DE2352465A1 - PROCESS FOR COLORING AND PRINTING TEXTILE MATERIALS - Google Patents
PROCESS FOR COLORING AND PRINTING TEXTILE MATERIALSInfo
- Publication number
- DE2352465A1 DE2352465A1 DE19732352465 DE2352465A DE2352465A1 DE 2352465 A1 DE2352465 A1 DE 2352465A1 DE 19732352465 DE19732352465 DE 19732352465 DE 2352465 A DE2352465 A DE 2352465A DE 2352465 A1 DE2352465 A1 DE 2352465A1
- Authority
- DE
- Germany
- Prior art keywords
- fiber
- groups
- dyes
- case
- 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.)
- Pending
Links
- 239000004753 textile Substances 0.000 title claims description 21
- 239000000463 material Substances 0.000 title claims description 17
- 238000000034 method Methods 0.000 title claims description 14
- 238000004040 coloring Methods 0.000 title description 3
- 239000000975 dye Substances 0.000 claims description 26
- 239000000835 fiber Substances 0.000 claims description 22
- 239000004952 Polyamide Substances 0.000 claims description 14
- 229920002647 polyamide Polymers 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000000981 basic dye Substances 0.000 claims description 11
- 238000004043 dyeing Methods 0.000 claims description 9
- 210000002268 wool Anatomy 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- 239000011737 fluorine Substances 0.000 claims description 5
- 229920002239 polyacrylonitrile Polymers 0.000 claims description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 8
- 239000004744 fabric Substances 0.000 description 6
- 125000000129 anionic group Chemical group 0.000 description 5
- -1 polymethylene Polymers 0.000 description 5
- 230000002378 acidificating effect Effects 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 241000251730 Chondrichthyes Species 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 239000000986 disperse dye Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- PKALEBFTSZCHGU-UHFFFAOYSA-M n,n-diethyl-4-[2-(1,3,3-trimethylindol-1-ium-2-yl)ethenyl]aniline;chloride Chemical compound [Cl-].C1=CC(N(CC)CC)=CC=C1\C=C\C1=[N+](C)C2=CC=CC=C2C1(C)C PKALEBFTSZCHGU-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- SDGNNLQZAPXALR-UHFFFAOYSA-N 3-sulfophthalic acid Chemical compound OC(=O)C1=CC=CC(S(O)(=O)=O)=C1C(O)=O SDGNNLQZAPXALR-UHFFFAOYSA-N 0.000 description 1
- 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 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N Caprolactam Natural products O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005354 coacervation Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- SKKIWNWLPWAHTF-UHFFFAOYSA-L disodium;5-(4-acetamidoanilino)-8-amino-9,10-dioxoanthracene-1,2-disulfonate Chemical compound [Na+].[Na+].C1=CC(NC(=O)C)=CC=C1NC1=CC=C(N)C2=C1C(=O)C(C=CC(=C1S([O-])(=O)=O)S([O-])(=O)=O)=C1C2=O SKKIWNWLPWAHTF-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- JLFNLZLINWHATN-UHFFFAOYSA-N pentaethylene glycol Chemical compound OCCOCCOCCOCCOCCO JLFNLZLINWHATN-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002759 woven fabric Substances 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
- 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
- D06P1/0028—Dyeing with a coacervate system
-
- 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
- D06P1/628—Compounds containing nitrogen
-
- 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
- D06P1/64—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 without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/647—Nitrogen-containing carboxylic acids or their salts
-
- 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
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/041—Material containing basic nitrogen containing amide groups using basic 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
- 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
- D06P3/70—Material containing nitrile groups
- D06P3/76—Material containing nitrile groups using basic 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
- 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
- D06P3/82—Textiles which contain different kinds of fibres
- D06P3/8204—Textiles which contain different kinds of fibres fibres of different chemical nature
- D06P3/8271—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing amide and nitrile groups
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Description
DIpWn91RWIRTH-DnV-SCHMtED-KOWARZlK Dipping. G. DANNENBERG ■ Dr. P. WEINHOLD · Dr, D. GUDELDIpWn 91 RWIRTH-DnV-SCHMtED-KOWARZlK Dipping. G. DANNENBERG ■ Dr. P. WEINHOLD · Dr, D. GUDEL
281134 6FRANKFUBTAMMAiN281134 6FRANKFUBTAMMAiN
TELEFON C0611)TELEPHONE C0611)
267014 GH. ESCHENHEIMER STHASSE 33267014 GH. ESCHENHEIMER STHASSE 33
Pase, 150-3451
Wd/Seh Pase, 150-3451
Wd / Seh
SAHBOZ JUG.
B a se 1
SchweizSAHBOZ JUG. B a se 1
Switzerland
Verfahren 2ürft Färben und Bedrucken von textlien MaterialienProcess 2 may dye and print textiles materials
Die vorliegende Erfindung betrifft ein Verfahren zum Färben und Bedrücken von textlien Materialien, wobei diese durch entsprechende Vorbehandlung mit basischen Farbstoffen so gefärbt werden können, dass die Anfärbbarkeit verbessert wird.The present invention relates to a method for Dyeing and printing of textile materials, whereby this by appropriate pretreatment with basic Dyes can be colored so that the dyeability is improved.
— 409818/1092- 409818/1092
- 2 - ' Case 150-3431 - 2 - ' Case 150-3431
Textile Materialien wie Gewebe oder Gewirke die einerseits basisch anfärbbare Pasern oder Fäden und andererseits sauer anfärbbare Fasern oder Fäden wie natürliche oder synthetische Polyamide enthalten, bieten Schwierigkeiten beim Färben oder Bedrucken. Bei der Verwendung von basischen Farbstoffen alleine oder im Gemisch mit anionischen Farbstoffen werden ungenügende Resultate erzielt/ da es nicht möglich ist, sov;ohl die basisch als auch die sauer anfärbbaren Anteile des textilen Materiales gleich tief oder nuancengleich anzufärben bzw. zu bedrucken und gleichzeitig gute Echtheitseigenschaften wie die Wasch-, Schweiss- oder Wasserechtheit zu erreichen. V/erden nur basische bzw. kationische Farbstoffe eingesetzt, so ist die Anfärbung des Wollanteils ungenügend, da diese Farbstoffklasse die Wolle nur anschmutzt und nicht echt färbt, wobei schlechte Echtheiten und ein schippriges Aussehen der gefärbten Stellen resultieren. Wird wiederum eine Mischung aus kationischen und anionischen Farbstoffen eingesetzt, so ist die Anschmutzung des Kollanteils durch den kationischen Farbstoff unvermeidlich und die Echtheiten dementsprechend ungenügend. Zudem zeigen Druckpasten, die Mischungen aus anionischen und kationischen Farbstoffen enthalten, nur sehr begrenzteTextile materials such as woven or knitted fabrics, on the one hand basic dyeable fibers or threads, and on the other hand Acid-dyeable fibers or threads, such as natural or synthetic polyamides, present difficulties when dyeing or printing. When using basic dyes alone or in a mixture with anionic ones Inadequate results are obtained from dyes / since it is not possible to use both the basic and the acid-dyeable parts of the textile material the same to be colored or printed deeply or with the same nuances and to achieve good fastness properties such as washing, perspiration or water fastness at the same time. If only basic or cationic dyes are used, the dyeing of the wool content is insufficient, because this class of dyes only soils the wool and does not dye fast, resulting in poor fastness properties and a flaky appearance of the dyed areas. If, in turn, a mixture of cationic and anionic dyes is used, the soiling of the Collar content inevitable due to the cationic dye and the fastness properties are accordingly inadequate. In addition show printing pastes containing mixtures of anionic and cationic dyes only to a very limited extent
4 09 8 1.8/1.0 9.24 09 8 1.8 / 1.0 9.2
- 3 - Case 150-3431- 3 - Case 150-3431
Lagerstabilitat, indem irreversible Reaktionen wie z.B. Ausfällungen, auftreten.Storage stability by irreversible reactions such as precipitation, occur.
Zur Erzeugung von Mehrfarbeneffekten auf natürlichem und synthetischem Polyamidfasermaterialf ist es schon bekannt, das Polyamidfasermateriäl mit einer wässrigen Lösung von mindestens einer farblosenf faserreaktiven Verbindung vor-2ubehanäeln und dann mit nichtbehandeltem und/oder mit mindestens einem andersartig vorbehandelten Fasermaterial zu verarbeiten und mit einem faseraffinen Farbstoff oder Gemisch solcher Farbstoffe zu färben.For the production of multicolour effects on natural and synthetic polyamide fiber material, it is already known to f, the Polyamidfasermateriäl process with an aqueous solution of at least one colorless f fiber-reactive compound prior-2ubehanäeln and then with untreated and / or with at least one otherwise pretreated fiber material and having an affinity for the fiber To dye dye or mixture of such dyes.
Es ist weiter auch schon bekannt, dass zum Ton-in-Ton Färben von Gemischen aus einem Elastomer-/Polyamid-Textilfasergemisch z.B. einem Stretch-Mischgewebe aus Polyurethan- und Polyamidfasergemisch, das Fasergemisch mit einem anionischen Blockierungsmittel vorzubehandeln und dann mit einem hydrophilen Farbstoff zu färben.It is also known that for tone-on-tone Dyeing of mixtures of an elastomer / polyamide textile fiber mixture E.g. a stretch blended fabric made of a polyurethane and polyamide fiber blend, the fiber blend with an anionic one Pre-treating blocking agents and then coloring with a hydrophilic dye.
Schliesslich ist es bekannt,t Textilmaterial aus natürlichen Polyamiden gegen anionische Farbstoffe durch Behandlung mit farblosen faserreaktiven Verbindungen zu reservieren. Die mit diesen Verbindungen behandelten Textilien aus natürlichem Polyamid zeigen dann eine erhöhte Anfärbbarkeit für basische Farbstoffe.Finally, it is known that textile material made of natural polyamides t reserve against anionic dyes by treatment with the colorless fiber-reactive compounds. The textiles made of natural polyamide treated with these compounds then show an increased dyeability for basic dyes.
409818/1092409818/1092
- 4 - . Case 15O-3431 - 4 -. Case 15O-3431
Es wurde nun gefunden, dass es möglich ist, sauer anfärbbare Fasern, Fäden oder daraus hergestellte Textilien vor allem auf Basis natürlicher oder synthetischer Polyamide durch eine Vorbehandlung derart zu modifizieren/ dass diese nun auch im Gemisch mit modifizierten Polyacrylnitril- oder Polyesterfasern unter Umgehung der erwähnten Nachteile mit basische Farbstoffe enthaltenden' Färbeflotten oder Druckpasten gefärbt oder bedruckt werden können.It has now been found that it is possible to stain acidic Fibers, threads or textiles made from them, primarily based on natural or synthetic polyamides to be modified by a pretreatment in such a way / that this is now also mixed with modified polyacrylonitrile or polyester fibers, circumventing the disadvantages mentioned, with dye liquors containing basic dyes or printing pastes can be colored or printed.
Die vorliegende Erfindung bezieht sich auf ein Verfahren zum Färben und Bedrucken von textlien Materialien, welche, sowohl basisch anfärbbare Fasern als auch solche aus natürlichen oder synthetischen Polyamiden enthalten/ welches dadurch gekennzeichnet ist, dass man vor dem Färbe- oder Druckprozess mit einer basische Farbstoffe enthaltendenThe present invention relates to a method for dyeing and printing textile materials, which, both basic dyeable fibers and those made of natural or synthetic polyamides / which is characterized in that one before the dyeing or Printing process with a basic dye containing
Farbflotte das textile Material mit Flotten oder Pasten, enthaltend eine Lösung oder Dispersion einer oder mehrerer solcher farbloser, faserreaktiver Verbindung, die mit Polyamidfasern zu reagieren vermögen und Carbonsäure- oder Sulfonsäuregruppen im Molekül enthalten, vorbehandelt und diese fixiert.Dye liquor the textile material with liquors or pastes containing a solution or dispersion of one or more such colorless, fiber-reactive compound that is able to react with polyamide fibers and carboxylic acid or Containing sulfonic acid groups in the molecule, pretreated and fixed them.
409818/1092409818/1092
- 5 - Case 150-3431- 5 - Case 150-3431
Die Erfindung betrifft im weiteren die so erhaltenen gefärbten textlien Materialien sowie die aus derartigen behandelten textlien Materialien hergestellten Gewebte, Gewirke/ Teppiche, Vliese etc.The invention also relates to the colored ones obtained in this way textile materials as well as woven fabrics made from such treated textile materials, Knitted fabrics / carpets, fleeces etc.
Basisch anfärbbare Fasern, Fäden oder daraus hergestellte lextilien sind vor allem modifizierte Polyacrylnitrilfasern und modifizierte Polyesterfasern, welche "bereits "bekannt sind, z.B solche, die Sulfonsäuregruppen, wie sie unter Verwendung von SuIfophthaisäure entstehen, oder Carboxylgruppen als Substituenten in der Kette enthalten. Sauer anfärbbare Fasern, Fäden oder daraus hergestellte Textilien sind vor allem natürliche Polyamide wie Wolle oder Seide aber auch Leder, sowie synthetische Polyamide. Zu letzteren zählen beispielsweise die polymeren Produkte des /*-Caprolactams, wie auch die Kondensationsprodukte von Dikarbonsäuren wie PoIymethylendikarbonsäuren, wie die Adipinsäure und Polymethylendiamine wie Hexamethylendiamin. Solche Produkte sind als Nylon 6# Nylon 7, Nylon 66, Nylon 76, Nylon 6IO usw. bekannte Basically dyeable fibers, threads or textiles made therefrom are above all modified polyacrylonitrile fibers and modified polyester fibers which are "already" known, for example those which contain sulfonic acid groups, as formed using sulfophthalic acid, or carboxyl groups as substituents in the chain. Acid-dyeable fibers, threads or textiles made from them are primarily natural polyamides such as wool or silk, but also leather and synthetic polyamides. The latter include, for example, the polymeric products of / * - caprolactam, as well as the condensation products of dicarboxylic acids such as polymethylene dicarboxylic acids such as adipic acid and polymethylene diamines such as hexamethylene diamine. Such products are known as nylon 6 #, nylon 7, nylon 66, nylon 76, nylon 6IO, and so on
Unter farblosen, faserreaktiven.Verb indungen sind insbesondere Verbindungen zu verstehen, in denen ein beliebiger, gegebenenfalls substituierter und/oder Hetero-Among colorless, fiber-reactive compounds are in particular To understand compounds in which any, optionally substituted and / or hetero-
409818/1092409818/1092
~ 6 - Case 150-3431 ~ 6 - Case 150-3431
atome enthaltender, farbloser organischer Rest, der vorzugsweise nicht bemerkenswert flüchtig sein soll, an eine Gruppe gebunden ist, die leicht mit einem Stickstoffatom des Polyamids zur Reaktion gebracht v/erden kann. Solche Gruppen enthalten z.B. reaktionsfähige Halogenatome, insbesondere Fluor-, Chlor- oder Bromatome oder eine oderAtoms-containing, colorless organic residue, which should preferably not be noticeably volatile, to a Group is bonded which can easily be reacted with a nitrogen atom of the polyamide. Such Groups contain, for example, reactive halogen atoms, in particular fluorine, chlorine or bromine atoms or one or
mehrere C-C-Doppelbindungen. Bevorzugte reaktive Gruppen sind z.B. halogenhaltige Triaziny!gruppen, insbesondere Dihalogentriazinylgruppen, aber auch Trihalogenpyrimidyl-, Carbonsäurehalogenid- oder Sulfonsäurehalogenidgruppen. Solche Verbindungen entsprechen zum Beispiel der Formelseveral C-C double bonds. Preferred reactive groups are e.g. halogen-containing triaziny groups, in particular Dihalotriazinyl groups, but also trihalopyrimidyl, carboxylic acid halide or sulfonic acid halide groups. Such compounds correspond, for example, to the formula
Hai—f Shark f
N NN N
HaiShark
v/orin Hai Fluor, Chlor oder Brom, X eine Gruppe der Formelv / orin shark fluorine, chlorine or bromine, X is a group of formula
SO3HSO 3 H
COOH ·COOH
SO3HSO 3 H
—O-O
COOHCOOH
SO5HSO 5 H
-NH-NH
409818/1092409818/1092
cooircooir
—NH—NH
\jrf\Zs\ V.COOID& » \ jrf \ Zs \ V.COOID & »
SAD ORIGINALSAD ORIGINAL
- 7 - Case' 150-3431- 7 - Case '150-3431
;ΟΙΟΗ$Ρ3Το. odcr ; ΟΙΟΗ $ Ρ3Το. or
η 1, 2 oder 3 und R eine Alky!gruppe mit 1-4 Kohlenstoffatomen bedeuten, die -SO3H- und -COOH-Gruppen vorzugsweise nicht in ortho-Stellung "zum Sauerstoff- oder Imino-Brückenglied an den aromatischen Kern gebunden sind und die aromatischen Kerne z.B. Halogenatome, wie Fluor, Chlor, Brom, Nitro-, Cyan- oder Alkyl- oder Alkoxygruppen mit 1-4 Kohlenstoffatoraen als weitere Substi·'-tuenten tragen können.η 1, 2 or 3 and R is an alkyl group with 1-4 carbon atoms, the -SO 3 H and -COOH groups are preferably not bonded to the aromatic nucleus in the ortho position "to the oxygen or imino bridge member and the aromatic nuclei, for example, halogen atoms such as fluorine, chlorine, bromine, nitro, cyano or alkyl or alkoxy groups with 1-4 carbon atoms can carry as further substituents.
Für die Herstellung und Applikation der Flotten und Pasten kann für die erfindungsgemässe Anwendung für Textilien g die Fasergeiaisehe aus basisch und sauer anfärbbaren Anteilen enthalten, analog verfahren werden, wie dies bereits in der Schweizerischen Patentschrift Nr, 525997 beschrieben ist,," Die in der vorgenannten Patentschrift in den Beispielen aufgeführten spezifischen farblosen, faserreaktiven Verbindungen sind erfindungsgemäss ebexrfalls gut verwertbar.For the production and application of the liquors and pastes, for the use according to the invention for textiles g containing the fiber gelatin from basic and acid-dyeable components, the procedure is analogous to that already described in Swiss Patent No. 525997 ,, "The in the aforementioned The specific colorless, fiber-reactive compounds listed in the examples can also be used well according to the invention.
Die Färbeflotte oder die Druckpaste kann auch als Koazervatsystem vorliegen. Ein besonderes i-5erkmal des erfindungsgeraässen Verfahrens ist es, dass die erwähnten tex-The dye liquor or the printing paste can also be used as a coacervate system are present. A special i-5 feature of the invention device Procedure is that the mentioned text
409818/1092409818/1092
- 8 - Case 150-3431- 8 - Case 150-3431
feilen Materialien^ welche basisch und sauer anfärbbaren Anteil enthalten, ausschliesslich mit basischen Farbstoffen gefärbt oder bedruckt v/erden können. Basische Farbstoffe, die zum Färben von Polyacrylfasern empfohlen v/erden, sind z.B. in Colour Index, Third Edition, Band I., Seiten 1607-1688 aufgezählt. Innerhalb der vorliegenden Erfindung liegt es auch solche textile Materialien zu verwenden, die neben basisch und sauer anfärbbaren Komponenten auch z.B. noch Polyesterfasern enthalten, die mit Dispersionsfarbstoffen anfärbbar sind. Ebenso können die Farbstofflotten oder Pasten neben dem basischen Farbstoff oder den basischen Farbstoffen auch saure Farbstoffe, Dispersionsfarbstoffe, Pigmente und weitere Hilfsmittel enthalten.filing materials ^ which can be dyed alkaline and acidic Contain portion, can only be colored or printed with basic dyes. Basic dyes, which are recommended for dyeing polyacrylic fibers, are e.g. in Color Index, Third Edition, Volume I., pages 1607-1688 listed. Such textile materials are also within the present invention to use which, in addition to basic and acidic dyeable components, also contain e.g. polyester fibers, which can be dyed with disperse dyes. Likewise, the dye liquors or pastes in addition to the basic dye or the basic dyes also acidic dyes, disperse dyes, pigments and contain additional aids.
Man färbt oder bedruckt unter den üblichen bekannten Bedingungen, 2.B. kontinuierlich. In den nachfolgenden Beispielen bedeuten Teile Gewichtsteile, Prozente Gewichtsprozente, Grade Celsiüsgrade.One dyes or prints under the usual known conditions, 2.B. continually. In the examples below Parts mean parts by weight, percentages mean percentages by weight, degrees of Celsius.
409818/1092409818/1092
- 9 - ' Case 150-3431 .- 9 - 'Case 150-3431.
B e i s ρ i' e T ' 1 - B ice ρ i 'e T' 1 -
Ein Gewirke, bestehend aus 50 % modifizierter Polyacryl-Tiitrilfaser und 5O % Wolle wird in einem Bad vorbehandelt. Das Behandlungsbad enthält/ bei einem Flottenverhältnis von 1:35, 4 % 2r4-Dichlor~6- (ßhenylamino-41—Sulfonsäure) -1,3,5-triazin- (berechnet auf das Warengewicht). Der pH-Wert wird mit Ameisensäure auf 4?5 eingestellt. Das Bad wird dann auf 6O°C erwärmt, das Gewirke zugegeben und im Bad leicht bewegt. Die Temperatur wird auf 800C gesteigert und die Behandlung eine Stunde fortgesetzt. Anschliessend wird der pH-Wert mit Ammoniak auf 9 eingestellt und das Gewebe so weitere 20 Minuten behandelt. Zum Schluss wird warm und kalt gespült und getrocknet. Das so vorbehandelte Material wird mit einer Druckpaste bedruckt, die 2O g des Farbstoffes CI. Basic Violet 16,A knitted fabric consisting of 50% modified polyacrylic-titanium fiber and 50% wool is pretreated in a bath. The treatment bath contains / with a liquor ratio of 1:35, 4% 2 r 4-dichloro-6- (phenylamino-4 1 -sulfonic acid) -1,3,5-triazine- (calculated on the weight of the goods). The pH value is adjusted to 4 ? With formic acid. 5 set. The bath is then heated to 60 ° C., the knitted fabric is added and it is gently agitated in the bath. The temperature is increased to 80 ° C. and the treatment is continued for one hour. The pH is then adjusted to 9 with ammonia and the tissue is treated in this way for a further 20 minutes. Finally, it is rinsed warm and cold and dried. The material pretreated in this way is printed with a printing paste, the 20 g of the dye CI. Basic Violet 16,
Const. No. 48.013Const. No. 48.013
50 g Johannisbrotkernmehl, veräthert (Kandels-50 g locust bean gum, etherified (candy
produkt), • 30 g Benzylalkohol,product), • 30 g benzyl alcohol,
2,5 g Weinsäure,
897,5 g Wasser,2.5 g tartaric acid,
897.5 g water,
enthält. Nach dem Druck wird die Ware getrocknet und 30 Minuten mit Darapf von 0,5 atü gedämpft. Die so fixierten Drucke v/erden zunächst kalt gespült, bei 50°Ccontains. After printing, the goods are dried and steamed for 30 minutes with a steam of 0.5 atmospheres. The so fixed Prints are first rinsed cold at 50 ° C
" 409818/1092 ·"409818/1092
- 10 - ' Case 150-3431- 10 - 'Case 150-3431
geseift, gespült und getrocknet. Die resultierenden Drucke zeigen eine gleichmässige Anfärbung des Polyacrylnitrils und Wollanteils sov/ie gute Gebrauchsechtheiten.soaped, rinsed and dried. The resulting prints show uniform coloring of the polyacrylonitrile and wool content as well as good fastness properties.
B e i s ρ i e 1 B e i s ρ i e 1 22
Ein Gewebe, welches zu 40 % aus modifizierter Polyacrylnitrilfaser und 60 % Wolle besteht, wird wie in Eeispiel 1 vorbehandelt und anschliessend mit einer Druckpaste, die als Koazervatsystem vorliegt, behandelt. Diese Druckpaste wird folgendermassen hergestellt:A fabric which consists of 40% modified polyacrylonitrile fiber and 60% wool is pretreated as in Example 1 and then treated with a printing paste which is present as a coacervate system. This printing paste is produced as follows:
10 Teile Nonyl-phenyl-pentaglykoläther10 parts of nonyl phenyl pentaglycol ether
undand
50 Teile einer 20%igen, wässrigen Lösung von Ricinoleinsäure- und Oleinsäureestersulfonatnatriumsalz werden in50 parts of a 20% aqueous solution of ricinoleic acid and oleic acid ester sulfonate sodium salt are used in
•5OO Teilen Verdickung, bestehend aus 22%.Kristallgummi , 13% aufgeschlossene Stärke und 65% V/asser mit Hi.lfe eines Propellerrührers bei Raumtemperatur eingerührt, v/obei sich zv/ei wässrige Phasen bilden nach dem Grundsatz der Koazervation. 5 Teile Weinsäure 50%ig wird zugegeben, ansehlies-• 5OO parts of thickening, consisting of 22% crystal rubber , 13% digested starch and 65% v / ater with the aid of a propeller stirrer stirred in at room temperature, v / obei zv / ei aqueous phases form after Principle of coacervation. 5 parts tartaric acid 50% is added, then
send werden
5 Teile des Farbstoffes C.I„ Basic Violet 16, undbe send
5 parts of the dye CI "Basic Violet 16, and
4Q98m7-i0924Q98m7-i092
11 - Case 150-343111 - Case 150-3431
3 Teile des Farbstoffes C.I. Acid Blue 23 in .427....TeIIe- heissem Kasser zugegeben und öle so3 parts of the dye C.I. Acid Blue 23 in .427 .... TeIIe added to the hot pot and oil like that
1000 Teile erhaltene Lösung gut gerührt«1000 parts of the solution obtained, stirred well «
Claims (7)
vox"2ugsvfeise nicht in ortho-Stellung zum Sauerstoff oder Imino-Brückenglied an den aromatischen Kern ge bunden sind und die aromatischen Kerne z.B. Halogen atome, wie Fluor, Chlor, Brom, Nitro-, Cyan- oder
Alkyl- oder Alkoxygruppen mit 1-4 Kohlenstoffatomenη 1, 2 or 3 and R is an Alky! group with 1-4 carbon atoms, the --SO 3 H and -COOH groups
vox "2ugsvfeise are not bound to the aromatic nucleus in the ortho position to the oxygen or imino bridge member and the aromatic nuclei, for example, halogen atoms, such as fluorine , chlorine, bromine, nitro, cyano or
Alkyl or alkoxy groups with 1-4 carbon atoms
werden» - 'as further substituents can be used
will" - '
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1547372A CH556943A (en) | 1972-10-23 | 1972-10-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2352465A1 true DE2352465A1 (en) | 1974-05-02 |
Family
ID=4409380
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19732352465 Pending DE2352465A1 (en) | 1972-10-23 | 1973-10-19 | PROCESS FOR COLORING AND PRINTING TEXTILE MATERIALS |
Country Status (8)
Country | Link |
---|---|
BE (1) | BE806372A (en) |
CH (1) | CH556943A (en) |
DE (1) | DE2352465A1 (en) |
ES (1) | ES419821A1 (en) |
FR (1) | FR2203907B1 (en) |
GB (1) | GB1444426A (en) |
IT (1) | IT1008582B (en) |
NL (1) | NL7314403A (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5795354A (en) * | 1987-03-25 | 1998-08-18 | Commonwealth Scientific And Industrial Research Organization | Process for dyeing wool and other keratin fibres |
ZA907220B (en) * | 1989-09-11 | 1991-07-31 | Invicta Group Ind Pty Ltd | Textile treatment |
WO1991010006A1 (en) * | 1990-01-02 | 1991-07-11 | Invicta Group Industries Pty Ltd | Textile treatment |
US5571444A (en) * | 1989-09-11 | 1996-11-05 | Invicta Group Industries Pty Ltd. | Textile treatment |
AU641181B2 (en) * | 1989-09-11 | 1993-09-16 | Sandoz Ltd. | Textile treatment using triazine as binding agent and sulfonated aromatic hydroxy as barrier agent |
AU688268B2 (en) * | 1992-08-12 | 1998-03-12 | Clariant Finance (Bvi) Limited | Method of increasing the spf rating and compounds suitable for increasing the spf rating of fibre or fabric |
US20050204487A1 (en) * | 2004-03-18 | 2005-09-22 | Reiyao Zhu | Dyeing of modacrylic/aramid fiber blends |
US8236385B2 (en) | 2005-04-29 | 2012-08-07 | Kimberly Clark Corporation | Treatment of substrates for improving ink adhesion to the substrates |
JP2024507613A (en) | 2020-12-18 | 2024-02-21 | アルフローマ アイピー ゲゼルシャフト ミット ベシュレンクテル ハフツング | Printing of mixed fibers, woven and non-woven or knitted fabrics |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1026759A (en) * | 1949-07-14 | 1953-05-04 | Basf Ag | Process for producing tone-on-tone or multicolored effects on fabrics |
GB1161411A (en) * | 1965-11-01 | 1969-08-13 | Ici Ltd | A process for Dyeing Textile Materials and the Textile Materials so obtained |
GB1161005A (en) * | 1967-01-07 | 1969-08-13 | Geigy Uk Ltd | Dyeing Process |
FR1574077A (en) * | 1968-04-11 | 1969-07-11 |
-
1972
- 1972-10-23 CH CH1547372A patent/CH556943A/xx unknown
-
1973
- 1973-10-19 GB GB4874373A patent/GB1444426A/en not_active Expired
- 1973-10-19 DE DE19732352465 patent/DE2352465A1/en active Pending
- 1973-10-19 NL NL7314403A patent/NL7314403A/xx not_active Application Discontinuation
- 1973-10-20 ES ES419821A patent/ES419821A1/en not_active Expired
- 1973-10-22 BE BE136946A patent/BE806372A/en unknown
- 1973-10-23 FR FR7337735A patent/FR2203907B1/fr not_active Expired
- 1973-10-23 IT IT5327873A patent/IT1008582B/en active
Also Published As
Publication number | Publication date |
---|---|
FR2203907B1 (en) | 1977-08-19 |
CH556943A (en) | 1974-12-13 |
FR2203907A1 (en) | 1974-05-17 |
BE806372A (en) | 1974-04-22 |
IT1008582B (en) | 1976-11-30 |
CH1547372A4 (en) | 1974-02-15 |
NL7314403A (en) | 1974-04-25 |
ES419821A1 (en) | 1976-08-01 |
GB1444426A (en) | 1976-07-28 |
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