CH91275A - Process for the preparation of an acidic dye containing chromium. - Google Patents
Process for the preparation of an acidic dye containing chromium.Info
- Publication number
- CH91275A CH91275A CH91275DA CH91275A CH 91275 A CH91275 A CH 91275A CH 91275D A CH91275D A CH 91275DA CH 91275 A CH91275 A CH 91275A
- Authority
- CH
- Switzerland
- Prior art keywords
- chromium
- preparation
- dye
- acidic dye
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines chromhaltigen sauren Farbstoffes. Es wurde gefunden, dar rnan den rnetall- empfindlichen Azofarbstoff aus der brornierten Diazoverbindung der 1-Arnino-2-oxyrraplrtalirr- 4-sulfosäure und u-Naphtol durch Behandeln mit den chromhaltigen Komplexverbindungen,
welche durch Einwirkung von hydroxylgrup- penhaltigen organischen Verbindungen auf alkalische Chromhydroxydsuspensionen erhal ten werden, in einen chromhaltigen sauren Farbstoff überführen kann, welcher das Chrom in maskierter Bindung enthält, indem das selbe aus der wässerigen Lösung durch Soda, Natronlauge oder Ammoniak nicht gefällt wird. Der Farbstoff ist wasserlöslich, säure beständig, nicht kupfererrrpfindlich und färbt animalische Fasern aus saurem Bad in blauen, walk- und lichtechten Tönen an.
<I>Beispiel</I> In 600 Teilen einer Chronihydroxydlry- dratpaste, enthaltend 76,5 Teile Cr=03, löst man unterhalb<B>700</B> 267 Teile Ätzkali. Hier auf gibt man 90 Teile Glyzerin hinzu und erhitzt zum Kochen, bis vollständige Lösung eingetreten ist.
Sodann -,erdünnt man auf <B>1100</B> Voluniteile, versetzt mit 173 Teilen des FarbstQffes aus der bromiurten Diazoverbirr- dung der 1-Amino-2-ox3-naphtalin--l-ulfosäure und a-Naphtol und kocht das Ganze einige Stunden am Riichflrrsskiililei# weiter,
bis der Farbstoff vollständig in seine Chromverbin- dung übergegangen ist. Ist dies erreicht. so verdünnt man mit 3300 Teilen kaltem Was ser und salzt den entstandenen Farbstoff aus, nachdem der tltzall@aliüberschul:, mit -Mineral- säure neutralisiert worden ist.
Statt (xlyzerin können auch andere hydroxylgruppenhaltige organische Verbindungen wie Clly-hol, Tannin, Gallussäure, Zuckerarten, Kohlenhydrate, ver wendet werden.
Process for the preparation of an acidic dye containing chromium. It has been found that the metal-sensitive azo dye from the brominated diazo compound of 1-amino-2-oxyrrapidal-4-sulfonic acid and u-naphthol by treatment with the chromium-containing complex compounds,
which are obtained by the action of hydroxyl group-containing organic compounds on alkaline chromium hydroxide suspensions, can be converted into a chromium-containing acidic dye which contains the chromium in masked bond, as the same is not precipitated from the aqueous solution by soda, sodium hydroxide or ammonia. The dye is water-soluble, acid-resistant, not sensitive to copper and stains animal fibers from an acid bath in blue, mill-fast and light-fast shades.
<I> Example </I> In 600 parts of a chronihydroxydrate paste containing 76.5 parts of Cr = 03, <B> 700 </B> 267 parts of caustic potash are dissolved. 90 parts of glycerine are added and the mixture is heated to a boil until it has completely dissolved.
Then -, you dilute to <B> 1100 </B> parts by volume, add 173 parts of the coloring agent from the brominated diazo compound of 1-amino-2-ox3-naphthalene-l-sulfonic acid and a-naphthol and boil it Whole a few hours on the Riichflrrrsskiilei #,
until the dye has completely converted into its chromium compound. Is this achieved. so you dilute with 3300 parts of cold water and salt out the resulting dye, after the tltzall @ aliüberul :, has been neutralized with mineral acid.
Instead of (xlycerin), other organic compounds containing hydroxyl groups, such as cyllyhol, tannin, gallic acid, types of sugar, carbohydrates, can also be used.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH77248T | 1920-03-30 | ||
CH91275T | 1920-03-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH91275A true CH91275A (en) | 1921-10-17 |
Family
ID=25702033
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH91275D CH91275A (en) | 1920-03-30 | 1920-03-30 | Process for the preparation of an acidic dye containing chromium. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH91275A (en) |
-
1920
- 1920-03-30 CH CH91275D patent/CH91275A/en unknown
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