JPS5847513B2 - Natsusen Narabini Senshiyokunokochiyakuhou - Google Patents
Natsusen Narabini SenshiyokunokochiyakuhouInfo
- Publication number
- JPS5847513B2 JPS5847513B2 JP50039299A JP3929975A JPS5847513B2 JP S5847513 B2 JPS5847513 B2 JP S5847513B2 JP 50039299 A JP50039299 A JP 50039299A JP 3929975 A JP3929975 A JP 3929975A JP S5847513 B2 JPS5847513 B2 JP S5847513B2
- Authority
- JP
- Japan
- Prior art keywords
- foam
- liquid
- fixing
- amount
- dye
- 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
- 239000006260 foam Substances 0.000 claims description 69
- 238000000034 method Methods 0.000 claims description 38
- 239000007788 liquid Substances 0.000 claims description 22
- 239000002657 fibrous material Substances 0.000 claims description 21
- 239000004753 textile Substances 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 16
- 238000004043 dyeing Methods 0.000 claims description 9
- 230000008569 process Effects 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 5
- 229920003043 Cellulose fiber Polymers 0.000 claims description 3
- 239000012209 synthetic fiber Substances 0.000 claims description 2
- 229920002994 synthetic fiber Polymers 0.000 claims description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- 239000000975 dye Substances 0.000 description 19
- 239000004744 fabric Substances 0.000 description 10
- 239000007791 liquid phase Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 235000011121 sodium hydroxide Nutrition 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 239000000984 vat dye Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 235000002639 sodium chloride Nutrition 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- -1 lauryl alcohol Chemical class 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 239000000985 reactive dye Substances 0.000 description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
- 239000011550 stock solution Substances 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000006265 aqueous foam Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- NXYNTHCSPIVNNX-SAIUNTKASA-N leucoester Natural products CCCCCCCCCCCCCCCC(=CCOC(=O)CCC[C@H](C)CCC[C@H](C)CCC(C)C)C NXYNTHCSPIVNNX-SAIUNTKASA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 235000019353 potassium silicate Nutrition 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 235000013912 Ceratonia siliqua Nutrition 0.000 description 1
- 240000008886 Ceratonia siliqua Species 0.000 description 1
- 229910006127 SO3X Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical group 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000010446 mirabilite Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/58—Material containing hydroxyl groups
- D06P3/60—Natural or regenerated cellulose
- D06P3/68—Preparing azo dyes on the material
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B19/00—Treatment of textile materials by liquids, gases or vapours, not provided for in groups D06B1/00 - D06B17/00
- D06B19/0088—Treatment of textile materials by liquids, gases or vapours, not provided for in groups D06B1/00 - D06B17/00 using a short bath ratio liquor
- D06B19/0094—Treatment of textile materials by liquids, gases or vapours, not provided for in groups D06B1/00 - D06B17/00 using a short bath ratio liquor as a foam
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/22—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using vat dyestuffs including indigo
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/62—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds with sulfate, sulfonate, sulfenic or sulfinic groups
- D06P1/621—Compounds without nitrogen
- D06P1/627—Sulfates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/673—Inorganic compounds
- D06P1/67333—Salts or hydroxides
- D06P1/6735—Salts or hydroxides of alkaline or alkaline-earth metals with anions different from those provided for in D06P1/67341
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/673—Inorganic compounds
- D06P1/67383—Inorganic compounds containing silicon
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/96—Dyeing characterised by a short bath ratio
- D06P1/965—Foam dyeing
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/58—Material containing hydroxyl groups
- D06P3/60—Natural or regenerated cellulose
- D06P3/66—Natural or regenerated cellulose using reactive dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Coloring (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Treatment Of Fiber Materials (AREA)
Description
【発明の詳細な説明】
建染め染料、ロイコエステル建染め染料及び反応染料の
顕色のための二相法に於ては、該方法の第二段階、すな
わち固着用化学薬品を、パジングもしくは捺染された繊
維物に適用する段階に於で特に困難が発生する。DETAILED DESCRIPTION OF THE INVENTION In the two-phase process for the development of vat dyes, leucoester vat dyes and reactive dyes, the second step of the process, the fixing chemicals, is applied to the padding or printing process. Particular difficulties arise in the application stage to coated textiles.
すなわち、化学薬品を含有する液の供給の正確な配量が
常に困難である。That is, accurate metering of the supply of liquids containing chemicals is always difficult.
当業界に於ではパジング法、スロツプパジング法、クロ
スパジング法及びスプレー法が公知である。Padding methods, slop padding methods, cross padding methods and spray methods are well known in the art.
化学薬品を均一に適用する必要性が大きい場合には、例
えば多過ぎるパジング液が繊維材料上に達して、捺染が
それによってにじみ出るかも知れず、これによりみにく
い織物面が作り出される危険が太いにある。If there is a great need for an even application of chemicals, there is a strong risk, for example, that too much padding liquid may reach the textile material and the print may thereby bleed, thereby creating an unsightly textile surface. .
この危険を少くするためには、固着液に相当量の無機塩
を添加し上記のすべての種類の染料のうちの適用された
染料の溶解度を低下させる。In order to reduce this risk, considerable amounts of inorganic salts are added to the fixing solution to reduce the solubility of the applied dyes of all the above-mentioned types of dyes.
染料の固着に本当に必要な液量は、一般に従来慣用の方
法で使用されてきた総液量よりも著しく少い。The amount of liquid actually required for dye fixation is generally significantly less than the total amount of liquid used in conventional methods.
それ故、それ自体不要な塩による廃水汚染をも含めてあ
らゆる困難は、適用される液相の量を少くすることによ
り避けられる。Therefore, all difficulties, including wastewater contamination with salts which are themselves unnecessary, are avoided by reducing the amount of liquid phase applied.
西ドイツ国特許出願公開第2145827号及び同第2
243865号によれば、繊維材料を泡沫の使用下にバ
ッチ法で染色または仕上げすることは公知である。West German Patent Application No. 2145827 and No. 2
According to No. 243,865, it is known to dye or finish textile materials in a batch process using foam.
同じく定期刊行物” Textilveredlung
”6 ( 1 9 7 1 )、第11号、708−
711頁には、起泡した染液を使用し、且つ遠心力の利
用下に繊維材料をパッチ法で染色することができる方法
が知られている。Similarly periodical “Textilveredlung”
"6 (1971), No. 11, 708-
On page 711, a method is known in which fiber materials can be dyed by a patch method using a foamed dye liquor and using centrifugal force.
最後に、西ドイツ国特許出願公開第2214377号に
従い、染料及び/または仕上げ剤並びにそれらの固着の
ために場合により必要な化学薬品を泡の形態で平面的繊
維構造物に適用することがすでに記載されている。Finally, it has already been described in accordance with DE 22 14 377 A1 to apply dyes and/or finishing agents and any necessary chemicals for their fixation to planar fiber structures in the form of foam. ing.
しかしこの最後にあげた処理法に於では、液体の適用量
を少くするという利点を必要ともしなければ利用もして
ない。However, in this last-mentioned process, the advantage of reducing the amount of liquid applied is not needed or utilized.
更に、この方法では染色及び仕上げのために泡沫を使用
するが、その際上記二つの加工法を、事情によっては同
時に実施し、且つ望むならば模様付け及び多色染色効果
を作り出すことができる。Furthermore, this method uses foam for dyeing and finishing, with the two processing methods described above optionally being carried out simultaneously and making it possible to create patterning and multicolored dyeing effects if desired.
この方法ではマイグレーション現象はさげられる。This method reduces the migration phenomenon.
西ドイツ国特許出願公開第2214377号の場合には
1段階染色法が問題にされているが、この場合には均一
な染色を得ることは極めて困難である。In the case of German Patent Application No. 2 214 377, a one-stage dyeing method is considered, but in this case it is extremely difficult to obtain a uniform dyeing.
というのは繊維材料の・・ンドリンク及び均一な泡沫の
施与−従って繊維材料への完全に均一な液の移行は実施
が著しく困難になるからである。This is because the linking of the fiber material and the application of a homogeneous foam - and therefore a completely homogeneous transfer of liquid to the fiber material - are extremely difficult to implement.
本発明者は、セルローズ繊維材料及びそれと合成繊維と
の混合物上に染色及び捺染を固着するためのあらゆる二
相法が、化学薬品含有の水性液の代りに染料の固着に必
要な量の化学薬品を(その液相と空気より成る)泡沫と
して、特に液体の少ない状態で、あらかじめ捺染または
パジングされた繊維材料に施与することにより行なわれ
つることを見い出した。The inventors have discovered that any two-phase method for fixing dyeings and prints on cellulose fiber materials and their mixtures with synthetic fibers can be used in which the amount of chemicals required for fixing the dye is used instead of a chemical-containing aqueous liquid. It has been found that this can be done by applying the foam as a foam (consisting of its liquid phase and air), especially in a liquid-poor state, to previously printed or padded textile materials.
上記の新規な適用法に関しては、泡沫の液相中に於ける
固着剤の濃度が或る程度高いことがたしかに必要ではあ
るが、固着用液の使用量の低減が同時に可能となる。Regarding the above-mentioned novel application method, although it is certainly necessary that the concentration of the fixing agent in the liquid phase of the foam be to some extent high, it is possible at the same time to reduce the amount of the fixing liquid used.
従って、全体としては、例えば20%液相を例えば5乃
至15%の泡沫の形で適用する場合には、通常の使用量
の例えば10%も化学薬品の量を低減させることができ
る。Overall, therefore, when applying, for example, a 20% liquid phase in the form of a foam of, for example, 5 to 15%, the amount of chemicals can be reduced, for example, by as much as 10% of the usual amount used.
泡沫の液相は1 0 0 ?/lまでの炭酸ナトリウム
、1l当り200crAのNaOH(38°Be)また
は1l当り400cniの水ガラス(500Be)を含
むことができる。Is the liquid phase of foam 100? /l of sodium carbonate, 200 crA of NaOH (38°Be) per liter or 400 cni of water glass (500Be) per liter.
普通は水ll中に炭酸ナトリウム802及び水酸化ナト
リウム5zを含む標準的アルカリ性液相が使用される。A standard alkaline liquid phase is used, usually comprising 802 ml of sodium carbonate and 5 z of sodium hydroxide.
更に、本方法により使用に供される。Furthermore, the method provides for use.
固着用化学薬品の泡沫形態は、該化学薬品の完全且つ均
一な分配を可能ならしめる。The foam form of the fixing chemical allows complete and uniform distribution of the chemical.
更に、泡沫の特に少い水含量一極端な場合には1%以下
の水含量のことさえある一の故に、化学薬品の量を完全
に正確に計量することが町能である。Moreover, because of the particularly low water content of the foam, in extreme cases even less than 1% water content, it is impossible to meter the amount of chemicals with complete accuracy.
粘稠な泡沫は決して液体の性質を有せず、従ってこの固
着法に於では捺染はにじみ出ることはあり得ない。A viscous foam never has liquid properties, so the print cannot ooze out with this fixing method.
捺染は鮮明な輪郭を有する。The print has clear outlines.
本発明方法において、パジングされた染料がこの泡沫に
溶解されて除去されることはありえない。In the method of the invention, it is impossible for the padded dye to be dissolved in this foam and removed.
この方法では、例えばベンジンエマルジョンを用いて作
られた捺染物も泡沫により処理され5る。In this method, prints made, for example, with benzene emulsions are also treated with foam.
起泡エマルジョンの適用も可能である。The application of foamed emulsions is also possible.
しかし、特許請求の範囲に記載された方法により工業的
に申し分のない一連の処理工程及び均一且つ一様な泡沫
の施与を保証するためには、繊維材料上の泡沫濃度を余
り低くしないようにすることが効果的である。However, in order to ensure an industrially satisfactory sequence of processing steps and a homogeneous and even foam application with the claimed method, the foam concentration on the textile material must not be too low. It is effective to do so.
しかし泡沫が多いということは液体が多いことを意味す
るので捺染物のシャープな輪郭線がぼけるおそれがある
。However, a large amount of foam means a large amount of liquid, which may blur the sharp outlines of the printed material.
それ故に、この様な場合、例えば食塩または芒硝の如き
無機塩10%までを泡沫の液相に加えるかまたは捺染ペ
ースト中に凝固し得る粘稠剤を使用して処理するのがよ
℃・。It is therefore advisable in such cases to add up to 10% of an inorganic salt, such as common salt or mirabilite, to the liquid phase of the foam or to use a thickening agent which can coagulate into the printing paste.
冒頭に述べた技術水準とは異なり、本発明の場合には染
料溶液は一般に慣用の技術及び方法で、パジングによる
か或は捺染により繊維材料に適用される。In contrast to the state of the art mentioned at the outset, in the present case the dye solution is generally applied to the textile material by conventional techniques and methods, by padding or by printing.
染料固着に必要なアルカリまたは酸のみが泡沫として施
与される。Only the alkali or acid necessary for dye fixation is applied as a foam.
こうすることにより、適用法の第二段階に於て、従来可
能であると考えられていたよりも僅かなアルカリ量の配
量が行える。This allows a lower amount of alkali to be dosed in the second stage of the application process than previously thought possible.
アルカリ性の固着液を用L・る通常のパジング法の場合
には、最少限50%の水が繊維材料上に達し、従って染
料が流れ出すのを阻止するために、必ずしも必要でない
塩をこの水に加えねばならなかった。In the case of conventional padding methods using alkaline fixing liquids, a minimum of 50% of the water reaches the textile material, and therefore salt, which is not necessarily necessary, is added to this water to prevent the dye from leaching out. I had to add it.
その上、水量の低減は、塩溶液を5すくすることを呵能
にするので化学薬品は次の二つの効果により節約される
。Additionally, the reduction in water volume allows for less salt solution to be required, so chemicals are saved in two ways.
すなわち、液が少くなり且つ塩濃度が低くなる。That is, the amount of liquid becomes smaller and the salt concentration becomes lower.
西ドイツ国特許出願公開第2214377号による固着
用助剤と共に染料を適用する一段階法と異なり、本発明
による二段階法に於では、パジング液または捺染ペース
トの安定性が本来的に保障される。In contrast to the one-stage process according to DE 22 14 377, in which the dye is applied together with fixing aids, in the two-stage process according to the invention the stability of the padding liquid or printing paste is inherently guaranteed.
前述のレベリングの問題も起らない。というのは水性パ
ジング液または捺染ペーストはいずれの場合にも均一に
施与されるからである。The leveling problem mentioned above does not occur either. This is because the aqueous padding liquid or printing paste is applied uniformly in each case.
固着用化学薬品の泡沫状での施与(第二段階)は、繊維
材料の全体に亘って固着用化学薬品の最小量が存在しな
げればならないという点でのみ染料固着の均一性に影響
を及ぼす。The application of the fixing chemical in the form of a foam (second stage) influences the uniformity of dye fixation only in that a minimum amount of fixing chemical must be present throughout the textile material. effect.
このことは機械技術的には著しく簡単に実現される。This is achieved mechanically with great ease.
固着用化学薬品の過配量は染着率に悪影響がない。Overdosing of fixing chemicals has no negative effect on the dyeing rate.
本発明方法の実施のためには、公知の方法、例えば泡沫
消火器の方法により安定な(長時間存続する)泡沫を製
造し、その際、泡の自発的崩壊に配慮する必要がないよ
うにするのが好ましい。In order to carry out the method of the invention, a stable (long-lasting) foam is produced by known methods, for example the method of foam fire extinguishers, so that there is no need to take into account spontaneous collapse of the foam. It is preferable to do so.
発泡剤としては、好ましくは一般式
R一〇−SO3H−N(CH2−CH2−OH) 3(
ここにRは12−14個の炭素原子を有するアルキル基
である。The blowing agent preferably has the general formula R10-SO3H-N(CH2-CH2-OH)3(
Here R is an alkyl group having 12-14 carbon atoms.
)なるトリエタノールアミンアルアルキルスルフエート
に基づく物、一般式R−O−(CH2−CH2−O)n
−SO3X(ここにRは前記と同一の意味を有し、Xは
アルカリ金属またはアンモニウムイオン、nは2乃至5
の数を意味する。) based on triethanolamine aralkyl sulfate, with the general formula R-O-(CH2-CH2-O)n
-SO3X (where R has the same meaning as above, X is an alkali metal or ammonium ion, n is 2 to 5
means the number of
)なるアルキルポリグリコールエーテルスルフエート、
及び混合比の制限のないこれらの混合物が適している。) alkyl polyglycol ether sulfate,
and mixtures thereof without any restriction on the mixing ratio are suitable.
この泡沫原液の製造のための溶剤として特にブチルジグ
リコールが使用され、且つ泡沫安定化剤として少量の脂
肪アルコール、例えばラウリルアルコールが併用される
。In particular, butyl diglycol is used as the solvent for the preparation of the foam concentrate, and small amounts of fatty alcohols, such as lauryl alcohol, are used as foam stabilizers.
この泡沫原液は、長期間存続する泡沫を得るために、0
. 5−3%の濃度で水性固着液に加えられる。This foam stock solution has a zero
.. It is added to the aqueous fixing solution at a concentration of 5-3%.
捺染ペーストまたはパジング液は染料の外に好ましくは
、泡沫崩壊性の(場合により行なわれる乾燥工程のため
に非揮発性の)助剤、例えば珪素を基体とする助剤を含
み、この助剤は繊維材料と接触した際に泡沫を崩壊させ
、その際泡沫の全量がその液体中に含まれる固着剤と共
に吸収されて利用されるようになる。The printing paste or padding liquid preferably contains, in addition to the dyestuff, foam-disintegrating (non-volatile due to the optional drying process) auxiliaries, for example silicon-based auxiliaries. The foam collapses upon contact with the fibrous material, the entire amount of the foam being absorbed and utilized together with the binding agent contained in the liquid.
本発明による固着法は主として、反応染料による染色及
び捺染の固着に使用される。The fixing method according to the invention is primarily used for fixing dyeings and prints with reactive dyes.
この場合、これに必要kアルカリは、苛性ソーダ、水ガ
ラスまたはソーダとして泡沫の形で適用される。In this case, the alkali required for this is applied in foam form as caustic soda, water glass or soda.
本発明方法によれば、建染染料を使用するためにソーダ
アルカリ性の還元剤系を発泡させることもできる。According to the method of the invention, it is also possible to foam soda-alkaline reducing agent systems for the use of vat dyes.
ナフトレート及び安定化されたジアゾ化合物の組み合せ
より成る染料の固着及び顕色のためには、例えば、液相
中に10%のギ酸を含む5%の泡沫を施与する。For fixation and development of dyes consisting of a combination of naphthlates and stabilized diazo compounds, for example, a 5% foam containing 10% formic acid is applied in the liquid phase.
この場合、このように処理された繊維材料を60秒間空
気にさらすことが、あらかじめ捺染した繊維材料上の染
料の顕色のために十分である。In this case, exposing the textile material treated in this way to air for 60 seconds is sufficient for the development of the dye on the previously printed textile material.
建染染料で捺染した繊維材料を固着用化学薬品と共に供
給する場合には、適当な消泡剤を捺染ペーストに添加す
るのが特に有効である。When textile materials printed with vat dyes are supplied together with fixing chemicals, it is particularly advantageous to add suitable defoamers to the printing paste.
とい5のは、閉じこめられた空気による悪影響を取り除
くために空気を含む泡沫はこれがスチーマーに入る前に
崩壊させなげればならない。Fifth, the air-containing foam must be collapsed before it enters the steamer in order to eliminate the negative effects of trapped air.
本発明を実施するための有利な装置の配置の例は、添加
の図面第1乃至第4図によりその概略が示される。Examples of advantageous equipment arrangements for carrying out the invention are shown schematically in the accompanying drawings, FIGS. 1-4.
ここに使用された数字は下記の意味を有する:
1.繊維材料
2、エンドレスのラハークロス
3.駆動町能な搬送用ロール
4.泡沫容器
5,処理剤を含む泡沫
6.泡沫と繊維材料との接触区間
7.接触区間6の長さを変えるためのカバーシ一ト
8.高さを調節できるドクターブレード
9,泡沫供給管
10.繊維材料用案内ロール
11.泡沫出口用の細隙ノズル
12,傾斜面
13枠
14.泡沫施与用ロール
新規方法の有利な一つの実施態様は、処理剤を含またせ
泡沫を高いローラーを有する箱の中に入れそして濡れ難
いドクタープレートを繊維材料上のあらかじめ定められ
た高さに保持することにより成る。The numbers used herein have the following meanings: 1. Fiber material 2, endless lahar cloth 3. Driving conveyor roll 4. Foam container 5, foam containing treatment agent 6. Contact zone between foam and fiber material7. Cover sheet 8 for varying the length of the contact section 6. Doctor blade 9 with adjustable height, foam supply pipe 10. Guide roll for textile materials 11. Slit nozzle 12 for foam outlet, inclined surface 13 frame 14. Roll for Foam Application One advantageous embodiment of the novel method is that the foam impregnated with the treatment agent is placed in a box with tall rollers and a non-wetting doctor plate is held at a predetermined height above the textile material. It consists of doing.
泡沫を上記容器に連続的または不連続的に供給するか或
はそれを容器の下部に於で定常的にまたはバッチ的に発
生させると有利であることが判った。It has been found to be advantageous to feed the foam continuously or discontinuously into the vessel or to generate it in the lower part of the vessel constantly or batchwise.
そこで上記容器中に於て繊維材料を、一この繊維材料は
ロールまたはロール系にかけられた搬送用ベルトにより
供給される一泡沫中へ多かれ少なかれ浸漬する。In the vessel, the fibrous material is then more or less immersed in a foam which is fed by a roll or a conveying belt over a system of rolls.
泡沫の吸収量は上記二つの態様に於で、泡沫と供給され
る布地との接触時間によっても大いに影響される。The amount of foam absorbed in the two embodiments described above is also greatly influenced by the contact time of the foam with the applied fabric.
このことは、薄地の繊維材料が少量の泡沫を必要とする
場合に、繊維材料と泡沫供給との間の接触区間を部分的
に覆うことにより、第1図に示された形で簡単に行なわ
れる。If the thin textile material requires a small amount of foam, this can easily be done in the manner shown in FIG. 1 by partially covering the contact zone between the textile material and the foam supply. It will be done.
接触区間の変更は、繊維材料搬送速度の変化に対する適
合をも一層容易にする。Changing the contact section also makes it easier to adapt to changes in the fiber material conveying speed.
最も簡単な方法では、繊維材料を傾斜面上に泡沫と一緒
に供給し、その際通常、傾斜面はドクターブレードであ
るか或はドクターブレードの代用となる。In the simplest method, the fiber material is fed together with the foam onto an inclined surface, the inclined surface usually being a doctor blade or a substitute for a doctor blade.
かような二通りの配置は第2図及び第3図より明らかで
ある。Such two arrangements are clear from FIGS. 2 and 3.
最後に第4図は、泡沫のための適用装置としてのロール
対を示す。Finally, FIG. 4 shows a pair of rolls as an application device for foam.
この配置によれば、一つのロールの外周面上に泡沫がも
たらされ、そのロールの回転によりそこから泡沫が運ば
れ、そしてロール対のニツプ部で繊維材料に移行し、繊
維材料はもう一つのロールの回りを案内されている。According to this arrangement, foam is provided on the outer circumferential surface of one roll, from which it is carried by the rotation of that roll, and transferred to the fibrous material at the nip of the pair of rolls; being guided around two rolls.
二つのロールの距離から布地への泡沫の施与厚み(泡沫
高さ)が決まる。The thickness of foam applied to the fabric (foam height) is determined by the distance between the two rolls.
下記の例により本発明による実施方法が更に詳細に説明
される。The examples below explain the implementation according to the invention in more detail.
例中、使用せる染料に対して記載するカラーインデック
ス番号はこのインデックスの1971年版から採録した
。In the examples, the color index numbers listed for the dyes used were taken from the 1971 edition of this index.
使用した百分率は重量%を意味する。The percentages used mean % by weight.
例1
重量が200P/m”の木綿メリヤスを
リアクテイブブル−19−C,I,厘 15P61
200
第一燐酸ナトリウム 2♂アル
ギン酸ナトリウム(5%水溶液’) 483?及び
水 500グ1000f
を含む捺染ペーストで捺染する。Example 1 Reactive blue-19-C, I, 15P61 cotton stockinette with a weight of 200P/m"
200 Sodium monophosphate 2♂Sodium alginate (5% aqueous solution') 483? and printing with a printing paste containing 500g and 1000f of water.
乾燥後、繊維材料上に、第4図による装置を用いて、5
%の水性泡沫一その液相は30%苛性7−ダ液10%及
びトリエタノールアミンーココヤン脂肪酸硫酸塩を基体
とする泡沫原液1%を含む一を適用する。After drying, on the fiber material, using the apparatus according to FIG.
% of an aqueous foam, the liquid phase of which is 30%, containing 10% of a caustic 7-D solution and 1% of a foam stock solution based on triethanolamine-cocoyang fatty acid sulfate is applied.
液のピックアップは20%で、これは30%水酸化ナト
リウム溶液4ml.が繊維材料im2上にもたらされた
ことを意味する。The liquid pickup is 20%, which is 4ml of 30% sodium hydroxide solution. is applied on the fiber material im2.
泡沫適用を実施する場合には、離して駆動される二つの
ロールの間隔は約1間である。When carrying out foam application, the distance between two rolls driven apart is about 1.
これが泡沫層の高さを規定する。This defines the height of the foam layer.
2個のロールは互に異なる速度で駆動されることができ
、その際泡沫を搬送するロールの方が速く回転するのが
好まし(・。The two rolls can be driven at different speeds, with the roll transporting the foam preferably rotating faster.
その場合、第2番目のロールの駆動を第1のロールによ
っても行うことができる。In that case, the second roll can also be driven by the first roll.
最も簡単な場合には、力の伝達はロールとロールを互に
押しつげ合うことによって実施され、その場合1つのロ
ールの両端にそれぞれ少くとも20CTL巾の布片を巻
きつける。In the simplest case, the force transmission is carried out by pressing the rolls against each other, each end of a roll being wrapped with a strip of cloth having a width of at least 20 CTL.
この巻きつげた層は、織物を導く位置に於ける2個のロ
ールの間隔に相当する厚さでなければならない。This rolled layer must have a thickness corresponding to the distance between the two rolls at the point where the fabric is guided.
かくして泡沫層を施与された繊維材料を、装置中に放置
後、スチーマーに供給し、そこで20秒間ioo℃の蒸
気で処理する。After leaving the fibrous material thus provided with a foam layer in the device, it is fed into a steamer and treated there with steam at io0° C. for 20 seconds.
洗滌及び乾燥後白地に青色の捺染が得られる。After washing and drying, a blue print is obtained on a white background.
例2
400P/m2の木綿タオル布地を染料、バット( v
at )オレンジ7 C, I, A.7 1 1
0 5の252で捺染した。Example 2 400P/m2 cotton towel fabric was dyed and vat (v
at) Orange 7 C, I, A. 7 1 1
Printed with 252 of 05.
捺染ペーストは、上記染料の外に粘稠剤として(10%
水性溶液の形の)澱粉工一テル50グ及びシリコーン消
泡剤0.52を含む。The printing paste contains, in addition to the above dye, a thickening agent (10%
50 grams of starch powder (in the form of an aqueous solution) and 0.52 grams of silicone defoamer.
捺染ユニットを出た後、また濡れている繊維材料に第1
図に記載の装置により、トリエタノールアミンーココヤ
シ脂肪酸硫酸塩及びココヤシ脂肪酸トリグリコールエー
テル硫酸塩のアンモニウム塩よりなる混合物(1:1)
2%の添加下に製造された5%水性泡沫を施与する。After leaving the printing unit, the wet textile material is again
A mixture (1:1) of triethanolamine-coco fatty acid sulfate and ammonium salt of coconut fatty acid triglycol ether sulfate was prepared using the apparatus shown in the figure.
A 5% aqueous foam prepared with a 2% addition is applied.
この泡沫の液相は5%苛性ソーダ溶液より或り、この中
には更に5%亜二チオン酸ナトリウムを溶解している。The liquid phase of the foam consists of a 5% caustic soda solution in which an additional 5% sodium dithionite is dissolved.
泡沫層の厚さは一第1図に於けるドクターブレードによ
り調節され−1.6關である。The thickness of the foam layer is adjusted by the doctor blade in FIG. 1 to -1.6 degrees.
泡沫供給装置を出ると直ちに泡沫は崩解し、そして水性
相が捺染された繊維材料に吸収される。Immediately after leaving the foam supply device, the foam disintegrates and the aqueous phase is absorbed into the printed fiber material.
液のピックアップは20%で、これは5%苛性ンーダ溶
液80mlが繊維材料1 m”にもたらされたことを意
味する。The liquid pick-up was 20%, which means that 80 ml of 5% caustic soda solution was delivered to 1 m'' of textile material.
泡沫適用後直ちに繊維材料を、乾燥せずにスチーマーに
入れ、そしてその中で1分間120℃の蒸気で処理する
。Immediately after applying the foam, the fiber material is placed, without drying, in a steamer and treated therein with steam at 120° C. for 1 minute.
かくして処理された繊維材料のす又ぎ、酸化及び洗滌の
後、白地に明るいオレンジ色の捺染が得られる。After rinsing, oxidizing and washing the fiber material thus treated, a bright orange print on a white background is obtained.
例3
3soP/mの亜麻布を、リアクティプイエロ17
C,I,A.18852を使用する以外は例1と同様に
して捺染ペーストを用いて捺染し、第3図に示す如く、
例lと同じ泡沫を施与する。Example 3 Linen cloth with 3soP/m is made of reactipuiero 17
C, I, A. Printing was carried out using the printing paste in the same manner as in Example 1 except that 18852 was used, and as shown in Fig. 3,
Apply the same foam as in Example 1.
液のピックアップは15%で、これは苛性ソーダ溶液5
2.5mlが繊維材料in上にもたらされたことを意味
する。The liquid pickup is 15%, which is 5% of the caustic soda solution.
This means that 2.5 ml was brought onto the fiber material in.
泡沫の厚さは約ITtrILであった。泡沫を施与しそ
してドクターブレードで処理した亜麻布を加熱チャンネ
ル中に60℃に於て導入し、そこで10分間貯蔵し、最
後に洗滌する。The thickness of the foam was approximately ITtrIL. The linen cloth applied with foam and treated with a doctor blade is introduced into a heating channel at 60° C., stored there for 10 minutes and finally washed.
半白の地にゴールデンイエローの柄が得られる。A golden yellow pattern is obtained on a semi-white background.
例4
アゾイツクカップリング戒分2−C.I,A37505
の15ft及び
ジアゾアミノ化合物として安定化された、そのジアゾニ
ウム塩の形のp−ニトロアニリン10グの混合物を2%
苛性ソーダ液le中に溶解し、そしてイナゴマメ粉で粘
稠化する。Example 4 Azoitsuku Coupling Precept 2-C. I, A37505
2% of a mixture of 15 ft of and 10 g of p-nitroaniline in the form of its diazonium salt stabilized as a diazoamino compound.
Dissolve in caustic soda solution and thicken with carob flour.
この捺染ペーストを125P/fflの重さを有するス
テーブルファイバー織物上に捺染し、これを乾燥する。This printing paste is printed onto a stable fiber fabric having a weight of 125 P/ffl and dried.
次いで10%水性ギ酸をココヤシ脂肪酸一トリグリコー
ルエーテルスルフエートのアンモニウム塩を基体とする
1.2%泡沫原液の添加下に発泡させ、そして第2図に
記載した装置を用いて繊維材料に施与する。10% aqueous formic acid was then foamed with the addition of a 1.2% foam stock solution based on the ammonium salt of coconut fatty acid monotriglycol ether sulfate and applied to the textile material using the apparatus described in FIG. give
液のピックアップは30%で、これは繊維材料lm上に
純粋なギ酸3752のピックアップに相当する。The liquid pick-up is 30%, which corresponds to the pick-up of pure formic acid 3752 on the fiber material lm.
泡沫の厚さは約1mrrtであった。The thickness of the foam was approximately 1 mrrt.
泡沫をドクターブレードにより処理した後、繊維材料を
60秒間空気にさらし、その際色調は極めて強く顕色さ
れる。After treating the foam with a doctor blade, the fiber material is exposed to air for 60 seconds, during which the color tone develops very strongly.
染料の顕色は赤外線により加熱することによっても強め
ることができる。The color development of the dye can also be enhanced by heating with infrared rays.
白地に赤色の捺染が得られる。A red print is obtained on a white background.
本発明は特許請求の範囲に記載の方法を要旨とするが、
尚実施の態様として下記を包含する。The gist of the present invention is the method described in the claims,
Note that the embodiments include the following.
(1)特許請求の範囲に記載の方法に於で、パジング液
または捺染ペーストが、繊維材料と泡沫との接触の際に
泡沫崩壊を惹起する泡沫崩壊剤を含有する方法。(1) A method according to the claims, wherein the padding liquid or the printing paste contains a foam disintegrating agent that causes foam collapse upon contact between the fiber material and the foam.
(2)特許請求の範囲に記載の方法に於で、セルロース
繊維及び混紡物中のセルロース部分の染色のために建染
め染料、ロイコエステル建染の染料、安定化アゾ染料ま
たは反応性染料を使用する方法。(2) In the method described in the claims, vat dyes, leucoester vat dyes, stabilized azo dyes, or reactive dyes are used for dyeing cellulose fibers and cellulose parts in blended fabrics. how to.
【図面の簡単な説明】
添付の図面第1〜4図は、本発明方法を実施するための
装置の横断面を示したものである。BRIEF DESCRIPTION OF THE DRAWINGS Figures 1 to 4 of the accompanying drawings show a cross-section of an apparatus for carrying out the method of the invention.
Claims (1)
の二相法による染色並びに捺染を固着する方法に於て、
染料の固着に必要な量の化学薬品を特に液体の少い状態
で泡沫として、あらかじめ捺染またはパジングされた繊
維材料に施与することを特徴とする方法。1. In a method for fixing dyeing and printing of cellulose fiber materials and mixtures thereof with synthetic fibers by a two-phase method,
A process characterized in that the amount of chemical necessary for dye fixation is applied, particularly as a foam in a low-liquid state, to the previously printed or padded textile material.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742416259 DE2416259C3 (en) | 1974-04-03 | Process for fixing dyeings or prints on textile goods |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS50135381A JPS50135381A (en) | 1975-10-27 |
| JPS5847513B2 true JPS5847513B2 (en) | 1983-10-22 |
Family
ID=5912072
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50039299A Expired JPS5847513B2 (en) | 1974-04-03 | 1975-04-02 | Natsusen Narabini Senshiyokunokochiyakuhou |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS5847513B2 (en) |
| AR (1) | AR205639A1 (en) |
| AT (1) | AT352673B (en) |
| BE (1) | BE827528A (en) |
| CA (1) | CA1051613A (en) |
| CH (2) | CH408675A4 (en) |
| DD (1) | DD117260A5 (en) |
| ES (1) | ES436112A1 (en) |
| FR (1) | FR2266766B1 (en) |
| GB (1) | GB1493683A (en) |
| IT (1) | IT1034768B (en) |
| NL (1) | NL7503730A (en) |
| ZA (1) | ZA751744B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63104214U (en) * | 1986-12-26 | 1988-07-06 | ||
| JPH02227321A (en) * | 1989-03-01 | 1990-09-10 | Kanto Auto Works Ltd | Automatic sun visor for vehicle |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2051885B (en) * | 1978-09-19 | 1982-10-20 | United Merchants & Mfg | Method for treating textile materials |
| DE2935413C2 (en) * | 1979-09-01 | 1986-02-27 | Küsters, Eduard, 4150 Krefeld | Device for the continuous treatment of a textile or similar material web with a treatment medium in foam form |
| DE3044409C2 (en) * | 1980-11-26 | 1983-04-28 | Mathias 4815 Schloss Holte Mitter | Device for the continuous application of a liquor in the form of foam onto a preferably textile web |
| DE3446421A1 (en) * | 1984-12-20 | 1986-07-03 | Hoechst Ag, 6230 Frankfurt | METHOD FOR FIXING PRINTS AND BLOCK COLORING WITH REACTIVE DYES IN HANGING LOOP DAMPERS |
-
1975
- 1975-01-01 AR AR258221A patent/AR205639A1/en active
- 1975-03-20 ZA ZA00751744A patent/ZA751744B/en unknown
- 1975-03-27 ES ES436112A patent/ES436112A1/en not_active Expired
- 1975-03-27 NL NL7503730A patent/NL7503730A/en not_active Application Discontinuation
- 1975-04-01 IT IT21905/75A patent/IT1034768B/en active
- 1975-04-01 AT AT243875A patent/AT352673B/en not_active IP Right Cessation
- 1975-04-01 DD DD185140A patent/DD117260A5/xx unknown
- 1975-04-01 CH CH408675D patent/CH408675A4/xx unknown
- 1975-04-01 CH CH408675A patent/CH584783B5/xx not_active IP Right Cessation
- 1975-04-02 GB GB13568/75A patent/GB1493683A/en not_active Expired
- 1975-04-02 JP JP50039299A patent/JPS5847513B2/en not_active Expired
- 1975-04-02 CA CA223,636A patent/CA1051613A/en not_active Expired
- 1975-04-03 FR FR7510425A patent/FR2266766B1/fr not_active Expired
- 1975-04-03 BE BE155062A patent/BE827528A/en not_active IP Right Cessation
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63104214U (en) * | 1986-12-26 | 1988-07-06 | ||
| JPH02227321A (en) * | 1989-03-01 | 1990-09-10 | Kanto Auto Works Ltd | Automatic sun visor for vehicle |
Also Published As
| Publication number | Publication date |
|---|---|
| DD117260A5 (en) | 1976-01-05 |
| FR2266766A1 (en) | 1975-10-31 |
| FR2266766B1 (en) | 1978-06-23 |
| AT352673B (en) | 1979-10-10 |
| CH584783B5 (en) | 1977-02-15 |
| GB1493683A (en) | 1977-11-30 |
| ATA243875A (en) | 1979-03-15 |
| CA1051613A (en) | 1979-04-03 |
| DE2416259B2 (en) | 1976-12-02 |
| IT1034768B (en) | 1979-10-10 |
| BE827528A (en) | 1975-10-03 |
| JPS50135381A (en) | 1975-10-27 |
| NL7503730A (en) | 1975-10-07 |
| AR205639A1 (en) | 1976-05-21 |
| CH408675A4 (en) | 1976-09-15 |
| DE2416259A1 (en) | 1975-10-16 |
| ZA751744B (en) | 1976-03-31 |
| ES436112A1 (en) | 1977-01-01 |
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