GB329014A - Improvements in the dyeing of regenerated cellulose materials - Google Patents

Improvements in the dyeing of regenerated cellulose materials

Info

Publication number
GB329014A
GB329014A GB416429A GB416429A GB329014A GB 329014 A GB329014 A GB 329014A GB 416429 A GB416429 A GB 416429A GB 416429 A GB416429 A GB 416429A GB 329014 A GB329014 A GB 329014A
Authority
GB
United Kingdom
Prior art keywords
acid
nitraniline
reduced
alkaline
naphtholsulphonic
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
Application number
GB416429A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB416429A priority Critical patent/GB329014A/en
Publication of GB329014A publication Critical patent/GB329014A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/02Disazo dyes
    • C09B35/039Disazo dyes characterised by the tetrazo component
    • C09B35/04Disazo dyes characterised by the tetrazo component the tetrazo component being a benzene derivative

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

329,014. Imperial Chemical Industries, Ltd., and Brightman, R. Feb. 7, 1929. Azo dyes. - Regenerated cellulose materials, e.g. viscose silks, are dyed in level violet-blue to blue shades by the application of disazo dyes obtained by coupling with a 1: 8- or 2 : 8-aminonaphthol mono- or di-sulphonic acid, a diazoazo compound produced by diazotizing the aminoazo compounds resulting from reduction of the nitro group or hydrolysis of the acetyl group of the mono-azo dyes of the type p-nitraniline, p-aminoacetanilide, or a nuclear substitution derivative thereof, other than an alkoxy derivative # a naphthol, a naphtholsulphonic acid, or an N- substituted 2 : 8-aminonaphtholsulphonic acid. In an example the nitro group of the dyestuff 4- nitraniline # (alkaline) 8-oxy-2 : 2<1>-dinaphthylamine-3 : 6-disulphonic acid is reduced with alkaline sodium sulphide, and the aminoazo product is diazotized and coupled (alkaline) with H-acid; the product dyes viscose silk blue. In a further example, a regenerated cellulose silk is dyed a bright blue in a dyebath containing Glauber's salt, soap, soda ash, and the dyestuff obtained by coupling (alkaline) with 1 : 8-aminonaphthol- 2 : 4-disulphonic acid, the diazo compound from the aminoazo product of reduction of the dyestuff 4-nitraniline # 1 : 4-naphtholsulphonic acid. A table is also given showing the shades obtained on viscose silk with the following dyestuffs : 4-nitraniline or 2-chloro-4-nitraniline # 1 :4-naphtholsulphonic acid (reduced) # (alkaline) 1: 8-aminonaphthol-2 : 4-disulphonic acid; 4-nitraniline-2-sulphonic acid # 2-naphthol (reduced), 4-nitramline # (alkaline) benzoyl- 2 : 8 : 6-acid (reduced), 2-chloro-4-nitraniline # (alkaline) 8-oxy-2-2<1>-dinaphthylamine-3: 6-disulphonic acid (reduced), or 5-nitro-2-toluidine # 2: 7-naphtholsulphonic acid (reduced) # (alkaline) H-acid; 4-nitraniline-2-sulphonic acid # 1 : 4-naphtholsulphonic acid (reduced), or 4- nitraniline # 1: 5- or 1 3-nitraniline-2-sulphonic acid # 2-naphthol (reduced) # (alkaline) 1 : 8 : 4-acid; 4-aminoacetanilide # 2 : 6-naphtholsulphonic acid (hydrolyzed) # (alkalme) 1: 8: 4-acid; 4-nitraniline # 1: 4- naphtholsulphonic acid (reduced) # (alkaline) 2 : 8-aminonaphthol-3 : 6-disulphonic acid. A similar table in the Provisional Specification shows the shades obtained on viscose silk with the following additional dyestuffs :-4-aminoacetanilide # 8-oxy-2: 2<1>-dinaphthylamine- 3 :6-disulphonic acid (hydrolyzed) # H-acid; 4-aminoacetanilide-2-sulphonic acid # 8-oxy- 2: 2<1>-dinaphthylamine-3 : 6-disulphonic acid or phenyl-2 : 8 : 6-acid (hydrolyzed) # H-acid; 4- nitraniline # 1 : 4-naphtholsulphonic acid (reduced) # 2 : 8 : 6-acid; 4-nitraniline-2-sulphonic acid # 2-naphthol (reduced) # 1 : 8-aminonaphthol-2 : 4-disulphonic acid; 4- nitraniline-2-sulphonic acid # phenyl-2 : 8 : 6- acid (reduced) # H-acid.
GB416429A 1929-02-07 1929-02-07 Improvements in the dyeing of regenerated cellulose materials Expired GB329014A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB416429A GB329014A (en) 1929-02-07 1929-02-07 Improvements in the dyeing of regenerated cellulose materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB416429A GB329014A (en) 1929-02-07 1929-02-07 Improvements in the dyeing of regenerated cellulose materials

Publications (1)

Publication Number Publication Date
GB329014A true GB329014A (en) 1930-05-07

Family

ID=9771917

Family Applications (1)

Application Number Title Priority Date Filing Date
GB416429A Expired GB329014A (en) 1929-02-07 1929-02-07 Improvements in the dyeing of regenerated cellulose materials

Country Status (1)

Country Link
GB (1) GB329014A (en)

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