DE1247261B - Process for dyeing structures made of hydrophobic materials - Google Patents
Process for dyeing structures made of hydrophobic materialsInfo
- Publication number
- DE1247261B DE1247261B DEF36061A DEF0036061A DE1247261B DE 1247261 B DE1247261 B DE 1247261B DE F36061 A DEF36061 A DE F36061A DE F0036061 A DEF0036061 A DE F0036061A DE 1247261 B DE1247261 B DE 1247261B
- Authority
- DE
- Germany
- Prior art keywords
- hydrophobic materials
- structures made
- dyeing
- quinone
- dyeing structures
- 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
- 238000004043 dyeing Methods 0.000 title claims description 7
- 230000002209 hydrophobic effect Effects 0.000 title claims description 4
- 239000000463 material Substances 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 4
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 9
- UKLNMMHNWFDKNT-UHFFFAOYSA-M sodium chlorite Chemical compound [Na+].[O-]Cl=O UKLNMMHNWFDKNT-UHFFFAOYSA-M 0.000 claims description 3
- 229960002218 sodium chlorite Drugs 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- -1 alkali metal dichromate Chemical class 0.000 claims description 2
- 150000001491 aromatic compounds Chemical class 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 238000010186 staining Methods 0.000 claims 1
- 238000009835 boiling Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000000835 fiber Substances 0.000 description 4
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 4
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 2
- RLQZIECDMISZHS-UHFFFAOYSA-N 2-phenylcyclohexa-2,5-diene-1,4-dione Chemical compound O=C1C=CC(=O)C(C=2C=CC=CC=2)=C1 RLQZIECDMISZHS-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 235000010265 sodium sulphite Nutrition 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
- D06P1/008—Preparing dyes in situ
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Description
DEUTSCHESGERMAN
PATENTAMTPATENT OFFICE
Int. Cl.;Int. Cl .;
D 06pD 06p
Deutsche Kl.: 8 m-1/01German class: 8 m-1/01
Nummer: 1247261 Number: 1247261
Aktenzeichen: F 36061IV c/8 mFile number: F 36061 IV c / 8 m
Anmeldetag: 4. November 1960 Filing date: November 4 , 1960
Auslegetag: 17. August 1967 Opened on: August 17 , 1967
Gegenstand des Patentes 1139 810 ist ein Verfahren zum Färben von Gebilden, wie Fäden, Fasern, Folien, Bändern u.dgl., aus hydrophoben Materialien, wie aromatischen Polyestern, insbesondere Polyäthylenterephthalaten, synthetischen Polyamiden und Polyurethanen, Polyacrylnitril und dessen Mischpolymerisaten, Celluloseestern und Polyolefinen, wobei man die zu färbenden Gebilde zunächst mit primäre und/oder sekundäre Aminogruppen enthaltenden aromatischen Verbindungen und anschließend mit Chinonen behandelt.The subject of patent 1139 810 is a process for dyeing structures such as threads, fibers, foils, tapes, etc., made of hydrophobic materials such as aromatic polyesters, in particular polyethylene terephthalates, synthetic polyamides and polyurethanes, polyacrylonitrile and its copolymers, cellulose esters and polyolefins , whereby the structures to be colored are first treated with aromatic compounds containing primary and / or secondary amino groups and then treated with quinones.
In weiterer Bearbeitung des im Hauptpatent näher erläuterten Erfindungsgedankens wurde nun gefunden, daß man in vielen Fällen besonders günstige Ergebnisse erzielt, wenn man den Färbebädern bzw. Klotzflotten, welche die Chinonkomponenten enthalten, noch AlkaIibichromat in Gegenwart von Säure oder Natriumchlorit, zusetzt. Hiermit wird ein vorzeitiger und unerwünschter Verbrauch an Chinonkomponente, bevor diese auf die Faser aufzieht bzw. mit der Aminkomponente zum Farbstoff entwickelt wird, vermieden und damit die Farbstoffausbeuteund die Qualität der erzielten Färbung besonders hinsichtlich der Reibechtheit verbessert.In further processing of the inventive concept explained in more detail in the main patent, it has now been found that in many cases particularly favorable results are achieved if the dyebaths or Padding liquors which contain the quinone components, or alkali dichromate in the presence of acid or sodium chlorite. This prevents premature and undesirable consumption of the quinone component, before it is absorbed onto the fiber or developed into a dye with the amine component is avoided, and thus the dye yield and the quality of the dyeing achieved, particularly with regard to it the rubbing fastness improved.
Verfahren zum Färben von Gebilden
aus hydrophoben MaterialienProcess for coloring structures
made of hydrophobic materials
Zusatz zum Patent: 1139 810 Addendum to the patent: 1139 810
Anmelder:Applicant:
Farbenfabriken Bayer Aktiengesellschaft,
LeverkusenPaint factories Bayer Aktiengesellschaft,
Leverkusen
Als Erfinder benannt:Named as inventor:
Dr. Max Schwarz, Leverkusen;Dr. Max Schwarz, Leverkusen;
Dr. Walter Wunder, Köln-Flittard;Dr. Walter Wunder, Cologne-Flittard;
Dr. Winfried Kruckenberg, LeverkusenDr. Winfried Kruckenberg, Leverkusen
5 g Polyäthylenglykolterephthalatfaser in Form von Strangware werden in einem Bad von 200 ml Wasser mit 0,4 g 4-Amino-2'-methoxydiphenylamin unter Zusatz von 0,4 g eines üblichen Dispergiermittels, 2 g/1 Natriumsulfid und 3 g/1 Trichlorbenzol 1 bis 1V2 Stunden bei Kochtemperatur behandelt. Nach einer Zwischenspülung der Ware wird der Farbstoff in einem Bad von 200 ml Wasser mit 0,2 g 2,5-Dichlorchinon, 0,05 g Kahumbichromat und 0,05 g Schwefelsäure während einer halben Stunde bei Kochtemperatur entwickelt. 5 g Polyäthylenglykolterephthalatfaser in the form of hanks are -methoxydiphenylamin in a bath of 200 ml of water with 0.4 g of 4-amino-2 ', with the addition of 0.4 g of a conventional dispersing agent, 2 g / 1 sodium sulfide and 3 g / 1 trichlorobenzene Treated for 1 to 1½ hours at boiling temperature. After an intermediate rinse of the goods, the dye is developed in a bath of 200 ml of water with 0.2 g of 2,5- dichloroquinone, 0.05 g of potassium dichromate and 0.05 g of sulfuric acid for half an hour at boiling temperature.
Nach einer reduktiven Nachbehandlung erhält man eine schwarze Färbung mit ausgezeichneten Echtheiten. Bei Verwendung von 0,5 g Phenylbenzochinon an Stelle von 2,5-Dichlorchinon erhält man eine blaugraue Färbung.After a reductive aftertreatment, a black dyeing with excellent fastness properties is obtained. If 0.5 g of phenylbenzoquinone is used instead of 2,5- dichloroquinone, a blue-gray color is obtained.
5 g Polyäthylenglykolterephthalatfaser werden, wie im Beispiel 1 beschrieben, vorbehandelt. Die Entwicklung des Farbstoffs erfolgt in einem Bad von 200 ml Wasser, welches mit 0,5 g Salzsäure angeteigtes Benzochinon (0,25 g) und 0,2 g Kaliumbichromat enthält, während 30 Minuten bei Kochtemperatur. 5 g of polyethylene glycol terephthalate fibers are, as described in Example 1 , pretreated. The dye is developed in a bath of 200 ml of water, which contains benzoquinone (0.25 g) made into a paste with 0.5 g of hydrochloric acid and 0.2 g of potassium dichromate, for 30 minutes at boiling temperature.
Man erhält eine schwarze Färbung mit guten Echtheiten nach der üblichen reduktiven Nachbehandlung.A black dyeing with good fastness properties is obtained after the customary reductive aftertreatment.
g Polyäthylenglykolterephthalatfaser werden in einem Bad von 200 ml Wasser mit 0,4 g 4-Benzoylammo-2,5-dimethoxyanüin, 0,4 g eines üblichen Dispergiermittels, 2 g/1 Natriumsulfit und 3 g/1 Trichlorbenzol 1 bis IVi Stunden bei Kochtemperatur behandelt. Nach einer Zwischenspülung der Ware wird der Farbstoff in einem Bad von 200 ml Wasser mit 0,2 g 2,5-Dichlorchinon und .0,2 g Natriumchlorit während einer halben Stunde bei Kochtemperatur entwickelt.g of polyethylene glycol terephthalate fiber are placed in a bath of 200 ml of water with 0.4 g of 4- benzoylammo -2,5 -dimethoxyanüin, 0.4 g of a conventional dispersant, 2 g / 1 sodium sulfite and 3 g / 1 trichlorobenzene for 1 to 1.5 hours at boiling temperature treated. After an intermediate rinse of the goods, the dye is developed in a bath of 200 ml of water with 0.2 g of 2,5- dichloroquinone and .0.2 g of sodium chlorite for half an hour at boiling temperature.
Nach einer reduktiven Nachbehandlung erhält man eine braunschwarze Färbung mit guten Echtheiten.After a reductive aftertreatment, a brown-black dyeing with good fastness properties is obtained.
Claims (1)
Deutsche Auslegeschrift Nr. 1079 587. Considered publications:
German publication No. 1079 587.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF36061A DE1247261B (en) | 1960-06-23 | 1960-11-04 | Process for dyeing structures made of hydrophobic materials |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1960F0031493 DE1139810B (en) | 1960-06-23 | 1960-06-23 | Process for dyeing structures made of hydrophobic materials |
| DEF36061A DE1247261B (en) | 1960-06-23 | 1960-11-04 | Process for dyeing structures made of hydrophobic materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1247261B true DE1247261B (en) | 1967-08-17 |
Family
ID=7096294
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF36061A Pending DE1247261B (en) | 1960-06-23 | 1960-11-04 | Process for dyeing structures made of hydrophobic materials |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE1247261B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1284933B (en) * | 1960-11-10 | 1968-12-12 | Bayer Ag | Process for dyeing structures made of hydrophobic materials |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1079587B (en) * | 1957-01-15 | 1960-04-14 | Hoechst Ag | Process for the production of real black coloring on textile material or foils from high-melting, linear polyesters containing six-membered carbocycles |
-
1960
- 1960-11-04 DE DEF36061A patent/DE1247261B/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1079587B (en) * | 1957-01-15 | 1960-04-14 | Hoechst Ag | Process for the production of real black coloring on textile material or foils from high-melting, linear polyesters containing six-membered carbocycles |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1284933B (en) * | 1960-11-10 | 1968-12-12 | Bayer Ag | Process for dyeing structures made of hydrophobic materials |
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