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US4251415A Expired / Lapsed US ⏱️ 0.0 years remaining

Paint composition for cationic electrodeposition process

Assignee: Nippon Soda Co Ltd
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Filing: 1979-06-21
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Granted: 1981-02-17
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Expires: 1999-06-21
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Abstract

Abstract A paint composition for cationic electrodeposition process comprises a producing step in which a polymer of conjugated diene having carboxyl group at molecular terminal position or a copolymer of the said conjugated diene and vinyl monomer is made to react with an epoxy resin by a type of condensate of bisphenol A - epichlorohydrin and further, the resulting reaction compound is made to react with a primary amine compound or a secondary amine compound and thereby a reaction compound (component 1) is obtained and furthermore, the said reaction compound (component 1) is made to react with a partial block isocyanate compound (component 2) and this final reaction compound is used for an ingredient of the paint composition as a film forming material.

Inventors

  • 👤 Hisao Nakada
  • 👤 Michisuke Harada
  • 👤 Seiji Yoshikoshi

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 12:36
CPC Classifications
C; C09; C09D; C09D5/00; C09D5/44; C09D5/4419; C09D5/443; C09D5/4434; C09D5/4438; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/67; C08G18/69; C08G59/00; C08G59/18; C08G59/182; C08G59/186; C08G59/40; C08G59/50; C08G59/56; C09D163/00; Y; Y10; Y10S; Y10S524/00; Y10S524/901; Y10S525/00; Y10S525/911

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 231 words
A paint composition for cationic electrodeposition in the form of an aqueous solution or dispersion, essentially prepared by: (a) reacting a carboxyl terminated polymer of a conjugated diene or a carboxyl terminated copolymer of a conjugated diene and vinyl monomer with a bisphenol A-epichlorohydrin epoxy resin condensate, in an amount of at least one equivalent part of the epoxy group of the latter in proportion to one equivalent part of the carboxyl group of the former at a temperature of about 80° C. to about 200° C. until the carboxyl group may be substantially eliminated to produce a reaction intermediate; (b) reacting said intermediate with a primary amine or a secondary amine compound, in an amount of not more than one equivalent part of said amine compound in proportion to one equivalent part of the epoxy group of said intermediate at a temperature of about 50° C. to about 150° C. to obtain an epoxy-amine adduct first component having an amine value of 20 to 200; (c) reacting said first component with a partial block isocyanate compound as a second component, the ratio of said first and second components being selected as 99 to 55 percent by weight of the former to 1 to 50 percent by weight of the latter component; and, (d) neutralizing the resultant resin with an acid to render the resultant resin soluble or dispersible in water.
Claim 2
Dependent Claim 231 words
A paint composition for cationic electrodeposition in the form of an aqueous solution or dispersion, essentially prepared by: (a) reacting a carboxyl terminated polymer of a conjugated diene or a carboxyl terminated copolymer of a conjugated diene and vinyl monomer with a bisphenol A-epichlorohydrin epoxy resin condensate, in an amount of at least one equivalent part of the epoxy group of the latter in proportion to one equivalent part of the carboxyl group of the former at a temperature of about 80° C. to about 200° C. until the carboxyl group may be substantially eliminated to produce a reaction intermediate; (b) reacting said intermediate with a primary amine or a secondary amine compound, in an amount of not more than one equivalent part of said amine compound in proportion to one equivalent part of the epoxy group of said intermediate at a temperature of about 50° C. to about 150° C. to obtain an epoxy-amine adduct first component having an amine value of 20 to 200; (c) reacting said first component with a partial block isocyanate compound as a second component, the ratio of said first and second components being selected as 99 to 55 percent by weight of the former to 1 to 50 percent by weight of the latter component; and, (d) neutralizing the resultant resin with an acid to render the resultant resin soluble or dispersible in water.

References Cited (Backward Citations)

US3894113A Cited
US3686359A Cited
US3823107A Cited
US3707583A Cited
US4107116A Cited
SU514879A1 Cited
US3926904A Cited
US3926903A Cited
US4130546A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-02-17 1984-08-18 1985-02-17 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-02-17 1988-08-18 1989-02-17 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-02-17 1992-08-18 1993-02-17 $7700.00 Window Closed / Lapsed

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