GB926975A - Process for dyeing and padding hydrophobic materials - Google Patents
Process for dyeing and padding hydrophobic materialsInfo
- Publication number
- GB926975A GB926975A GB2289061A GB2289061A GB926975A GB 926975 A GB926975 A GB 926975A GB 2289061 A GB2289061 A GB 2289061A GB 2289061 A GB2289061 A GB 2289061A GB 926975 A GB926975 A GB 926975A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- dichloro
- benzoquinone
- diimine
- diphenylamine
- 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
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/32—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using oxidation dyes
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Abstract
Materials of aromatic polyesters, polyamides, polyurethanes, polyacrylonitrile and its copolymerisates, cellulose esters and polyolefins are dyed mainly dark shades, particularly black, by treating consecutively (in either sequence) with aromatic compounds containing primary and/or secondary amino groups or their salts and with (a) quinones or (b) N-haloquinone-imines or N,N1-dihaloquinone-diimines of optionally substituted quinones or (c) with compounds containing the grouping <FORM:0926975/IV(a)/1> in a non-aromatic carbocyclic ring, where X and Y denote carbon-carbon bonds or hydrogen or halogen atoms; alternatively with (d) compounds convertible into quinoid compounds by action of oxidizing agents and (e) organic or inorganic oxidizing agents, or mixtures of (a) and/or (b) and/or (c) and/or (d) and (e). The amino group containing compounds specified are: 4-amino-diphenylamine, 4-amino-41-methoxy-diphenylamine, 1,8-diamino-naphthalene, benzidine, 4-amino-naphthalene-1,11-azo-41-aminobenzene, 3-methoxy-4-aminodiphenylamine, 4-amino-41-cyclohexyl-diphenylamine, 4-amino-41-methyl-diphenylamine, 4-amino-41-naphthyl-diphenylamine, 2,4-diamino-diphenylamine, diamisidine, m-phenylenediamine, 4-amino-2-chloro-41-(N-dihydroxyethyl)-amino-1,11 -azobenzene, 4-benzoylamido-2,5-dimethoxy-1-aminobenzene, N,N1-bis-(4-aminophenyl)-4,41-diaminodiphenylamine, N,N1-bis-(4-aminophenyl)-4,41-diaminodiphenylether, N,N1-bis-(4-aminophenyl)-4,41-diamino-diphenylmethane, 4,41-diaminostilbene, N,N1-bis-(4-aminophenyl)-4,41-diaminostilbene, N,N1-bis-(4-aminophenyl)-4,41-diamino-3, 31-dimethoxy-diphenyl, 1-phenylamino-4-amino-naphthalene, 4,41-diamino-azobenzene, 4-(41-amino-phenylamino)-benzophenone and 1-(41-amino-phenylamino)-2-methoxy benzene. Specified (a) are: benzoquinone-(1,4), naphthoquinone-(1,4), 2,5-dichlorobenzoquinone-(1,4), 2,3,5,6-tetrachlorobenzoquinone-(1,4), 2,6-dichlorobenzoquinone-(1,4), 2,3,6-trichlorobenzoquinone-(1,4), the corresponding bromine derivatives, 1,2-benzo- or naphthoquinone or their derivatives, 2-phenyl-1,4- or 1,2-benzoquinone, diphenylquinone and their substitution products. Specified (b) are: N,N1-dichloro-p-benzoquinone-imine, 2,6-dichloro-4-monochloriminobenzoquinone, 2,5- and 2,6-dichloro-N,N1-dichloro-p-benzoquinone-diimine, 2-chloro-N,N1-dichloro-p-benzoquinone-diimine, 2,5-dichloro-N-chloro-N1-acetyl-p-benzoquinone-diimine, N-chloro-N1-acetyl-p-benzoquinone-diimine, N-methyl-N1-chloro-p-benzoquinone-diimine, 2-methyl-4-monochlorimino-p-benzoquinone, N,N1-dichloro-diphenylquinone-diimine and naphthoquinone-1,4-dichloro-diimine. Specified (c) are: cyclohexanone, cyclohexane-dienone, heptachlorocyclohexenone, pentachlorotetralone and hexachlorocyclohexadienone. Specified (d) are: p-benzohydroquinone, p-phenylenediamine, 1,4-naphthylene-diamine, 1,4-dihydroxynaphthalene, monochlorohydroquinone, 2,6- and 2,5-dichloro-hydroquinone, p-aminophenyl, monochlorophenylene-1,4-diamine, 2- and 3-chloro-4-amino-phenol, 2,6-dichloro-4-aminophenol, 2,5-dichloro-p-phenylene-diamine, 2-nitro-4-aminophenol, 4-amino-phenol sulphate, o-phenylenediamine, phenylenediamine, o-amino-phenol, pyrocatechol and 1-amino-2-hydroxy-3-chlorobenzene and specified (e) are: benzoyl peroxide, acetyl peroxide, alkali metal bichromates, permanganates and persulphates and sodium chlorite with or without an acid or alkali. The components may be applied as an aqueous solution or dispersion at temperatures of up to 140 DEG C. in the presence of normal carriers, emulsifying and dispersing agents. The amino group containing compound may be stabilized with a reducing agent and if it is in the form of a salt, the free base is liberated by the addition of an alkali. Between the two application stages described above may be interposed drying, thermofixing and soaping steps. An after-treatment with alkaline reducing agents or acidic oxidizing agents may also be included. Many examples of dyeing are given. Specifications 414,932, 645,594 and 870,045 are referred to.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1960F0031493 DE1139810B (en) | 1960-06-23 | 1960-06-23 | Process for dyeing structures made of hydrophobic materials |
DEF32166A DE1145137B (en) | 1960-09-21 | 1960-09-21 | Process for dyeing structures made of hydrophobic materials |
DEF32517A DE1284933B (en) | 1960-11-10 | 1960-11-10 | Process for dyeing structures made of hydrophobic materials |
DEF32818A DE1169411B (en) | 1960-12-22 | 1960-12-22 | Process for dyeing structures made of hydrophobic materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB926975A true GB926975A (en) | 1963-05-22 |
Family
ID=27436878
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2289061A Expired GB926975A (en) | 1960-06-23 | 1961-06-23 | Process for dyeing and padding hydrophobic materials |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE604976A (en) |
CH (1) | CH376471A (en) |
GB (1) | GB926975A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3441363A (en) * | 1965-10-07 | 1969-04-29 | Sandoz Ag | Dyeing of hydrophobic materials |
WO2001003651A2 (en) * | 1999-07-13 | 2001-01-18 | Henkel Kommanditgesellschaft Auf Aktien | Agent for dyeing fibres containing keratin |
AT505137B1 (en) * | 2007-04-16 | 2009-01-15 | Hinrichs Karl Heinz Dipl Ing | COMBINED AIR WATER HEAT EXCHANGER |
-
1961
- 1961-06-14 BE BE604976A patent/BE604976A/en unknown
- 1961-06-23 CH CH739561A patent/CH376471A/en unknown
- 1961-06-23 GB GB2289061A patent/GB926975A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3441363A (en) * | 1965-10-07 | 1969-04-29 | Sandoz Ag | Dyeing of hydrophobic materials |
WO2001003651A2 (en) * | 1999-07-13 | 2001-01-18 | Henkel Kommanditgesellschaft Auf Aktien | Agent for dyeing fibres containing keratin |
WO2001003651A3 (en) * | 1999-07-13 | 2001-07-12 | Henkel Kgaa | Agent for dyeing fibres containing keratin |
AT505137B1 (en) * | 2007-04-16 | 2009-01-15 | Hinrichs Karl Heinz Dipl Ing | COMBINED AIR WATER HEAT EXCHANGER |
Also Published As
Publication number | Publication date |
---|---|
CH376471A (en) | 1963-12-31 |
BE604976A (en) | 1961-12-14 |
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