Multilayer coating with a primer-surfacer of a nonaqueous coating material comprising at least two different polyesters
Method for producing a multicoat coating comprises: applying a primer-surfacer coat (I) to an optionally pretreated substrate, curing coat (I), applying a basecoat (II) to coat (I), optionally curing the basecoat (II), applying a clearcoat (III) to basecoat (II), and curing basecoat (II) and/or clearcoat (III), wherein coat (I) is obtained by applying a nonaqueous, solventborne coating material comprising by weight: at least 20% of at least one organic solvent, at least 8% of at least one first polyester (A1), having a glass transition temperature of at least 20° C. and an acid number of 0 to 40 mg KOH/g; at least 8% by weight of at least one second polyester (A2), different from (A1) and having a glass transition temperature of not more than 10° C.; at least one crosslinker (B); and at least 8% of one or more fillers and/or pigments (C).
1. A method for producing a multicoat coating comprising:
(i) applying a primer-surfacer coat (I) to an optionally pretreated substrate,
(ii) curing the primer-surfacer coat (I),
(iii) applying a basecoat (II) to the cured primer-surfacer coat (I),
(iv) optionally curing the basecoat (II),
(v) applying a clearcoat (III) to the cured or uncured basecoat (II), and
(vi) curing the clearcoat (III) or the basecoat and the clearcoat if the basecoat was not cured in step (iv),
wherein the primer-surfacer coat (I) is obtained by applying a nonaqueous, solventborne coating material (F) comprising:
at least 20% by weight, based on the total coating material (F), of at least one organic solvent, and also
(A1) from 9% to below 30% by weight, based on the total coating material (F), of at least one first polyester (A1), having a glass transition temperature of at least 20° C. and an acid number of 0 to 40 mg KOH/g,
(A2) from 9% to below 30% by weight, based on the total coating material (F), of at least one second polyester (A2), different from (A1) and having a glass transition temperature of not more than 10° C. and an acid number of 5 to 50 mg KOH/g,
(B) at least one crosslinker (B), and
(C) at least 8% by weight, based on the total coating material (F), of one or more fillers and/or pigments (C);
wherein the nonaqueous, solventborne coating material (F) is storage-stable wherein on storage at 40° C. for four weeks, viscosity of (F) measured at 23° C. is not more than twice the viscosity of (F) immediately after preparation;
wherein the coating material (F) has a weight ratio of polyester (A1) to polyester (A2) of 0.7 to 1.2; and
wherein the coating material (F) further comprises an epoxy resin and wherein (A1) is obtained from the reaction of: neopentyl glycol ester of hydroxypivaloyl acid, neopentyl glycol, isophthalic acid or anhydride, and tetrahydrophthalic acid or anhydride, and subsequent reaction with: trimellitic acid or anhydride, and phthalic acid or anhydride; and (A2) is obtained from the reaction of: ethoxylated bisphenol A derivative, neopentyl glycol, and trimethylolpropane with: adipic acid, and trimellitic acid or anhydride.
2. The method according to claim 1 , wherein the optionally pretreated substrate is a metallic substrate.
3. The method according to claim 1 , wherein the optionally pretreated substrate is an automobile body or a part thereof.
4. A multicoat coating obtainable by the method according to claim 1 .
5. The multicoat coating according to claim 4 , wherein the glass transition temperature of the coating material (F) is at least 35° C.
6. The multicoat coating according to claim 4 , wherein the polyester (A1) has an acid number of 0 to 30 mg KOH/g.
7. The multicoat coating according to claim 4 , wherein the polydispersity (Mw/Mn) of the first polyester (A1) is 5 or below, and the polydispersity (Mw/Mn) of the second polyester (A2) is 5 or above.
8. The multicoat coating according to claim 4 , wherein the crosslinker or crosslinkers (B) are selected from the group consisting of blocked polyisocyanates, melamine-formaldehyde resins and benzoguanamine-formaldehyde resins.
9. The multicoat coating according to claim 4 , wherein the coating material (F) comprises at least one blocked isocyanate and at least one amino resin as crosslinker (B).
10. The multicoat coating according to claim 4 , wherein the coating material (F) has a weight ratio of fillers and/or pigments (C) to binders (A1+A2+B) of (C):(A1+A2+B)=0.5 to 1.2.
11. The multicoat coating according to claim 4 , wherein the filler or fillers and/or pigment or pigments (C) are selected from the group consisting of silicates, calcium carbonates, calcium magnesium carbonates, barium carbonate, carbon black, barium sulfates, calcium sulfate, aluminum hydroxide, magnesium hydroxide, titanium dioxide and silicas.
12. A substrate coated with the multicoat coating according to claim 4 .
13. The substrate according to claim 12 that a metallic substrate.
14. The substrate according to claim 13 that is an automobile body or part thereof.
15. The method according to claim 1 , wherein the at least one crosslinker (B) is selected from the group consisting of a blocked isocyanate and an amino resin.
16. The method according to claim 1 , wherein (iii) comprises applying the basecoat (II) directly to the cured primer-surfacer coat (I).
17. The method according to claim 1 , wherein the at least one first polyester (A1) is present in an amount of from 10% to below 30% by weight.
18. A method for producing a multicoat coating comprising:
(i) applying a primer-surfacer coat (I) to an optionally pretreated substrate,
(ii) curing the primer-surfacer coat (I),
(iii) applying a basecoat (II) to the cured primer-surfacer coat (I),
(iv) optionally curing the basecoat (II),
(v) applying a clearcoat (III) to the cured or uncured basecoat (II), and
(vi) curing the clearcoat (III) or the basecoat and the clearcoat if the basecoat was not cured in step (iv),
wherein the primer-surfacer coat (I) is obtained by applying a nonaqueous, solventborne coating material (F) comprising:
at least 20% by weight, based on the total coating material (F), of at least one organic solvent, and also
(A1) from 9% to below 30% by weight, based on the total coating material (F), of a first polyester (A1), having a glass transition temperature of at least 20° C. and an acid number of 0 to 40 mg KOH/g, the first polyester (A1) obtained from the reaction of: neopentyl glycol ester of hydroxypivaloyl acid, neopentyl glycol, isophthalic acid, and tetrahydrophthalic anhydride, and subsequent reaction with trimellitic anhydride and phthalic anhydride;
(A2) from 9% to below 30% by weight, based on the total coating material (F), of a second polyester (A2), different from (A1) and having a glass transition temperature of not more than 10° C. and an acid number of 5 to 50 mg KOH/g, the second polyester (A2) obtained from the reaction of: ethoxylated bisphenol A derivative, neopentyl glycol, and trimethylolpropane with: adipic acid and trimellitic anhydride;
(B) at least one crosslinker (B) selected from the group consisting of blocked polyisocyanates and melamine-formaldehyde resins, and
(C) at least 8% by weight, based on the total coating material (F), of one or more fillers and/or pigments (C);
wherein the coating material (F) has a weight ratio of polyester (A1) to polyester (A2) of 0.9 to 1.2.
19. The method of claim 18 , wherein the coating material (F) further comprises an epoxy resin.
20. The method of claim 18 , wherein the at least one first polyester (A1) is present in an amount of from 10% to below 30% by weight.