GB1217002A - Electrodeposition of resins - Google Patents

Electrodeposition of resins

Info

Publication number
GB1217002A
GB1217002A GB627168A GB627168A GB1217002A GB 1217002 A GB1217002 A GB 1217002A GB 627168 A GB627168 A GB 627168A GB 627168 A GB627168 A GB 627168A GB 1217002 A GB1217002 A GB 1217002A
Authority
GB
United Kingdom
Prior art keywords
resin
epoxide
polyether
carboxyl groups
dispersion
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
GB627168A
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.)
DeSoto Inc
Original Assignee
DeSoto 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 DeSoto Inc filed Critical DeSoto Inc
Publication of GB1217002A publication Critical patent/GB1217002A/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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/44Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
    • C09D5/4419Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications with polymers obtained otherwise than by polymerisation reactions only involving carbon-to-carbon unsaturated bonds
    • C09D5/4423Polyesters, esterified polyepoxides
    • C09D5/4426Esterified polyepoxides
    • 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
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • C08G65/2603Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
    • C08G65/2615Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen the other compounds containing carboxylic acid, ester or anhydride groups
    • 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
    • C09D161/00Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
    • C09D161/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • 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
    • C08F2810/20Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently

Abstract

1,217,002. Coatings. DESOTO, Inc. 8 Feb., 1968 [10 Feb., 1967; 28 April, 1967], No. 6271/ 68. Heading B2E. [Also in Divisions C3 and C7] An electrically-conductive body is coated with a resin by immersing the body in an aqueous dispersion of a hydrophilic resin having an acid number of 8 to 70 and being a linear resin containing carboxyl groups and hydroxyl groups, the latter having been formed by reaction of some of the carboxyl groups with an epoxide and being positioned remote from the backbone of the resin, the resin being in the form of a salt with a base to provide dispersed particles of size less than 0.5 micron, passing a unidirectional current through the dispersion with the body as anode to form a film thereon and baking the film to cure it. The dispersion may also contain a waterinsoluble thermosetting aminoplast resin. The hydrophilic resin may be derived from a polyhydric polyether or an addition polymer. The polyether is preferably an aliphatic polycyolic polyether of the formula where n is 10 to 14. This is partially esterified with a monocarboxylic acid and the hydroxy ester is then reacted with a polybasic acid anhydride to provide carboxyl groups without cross-linking the resin. The product is then reacted with an epoxide in stoichiometric deficiency to form a hydroxy ester containing carboxyl groups. The epoxide is preferably a mono-epoxide but may comprise additionally or solely a polyepoxide, e.g. a diglycidyl ether of bis-phenol. The polyether may also comprise, instead of the above polycyclic compounds, glycidyl ethers of aromatic compounds or of glycols. The addition polymers which may be used are copolymers of hydroxyl-containing ethylenic compounds and carboxylcontaining ethylenic compounds. The first group includes hydroxyalkyl acrylates, methacrylates, maleates, crotonates and norbornene and alkyl, methalkyl and orotyl alcohols. The second group includes acrylic, methacrylic, crotonic, itaconic, maleic and fumaric acids and monobutyl maleate. The copolymers are reacted with epoxides as above. The aminoplast resin may be a urea-, melamine- or benzoguanamine-formaldehyde condensate in amount up to 40% by weight of total resin. A pigment, e.g. TiO 2 , and organic solvents may also be present. The base which may be used to convert the resin to a salt may be ammonia but is preferably an amine. The dispersion preferably contains 5 to 15% solids and may be maintained at a pH of up to 10. Voltages of at least 200 are suitable. In Example 1, a metal tank serves as cathode and steel and aluminium panels treated with zinc phosphate are used as the anodes for coating. The voltage is run up from zero to 500. The film is baked at 400‹ F. to cure.
GB627168A 1967-02-10 1968-02-08 Electrodeposition of resins Expired GB1217002A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US61504867A 1967-02-10 1967-02-10
US63448067A 1967-04-28 1967-04-28

Publications (1)

Publication Number Publication Date
GB1217002A true GB1217002A (en) 1970-12-23

Family

ID=27087398

Family Applications (1)

Application Number Title Priority Date Filing Date
GB627168A Expired GB1217002A (en) 1967-02-10 1968-02-08 Electrodeposition of resins

Country Status (8)

Country Link
JP (1) JPS5031177B1 (en)
BE (1) BE710605A (en)
DE (1) DE1720537B1 (en)
ES (1) ES350352A1 (en)
FR (1) FR1560607A (en)
GB (1) GB1217002A (en)
NL (1) NL153266B (en)
NO (1) NO126138B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4122053A (en) * 1971-08-11 1978-10-24 Ppg Industries, Inc. Electrodepositable micellar dispersions
WO2007048396A2 (en) * 2005-10-27 2007-05-03 Construction Research & Technology Gmbh Carboxylic acid derivatives, method for the production thereof, and use thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4122053A (en) * 1971-08-11 1978-10-24 Ppg Industries, Inc. Electrodepositable micellar dispersions
WO2007048396A2 (en) * 2005-10-27 2007-05-03 Construction Research & Technology Gmbh Carboxylic acid derivatives, method for the production thereof, and use thereof
WO2007048396A3 (en) * 2005-10-27 2008-06-19 Constr Res & Tech Gmbh Carboxylic acid derivatives, method for the production thereof, and use thereof

Also Published As

Publication number Publication date
NO126138B (en) 1972-12-27
NL153266B (en) 1977-05-16
DE1720537B1 (en) 1973-02-01
FR1560607A (en) 1969-03-21
NL6801854A (en) 1968-08-12
ES350352A1 (en) 1969-11-16
JPS5031177B1 (en) 1975-10-08
BE710605A (en) 1968-06-17

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