IP Library Granted Patent US 7,686,878
Granted Patent B2
US 7,686,878 · App. 11/295,083 · Granted Mar 30, 2010

Coating composition containing a low VOC-producing silane

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Quick Facts
Patent No.
US 7,686,878
App. No.
11/295,083
Granted
Mar 30, 2010
Kind
B2
Abstract

A coating composition is provided which includes an adhesion promoter or a crosslinker silane which, upon hydrolysis, of its hydrolyzable sites, produces a reduced amount of volatile organic compound compared to that produced by the hydrolysis of a silane possessing an equivalent number of hydrolyzable sites all of which are hydrolyzable alkoxy groups.

Claims (64)

1. A coating composition which comprises an adhesion-promoting amount or crosslinking effective amount of a silane which, upon hydrolysis of its hydrolyzable sites, produces an organic compound selected from the group consisting of acetylenic glycols, polyalkoxylated variants of acetylenic glycols, hydroxycarboxylic acids and ester alcohols wherein the silane has the general formula:

Y[-G(—SiX u Z c w ) s ] r   (Formula 1)

wherein

each occurrence of G is independently chosen from a set of groups comprising a polyvalent group derived by substitution of one or more hydrogen atoms of an alkyl, alkenyl, aryl or aralkyl group, or a molecular component which can be obtained by removal of one or more hydrogen atoms of a heterocarbon, with G containing from about 1 to about 30 carbon atoms;

each occurrence of X is independently selected from the group consisting of a monovalent alkoxy group derived from acetylenic glycols, polyalkoxylated variants of acetylenic glycols, hydroxycarboxylic acid and ester alcohols;

each occurrence of Z C is independently selected from the group consisting of —O(R 10 CR 11 ) f O—, —NR 4 -L 1 -NR 5 —, and —OC(═O)R 10 CR 11 C(═O)O—, wherein each occurrence of R 10 and R 11 is independently R and each occurrence of L 1 is independently G;

each occurrence of R is chosen independently from the set of groups consisting of hydrogen, and organic groups having 1 to about 20 carbon atoms and selected from straight alkyl, cyclic alkyl, branched alkyl, alkenyl, aryl, aralkyl, an ether, a polyether and molecular components obtained by removal of one or more hydrogen atoms of a heterocarbon;

each occurrence of R 4 and R 5 is independently given by one of the structures listed for R

each occurrence of the subscript f is an integer from 1 to about 15;

each occurrence of the subscript u is an integer equal to 1;

each occurrence of the subscript w is an integer equal to 1;

each occurrence of the subscript r is an integer from 1 to about 6;

each occurrence of the subscript s is an integer from 1 to about 6; and,

each occurrence of Y is a functional group of valence r.

2. The composition of claim 1 wherein Y is selected from the group consisting of a univalent functional group, a divalent functional group, a trivalent functional group, a tetravalent functional group and a polyvalent functional group.

3. The composition of claim 2 wherein the univalent functional group is selected from the group consisting of CH 2 ═CH—, CHR═CH—, CR 2 ═CH—, mercapto, acryloxy, methacryloxy, acetoxy, —O—CH 2 —C 2 H 3 O, —CH 2 —CH 2 —C 6 H 9 O, —C 6 H 9 O, —CR 6 (—O—)CR 4 R 5 , —OH, —NR 4 C(═O)OR 5 , —OC(═O)NR 4 R 5 , —NR 4 C(═O)SR 5 , —SC(═O)NR 4 R 5 , —NR 4 C(═S)OR 5 , —OC(═S)NR 4 R 5 , —NR 4 C(═S)SR 5 , —SC(═S)NR 4 R 5 , maleimide, maleate, substituted maleate, fumarate, substituted fumarate, —CN, citraconimide, , —OCN, —N═C═O, —SCN, —N═C═S, —OR 4 , —F, —Cl, —Br; —I, —SR 4 , —S—SR 4 , —S—S—SR 4 , —S—S—S—SR 4 , —S—S—S—S—SR 4 , —S—S—S—S—S—SR 4 , —S x R 4 , —SC(═S)OR 4 , —SC(═S)SR 4 , —SC(═O)SR 4 , —NR 4 C(═O)NR 5 R 6 , —NR 4 C(═S)NR 5 R 6 , R 4 C(═O)NR 5 —, —C(═O)NR 4 R 5 —, R 4 C(═S)NR 4 —, melamine, cyanurato, —NH 2 , —NHR 4 , —NR 4 R 5 , —NR 4 -L 1 -NR 5 R 6 , —NR 4 -L 1 (—NR 5 R 6 ) 2 , —NR 4 -L 1 -NR 5 -L 2 -NR 6 R 7 , —NR 4 -L 1 (—NR 5 R 6 ) 3 , —NR 4 -L 1 -NR 5 -L 2 -NR 6 -L 3 -NR 7 R 8 and —NR 4 -L 1 -N(-L 2 NR 5 R 6 ) 2 ;

the divalent functional group is selected from the group consisting of -(-)C (—O—)CR 4 R 5 , —CR 5 (—O—)CR 4 —, —O(R 10 CR 11 ) f O—, -(-) NC(═O)OR 5 , —OC(═O)NR 4 —, -(-) NC(═O)SR 5 , —SC(═O)NR 4 —, -(-)NC(═S)OR 5 , —OC(═S)NR 4 —, -(-) NC(═S)SR 5 , —SC(═S)NR 4 —, —O—, maleate, substituted maleate, fumarate, substituted fumarate, —S—, —S—S—, —S—S—S—, —S—S—S—S—, —S—S—S—S—S—, —S—S—S—S—S—S—, —S x —, —SC(═S)O—, —SC(═S)S—, —SC(═O)S—, -(-) NC(═O)NR 4 R 5 , —NR 4 C(═O)NR 5 —, -(-)NC(═S)NR 4 R 5 , —NR 4 C(═S)NR 5 —, R 4 C(═O)N(-)-, —C(═O)NR 4 —, R 4 C(═S)N(-)-, divalent melamine, divalent cyanurato, —NH—, —NR 4 —, -(-)N-L 1 -NR 4 R 5 , —NR 4 -L 1 -NR 5 —, (-)NR 4 ) 2 -L 1 -NR 5 R 6 , -(-)N-L 1 -NR 5 -L 2 -NR 6 R 7 , —NR 4 -L 1 -N(-)-L 2 -NR 5 R 6 , —NR 4 -L 1 -NR 5 -L 2 -NR 6 —, -(-)N-L 1 -(NR 5 R 6 ) 3 , (—NR 4 ) 2 -L 1 -(NR 5 R 6 ) 2 , -(-) N-L 1 -NR 4 -L 2 -NR 5 -L 3 -NR 6 R 7 , —NR 4 -L 1 -N(-)-L 2 -NR 5 -L 3 -NR 6 R 7 , —NR 4 -L 1 -NR 5 -L 2 -N(-)-L 3 -NR 6 R 7 , —NR 4 -L 1 -NR 5 -L 2 -NR 6 -L 3 -NR 7 —, -(-)N-L 1 -N(-L 2 NR 5 R 6 ) 2 and (—NR 4 L 1 -) 2 N-L 2 NR 5 R 6 ;

the trivalent functional group is selected from the group consisting of -(-)C (—O—)CR 4 —, -(-)NC(═O)O—, -(-)NC(═O)S—, -(-)NC(═S)O—, -(-)NC(═S)S—, -(-)NC(═O)NR 4 —, -(-)NC(═S)NR 4 —, —C(═O)N(-)-, —C(═S)N(-)-, trivalent melamino; trivalent cyanurato, —N(-)-, -(-)N-L 1 -NR 4 —, (—NR 4 ) 3 -L 1 , (—NR 4 ) 2 -L 1 -NR 5 —, -(-)N -L 1 -N(-)-L 2 -NR 3 R 4 , —NR 4 -L 1 -N(-)-L 2 -NR 5 —, -(-)N-L 1 -NR 4 -L 2 -NR 5 —, -(-)N-L 1 -N(-)-L 2 -NR 5 -L 3 -NR 3 R 4 , —NR 4 -L 1 -N(-)-L 2 -N(-)-L 3 -NR 3 R 4 , -(-)N-L 1 -NR 5 -L 2 -N(-)-L 3 -NR 3 R 4 , —NR 4 -L 1 -N(-)-L 2 -NR 3 -L 3 -NR 4 —, -(-)N-L 1 -N(-L 2 NR 3 R 4 )(-L 2 NR 5 —) and (—NR 4 L 1 -) 3 N;

the tetravalent functional group is selected from the group consisting of -(-)C (—O—)C (-)-, -(-)NC(═O)N(-)-, -(-)NC(═S)N(-)-, tetravalent melamino, -(-)N-L 1 -N(-)-, (—NR 4 ) 4 -L 1 , (—NR 4 ) 2 -L 1 -N(-)-, -(-)N-L 1 -N(-)-L 2 NR 3 —, -(-)N-L 1 -NR 4 -L 2 (-)-, -(-)N-L 1 -N(-)-L 2 -N (-)-L 3 -NR 4 R 3 , —NR 4 -L 1 -N(-)-L 2 -N(-)-L 3 -NR 3 —, -(-)N-L 1 -NR 4 -L 2 -NR 3 -L 3 -N(-)- and -(-)N-L 1 -N (-L 2 NR 3 —) 2 ; and,

the polyvalent functional group is selected from the group consisting of polyvalent hydrocarbon groups, (—NR 3 )(—N—) 2 C 3 N 3 , (—N—) 3 C 3 N 3 , -(-)N-L 1 -N(-)-L 2 -N(-)-, -(-)N-L 1 -N(-)-L 2 -N(-)-L 3 -NR 3 —, -(-)N-L 1 -NR 3 -L 2 -N(-)-L 3 -N(-)-, [-(-)N-L 1 -] 2 N-L 2 NR 3 —, -(-)N-L 1 -N(-)-L 2 -N(-)-L 3 -N(-)- and [-(-)N-L 1 -] 3 ,

wherein each occurrence of L 1 , L 2 , and L 3 is selected independently from the set of structures given above for G, each occurrence of R 3-8 is independently given by one of the structures listed above for R and x is independently an integer from 1 to 10.

4. The composition of claim 1 wherein G is selected from the group consisting of diethylene cyclohexane, 1,2,4-triethylene cyclohexane, diethylene benzene, phenylene, —(CH 2 ) m -wherein m is 1 to 12 and CH 2 (CH 2 ) q CH(CH 3 )— wherein q is zero to 17.

5. The composition of claim 1 wherein R and R 10 and R 11 are independently selected from the group consisting of methyl, ethyl, propyl, isopropyl, octenyl, cyclohexyl, butyl, phenyl, benzyl, tolyl, allyl, methoxyethyl, ethoxyethyl, dimethylaminoethyl and cyanoethyl.

6. The composition of claim 1 wherein R 10 and R 11 are each independently selected from a group consisting of hydrogen, methyl and ethyl.

7. The composition of claim 1 wherein R 4 and R 5 are independently selected from the group consisting of hydrogen, methyl, ethyl and propyl.

8. The composition of claim 3 wherein R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are independently selected from the group consisting of phenyl, methyl, butyl, H and ethyl.

9. The composition of claim 1 wherein X is a group derived from glycolic acid or a group derived from 2,2,4-trimethyl-1,3-propanediol monoisobutyrate.

10. The composition of claim 1 wherein Z c is selected from the group consisting of divalent alkoxy groups derived from the diols consisting of ethylene glycol, propylene glycol, neopentyl glycol, 1,3-propanediol, 2-methyl-1,3-propanediol, 1,3-butanediol, 1,4 butanediol, 2-methyl-2,4-pentanediol, cyclohexane dimethanol and pinacol.

11. The composition of claim 1 wherein Z c is a moiety derived from a diol selected from the group of diols consisting of 1,3-propanediol, 2-methyl-1,3-propanediol, 1,3-butanediol and 2-methyl-2,4-pentanediol;

R is independently selected from the group consisting of an alkyl of C 1 to C 4 and H; and,

G is a divalent straight chain alkyl of 2 to 18 carbon atoms.

12. The composition of claim 1 wherein G is a C 2 -C 12 straight-chain alkyl derivative.

13. The composition of claim 1 wherein is R is an alkyl of C 1 to C 4 or H, and G is a divalent straight chain alkyl of 2 to 18 carbon atoms.

14. The composition of claim 1 wherein the silane is present in the range of from about 0.1 to about 30 weight percent of the composition.

15. The composition of claim 14 wherein the silane is present in the range of from about 0.1 to about 10 weight percent of the composition.

16. The composition of claim 1 wherein the composition further comprises an emulsifier.

17. The composition of claim 16 wherein the emulsifier is selected from the group consisting of nonionic, anionic, cationic, amphoteric surfactants, and mixtures thereof.

18. The composition of claim 16 wherein the emulsifier has an HLB of less than about 4 to about 17.

19. The composition of claim 1 wherein the pH of the composition is in the range of from about 5.5 to about 8.5.

20. The composition of claim 1 wherein the composition further comprises a catalyst.

21. The composition of claim 20 wherein the catalyst is selected from the group consisting of organotitanate, organotin, chelated titanium, aluminum and zirconium compounds, and combinations thereof.

22. The composition of claim 20 wherein the catalyst is present in an amount of about 0.05 to about 5 percent of the coating composition.

23. The composition of claim 1 wherein the composition further comprises one or more of a wetting agent, a filler, a thixotrope, a pigment, a plasticizer, a coalescing agent, a biocide, a fungicide, a UV inhibitor, an anti-oxidant and a moisture barrier resin.

24. A silane of general Formula (1):

Y[-G(—SiX u Z c w ) s ] r   (Formula 1)

wherein

each occurrence of G is independently chosen from a set of groups comprising a polyvalent group derived by substitution of one or more hydrogen atoms of an alkyl, alkenyl, aryl or aralkyl group, or a molecular component which can be obtained by removal of one or more hydrogen atoms of a heterocarbon, with G containing from about 1 to about 30 carbon atoms;

each occurrence of X is independently selected from the group consisting of a monovalent alkoxy group derived from acetylenic glycols, polyalkoxylated variants of acetylenic glycols, hydroxycarboxylic acids and ester alcohols;

each occurrence of Z c is independently selected from the group consisting of —O(R 10 CR 11 ) f O—, —NR 4 -L 1 -NR 5 —, and —OC(═O)R 10 CR 11 C(═O)O—, wherein each occurrence of R 10 and R 11 is independently R and each occurrence of L 1 is independently G;

each occurrence of R is chosen independently from the set of groups consisting of hydrogen, and organic groups having 1 to about 20 carbon atoms and selected from straight alkyl, cyclic alkyl, branched alkyl, alkenyl, aryl, aralkyl, an ether, a polyether and molecular components obtained by removal of one or more hydrogen atoms of a heterocarbon;

each occurrence of R 4 and R 5 is independently given by one of the structures listed for R

each occurrence of the subscript f is an integer from 1 to about 15;

each occurrence of the subscript u is an integer equal to 1;

each occurrence of the subscript w is an integer equal to 1,

each occurrence of the subscript r is an integer from 1 to about 6;

each occurrence of the subscript s is an integer from 1 to about 6;

each occurrence of Y is a functional group of valence r.

25. The silane of claim 24 , wherein Y is a univalent functional group selected from the group consisting of CH 2 ═CH—, CHR═CH—, CR 2 ═CH—, mercapto, acryloxy, methacryloxy, acetoxy, —O—CH 2 —C 2 H 3 O, —CH 2 —CH 2 —C 6 H 9 O, —C 6 H 9 O, —CR 6 (—O—)CR 4 R 5 , —OH, —NR 4 C(═O)OR 5 , —OC(═O)NR 4 R 5 , —NR 4 C(═O)SR 5 , —SC(═O)NR 4 R 5 , —NR 4 C(═S)OR 5 , —OC(═S)NR 4 R 5 , —NR 4 C(═S)SR 5 , —SC(═S)NR 4 R 5 , maleimide, maleate, substituted maleate, fumarate, substituted fumarate, —CN, citraconimide, , —OCN, —N═C═O, —SCN, —N═C═S, —OR 4 , —F, —Cl, —Br; —I, —SR 4 , —S—SR 4 , —S—S—SR 4 , —S—S—S—SR 4 , —S—S—S—S—SR 4 , —S—S—S—S—S—SR 4 , —S x R 4 , —SC(═S)OR 4 , —SC(═S)SR 4 , —SC(═O)SR 4 , —NR 4 C(═O)NR 5 R 6 , —NR 4 C(═S)NR 5 R 6 , R 4 C(═O)NR 5 —, —C(═O)NR 4 R 5 —, R 4 C(═S)NR 4 —, melamine, cyanurato, —NH 2 , —NHR 4 , —NR 4 R 5 , —NR 4 -L 1 -NR 5 R 6 , —NR 4 -L 1 (—NR 5 R 6 ) 2 , —NR 4 -L 1 -NR 5 -L 2 -NR 6 R 7 , —NR 4 -L 1 (—NR 5 R 6 ) 3 , —NR 4 -L 1 -NR 5 -L 2 -NR 6 -L 3 -NR 7 R 8 and —NR 4 -L 1 -N(-L 2 NR 5 R 6 ) 2 ;

or Y is a divalent functional group selected from the group consisting of -(-)C(—O—)CR 4 R 5 , —CR 5 (—O—)CR 4 —, —O(R 10 CR 11 ) f O—, -(-)NC(═O)OR 5 , —OC(═O)NR 4 —, -(-)NC(═O)SR 5 , —SC(═O)NR 4 —, -(-)NC(═S)OR 5 , —OC(═S)NR 4 —, -(-)NC(═S)SR 5 , —SC(═S)NR 4 —, —O—, maleate, substituted maleate, fumarate, substituted fumarate, —S—, —S—S—, —S—S—S—, —S—S—S—S—, —S—S—S—S—S—, —S—S—S—S—S—S—, —S x —, —SC(═S)O—, —SC(═S)S—, —SC(═O)S—, -(-)NC(═O)NR 4 R 5 , —NR 4 C(═O)NR 5 —, -(-)NC(═S)NR 4 R 5 , —NR 4 C(═S)NR 5 —, R 4 C(═O)N(-)-, —C(═O)NR 4 —, R 4 C(═S)N(-)-, divalent melamine, divalent cyanurato, —NH—, —NR 4 —, -(-)N-L 1 -NR 4 R 5 , —NR 4 -L 1 -NR 5 —, (-)NR 4 ) 2 -L 1 -NR 5 R 6 , -(-)N-L 1 -NR 5 -L 2 -NR 6 R 7 , —NR 4 -L 1 -N(-)-L 2 -NR 5 R 6 , —NR 4 -L 1 -NR 5 -L 2 NR 6 —, -(-)N-L 1 -(NR 5 R 6 ) 3 , (—NR 4 ) 2 -L 1 -(NR 5 R 6 ) 2 , -(-)N-L 1 -NR 4 -L 2 -NR 5 -L 3 -NR 6 R 7 , —NR 4 -L 1 -N(-)-L 2 -NR 5 -L 3 -NR 6 R 7 , —NR 4 -L 1 -NR 5 -L 2 -N(-)-L 3 -NR 6 R 7 , —NR 4 -L 1 -NR 5 -L 2 -NR 6 -L 3 -NR 7 —, -(-)N-L 1 -N(-L 2 NR 5 R 6 ) 2 and (—NR 4 L 1 -) 2 N-L 2 NR 5 R 6 ;

or Y is a trivalent functional group selected from the group consisting of -(-)C(—O—)CR 4 —, -(-)NC(═O)O—, -(-)NC(═O)S—, -(-)NC(═S)O—, -(-)NC(═S)S—, -(-)NC(═O)NR 4 —, -(-)NC(═S)NR 4 —, —C(═O)N (-)-, —C(═S)N(-)-, trivalent melamino; trivalent cyanurato, —N(-)-, -(-)N-L 1 -NR 4 —, (—NR 4 ) 3 -L 1 , (—NR 4 ) 2 -L 1 -NR 5 —, -(-)N-L 1 -N(-)-L 2 -NR 3 R 4 , —NR 4 -L 1 -N(-)-L 2 -NR 5 —, -(-)N-L 1 -NR 4 -L 2 -NR 5 —, -(-)N-L 1 -N(-)-L 2 -NR 5 -L 3 -NR 3 R 4 , —-NR 4 -L 1 -N (-)-L 2 -N(-)-L 3 -NR 3 R 4 , -(-)N-L 1 -NR 5 -L 2 -N(-)-L 3 -NR 3 R 4 , —NR 4 -L 1 -N(-)-L 2 -NR 3 -L 3 -NR 4 —, -(-)N-L 1 -N(-L 2 NR 3 R 4 )(-L 2 NR 5 —) and (—NR 4 L 1 —) 3 N;

or Y is a tetravalent functional group selected from the group consisting of -(-)C (—O—)C(-)-, -(-)NC(═O)N(-)-, -(-)NC(═S)N(-)-, tetravalent melamino, -(-)N-L 1 -N(-)-, (—NR 4 ) 4 -L 1 , (—NR 4 ) 2 -L 1 -N(-)-, -(-)N-L 1 -N(-)-L 2 NR 3 —, -(-)N-L 1 NR 4 -L 2 (-)-, -(-)N-L 1 -N(-)-L 2 -N (-)-L 3 -NR 4 R 3 , —NR 4 -L 1 - -N (-)-L 2 -N(-)-L 3 -NR 3 —, -(-)N-L 1 -NR 4 -L 2 -NR 3 -L 3 -N(-)- and -(-)N-L 1 -N (-L 2 NR 3 —) 2 ; and,

or Y is a polyvalent functional group selected from the group consisting of polyvalent hydrocarbon groups, (—NR 3 )(—N—) 2 C 3 N 3 , (—N—) 3 C 3 N 3 , -(-)N-L 1 -N(-)-L 2 -N(-)-, -(-)N-L 1 -N(-)-L 2 -N(-)-L 3 -NR 3 —, -(-)N-L 1 -NR 3 -L 2 -N(-)-L 3 -N(-)-, [-(-)N-L 1 -] 2 N-L 2 NR 3 —, -(-)N-L 1 -N(-)-L 2 -N(-)-L 3 -N(-)- and [-(-)N-L 1 -] 3 , wherein each occurrence of L 1 , L 2 , and L 3 is selected independently from the set of structures given above for G, each occurrence of R 3-8 is independently given by one of the structures listed above for R and x is independently an integer from 1 to 10.

26. The silane of claim 24 , wherein R 10 and R 11 are each independently selected from a group consisting of hydrogen, methyl and ethyl.

27. The silane of claim 25 , wherein R 3 ,R 4 , R 5 , R 6 , R 7 and R 8 are each independently selected from the group consisting of phenyl, methyl, butyl, H and ethyl.

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