CH167803A - Process for the preparation of a chromium-containing azo dye. - Google Patents
Process for the preparation of a chromium-containing azo dye.Info
- Publication number
- CH167803A CH167803A CH167803DA CH167803A CH 167803 A CH167803 A CH 167803A CH 167803D A CH167803D A CH 167803DA CH 167803 A CH167803 A CH 167803A
- Authority
- CH
- Switzerland
- Prior art keywords
- chromium
- azo dye
- oxynaphthalene
- preparation
- sulfuric acid
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/01—Complex metal compounds of azo dyes characterised by the method of metallisation
Description
Verfahren zur Herstellung eines ehromhaltigen Azofarbstoffes. Es wurde gefunden, dass man einen chrom- haltigen Azofarbstoff herstellen kann, wenn man den Azofarbstoff aus nitrierter 1-Diazo- 2-oxynaphthalin-4-sulfonsäLire und 2-Oxy- naphthalin mit einem ehromabgebenden Mittel in solchen Mengen,
dass der ehromierbaren Gruppe des Farbstoffmoleküls weniger als <B>1</B> Atom Chrom entspricht, sowie in Gegen wart löslicher Salze organischer Säuren be handelt.
Der erhaltene ehromhaltige Azofarbstoff löst sich leicht in Wasser und färbt Wolle aus schwefelsaurem oder aus organischsaurem- schwefelsaurem Bade in schwarzen Tönen von vorzüglichen Echtheiten.
<I>Beispiel:</I> 46,1 Teile des Azofarbstoffes aus nitrier ter 1-Diazo-2-oxynaplithalin-4-sulfonsäure und 2-Oxynaphthalin werden mit<B>1000</B> Teilen Wasser verrührt. Dann gibt man 4 Teile <B>30</B> '/oige Natronlauge, 12 Teile Natrium- formiat und eine Chromfluoridlösung, deren Gehalt<B>5,32</B> Teilen Cr20s entspricht, zu.
Hierauf wird das Ganze<B>5</B> Stunden unter Rückflusskühlung gekocht und die entstan- derie seliwarzviolett gefärbte Lösung auf dem Wasserbade im Vakuum eingedampft.
Zu demselben Farbstoffe gelangt man, wenn statt Chromfluorid andere chromab gebende Mittel, wie zum Beispiel Chrom- azetat, Chromformiat, benzolsulfonsaures Chrom oder Gemische solcher Chromierungs- mittel verwendet werden.
Ebenso wird der gleiche Farbstoff er halten, wenn das im Beispiel verwendete Natriumformiat durch andere lösliche Salze, organischer Säuren, wie zum Beispiel durch Natriumazetat oder durch Natriumoxalat er setzt wird.
Process for the preparation of an azo dye containing Ehrom. It has been found that a chromium-containing azo dye can be produced if the azo dye is prepared from nitrated 1-diazo-2-oxynaphthalene-4-sulfonic salts and 2-oxynaphthalene with an honor-releasing agent in amounts
that the honorable group of the dye molecule corresponds to less than <B> 1 </B> atom of chromium, and is treated in the presence of soluble salts of organic acids.
The azo dye containing Ehrom dissolves easily in water and dyes wool from sulfuric acid or from organic acid-sulfuric acid bath in black shades with excellent fastness properties.
<I> Example: </I> 46.1 parts of the azo dye from nitrated 1-diazo-2-oxynaplithalin-4-sulfonic acid and 2-oxynaphthalene are stirred with <B> 1000 </B> parts of water. Then 4 parts of <B> 30 </B> '/ o sodium hydroxide solution, 12 parts of sodium formate and a chromium fluoride solution, the content of which corresponds to <B> 5.32 </B> parts of Cr20s, are added.
The whole thing is then refluxed for <B> 5 </B> hours and the resulting seliwarz-violet colored solution is evaporated on the water bath in a vacuum.
The same colorant is obtained if, instead of chromium fluoride, other chromium-releasing agents, such as chromium acetate, chromium formate, benzenesulfonic acid chromium or mixtures of such chromating agents, are used.
Likewise, the same dye is obtained if the sodium formate used in the example is replaced by other soluble salts, organic acids, such as sodium acetate or sodium oxalate.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH167803T | 1933-01-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH167803A true CH167803A (en) | 1934-03-15 |
Family
ID=4420157
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH167803D CH167803A (en) | 1933-01-25 | 1933-01-25 | Process for the preparation of a chromium-containing azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH167803A (en) |
-
1933
- 1933-01-25 CH CH167803D patent/CH167803A/en unknown
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