IP Library Granted Patent US 8,673,999
Granted Patent B2
US 8,673,999 · App. 13/577,668 · Granted Mar 18, 2014

Water based primer composition for isocyante and silane functional adhesives

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Quick Facts
Patent No.
US 8,673,999
App. No.
13/577,668
Granted
Mar 18, 2014
Kind
B2
Abstract

The present invention is directed to a unique solution for promoting adhesion of substrates to adhesives containing a prepolymer having isocyanate, silane or both functional groups. The solution comprises a composition comprising: a) from about 0.05 to about 10.0 parts by weight of a hydrolysate of one or more of alkoxysilyl amines; b) from about 0.05 to about 1.0 parts by weight of one of more alkoxylated alcohols, alkoxysilyl terminated alkoxylated alcohols, fatly acids or fatty acid esters; and, c) from about 80 to about 99.9 parts by weight of water: wherein the composition contains 100 parts by weight and the composition exhibits a pH of about 9 to about 12.

Claims (58)

1. A composition comprising a stable solution of:

a) from about 0.05 to about 10.0 parts by weight of a hydrolysate of one or more alkoxysilyl amines;

b) from about 0.05 to about 1.0 parts by weight of one or more alkoxylated alcohols, alkoxysilyl terminated alkoxylated alcohols, fatty acids or fatty acid esters; and,

c) from about 90 to about 99.9 parts by weight of water:

wherein the composition contains 100 parts by weight and the composition exhibits a ph of about 9 to about 12.

2. A composition according to claim 1 wherein the one or more alkoxysilyl amines comprise one or more alkoxysilyl alkyl amines, alkoxysilyl polyalkylamines or bis(alkoxysilyl)amines.

3. The composition according to claim 1 wherein part b) comprises one or more alkoxylated alcohols or alkoxysilyl terminated alkoxylated alcohols.

4. The composition according to claim 1 wherein part b) comprises a mixture of two or more alkoxylated alcohols.

5. The composition according to claim 1 wherein the one or more alkoxylated alcohols correspond to the formula;

wherein:

R 7 —(OCH 2 ) 3 O) a ((CH 2 ) 2 O) b —H) c

and the one or more alkoxysilyl terminated alkoxylated alcohols correspond to the formula

wherein:

R 3 is separately in each occurrence a C 1-4 alkyl group;

R 4 is separately in each occurrence a C 1-4 alkyl group;

R 7 is separately in each occurrence a C 1-20 straight or branched chain alkyl or alkenyl group: R 8 is a C 1-20 hydrocarbylene group;

X is a direct bond or a linking group formed by the reaction of alkoxylated alcohols with an alkoxy silane having a group reactive with a hydroxyl compound;

a is separately in each occurrence is an integer of about 1 to about 3;

b is separately in each occurrence an integer of about 2 to about 10;

c is separately in each occurrence an integer of about 1 to about 6;

f is separately in each occurrence 0 or 1;

Y is separately in each occurrence an integer of from 1 to 3; and

Z is separately and integer of from 0 to 2 provided that Z=3−Y.

6. The composition according to claim 1 wherein the alkoxylated alcohols are derived from seed oils.

7. The composition according to claim 1 wherein the hydrolysate of one or more of alkoxysilyl amines is present in an amount of about 0.5 to about 5.0 parts by weight.

8. A composition according to claim 1 wherein the composition comprises less than 1 percent by weight of organic based solvents.

9. A kit comprising a composition according to claim 1 and an adhesive comprising a prepolymer containing isocyanate functional groups, silane groups or a mixture thereof.

10. A kit according to claim 9 wherein the adhesive comprises a prepolymer containing isocyanate functional groups and the prepolymer further contains silane functional groups or the adhesive further contains a silane functional group containing compound.

11. A process comprising:

a) applying a composition according to claim 1 to a surface of a first substrate; and

b) wiping the applied composition off of the surface of the first substrate or allowing a major portion of the water in the composition to evaporate off of the surface of the first substrate.

12. A process according to claim 11 wherein the applied composition is wiped off of the surface of the first substrate.

13. A process according to claim 11 wherein the water in the applied composition is allowed to evaporate off of the surface of the substrate.

14. A process according to claim 13 wherein the water is allowed to evaporate off for at least about 10 seconds.

15. A process according to claim 11 which further comprises contacting the first substrate with an adhesive containing a prepolymer having isocyanate, silane or both functional groups and a second substrate wherein the adhesive is applied to the portion of the surface of the first substrate to which the composition was applied and the adhesive is disposed between the first and the second substrates.

16. A process according to claim 15 wherein the time period between applying the composition to the first surface and contacting the first surface with the adhesive is from about 20 seconds to 8 days.

17. A process according to claim 15 wherein the first substrate is glass or glass having a ceramic or organic frit on the portion of the surface which is bonded to the second substrate.

18. A process according to claim 17 where in the glass substrate is a window and the second substrate is a flange in a vehicle adapted to hold the window in place in the vehicle or the substrate is a window frame in a building.

19. A composition comprising a stable solution of:

a) from about 0.05 to about 10.0 parts by weight of a hydrolysate of one or more alkoxysilyl amines;

b) from about 0.05 to about 1.0 parts by weight of one or more alkoxylated alcohols, alkoxysilyl terminated alkoxylated alcohols, fatty acids or fatty acid esters; and,

c) from about 90 to about 99.9 parts by weight of water:

wherein the composition contains 100 parts by weight and the composition exhibits a ph of about 9 to about 12 and the alkoxysilyl amines correspond to the formula;

the alkoxysilyl polyalkylamines correspond to the formula;

and, the bis(alkoxysilyl)amines correspond to the formula;

wherein:

R 2 is separately in each occurrence a C 1-20 hydrocarbyl group;

R 3 is separately in each occurrence a C 1-4 alkyl group;

R 4 is separately in each occurrence a C 1-4 alkyl group;

W is seperately in each occurrence an integer of from about 1 to about 10;

X is separately in each occurrence an integer of from 1 to 4;

Y is separately in each occurrence an integer of from 1 to 3; and

Z is separately and integer of from 0 to 2 provided that X=3−Y.

20. A composition comprising a stable solution of:

a) from about 0.05 to about 10.0 parts by weight of a hydrolysate of one or more alkoxysilyl amines;

b) one or more alkoxylated alcohols, alkoxysilyl terminated alkoxylated alcohols, fatty acids or fatty acid esters present in an amount of from about 0.08 to about 0.12 parts by weight, and

c) from about 90 to about 99.9 parts by weight of water:

wherein the composition contains 100 parts by weight and the composition exhibits a ph of about 9 to about 12.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2024
From: DOW GLOBAL TECHNOLOGIES LLC
To: THE DOW CHEMICAL COMPANY
Reel/Frame 069923/0030 →
CHANGE OF LEGAL ENTITY Recorded Sep 10, 2024
From: DDP SPECIALTY ELECTRONIC MATERIALS US, INC
To: DDP SPECIALTY ELECTRONIC MATERIALS US, LLC
Reel/Frame 068907/0881 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2024
From: THE DOW CHEMICAL COMPANY
To: DDP SPECIALTY ELECTRONIC MATERIALS US, INC
Reel/Frame 068922/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2013
From: SCHMATLOCH, STEFAN
To: DOW EUROPE GMBH
Reel/Frame 031277/0247 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2013
From: DOW EUROPE GMBH
To: THE DOW CHEMICAL COMPANY
Reel/Frame 031277/0539 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2013
From: THE DOW CHEMICAL COMPANY
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 031277/0678 →