GB976084A - Pigment preparations - Google Patents

Pigment preparations

Info

Publication number
GB976084A
GB976084A GB766061A GB766061A GB976084A GB 976084 A GB976084 A GB 976084A GB 766061 A GB766061 A GB 766061A GB 766061 A GB766061 A GB 766061A GB 976084 A GB976084 A GB 976084A
Authority
GB
United Kingdom
Prior art keywords
radical
dyes
resins
grinding
aliphatic
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
GB766061A
Inventor
Werner Albert Ritter
Kurt Hofer
Karl Ulrich Steiner
Erwin Hess
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.)
Sandoz AG
Original Assignee
Sandoz 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 Sandoz AG filed Critical Sandoz AG
Publication of GB976084A publication Critical patent/GB976084A/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
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D17/00Pigment pastes, e.g. for mixing in paints
    • 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
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0071Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
    • 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
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0071Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
    • C09B67/0084Dispersions of dyes
    • C09B67/0085Non common dispersing agents
    • C09B67/0086Non common dispersing agents anionic dispersing agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Paints Or Removers (AREA)

Abstract

A pigment preparation contains as dispersing agent at least one compound of the general formula <FORM:0976084/C1/1> where R = a hydrocarbon radical which may be substituted, A=an alkylene radical having 1 or 2 carbon atoms, n=an integer up to 80, and X=hydrogen or a radical which dissociates as a cation in water, R may be an aliphatic straight chain or branched radical, e.g. dodecyl or tridecyl or mixtures thereof, or an alkyl aryl radical in which the aryl radical is mono- or multi-nuclear, or an alkyl cycloalkyl radical. X may be sodium, potassium, ammonium or an aliphatic, cyclic or hydroxyamine. Other substances which may be present include polyglycol ethers of the formula <FORM:0976084/C1/2> where R has the meaning as in (I) and y is 1 to 50, aliphatic diols and ethers thereof, 2-methyl-2-hydroxy pentanone-4, dimethyl sulphoxide, butyrolacetone, tetrahydrofurfuryl alcohol, condensation products of formaldehyde and naphthalene sulphonic acids, sulphuric acid esters of fatty alcohols, alkyl aryl sulphonates, sulphosuccinic acid dialkyl esters with straight chain or branched alkyl radicals, keto-alcohols and lactones. The pigments (e.g. up to 5 microns) may be organic or inorganic and may be coloured, e.g. metal free or metal-containing, unhalogenated or halogenated phthalocyanines, azo dyes, dioxazine derivatives, anthraquinone, dyes, nitroso dyes, basic dyes, quinacridine-7,14 diones, perylenetetracarboxylic acid diimides, titanium dioxide, barium sulphate, china clay, calcium carbonate, carbon black, oxides and hydrated oxides of iron, chromium, lead or manganese and cadmium sulphide. Infusorial earth and silicon oxides may be included. The preparation may be prepared by grinding the pigment in an organic liquid, roller milling, adding dispersing agent (I) and other additives, homogenizing, grinding and adding an agent to improve the odour; or by mixing all the components and grinding simultaneously. The preparations may be incorporated in oil or water paints based on natural resins, casein, chlorinated rubber or synthetic resins. Specification 793,113 is referred to.ALSO:Paint is prepared by incorporating into styrene-butadiene polymers, polyacrylates, polymethacrylates, polyvinyl acetate, polyvinyl propionate, phenol resins, urea resins, melamine resins, cyclohexanone resins, alkyd resins, unsaturated polyester resins, polyurethane resins or epoxy resins a pigment preparation containing as dispersing agent at least one compound of the general formula <FORM:0976084/C3/1> where R=a hydrocarbon radical which may be substituted, A=an alkylene radical having 1 or 2 carbon atoms, n=an integer up to 80, and X= hydrogen or a radical which dissociates as a cation in water. R may be an aliphatic straight chain or branched radical, e.g. dodecyl or tridecyl or mixtures thereof, or an alkyl aryl radical in which the aryl radical is mono- or multi-nuclear, or an alkyl cycloalkyl radical. X may be sodium, potassium, ammonium or an aliphatic, cyclic or hydroxyamine. Other substances which may be present include polyglycol ethers of the formula <FORM:0976084/C3/2> where R has the meaning as in (I) and y is 1 to 50, aliphatic diols and ethers thereof, 2-methyl-2-hydroxy pentanone-4, dimethyl sulphoxide buryrolacetone, tetrahydrofurfuryl alcohol, condensation products of formaldehyde and naphthalene sulphonic acids, sulphuric acid esters of fatty alcohols, alkyl aryl sulphonates, sulphosuccinic acid dialkyl esters with straight chain or branched alkyl radicals, keto-alcohols and lactones. The pigments (e.g. up to 5 microns) may be organic or inorganic and may be coloured, e.g. metal free or metal-containing, unhalogenated or halogenated phthalocyanines, azo dyes, dioxarine derivatives, anthraquinone, dyes, nitroso dyes, basic dyes, quinaceridine-7, 14 diones, perylenetetracarboxylic acid diimides, titanum dioxide, barium sulphate, china clay, calcium carbonate, carbon black, oxides and hydrated oxides of iron, chromium, lead or manganese and cadmium sulphide. Infusorial earth and silicon oxides may be included. The resins may be dissolved or dispersed in water or vegetable oils. The preparation may be prepared by grinding the pigment in an organic liquid, roller milling, adding dispersing agent (I) and other additives, homogenising, grinding and adding an agent to improve the odour; or by mixing all the components and grinding simultaneously. Specification 793,113 is referred to.ALSO:A pigment preparation contains as dispersing agent at least one compound of the general formula <FORM:0976084/C4-C5/1> where R = a hydrocarbon radical which may be substituted, A = an alkylene radical having 1 or 2 carbon atoms, n = an integer up to 80, and X = hydrogen or a radical which dissociates as a cation in water. R may be an aliphatic straight chain or branched radical, e.g. dodecyl or tridecyl or mixtures thereof, or an alkyl aryl radical in which the aryl radical is mono- or multi-nuclear, or an alkyl cycloalkyl radical. X may be sodium, potassium, ammonium or an aliphatic, cyclic or hydroxyamine. Other substances which may be present include polyglycol ethers of the formula R-(OC2H4)y-O-CH2-CH2OH (II) where R has the meaning as in (I) and y is 1 to 50, aliphatic diols and ethers thereof, 2-methyl-2-hydroxy pentanone-4, dimethyl sulphoxide, buryrolacetone, tetrahydrofurfuryl alcohol, condensation products of formaldehyde and naphthalene sulphonic acids, sulphuric acid esters of fatty alcohols, alkyl aryl sulphonates, sulphosuccinic acid dialkyl esters with straight chain or branched alkyl radicals, keto-alcohols and lactones. The pigments (e.g. up to 5 microns) may be organic or inorganic and may be coloured, e.g. metal free or metal-containing, unhalogenated or halogenated phthalocyanines, azo dyes, dioxazine derivatives, anthraquinone, dyes, nitroso dyes, basic dyes, quinacridine-7,14 diones, perylenetetracarboxylic acid diimides, titanium dioxide, barium sulphate, china clay, calcium carbonate, carbon black, oxides and hydrated oxides of iron, chromium, lead or manganese and cadmium sulphide. Infusorial earth and silicon oxides may be included. The preparation may be prepared by grinding the pigment in an organic liquid, roller milling, adding dispersing agent (I) and other additives, homogenizing, grinding and adding an agent to improve the odour; or by mixing all the components and grinding simultaneously. The preparations may be incorporated in oil, or water paints based on natural resins, casein, chlorinated rubber or synthetic resins. Specification 793,113 is referred to.ALSO:A pigment preparation contains as dispersing agent at least one compound of the general formula: <FORM:0976084/B1-B2/1> where R is a hydrocarbon radical which may be substituted, A is an alkylene radical having 1 or 2 carbon atoms, n is an integer up to 80, and X is hydrogen or a radical which dissociates as a cation in water. R may be an aliphatic straight chain or branched radical, e.g. dodecyl or tridecyl or mixtures thereof, or an alkyl aryl radical in which the aryl radical is mono- or multi-nuclear, or an alkyl cycloalkyl radical. X may be sodium, potassium, ammonium or an aliphatic, cyclic or hydroxyamine. Other substances which may be present include polyglycol ethers of the formula: R-(OC2H4)y-O-CH2-CH2OH where R has the meaning as in (I) and y is 1 to 50, aliphatic diols and ethers thereof, 2-methyl-2-hydroxy pentanone-4, dimethyl sulphoxide, butyrolacetone, tetrahydrofurfuryl alcohol, condensation products of formaldehyde and naphthalene sulphonic acids, sulphuric acid esters of fatty alcohols, alkyl aryl sulphonates, sulphosuccinic acid dialkyl esters with straight chain or branched alkyl radicals, keto-alcohols and lactones. The pigments (e.g. up to 5 microns) may be unhalogenated or halogenated phthalocyanines, azo dyes, dioxarine derivatives, anthraquinone dyes, nitroso dyes, basic dyes, quinacridine-7,14 diones and perylenetetracarboxylic acid diimides. The preparation may be prepared by grinding the pigment in an organic liquid, roller milling, adding dispersing agent (I) and other additives, homogenizing, grinding and adding an agent to improve the odour; or by mixing all the components and grinding simultaneously. Specification 793,113 is referred to.
GB766061A 1960-03-04 1961-03-02 Pigment preparations Expired GB976084A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH251460A CH387202A (en) 1960-03-04 1960-03-04 Pigment preparations

Publications (1)

Publication Number Publication Date
GB976084A true GB976084A (en) 1964-11-25

Family

ID=4235491

Family Applications (1)

Application Number Title Priority Date Filing Date
GB766061A Expired GB976084A (en) 1960-03-04 1961-03-02 Pigment preparations

Country Status (4)

Country Link
CH (1) CH387202A (en)
DE (1) DE1211578B (en)
ES (1) ES265332A1 (en)
GB (1) GB976084A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3628976A (en) * 1967-11-03 1971-12-21 Ciba Geigy Ag Process of making perylene pigments
US3663229A (en) * 1966-10-12 1972-05-16 Agfa Gevaert Nv Photographic elements containing carboxyalkyl polyglycol ethers and esters
US5091013A (en) * 1987-02-12 1992-02-25 Miyoshi Kasei Co., Ltd. Moisture holding pigment and a cosmetic containing such a pigment
GB2458772A (en) * 2008-04-02 2009-10-07 Kansai Paint Co Ltd An Aqueou Coating

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2244777C3 (en) * 1972-09-13 1975-03-27 Bayer Ag, 5090 Leverkusen Aqueous pigment dispersions and their use
GB2035384B (en) * 1978-10-16 1982-12-01 Ici Ltd Stabilised aqueous dyestuff dispersions
DE102011010580A1 (en) 2011-02-08 2012-07-12 Clariant International Ltd. Aqueous pigment preparation useful e.g. for coloration of macromolecular materials, comprises inorganic white or colored pigment, polyglycol ether carboxylate, nonionic, anionic or amphoteric wetting and dispersing additive, and water

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2745857A (en) * 1952-02-23 1956-05-15 Dow Chemical Co Glycolic acid ethers of polyoxypropylene compounds and method of preparation
US2809122A (en) * 1954-06-24 1957-10-08 Sherwin Williams Co Dual purpose tinting base

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3663229A (en) * 1966-10-12 1972-05-16 Agfa Gevaert Nv Photographic elements containing carboxyalkyl polyglycol ethers and esters
US3628976A (en) * 1967-11-03 1971-12-21 Ciba Geigy Ag Process of making perylene pigments
US5091013A (en) * 1987-02-12 1992-02-25 Miyoshi Kasei Co., Ltd. Moisture holding pigment and a cosmetic containing such a pigment
GB2458772A (en) * 2008-04-02 2009-10-07 Kansai Paint Co Ltd An Aqueou Coating
GB2458772B (en) * 2008-04-02 2011-06-22 Kansai Paint Co Ltd Aqueous coating composition
US8053084B2 (en) 2008-04-02 2011-11-08 Kansai Paint Co., Ltd. Aqueous coating composition
CN101550308B (en) * 2008-04-02 2013-04-03 关西涂料株式会社 Aqueous coating composition

Also Published As

Publication number Publication date
ES265332A1 (en) 1961-09-01
CH387202A (en) 1965-01-31
DE1211578B (en) 1966-03-03

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