GB826009A - Coating compositions - Google Patents

Coating compositions

Info

Publication number
GB826009A
GB826009A GB3117855A GB3117855A GB826009A GB 826009 A GB826009 A GB 826009A GB 3117855 A GB3117855 A GB 3117855A GB 3117855 A GB3117855 A GB 3117855A GB 826009 A GB826009 A GB 826009A
Authority
GB
United Kingdom
Prior art keywords
phthalate
butyl
ethyl
vinyl
methyl
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
GB3117855A
Inventor
Bernard James Balfe
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB3117855A priority Critical patent/GB826009A/en
Publication of GB826009A publication Critical patent/GB826009A/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
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/10Homopolymers or copolymers of methacrylic acid esters
    • C09D133/12Homopolymers or copolymers of methyl methacrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride

Abstract

Surfaces, e.g. steel surfaces and those of cars, are sprayed and coated with a composition comprising a methyl methacrylate polymer or copolymer of molecular weight 60,000-100,000; a vinyl chloride/vinyl acetate resin in a proportion of 1 to 5 parts of methacrylate per part of vinyl resin and a plasticizer in a proportion of from 0 to 0.3 part per part of total polymer, all dissolved in a solvent of boiling-point 130-250 DEG C. The plasticizer may be dibutyl phthalate, dicyclohexanyl phthalate, dibenzyl sebacate, butyl benzyl phthalate, trichloroethyl phosphate, methyl phthalyl ethyl glycolate, polypropylene glycol adipate, lauric or benzoic acid modified polypropylene glycol adipate or certain blends thereof. Various solvent blends are mentioned incorporating benzene, toluene, xylene, methyl ethyl and methyl isobutyl ketone, acetone, petroleum ether and high boiling (130-250 DEG C.) solvents such as isophorone, diacetone alcohol, ethyl lactate, butyl acetate or lactate, ethyl ethylene glycol acetate or ethylene glycol butyl ether. The compositions may also comprise pigments such as rutile titanium dioxide, Deep Brunswick Green, Maroon MS, Kosmolac Carbon Black, Carbolac No. 2, Neo Spectra Mark II, barium chromate, Waxoline Black C.O. paste and other components such as linseed oil, monoglyceride and copper butyl phthalate. Specification 478,323, [Group IV], is referred to.ALSO:A sprayable coating composition comprises (1) methyl methacrylate polymer, or copolymer with acrylic or methacrylic p acids, of molecular weight 60,000-100,000; (2) a vinyl chloride/vinyl acetate resin in a proportion of 1-5 parts of methacrylate per part of vinyl resin; (3) a plasticizer in a proportion of from 0 to 0.3 part per part of total polymer; and (4) a solvent of boiling-point 130-250 DEG C. at atmospheric pressure. The preferred vinyl resin is a terpolymer of vinyl acetate, vinyl chloride and vinyl alcohol, and suitable plasticizers are dibutyl phthalate, dicyclohexanyl phthalate, dibenzyl sebacate, butyl benzyl phthalate, trichloroethyl phosphate, methyl phthalyl ethyl glycolate, polypropylene glycol adipate, polypropylene glycol adipate modified with lauric acid or with benzoic acid and certain blends thereof. Various solvent blends are mentioned incorporating benzene, toluene, xylene, methyl ethyl and methyl isobutyl ketone, acetone, petroleum ether, and high boiling (130-250 DEG C.) solvents such as isophorone, diacetone alcohol, ethyl lactate, butyl acetate or lactate, ethyl ethylene glycol acetaet or ethylene glycol butyl ether. The compositions may also comprise pigments such as rutile titanium dioxide, barium chromate, "Waxoline" Black C.O. Paste, Deep Brunswick Green, Maroon MS, Kosmolac Carbon Black, Carbolac No. 2, and Neo Spectra Mark II and other components such as linseed oil, monoglyceride and copper butyl phthalate and may be used in the automobile industry as car finishes. Specification 478,323, [Group IV], is referred to.
GB3117855A 1955-11-01 1955-11-01 Coating compositions Expired GB826009A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3117855A GB826009A (en) 1955-11-01 1955-11-01 Coating compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3117855A GB826009A (en) 1955-11-01 1955-11-01 Coating compositions

Publications (1)

Publication Number Publication Date
GB826009A true GB826009A (en) 1959-12-23

Family

ID=10319170

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3117855A Expired GB826009A (en) 1955-11-01 1955-11-01 Coating compositions

Country Status (1)

Country Link
GB (1) GB826009A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1287238B (en) * 1965-04-09 1969-01-16 Permalux Company Use of a mixture for coating polyvinyl and polyester surfaces
GB2147307A (en) * 1983-09-09 1985-05-09 Dulux Australia Ltd Thermo plastic coating compositions
US8071685B2 (en) 2005-12-09 2011-12-06 Rutgers, The State University Of New Jersey Method of recycling paints as a component of an immiscible polymer blend
CN113930120A (en) * 2021-11-29 2022-01-14 河南蓝翎环科防水材料有限公司 High-strength explosion-proof protective coating and production process thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1287238B (en) * 1965-04-09 1969-01-16 Permalux Company Use of a mixture for coating polyvinyl and polyester surfaces
GB2147307A (en) * 1983-09-09 1985-05-09 Dulux Australia Ltd Thermo plastic coating compositions
US8071685B2 (en) 2005-12-09 2011-12-06 Rutgers, The State University Of New Jersey Method of recycling paints as a component of an immiscible polymer blend
US8436099B2 (en) 2005-12-09 2013-05-07 Rutgers The State University Of New Jersey Method of recycling paints as a component of an immiscible polymer blend
CN113930120A (en) * 2021-11-29 2022-01-14 河南蓝翎环科防水材料有限公司 High-strength explosion-proof protective coating and production process thereof
CN113930120B (en) * 2021-11-29 2022-05-13 河南蓝翎环科防水材料有限公司 High-strength explosion-proof protective coating and production process thereof

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