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US4081492A Expired / Lapsed US ⏱️ 0.0 years remaining

Hardenable coating compositions

Assignee: Bayer AG
•
Filing: 1976-07-22
•
Granted: 1978-03-28
•
Expires: 1996-07-22
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Abstract

Abstract A coating composition comprising as binder a reaction product of a polyepoxide with more than one 1,2-epoxide group per molecule, wherein its epoxide groups have been reacted A. with 0.01 to 0.5 NH-equivalents, based on one epoxide equivalent, of ammonia or of an aliphatic or cycloaliphatic primary or secondary amine or of an amino carboxylic acid or of a mixture of the aforementioned nitrogen compounds; and subsequently B. with 0.40 to 0.90 carboxyl equivalents, based on one epoxide equivalent, of acrylic acid or methacrylic acid or of a mixture of acrylic amd methacrylic acid; and finally C. with 0.09 to 0.50 carboxyl equivalents, based on one epoxide group, of a saturated aliphatic, a cycloaliphatic or an aromatic carboxylic acid, so that at least 80% of the epoxide groups originally present have been reacted through these three component stages. The binder may be used alone or together with additional monomers by radicals forming compounds or preferably by photopolymerization in the presence of a photoinitiator.

Inventors

  • 👤 Hans-Joachim Traenckner
  • 👤 Karl Fuhr
  • 👤 Hans Jurgen Rosenkranz
  • 👤 Manfred Patheiger, deceased
  • 👤 Hans Rudolph

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 20:38
CPC Classifications
C; C08; C08F; C08F299/00; C08F299/02; C08F299/026; C08F299/028; Y; Y10; Y10S; Y10S522/00; Y10S522/909

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 129 words
A coating composition comprising as binder a reaction product of a polyepoxide with more than one 1,2-epoxide group per molecule, wherein its epoxide groups have been reacted a. with 0.01 to 0.5 NH-equivalents, based on one epoxide equivalent of ammonia or of an aliphatic or cycloaliphatic primary amine or of ε-aminocaproic acid or of a mixture of the aforementioned nitrogen compounds; and subsequently b. with 0.40 to 0.90 carboxyl equivalents, based on one epoxide equivalent, of acrylic acid or methacrylic acid or of a mixture of acrylic and methacrylic acid; and finally c. with 0.09 to 0.50 carboxyl equivalents, based on one epoxide group, of a saturated aliphatic, monocarboxylic acid, so that at least 80% of the epoxide groups originally present have been reacted through these three component stages.
Claim 2
Dependent Claim 129 words
A coating composition comprising as binder a reaction product of a polyepoxide with more than one 1,2-epoxide group per molecule, wherein its epoxide groups have been reacted a. with 0.01 to 0.5 NH-equivalents, based on one epoxide equivalent of ammonia or of an aliphatic or cycloaliphatic primary amine or of ε-aminocaproic acid or of a mixture of the aforementioned nitrogen compounds; and subsequently b. with 0.40 to 0.90 carboxyl equivalents, based on one epoxide equivalent, of acrylic acid or methacrylic acid or of a mixture of acrylic and methacrylic acid; and finally c. with 0.09 to 0.50 carboxyl equivalents, based on one epoxide group, of a saturated aliphatic, monocarboxylic acid, so that at least 80% of the epoxide groups originally present have been reacted through these three component stages.
Claim 3
Dependent Claim 15 words
A coating composition as claimed in claim 1, wherein the polyepoxide is a bisphenol-A-polyglycidyl ether.

References Cited (Backward Citations)

US3256226A Cited
US3971834A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-03-27 1981-09-26 1982-03-28 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-03-27 1985-09-26 1986-03-28 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-03-27 1989-09-26 1990-03-28 $7700.00 Window Closed / Lapsed

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