JPS62282085A - Post-treatment of dyed article - Google Patents
Post-treatment of dyed articleInfo
- Publication number
- JPS62282085A JPS62282085A JP61120965A JP12096586A JPS62282085A JP S62282085 A JPS62282085 A JP S62282085A JP 61120965 A JP61120965 A JP 61120965A JP 12096586 A JP12096586 A JP 12096586A JP S62282085 A JPS62282085 A JP S62282085A
- Authority
- JP
- Japan
- Prior art keywords
- dyed
- fibers
- dyes
- dye
- bath
- 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
- 238000011282 treatment Methods 0.000 title description 10
- 239000000835 fiber Substances 0.000 claims description 52
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 20
- 230000002209 hydrophobic effect Effects 0.000 claims description 15
- 238000004043 dyeing Methods 0.000 claims description 14
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 11
- -1 alkali metal salt Chemical class 0.000 claims description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- 229960005070 ascorbic acid Drugs 0.000 claims description 5
- 238000012805 post-processing Methods 0.000 claims description 4
- 239000002211 L-ascorbic acid Substances 0.000 claims description 3
- 235000000069 L-ascorbic acid Nutrition 0.000 claims description 3
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 claims 1
- 235000010350 erythorbic acid Nutrition 0.000 claims 1
- 229940026239 isoascorbic acid Drugs 0.000 claims 1
- 239000000975 dye Substances 0.000 description 23
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 239000004744 fabric Substances 0.000 description 17
- 229920000728 polyester Polymers 0.000 description 16
- 238000005406 washing Methods 0.000 description 14
- 229920000742 Cotton Polymers 0.000 description 13
- 239000000986 disperse dye Substances 0.000 description 13
- 239000000985 reactive dye Substances 0.000 description 8
- 229920003043 Cellulose fiber Polymers 0.000 description 7
- 238000004140 cleaning Methods 0.000 description 7
- 238000002845 discoloration Methods 0.000 description 7
- 235000011121 sodium hydroxide Nutrition 0.000 description 7
- RWSOTUBLDIXVET-UHFFFAOYSA-M hydrosulfide Chemical compound [SH-] RWSOTUBLDIXVET-UHFFFAOYSA-M 0.000 description 6
- 210000002268 wool Anatomy 0.000 description 6
- 239000002759 woven fabric Substances 0.000 description 6
- 229920000297 Rayon Polymers 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000011109 contamination Methods 0.000 description 5
- 239000000982 direct dye Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000002964 rayon Substances 0.000 description 5
- 150000001340 alkali metals Chemical class 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000980 acid dye Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000003672 processing method Methods 0.000 description 3
- 230000001603 reducing effect Effects 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 238000010186 staining Methods 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 2
- 241000280258 Dyschoriste linearis Species 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 238000011437 continuous method Methods 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- SAQSTQBVENFSKT-UHFFFAOYSA-M TCA-sodium Chemical compound [Na+].[O-]C(=O)C(Cl)(Cl)Cl SAQSTQBVENFSKT-UHFFFAOYSA-M 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 229920006221 acetate fiber Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010018 discharge printing Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium erythorbate Chemical compound [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 1
- 235000010352 sodium erythorbate Nutrition 0.000 description 1
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 1
- 235000019187 sodium-L-ascorbate Nutrition 0.000 description 1
- 239000011755 sodium-L-ascorbate Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000004094 surface-active agent 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】
3、発明の詳細な説明
「産業上の利用分野」
本発明は染色物の後処理法に関する。更に詳しくは疎水
性繊維又は疎水性繊維と親水性繊維との混合繊維の染色
物を後処理する方法に関する。Detailed Description of the Invention 3. Detailed Description of the Invention "Field of Industrial Application" The present invention relates to a post-treatment method for dyed products. More specifically, the present invention relates to a method for post-processing dyed products of hydrophobic fibers or mixed fibers of hydrophobic fibers and hydrophilic fibers.
「従来の技術」
各種の繊維製品は染色処理後、未固着染料の除去等の目
的で水洗、湯洗、ソーピンク等の処理を行い堅牢度の向
上が図られている。"Prior Art" After dyeing, various textile products are subjected to treatments such as water washing, hot water washing, and saw pinking to remove unfixed dyes in order to improve their fastness.
更に、アルカリ耐性、還元耐性の強い繊維製品の染色物
の場合には還元洗浄の工程も施こされる。Furthermore, in the case of dyed textile products with strong alkali resistance and reduction resistance, a reduction washing process is also performed.
この還元洗浄工程は一般には苛性ソーダとハイドロサル
ファイドを併用した水浴中で行われる。しかしながらハ
イドロサルファイドが強力な還元剤である事及び・・イ
ドロサルファイトを水中において安定に維持するために
大量の苛性ソーダが必要である事などによって前記した
ようなハイドロサルファイトド苛性ソーダを併用する還
元洗浄法の適用は繊維及び用いられる染料がこれらの薬
剤に十分耐性を有する繊維類の染色物に限られる。この
ため例えばポリエステル繊維(疎水性繊維)とセルロー
ス繊維(親水性繊維、木綿、レーヨン、麻等)の混紡品
を浸染法で染色加工を行う場合は、まず第−浴でポリエ
ステル繊維側を分散染料で高温高圧法又はキャリヤー法
で染色を行い、続いて苛性ソーダ及び−・イドロサルフ
ァイトを用いてアルカリ還元洗浄を行う。この工程でセ
ルロース繊維へ汚染した分散染料を還元分解しアルカリ
浴へ可溶化又は分散させる。次いで水洗、湯洗を行い、
アルカリ剤や還元剤を除去する。続いて第二浴でセルロ
ース繊維側を反応染料又は直接染料等で染色し水洗、湯
洗、ソーピングを行い、乾燥させ仕上げる。この長い工
程を工程短縮の目的で、分散染料でポリエステル繊維側
を反応染料又は直接染料でセルロース繊維側を同浴で染
色し、苛性ソーダ、ハイドロサルファイドによる還元洗
浄を行うとするとセルロース繊維側に染着した反応染料
、直接染料は還元分解等により大きな変色を起こしてし
まい不都合な結果となる。This reduction cleaning step is generally carried out in a water bath using a combination of caustic soda and hydrosulfide. However, because hydrosulfide is a strong reducing agent and a large amount of caustic soda is required to keep hydrosulfite stable in water, reduction cleaning using hydrosulfite and caustic soda as described above is recommended. The application of the method is limited to the dyeing of textiles where the fibers and the dyes used are sufficiently resistant to these agents. For this reason, for example, when dyeing a blended product of polyester fiber (hydrophobic fiber) and cellulose fiber (hydrophilic fiber, cotton, rayon, linen, etc.) using the dyeing method, first dye the polyester fiber side with disperse dye in the first bath. Dyeing is carried out using a high temperature and high pressure method or a carrier method, followed by alkaline reduction cleaning using caustic soda and hydrosulfite. In this step, the disperse dye that has contaminated the cellulose fibers is reduced and decomposed and solubilized or dispersed in an alkaline bath. Next, wash with water and hot water,
Remove alkaline agents and reducing agents. Next, in the second bath, the cellulose fiber side is dyed with a reactive dye or a direct dye, washed with water, hot water, soaped, and dried to finish. In order to shorten this long process, if we dye the polyester fiber side with a disperse dye and the cellulose fiber side with a reactive dye or direct dye in the same bath, and perform reduction cleaning with caustic soda and hydrosulfide, the dyeing will occur on the cellulose fiber side. The reactive dyes and direct dyes caused by reductive decomposition etc. cause large discoloration, resulting in unfavorable results.
疎水性繊維のみからなる繊維製品の染色物であってもこ
のような苛性ソーダ及び−・イドロサルファイトを用い
るアルカリ還元洗浄の工用
程は未固着染料の除去に極めて有狗な方法であるという
ものの前記したようにその強アルカリ性及び強還元性の
ために疎水性繊維の中でもポリエステル繊維を除いてア
セテート繊維等には強度劣化等の理由から採用できない
問題がある。Even for dyed textile products made only of hydrophobic fibers, the process of alkaline reduction cleaning using caustic soda and hydrosulfite is an extremely effective method for removing unfixed dyes. As mentioned above, due to their strong alkalinity and strong reducing properties, among hydrophobic fibers, acetate fibers and the like, with the exception of polyester fibers, have a problem in that they cannot be used for reasons such as strength deterioration.
一方親水性繊維のうち、セルロース繊維染色物は苛性ソ
ーダ、ハイドロサルファイドの処理により分解・変色を
起こす事、又羊毛、絹等の蛋白繊維染色物も分解による
変色や繊維強度の劣化を生ずるため採用出来ない。尚、
ポリエステル繊維/羊毛混紡品の二浴染色法において、
分散染料によるポリエステル染色後、アルカリ剤の強度
を弱めるためアンモニア水ヲ用いてハイドロサルファイ
ドによル還元洗浄を行う場合があるが、ハイドロサルフ
ァイドの安定性が不十分であるという問題がある。On the other hand, among hydrophilic fibers, dyed cellulose fibers are subject to decomposition and discoloration when treated with caustic soda and hydrosulfide, and dyed protein fibers such as wool and silk also cannot be used because they cause discoloration and deterioration of fiber strength due to decomposition. do not have. still,
In the two-bath dyeing method for polyester fiber/wool blend products,
After dyeing polyester with disperse dyes, reduction cleaning is sometimes performed with hydrosulfide using aqueous ammonia to weaken the strength of the alkaline agent, but there is a problem that the stability of hydrosulfide is insufficient.
「発明が解決しようとする問題点」
疎水性繊維又は疎水性繊維と親水性繊維との混合繊維の
染色物を堅牢変向上等の目的の為に後処理するにあたっ
てその繊維の種類及び染色に使用された染料の種類に制
限をうけることな(実施出来るような方法の開発が望ま
れている。``Problem to be solved by the invention'' Type of fiber and use for dyeing when post-processing dyed products of hydrophobic fibers or mixed fibers of hydrophobic fibers and hydrophilic fibers for the purpose of improving fastness, etc. It is desired to develop a method that can be implemented without being restricted by the type of dye used.
「問題点を解決するための手段」
本発明者らは前記したような問題点を解決すべく鋭意努
力を重ねた結果本発明に至ったものである。即ち本発明
は疎水性繊維又は疎水性繊維と親水性繊維との混合繊維
の染色物ス
をL−アスコルビン酸、イソア斧コルビン酸又はそれら
のアルカリ金属塩を含有するアルカリ性の水浴中で処理
することを特徴とする染色物の後処理法を提供する。"Means for Solving the Problems" The present inventors have made extensive efforts to solve the above-mentioned problems, and as a result they have arrived at the present invention. That is, the present invention involves treating a dyed product of hydrophobic fibers or mixed fibers of hydrophobic fibers and hydrophilic fibers in an alkaline water bath containing L-ascorbic acid, isoaxcorbic acid, or an alkali metal salt thereof. Provided is a post-processing method for dyed products characterized by the following.
本発明の詳細な説明する。The present invention will be described in detail.
本発明において疎水性繊維としてはポリエチレンテレフ
タレート、ポリエチレンテレフタレートを主体とするポ
リエステル、酸性ポリエステル、セルロースジアセテー
ト、セルローストリアセテート、ポリアミド、ポリアク
リル等が挙げられる。In the present invention, examples of the hydrophobic fiber include polyethylene terephthalate, polyester mainly composed of polyethylene terephthalate, acidic polyester, cellulose diacetate, cellulose triacetate, polyamide, and polyacrylic.
これらの繊維の染色物は分散染料、カチオン染料、酸性
染料等を用いて通常の染色法をよって得られるものであ
るが染料としては特にアルカリ可溶性基を有したアルカ
リ可抜性染料、還元され易い基を有した還元防抜染用染
料が適している。The dyed products of these fibers are obtained by ordinary dyeing methods using disperse dyes, cationic dyes, acid dyes, etc., but the dyes are particularly alkali-removable dyes with alkali-soluble groups, which are easily reduced. Suitable are dyes for reduction-resistant discharge printing which have groups.
又親水性繊維として、木綿、麻、レーヨン等のセルロー
ス繊維、羊毛、絹等の蛋白繊維等が挙げられる。Examples of hydrophilic fibers include cellulose fibers such as cotton, linen, and rayon, and protein fibers such as wool and silk.
これらの染色物は反応染料、直接染料、酸性染料等を用
いて通常の染色法を行って得られるものである。These dyed products are obtained by conventional dyeing methods using reactive dyes, direct dyes, acid dyes, and the like.
更に疎水性繊維と親水性繊維との混合繊維の染色物は各
々の繊維に染着性を有する複数のタイプの染料(例えば
分散染料と直接染料、分散染料と反応染料、塩基性染料
と酸性染料等)を用いて通常の方法により望ましくは一
浴染色法によってえられる。Furthermore, dyeing of mixed fibers of hydrophobic fibers and hydrophilic fibers involves the use of multiple types of dyes that can dye each fiber (for example, disperse dyes and direct dyes, disperse dyes and reactive dyes, basic dyes and acid dyes). etc.) by a conventional method, preferably by a one-bath dyeing method.
染色物をえるための繊維類の形態としては、交編品、交
織品、混紡品等あるいはワタ、トウ、糸、編物、織物等
がある。Examples of the forms of fibers used to obtain dyed products include interlaced knitted products, interwoven woven products, blended products, cotton, tow, yarn, knitted fabrics, and woven fabrics.
本発明の方法ではL−アスコルビン酸、イソアスコルヒ
ン酸又はこれらのアルカリ金属塩が使用され、アルカリ
金属の例としてはナトリウム、カリウム、リチウム等が
あげられる。特にL−アスコルビン酸ナトリウム及びイ
ソアスコルビン酸ナトリウム塩が溶解性、還元力、経済
性の点より適している。なおこれらは2種以上を混合し
て用いてもよい。その使用量は水浴中に0.1〜I O
g/、、7i! 好ましくは0.5〜5 g/A添加
するのが好適である。In the method of the present invention, L-ascorbic acid, isoascorhinic acid, or alkali metal salts thereof are used, and examples of alkali metals include sodium, potassium, lithium, and the like. In particular, sodium L-ascorbate and sodium isoascorbate are suitable in terms of solubility, reducing power, and economy. In addition, these may be used in combination of two or more types. Its usage amount is 0.1 to IO in water bath
g/,,7i! It is preferable to add 0.5 to 5 g/A.
アルカリ性の水浴を構成するアルカリ剤としては例えば
0.05%水溶液でpH値8以上を示す塩基、即ち、ア
ルカリ及びアルカリ土類金属の水酸化物(例えば水酸化
す) IJウム、水酸化カリウム)、アルカリ金属と無
機弱酸のアルカリ塩(例えば、アルカリ金属の炭酸塩、
重炭酸塩、リン酸塩、ケイ酸塩)、アルカリ金属と有機
酸との塩(例えばアルカリ金属のギ酸塩)、アンモニア
又は脂肪族アミン(例えば、トリエチルアミン及びその
誘導体、エタノールアミン及びその誘導体、ジェタノー
ルアミン及びその誘導体、トリエタノールアミン)、又
加熱によりアルカリを発生する潜在アルカリ例えばトリ
クロル酢酸ソーダ等カ挙げられ、これらは単独又は二種
以上併用する事ができる。そのような条件を得るための
通常の処理法での使用量は0.1〜] Og/fflに
0.5〜5g/!である。Examples of alkaline agents constituting the alkaline water bath include bases that exhibit a pH value of 8 or higher in a 0.05% aqueous solution, i.e., alkali and alkaline earth metal hydroxides (e.g. hydroxide, potassium hydroxide). , alkali salts of alkali metals and inorganic weak acids (e.g. carbonates of alkali metals,
salts of alkali metals and organic acids (e.g. alkali metal formates), ammonia or aliphatic amines (e.g. triethylamine and its derivatives, ethanolamine and its derivatives, (tanolamine and its derivatives, triethanolamine), and latent alkalis that generate alkali upon heating, such as sodium trichloroacetate, and these may be used alone or in combination of two or more. The amount used in the usual processing method to obtain such conditions is 0.1 to 0.5 to 5 g/ffl! It is.
処理温度はアルカリ剤の種類や量、又アスコルビン酸の
種類や量により20〜100℃で変動させることができ
るが、繊維と染料の性質、物性より一般には、40〜9
0℃が適当である。The treatment temperature can be varied from 20 to 100 degrees Celsius depending on the type and amount of the alkali agent and the type and amount of ascorbic acid, but it is generally 40 to 9 degrees Celsius depending on the properties and physical properties of the fiber and dye.
0°C is suitable.
処理法としてはバッチ法、連続法の(・ずれも採用出来
るがバッチ法の場合には浴比1:10〜]:]OOで5
〜60分好ましくは10〜20分処理する。又連続法の
場合にはやや高目の温度例えば70〜80℃で1〜10
分好ましくは2〜5分処理する。The processing method is a batch method or a continuous method.
Process for ~60 minutes, preferably 10-20 minutes. In addition, in the case of a continuous method, a slightly higher temperature of 1 to 10
Preferably 2 to 5 minutes.
洗浄時に、染料のアルカリ及び還元作用による可溶化、
分解物が、処理物へ再付着するのを防止するため、界面
活性剤その他を添加する事も可能である。During washing, the dye is solubilized by alkali and reducing action,
In order to prevent the decomposed products from re-adhering to the treated material, it is also possible to add a surfactant or the like.
本発明の特徴点をポリエステル繊維/木綿混紡品の染色
物の例をもってまとめると表1の如くである。The characteristics of the present invention are summarized in Table 1 with examples of dyed polyester fiber/cotton blend products.
表1゜
即ちポリエステル繊維等の素材に染着した分散染料に対
しては何ら悪い作用も与えないが未染着染料には極めて
有効に働きこれらは容易に分解除去される。Table 1: In other words, it does not have any negative effect on disperse dyes dyed on materials such as polyester fibers, but it works extremely effectively on undyed dyes, which are easily decomposed and removed.
又アルカリ性下でのアスコルビン酸は木綿に染着した反
応染料にはほとんど影響を与えず未染着の反応染料を分
解除去する作用を示す。In addition, ascorbic acid under alkaline conditions shows the effect of decomposing and removing undyed reactive dyes while having almost no effect on reactive dyes dyed on cotton.
以下実施例によって本発明の詳細な説明するが本発明は
これらに限定されるものではない。実施例の中での″部
nは重量部、1%1.は重量%、温度は摂氏温度である
。The present invention will be described in detail below with reference to Examples, but the present invention is not limited thereto. In the examples, "part n" is part by weight, 1% 1. is weight %, and temperature is in degrees Celsius.
実施例1〜5゜
耐熱ジアセテート/レーヨンの交織布に下記組成の色糊
な大同エンジニアリン羨オートスクリーンを用いて、水
玉模様に印捺し、70℃で10分間中間乾燥を行い、1
00〜103℃で15〜20分間の蒸熱処理により染料
を固着させた。Examples 1 to 5 A polka dot pattern was printed on a heat-resistant diacetate/rayon mixed woven fabric using a dyed Daido Engineering Autoscreen with the following composition, and intermediate drying was performed at 70°C for 10 minutes.
The dye was fixed by steaming at 00-103°C for 15-20 minutes.
固着布(捺染布)を7分割し各処理条件で処理した結果
、水玉部の変色度及び白湯の汚染度は表2の如き結果と
なった。The fixed cloth (printed cloth) was divided into seven parts and treated under each treatment condition, and the results of the degree of discoloration of the polka dots and the degree of contamination of hot water were as shown in Table 2.
(色 糊)
KP Black GD−8paste
l 5部水
35〃計
100部本発明の方法による処理物は、
■ 耐熱ジアセテート側は、
・水玉部は真黒色を呈し変色がない
・白湯部は汚染がなく美麗である
・繊維強度劣化は殆んどない
■ レーヨン側は、
・分散染料の汚染は除去され美麗である・繊維強度劣化
も殆んどない
という結果であり、優れた処理物を得た。(Color glue) KP Black GD-8paste
l 5 parts water
35 total
100 parts The product treated by the method of the present invention is as follows: ■ The heat-resistant diacetate side: - The water droplet part is jet black and has no discoloration - The hot water part is beautiful with no contamination - There is almost no deterioration in fiber strength ■ Rayon On the other hand, the results were as follows: - Disperse dye stains were removed and the fabric was beautiful - There was almost no deterioration in fiber strength, and an excellent treated product was obtained.
* 水玉部の色相
◎・・・・・・変色なく黒色を呈すもの×・・・・・・
著しい変色を起こしたもの** 白湯汚染度
◎・・・・・・白湯の汚染が殆んどないもの×・・・・
・・白湯の汚染が著しく太きいもの実施例6゜
(縦糸)木綿/(横糸〕耐熱ジアセテート、ポリエステ
ル(三菱レーヨン製)の交織布に下記組成の色糊なスク
リーン捺染機を用いて花柄にn−し、70℃で10分間
中間乾燥を行い、続いて175℃、8分間のHTS(過
熱蒸気)処理を施し染料の固着処理を行った。* Hue of the polka dots ◎...Things that exhibit black without discoloration×...
Items with significant discoloration ** Level of hot water contamination ◎... Items with almost no pollution in the hot water ×...
・・Contamination with hot water is extremely heavy Example 6: Floral patterns are printed on a mixed woven fabric of (warp) cotton/(weft) heat-resistant diacetate and polyester (manufactured by Mitsubishi Rayon) using a screen printing machine with the following composition. After drying at 70° C. for 10 minutes, the dye was fixed by HTS (superheated steam) treatment at 175° C. for 8 minutes.
得られた固着布(捺染布)を7分割し各処理条件で処理
し表3の如き結果を得た。The obtained fixed cloth (printed cloth) was divided into seven parts and treated under each treatment condition, and the results shown in Table 3 were obtained.
(色 糊〕
Kayacelon React Red CN−3B
2部(反応染料、日本化薬製)
Kayalon Po1yester Red BD−
8Pa5te 4 ’(分散染料、日本化薬
製)
尿素 15#
熱湯(pH7〜7.3) ’ 29部100
部
* 花柄部の色相
◎・・・・・・変退色がなく赤色を呈すもの×・・・・
・・変退色を起こしたもの
** 白湯汚染度
◎・・・・・・白湯の汚染が殆んどないもの○・・・・
・・ 〃 僅かあるもの8°゛°゛°
著しく太き〜・もの実施例12゜
(表地)ポリエステル繊維/(裏地)木綿のリバーシブ
ル編物5gを、浴比1:30で下記染浴を用いてpH7
,130℃で60分の染色を行った。(Color glue) Kayacelon React Red CN-3B
2 parts (reactive dye, manufactured by Nippon Kayaku) Kayalon Polyester Red BD-
8Pa5te 4' (disperse dye, manufactured by Nippon Kayaku) Urea 15# Boiling water (pH 7-7.3)' 29 parts 100
Part * Hue of the flower stalk ◎... Red color with no change or fading ×...
・・Things that have changed color and faded ** Level of hot water contamination ◎・・・・Things that have almost no pollution in hot water ○・・・
・・・ 〃 Only a few 8°゛°゛°
Extremely thick Example 1 5g of reversible knitted fabric of 2゜(outer material) polyester fiber/(lining material) cotton was dyed at pH 7 using the following dye bath at a bath ratio of 1:30.
, staining was carried out at 130°C for 60 minutes.
得られた染色さ終た編物を下記洗浄浴 で70℃、10分処理し水洗、乾燥した。The resulting dyed knitted fabric is washed in the following washing bath. The sample was treated at 70°C for 10 minutes, washed with water, and dried.
リバーシブル編物の表地は赤で裏地は黄色の美麗な堅牢
染色物を得た。洗浄処理前は、裏地の木綿に分散染料に
よる赤色の汚染が著しく、橙色を呈していたが洗浄処理
によりこれらは除去された。A beautiful fast-dyed reversible knitted fabric was obtained, with the outer material being red and the lining being yellow. Before the washing process, the cotton lining had significant red stains caused by the disperse dye, giving it an orange color, but these were removed by the washing process.
実施例13゜
ポリエステル繊維/羊毛(50150)混紡織物を下記
の染料、薬剤
を添加した浴でpH5,105℃で60分染色を行った
。得られた染色された織物を下記洗浄浴で60℃、15
分処理し水洗、乾燥した。Example 1 A 3° polyester fiber/wool (50150) blended fabric was dyed in a bath containing the following dyes and chemicals at pH 5 and 105° C. for 60 minutes. The obtained dyed fabric was washed at 60°C for 15 minutes in the following washing bath.
It was separated, washed with water, and dried.
ポリエステル繊維は橙色に、羊毛は赤色に染色された織
物を得た。A fabric was obtained in which the polyester fiber was dyed orange and the wool was dyed red.
洗浄処理前の染色された織物は、羊毛に分散染料による
橙色の汚染がみられ、ぐすんだ色調であったが、洗浄処
理によりそれらが除去された。The dyed fabric before washing had a dull tone with orange stains caused by disperse dyes in the wool, but these were removed by washing.
実施例14゜
アクリル繊維/木綿(50150)混紡織物を下記染料
、薬剤
を添加した染浴で、浴比1:20.pH7,97°Cで
60分染色を行った。Example 14 Acrylic fiber/cotton (50150) blended fabric was dyed in a dye bath containing the following dyes and chemicals at a bath ratio of 1:20. Staining was performed at pH 7 and 97°C for 60 minutes.
得られた織物を下記洗浄浴 で60℃、15分処理し、水洗、乾燥した。The resulting fabric was subjected to the following cleaning bath. The sample was treated at 60°C for 15 minutes, washed with water, and dried.
アクリル繊維側は青色に、木綿側は黄色に染色された織
物を得た。洗浄処理前の染色された織物は木綿側にカチ
オン染料による青色の汚染があり、色調が暗んだ黄色で
あったが、洗浄処理によりそれらは除去された。A fabric was obtained in which the acrylic fiber side was dyed blue and the cotton side was dyed yellow. Before washing, the dyed fabric had blue stains caused by cationic dyes on the cotton side, giving it a dark yellow color, but these were removed by washing.
実施例15
縦糸ポリエステルff11m、/横糸木綿の交織布を下
記パッド浴
にパッドし、マングルで95%に絞った。続いて100
℃、3分間中間乾燥を行い、次いで200°C190秒
間熱風処理を行った。得られた染色された織布を下記処
理浴
で80℃、5分処理し水洗、乾燥した。Example 15 A mixed woven fabric of warp polyester ff 11m/weft cotton was padded in the following pad bath and squeezed to 95% with a mangle. followed by 100
Intermediate drying was performed at 200° C. for 3 minutes, followed by hot air treatment at 200° C. for 190 seconds. The obtained dyed woven fabric was treated in the following treatment bath at 80° C. for 5 minutes, washed with water, and dried.
縦糸は青色、横糸は赤色に染色された交織布を得た。洗
浄処理前は木綿側に青色分散染料による汚染がみられた
が、洗浄処理により除去された。A mixed woven fabric was obtained in which the warp threads were dyed blue and the weft threads were dyed red. Before the washing process, staining with blue disperse dye was observed on the cotton side, but it was removed by the washing process.
「発明の効果」
疎水性繊維又は疎水性線維と親水性繊維との混合繊維の
染色物を堅牢変向上等の目的でなされる後処理において
その繊維の種類及び該染色物を得るために使用された染
料の種類に制限をうけることなく適用可能な処理法が確
立された。"Effects of the Invention" In post-treatment of dyed products of hydrophobic fibers or mixed fibers of hydrophobic fibers and hydrophilic fibers for the purpose of improving fastness, etc., the type of fiber and the type of dyed product used to obtain the dyed product are A processing method has been established that can be applied to any type of dye.
Claims (1)
維の染色物をL−アスコルビン酸、イソアスコルビン酸
又はそれらのアルカリ金属塩を含有するアルカリ性の水
浴中で処理することを特徴とする染色物の後処理法。1 Dyeing characterized by treating a dyed product of hydrophobic fibers or mixed fibers of hydrophobic fibers and hydrophilic fibers in an alkaline water bath containing L-ascorbic acid, isoascorbic acid, or an alkali metal salt thereof. Post-processing methods for things.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61120965A JPS62282085A (en) | 1986-05-28 | 1986-05-28 | Post-treatment of dyed article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61120965A JPS62282085A (en) | 1986-05-28 | 1986-05-28 | Post-treatment of dyed article |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62282085A true JPS62282085A (en) | 1987-12-07 |
Family
ID=14799389
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61120965A Pending JPS62282085A (en) | 1986-05-28 | 1986-05-28 | Post-treatment of dyed article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62282085A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108779602A (en) * | 2016-01-04 | 2018-11-09 | 尼克瓦格斯有限公司 | improved method for removing textile dyes |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50155782A (en) * | 1974-06-11 | 1975-12-16 | ||
JPS5915584A (en) * | 1982-07-13 | 1984-01-26 | 三井東圧化学株式会社 | Post-treatment of fiber |
-
1986
- 1986-05-28 JP JP61120965A patent/JPS62282085A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50155782A (en) * | 1974-06-11 | 1975-12-16 | ||
JPS5915584A (en) * | 1982-07-13 | 1984-01-26 | 三井東圧化学株式会社 | Post-treatment of fiber |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108779602A (en) * | 2016-01-04 | 2018-11-09 | 尼克瓦格斯有限公司 | improved method for removing textile dyes |
JP2019506545A (en) * | 2016-01-04 | 2019-03-07 | ニクワックス リミテッド | How to remove dye |
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