GB452006A - A process of dyeing - Google Patents
A process of dyeingInfo
- Publication number
- GB452006A GB452006A GB4367/35A GB436735A GB452006A GB 452006 A GB452006 A GB 452006A GB 4367/35 A GB4367/35 A GB 4367/35A GB 436735 A GB436735 A GB 436735A GB 452006 A GB452006 A GB 452006A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyed
- hour
- aqueous solution
- dyestuff
- fluorindine
- 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
- C09B17/00—Azine dyes
- C09B17/06—Fluorindine or its derivatives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Substantive dyes, dyeing with; regenerated celluloses, dyeing.--Cellulosic material is dyed directly with an alkali salt of a sulphonic acid of a diarylfluorindine of the general formula <FORM:0452006/IV/1> (R representing aryl radicles which may be the same as or different from those otherwise present) which contains either negative groups or (as the R's or as the aryl groups) polynuclear ring systems or both, and which may be halogenated. Specified negative groups are nitro, CO-alkyl, CO-aryl, carboxyl and quinone groups and specified ring systems are those of naphthalene, diphenyl, stilbene, pyrene and anthracene. The dyestuffs are obtainable as described in Specification 442,732. The following examples are specified: (1) To a melt of p-aminodiphenyl (10 parts) at 90 DEG C. are added slowly, with stirring, p-aminodiphenyl hydrochloride (1 part) and p-nitrosophenol (1 part) and the whole is cooled to 70 DEG C. and alcohol is added to precipitate crystals which are filtered and washed; these are dissolved in nitrobenzene, the solution is boiled for \ba1/2\be hour with an addition of lead dioxide and the fluorindine which separates on cooling is sulphonated; cotton is dyed a clear blue by treatment for 1 hour in an aqueous solution at 85--90 DEG C. containing the dyestuff product, sodium chloride and an alkylnaphthalenesulphonate obtainable as described in Specification 246,817, [Class 2 (iii)]; (2) The fluorindine obtained from 3 - aminopyrene and p - quinonedianil, as described in example 3 of Specification 442,732, is sulphonated; cotton yarn is dyed green, fast to light by treatment for 1 hour in an aqueous solution at 90--95 DEG C. containing the dyestuff product, sodium chloride and sodium carbonate; (3) Viscose yarn is similarly dyed with the dyestuff of (2) in an aqueous solution at 85--90 DEG C. containing sodium sulphate and Marseilles soap; (4) Mercerized cotton fabric is dyed grey by treatment for 1 hour in an aqueous solution at 85--90 DEG C. containing a dyestuff obtained as in (2) but with stronger sulphonation, sodium chloride and sodium carbonate. The Specification as open to inspection under Sect. 91 comprises also the use of alkali salts of sulphonic acids of fluorindine compounds in general. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE452006X | 1934-02-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB452006A true GB452006A (en) | 1936-08-11 |
Family
ID=6538588
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4367/35A Expired GB452006A (en) | 1934-02-10 | 1935-02-11 | A process of dyeing |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB452006A (en) |
-
1935
- 1935-02-11 GB GB4367/35A patent/GB452006A/en not_active Expired
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