GB839480A - Relating to coating compositions - Google Patents

Relating to coating compositions

Info

Publication number
GB839480A
GB839480A GB1186757A GB1186757A GB839480A GB 839480 A GB839480 A GB 839480A GB 1186757 A GB1186757 A GB 1186757A GB 1186757 A GB1186757 A GB 1186757A GB 839480 A GB839480 A GB 839480A
Authority
GB
United Kingdom
Prior art keywords
butyl
peroxide
methacrylate
methyl
toluene
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
GB1186757A
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 GB839480A publication Critical patent/GB839480A/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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)

Abstract

Coating compositions (see Group IV (a)) comprising a liquid carrier and as the predominant resinous component an interpolymer of 50 to 90% by weight of methyl methacrylate and 10 to 50% by weight of another alkyl ester of an ethylenically unsaturated carboxylic acid, said interpolymer having a viscosity of 25 to 320 centistokes when measured at 25 DEG C. as a solution of 25% solids in toluene, may be coated on wood, plastic and metal, e.g. car body panels. The metal may be unprimed, primed and coated with highly pigmented surfacers and undercoats, or with a single primer-surfacer composition comprising nitrocellulose, polyvinyl acetal, alkyd resins or shellac, the base coats being baked before applying top coats according to the invention. Examples describe the application by spraying of (vii) a composition comprising a methyl methacrylate-ethyl acetate copolymer, butyl benzyl phthalate, titanium dioxide, toluene and monoethyl ether of ethylene glycol acetate to primed steel panels; (viii) compositions comprising a methyl methacrylate-ethyl acrylate copolymer, titanium dioxide, polyethylene, butyl benzyl phthalate, toluene and monoethyl ether of ethylene glycol acetate to metal panels which had been "Bonderised" (Registered Trade Mark), primed, coated with a highly pigmented surfacer and a filler prepared from nitrocellulose, a soya oil modified alkyd resin and chlorinated biphenyl; and (ix) compositions comprising a methyl methacrylate-n-butyl methacrylate copolymer, titanium dioxide, phthalocyanine blue, carbon black, butyl benzyl phthalate, toluene and the monoethyl ether of ethylene glycol acetate to primed steel panels.ALSO:Coating compositions comprise a liquid carrier and as the predominant resinous component an interpolymer of 50 to 90% by weight of methyl methacrylate and 10 to 50% by weight of another alkyl ester of an ethylenically unsaturated carboxylic acid, said interpolymer having a viscosity of 25 to 320 centistokes when measured at 25 DEG C. as a solution of 25% solids in toluene. Specified alkyl esters are ethyl acrylate, propyl acrylate, butyl acrylate, octyl acrylate, ethyl methacrylate, n-butyl methacrylate, hexyl methacrylate, octyl methacrylate, lauryl methacrylate, mixed octyl and decyl methacrylates, dimethyl itaconate, diethyl itaconate and dibutyl itaconate. Minor amounts of additional comonomers, e.g. N-t.-butyl acrylamide and methacrylic acid (Example VI), may also be used. The interpolymers may be prepared by polymerization in solution, emulsion or suspension, e.g. in the presence of protective colloids such as polyvinyl alcohol, sodium polyacrylate, polyacrylamide, bentonite, starch or magnesium silicate, in the presence of catalysts, e.g. acetyl peroxide, benzoyl peroxide, lauroyl peroxide, acetyl benzoyl peroxide, hydroxyheptyl peroxide, 2,4-dichlorobenzoyl peroxide, dicumyl peroxide, di-t-butyl peroxide, p-chlorobenzoyl peroxide, cyclohexyl hydroperoxide, cumene hydroperoxide, t-butyl hydroperoxide, methyl cyclohexyl hydroperoxide, methyl ethyl ketone peroxide, cyclohexanone peroxide, methyl amyl ketone peroxide, peracetic acid, t-butyl peracetate, t-butyl permaleic acid, di-t-butyl perphthalate, t-perphthalic acid, potassium persulphate, ammonium persulphate, a ,a -azo-diisobutyronitrile and p-methoxy phenyl diazo-thio-(2-naphthyl) ether, buffers, e.g. mono- and disodium phospahtes, and chain transfer agents, e.g. dodecyl mercaptan, tertiary dodecyl mercaptan, octyl mercaptan, hexyl mercaptan, carbon tetrachloride, allyl acetate, allyl carbamate, isopropyl benzene, butyl chloride, acetic acid and dioxane. The polymers may be dissolved in solvents, e.g. toluene, xylene, acetone, methyl ethyl ketone, methyl amyl ketone, monoethyl ether of glycol acetate, ethyl acetate, isopropyl acetate, amyl acetate, heptane, octane, methyl alcohol, isopropyl alcohol, amyl alcohol and diacetone alcohol, together with plasticizers, e.g. butyl benzyl phthalate, tricresyl phosphate, dioctyl phthalate, dicyclohexyl phthalate, di-3,5,5-trimethyl hexyl phthalate, butyl cyclohexyl phthalate, epoxidized oils and castor oil acetoacetate, pigments, e.g. carbon black, titanium dioxide, phthalocyanine greens and blues, metal oxides and sulphides and metal, e.g. aluminium, flake pigments, fillers and extenders, e.g. talc, kieselguhr, clays, silicates and diatomaceous earth, silicones, nitrocellulose, polyvinyl acetal resins and polyethylene. The composition may be coated on bare or primed metal, e.g. car bodies, wood and plastics.
GB1186757A 1956-05-14 1957-04-11 Relating to coating compositions Expired GB839480A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US58447456A 1956-05-14 1956-05-14

Publications (1)

Publication Number Publication Date
GB839480A true GB839480A (en) 1960-06-29

Family

ID=24337460

Family Applications (2)

Application Number Title Priority Date Filing Date
GB1186757A Expired GB839480A (en) 1956-05-14 1957-04-11 Relating to coating compositions
GB1698462A Expired GB991802A (en) 1956-05-14 1962-05-03 Coating compositions

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB1698462A Expired GB991802A (en) 1956-05-14 1962-05-03 Coating compositions

Country Status (5)

Country Link
BE (1) BE557326A (en)
CH (1) CH368570A (en)
FR (1) FR1175483A (en)
GB (2) GB839480A (en)
NL (2) NL97015C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3198654A (en) * 1961-12-21 1965-08-03 Pittsburgh Plate Glass Co Coating system
GB2155943A (en) * 1984-03-20 1985-10-02 Erba Farmitalia Composition for mounting microscope slide specimens
EP1500689A1 (en) * 2003-07-24 2005-01-26 Celanese Emulsions GmbH Coating composition and method for its preparation

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1396128A (en) * 1971-07-16 1975-06-04 Monier Research Dev Pty Ltd Acrylic polymers and acrylic coatings
CA2021957A1 (en) * 1989-09-11 1991-03-12 Hans G. Feichtmeier Abrasion resistant ionomeric film
CN108948888A (en) * 2018-08-19 2018-12-07 柳州市家富连装饰有限公司 A kind of indoor decoration water paint and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3198654A (en) * 1961-12-21 1965-08-03 Pittsburgh Plate Glass Co Coating system
GB2155943A (en) * 1984-03-20 1985-10-02 Erba Farmitalia Composition for mounting microscope slide specimens
EP1500689A1 (en) * 2003-07-24 2005-01-26 Celanese Emulsions GmbH Coating composition and method for its preparation

Also Published As

Publication number Publication date
CH368570A (en) 1963-04-15
BE557326A (en)
NL97015C (en)
GB991802A (en) 1965-05-12
FR1175483A (en) 1959-03-26
NL216873A (en)

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