GB874620A - Process for dyeing organic products with pigment dyestuffs - Google Patents

Process for dyeing organic products with pigment dyestuffs

Info

Publication number
GB874620A
GB874620A GB14816/58A GB1481658A GB874620A GB 874620 A GB874620 A GB 874620A GB 14816/58 A GB14816/58 A GB 14816/58A GB 1481658 A GB1481658 A GB 1481658A GB 874620 A GB874620 A GB 874620A
Authority
GB
United Kingdom
Prior art keywords
amino
anthraquinoid
condensation product
residue
mols
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
GB14816/58A
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
Ciba AG
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 Ciba AG filed Critical Ciba AG
Publication of GB874620A publication Critical patent/GB874620A/en
Expired legal-status Critical Current

Links

Classifications

    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/28—Colorants ; Pigments or opacifying agents
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477—Six-membered rings
    • C08K5/3492—Triazines
    • C08K5/34922—Melamine; Derivatives thereof
    • 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
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/36—Dyes with acylated amino groups
    • C09B1/46—Dyes with acylated amino groups the acyl groups being residues of cyanuric acid or an analogous heterocyclic compound
    • C09B1/467—Dyes with acylated amino groups the acyl groups being residues of cyanuric acid or an analogous heterocyclic compound attached to two or more anthraquinone rings
    • 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
    • C09B6/00—Anthracene dyes not provided for above
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00—General methods for the manufacture of artificial filaments or the like
    • D01F1/02—Addition of substances to the spinning solution or to the melt
    • D01F1/06—Dyes
    • 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
    • D06P1/44—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 insoluble pigments or auxiliary substances, e.g. binders

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Textile Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Coloring (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Organic products such as lacquers, plastic compositions, and natural and artificial fibres are coloured with a pigment dyestuff of the formula: <FORM:0874620/IV (a)/1> wherein each A represents an anthraquinoid residue and Z represents an amino group which may be substituted by, for example, an ethyl group, a benzene residue or another anthraquinoid residue. The anthraquinoid residues may contain as a nuclear substituent a methoxy or benzoylamino group. Examples describe the use of the above pigments for colouring (1) a composition comprising polyvinyl chloride, dioctyl phthalate, cadmium stearate and titanium dioxide which is rolled to form a foil, (2) a nitrocellulose lacquer containing titanium dioxide, (3) acetyl cellulose which is then dissolved in acetone and dry-spun into filaments, (6) an alkyd-melamine bakeable lacquer containing titanium dioxide and (7) viscose which is then spun into filaments. Example 8 describes the dyeing of cotton from a bath containing, in addition to the pigment dyestuff, an isobutyl acrylate-acrylonitrile-acrylic acid copolymer latex, an aqueous emulsion of a methylol-melamine allyl ether modified with soya bean fatty acid, a water-soluble methyl ether of a urea-formaldehyde condensation product and formic acid. Example 9 describes a textile printing paste containing an aqueous binding agent and an ethylene oxide-nonyl phenol condensation product, in addition to the pigment dyestuff which has been incorporated into a composition comprising a solution of a melamine-formaldehyde condensation product etherified with butanol, a vinyl chloride-vinyl acetate copolymer plasticized with dioctadecyl phthalate and xylene. The pigment dyestuffs employed in the examples are those prepared from 1 mol of cyanuric chloride and 3 mols of 1-amino-, 1-amino-5-benzoylamino-, 1-amino-6-chloro-, 1-amino-6(7)-methoxy-and 1-amino-4-phenylamino-anthraquinone or 3 mols of 5-amino-isothiazoleanthrone or of 4-aminoantraquinone-1(N), -2-benzacridone. Others described are of the formula: <FORM:0874620/IV (a)/2> Specification 375,056 is referred to.ALSO:Natural and artificial fibres (including paper pulp) are coloured with a pigment dyestuff of the formula:- <FORM:0874620/IV(c)/1> wherein each A represents an anthraquinoid residue and Z represents an amino group which may be substituted by, for example, an ethyl group, a benzene residue or another anthraquinoid residue. The anthraquinoid residues may contain as a nuclear substituent a methoxy or benzoylamino group. Example 8 describes the dyeing of cotton from a bath containing, in addition to the pigment dyestuff, an isobutyl acrylate-acrylonitrile-acrylic acid copolymer latex, an aqueous emulsion of a methylolmelamine allyl ether modified with soya bean fatty acid, a water-soluble methyl ether of a urea-formaldehyde condensation product and formic acid. Example 9 describes a textile printing paste containing an aqueous binding agent and an ethylene oxide-nonyl phenol condensation product, in addition to the pigmentdyestuff which has been flushed with a composition comprising a solution of a melamineformaldehyde condensation product etherified with butenol, a vinyl chloride-vinyl acetate copolymer plasticized with dioctadecyl phthalate and xylene. The pigment dyestuffs employed in the examples are those prepared from 1 mol of cyanuric chloride and 3 mols of 1-amino-, 1-amino-5-benzoylamino-, 1-amino- 6-chloro-, 1-amino- 6(7)-methoxy- and 1-amino- 4-phenylamino-anthraquinone or 3 mols of 5-aminoisothiazoleanthrone or of 4-aminoanthraquinone-1(N), -2-benzacridone. Others described are of the formula:- <FORM:0874620/IV(c)/2> Specification 375,056 is referred to.
GB14816/58A 1957-05-08 1958-05-08 Process for dyeing organic products with pigment dyestuffs Expired GB874620A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH874620X 1957-05-08

Publications (1)

Publication Number Publication Date
GB874620A true GB874620A (en) 1961-08-10

Family

ID=4544305

Family Applications (1)

Application Number Title Priority Date Filing Date
GB14816/58A Expired GB874620A (en) 1957-05-08 1958-05-08 Process for dyeing organic products with pigment dyestuffs

Country Status (4)

Country Link
BE (1) BE567462A (en)
CH (1) CH348547A (en)
DE (1) DE1110403B (en)
GB (1) GB874620A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2000159A (en) * 1977-06-14 1979-01-04 Ciba Geigy Ag Process for dyeing high-molecular organic material in the melt
US4492790A (en) * 1981-01-31 1985-01-08 Bayer Aktiengesellschaft Vat dyestuffs of the trisanthraquinonylaminotriazine series

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1288788B (en) * 1959-05-06 1969-02-06 Ciba Geigy Coloring of high molecular weight organic products in bulk
US4329456A (en) * 1979-05-17 1982-05-11 Ciba-Geigy Ag Process for the preparation of vat dyes
DE3103312A1 (en) * 1981-01-31 1982-08-26 Bayer Ag, 5090 Leverkusen TRISANTHRACHINONYLAMINOTRIAZINE COMPOUNDS AND THE PRODUCTION AND USE THEREOF AS A COPPER DYE

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB691507A (en) * 1951-05-23 1953-05-13 American Cyanamid Co Triazine vat dyes
DE933144C (en) * 1951-12-07 1955-09-22 Ciba Geigy Process for dyeing or printing cellulose-containing materials and dye preparations suitable for its implementation

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2000159A (en) * 1977-06-14 1979-01-04 Ciba Geigy Ag Process for dyeing high-molecular organic material in the melt
GB2000159B (en) * 1977-06-14 1982-01-27 Ciba Geigy Ag Process for dyeing high-molecular organic material in the melt
US4492790A (en) * 1981-01-31 1985-01-08 Bayer Aktiengesellschaft Vat dyestuffs of the trisanthraquinonylaminotriazine series

Also Published As

Publication number Publication date
DE1110403B (en) 1961-07-06
BE567462A (en)
CH348547A (en) 1960-08-31

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