CH145853A - Process for the production of a metal-containing dye. - Google Patents
Process for the production of a metal-containing dye.Info
- Publication number
- CH145853A CH145853A CH145853DA CH145853A CH 145853 A CH145853 A CH 145853A CH 145853D A CH145853D A CH 145853DA CH 145853 A CH145853 A CH 145853A
- Authority
- CH
- Switzerland
- Prior art keywords
- metal
- dye
- violet
- production
- aluminum
- 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
- C09B45/22—Monoazo compounds containing other metals
-
- 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
- C09B45/18—Monoazo compounds containing copper
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Description
Verfahren zur Herstellung eines metallhaltigen Farbstoffes. Es wurde gefunden, dass man einen neuen metallhaltigen Farbstoff erhält, wenn man den Farbstoff aus diazotiertem 5-Nitro-2- amino-l-phenol und ss-Naphtlrol mit einem eisen-, aluminium- und kupferhaltigen Pro dukt, das durch Einwirkung einer hydroxyl- gruppenhaltigen organischen Verbindung auf Eisen-, Aluminium- und Kupferverbin dungen in Gegenwart von Alkalien erhalten wird, behandelt.
Der neue metallhaltige Farbstoff ist in Wasser sehr schwer, in Natronlauge etwas mit braunroter Farbe löslich. In konzentrier ter Schwefelsäure löst er sich violett, und aus der ebenfalls violetten Lösung in Zapon- lack erhält man auf Metallfolien violette Anstriche von sehr guter Lichtechtheit.
<I>Beispiel:</I> 6,18 Gewichtsteile des Farbstoffes aus dianotiertem 5-Nitro-2-amino-l-phenol und l Naphthol werden in 500 Teilen Wasser und <B>10</B> Teilen Natronlauge von<B>36'</B> Be gelöst und mit einer glyzerinhaltigon, alkalischen Lösung aus 0,65 Teilen Eisenchlorid, 0,69 Teilen Aluminiumsulfat und 3,0 Teilen kri stallisiertem Kupfersulfat in 50 Teilen Was ser, 5 Teilen Glyzerin und 20 Teilen Natron lauge (36 B6) kurze Zeit am Rückfluss zum Kochen erhitzt. Nach dem Erkalten des Reaktionsgemisches wird mit Essigsäure neutralisiert und der abgeschiedene Farbstoff filtriert, ausgewaschen und bei mässiger Tem peratur getrocknet.
Ein gleiches Produkt wird erhalten, wenn statt Glyzerin andere hydroxylgruppenhaltige organische Verbindungen, wie Glykol, Tannin, Gallussäure, Zuckerarten, Kohlenhydrate, ver wendet werden.
Process for the production of a metal-containing dye. It has been found that a new metal-containing dye is obtained if the dye is made from diazotized 5-nitro-2-amino-1-phenol and ss-naphtholrol with an iron, aluminum and copper-containing product that is produced by the action of a hydroxyl - Group-containing organic compound on iron, aluminum and copper compounds in the presence of alkalis is obtained treated.
The new metal-containing dye is very difficult in water and somewhat soluble in caustic soda with a brownish-red color. It dissolves violet in concentrated sulfuric acid, and the violet solution in Zapon varnish gives violet coatings of very good lightfastness on metal foils.
<I> Example: </I> 6.18 parts by weight of the dye from dianotized 5-nitro-2-amino-1-phenol and 1 naphthol are mixed with 500 parts of water and 10 parts of sodium hydroxide solution > 36 '</B> Be dissolved and with a glycerin-containing, alkaline solution of 0.65 parts of ferric chloride, 0.69 parts of aluminum sulfate and 3.0 parts of kri-crystallized copper sulfate in 50 parts of water, 5 parts of glycerin and 20 parts of sodium hydroxide (36 B6) heated to reflux for a short time. After the reaction mixture has cooled, it is neutralized with acetic acid and the deposited dye is filtered, washed and dried at a moderate temperature.
The same product is obtained if, instead of glycerine, other organic compounds containing hydroxyl groups, such as glycol, tannin, gallic acid, types of sugar, carbohydrates, are used.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH145853T | 1928-10-05 | ||
CH141535T | 1929-07-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH145853A true CH145853A (en) | 1931-03-15 |
Family
ID=25713807
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH145853D CH145853A (en) | 1928-10-05 | 1928-10-05 | Process for the production of a metal-containing dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH145853A (en) |
-
1928
- 1928-10-05 CH CH145853D patent/CH145853A/en unknown
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