrics, etc., or blends of cotton fibers with other fibers, blended fibers, mixed knitted fabrics, etc.
本発明で用いられるカチオン性ポリマー系固着剤(ポリ
アミン系、ジシアンジアミド系等)は、共有結合で反応
し得る反応基を有しておらず、水素結合、イオン結合及
び配位結合等によって、繊維又は染料と結合して酸加水
分解堅牢度を増進せしめ、かつ加水分解型タンニンを染
色物に固定せしめる作用を有する。The cationic polymer-based fixing agent (polyamine-based, dicyandiamide-based, etc.) used in the present invention does not have a reactive group that can react with covalent bonds, and is able to bind fibers or It binds to dyes to improve fastness to acid hydrolysis and has the effect of fixing hydrolyzable tannins to dyed materials.
具体的には、ポリアミン−ジシアンジアミド反応生成物
、ポリアミン−ジシアンジアミド−尿素反応生成物、グ
アニジン類−ホルマリン反応生成物、ジシアンジアミド
−尿素−ホルマリンの反応生成物、ポリアミンスルホン
及びニトリル重合物等である。これらの多くは市販され
ており、それがそのまま用いられる。Specifically, they include polyamine-dicyandiamide reaction products, polyamine-dicyandiamide-urea reaction products, guanidines-formalin reaction products, dicyandiamide-urea-formalin reaction products, polyamine sulfones, and nitrile polymers. Many of these are commercially available and can be used as is.
これらの固着剤のうち、特に望ましいものはその還元力
が染料に比して強い固着剤である。還元力が強い程加水
分解型タンニンによる塩素堅牢度増進の効果がより強く
発揮される。強い還元力とは、固着剤自身の酸化される
速度が速く、かつその酸化還元電位が低いことを意味す
る。しかし、還元力の弱い固着剤でも、加水分解型タン
ニンを併用することにより、該固着剤を単独に使用する
場合に比して、塩素堅牢度は大きく増進される。Among these fixing agents, particularly desirable ones are fixing agents whose reducing power is stronger than that of dyes. The stronger the reducing power, the stronger the effect of improving chlorine fastness by hydrolyzed tannins. Strong reducing power means that the fixing agent itself is oxidized at a high rate and its redox potential is low. However, even when a fixing agent with a weak reducing power is used in combination with a hydrolyzable tannin, the chlorine fastness is greatly improved compared to when the fixing agent is used alone.
加水分解型タンニンとしては、五倍子タンニン、タラタ
ンニン、没食子タンニン等があり、反応性染料より先に
酸化を受けることにより、反応性染料そのものが酸化さ
れるのを防ぐ効果を有している。Hydrolyzable tannins include fivefold tannin, cod tannin, gallic tannin, and the like, which have the effect of preventing the reactive dye itself from being oxidized by being oxidized before the reactive dye.
カチオン性ポリマー系固着剤と加水分解型タンニンを混
和せしめてなる組成物は、通常カチオン性ポリマー系固
着剤を酸性で水に溶解し該固着剤の塩の水溶液を作り、
他方、加水分解型タンニンを水に溶解しタンニン水溶液
とし、両者を均一混和すればよい。その混合比は特に限
定はないが、組成物中に混和された加水分解型タンニン
の処理量が綿繊維製品に対し0.1〜1%o、w、f、
になるように固着剤に混和すればよい。A composition formed by mixing a cationic polymer-based adhesive and a hydrolyzable tannin is usually prepared by dissolving the cationic polymer-based adhesive in water with acidity to form an aqueous solution of the salt of the adhesive.
On the other hand, a hydrolyzed tannin may be dissolved in water to form an aqueous tannin solution, and both may be uniformly mixed. The mixing ratio is not particularly limited, but the amount of hydrolyzable tannin mixed in the composition is 0.1 to 1% o, w, f, based on the cotton fiber product.
You just need to mix it with the fixing agent so that it becomes .
本発明の組成物を用いて綿繊維製品を処理する場合、そ
の処理条件は反応性染料の種類、染色の濃度などにより
多少異なるが、組成物を0.1〜10%o、w、f1、
好ましくは0.5〜4チo、w、f、、浴比1:10〜
1:30で使用する。処理温度は5〜80℃であり、処
理時間は10〜30分、処理pHは2〜6である。When treating cotton fiber products using the composition of the present invention, the treatment conditions vary somewhat depending on the type of reactive dye, dyeing concentration, etc.
Preferably 0.5 to 4 thio, w, f, bath ratio 1:10 to
Use at 1:30. The treatment temperature is 5 to 80°C, the treatment time is 10 to 30 minutes, and the treatment pH is 2 to 6.
また、カチオン性ポリマー系固着剤で処理する際に加水
分解型タンニンを併用する場合は、綿繊維製品をまずカ
チオン性ポリマー系固着剤で処理し、次いで加水分解型
タンニンで処理するか、又はカチオン性ポリマー系固着
剤と加水分解型タンニンで同時に処理する。その処理条
件は組成物を用いる場合と略同様である。In addition, if hydrolyzable tannins are used in conjunction with treatment with a cationic polymer-based binding agent, the cotton fiber product must first be treated with the cationic polymer-based adhesive and then treated with hydrolyzable tannins, or Simultaneously treated with a polymeric fixing agent and hydrolyzable tannin. The processing conditions are substantially the same as those when using the composition.
以上のようにして得られた染色物を更に金属塩で処理す
ることが望ましい。金属塩処理によって加水分解型タン
ニンは、染色物により強固に固定化され、ソーピング工
程時またはくシ返し洗濯時に順次脱落し、その効果の低
減をきたすことが防げる。長期間の塩素堅牢度を問題に
しない製品においては、金属塩処理は必要ではない。It is desirable to further treat the dyed product obtained as described above with a metal salt. Hydrolyzable tannins are firmly fixed in the dyed material by the metal salt treatment, and can be prevented from falling off during the soaping process or repeated washing, thereby reducing its effectiveness. Metal salt treatment is not necessary for products where long-term chlorine fastness is not an issue.
金属塩としては、吐酒石、塩化アンチモン、酒石酸アン
チモンナトリウム、塩化第一スズ、塩イヒ第二スズ、塩
化アルミニウム、硫酸アルミニウム、硫酸第一鉄、硫酸
第二鉄、塩化亜鉛、硫酸銅などがあげられるが、吐酒石
、酒石酸アンチモンナトリウム、塩化アルミニウムなど
が好ましい。Metal salts include tartarite, antimony chloride, sodium antimony tartrate, stannous chloride, stannic chloride, aluminum chloride, aluminum sulfate, ferrous sulfate, ferric sulfate, zinc chloride, copper sulfate, etc. Among them, tartarite, sodium antimony tartrate, aluminum chloride, etc. are preferred.
金属塩による処理条件は、加水分解型タンニンの0,1
〜0.5倍量、好ましくは0.25〜0.5倍量の金属
塩を使用するが、その他は上述の他の処理と同様である
。The treatment conditions with metal salts are 0, 1 of hydrolyzed tannin.
~0.5 times the amount of metal salt, preferably 0.25 to 0.5 times the amount of metal salt is used, but otherwise the same as the other treatments described above.
本発明によれば、従来のカチオン性ポリマー系固着剤の
みでは得られない塩素堅牢度の飛躍的な増進を達成する
ことができる。また、加水分解型タンニンを用いたこと
による色相、湿潤堅牢度及び酸加水分解堅牢度に及ぼす
悪影響は認められないO
本発明を更に詳細に説明するために、以下に実施例を示
す。According to the present invention, it is possible to achieve a dramatic improvement in chlorine fastness, which cannot be obtained with conventional cationic polymer-based fixing agents alone. In addition, no adverse effects on hue, wet fastness, and acid hydrolytic fastness due to the use of hydrolyzable tannins were observed. In order to explain the present invention in more detail, Examples are shown below.
実施例1
ポリアミン系固着剤サンフィックス555(三洋化成製
)10部を50チ酢酸58部及びエチレングリコール3
0部に溶解し、この中にタラタンニン2部を加えて攪拌
溶解させ、組成物100部を得た。Example 1 10 parts of polyamine adhesive Sanfix 555 (manufactured by Sanyo Chemical Co., Ltd.), 58 parts of 50 thiacetic acid and 3 parts of ethylene glycol
0 parts, 2 parts of cod tannin was added thereto, and stirred and dissolved to obtain 100 parts of a composition.
本組成物は水に澄明に溶解した0
実施例2
ポリアミン系固着剤スープラフイツクスDFC(日本染
化製)10部を50%酢酸58部及びエチレンクリコー
ル30部に浴解し、この中に五倍子タンニン2部を加え
て攪拌溶解させ、組成物100部を得た。本組成物は水
に澄明に溶解した。Example 2 10 parts of the polyamine-based fixing agent Supra Fixtures DFC (manufactured by Nippon Senka Co., Ltd.) was dissolved in 58 parts of 50% acetic acid and 30 parts of ethylene glycol. 2 parts of five-fold tannin was added and dissolved with stirring to obtain 100 parts of a composition. The composition dissolved clearly in water.
実施例3
反応性染料ミカシオンブリリアントフ゛ル−R8(日本
化薬製) 4% (o、w、f、)で染色した綿ギャノ
くを、実施例1で得られた組成物を20%(o、w、f
、)含んだ処理浴中、浴比l:50、pH5、温度40
’Cで20分間浸漬処理に付し、水洗後風乾した。Example 3 Cotton gannoku dyed with 4% (o, w, f,) of the reactive dye Mikasion Brilliant File-R8 (manufactured by Nippon Kayaku) was dyed with 20% (o, w, f,) of the composition obtained in Example 1. ,w,f
,) in a treatment bath containing: bath ratio l:50, pH 5, temperature 40
'C for 20 minutes, washed with water and air-dried.
実施例4
実施例2で得られた組成物を用いる他は、実施例3と同
様に処理し、水洗後風乾した。Example 4 Except for using the composition obtained in Example 2, the same treatment as in Example 3 was carried out, followed by washing with water and air drying.
実施例5
反応性染料ミカシオンブリリアントプル−R54% (
oow、f、)で染色した綿ギャノ(を、ポリアミン系
固着剤サンフィックス555及びタラタンニンをそれぞ
れ2係(o、w、f、)及び0.4係(olw、f、)
含んだ処理浴中、浴比1:50、pH5、温度40°C
で20分間浸漬処理に付し、水洗後風乾した。Example 5 Reactive dye Mikasion Brilliant Pur-R54% (
Cotton gyano (oow, f,) was dyed with polyamine fixative Sanfix 555 and tartannin at 2 parts (o, w, f,) and 0.4 parts (olw, f,), respectively.
In the treatment bath containing: bath ratio 1:50, pH 5, temperature 40°C
The sample was soaked in water for 20 minutes, washed with water, and air-dried.
参考例1
反応性染料ミカシオンブリリアントブル−R54% (
0,w、f、)で染色した綿ギャノくを、ポリアミン系
固着剤サンフィックス555を2%(oow、f、)含
んだ処理浴中、浴比1:50.pH5、温度40°Cで
20分間浸漬処理に付し、水洗後風乾した。Reference example 1 Reactive dye Mikasion Brilliant Blue-R54% (
Cotton gyanoku dyed with 0, w, f, ) was placed in a treatment bath containing 2% (oow, f,) of the polyamine fixative Sunfix 555 at a bath ratio of 1:50. It was subjected to immersion treatment at pH 5 and temperature of 40°C for 20 minutes, washed with water, and then air-dried.
参考例2
固着剤としてポリアミン系固着剤スープラフイノクスD
FCを用いる他は、参考例1と同様に処理し、水洗後風
乾した。Reference example 2 Polyamine-based adhesive Supra Inox D as adhesive
The treatment was carried out in the same manner as in Reference Example 1 except that FC was used, and the sample was washed with water and air-dried.
参考例3
固着剤として五倍子タンニンを用いる他は、参考例1と
同様に処理し、水洗後風乾した。Reference Example 3 The same process as in Reference Example 1 was carried out except that five-fold tannin was used as a fixing agent, and the sample was washed with water and then air-dried.
実施例6〜8及び参考例4〜6
反応性染料チバクロンネイビーF−G(チバガイギー製
)3%(oow、 f、 )で染色した綿ギャバを、そ
れぞれ実施例3〜5及び参考例1〜3と同様の処理に付
し、水洗後風乾した。Examples 6 to 8 and Reference Examples 4 to 6 Cotton GABA dyed with reactive dye Cibacron Navy FG (manufactured by Ciba Geigy) 3% (oow, f, ) was used in Examples 3 to 5 and Reference Examples 1 to 6, respectively. It was subjected to the same treatment as in No. 3, washed with water, and then air-dried.
実施例9
実施例3〜8及び参考例1〜6で得られた処理済綿ギャ
バに対して、次の染色堅牢度試験を行なった。結果を下
記表に示す。Example 9 The following color fastness test was conducted on the treated cotton gabarries obtained in Examples 3 to 8 and Reference Examples 1 to 6. The results are shown in the table below.
塩素堅牢度試験
有効塩素soppmを含むpH8の緩衝液に試験片を浴
比1 : 100で浸漬し、25℃で2時間攪拌後、水
洗し乾燥した。試験片の変退色の判定はJIS−L−0
801の10によった。Chlorine Fastness Test A test piece was immersed in a pH 8 buffer containing soppm of available chlorine at a bath ratio of 1:100, stirred at 25°C for 2 hours, washed with water, and dried. Judgment of discoloration and fading of test piece is based on JIS-L-0
According to 801-10.
酸加水分解堅牢度試験
乳酸10 y/lの水溶液に、試験片及び添付白布(綿
)を浴比1 : 100で浸漬し、60°Cで20分間
攪拌後、水洗し乾燥した。本試験の添付白布の汚染の判
定はJ l5−L−0801の10によった。Acid hydrolysis fastness test The test piece and attached white cloth (cotton) were immersed in an aqueous solution of lactic acid 10 y/l at a bath ratio of 1:100, stirred at 60°C for 20 minutes, washed with water, and dried. The contamination of the attached white cloth in this test was determined according to J15-L-0801, 10.
洗濯堅牢度試験
JIS−L−1045A 2号に従って行なった。試験
片の変退色の判定及び添付白布の汚染の判定はJ l5
−L−0801の10によった。Washing fastness test was conducted according to JIS-L-1045A No. 2. Judgment of discoloration and fading of the test piece and judgment of contamination of the attached white cloth shall be made in accordance with J15.
- According to 10 of L-0801.
汗(アルカリ)堅牢度試験
JIS−L−0847A−1号に従った。添付白布の汚
染の判定はJIS−L−0801の10によった。Sweat (alkali) fastness test JIS-L-0847A-1 was followed. Contamination of the attached white cloth was determined according to JIS-L-0801 10.
結果から明らかなように、本発明の組成物及び方法によ
る処理布においては、塩素堅牢度が固着剤のみ又は加水
分解型タンニンのみによる処理布及び未処理布のいずれ
に比しても格段に増進されている。As is clear from the results, the chlorine fastness of the fabric treated with the composition and method of the present invention is significantly improved compared to both the fabric treated with only a fixing agent or only hydrolyzable tannin, and the untreated fabric. has been done.
尚、固着剤のみによる処理では未処理に比して低下する
傾向が認められ、加水分解型タンニンのみの処理ではあ
まシ改善されていない。In addition, when treated with only a fixing agent, there is a tendency for it to be lower than when untreated, and when treated only with hydrolyzable tannin, there is no significant improvement.
更に、酸加水分解堅牢度及び湿潤堅牢度は、固着剤のみ
の処理と同等の優れた効果が得られており、加水分解型
タンニンのみによる処理及び未処理に比して同等又は増
進されている。Furthermore, the acid hydrolytic fastness and wet fastness are as good as those treated with a fixing agent alone, and are equivalent or improved compared to those treated with only a hydrolyzable tannin and untreated. .
鑞 T 余 白)Tsui T extra white)
Claims (1)
ンニンを混和してなると〉を特徴とする反応性染料で染
色された綿繊維製品の染色堅牢度増進に用いる組成物。 (2)反応性染料で染色された綿繊維製品をカチオン性
ポリマー系固着剤で処理する際に加水分解型タンニンを
併用することを特徴とする染色堅牢度を増進する方法。[Scope of Claims] +11 A composition used for improving the color fastness of cotton textile products dyed with a reactive dye, characterized in that it contains a cationic polymer-based fixing agent and a hydrolyzable tannin. (2) A method for improving color fastness, which comprises using a hydrolyzable tannin in combination when treating a cotton fiber product dyed with a reactive dye with a cationic polymer fixing agent.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56102501A JPS584885A (en) | 1981-06-30 | 1981-06-30 | Composition and method for improving the fastness of dyed products |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56102501A JPS584885A (en) | 1981-06-30 | 1981-06-30 | Composition and method for improving the fastness of dyed products |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS584885A true JPS584885A (en) | 1983-01-12 |
Family
ID=14329149
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56102501A Pending JPS584885A (en) | 1981-06-30 | 1981-06-30 | Composition and method for improving the fastness of dyed products |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS584885A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2748281A1 (en) * | 1996-05-02 | 1997-11-07 | Protex Manuf Prod Chimiq | Improving resistance to bleaching of dyed fabrics |
| JP2005009059A (en) * | 2003-06-18 | 2005-01-13 | Komatsu Seiren Co Ltd | Fiber fabric excellent in chlorine fastness and method for producing the same |
-
1981
- 1981-06-30 JP JP56102501A patent/JPS584885A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2748281A1 (en) * | 1996-05-02 | 1997-11-07 | Protex Manuf Prod Chimiq | Improving resistance to bleaching of dyed fabrics |
| JP2005009059A (en) * | 2003-06-18 | 2005-01-13 | Komatsu Seiren Co Ltd | Fiber fabric excellent in chlorine fastness and method for producing the same |
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