GB988983A - Stoving lacquers - Google Patents

Stoving lacquers

Info

Publication number
GB988983A
GB988983A GB3560063A GB3560063A GB988983A GB 988983 A GB988983 A GB 988983A GB 3560063 A GB3560063 A GB 3560063A GB 3560063 A GB3560063 A GB 3560063A GB 988983 A GB988983 A GB 988983A
Authority
GB
United Kingdom
Prior art keywords
lacquer
monomer
oxaalkoxymethyl
copolymer
examples
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
GB3560063A
Inventor
Hermann Wesslau
Hans Wilhelm
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB988983A publication Critical patent/GB988983A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/62Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
    • 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
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/52Amides or imides
    • 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
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/52Amides or imides
    • C08F20/54Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
    • C08F20/58Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-acryloylmorpholine
    • 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
    • C08F22/00Homopolymers and 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 carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
    • C08F22/36Amides or imides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)

Abstract

A stoving lacquer contains water and, in dissolved form, at least one aqueous ammonia soluble polymeric substance which has the structure of a copolymer of:-(a) 2 to 30% by weight of at least one ethelenically unsaturated monomer having a carbonamide or carbonimide group whose nitrogen atom beans an oxaalkoxymethyl group, (b) 1 to 2o% by weight of at least one other ethelenically unsaturated monomer having a carboxyl group or a salt thereof, and (c) 50 to 97% by weight of at least one other ethelenically unsaturated monomer, the sum of the percentages under (a), (b) and (c) being 100. A long list of suitable types of oxaalkoxymethyl amides and imides (a) is given and N-[(3-oxabutoxy)-methyl]-acrylamide is exemplified. In the examples monomer (b) is acrylic acid or methacrylic acid, present as the N, N-dimethyl-N(2-hydroxy-ethyl)-amine salt; a number of others are specified. A long list including many different types of monomer (c) is given; those exemplified are: acrylonitrile, styrene, isobutyl acrylate, 2-ethylhexylacrylate, and 4-hydroxybutyl acrylate. Copolymerization catalysts employed are azodiisobutyronitrile and cumene hydroperoxide. Tertiary-dodecyl-mercaptan is also added in some of the examples. The copolymer is also made using, in place of monomer (a) either methacrylamide or monoacryloylurea and after polymerization converting the copolymer into the corresponding N-(oxaalkoxymethyl) derivative by treating with formaldehyde and ethanediol monomethyl ether and, in some examples, with maleic anhydride also. The lacquer may also contain other conventional stoving lacquer components such as other aqueous ammonia soluble polymers, aqueous dispersions of polymers, epoxy compounds, aminoplasts and their precondensates, phenoplasts and their precondensates, and alkyd resins; conventional additives such as soluble dyes, pigments and hexavalent chromium compounds; and, in addition to water, organic water-miscible solvents such as alcohols, esters, ethers and ketones. A number of these components and additives are specified of which titanium dioxide and the reaction product of 2,2 - bis - (p - hydroxyphenyl) - propane and 1-chloro-2,3-epoxypropane are exemplified. The pH of the lacquer may be adjusted with inorganic or organic bases conventional in aqueous storing lacquers. The lacquer may be applied to metals, wood, plastics or ceramics.ALSO:A stoving lacquer contains water and, in dissolved form, at least one aqueous ammonia soluble polymeric substance which has the structure of a copolymer of (a) 2-30% by weight of at least one ethylenically unsaturated monomer having a carbonamide or carbonimide group whose nitrogen atom bears an oxaalkoxymethyl group, (b) 1-20% by weight of at least one other ethylenically unsaturated monomer having a carboxyl group or a salt thereof, and (c) 50-97% by weight of at least one other ethylenically unsaturated monomer, the sum of the percentages under (a), (b) and (c) being 100. A long list of suitable types of oxaalkoxymethyl amides and imides (a) is given and N-[(3-oxabutoxy)-methyl]-acrylamide is exemplified. In the examples monomer (b) is acrylic acid or methacrylic acid, present as the N,N-dimethyl-N(2-hydroxyethyl)-amine salt; a number of others are specified. A long list including many different types of monomer (c) is given; those exemplified are: acrylonitrile, styrene, isobutyl acrylate, 2-ethylhexylacrylate, and 4-hydroxybutyl acrylate. Copolymerization catalysts employed are azodiisobutyronitrile and cumene hydroperoxide. Tertiary-dodecyl-mercaptan is also added in some of the examples. The copolymer is also made using, in place of monomer (a) either methacrylamide or monoacryloylurea and after polymerization converting the copolymer into the corresponding N-(oxaalkoxymethyl) derivative by treating with formaldehyde and ethanediol monomethyl ether and, in some examples, with maleic anhydride also. The lacquer may also contain other conventional stoving lacquer components such as other aqueous ammonia soluble polymers, aqueous dispersions of polymers, epoxy compounds, aminoplasts and their precondensates, phenoplasts and their precondensates, and alkyd resins: conventional additives such as soluble dyes, pigments and hexavalent chromium compounds; and, in addition to water, organic water-miscible solvents such as alcohols, esters, ethers and ketones. A number of these components and additives are specified of which titanium dioxide and the reaction product of 2,2-bis-(p-hydroxyphenyl)-propane and 1-chloro-2,3-epoxypropane are exemplified. The pH of the lacquer may be adjusted with inorganic or organic bases conventional in aqueous stoving lacquers. The lacquer may be applied to metals, e.g. aluminium, iron and magnesium, wood, plastics or ceramics. Articles which may be coated include vehicle bodies, ships, washing machines, refrigerators, boxes, cans and tubs.
GB3560063A 1962-09-11 1963-09-10 Stoving lacquers Expired GB988983A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB68802A DE1258996B (en) 1962-09-11 1962-09-11 Binder for stoving enamels, thermosetting impregnations, finishes and adhesives

Publications (1)

Publication Number Publication Date
GB988983A true GB988983A (en) 1965-04-14

Family

ID=6976041

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3560063A Expired GB988983A (en) 1962-09-11 1963-09-10 Stoving lacquers

Country Status (3)

Country Link
BE (1) BE637264A (en)
DE (1) DE1258996B (en)
GB (1) GB988983A (en)

Also Published As

Publication number Publication date
BE637264A (en)
DE1258996B (en) 1968-01-18

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