AQUEOUS COATING COMPOSITIONS AND PROCESS FOR THE PRODUCTION OF COATING LAYERS
Aqueous coating compositions with a resin solids consisting of 60 to 80 wt. % of binder solids and 20 to 40 wt. % of cross-linker solids, the binder solids consisting of 20 to 100 wt. % of binder C and 0 to 80 wt. % of one or more further binders and the cross-linker solids consisting of 80 to 100 wt. % of one or more aminoplast resins and 0 to 20 wt. % of one or more further cross-linkers, the sum of the respective wt. % equalling 100 wt. % and the binder C being produced by reacting a polyisocyanate A partially blocked by one or more monoalcohols A2 and having a content of free isocyanate groups of 0.5 to 10 wt. % with a resin B comprising a hydroxyl number of 50 to 250 mg KOH/g and a carboxyl number of 10 to 50 mg KOH/g at a molar ratio of hydroxyl groups of B to free isocyanate groups of A of at least 2:1.
1 . Aqueous coating compositions with a resin solids consisting of 60 to 80 wt. % of binder solids and 20 to 40 wt. % of cross-linker solids, the binder solids consisting of 20 to 100 wt. % of binder C and 0 to 80 wt. % of one or more further binders and the cross-linker solids consisting of 80 to 100 wt. % of one or more aminoplast resins and 0 to 20 wt. % of one or more further cross-linkers, the sum of the respective wt. % equalling 100 wt. % and the binder C being produced by reacting a polyisocyanate A partially blocked by one or more monoalcohols A2 and having a content of free isocyanate groups of 0.5 to 10 wt. % with a resin B comprising a hydroxyl number of 50 to 250 mg KOH/g and a carboxyl number of 10 to 50 mg KOH/g at a molar ratio of hydroxyl groups of B to free isocyanate groups of A of at least 2:1.
2 . The aqueous coating compositions of claim 1 , wherein the polyisocyanate A is an addition product prepared from one or more polyisocyanates A1 and a deficit of one or more monoalcohols A2, wherein the one or more polyisocyanates A1 are selected from the group consisting of diisocyanates with NCO groups bonded to non-aromatic carbon, trisisocyanatononane, polyisocyanates derived from the diisocyanates with NCO groups bonded to non-aromatic carbon and any combinations thereof.
3 . The aqueous coating compositions of claim 1 , wherein the content of the monoalcohol A2-blocked isocyanate groups is 0.1 to 0.5 mol per 100 g of binder C.
4 . The aqueous coating compositions of claim 1 , wherein resin B is an esterification product made of a polyurethane resin B1 with a carboxyl number of 50 to 200 mg KOH/g and a polyester polyol B2 with a hydroxyl number of 70 to 300 mg KOH/g and a carboxyl number of 0 to 30 mg KOH/g.
5 . The aqueous coating compositions of claim 1 , wherein the further binders are hydroxyl-functional.
6 . The aqueous coating compositions of claim 1 , wherein the same resin B which forms a structural element of the binder C is contained as a further binder or as the single further binder.
7 . The aqueous coating compositions of claim 1 , wherein the cross-linker solids consists of one or more aminoplast resins.
8 . The aqueous coating compositions of claim 7 , wherein the one or more aminoplast resins are aminoplast resins.
9 . A process for the production of a coating layer, comprising the following steps:
a) applying an aqueous coating composition of any one of the preceding claims to a substrate, and
b) thermally curing the coating layer at an object temperature which is not sufficient to cleave the monoalcohol(s) A2 from the blocked isocyanate groups of the binder C.
10 . The process of claim 9 , wherein the aqueous coating composition is applied and thermally cured to form a primer surfacer coating layer on an automotive substrate.