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DE410758C - Process for the production of washable and lightfast colors on the fiber - Google Patents

Process for the production of washable and lightfast colors on the fiber

Info

Publication number
DE410758C
DE410758C DEF48573D DEF0048573D DE410758C DE 410758 C DE410758 C DE 410758C DE F48573 D DEF48573 D DE F48573D DE F0048573 D DEF0048573 D DE F0048573D DE 410758 C DE410758 C DE 410758C
Authority
DE
Germany
Prior art keywords
fiber
mole
washable
production
mol
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
Application number
DEF48573D
Other languages
German (de)
Inventor
Dr Richard Stuesser
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
Farbenfabriken Vorm Friedr Bayer and Co
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 Farbenfabriken Vorm Friedr Bayer and Co filed Critical Farbenfabriken Vorm Friedr Bayer and Co
Priority to DEF48573D priority Critical patent/DE410758C/en
Application granted granted Critical
Publication of DE410758C publication Critical patent/DE410758C/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/58Material containing hydroxyl groups
    • D06P3/60Natural or regenerated cellulose
    • D06P3/64Natural or regenerated cellulose using mordant dyes or metallisable dyes

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)

Description

Verfahren zur Erzeugung wasch- und lichtechter Färbungen auf der Faser. Es ist bekannt, daß man durch Nachkupfern von gewissen Baumwollfarbstoffen auf der Faser eine bessere Wasch- und Lichtechtheit der Färbung erzielt (vgl. z. B. G. Schultz, Farbstofftabellen, 5. Aufl., S. 132 Nr. 410, 4.12; S. 133 Nr. 4.16, 417; S. 135 Nr. 424 usw.).Process for producing washable and lightfast dyeings on the fiber. It is known that by re-coppering certain cotton dyes on the fiber, a better wash and light fastness of the dyeing is achieved (see, for example, BG Schultz, dye tables, 5th edition, p. 1 32 No. 410, 4.12; p. 1 33 No. 4.16, 417; p. 135 No. 424 etc.).

Die so erhaltenen Färbungen genügen jedoch den Ansprüchen der Praxis nicht, da die Erhöhung der Waschechtheit nur eine geringe ist und sie bei wiederholtem Waschen zurückgeht; da dies auf einem Auslaugen des Kupfers beruht, geht damit auch die Lichtechtheit zurück.However, the dyeings obtained in this way meet practical requirements not, since the increase in wash fastness is only slight and it increases with repeated use Washing goes down; since this is based on a leaching of the copper, so is also possible the lightfastness back.

Es wurde nun gefunden, daß man auf der Faser, wie Baumwolle und Seide, dauerhafte, sehr licht- und waschechte Färbungen dadurch erhalten kann, daß man Azofarbstoffe aus der q..q.'-Diaminodiphenyl-3.3'-dicarb,onsäure auf der Faser nachkupfert. Die so erhaltenen Ausfärbungen besitzen die hohe Lichtechtheit der Küpenfarben und eine über das gewohnte Maß gesteigerte Waschechtheit, die in vielen Fällen so weit geht, daß sie an die Waschechtheit der Entwicklungs- und Eisfarben heranreicht. Beispiel i.It has now been found that on fibers, like cotton and silk, permanent, very light and washfast colorations can be obtained by Azo dyes from the q..q .'-diaminodiphenyl-3.3'-dicarb, onic acid re-coppered on the fiber. The colorations obtained in this way have the high lightfastness of the vat colors and a washfastness that is increased beyond the usual level, which in many cases goes so far goes that it comes close to the washing fastness of the developing and ice colors. Example i.

Der Disazofarbstoff aus i Mol. tetrazo- ' tierter 4#q.' - Diaminodiphenyl - 3#3' - dica.rbonsäure, i Mol. Aoetessig - o - chloranilid und i Mol. i-Amino-8-oxynaphthalin-4-sulfosäure wird in bekannter Weise mit 2 Prozent Soda und 2o Prozent Glaubersalz auf Baumwolle ausgefärbt, die Ausfärbung sodann, wie üblich, auf frischem Bade mit 2 bis 3 Prozent Kupfersulfat und 3 Prozent Essigsäure 20 Minuten heiß nachbehandelt, darauf kalt gespült und getrocknet.The disazo dye from i mol. Tetrazo- 'tated 4 # q.' - diaminodiphenyl - 3 # 3 '- dicarboxylic acid, 1 mol. Aoetoacetic - o - chloranilide and 1 mol. I-amino-8-oxynaphthalene-4-sulfonic acid is made in a known way with 2 percent soda and 2o percent Glauber's salt on cotton colored, the color then, as usual, on a fresh bath with 2 to 3 percent Copper sulfate and 3 percent acetic acid aftertreated hot for 20 minutes, then cold rinsed and dried.

Die Ausfärbung, ein Korinth, geht durch Nachkupfern in ein Dunkelgrün über. Beispiel 2.The color, a Corinth, turns into a dark green after copper plating above. Example 2.

Der aus i Mol. tetrazotierter 4.#.1'-Diaminodiphenyl-3.3'-dicarbon.säure, i Mol. Phenylß-naphthylamin und i Mol. i-Amino-8-oxynaphthalin-4.-sulfOsäure erhaltene Farbstoff liefert auf Baumwolle ein Violett. Wird er, wie in. Beispiel i angegeben, nachbehandelt, so erhält man ein Blau.The 4. #. 1'-diaminodiphenyl-3.3'-dicarboxylic acid, tetrazotized from 1 mol. one mole of phenylβ-naphthylamine and one mole of i-amino-8-oxynaphthalene-4-sulfoic acid Dye produces a purple color on cotton. If it is given, as in example i, post-treated, a blue is obtained.

Beispiel 3.Example 3.

Das Produkt aus 2 Mol. tetrazotierter 4.#¢'-Diaminodiphenyl - 3-3'- dicarbonsäure, 2 Mol. Phenyl - (3 - naphthylamin und i Mol. 5' 5'-Dioxy - 2.2'- dinaphthylamin-7#7' - disulfosäure liefert, auf dieselbe Weise ausgefärbt, ein Violett, nachbehandelt ein Blau.The product of 2 mol. Tetrazotized 4. # ¢ '-diaminodiphenyl - 3-3'- dicarboxylic acid, 2 mol. Phenyl - (3 - naphthylamine and 1 mol. 5 '5'-Dioxy - 2.2'- dinaphthylamine-7 # 7 '- disulfonic acid, colored in the same way, gives a violet, post-treated a blue.

Beispiel q..Example q ..

Der Farbstoff aus i Mol. tetrazotierter q.#4'-Diaminodiphenyl-3#3'-dica.rbonsäure, i Mol. Phenyl-(3-naphthylamin und z Mol. i-Oxynaphthalin-5-sulfosäure liefert auf Baumwolle direkt ein Violett, das durch Nachkupfern etwas nach Blau verschoben wird.The dye from 1 mole of tetrazotized q. # 4'-diaminodiphenyl-3 # 3'-dica.rboxylic acid, i mole. Phenyl- (3-naphthylamine and z mol. I-oxynaphthalene-5-sulfonic acid directly produces a violet color on cotton, which is somewhat blue due to re-coppering is moved.

Beispiel 5.Example 5.

Der aus i Mol. tetrazotierter 4..q.'-Diamnodiphenyl-3.3'-dicarbonsäure, i M o1. Phenylj3-naphthylamin und i Mol. Resorcin erhaltene Farbstoff liefert auf Baumwolle ein blaustichiges Rot, das beim Nachkupfern in ein Bordeaux übergeht.The 4..q .'-diamnodiphenyl-3.3'-dicarboxylic acid, tetrazotized from i mol, i M o1. Phenyl / 3-naphthylamine and 1 mole of resorcinol gives the dye Cotton is a bluish red that turns into a Bordeaux when re-coppering.

Beispiel 6.Example 6.

Der Farbstoff aus i Mol. derselben Tetrazoverbindung mit i Mol. Acetessig-o-chloranilid und i Mol. i-Phenyl-5-pyrazolon-3-carbonsäure gibt auf Baumwolle direkt ein Orange, das durch Nachkupfern in ein Gelbbraun übergeht.The dye from one mole of the same tetrazo compound with one mole of acetoacetic-o-chloroanilide and i mole of i-phenyl-5-pyrazolone-3-carboxylic acid gives an orange directly to cotton, which turns into a yellow-brown through re-coppering.

Beispiel 7.Example 7.

Der Farbstoff aus i Mol. derselben Tetrazoverbindung mit i Mol. Acetessiganilid und i Mol. Acetessiganilid-p-carbonsäure liefert auf Baumwolle direkt ein rotstichiges Gelb, das durch Nachbehandeln in ein braunstichiges Gelb übergeht.The dye from one mole of the same tetrazo compound with one mole of acetoacetanilide and 1 mole. Acetoacetanilide-p-carboxylic acid gives a reddish cast on cotton directly Yellow, which changes to a brownish yellow after treatment.

Claims (1)

PATENT-ANSPRUCH: Verfahren. zur Erzeugung wasch- und lichtechter Färbungen auf der Faser, dadurch gekennzeichnet, daß man Azofarb-. Stoffe aus der q.#q.'-Diaminodiphenyl-3#3'-dicarbonsäure auf der Faser nachkupfert.PATENT CLAIM: Process. for the creation of wash and lightfast dyeings on the fiber, characterized in that azo color. Substances from q. # Q .'-diaminodiphenyl-3 # 3'-dicarboxylic acid re-coppered on the fiber.
DEF48573D 1921-02-12 1921-02-12 Process for the production of washable and lightfast colors on the fiber Expired DE410758C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEF48573D DE410758C (en) 1921-02-12 1921-02-12 Process for the production of washable and lightfast colors on the fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF48573D DE410758C (en) 1921-02-12 1921-02-12 Process for the production of washable and lightfast colors on the fiber

Publications (1)

Publication Number Publication Date
DE410758C true DE410758C (en) 1925-03-16

Family

ID=7102324

Family Applications (1)

Application Number Title Priority Date Filing Date
DEF48573D Expired DE410758C (en) 1921-02-12 1921-02-12 Process for the production of washable and lightfast colors on the fiber

Country Status (1)

Country Link
DE (1) DE410758C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE751299C (en) * 1935-04-06 1953-01-19 Chemische Ind Ges Process for dyeing cellulose fibers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE751299C (en) * 1935-04-06 1953-01-19 Chemische Ind Ges Process for dyeing cellulose fibers

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