GB991028A - Coating compositions - Google Patents

Coating compositions

Info

Publication number
GB991028A
GB991028A GB5861/62A GB586162A GB991028A GB 991028 A GB991028 A GB 991028A GB 5861/62 A GB5861/62 A GB 5861/62A GB 586162 A GB586162 A GB 586162A GB 991028 A GB991028 A GB 991028A
Authority
GB
United Kingdom
Prior art keywords
styrene
copolymer
methyl methacrylate
interpolymer
oil
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
GB5861/62A
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.)
De Soto Chemical Coatings Inc
Original Assignee
De Soto Chemical Coatings Inc
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 De Soto Chemical Coatings Inc filed Critical De Soto Chemical Coatings Inc
Publication of GB991028A publication Critical patent/GB991028A/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
    • C09D133/24Homopolymers or copolymers of amides or imides
    • C09D133/26Homopolymers or copolymers of acrylamide or methacrylamide
    • 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
    • C08F8/14Esterification
    • 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
    • C08F8/28Condensation with aldehydes or ketones
    • 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
    • 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
    • C08F2810/00Chemical modification of a polymer
    • C08F2810/50Chemical modification of a polymer wherein the polymer is a copolymer and the modification is taking place only on one or more of the monomers present in minority

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Heat hardenable resin compositions comprise a copolymer of the ester reaction product of a resinous polyhydric alcohol and a drying oil or drying oil fatty acids and 5 to 45% by weight of the copolymer of copolymerizable ethylenically unsaturated monomer comprising a major proportion of methyl methacrylate, and an interpolymer of a carboxylic acid amide containing a CH2=C< group with at least one other ethylenically unsaturated monomer, the interpolymer having amido hydrogen atoms replaced by -ROR1, where R is a saturated C1-8 aliphatic hydrocarbon group having its free valencies on a single carbon atom and R1 is H or C1-8 alkyl. The copolymer may be derived from ester reaction products of linseed, coconut, cottonseed, dehydrated castor, tall, fish or soyabean oils or the acids therefrom and alkyds derived from dicarboxylic acids and alcohols containing at least three hydroxyl groups, e.g. glycerol or pentaerythritol, or copolymers of allyl or methallyl alcohol with styrene, halo or alkyl substituted styrenes or methyl methacrylate. Specified comonomers which may be used in minor proportions are styrene and substituted styrenes, and acrylic and methacrylic esters. The interpolymer may be derived from acrylamide, methacrylamide or itaconic acid diamide and styrene or substituted styrenes, acrylic or methacrylic esters, maleic anhydride, monoesters or diesters or olefins. The interpolymer is modified with an aldehyde, preferably formaldehyde and optionally etherified, e.g. with butanol. In examples, acrylamide is interpolymerized with (1 and 4) styrene and ethyl acrylate, (3) styrene, ethyl acrylate and methyl methacrylate, (5) ethyl acrylate, methyl methacrylate and 2-ethylhexyl acrylate, (6) vinyl toluene and ethyl acrylate and (7) styrene, methyl acrylate and 2-ethylhexyl acrylate, and the interpolymers reacted with formaldehyde in the presence of butanol; glycerol and phthalic acid are reacted with (12) dehydrated castor oil and (18) cottonseed oil, coconut oil and dehydrated castor oil fatty acids, and the products copolymerized with (13) methyl methacrylate and styrene and (16) methyl methacrylate; a styrene-allyl alcohol copolymer is reacted with (19) dehydrated castor oil and the product copolymerized with methyl methacrylate and styrene. The interpolymers and copolymers are admixed with conventional ingredients, e.g. titanium dioxide, talc, silica, solvents such as xylene and butanol and butylated melamine-formaldehyde resins to form enamels.ALSO:Metal substrates, e.g. steel and aluminium, may be coated with heat hardenable resin compositions comprising a copolymer of the ester reaction product of a resinous polyhydric alcohol and a drying oil or fatty acids therefrom and 5-45% by weight of the copolymer of ethylenically unsaturated monomer comprising a major proportion of methyl methacrylate, and an interpolymer of a carboxylic acid amide containing a CH2=C ? group with at least one copolymerizable monomer, said interpolymer having amido hydrogen atoms replaced by -ROR1 where R is a saturated aliphatic hydrocarbon group having its free valencies on a single carbon atom and R1 is H or C1-8 alkyl. The ester reaction product may be derived from a hydroxy polyester or allyl alcohol copolymer and linseed, coconut, cotton-seed, dehydrated castor, tall, fish or soya bean oil or acids therefrom. In examples aluminium strips are coated with high gloss enamels comprising (14) the copolymer of methyl methacrylate and styrene with an ester reaction product of glycerol, phthalic anhydride and dehydrated castor oil, a butylated formaldehyde modified interpolymer of acrylamide, styrene and ethyl acrylate, titanium dioxide and xylene, optionally together with (20) a butanol/xylene solution of a butylated melamine/formaldehyde resin; and a low gloss enamel comprising (15) the above copolymer and interpolymer, a styrene/allyl alcohol copolymer, xylene, talc, titanium dioxide and silica.
GB5861/62A 1961-02-16 1962-02-15 Coating compositions Expired GB991028A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US8966761A 1961-02-16 1961-02-16

Publications (1)

Publication Number Publication Date
GB991028A true GB991028A (en) 1965-05-05

Family

ID=22218933

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5861/62A Expired GB991028A (en) 1961-02-16 1962-02-15 Coating compositions

Country Status (1)

Country Link
GB (1) GB991028A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112759748A (en) * 2020-12-30 2021-05-07 长兴化学(天津)有限公司 Nano titanium dioxide modified alkyd resin and preparation method and application thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112759748A (en) * 2020-12-30 2021-05-07 长兴化学(天津)有限公司 Nano titanium dioxide modified alkyd resin and preparation method and application thereof

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