Hardenable coating compositions
First Claim
1. 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 reacteda. 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
subsequentlyb. 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
finallyc. 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.
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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.
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Citations
2 Claims
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1. 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
subsequentlyb. 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
finallyc. 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. - View Dependent Claims (2)
- -aminocaproic acid or of a mixture of the aforementioned nitrogen compounds; and
Specification
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- Resources
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Current AssigneeBayer AG
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Original AssigneeBayer AG
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InventorsTraenckner, Hans-Joachim, Rosenkranz, Hans Jurgen, Fuhr, Karl, Rudolph, Hans, Patheiger, deceased, Manfred
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Primary Examiner(s)Lieberman, Paul
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Application NumberUS05/707,875Time in Patent Office614 DaysField of Search260/836, 260/837US Class Current525/531CPC Class CodesC08F 299/028 photopolymerisable composit...Y10S 522/909 Solventless ink
