Claims
- 1. A clear, topcoat coating composition which is effective for application over a pigmented basecoat composition, the topcoat coating composition comprising a polymeric vehicle which comprises:
- a phenolic ester compound selected from the group consisting of a phenolic ester alcohol having the structural formula ##STR35## phenolic urethane having the structural formula ##STR36## a phenolic blocked isocyanate having the structural formula (a) ##STR37## phenolic blocked isocyanates having the structural formula (b) ##STR38## and mixtures thereof, wherein R.sub.4 is selected from the group consisting of hydrogen, halogen, hydroxyl, C.sub.1 to C.sub.8 alkyl and C.sub.1 to C.sub.8 alkoxy, R.sub.5 is selected from the group consisting of a direct bond, C.sub.1 to C.sub.20 organic radical having only carbon and hydrogen atoms, and a C.sub.1 to C.sub.20 organic radical which includes in its structure a substitution group selected from the group consisting of phenol, aliphatic hydroxyl, ester, ether, carbonate and combinations thereof, R.sub.6 is selected from the group consisting of hydrogen, a C.sub.1 to C.sub.20 organic radical, and a C.sub.1 to C.sub.20 organic radical which includes in its structure at least one ester linkage or a direct bond which forms with R.sub.7 part of a 5 or 6 carbon atom cyclic ring structure, R.sub.7 is CH.sub.2 R.sub.8 wherein R.sub.8 is selected from the group consisting of hydroxy, OR.sub.9, ##STR39## and R.sub.11, wherein R.sub.9 is selected from the group consisting of a primary aliphatic group containing 3 to 20 carbon atoms, a secondary aliphatic group containing 3 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms, a primary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage and a secondary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage, wherein R.sub.10, is selected from the group consisting of a primary aliphatic group containing 4 to 20 carbon atoms, a secondary aliphatic group containing 4 to 20 carbon atoms, a tertiary aliphatic group containing 4 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms and combinations thereof, wherein the primary, secondary and tertiary aliphatic groups include at least one ester linkage, and wherein R.sub.11 is selected from the group consisting of a C.sub.2 to C.sub.20 organic radical, a C.sub.2 to C.sub.20 organic radical which includes in its structure at least one ester linkage, a C.sub.2 to C.sub.20 organic radical which forms with R.sub.6 part of a 5 or 6 carbon atom cyclic ring structure, where y=1 to 20, y.sub.1 =1 to 4 and where R.sub.12 is selected from the group consisting of alkyl, an alkyl difunctional radical, alkenyl, alkenyl difunctional radical, aromatic and an aromatic difunctional radical and wherein the molecular weight of the phenolic ester alcohol is not more than about 1500 and the molecular weights of the phenolic urethane and phenolic blocked isocyanate are not more than about 50,000;
- a crosslinker blend comprising a polyisocyanate compound and an amino resin; and
- a polyol which is not a phenolic ester alcohol and is selected from the group consisting of a polyester polyol, an acrylic polyol, an alkyd polyol and mixtures thereof, the phenolic ester compound, crosslinker blend and polyol being in amounts which are effective for providing a cured clearcoat coating binder having a Tukon hardness of at least about 5 knoops at a film thickness of about 1.0 mil dry.
- 2. A clear topcoat coating composition as recited in claim 1, wherein the polymeric vehicle comprises at least about 0.3 equivalents of isocyanate functionality for about one equivalent of aliphatic hydroxyl in the polymeric vehicle and which isocyanate functionality is effective for reacting with the polyol and the hydroxyl functionality of the phenolic ester compound, and wherein the composition comprises from about 1.9 to about 12 equivalents of amino resin functional groups for every one equivalent of phenolic hydroxy and which amino resin functionality is effective for reacting with the polyol and the phenol hydroxyl functionality of the phenolic ester compound.
- 3. A clear topcoat coating composition as recited in claim 2, wherein the crosslinker blend has from about 0.8 to about 1.8 equivalents of isocyanate funtionality for one equivalent of aliphatic hydroxyl in the polymeric vehicle and from about 3 to about 5 equivalents of amino funtionality per equivalent of phenolic hydroxyl in the polymeric vehicle.
- 4. A clear topcoat coating composition as recited in claim 1, wherein polymeric vehicle comprises from about 40 to about 65 weight percent polyol, based upon the weight of the polymeric vehicle, from about 8 to about 50 weight percent phenolic urethane, based upon the weight of the polymeric vehicle, and from about 20 to about 50 weight percent crosslinker blend, based upon the weight of the polymeric vehicle.
- 5. A clear topcoat coating composition as recited in claim 1, wherein polymeric vehicle comprises from about 40 to about 65 weight percent polyol, based upon the weight of the polymeric vehicle, from about 5 to about 40 weight percent phenolic blocked isocyanate of formulas (a) and/or (b), based upon the weight of the polymeric vehicle, and from about 20 to about 50 weight percent crosslinker blend, based upon the weight of the polymeric vehicle.
- 6. A clear topcoat coating composition as recited in claim 1, wherein polymeric vehicle comprises from about 30 to about 70 weight percent polyol, based upon the weight of the polymeric vehicle, from about 5 to about 50 weight percent phenolic ester alcohol, based upon the weight of the polymeric vehicle, and from about 25 to about 50 weight percent crosslinker blend, based upon the weight of the polymeric vehicle.
- 7. A clear topcoat composition as recited in claim 1, wherein the polymeric vehicle comprises a phenolic urethane having the structural formula ##STR40##
- 8. A polymeric vehicle which is effective for providing a clear topcoat coating binder having a Tukon hardness of at least about 5 knoops, the polymeric vehicle comprising: a phenolic ester alcohol having the structural formula ##STR41## a crosslinker blend comprising a polyisocyanate compound and an amino resin; and
- a polyol which is not a phenolic ester alcohol and is selected from the group consisting of a polyester polyol, an acrylic polyol, an alkyd polyol and mixtures thereof, the polyol having a number average molecular weight of not more than about 20,000, the polymeric vehicle effective for providing a coating binder with from about 0.7 to about 20 weight percent, based upon the weight of the polymeric vehicle before crosslinking, carbamate linkages upon curing the polymeric vehicle and the polymeric vehicle comprising from about 1.9 to about 12 equivalent of aminoresin functional groups for every one equivalent of phenolic hydroxy in the polymeric vehicle and which amino resin functionality is effective for reacting with the polyol and the phenol hydroxyl functionality of the phenolic ester alcohol and R.sub.4 is selected from the group consisting of hydrogen, halogen, hydroxyl, C.sub.1 to C.sub.8 alkyl and C.sub.1 to C.sub.8 alkoxy, R.sub.5 is selected from the group consisting of a direct bond, C.sub.1 to C.sub.20 organic radical having only carbon and hydrogen atoms, and a C.sub.1 to C.sub.20 organic radical which includes in its structure a substitution group selected from the group consisting of phenol, aliphatic hydroxyl, ester, ether, carbonate and combinations thereof, R.sub.6 is selected from the group consisting of hydrogen, a C.sub.1 to C.sub.20 organic radical, and a C.sub.1 to C.sub.20 organic radical which includes in its structure at least one ester linkage or a direct bond which forms with R.sub.7 part of a 5 or 6 carbon atom cyclic ring structure, R.sub.7 is CH.sub.2 R.sub.8 wherein R.sub.8 is selected from the group consisting of hydroxy, OR.sub.9, ##STR42## and R.sub.11, wherein R.sub.9 is selected from the group consisting of a primary aliphatic group containing 3 to 20 carbon atoms, a secondary aliphatic group containing 3 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms, a primary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage and a secondary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage, wherein R.sub.10 is selected from the group consisting of a primary aliphatic group containing 4 to 20 carbon atoms, a secondary aliphatic group containing 4 to 20 carbon atoms, a tertiary aliphatic group containing 4 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms and combinations thereof, wherein the primary, secondary and tertiary aliphatic groups include at least one ester linkage, and wherein R.sub.11 is selected from the group consisting of a C.sub.2 to C.sub.20 organic radical, a C.sub.2 to C.sub.20 organic radical which includes in its structure at least one ester linkage, a C.sub.2 to C.sub.20 organic radical which forms with R.sub.6 part of a 5 or 6 carbon atom cyclic ring structure and wherein the molecular weight of the phenolic ester alcohol is not more than about 1500.
- 9. A polymeric vehicle as recited in claim 8, wherein the crosslinker blend has from about 0.8 to about 1.8 equivalents of isocyanate funtionality for one equivalent of aliphatic hydroxyl in the polymeric vehicle and from about 3 to about 5 equivalents of amino funtionality per equivalent of phenolic hydroxyl in the polymeric vehicle.
- 10. A polymeric vehicle as recited in claim 8, wherein polymeric vehicle comprises from about 30 to about 70 weight percent polyol, based upon the weight of the polymeric vehicle, from about 5 to about 50 weight percent phenolic ester alcohol, based upon the weight of the polymeric vehicle, and from about 25 to about 50 weight percent crosslinker blend, based upon the weight of the polymeric vehicle.
- 11. A polymeric vehicle as recited in claim 8 wherein the phenolic ester alcohol is ##STR43## wherein R.sub.14 is an alkyl having 8 carbon atoms.
- 12. A polymeric vehicle which is effective for providing a clear topcoat coating binder having a Tukon hardness of at least about 5 knoops, the polymeric vehicle comprising:
- phenolic urethane having the structural formula ##STR44## an amino crosslinking resin; a polyol which is not a phenolic ester alcohol and is selected from the group consisting of a polyester polyol, an acrylic polyol, an alkyd polyol and mixtures thereof, the polyol having a number average molecular weight of not more than about 20,000, the polymeric vehicle effective for providing a coating binder with from about 0.7 to about 20 weight percent, based upon the weight of the polymeric vehicle before crosslinking, carbamate linkages upon curing the polymeric vehicle and the polymeric vehicle comprising from about 1.9 to about 12 equivalent of amino resin functional groups for every one equivalent of phenolic hydroxy in the polymeric vehicle and which amino resin functionality is effective for reacting with the polyol and the phenol hydroxyl functionality of the phenolic urethane and R.sub.4 is selected from the group consisting of hydrogen, halogen, hydroxyl, C.sub.1 to C.sub.8 alkyl and C.sub.1 to C.sub.8 alkoxy, R.sub.5 is selected from the group consisting of a direct bond, C.sub.1 to C.sub.20 organic radical having only carbon and hydrogen atoms, and a C.sub.1 to C.sub.20 organic radical which includes in its structure a substitution group selected from the group consisting of phenol, aliphatic hydroxyl, ester, ether, carbonate and combinations thereof, R.sub.6 is selected from the group consisting of hydrogen, a C.sub.1 to C.sub.20 organic radical, and a C.sub.1 to C.sub.20 organic radical which includes in its structure at least one ester linkage or a direct bond which forms with R.sub.7 part of a 5 or 6 carbon atom cyclic ring structure, R.sub.7 is CH.sub.2 R.sub.8 wherein R.sub.8 is selected from the group consisting of hydroxy, OR.sub.9, ##STR45## and R.sub.11, wherein R.sub.9 is selected from the group consisting of a primary aliphatic group containing 3 to 20 carbon atoms, a secondary aliphatic group containing 3 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms, a primary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage and a secondary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage, wherein R.sub.10 is selected from the group consisting of a primary aliphatic group containing 4 to 20 carbon atoms, a secondary aliphatic group containing 4 to 20 carbon atoms, a tertiary aliphatic group containing 4 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms and combinations thereof, wherein the primary, secondary and tertiary aliphatic groups include at least one ester linkage, and wherein R.sub.11 is selected from the group consisting of a C.sub.2 to C.sub.20 organic radical, a C.sub.2 to C.sub.20 organic radical which includes in its structure at least one ester linkage, a C.sub.2 to C.sub.20 organic radical which forms with R.sub.6 part of a 5 or 6 carbon atom cyclic ring structure, where R.sub.12 is selected from the group consisting of alkyl, an alkyl difunctional radical, alkenyl, alkenyl difunctional radical, aromatic and an aromatic difunctional radical and wherein the molecular weight of the phenolic urethane is not more than about 50,000.
- 13. A polymeric vehicle as recited in claim 12, wherein the polymeric vehicle further includes an isocyanate compound to provide a crosslinker blend and the amino resin in the crosslinker blend is in an amount effective for providing from about 3 to about 5 equivalents of amino funtionality per equivalent of phenolic hydroxyl in the polymeric vehicle.
- 14. A polymeric vehicle as recited in claim 13, wherein polymeric vehicle comprises from about 40 to about 65 weight percent polyol, based on the weight of the polymeric vehicle, from about 8 to about 50 weight percent phenolic urethane, based on the weight of the polymeric vehicle and from about 20 to about 50 weight percent crosslinker blend based on the weight of the polymeric vehicle.
- 15. A polymeric vehicle as recited in claim 12 wherein the phenolic urethane is ##STR46## wherein R.sub.14 is an alkyl having 8 carbon atoms.
- 16. A polymeric vehicle which is effective for providing a clear topcoat coating binder having a Tukon hardness of at least about 5 knoops, the polymeric vehicle comprising:
- phenolic blocked isocyanates having the structural formula ##STR47## an amino crosslinking resin; and a polyol which is not a phenolic ester alcohol and is selected from the group consisting of a polyester polyol, an acrylic polyol, an alkyd polyol and mixtures thereof, the polyol having a number average molecular weight of not more than about 20,000, the polymeric vehicle effective for providing a coating binder with from about 0.7 to about 20 weight percent, based upon the weight of the polymeric vehicle before crosslinking, carbamate linkages upon curing the polymeric vehicle and the polymeric vehicle comprising from about 1.9 to about 12 equivalent of amino resin functional groups for every one equivalent of a deblocked phenolic hydroxy in the polymeric vehicle and which amino resin functionality is effective for reacting with the polyol and the phenol hydroxyl functionality which results from deblocking of the phenolic blocked isocyanate wherein R.sub.4 is selected from the group consisting of hydrogen, halogen, hydroxyl, C.sub.1 to C.sub.8 alkyl and C.sub.1 to C.sub.8 alkoxy, R.sub.5 is selected from the group consisting of a direct bond, C.sub.1 to C.sub.20 organic radical having only carbon and hydrogen atoms, and a C.sub.1 to C.sub.20 organic radical which includes in its structure a substitution group selected from the group consisting of phenol, aliphatic hydroxyl, ester, ether, carbonate and combinations thereof, R.sub.6 is selected from the group consisting of hydrogen, a C.sub.1 to C.sub.20 organic radical, and a C.sub.1 to C.sub.20 organic radical which includes in its structure at least one ester linkage or a direct bond which forms with R.sub.7 part of a 5 or 6 carbon atom cyclic ring structure, R.sub.7 is CH.sub.2 R.sub.8 wherein R.sub.8 is selected from the group consisting of hydroxy, OR.sub.9, ##STR48## and R.sub.11, wherein R.sub.9 is selected from the group consisting of a primary aliphatic group containing 3 to 20 carbon atoms, a secondary aliphatic group containing 3 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms, a primary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage and a secondary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage, wherein R.sub.1 O is selected from the group consisting of a primary aliphatic group containing 4 to 20 carbon atoms, a secondary aliphatic group containing 4 to 20 carbon atoms, a tertiary aliphatic group containing 4 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms and combinations thereof, wherein the primary, secondary and tertiary aliphatic groups include at least one ester linkage, and wherein R.sub.11 is selected from the group consisting of a C.sub.2 to C.sub.20 organic radical, a C.sub.2 to C.sub.20 organic radical which includes in its structure at least one ester linkage, a C.sub.2 to C.sub.20 organic radical which forms with R.sub.6 part of a 5 or 6 carbon atom cyclic ring structure, where y=1 to 20, y.sub.1 =1 to 4 and where R.sub.12 is a residue of a multifunctional isocyanate compound and wherein the molecular weight of the phenolic blocked isocyanate is not more than about 50,000.
- 17. A polymeric vehicle which is effective for providing a clear topcoat coating binder having a Tukon hardness of at least about 5 knoops, the polymeric vehicle comprising:
- phenolic blocked isocyanates having the structural formula ##STR49## an amino crosslinking resin; and a polyol which is not a phenolic ester alcohol and is selected from the group consisting of a polyester polyol, an acrylic polyol, an alkyd polyol and mixtures thereof, the polyol having a number average molecular weight of not more than about 20,000, the polymeric vehicle effective for providing a coating binder with from about 0.7 to about 20 weight percent, based upon the weight of the polymeric vehicle before crosslinking, carbamate linkages upon curing the polymeric vehicle and the polymeric vehicle comprising from about 1.9 to about 12 equivalent of amino resin functional groups for every one equivalent of a deblocked phenolic hydroxy in the polymeric vehicle and which amino resin functionality is effective for reacting with the polyol and the phenol hydroxyl functionality which results from deblocking of the phenolic blocked isocyanate wherein R.sub.4 is selected from the group consisting of hydrogen, halogen, hydroxyl, C.sub.1 to C.sub.8 alkyl and C.sub.1 to C.sub.20 alkoxy, R.sub.5 is selected from the group consisting of a direct bond, C.sub.1 to C.sub.20 organic radical having only carbon and hydrogen atoms, and a C.sub.1 to C.sub.20 organic radical which includes in its structure a substitution group selected from the group consisting of phenol, aliphatic hydroxyl, ester, ether, carbonate and combinations thereof, R.sub.6 is selected from the group consisting of hydrogen, a C.sub.1 to C.sub.20 organic radical, and a C.sub.1 to C.sub.20 organic radical which includes in its structure at least one ester linkage or a direct bond which forms with R.sub.7 part of a 5 or 6 carbon atom cyclic ring structure, R.sub.7 is CH.sub.2 R.sub.8 wherein R.sub.8 is selected from the group consisting of hydroxy, OR.sub.9, ##STR50## and R.sub.11, wherein R.sub.9 is selected from the group consisting of a primary aliphatic group containing 3 to 20 carbon atoms, a secondary aliphatic group containing 3 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms, a primary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage and a secondary aliphatic group containing 3 to 20 carbon atoms which includes at least one ester linkage, wherein R.sub.10 is selected from the group consisting of a primary aliphatic group containing 4 to 20 carbon atoms, a secondary aliphatic group containing 4 to 20 carbon atoms, a tertiary aliphatic group containing 4 to 20 carbon atoms, an aromatic group containing 6 to 20 carbon atoms and combinations thereof, wherein the primary, secondary and tertiary aliphatic groups include at least one ester linkage, and wherein R.sub.11 is selected from the group consisting of a C.sub.2 to C.sub.20 organic radical, a C.sub.2 to C.sub.20 organic radical which includes in its structure at least one ester linkage, a C.sub.2 to C.sub.20 organic radical which forms with R.sub.6 part of a 5 or 6 carbon atom cyclic ring structure, where y=1 to 20, and where R.sub.12 is a residue of a multifunctional isocyanate compound and wherein the molecular weight of the phenolic blocked isocyanate is not more than about 50,000.
- 18. A polymeric vehicle as recited in claims 16 or 17, wherein the polymeric vehicle further includes an isocyanate compound to provide a crosslinker blend and the amino resin in the crosslinker blend is in an amount effective for providing from about 3 to about 5 equivalents of amino functionality per equivalent of deblocked phenolic hydroxyl in the polymeric vehicle.
- 19. A polymeric vehicle as recited in claim 18, wherein polymeric vehicle comprises from about 40 to about 65 weight percent polyol, based upon the weight of the polymeric vehicle, from about 5 to about 40 weight percent phenolic blocked isocyanate, based upon the weight of the polymeric vehicle, and from about 20 to about 50 weight percent crosslinker blend, based upon the weight of the polymeric vehicle.
- 20. A polymeric vehicle as recited in claim 17 wherein the phenolic blocked isocyanate is ##STR51## wherein R.sub.14 is an alkyl having 8 carbon atoms.
BACKGROUND OF THE INVENTION
This application is a continuation in part application of Ser. No. 08/621,171 filed Mar. 21, 1996 allowed, which application is a continuation in part application of Ser. No. 08/424,205 filed Mar. 19, 1995, now U.S. Pat. No. 5,681,906. This application also is a continuation in part application of Ser. No. 08/621,177 filed Mar. 21, 1996, now U.S. Pat. No. 5,973,072 which application stems from provisional patent application Ser. No. 60/002,063 filed Aug. 9, 1995. Further, this application is a continuation in part application of Ser. No. 08/702,966 filed Aug. 26, 1996 abandoned.
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Continuation in Parts (2)
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Number |
Date |
Country |
| Parent |
621171 |
Mar 1996 |
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| Parent |
424205 |
Mar 1995 |
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Patent Grant
6103826
