DE1105837B - Dyeing of polyester fiber materials - Google Patents

Dyeing of polyester fiber materials

Info

Publication number
DE1105837B
DE1105837B DEF25424A DEF0025424A DE1105837B DE 1105837 B DE1105837 B DE 1105837B DE F25424 A DEF25424 A DE F25424A DE F0025424 A DEF0025424 A DE F0025424A DE 1105837 B DE1105837 B DE 1105837B
Authority
DE
Germany
Prior art keywords
dyeing
fiber materials
polyester fiber
diamino
anthraquinone
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
Application number
DEF25424A
Other languages
German (de)
Inventor
Dr Guenter Gehrke
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer AG
Original Assignee
Bayer AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Priority to DEF25424A priority Critical patent/DE1105837B/en
Priority claimed from GB3773060A external-priority patent/GB896307A/en
Publication of DE1105837B publication Critical patent/DE1105837B/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16Amino-anthraquinones
    • C09B1/20Preparation from starting materials already containing the anthracene nucleus
    • C09B1/22Dyes with unsubstituted amino groups

Description

DEUTSCHESGERMAN

Es wurde gefunden, daß, wenn man synthetische Fasermaterialien, die im wesentlichen aus Polyestern bestehen, mit l,4-Diamino-2-nitro-anthrachinon färbt, Färbungen guter Lichtechtheit erhalten werden. Dieses ist überraschend, weil l,4-Diamino-2-nitro-anthrachinon in Gegensatz zu Farbstoffen ähnlicher Konstitution, wie 1,4-Diamino-2-methoxy-, l,4-Diamino-5-nitro- und 1,4-Diamino-2,3-dichlor-anthrachinon, als Farbstoff für Celluloseacetat wegen seiner schlechten Lichtechtheit nicht in Frage kommt. It has been found that when using synthetic fiber materials consisting essentially of polyesters, dyes with 1,4-diamino-2-nitro-anthraquinone, dyeings of good lightfastness are obtained. This is surprising because 1,4-diamino-2-nitro-anthraquinone in contrast to dyes of a similar constitution, such as 1,4-diamino-2-methoxy-, 1,4-diamino-5-nitro- and 1,4-diamino-2,3-dichloro-anthraquinone, as a dye for cellulose acetate is out of the question because of its poor lightfastness.

Die Durchführung der Ausfärbung kann nach den Methoden erfolgen, die üblicherweise für das Färben von Polyesterfasermaterialien verwendet werden. Man kann die Ausfärbung also z. B. bei Kochtemperatur vornehmen, vorzugsweise in Gegenwart der üblicherweise verwendeten »Carrier«, wie Benzoesäure, Salicylsäure, Kresotinsäuremethylester, o- bzw. p-Oxydiphenyl oder Trichlorbenzol, oder aber man kann die Ausfärbungen auch bei erhöhter Temperatur unter Druck durchführen.The coloration can be carried out by the methods customarily used for dyeing of polyester fiber materials can be used. You can change the color z. B. at cooking temperature, preferably in the presence of the commonly used "carriers" such as benzoic acid, salicylic acid, Cresotinic acid methyl ester, o- or p-oxydiphenyl or Trichlorobenzene, or the coloration can also be carried out at elevated temperature under pressure.

Die Herstellung des l,4-Diamino-2-nitro-anthrachinon kann nach bekannten Verfahren erfolgen, wie sie z. B. in den deutschen Patentschriften 254 185 und 267 445 beschrieben werden. Die Farbstoffe werden vorteilhafterweise in einem feinen Verteilungszustand verwendet. Dieser feine Verteilungszustand kann nach einer der üblichen Methoden erreicht werden, z. B. durch Verpasten aus Schwefelsäure und durch Vermählen mit Dispergiermitteln. The preparation of the 1,4-diamino-2-nitro-anthraquinone can be carried out by known processes, such as those described, for. B. in German patents 254 185 and 267 445 are described. The dyes are advantageous used in a fine distribution state. This fine distribution state can be according to one of the common methods can be achieved, e.g. B. by pasting from sulfuric acid and by grinding with dispersants.

Beispielexample

1 kg Polyesterfasern, z. B. Polyäthylenglycolterephthalat, wird in einer Flotte von 20 bis 401 Wasser mit einer Suspension von 10 g l^-Diamino^-nitro-anthrachinon, das man vorteilhafterweise, z. B. durch Verpasten Färben von Polyesterfasermaterialien1 kg of polyester fibers, e.g. B. polyethylene glycol terephthalate is in a liquor of 20 to 401 of water a suspension of 10 g l ^ -diamino ^ -nitro-anthraquinone, that one advantageously, z. B. by paste dyeing of polyester fiber materials

Anmelder:Applicant:

Farbenfabriken Bayer Aktiengesellschaft, Leverkus en-B ay erwerkFarbenfabriken Bayer Aktiengesellschaft, Leverkus en-B ay erwerk

Dr. Günter Gehrke, Köln-Flittard,
ist als Erfinder genannt worden
Dr. Günter Gehrke, Cologne-Flittard,
has been named as the inventor

aus Schwefelsäure und durch Vermählen mit Dispergiermitteln, vorher in feine Verteilung gebracht hat, 2 Stunden bei 125° C unter Druck gefärbt. Man erhält eine kräftige blaugrüne Färbung von sehr guten Echtheiten. Färbt man bei 95 bis 100° C und setzt dem Färbebad einen »Carrier« zu, z. B. 500 g Benzoesäure, 100 g o- bzw. p-Oxydiphenyl, 100 g Trichlorbenzol oder 100 g Kresotinsäuremethylester, gegebenenfalls in emulgierter Form, so erhält man eine ähnliche Färbung.from sulfuric acid and by grinding with dispersants, has previously brought into fine distribution, dyed under pressure at 125 ° C for 2 hours. You get a strong one blue-green coloring of very good fastness properties. The dyeing is carried out at 95 to 100 ° C and the dyebath is used »Carrier« to, z. B. 500 g benzoic acid, 100 g o- or p-oxydiphenyl, 100 g of trichlorobenzene or 100 g of methyl cresotinate, optionally in emulsified form, see above a similar color is obtained.

Claims (1)

Patentanspruch:Claim: Verwendung von l,4-Diamino-2-nitro-anthrachinon zum Färben von Polyesterfasermaterialien.Use of 1,4-diamino-2-nitro-anthraquinone for dyeing polyester fiber materials. In Betracht gezogene Druckschriften:
Deutsche Patentschriften Nr. 254185, 267 445;
deutsche Auslegeschriften Nr. 1011848, 1014 962;
USA.-Patentschrift Nr. 2 757 064.
Considered publications:
German Patent Nos. 254185, 267 445;
German Auslegeschriften Nos. 1011848, 1014 962;
U.S. Patent No. 2,757,064.
DEF25424A 1958-04-05 1958-04-05 Dyeing of polyester fiber materials Pending DE1105837B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEF25424A DE1105837B (en) 1958-04-05 1958-04-05 Dyeing of polyester fiber materials

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEF25424A DE1105837B (en) 1958-04-05 1958-04-05 Dyeing of polyester fiber materials
GB3773060A GB896307A (en) 1960-11-02 1960-11-02 Process for the dyeing of polyester fibre materials

Publications (1)

Publication Number Publication Date
DE1105837B true DE1105837B (en) 1961-05-04

Family

ID=25974120

Family Applications (1)

Application Number Title Priority Date Filing Date
DEF25424A Pending DE1105837B (en) 1958-04-05 1958-04-05 Dyeing of polyester fiber materials

Country Status (1)

Country Link
DE (1) DE1105837B (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE254185C (en) *
DE267445C (en) *
US2757064A (en) * 1953-04-16 1956-07-31 Du Pont Polyester fibers dyed with anthraquinone dyes
DE1011848B (en) * 1955-12-24 1957-07-11 Hoechst Ag Process for dyeing fiber material made from high polymer polyesters
DE1014962B (en) * 1956-04-28 1957-09-05 Hoechst Ag Process for dyeing and printing shaped structures made of hydrophobic, organic high polymers which contain ester groups

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE254185C (en) *
DE267445C (en) *
US2757064A (en) * 1953-04-16 1956-07-31 Du Pont Polyester fibers dyed with anthraquinone dyes
DE1011848B (en) * 1955-12-24 1957-07-11 Hoechst Ag Process for dyeing fiber material made from high polymer polyesters
DE1014962B (en) * 1956-04-28 1957-09-05 Hoechst Ag Process for dyeing and printing shaped structures made of hydrophobic, organic high polymers which contain ester groups

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