IP Library Granted Patent US 7,405,259
Granted Patent B2
US 7,405,259 · App. 11/297,757 · Granted Jul 29, 2008

Silylated polymer derived from butadiene and solvent-resistant pressure sensitive adhesive composition containing same

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Quick Facts
Patent No.
US 7,405,259
App. No.
11/297,757
Granted
Jul 29, 2008
Kind
B2
Abstract

A silylated polymer contains repeating units derived from butadiene. The polymer when partially silylated is especially useful for pressure sensitive adhesives where it imparts superior solvent resistance performance thereto.

Claims (38)

1. A silylated polymer obtained by the process which comprises:

a) reacting hydroxyl-terminated polybutadiene and, optionally, chain extender and/or other polyol, with polyisocyanate in the presence of a monofunctional fluorine-containing organic compound possessing an isocyanate reactive functionality to provide isocyanate-terminated polyurethane prepolymer; and,

b) reacting the isocyanate-terminated polyurethane prepolymer with silane possessing hydrolyzable functionality and isocyanate-reactive functionality to provide silylated polyurethane prepolymer wherein less than all of the isocyanate groups of the isocyanate-terminated polyurethane prepolymer are silylated.

2. The silylated polymer of claim 1 wherein the silane is a primary or secondary aminosilane of the general formula:

X—R 1 —Si(R 2 ) x (OR 3 ) 3-x

wherein X is —SH or —NHR 4 in which R 4 is H, a monovalent hydrocarbon group of tip to 8 carbon atoms or —R 5 —Si(R 6 ) y (OR 7 ) 3-y , R 1 and R 5 each is the same or different divalent hydrocarbon group of up to 12 carbon atoms, optionally containing one or more heteroatoms, each R 2 and R 6 is the same or different monovalent hydrocarbon group of up to 8 carbon atoms, each R 3 and R 7 is the same or different alkyl group of up to 6 carbon atoms and x and y each, independently, is 0, 1 or 2.

3. The silylated polymer of claim 2 wherein the silane is a secondary amino silane.

4. The silylated polymer of claim 2 wherein the silane is a mercaptosilane.

5. The silylated polymer of claim 2 wherein the silane is selected from the group consisting of 2-mercaptoethyl trimethoxysilane, 3-mercaptopropyl trimethoxysilane, 2-mercaptopropyl triethoxysilane, 3-mercaptopropyl triethoxysilane, 2-mercaptoethyl tripropoxysilane, 2-mercaptoethyl tri sec-butoxysilane, 3-mercaptopropyl tri-t-butoxysilane, 3-mercaptopropyl triisopropoxysilane, 3-mercaptopropyl trioctoxysilane, 2-mercaptoethyl tri-2′-ethylhexoxysilane, 2-mercaptoethyl dimethoxy ethoxysilane, 3-mercaptopropyl methoxyethoxypropoxysilane, 3-mercaptopropyl dimethoxy methylsilane, 3-mercaptopropyl methoxy dimethylsilane, 3-mercaptopropyl ethoxy dimethylsilane, 3-mercaptopropyl diethoxy methylsilane, 3-mercaptopropyl cyclohexoxy dimethyl silane, 4-mercaptobutyl trimethoxysilane, 3-mercapto-3-methylpropyltrimethoxysilane, 3-mercapto-3-methylpropyl-tripropoxysilane, 3-mercapto-3-ethylpropyl-dimethoxy methylsilane, 3-mercapto-2-methylpropyl trimethoxysilane, 3-mercapto-2-methylpropyl dimethoxy phenylsilane, 3-mercaptocyclohexyl-trimethoxysilane, 12-mercaptododecyl trimethoxy silane, 12-mercaptododecyl triethoxy silane, 18-mercaptooctadecyl trimethoxysilane, 18-mercaptooctadecyl methoxydimethylsilane, 2-mercapto-2-methylethyl-tripropoxysilane, 2-mercapto-2-methylethyl-trioctoxysilane, 2-mercaptophenyl trimethoxysilane, 2-mercaptophenyl triethoxysilane, 2-mercaptotolyl trimethoxysilane, 2-mercaptotolyl triethoxysilane, 1-mercaptomethyltolyl trimethoxysilane, 1-mercaptomethyltolyl triethoxysilane, 2-mercaptoethylphenyl trimethoxysilane, 2-mercaptoethylphenyl triethoxysilane, 2-mercaptoethyltolyl trimethoxysilane, 2-mercaptoethyltolyl triethoxysilane, 3-mercaptopropylphenyl trimethoxysilane, 3-mercaptopropylphenyl triethoxysilane, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 4-aminobutyltriethoxysilane, N-methyl-3-amino-2-methylpropyltrimethoxysilane, N-ethyl-3-amino-2-methylpropyltrimethoxysilane, N-ethyl-3-amino-2-methylpropyldiethoxymethylsilane, N-ethyl-3-amino-2-methylpropyltriethoxysilane, N-ethyl-3-amino-2-methylpropylmethyldimethoxysilane, N-butyl-3-amino-2-methylpropyltrimethoxysilane, 3-(N-methyl-2-amino-1-methyl-1-ethoxy)-propyltrimethoxysilane, N-ethyl-4-amino-3,3-dimethylbutyldimethoxymethylsilane, N-ethyl-4-amino-3,3-dimethylbutyltrimethoxysilane, N-(cyclohexyl)-3-aminopropyltrimethoxysilane, N-(2-aminoethyl)-3-aminopropyltrimethoxysilane, N-(2-aminoethyl)-3-aminopropyltriethoxy-silane, N-(2-aminoethyl)-3-aminopropylmethyldimethoxysilane, aminopropyltriethoxysilane, bis-(3-trimethoxysilyl-2-methylpropyl)amine and N-(3′-trimethoxysilylpropyl)-3-amino-2-methylpropyltrimethoxysilane.

6. The silylated polyurethane of claim 2 wherein not more than about 95 percent of the isocyanate groups of the isocyanate-terminated polyurethane prepolymer are silylated.

7. A silylated polymer obtained by the process which comprises:

a) blending at least one hydroxyl-terminated polybutadiene diol possessing terminal hydroxyl groups bonded to carbon atoms adjacent to double bonded carbon atoms and a number average molecular weight of from 500 to 10,000 grams per mole, at least one hydroxyl-containing polybutadiene polyol possessing an average of from 2.4 to about 2.8 hydroxyl groups per molecule, and optionally, chain extender and/or other polyol,

b) reacting the mixture of step (a) with diisocyanate to provide hydroxyl-terminated polyurethane prepolymer possessing a molar ratio of NCO to OH of from about 0.3 to about 0.95; and,

c) reacting the hydroxyl-terminated polyurethane prepolymer of step (b) with isocyanatosilane possessing hydrolyzable functionality to provide silylated polyurethane possessing a level of silation of not more than 95 percent.

8. The silylated polyurethane of claim 7 wherein in step (c) not more than about 90 percent of the hydroxyl groups of the hydroxyl-terminated polyurethane prepolymer are silylated.

9. The silylated polyurethane of claim 7 wherein the hydroxyl terminated polyurethane in step (b) possesses a molar ratio of NCO to OH of from 0.5 to 0.9 and, step (c) is carried out in the additional presence of monofunctional hydroxyl-capping reactant to cap non-silylated hydroxyl groups in the silylated polyurethane.

10. The silylated polyurethane of claim 9 wherein in step (c) not more than about 90 percent of the hydroxyl groups of the hydroxyl-terminated polyurethane prepolymer are silylated.

11. A curable pressure sensitive adhesive composition comprising a pressure sensitive adhesive amount of at least one partially silylated polyurethane of claim 1 .

12. A curable pressure sensitive adhesive composition comprising a pressure sensitive adhesive amount of at least one partially silylated polyurethane of claim 7 .

13. The curable pressure sensitive adhesive composition of claim 11 comprising at least one additional component selected from the group consisting of filler, tackifier, silane adhesion promoter, plasticizer, solvent, thixotropic agent, U.V. stabilizer, antioxidant and curing catalyst.

14. A curable pressure sensitive adhesive composition comprising a pressure sensitive adhesive amount of at least one partially silylated polyurethane obtained by the process which comprises:

a) reacting hydroxyl-terminated polybutadiene and, optionally, chain extender and/or other polyol, with polyisocyanate to provide isocyanate-terminated polyurethane prepolymer; and,

b) reacting the isocyanate-terminated polyurethane prepolymer with silane possessing hydrolyzable functionality and isocyanate-reactive functionality to provide silylated polyurethane prepolymer wherein less than all of the isocyanate groups of the isocyanate-terminated polyurethane prepolymer are silylated; and,

c) carrying out step (b) in the additional presence of monofunctional isocyanate-capping reactant to cap non-silylated isocyanate groups in the silylated polyurethane, wherein the curable pressure sensitive adhesive composition further comprises a tackifying amount of MQ tackifier resin and a curing catalyst therefor.

15. The cured pressure sensitive adhesive composition of claim 11 .

16. The cured pressure sensitive adhesive composition of claim 14 .

17. The curable pressure sensitive adhesive composition of claim 12 comprising at least one additional component selected from the group consisting of filler, tackifier, silane adhesion promoter, plasticizer, solvent, thixotropic agent, U.V. stabilizer, antioxidant and curing catalyst.

18. A curable pressure sensitive adhesive composition comprising a pressure sensitive adhesive amount of at least one partially silylated polyurethane obtained by the process which comprises:

a) blending at least one hydroxyl-terminated polybutadiene diol possessing terminal hydroxyl groups bonded to carbon atoms adjacent to double bonded carbon atoms and a number average molecular weight of from 500 to 10,000 grams per mole, at least one hydroxyl-containing polybutadiene polyol possessing an average of from 2.4 to about 2.8 hydroxyl groups per molecule, and optionally, chain extender and/or other polyol,

b) reacting the mixture of step (a) with diisocyanate to provide hydroxyl-terminated polyurethane prepolymer possessing a molar ratio of NCO to OH of from about 0.3 to about 0.95; and,

c) reacting the hydroxyl-terminated polyurethane prepolymer of step (b) with isocyanatosilane possessing hydrolyzable functionality to provide silylated polyurethane possessing a level of silation of not more than 95 percent,

and wherein said curable pressure sensitive adhesive composition further comprises a tackifying amount of MQ tackifier resin and a curing catalyst therefor.

19. The cured pressure sensitive adhesive composition of claim 12 .

20. The cured pressure sensitive adhesive composition of claim 18 .

21. The cured pressure sensitive adhesive composition of claim 13 .

22. The cured pressure sensitive adhesive composition of claim 17 .

23. The silylated polymer of claim 1 wherein the monofunctional fluorine-containing organic compound possessing an isocyanate reactive functionality is a fluorinated alcohol.

24. The silylated polymer of claim 23 wherein the fluorinated alcohol has the formula HOCH 2 CH 2 (CF 2 ) ˜10 CF 3 .

Assignments (23)
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (063213/0472) Recorded Oct 22, 2025
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To: MOMENTIVE PERFORMANCE MATERIALS INC.
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FIRST LIEN TERM LOAN PATENT SECURITY AGREEMENT Recorded Mar 31, 2023
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 063213/0472 →
RELEASE OF SECURITY INTEREST Recorded Mar 30, 2023
From: KOOKMIN BANK NEW YORK
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 063197/0373 →
SECURITY INTEREST Recorded Mar 30, 2023
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: KOOKMIN BANK NEW YORK BRANCH
Reel/Frame 063197/0475 →
RELEASE OF SECURITY INTEREST Recorded Dec 24, 2020
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS COLLATERAL AGENT
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 054883/0855 →
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Reel/Frame 054387/0001 →
SECOND LIEN TERM LOAN PATENT AGREEMENT Recorded Jun 5, 2019
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: KOOKMIN BANK, NEW YORK BRANCH, AS ADMINISTRATIVE AGENT
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FIRST LIEN TERM LOAN PATENT AGREEMENT Recorded Jun 5, 2019
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: BNP PARIBAS, AS ADMINISTRATIVE AGENT
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TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded May 21, 2019
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To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 050304/0555 →
RELEASE OF SECURITY INTEREST Recorded May 15, 2019
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To: MOMENTIVE PERFORMANCE MATERIALS INC.
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RELEASE OF SECURITY INTEREST Recorded May 15, 2019
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To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 049249/0271 →
NOTICE OF CHANGE OF COLLATERAL AGENT - ASSIGNMENT OF SECURITY INTEREST IN INTELLECTUAL PROPERTY - SECOND LIEN Recorded Mar 6, 2015
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NOTICE OF CHANGE OF COLLATERAL AGENT - ASSIGNMENT OF SECURITY INTEREST IN INTELLECTUAL PROPERTY Recorded Mar 6, 2015
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TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Oct 30, 2014
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TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Oct 30, 2014
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To: MOMENTIVE PERFORMANCE MATERIALS INC.
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SECURITY INTEREST Recorded Oct 27, 2014
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SECURITY INTEREST Recorded Oct 27, 2014
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SECURITY AGREEMENT Recorded Apr 29, 2013
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PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
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SECURITY AGREEMENT Recorded May 31, 2012
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