GB414872A - Process for dyeing furs - Google Patents
Process for dyeing fursInfo
- Publication number
- GB414872A GB414872A GB15862/33A GB1586233A GB414872A GB 414872 A GB414872 A GB 414872A GB 15862/33 A GB15862/33 A GB 15862/33A GB 1586233 A GB1586233 A GB 1586233A GB 414872 A GB414872 A GB 414872A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- chromium
- phenol
- acid
- sulphonic acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/30—Material containing basic nitrogen containing amide groups furs feathers, dead hair, furskins, pelts
- D06P3/3058—Material containing basic nitrogen containing amide groups furs feathers, dead hair, furskins, pelts using metallisable or mordant dyes
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Abstract
Furs are dyed by treatment with a dyestuff containing metal in complex union after pre-treatment with a chrome mordant which imparts resistance to high temperature to the skin portion e.g. with chrome-alum, alkali bichromates, chromium sulphate and basic solutions of chromium oxide salts, and also with a chlorinating agent, e.g. alkali hypochlorite or phosphates which increase the capacity of the hair for taking up the dyestuff and promote even dyeing. Suitable dyestuffs are the mono-metal or poly-metal compounds, e.g. the chromium, copper, nickel, cobalt, titanium, vanadium, manganese and iron compounds, of mono- and polyazo-dyestuffs or the chromium compounds of the anthraquinone derivatives. Furs tanned with alum are treated in a bath containing chromium sulphate, they are then rinsed and fulled in a bath containing formic acid. After centrifuging, they are introduced into a bath containing Javelle liquor or chloride of lime together with some sulphite cellulose liquor. The furs are again centrifuged, fulled in a bath containing dilute formic acid and then introduced into the dye-bath which also contains formic acid. After dyeing, the furs are rinsed and treated on the flesh side with a solution of yolk of egg to keep them supple during drying. Orange shades are obtained with the chromium compound of 2 - amino - 1 - phenol - 4 : 6 - disulphonic acid --> 1-phenyl-3-methyl-5-pyrazolone and with the nickel compound from 4-chloro-2-amino-1-phenol-6-sulphonic acid --> resorcinol. Blue shades are obtained with the chromium compound of 1-amino-2-oxynaphthalene-4-sulphonic acid --> b -naphthol and with the chromium and copper compound from 5-nitro-2-amino-1-phenol --> 2-phenylamino-5-oxynaphthalene-7 sulphonic acid and with the primary disazo-dyestuff containing chromium and copper from 4-chloro-2-amino-1-phenol (2 mols) \sQ 5 : 5<1>-dioxy-2 : 2<1>-dinaphthylamine-7 : 7<1>-disulphonic acid. Yellow shades are obtained with the chromium compound from 4 - nitro - 2-amino - 1 - phenol - 6 - sulphonic acid --> acetoacetic acid anilide. Rose shades are obtained with the chromium compound from nitrated 1 - diazo - 2 - oxynaphthalene - 4 - sulphonic acid and 1-(3<1>-sulphamido)-phenyl - 3 - methyl - 5 - pyrazolone; red shades with the chromium compound from 2-amino-1-phenol-4 : 6-disulphonic acid --> 2 : 4-dioxyquinoline; bordeaux shades with the chromium compound from 4-chloro-2-amino-1-phenol-6-sulphonic acid --> 2 : 4-dioxyquinoline and with the chromium compound from 1 : 8-dioxyanthraquinone-disulphonic acid; brown shades with the chromium compound from 2-amino-1-phenol-4-sulphonic acid --> para-cresol or with the iron compound from 4-chloro-2-amino-1-phenol-6-sulphonic acid --> b -naphthol or with the chromium compound from 1 : 2-dioxy anthraquinone-4-sulphonic acid; violet-brown shades with the chromium compound from 4-nitro-2-amino-1-phenol-6-sulphonic acid --> b -naphthol; violet shades with the chromium compound from 4-chloro-2-amino-1-phenol --> 2-oxynaphthalene-6-sulphonic acid or with the copper compound from 1-amino-2-oxynaphthalene-4-sulphonic acid -->a -naphthol; blue-green shades with the chromium compound from 1 : 4 : 5 : 8-tetra-oxyanthraquinone-sulphonic acid; green shades with the chromium compound from 5-nitro-2-amino-1-phenol --> (acid) 2-naphthylamine-6-sulphonic acid; grey shades with the primary disazo dyestuff containing chromium from 5-nitro-2-amino-1-phenol --> (acid) 2-amino-5-oxynaphthalene-7-sulphonic acid (alkaline) \sM anthranilic acid and black shades with the chromium compound from nitrated 1-diazo-2-oxynaphthalene - 4 - sulphonic acid and b - naphthol. Specification 6841/00, [Class 15], is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH414872X | 1932-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB414872A true GB414872A (en) | 1934-08-16 |
Family
ID=4514533
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15862/33A Expired GB414872A (en) | 1932-06-02 | 1933-06-01 | Process for dyeing furs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB414872A (en) |
-
1933
- 1933-06-01 GB GB15862/33A patent/GB414872A/en not_active Expired
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