GB418622A - Manufacture of chromiferous dyestuffs - Google Patents

Manufacture of chromiferous dyestuffs

Info

Publication number
GB418622A
GB418622A GB2474/34A GB247434A GB418622A GB 418622 A GB418622 A GB 418622A GB 2474/34 A GB2474/34 A GB 2474/34A GB 247434 A GB247434 A GB 247434A GB 418622 A GB418622 A GB 418622A
Authority
GB
United Kingdom
Prior art keywords
acids
acid
chromium
azo
wool
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
GB2474/34A
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.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB418622A publication Critical patent/GB418622A/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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/01Complex metal compounds of azo dyes characterised by the method of metallisation

Landscapes

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

Abstract

Azo dyes, chromium compounds of; acid wool dyes, dyeing with.--Chromiferous azo dyestuffs are obtained by treating, in presence of a soluble salt of an organic acid, an azo dyestuff of the general formula HO--R1--N = N--R2, wherein R1 is a sulphonated naphthalene residue, R2 is a naphthol residue and the hydroxyl group of the residue R1 is in o-position to the azo bridge, with an agent yielding chromium used in such proportion that there is less than one atomic proportion of chromium for each chromable group in the dyestuff molecule. The products give fast level blue to black shades on animal fibres, e.g. wool or silk. The treatment may be effected in an open vessel or under pressure and with or without further additions such as an inorganic salt or organic or inorganic acid, in neutral or acid medium. Specified agents yielding chromium are the chloride, fluoride, sulphate, sulphite, acetate, formate, oxalate and benzenesulphonate or mixtures thereof. Specified soluble salts of organic acids are sodium, potassium or ammonium formate, acetate, propionate, oxalate, succinate, malonate, hexahydrobenzoate, hexahydrophthalate, o -benzylsulphonate, N-o -methylsulphonates and the corresponding salts of amino-, oxy- and aminooxy-acids, halogenated or nitrated acids, oxamino - acids, aminosulphonic acids of the benzene, naphthalene or anthracene series aminonaphtholsulphonic acids, benzoic and phthalic acids, oxybenzoic sulphosalicylic, sulphoaminosalicylic and sulphophthalic acids. The following examples are specified: (1) 46,1 parts by weight of the azo dyestuff from nitrated 1 : 2-diazonaphthol-4-sulphonic acid and 2-naphthol are boiled for 5 hours under reflux with a solution containing caustic soda, sodium formate and chromium fluoride corresponding to 5,32 parts of Cr2O3 and the solution is evaporated in vacuo; the product dyes wool fast black tints from a bath containing an organic acid and sulphuric acid. (2) 4,16 Parts of the azo dyestuff 2 : 1-aminonaphthol - 4 - sulphonic acid --> 2 - naphthol is boiled under reflux with a solution containing caustic soda, chromium formate corresponding to 0,42 part of Cr2O3, and the disodium salt of 1 - oxy - 4 - sulphobenzene - 2 - carboxylic acid, and the solution is filtered and concentrated and the dyestuff salted out; the product dyes wool fast marine blue tints. Examples of the dyeing processes for wool and loaded or unloaded silk are also given. Specifications 269,522, [Class 2 (iii)], 364,148, and 408,497 are referred to.
GB2474/34A 1933-01-25 1934-01-24 Manufacture of chromiferous dyestuffs Expired GB418622A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH418622X 1933-01-25

Publications (1)

Publication Number Publication Date
GB418622A true GB418622A (en) 1934-10-29

Family

ID=4514643

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2474/34A Expired GB418622A (en) 1933-01-25 1934-01-24 Manufacture of chromiferous dyestuffs

Country Status (1)

Country Link
GB (1) GB418622A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2417735A (en) * 1941-10-15 1947-03-18 Geigy Ag J R Method of chroming dyestuffs with ortho hydroxy carboxylic acid chromium complexes
US2428866A (en) * 1943-06-04 1947-10-14 Geigy Ag J R Chromable dyestuffs and a process of making same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2417735A (en) * 1941-10-15 1947-03-18 Geigy Ag J R Method of chroming dyestuffs with ortho hydroxy carboxylic acid chromium complexes
US2428866A (en) * 1943-06-04 1947-10-14 Geigy Ag J R Chromable dyestuffs and a process of making same

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