GB295594A - Manufacture of dyestuffs containing chromium - Google Patents

Manufacture of dyestuffs containing chromium

Info

Publication number
GB295594A
GB295594A GB23325/28A GB2332528A GB295594A GB 295594 A GB295594 A GB 295594A GB 23325/28 A GB23325/28 A GB 23325/28A GB 2332528 A GB2332528 A GB 2332528A GB 295594 A GB295594 A GB 295594A
Authority
GB
United Kingdom
Prior art keywords
dyestuff
acid
fast
hrs
heated
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
GB23325/28A
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 GB295594A publication Critical patent/GB295594A/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

295,594. Soc. of Chemical Industry in Basle. Aug. 13, 1927, [Convention date]. Azo dyes, soluble chromium compounds of.- Azo dyestuffs are converted into chromium compounds by treatment, in presence of a watersoluble sulphide, with hydrated chromium oxide with or without pressure, a protective colloid or an organic or inorganic salt being added if necessary. In some cases the presence of organic agents such as glucose, soluble degradation products of starch or cellulose, glycerine, sulphitecellulose lye, or lignin-sulphonic acid favours the reaction. When the parent dyestuffs contain nitro groups the products may contain amino, azo, or azoxy groups according to the proportion of reducing agent used. The products give fast dyeings on vegetable, animal, or regenerated cellulose fibres and are suitable for colouring varnishes. The following examples are specified. (1) A paste containing the dyestuff 6-nitro-2- aminophenol-4-sulphonic ->- #-naphthol is. heated for 12-15 hrs. at 90-100‹ C. with sodium sulphide, chromium hydroxide paste, and sulphite cellulose lye; the separated dyestuff dyes wool from a sulphuric acid bath a. fast brownviolet. (2) The same dyestuff paste is heated for 15 hrs. at 90-100‹ C. with sodium sulphide, chromium hydroxide paste and caustic soda lye; the separated dyestuff dyes wool from a sulphuricacid bath a fast brown-violet, and may be diazotized and coupled with #-naphthol to produce a disazo dyestuff which dyes silk from an acetic acid bath a fast black-blue. (3) A paste containing the sodium salt of the dyestuff 4-chloro-2- aminophenol # 1-(m-sulphamido) phenyl-3- methyl-5-pyrazolone is heated for 6 hrs. under pressure with sodium sulphide, chromium hydroxide paste, and water; the separated dyestuff dyes wool from a sulphuric acid bath a fast red-orange; the corresponding chromium compounds of the dyestuffs 1 : 2-aminonaphthol-4- sulphoxiic acid # 1-phenyl-3-methyl-5-pyrazolone or 1-(m-nitro)-phenyl-3-methyl-5-pyrazolone dye wool fast red tints, and that of a dyestuff chloraminophenolsulphonic acid # 1-phenyl-3- methyl-5-pyrazolone dyes wool fast orange-red. (4) The dyestuff 4-chloro-2-aminophenol # barbituric acid is heated for 8 hrs. at 80-90‹ C. with sodium sulphide, chromium hydroxide paste, caustic soda. lye, sugar, and water; the separated dyestuff dyes wool a fast orange; if the heating is for 4 hrs. at 110-115‹ C. the product dyes a brown-orange. (5) The sodium, salt of the dyestuff 4-nitro-2-aminophenol # #-napbthol is heated for 16 hrs. at 90-100‹ C. with sodium sulphide, chromium hydroxide paste. caustic soda lye, and water: the product, treated with formalehyde and bisulphite, dyes silk and wool fast violet-black. (6) The sodium salt of the dyestuff from the nitrated diazo compound of 1 : 2-aminonaphthol-4-sulphonic acid and 1 : 4-naphtholsulphonic acid is heated for 3 hrs. at 90-100‹ C. with sodium sulphide, chromium hydroxide paste, sugar, and water; the product dyes wool and silk fast blue-grey. (7) The sodium salt of the dyestuff 1 : 2-aminonaphthol-4- sulphonic acid # 1-naphthol-4- : 8-disulphonic acid is heated for 12 hours at 90-100‹ C. with sodium sulphide, chromium hydroxide paste, and water; the product dyes wool a fast blue.-grey. (8) The sodium salt of the dyestuff 2 : 1-aminonaphthol-4 : 8-disulphonic acid # barbituric acid is heated for 16-20 hrs. at 90-100‹ C. with sodium sulphide, chromium hydroxide paste, caustic potash, glycerine, and water; the product dyes wool a fast. bluish red. (9) The disodium salt of the dyestuff 5-nitro-2-aminophenol -> phenyl- 2 : 5: 7-acid is heated for 16 hrs. at 90-100‹ C. with sodium sulphide, chromium hydroxide paste, and glycol; the product dyes cotton a bluegrey. (10) A paste containing the dyestuff from the nitrated diazo compounds of 1 : 2-aminonaphthol-4-sulphonic acid and #-naphthol is heated for 12 hrs. at 80-85‹ C. with sodium sulphide, chromium hydroxide paste, and caustic potash; the product dyes wool and silk fast blue-grey. (11) and (12). Wool and silk are, dyed in acid baths containing the. lyestuffs of examles (3) and (6) respectively. (13) Cotton is dyed in a Glauber's salt bath containing the dyestuff of example (9). (14). 2 per cent of the dyestuff of example (3) is incorporated in a hot celluloid varnish. (15) Artificial silk, e.g. viscose, is dyed in a bath containing salt, which is neutral, feebly alkaline, or feebly acid with acetic acid.
GB23325/28A 1927-08-13 1928-08-13 Manufacture of dyestuffs containing chromium Expired GB295594A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH295594X 1927-08-13

Publications (1)

Publication Number Publication Date
GB295594A true GB295594A (en) 1929-11-13

Family

ID=4488929

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23325/28A Expired GB295594A (en) 1927-08-13 1928-08-13 Manufacture of dyestuffs containing chromium

Country Status (1)

Country Link
GB (1) GB295594A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1267358B (en) * 1958-07-30 1968-05-02 Ici Ltd Process for the production of metallized azo dyes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1267358B (en) * 1958-07-30 1968-05-02 Ici Ltd Process for the production of metallized azo dyes

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