CH93740A - Process for the preparation of a chromium compound of a mordant dye. - Google Patents
Process for the preparation of a chromium compound of a mordant dye.Info
- Publication number
- CH93740A CH93740A CH93740DA CH93740A CH 93740 A CH93740 A CH 93740A CH 93740D A CH93740D A CH 93740DA CH 93740 A CH93740 A CH 93740A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- chromium compound
- mordant dye
- parts
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 3
- 150000001845 chromium compounds Chemical class 0.000 title description 2
- 239000000983 mordant dye Substances 0.000 title description 2
- 238000002360 preparation method Methods 0.000 title description 2
- 239000000975 dye Substances 0.000 claims description 8
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 239000000980 acid dye Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 150000008049 diazo compounds Chemical class 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paper (AREA)
Description
Verfahren zur Herstellung einer Clironiverbinduneines Beizenfarbstoffes. Es wurde gefunden, dass man eine technisch wertvolle Clirotnverbinclurig Herstellen kann, wenn rnan die Diazoverbindung der 1-1linine@- 2-oxynaphtalin-4-sulfosäare reit 1-Oxy-5 : 8 dichlornaplitalin kuppelt und den so erhaltenen Farbstoff mit chromabgebenden Mitteln be handelt.
Die so erhaltene Chromverbindung stellt einen wertvollen Säurefarbstoff dar, der Wolle in sehr egalen, licht- und walkecliten blauen Tönen färbt.
Beispiel: 106.5 Teile 1-Oxy-5:8-dicliloi-naphtalin werden in überschüssiger Natronlauge geli;st und bei niedriger Temperatur mit einer w;iI.i- rigen Suspension von 130 Teilen diazotierter 1-Amino-2-oxyriaphtaliii-4-sulfosäure versetzt.
31.111 rührt, bis die 1)iazove,-bindiingverschwun- den ist, verdünnt finit Nasser, stellt eben mineralsauer finit Salzsäure ein Lind salzt den gebildeten Farbstoff aus.
463 Teile dieses Farbstoffes werden nun in 1000 Teile einer wässrigen Lösung, ent- haltend 76.;5 Teile Chromoxyd, 22.1,5 Teile Ätznatron und 112.5 Teile Glycei#in einge tragen und 10 Stunden ain Rüch$uhkühler gekocht. Hierauf wird mit der dreifachen @@'assernienge verdünnt, das fr-eigeworderie .@tzkali reit Mineralsäure eben neutralisiert,
der entstandene chromhaltige Farbstoff aus- ges@iIzen, filtriert und guti-ocl@net.
Process for the preparation of a clironi compound of a mordant dye. It has been found that a technically valuable compound can be produced if the diazo compound of the 1-1linine @ - 2-oxynaphthalene-4-sulfosäare is coupled with 1-oxy-5: 8 dichloromaplitaline and the dye thus obtained is treated with chromium-releasing agents .
The chromium compound obtained in this way is a valuable acid dye that dyes wool in very even, light and milled blue tones.
Example: 106.5 parts of 1-oxy-5: 8-dicliloi-naphthalene are dissolved in excess sodium hydroxide solution and treated at low temperature with an aqueous suspension of 130 parts of diazotized 1-amino-2-oxyriaphtaliii-4- sulfonic acid added.
31.111 stirs until the 1) iazove, -bindiing has disappeared, dilutes finite water, just adds mineral acid finite hydrochloric acid and saltes out the dye formed.
463 parts of this dye are then introduced into 1000 parts of an aqueous solution containing 76.5 parts of chromium oxide, 22.1.5 parts of caustic soda and 112.5 parts of glycine and boiled in a cooler for 10 hours. Then it is diluted with threefold @@ 'assernienge, the fr-eigeworderie. @ Tzkali reit mineral acid is neutralized,
the resulting chromium-containing dye is extracted, filtered and guti-ocl @ net.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH93740T | 1921-02-12 | ||
| CH93279T | 1921-02-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH93740A true CH93740A (en) | 1922-03-16 |
Family
ID=25704639
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH93740D CH93740A (en) | 1921-02-12 | 1921-02-12 | Process for the preparation of a chromium compound of a mordant dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH93740A (en) |
-
1921
- 1921-02-12 CH CH93740D patent/CH93740A/en unknown
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