GB332545A - Improvements in the dyeing of regenerated cellulose materials - Google Patents
Improvements in the dyeing of regenerated cellulose materialsInfo
- Publication number
- GB332545A GB332545A GB1225229A GB1225229A GB332545A GB 332545 A GB332545 A GB 332545A GB 1225229 A GB1225229 A GB 1225229A GB 1225229 A GB1225229 A GB 1225229A GB 332545 A GB332545 A GB 332545A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- aminonaphtholsulphonic
- acids
- alkaline
- chloraniline
- 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
-
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/025—Disazo dyes containing acid groups, e.g. -COOH, -SO3H, -PO3H2, -OSO3H, -OPO2H2; Salts thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
332,545. Imperial Chemical Industries, Ltd., and Brightman, R. April 19, 1929. Azo dyes.-Regenerated cellulose materials are dyed in level shades ranging from orange and red to bluish violet and blue by the application of secondary disazo dyes of the type monamine of the benzene series not containing a nitro group # (alkaline) an aminonaphtholsulphonic acid # end component. When the end component is an aminonaphtholsulphonic acid it is coupled in alkaline solution. The use of dyestuffs of the type aminosalicycic acids or their homologues # the usual middle components # 1: 8-dihydroxynaphthalene, 1: 8-aminonaphtholsulphonic acids or N-substitution products thereof, naphtholsulplsanic acids, naphthylaminesulphonic acids, or N-substitution products of the latter, and the use of secondary disazo dyestuffs having as and component an N-substituted 2: 8-aminonaphtholsulphonic acid are excluded from the invention. In an example, viscose silk is dyed violet-brown by treatment with the dyestuff pchloraniline # (alkaline) 2 : 8 : 6-aminonaphtholsulphonic acid # (alkaline) 2: 8: 6-aminonaphtholsulphonic acid. A table is also given showing, the shades obtained on viscose silk with the following dyestuffs :-p-Chloraniline # 2: 5: 7-acid # #-naphthol or nitro-m-phenylenediamine, m-aminobenzoic acid # 2 : 8 : 6- acid # #-naphthol, p-chloraniline # 2 : 8 : 6- acid # nitro-m-phenylenediamine or salicylic acid, o-anisidine # 1 : 5: 7-acid or 2:5:7- acid # 1 : 8-aminonaphthol-2 : 4-disulphonic acid, o-anisidine # 2: 8: 6-acid # 1:8:4- acid, p-chloraniline # H-acid # #-naphthol, m-aminobenzoic acid # 2 : 8 : 6-acid # salicylic acid, o-anisidine # 1 : 8 : 4-acid # 2 ; 8 : 6-acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1225229A GB332545A (en) | 1929-04-19 | 1929-04-19 | Improvements in the dyeing of regenerated cellulose materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1225229A GB332545A (en) | 1929-04-19 | 1929-04-19 | Improvements in the dyeing of regenerated cellulose materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB332545A true GB332545A (en) | 1930-07-21 |
Family
ID=10001145
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1225229A Expired GB332545A (en) | 1929-04-19 | 1929-04-19 | Improvements in the dyeing of regenerated cellulose materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB332545A (en) |
-
1929
- 1929-04-19 GB GB1225229A patent/GB332545A/en not_active Expired
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