GB911050A - Polymerisable compositions - Google Patents

Polymerisable compositions

Info

Publication number
GB911050A
GB911050A GB1753160A GB1753160A GB911050A GB 911050 A GB911050 A GB 911050A GB 1753160 A GB1753160 A GB 1753160A GB 1753160 A GB1753160 A GB 1753160A GB 911050 A GB911050 A GB 911050A
Authority
GB
United Kingdom
Prior art keywords
epoxypropyl
dimethylaminomethyl
copolymer
tri
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
GB1753160A
Inventor
Alan James Becalick
Robert Paul Gentles
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 GB1753160A priority Critical patent/GB911050A/en
Publication of GB911050A publication Critical patent/GB911050A/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
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins

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)
  • Epoxy Resins (AREA)

Abstract

Phosphated and tin-plated steel plates are spray coated with compositions comprising a copolymer of methyl methacrylate, coconut palm kernel alcohol methacrylate and methacrylic acid, titanium dioxide, diphenylol propane diglycidyl ether, oxypropylated diethyl amino propylamine, xylene and butanol and:-(1) and (3) a phthalic anhydride-polypropylene glycol reaction product and (2) succinic anhydride and polypropylene glycol and heated.ALSO:A polymerizable composition comprises a copolymer of methyl metahcrylate with from 1 to 10% by weight of the copolymer of a polymerizable carboxylic acid and optionally an alkyl methacrylate wherein the alkyl radical contains from 4 to 16 carbon atoms, a polyepoxy compound, a basic organic catalyst, a solvent and as plasticizer an acid ester obtained by the reaction of one molecular proportion of polypropylene glycol and substantially two molecular proportions of phthalic or succinic anhydride. Specified polymerizable carboxylic acids are acrylic, crotonic, fumaric, maleic and itaconic acids. Specified polyepoxides which may be admixed with monoepoxides, e.g. phenyl-2:3-epoxypropyl ether and 2:3-epoxypropyl-N-phenylcarbamate are 1:2-3:4-diepoxybutane, 1:2-5:6-diepoxy-2:5-dimethyl hexane, methyl di(2:3-epoxypropyl)acetate, 1:4-divinylbenzene diepoxide, di(2:3-epoxypropyl)ether, glycerol tri-(2:3-epoxypropyl)ether, m- and p-di(2:3-epoxypropyl)benzenes, 2:2-di[4-(2:3-epoxypropoxy)-phenyl] propane, N:N-di(2:3-epoxypropyl) sebacate, (2:3-epoxypropyl) sebacate dimer, di-(2:3-epoxypropyl)itaconate, di(2:3-epoxypropyl)-isophthalate, tri(2:3-epoxypropyl)trimesate, N:N-di(2:3-epoxypropyl)-p-toluene sulphonamide and condensation products of epichlorhydrin or glycerol dichlorhydrin with polyhydric phenols and phenolaldehyde condensates. Specified catalyst are 2:4:6-tri(dimethylaminomethyl)phenol, triethylamine, dimethylaniline, pyridine, N:N-dimethyl: 3-propanediamine, diethylene triamine, 2:5di(dimethylaminomethyl)quinol, N:N-dimethylcyclohexylamine, N:N-dimethylbenzylamine, N:N:N1:N1-tetramethylhexamethylenediamine, 2-(dimethylaminomethyl)-cyclohexane, phenyl-2-(dimethylamino)ethyl ketone, di[2-)diethylamino)ethyl]-adipate, N-ethylhexamethyleneimine, hexamethyleneimine, N-methylbenzylamine, ben. zyltrimethyl ammonium hydroxide, benzyl trimethyl ammonium acetate, the triacetate of 2:4:6-tri(dimethylaminomethyl)phenol and oxyalkylated amines. Solvents specified are xylene, butanol, toluene, methyl ethyl ketone and ethyl acetate. The examples disclose reactive compositions comprising polyesters derived from polypropylene glycol and:-(1) and (3) phthalic anhydride and (2) succinic anhydride in admixture with a copolymer of methyl methacrylate, coconut palm kernel alcohol methacrylate and methacrylic acid, titanium dioxide, diphenyl propane diglycidyl ether, oxypropylated diethylaminopropylamine, xylene and butanol, the mixtures being applied to steel panels and aired by heating. Specification 809,658 is referred to.
GB1753160A 1960-05-18 1960-05-18 Polymerisable compositions Expired GB911050A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1753160A GB911050A (en) 1960-05-18 1960-05-18 Polymerisable compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1753160A GB911050A (en) 1960-05-18 1960-05-18 Polymerisable compositions

Publications (1)

Publication Number Publication Date
GB911050A true GB911050A (en) 1962-11-21

Family

ID=10096802

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1753160A Expired GB911050A (en) 1960-05-18 1960-05-18 Polymerisable compositions

Country Status (1)

Country Link
GB (1) GB911050A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4859758A (en) * 1987-11-16 1989-08-22 The Sherwin-Williams Company Acid-functional polymers derived from cellulose ester-unsaturated alcohol copolymers, which are reacted with cyclic anhydrides
US5043220A (en) * 1987-11-16 1991-08-27 The Sherwin-Williams Company Substrate coated with a basecoat and/or a clearcoat of an acid-functional compound, an anhydride-functional compound, an epoxy-functional compound and a hydroxy-functional compound
US5411809A (en) * 1987-11-16 1995-05-02 The Sherwin-Williams Company Reactive coatings comprising an acid-functional compound, an anhydride-functional compound and an epoxy-functional compound

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4859758A (en) * 1987-11-16 1989-08-22 The Sherwin-Williams Company Acid-functional polymers derived from cellulose ester-unsaturated alcohol copolymers, which are reacted with cyclic anhydrides
US5043220A (en) * 1987-11-16 1991-08-27 The Sherwin-Williams Company Substrate coated with a basecoat and/or a clearcoat of an acid-functional compound, an anhydride-functional compound, an epoxy-functional compound and a hydroxy-functional compound
US5411809A (en) * 1987-11-16 1995-05-02 The Sherwin-Williams Company Reactive coatings comprising an acid-functional compound, an anhydride-functional compound and an epoxy-functional compound
US5580926A (en) * 1987-11-16 1996-12-03 The Sherwin-Williams Company Reactive coatings comprising an acid-functional compound, an anhydride-functional compound, an epoxy-functional compound and a hydroxy-functional compound

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