JPS5825792B2 - Color resist dyeing method - Google Patents
Color resist dyeing methodInfo
- Publication number
- JPS5825792B2 JPS5825792B2 JP52048680A JP4868077A JPS5825792B2 JP S5825792 B2 JPS5825792 B2 JP S5825792B2 JP 52048680 A JP52048680 A JP 52048680A JP 4868077 A JP4868077 A JP 4868077A JP S5825792 B2 JPS5825792 B2 JP S5825792B2
- Authority
- JP
- Japan
- Prior art keywords
- dyeing
- resist
- dye
- printing
- polyvalent metal
- 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
Links
- 238000004043 dyeing Methods 0.000 title claims description 39
- 238000000034 method Methods 0.000 title claims description 27
- 150000002736 metal compounds Chemical class 0.000 claims description 19
- 238000007639 printing Methods 0.000 claims description 17
- 150000005846 sugar alcohols Polymers 0.000 claims description 9
- 239000004753 textile Substances 0.000 claims description 9
- 238000009835 boiling Methods 0.000 claims description 4
- 239000000975 dye Substances 0.000 description 45
- 230000000694 effects Effects 0.000 description 9
- 239000000835 fiber Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 150000002739 metals Chemical class 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- 239000004744 fabric Substances 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 230000003247 decreasing effect Effects 0.000 description 5
- 239000000986 disperse dye Substances 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000013522 chelant Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- -1 etc. Substances 0.000 description 3
- 238000010021 flat screen printing Methods 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 230000003321 amplification Effects 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 238000003199 nucleic acid amplification method Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000004094 surface-active agent Substances 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
- OKZNPGWYVNZKKZ-UHFFFAOYSA-N 1,5-dihydroxy-4,8-bis(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=C(NC)C=CC(O)=C2C(=O)C2=C1C(O)=CC=C2NC OKZNPGWYVNZKKZ-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical class [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000009990 desizing Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000004044 disperse dyeing Methods 0.000 description 1
- TUXJTJITXCHUEL-UHFFFAOYSA-N disperse red 11 Chemical compound C1=CC=C2C(=O)C3=C(N)C(OC)=CC(N)=C3C(=O)C2=C1 TUXJTJITXCHUEL-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 230000021148 sequestering of metal ion Effects 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
Landscapes
- Coloring (AREA)
Description
【発明の詳細な説明】
本発明は着色防染法に関するものであり、更に詳しくは
多価金属化合物を防染剤として用いる繊維製品の着色防
染における改良に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a color resist dyeing method, and more particularly to improvements in color resist dyeing of textile products using a polyvalent metal compound as a resist dye.
その目的は防染性を損うことなく着色染料のビルドアン
プ性を向上して鮮明性の優れた着色防染面を得るにある
。The purpose is to improve the build amplification properties of colored dyes without impairing the resist properties, and to obtain a colored resist-dyed surface with excellent clarity.
従来、ポリエステル、セルロースアセテートのような合
成繊維製品の防染法として活性炭素、活性白土、ワック
ス等を用いる物理的防染法、塩化第一錫のような還元剤
や多価金属化合物のような染料とのキレート形成剤等を
用いる化学的防染法が知られている。Conventionally, as a resist dyeing method for synthetic fiber products such as polyester and cellulose acetate, physical resist dyeing methods using activated carbon, activated clay, wax, etc., and reducing agents such as stannous chloride and polyvalent metal compounds have been used. A chemical resist dyeing method using a chelate forming agent or the like with a dye is known.
そしてオートスクリーン捺染における連続捺染性、操業
安定性等の点から多価金属化合物を用いる化学的防染法
が特に注目されるようになった。From the viewpoint of continuous printing performance, operational stability, etc. in autoscreen printing, chemical resist dyeing methods using polyvalent metal compounds have attracted particular attention.
しかし、多価金属化合物な防染剤として用いる着色防染
法も従来の高圧スチーム法による染着処理では良好な着
色防染効果を与えるものの、近年連続操業性、経済性の
観点から多用されつつある高圧スチーム法あるいはサー
モゾール法においては着色防染における着色染料のビル
ドアツプ性、鮮明性が不充分であり、著しく品位を損っ
た捺染品を生じる欠点を有している。However, although the colored resist dyeing method using a polyvalent metal compound as a resist dye gives a good colored resist dyeing effect in the conventional high-pressure steam dyeing process, in recent years it has been increasingly used from the viewpoint of continuous operation and economic efficiency. Certain high-pressure steam methods and thermosol methods have the disadvantage that the build-up properties and sharpness of colored dyes in color resist dyeing are insufficient, resulting in printed products of significantly inferior quality.
本発明者等はその原因の究明と解決法について鋭意研究
の結果、高温スチーム法またはサーモゾール法における
着色防染面の着色柄部の色相が不鮮明かつビルドアツプ
性が不充分となる原因として染料固着時の温度、時間は
もちろんのこと、その他に捺染糊中に含有される多価金
属化合物の種類釦よび量、捺染布中に含有される水分量
等も鮮明性、ビルドアツプ性に大きく影響することを知
った。As a result of intensive research into the cause and solution, the present inventors found that dye fixation is the cause of the indistinct hue of the colored pattern on the colored resist dyeing surface and insufficient build-up properties in the high-temperature steam method or thermosol method. It is known that not only the temperature and time of printing, but also the type and amount of polyvalent metal compounds contained in the printing paste, the amount of water contained in the printed fabric, etc. greatly affect the clarity and build-up performance. Knew.
すなわち、多価金属化合物を含有する防染糊を用いる着
色防染において、高温スチームまたはサーモゾール発色
時の着色染料の不鮮明化あるいはビルドアツプ性不良現
象は微量水分下における染料の繊維への拡散移行性低下
むよび多価金属化合物と染料間における化学的結合もし
くは物理的結合、多価金属化合物による染料の分散性低
下等に起因する繊維への染料の染着抑制が主因であるも
のと考えられる。In other words, in color resist dyeing using a resist dye containing a polyvalent metal compound, the phenomenon of blurring of the colored dye or poor build-up during high-temperature steam or thermosol coloring is due to a decrease in the diffusion and transfer of the dye to the fibers in the presence of trace amounts of moisture. The main cause is thought to be the chemical or physical bond between the polyvalent metal compound and the dye, and the inhibition of dye adhesion to the fibers due to a decrease in the dispersibility of the dye due to the polyvalent metal compound.
しかし、染料固着時の布の含有水分率増加がほとんど期
待できない高温スチーム法あるいはサーモゾール法によ
る着色防染KL−いては、通常捺染における高温スチー
ム法あるいはサーモゾール法による固着において優れた
染着促進効果を発揮するキャリヤー、界面活性剤、吸湿
剤(塩化ナトリウム、尿素)等を着色防染期に添加して
もほとんどまたは全く効果がないばかりかキャリヤー、
界面活性剤等の多くは防染性を著しく低下させるという
致命的欠点を有する。However, in the case of colored resist dyeing KL using high-temperature steam or thermosol methods, which can hardly be expected to increase the moisture content of the fabric during dye fixation, the excellent dyeing promotion effect of high-temperature steam or thermosol dye fixation in normal textile printing is not expected. Adding carriers, surfactants, moisture absorbers (sodium chloride, urea), etc. during the coloring and resisting stage has little or no effect;
Many surfactants have the fatal drawback of significantly reducing dye resistance.
本発明者等はこのような欠点のない着色防染法につき更
に鋭意研究の結果、本発明の方法に到達したものである
。The inventors of the present invention have further conducted intensive research into a colored resist dyeing method that does not have such drawbacks, and have arrived at the method of the present invention.
すなわち、本発明は繊維製品に沸点が150℃以上かつ
分子量が800以下の多価アルコール類と多価金属化合
物を含む防染糊を柄状に印捺し、次いで捺染糊をオーバ
ープリントした後、高温スチーム法もしくはサーモゾー
ル法により染料固着することを特徴とする着色防染法で
ある。That is, in the present invention, a resist dyeing paste containing a polyhydric alcohol with a boiling point of 150° C. or more and a molecular weight of 800 or less and a polyvalent metal compound is printed on a textile product in the form of a pattern, then overprinted with the printing paste, and then heated at a high temperature. This is a colored resist dyeing method characterized by fixing the dye using a steam method or a thermosol method.
本発明の方法によるときは差色染料のビルドアンプ性、
鮮明性を著しく向上すると共に多価金属化合物による防
染性を何ら損うことがないことから極めて商品価値の高
い優れた着色防染品を提供することができる。When using the method of the present invention, the build amplification property of the differential color dye,
It is possible to provide an excellent colored resist-dyed product with extremely high commercial value, since the clarity is significantly improved and the resist-dyeing property of the polyvalent metal compound is not impaired in any way.
また濃染剤としてキャリヤーを使用するときに見られる
耐光堅牢度低下、脱糊性低下、防染性低下等の欠点や染
料凝集、フィルム強度低下に起因する汚れ等の欠点がな
いばかりか、脱糊性等が改善できる利点を“有する。In addition, there are no disadvantages such as decreased light fastness, decreased desizing ability, and decreased dye resistance that occur when using a carrier as a deep dyeing agent, as well as stains caused by dye aggregation and decreased film strength. It has the advantage of improving adhesive properties, etc.
更に吸湿剤として塩化ナトリウム、尿素等を使用すると
きに見られるスクリーン目詰り、pH変化に伴うキレー
ト結合能低下による防染性低下、型際不良等の欠点もな
い。Furthermore, there are no disadvantages such as screen clogging, decrease in dye resistance due to decrease in chelate binding ability due to pH change, and mold border failure that occur when using sodium chloride, urea, etc. as a moisture absorbent.
本発明の方法により優れたビルドアツプ性、鮮明性が得
られ、しかも防染性が低下しない理由については明らか
でないが、特定の多価アルコール類が多価金属化合物と
差色染料間の物理的、化学的結合性を抑制すると共に多
量の多価金属化合物の存在下かつ水の不存在下において
も効果的に差色染料を分散または酵解状態に保持するこ
とにより差色染料の染着を促進し、しかも捺染(返し捺
染)横巾の染料と多価金属化合物とのキレート反応は妨
害しないために優れた防染効果を維持するためと考えら
れる。Although it is not clear why the method of the present invention provides excellent build-up properties and sharpness without deteriorating resisting properties, it is clear that certain polyhydric alcohols have a physical effect between polyvalent metal compounds and differential color dyes. Promotes dyeing of differential color dyes by suppressing chemical bonding and effectively maintaining differential color dyes in a dispersed or fermented state even in the presence of large amounts of polyvalent metal compounds and in the absence of water. However, this is thought to be because the chelate reaction between the dye and the polyvalent metal compound in the textile printing (reverse printing) width is not interfered with, thereby maintaining an excellent resist dyeing effect.
本発明の方法を更に詳しく説明すると、用いる多価アル
コール類としては沸点が150℃かつ分子量が800以
下の多価アルコール類であり、具体的にはエチレングリ
コール、ジエチレングリコール、フロピレンクリコール
、シフロピレンクリコール、ポリエチレンクリコール、
ポリプロピレングリコール、多価アルコール、エチレン
オキシド付加体、グリセリン、ポリグリセリン、多価ア
ルコール、プロピレンオキシド付加体等が例示されるが
、特に200℃以上の沸点を有し、かつ分子量が500
以下の多価アルコール類が好ましく、就中グリセリン、
ポリプロピレングリコール、グリセリン、プロピレンオ
キシド付加体が特に好ましい。To explain the method of the present invention in more detail, the polyhydric alcohols used have a boiling point of 150°C and a molecular weight of 800 or less, and specifically, ethylene glycol, diethylene glycol, flopylene glycol, and sifropylene. glycol, polyethylene glycol,
Examples include polypropylene glycol, polyhydric alcohol, ethylene oxide adduct, glycerin, polyglycerin, polyhydric alcohol, propylene oxide adduct, etc., and in particular, those having a boiling point of 200°C or higher and a molecular weight of 500°C.
The following polyhydric alcohols are preferred, especially glycerin,
Particularly preferred are polypropylene glycol, glycerin, and propylene oxide adducts.
その使用量は多価金属化合物の種類、量等によっても異
なるが、通常防染糊に対し2〜lO重量部であり、好ま
しくは4〜8重量部である。The amount used varies depending on the type and amount of the polyvalent metal compound, but is usually 2 to 10 parts by weight, preferably 4 to 8 parts by weight, based on the resist dyeing paste.
また、用いる多価金属化合物としてはキレート形成能を
有する全ての多価金属、たとえば銅、アルミニウム、鉄
、クロム、コバルト、ニッケル、バリウム、カルシウム
等の硫酸塩、硝酸塩、酢酸塩、炭酸塩、・・ロゲン化物
、水酸化物等が挙げられ、一種または二種以上の組合せ
で使用されるが、特に酸性を示す化合物とアルカリ性を
示す化合物とを併用するのが防染効果から好ましい。In addition, the polyvalent metal compounds to be used include all polyvalent metals that have chelate-forming ability, such as sulfates, nitrates, acetates, carbonates, etc. of copper, aluminum, iron, chromium, cobalt, nickel, barium, calcium, etc.・Rogenides, hydroxides, etc. may be used, and they may be used singly or in combination of two or more, but it is particularly preferable to use a combination of an acidic compound and an alkaline compound from the viewpoint of the resisting effect.
その使用量は目標とする防染効果、淡色防染〜中濃色防
染によって異なるが通常防染糊に対し5〜50重量部で
あり、好ましくは15〜35重量である。The amount used varies depending on the desired resist dyeing effect and light resist dyeing to medium dark resist dyeing, but is usually 5 to 50 parts by weight, preferably 15 to 35 parts by weight, based on the resist dyeing paste.
本発明VCかいては上記多価アルコール類、多価金属化
合物、差色用染料に元糊、所望により助剤(pH調節剤
、金属イオン封鎖剤、両性界面活性剤)等からなる防染
糊を柄状に印捺した後、更に防染するべき染料を含有す
る捺染糊をオーバープリントし、乾朦してから高温スチ
ームあるいはサーモゾール法によって染料の固着処理を
行う。The VC of the present invention is a resist dyeing paste consisting of the above-mentioned polyhydric alcohols, polyvalent metal compounds, dyes for different colors, base paste, and optionally auxiliary agents (pH adjuster, metal ion sequestering agent, amphoteric surfactant), etc. After printing into a pattern, a printing paste containing the dye to be resist-dyed is overprinted, and after drying, the dye is fixed using high-temperature steam or thermosol method.
本発明を適用する繊維製品としては特にポリエステル、
ポリアミド、アセテートのような疎水性繊維含有製品、
疎水性合成樹脂で処理された親水性繊維またはガラス繊
維含有製品、エーテル化またはエステル化されたヒドロ
キシル基含有繊維製品、ポリオールまたはその誘導体類
、アミド化合物、芳香族化合物、アルキレンオキシド付
加型非イオン性化合物等によって前処理されたセルロー
ス、絹、ポリビニルアルコール等の親水性繊維含有製品
のような分散染料可染性繊維製品、またはイオン染料と
該イオンに対し反対荷電を有する化合物とのコンプレッ
クスのような分散型染料に可染性の繊維製品が好ましく
、就中ポリエステル繊維製品が好ましい。In particular, the textile products to which the present invention is applied include polyester,
Products containing hydrophobic fibers such as polyamide, acetate,
Products containing hydrophilic fibers or glass fibers treated with hydrophobic synthetic resins, etherified or esterified hydroxyl group-containing textile products, polyols or their derivatives, amide compounds, aromatic compounds, alkylene oxide-added nonionic products Disperse dye dyeable textile products, such as products containing hydrophilic fibers such as cellulose, silk, polyvinyl alcohol, etc., pretreated with compounds, etc., or complexes of ionic dyes and compounds with opposite charges to the ions. Fiber products dyeable with disperse dyes are preferred, and polyester fiber products are particularly preferred.
繊維製品には、繊維、トウ、整経状糸状、編織物、不織
布、合成紙、敷物、テープ等を包含する。Textile products include fibers, tows, warped threads, knitted fabrics, nonwoven fabrics, synthetic papers, rugs, tapes, and the like.
また本発明において防染することのできる染料としては
多価金属によりキレート化できる化学構造を有する染料
、多価金属と作用して分散効果を消失する分散剤によっ
て分散された染料等が挙げられるが、具体的には多価金
属と反応し得るアニオン基含有染料、分散染料、多価金
属と反応し得るアニオン活性剤で分散された分散染料、
アニオン染料とカチオン化合物とのコンプレックス、カ
チオン染料とアニオン化合物とのコンプレックス等が例
示される。In addition, dyes that can be resist-dyed in the present invention include dyes having a chemical structure that can be chelated with polyvalent metals, dyes dispersed with dispersants that interact with polyvalent metals, and lose their dispersion effect, etc. , specifically anionic group-containing dyes and disperse dyes that can react with polyvalent metals, disperse dyes dispersed with anionic activators that can react with polyvalent metals,
Examples include a complex between an anionic dye and a cationic compound, a complex between a cationic dye and an anionic compound, and the like.
しかし、特に多価金属と反応してキレート化できる化学
構造を有する分散染料が等が例示される。However, examples include disperse dyes having a chemical structure that can react with and chelate polyvalent metals.
また着色防染KL−ける着色染料としては多価金属と反
応しないかまたは反応性の小さい染料が挙げられるが、
ことに多価金属と反応してキレート化しないか、または
し難い分散染かくして多価金属化合物を用いる防染KL
−いて、高温スチーム法あるいはサーモゾール法による
染料固着により能率的に、かつ鮮明性、ビルドアンプ性
の優れた着色防染品を得ることができる。In addition, dyes that do not react with polyvalent metals or have low reactivity can be used as coloring dyes for color resist dyeing KL-.
In particular, disperse dyeing that does not or is difficult to react with polyvalent metals and thus resists KL using polyvalent metal compounds.
- By fixing the dye using a high temperature steam method or a thermosol method, it is possible to efficiently obtain a colored resist-dyed product with excellent clarity and build-up properties.
以下、実施例により本発明を説明する。The present invention will be explained below with reference to Examples.
なお、実施例中の部釦よび釦ま重量部釦よび重量部であ
る。In addition, the parts and buttons in the examples are parts by weight.
実施例 l
ポリエステル加工糸織物(スェード)上に下記処方の防
染槻a)、(b)をそれぞれ用いてフラットスクリーン
捺染機により柄状に印捺した。Example 1 A pattern was printed on a polyester processed yarn fabric (suede) using a flat screen printing machine using resist dyes a) and (b) having the following formulations.
次いでC,I、ディスバーズフルー26 6部、ローカ
ストビーンガム系糊剤7部、水70部よりなる捺染糊で
全面にオーバープリントし、乾燥してから175℃で1
0分間高温スチーミングし、水洗、ンーピング、水洗、
乾燥した。Next, the entire surface was overprinted with a printing paste consisting of C, I, 6 parts of Disbirds Flu 26, 7 parts of a locust bean gum paste, and 70 parts of water, dried, and then printed at 175°C for 1 hour.
Steam at high temperature for 0 minutes, rinse with water, soak, rinse with water,
Dry.
その結果、防染糊(a)を用いた本発明は青色地にオレ
ンジ色の極めて鮮明かつビルドアツプ性の優れた着色防
染品が得られた。As a result, in the present invention using the resist dyeing paste (a), a colored resist dyed product with an extremely clear orange color on a blue background and excellent build-up properties was obtained.
これに対し、防染糊(b)を用いた比較例は差色染料の
鮮明性、ビルドアツプ性が不充分であった。On the other hand, in the comparative example using resist dyeing paste (b), the sharpness of the differential color dye and the build-up property were insufficient.
なお、染料固着を200℃、90秒間のサーモゾールに
代えて実施したところ、同様の結果が得られた。Note that similar results were obtained when dye fixation was carried out at 200° C. for 90 seconds instead of using thermosol.
実施例 2
ポリエステル繊維100φからなる加工糸織物上に下記
処方の防染糊を用いてフラットスクリーン捺染機により
柄状に印捺した。Example 2 A resist dyeing paste having the following formulation was printed into a pattern on a textured yarn fabric made of 100φ polyester fibers using a flat screen printing machine.
次いでC,I、ディスバーズイエロー82部、C,I、
ディスバーズレッド146.25部、C,I、ディスパ
ーズブルー26 1部、グアガム系糊剤8部、水86部
5部よりなる捺染糊をそれぞれ全面にオーバープリント
し、乾燥してから高温スチーム−により180°Cで8
分間蒸熱した後、水洗、乾燥した。Next, C, I, 82 parts of Disbirds Yellow, C, I,
A printing paste consisting of 146.25 parts of Disperse Red, 1 part of Disperse Blue 26, 8 parts of guar gum paste, and 5 parts of 86 parts of water was overprinted on the entire surface, dried, and then heated with high temperature steam. 8 at 180°C
After steaming for a minute, it was washed with water and dried.
その結果を表−1に示した。その結果、本発明の方法に
より、差色染料の鮮明性、ビルドアツプ性が著しく改善
され、優れた着色防染面が得られた。The results are shown in Table-1. As a result, by the method of the present invention, the sharpness and build-up property of the differential color dye were significantly improved, and an excellent colored resist dyed surface was obtained.
本発明においても特にグリセリン、分子量300以下の
ポリプロピレングリコールが優れていた。In the present invention, particularly glycerin and polypropylene glycol having a molecular weight of 300 or less were excellent.
これに対しキャリヤー類を用いた比較例A7〜10は防
染性が著しく低下した。On the other hand, in Comparative Examples A7 to A10 in which carriers were used, the resistance to dyeing was significantly reduced.
また高温スチーム用の通常濃染剤を用いた比較例/16
11〜19は多少ビルドアツプ性が向上するものもある
が、大部分は防染性を低下させ、着色防染面の品位を著
しく低下させた。Comparative example/16 using a normal dyeing agent for high-temperature steam
Some of Nos. 11 to 19 improved the build-up property to some extent, but most of them lowered the resistance to dyeing and markedly deteriorated the quality of the colored resistance surface.
更に塩化す) I)ラム、尿素等の吸湿弁jは着防差色
の鮮明化ビルドアツプ性の向上には全く効果がないばか
りかスクリーンの目詰まり等により連続捺染性が低下す
る等の欠点を生じた。I) Moisture absorption valves such as ram, urea, etc. are completely ineffective in improving the sharpness of color retention and build-up properties, and they also have drawbacks such as decreased continuous printing performance due to screen clogging, etc. occured.
実施例 3
ポリエステル100俤織物上に下記処方の防染ぶ※糊を
用いてフラットスクリーン捺染機により柄状に印捺した
。Example 3 A pattern was printed on a 100-pound polyester fabric using a flat screen printing machine using a resist-dyeing paste with the following formulation.
次いで実施例2と同じ処方の捺染糊を用いて全面にオー
バープリントし、乾燥してから高温スチーマ−により1
75℃、8分間蒸熱処理し、水洗、ンーピング、水洗、
乾燥した。Next, the entire surface was overprinted using a printing paste with the same formulation as in Example 2, and after drying, it was coated with a high temperature steamer.
Steamed at 75°C for 8 minutes, washed with water, dumped, washed with water,
Dry.
その結果を表−2に示す。The results are shown in Table-2.
その結果、本発明の方法による捺染品は茶色地にオレン
ジ色の鮮明性、ビルドアツプ性ともに優れた着色防染面
を得た。As a result, the printed product obtained by the method of the present invention had a colored resist surface that was excellent in both orange clarity and build-up property on a brown background.
一方市販の高温スチーム用濃染剤を用いた比較角マ差色
のビルドアップか不充分であるばかりか防染性が著しく
低下し、鮮明着色防染品を得ることができなかった。On the other hand, in comparison with the use of a commercially available deep dyeing agent for high-temperature steam, the build-up of the square difference color was not only insufficient, but also the resistance to dyeing was markedly reduced, making it impossible to obtain a brightly colored resist-dyed product.
なか、通常プリントに釦ける高温スチームにおいては表
−3に示すように比較例で用いたキャリヤー、濃染剤、
吸湿剤の濃染効果が逆に大きいことから多価アルコール
類によって得られる効果は多価金属化合物を用いる着色
防染に特有の効果である。Among them, as shown in Table 3, in the high-temperature steam that is normally used for printing, the carrier, deep dye,
On the contrary, the effect obtained by polyhydric alcohols is unique to colored resist dyeing using polyvalent metal compounds, since the moisture absorbing agent has a strong dyeing effect.
Claims (1)
0以下の多価アルコール類と多価金属化合物を含む防染
糊を柄状に印捺し、次いで捺染糊をオーバープリントし
た後、高温スチームもしくはサーモゾール法により染料
固着することを特徴とする着色防染法。1 Textile products with a boiling point of 150°C or higher and a molecular weight of 80
Colored resist dyeing characterized by printing resist dyeing paste containing 0 or less polyhydric alcohols and polyvalent metal compounds in a pattern, then overprinting the printing paste, and then fixing the dye by high temperature steam or thermosol method. Law.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52048680A JPS5825792B2 (en) | 1977-04-26 | 1977-04-26 | Color resist dyeing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP52048680A JPS5825792B2 (en) | 1977-04-26 | 1977-04-26 | Color resist dyeing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS53134984A JPS53134984A (en) | 1978-11-25 |
| JPS5825792B2 true JPS5825792B2 (en) | 1983-05-30 |
Family
ID=12810023
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP52048680A Expired JPS5825792B2 (en) | 1977-04-26 | 1977-04-26 | Color resist dyeing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5825792B2 (en) |
-
1977
- 1977-04-26 JP JP52048680A patent/JPS5825792B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS53134984A (en) | 1978-11-25 |
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