GB1344725A - Water dispersible coating compositions - Google Patents

Water dispersible coating compositions

Info

Publication number
GB1344725A
GB1344725A GB2664071A GB2664071A GB1344725A GB 1344725 A GB1344725 A GB 1344725A GB 2664071 A GB2664071 A GB 2664071A GB 2664071 A GB2664071 A GB 2664071A GB 1344725 A GB1344725 A GB 1344725A
Authority
GB
United Kingdom
Prior art keywords
acid
vinyl
ether
styrene
methacrylic acid
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
GB2664071A
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.)
Dow Chemical Co
Original Assignee
Dow Chemical 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 Dow Chemical Co filed Critical Dow Chemical Co
Publication of GB1344725A publication Critical patent/GB1344725A/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
    • C09D125/00Coating 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 an aromatic carbocyclic ring; Coating compositions based on derivatives of such polymers
    • C09D125/02Homopolymers or copolymers of hydrocarbons
    • C09D125/04Homopolymers or copolymers of styrene
    • C09D125/08Copolymers of styrene
    • C09D125/14Copolymers of styrene with unsaturated esters
    • 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
    • C09D157/00Coating compositions based on unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C09D157/06Homopolymers or copolymers containing elements other than carbon and hydrogen
    • C09D157/10Homopolymers or copolymers containing elements other than carbon and hydrogen containing oxygen atoms
    • 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)
  • Chemical Kinetics & Catalysis (AREA)
  • Paints Or Removers (AREA)

Abstract

1344725 Water dispersible curable coating compositions DOW CHEMICAL CO 19 April 1971 [20 April 1970] 26640/71 Headings C3P and C3B A curable coating composition comprises a solution of a vinyl polymer containing pendant carboxylic acid groups, at least half of which are neutralized by ammonia and/or a volatile amine in which the nitrogen atom is not attached directly to an aromatic ring, and a cross-linking agent containing more than one aziridinyl hydroxyalkyl ether or ester group per molecule in a solvent consisting of or containing a watermiscible glycol ether. The composition preferably contains 0À1 to 10 aziridinyl equivalents per carboxyl or carboxylate equivalent, and at least 15% by weight of the glycol ether, based on the cross-linking agent. The polymer may be an interpolymer of monovinyl monomers 1 to 50% by weight of which contain at least one carboxylic acid or carboxylate group. Suitable carboxyl monomers are acrylic acid, methacrylic acid, maleic acid, itaconic acid, fumaric acid and the half-esters and half-amides of the dicarboxylic acids. Monomers which may be copolymerized with these include: styrene, vinyl toluene, alphamethyl styrene, halogenated styrenes, t-butyl styrene, esters of acrylic and methacrylic acids, vinyl halides, vinyl acetate, acrylamide, acrylonitrile and methyl vinyl ether, and mixtures thereof. The ammonium or amine salt groups may be introduced by adding the ammonia or amine to a solution of the polymer which contains carboxylic acid groups. The crosslinking agent preferably contains more than one group of the formula where each of R 1 and R 2 is hydrogen or C 1-3 alkyl. In the examples the vinyl polymer is (1), (2), (4) and (6) a copolymer of styrene, methyl methacrylate, butyl acrylate and methacrylic acid which has been reacted with aqueous ammonia; (3) the copolymer of Example (1) which has been reacted with morpholine, triethylamine, dibutylamine, benzylmethylamine, diethyl ethanolamine, N,N- dimethylaminoethylamine, diethanolamine or ethanolamine; (5) a copolymer of (a) styrene, methacrylic acid and 2-ethyl hexyl acrylate, (b) methyl methacrylate, acrylic acid and butylacrylate, (c) vinyl chloride, monobutyl maleate and ethyl acrylate, (d) methyl methacrylate and 2-hydroxyethyl acrylate phthalate half-ester, (e) methyl methacrylate, methacrylic acid and 2-ethylhexyl acrylate and (f) methacrylic acid and butyl methacrylate, each neutralized with ammonia. In Example (6) the coating solution also contains a polyglycidyl ether of bisphenol A. The cross-linking agents may be prepared by reacting a polyepoxide which is a glycidyl ether or ester with an alkyleneimine. In specific examples ethyleneimine is reacted with a diglycidyl ether of bisphenol A or with a diglycidyl ester of tetrahydrophthalic acid.
GB2664071A 1970-04-20 1971-04-19 Water dispersible coating compositions Expired GB1344725A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US3022470A 1970-04-20 1970-04-20

Publications (1)

Publication Number Publication Date
GB1344725A true GB1344725A (en) 1974-01-23

Family

ID=21853168

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2664071A Expired GB1344725A (en) 1970-04-20 1971-04-19 Water dispersible coating compositions

Country Status (7)

Country Link
AU (1) AU2698771A (en)
BE (1) BE766010A (en)
BR (1) BR7102259D0 (en)
DE (1) DE2118862A1 (en)
FR (1) FR2089648A5 (en)
GB (1) GB1344725A (en)
NL (1) NL7105060A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104284698A (en) * 2012-04-04 2015-01-14 玛德瑞福科学有限公司 Coating compositions for proteinaceous substrates and methods of priming and topcoating proteinaceous substrates therewith
WO2021148570A1 (en) * 2020-01-22 2021-07-29 Covestro (Netherlands) B.V. Multi-aziridine compound
US11878969B2 (en) 2018-07-23 2024-01-23 Covestro (Netherlands) B.V. Multi-aziridine compound

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU421205B (en) * 1905-09-23 1906-07-24 Edward George Mills An improved food for calves and stock, and method of manufacture of same

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104284698A (en) * 2012-04-04 2015-01-14 玛德瑞福科学有限公司 Coating compositions for proteinaceous substrates and methods of priming and topcoating proteinaceous substrates therewith
US9271914B2 (en) 2012-04-04 2016-03-01 Mad River Science Primecoat compositions for proteinaceous substrates and methods of priming proteinaceous substrates therewith
US9636287B2 (en) 2012-04-04 2017-05-02 Mad River Science Primecoat compositions for proteinaceous substrates and methods of priming proteinaceous substrates therewith
US11878969B2 (en) 2018-07-23 2024-01-23 Covestro (Netherlands) B.V. Multi-aziridine compound
WO2021148570A1 (en) * 2020-01-22 2021-07-29 Covestro (Netherlands) B.V. Multi-aziridine compound
WO2021148569A1 (en) * 2020-01-22 2021-07-29 Covestro (Netherlands) B.V. Multi-aziridine compound

Also Published As

Publication number Publication date
FR2089648A5 (en) 1972-01-07
BE766010A (en) 1971-10-20
NL7105060A (en) 1971-10-22
AU2698771A (en) 1972-09-28
BR7102259D0 (en) 1973-03-08
DE2118862A1 (en) 1971-11-04

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Legal Events

Date Code Title Description
PS Patent sealed
PLNP Patent lapsed through nonpayment of renewal fees