CH172592A - 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
- CH172592A CH172592A CH172592DA CH172592A CH 172592 A CH172592 A CH 172592A CH 172592D A CH172592D A CH 172592DA CH 172592 A CH172592 A CH 172592A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- chromium
- dye
- black
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>169696-</B> Verfahren zur Herstellung eines ehroinhaltigei) Azofarbstoffes. Es wurde gefunden, dass man einen ehrom- haltigen Azofarbstoff aus dem Azofarbstoff, der durch Kuppeln von nitrierter 1-Diazo-2- gxyriaphthaliii-4-sulfonsäure und 2-Oxynaph- bhalin entsteht, erhalten kann, wenn man diesen Azofarbstoff,
ein Chromierungsmittel und eine hydroxylgruppenhaltige organische Verbindung in ätzalkalischem Medium auf- ginander einwirken lässt.
Der erhaltene ehromhaltige Farbstoff stellt ein schwarzes Pulver dar, das sich in Wasser mit braunviolett-schwarzer Farbe löst. In 10 '/oiger Sodalösung sowie 10 %iger Natron- lauge löst er sich nur sehr schwer. Er färbt Wolle aus organischsaurem-schwefelsaurem Bade in schwarzen Tönen von guten Echt- heiten.
<I>Beispiel:</I> 46,1 Teile des Azofarbstoffes aus nitrier ter 1-Diazo-2-oxynaphthaliii-4-sulfonsäure und 2-Oxynaphthalin werden in eine Natrium- ehromitlösung eingerührt, die aus<B>70</B> Teilen <B>8</B> %iger Chromoxydhydratpaste, entsprechend <B>5,7</B> Teilen Cr20s, <B>110</B> Teilen<B>30</B> 1/oiger Na tronlauge und 20 Teilen Zucker frisch bereitet wurde.
Man verdünnt mit 120 Teilen Wasser, erhitzt unter Rühren<B>6</B> Stunden auf<B>75-800</B> Lind hierauf<B>3</B> Stunden auf 80-900. Die Reaktionsmasse wird in<B>1500</B> Teile heisses Wasser ausgetragen, mit schwach verdünnter Ameisensäure kräftig lakmussauer gestellt, von unlöslichen Anteilen abfiltriert Lind das Filtrat im Vakuum zur Trockne verdampft.
Zu dem selben Farbstoffe gelangt man, wenn man, statt"den Azofarbstoff mit solchen Komplexverbindungen zu behandeln, die durch Einwirkung von hydroxylgruppenhaltigen organischen Verbindungen auf ätzalkali- sehe Chromhydroxydsuspensionen entstehen, Ohromsalze sowie überschüssige Ätzalkalien zusammen mit den hydroxylgruppenhaltigen organischen Verbindungen und dem Azofarb- Stoffe erwärmt.
Additional patent to main patent no. <B> 169696- </B> Process for the production of an ehroinhaltigei) azo dye. It has been found that an azo dye containing Ehrom can be obtained from the azo dye which is formed by coupling nitrated 1-diazo-2-gxyriaphthaliii-4-sulfonic acid and 2-oxynaphbhalin if this azo dye,
a chromating agent and an organic compound containing hydroxyl groups act on one another in an alkaline medium.
The resulting Ehrom-containing dye is a black powder which dissolves in water with a brown-violet-black color. It dissolves only with great difficulty in 10% soda solution and 10% sodium hydroxide solution. It dyes wool from organic acid-sulfuric acid bath in black shades of good fastness.
<I> Example: </I> 46.1 parts of the azo dye from nitrated 1-diazo-2-oxynaphthalene-4-sulfonic acid and 2-oxynaphthalene are stirred into a sodium eromite solution which is composed of <B> 70 </ B > Parts <B> 8 </B>% chromium oxide hydrate paste, corresponding to <B> 5.7 </B> parts Cr20s, <B> 110 </B> parts <B> 30 </B> 1 /% sodium hydroxide solution and 20 parts of sugar was freshly made.
The mixture is diluted with 120 parts of water and heated for <B> 6 </B> hours to <B> 75-800 </B> and then <B> 3 </B> hours to 80-900 while stirring. The reaction mass is poured out in 1500 parts of hot water, strongly lacquered with weakly dilute formic acid, insoluble components are filtered off and the filtrate is evaporated to dryness in vacuo.
The same dyestuff is obtained if, instead of "treating the azo dyestuff with such complex compounds that are formed by the action of hydroxyl-containing organic compounds on caustic alkali chromium hydroxide suspensions, ohrom salts and excess caustic alkalis are heated together with the hydroxyl-containing organic compounds and the azo dyes .
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH172592T | 1933-04-03 | ||
CH169696T | 1933-04-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH172592A true CH172592A (en) | 1934-10-15 |
Family
ID=25718773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH172592D CH172592A (en) | 1933-04-03 | 1933-04-03 | Process for the preparation of a chromium-containing azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH172592A (en) |
-
1933
- 1933-04-03 CH CH172592D patent/CH172592A/en unknown
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