[go: up one dir, main page]

GB1123303A - Production of pigmented resinous compositions - Google Patents

Production of pigmented resinous compositions

Info

Publication number
GB1123303A
GB1123303A GB24076/66A GB2407666A GB1123303A GB 1123303 A GB1123303 A GB 1123303A GB 24076/66 A GB24076/66 A GB 24076/66A GB 2407666 A GB2407666 A GB 2407666A GB 1123303 A GB1123303 A GB 1123303A
Authority
GB
United Kingdom
Prior art keywords
acid
ester
polymer
methacrylate
hydroxy
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
GB24076/66A
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.)
PPG Industries Inc
Original Assignee
Pittsburgh Plate Glass Co
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 Pittsburgh Plate Glass Co filed Critical Pittsburgh Plate Glass Co
Publication of GB1123303A publication Critical patent/GB1123303A/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
    • C09D157/00Coating compositions based on unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/30Introducing nitrogen atoms or nitrogen-containing groups
    • 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
    • C09B67/006Preparation of organic pigments
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09CTREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/44Carbon
    • C09C1/48Carbon black
    • C09C1/56Treatment of carbon black ; Purification
    • 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
    • C09D157/00Coating compositions based on unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C09D157/04Copolymers in which only the monomer in minority is defined
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/22Rheological behaviour as dispersion, e.g. viscosity, sedimentation stability
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2800/00Copolymer characterised by the proportions of the comonomers expressed
    • C08F2800/20Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)

Abstract

Pigmented compositions comprise a pigment dispersed in a vehicle comprising an iminemodified polymer containing at least 0.1% by weight of carboxylic acid units which have been reacted with an alkylenimine or substituted alkylenimine. Pigments which may be used include carbon black, titanium dioxide, phthalocyanine blue or green, red or yellow iron oxide, transparent orange or red iron oxide, indo red or yellow, molybdate orange, monastral violet, ultramarine blue and cadmium red. The polymer which is iminated is preferably an interpolymer of an ester of an ethylenically unsaturated carboxylic acid; the acid component may be copolymerized with such ester or be present in another polymer which is blended with the ester polymer. Other acid polymers which may be iminated include alkyds, e.g. the product derived from coconut fatty acid, trimethylol ethane, p-t-butylbenzoic acid and phthalic anhydride, and other polycarboxylic acid resins. Suitable acid monomers which may be used in, or with, the ester polymers are acrylic, methacrylic and related a -substituted acrylic acids, maleic acid, fumaric acid and half-esters of such dibasic acids, crotonic acid, 3-butenoic acid, tiglic acid and itaconic acid and its half-esters; copolymerizable fatty acids such as dehydrated castor oil acids may also be used. The ester component of the polymer may be an alkyl methacrylate or an hydroxy alkyl ester of an ethylenically unsaturated carboxylic acid; additional units of the polymer are derived, for example, from alkyl acrylates, acrylonitrile, methacrylonitrile, butadiene, vinyl acetate, vinyl chloride, dibutyl maleate, styrene vinyl toluene, a -alkyl styrenes, dibutyl maleate, glycidyl methacrylate or dimethylbenzyl acrylate. The iminating agent is an alkylenimine which may contain substituents such as aryl, alkaryl, aralkyl, cyano, halo, amino, hydroxy, alkoxy, carbalkoxy and nitrile; preferred compounds are those of 2 to 4 carbon atoms, e.g. ethylenimine, 1,2 - propylenimine and N-(2 - hydroxy ethyl) - ethylenimine. Imination is effected by heating the components, e.g. at 50-150 DEG C. and may take place during or after polymerization. Polymerization of the starting monomers is generally effected using a peroxy catalyst, e.g. cumene hydroperoxide or benzoyl peroxide, or an azo catalyst, and in the presence of an organic solvent, e.g. xylene/butanol or toluene, which remains as part of the dispersing vehicle; a mercaptan may also be present. Additional solvent may also be included in the pigment composition, e.g. butanol, toluene, xylene, acetone, methyl ethyl ketone or ethylene glycol ethyl ether acetate. p-Phenylenediamine may also be added, and in one example a carbon black dispersion is formulated into a black enamel by mixing with a butylated melamine-formaldehyde resin, and cured coatings are prepared therefrom.ALSO:In an Example, steel panels are sprayed with a black enamel composition comprising in an organic solvent (a) an interpolymer of n-butyl methacrylate, methyl methacrylate, ethyl acrylate, 2-hydroxy-n-propyl methacrylate and methacrylic acid, wherein the acid groups have been reacted with 1,2-propylenimine (b) carbon black (c) p-phenylene diamine and (d) butylated melamine-formaldehyde resin, and then baked at 250 DEG C. for 30 minutes. In similar Examples (i) the 1, 2-propylenimine is replaced by ethylenimine and (ii) component (c) is omitted.
GB24076/66A 1965-06-01 1966-05-31 Production of pigmented resinous compositions Expired GB1123303A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US46049765A 1965-06-01 1965-06-01

Publications (1)

Publication Number Publication Date
GB1123303A true GB1123303A (en) 1968-08-14

Family

ID=23828950

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24076/66A Expired GB1123303A (en) 1965-06-01 1966-05-31 Production of pigmented resinous compositions

Country Status (7)

Country Link
AT (1) AT278210B (en)
BE (1) BE681937A (en)
CH (1) CH465859A (en)
DE (1) DE1669253A1 (en)
GB (1) GB1123303A (en)
NL (1) NL6607487A (en)
SE (1) SE324024B (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4451608A (en) * 1982-06-30 1984-05-29 Union Carbide Corporation Amphoteric acrylic ester based latexes
GB2135318A (en) * 1983-01-29 1984-08-30 Nippon Paint Co Ltd Resinous composition for coating use
US4563492A (en) * 1983-01-29 1986-01-07 Hirotoshi Umemoto Resinous composition which is useful for the dispersion difficulty dispersible coloring matter
WO2013083747A1 (en) * 2011-12-08 2013-06-13 Dow Corning Corporation Treatment of carbon based filler
US9000088B2 (en) 2011-12-08 2015-04-07 Dow Corning Corporation Hydrolysable silanes and elastomer compositions containing them
US9080057B2 (en) 2011-12-08 2015-07-14 Dow Corning Corporation Treatment of filler with silane
US9321792B2 (en) 2011-12-08 2016-04-26 Dow Corning Corporation Hydrolysable silanes
US9440997B2 (en) 2011-12-08 2016-09-13 Dow Corning Corporation Hydrolysable silanes

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4451608A (en) * 1982-06-30 1984-05-29 Union Carbide Corporation Amphoteric acrylic ester based latexes
GB2135318A (en) * 1983-01-29 1984-08-30 Nippon Paint Co Ltd Resinous composition for coating use
US4563492A (en) * 1983-01-29 1986-01-07 Hirotoshi Umemoto Resinous composition which is useful for the dispersion difficulty dispersible coloring matter
WO2013083747A1 (en) * 2011-12-08 2013-06-13 Dow Corning Corporation Treatment of carbon based filler
CN103987795A (en) * 2011-12-08 2014-08-13 道康宁公司 Treatment of carbon based filler
US9000088B2 (en) 2011-12-08 2015-04-07 Dow Corning Corporation Hydrolysable silanes and elastomer compositions containing them
US9080057B2 (en) 2011-12-08 2015-07-14 Dow Corning Corporation Treatment of filler with silane
US9321792B2 (en) 2011-12-08 2016-04-26 Dow Corning Corporation Hydrolysable silanes
US9440997B2 (en) 2011-12-08 2016-09-13 Dow Corning Corporation Hydrolysable silanes

Also Published As

Publication number Publication date
NL6607487A (en) 1966-12-02
CH465859A (en) 1968-11-30
AT278210B (en) 1970-01-26
DE1669253A1 (en) 1970-10-01
BE681937A (en) 1966-12-01
SE324024B (en) 1970-05-19

Similar Documents

Publication Publication Date Title
US3940353A (en) Pigment dispersions and lacquers containing copolymer of isobornyl methacrylate
US4144212A (en) Air-curing copolymer latices
US3536687A (en) Polymers and copolymers from cyclohexenyl-alkyl alcohol ester of alpha,beta-unsaturated acids
US4016332A (en) Mercaptan blocked thermosetting copolymers
GB1340179A (en) Polymeric materials and dispersions containing them
GB1109643A (en) Interpolymers and coating compositions made therefrom
GB1123303A (en) Production of pigmented resinous compositions
US3681298A (en) Copolymer containing isobornyl methacrylate
US8809446B2 (en) Substituted 3-oxopentanoates and their uses in coating compositions
US3256233A (en) Water-base coating composition of emulsified polymer solids and styrenemaleic interpolymer
KR960014279A (en) Copolymers comprising cyclic or polycyclic monomers with specific isomer distributions and their use in paint compositions
EP0006935B1 (en) Modified copolymers, process for their production and their use
EP0072127B1 (en) Autoxidizable polymer compositions, articles made therefrom and processes for making both
US4670521A (en) Process for producing tertiary amino group-containing vinyl polymers and curable resin compositions based on these polymers
USRE30530E (en) Polymerizable monomers
US4812549A (en) Resinous composition comprising an acrylic resin having end carboxyl bearing long pendant groups and preparation thereof
JPH08509768A (en) Thermosetting coating composition
US3296175A (en) Polymer latices which have high viscosities and coating composition containing the same
US3203935A (en) Polymeric compositions of terpolymers reacted with aminohydroxy compounds
US4031290A (en) Mercaptan blocked thermosetting copolymers
GB838656A (en) Production of resinous compositions
US4310453A (en) Pigment dispersions containing copolymer of oxazolidinylalkyl or oxazolidinylalkoxyalkyl (meth)acrylate
US3108088A (en) Resinous compositions comprising a styrene polymer and an aldehyde modified interpolymer of an acid amide and a vinyl monomer and articles coated therewith
US3085076A (en) Heat curable composition comprising a latex of a carboxylated diene polymer, primary metal drier, and a secondary curing agent and a latex paint thereof
US2850469A (en) Soluble interpolymers of ethylenic monomers and polyesters of alphabeta ethylenic polycarboxylic acids