IP Library › Granted Patent US 10,920,021
Granted Patent B2
US 10,920,021 · App. 16/148,766 · Granted Feb 16, 2021

Silicone compositions

Inventors: Jianfeng Zhang (Shrewsbury, MA); Michael J. Tzivanis (Chicopee, MA); Xipeng Liu (Concord, MA); Jian L. Ding (Glastonbury, CT)
Assignee: Saint-Gobain Performance Plastics Corporation
C08G77/08C08L83/06C09J183/06C08G77/12C08G77/14
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Quick Facts
Patent No.
US 10,920,021
App. No.
16/148,766
Granted
Feb 16, 2021
Kind
B2
Abstract

This disclosure relates to polymerizable silicone compositions, methods for polymerizing such compositions, and to polymerized silicone compositions formed thereby. In one embodiment, a polymerizable composition includes one or more first organosiloxanes or organosilanes, each comprising a plurality of silicon hydride functional groups, one or more second organosiloxanes or organosilanes, each comprising a plurality of reactive heterocycloalkyl functional groups; and one or more third organosiloxanes or organosilanes, each comprising at least about one silicon hydride functional group and at least about one reactive heterocycloalkyl functional group; and an effective amount of a borane catalyst, present, for example, in an amount within the range of 0.0005 wt % to about 10 wt %, wherein the ratio of reactive heterocycloalkyl functional groups to reactive silicon hydride functional groups in the composition is in the range of 1:5 to 5:1. The compositions and methods are useful, for example, in adhesive and sealing applications.

Claims (140)

1. A polymerizable composition comprising

one or more organosiloxanes, the one or more organosiloxanes comprising

one or more first organosiloxanes, each comprising a plurality of silicon hydride functional groups but lacking reactive heterocycloalkyl functional groups, present in an amount within the range of about 0.05 wt % to about 99.95 wt %; and

one or more second organosiloxanes, each comprising a plurality of reactive heterocycloalkyl functional groups but lacking reactive silicon hydride functional groups, present in an amount within the range of about 0.05 wt % to about 99.95 wt %; and

an effective amount of a borane catalyst, present in an amount within the range of 0.0005 wt % to about 10 wt %,

wherein the ratio of reactive heterocycloalkyl functional groups to reactive silicon hydride functional groups in the composition is in the range of 1:5 to 5:1.

2. A polymerizable composition according to claim 1 , wherein each heterocycloalkyl functional group is an epoxide.

3. A polymerizable composition according to claim 1 , wherein the one or more first organosiloxanes are present in a total amount of about 25 wt % to about 90 wt %.

4. A polymerizable composition according to claim 1 , wherein at least one of the first organosiloxanes is a compound of Formula I-A:

wherein:

each of R 1 , R 2 , and R 3 is independently hydrogen, C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

each of R 4 , R 5 , and R 6 is independently C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

each of R 7 , R 9 , R 10 , and R 12 is independently hydrogen or C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

R 8 is hydrogen, O, or C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

R 11 is a covalent bond to R 8 if R 8 is O and is otherwise hydrogen or C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon; and

each of X, Y, and Z is independently 0-20,000, provided that at least one of X, Y and Z is not zero, and that the molecule bears at least two reactive silicon hydride groups.

5. A polymerizable composition according to claim 1 , wherein the one or more first organosiloxanes comprise one or more of hydride-terminated PDMS; methylhydrosiloxane-dimethylsiloxane copolymer; polymethylhydrosiloxanes; and methylhydrogen silicone fluid (side chain type); 2,4,6,8-tetramethylcyclotetrasiloxane; and methylhydrosiloxane-phenylmethylsiloxane copolymer.

6. A polymerizable composition according to claim 1 , wherein the one or more second organosiloxanes are present in a total amount of about 25 wt % to about 90 wt %.

7. A polymerizable composition according to claim 1 , wherein at least one of the second organosiloxanes is a compound of Formula II-A:

wherein:

each of R 21 , R 22 , R 23 , R 27 , and R 30 is independently C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon, R A or R B ;

R A is

in which

each of Q 1 and T 1 is independently O, or S;

R C is C 1 -C 20 hydrocarbonylene;

each of R D and R E is independently C 1 -C 6 hydrocarbonylene or a covalent bond;

r is 0 or 1; and

R F is C 1 -C 6 hydrocarbonylene;

R B is

in which

each of Q 2 and T 2 is independently O, or S;

R G is C 1 -C 20 hydrocarbonylene;

each of R H and R J is independently C 1 -C 5 hydrocarbonylene;

r is 0 or 1;

R K is C 1 -C 6 hydrocarbonylene if r is 1; and

R K is C 1 -C 6 hydrocarbonylene or a covalent bond if r is 0;

each of R 24 , R 25 , and R 26 is independently C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

each of R 29 and R 32 is independently hydrogen or C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

R 28 is O, or C 1 -C 60 hydrocarbon;

R 31 is a covalent bond to R 28 if R 28 is O, or is otherwise C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

each of A, B, and C is independently 0-20,000, provided that at least one of A, B and C is not zero, and that the molecule bears at least two reactive heterocycloalkyl groups.

8. A polymerizable composition according to claim 1 , wherein the one or more second organosiloxanes comprise one or more of epoxide-terminated polysiloxanes; epoxycyclohexylethylmethylsiloxane-dimethylsiloxane copolymer; 2,4,6,8-tetramethyl-2,4,6,8-tetrakis(propyl glycidyl ether)cyclotetrasiloxane; and epoxy-modified side-chain type silicone fluids (e.g., epoxypropoxypropyl)methylsiloxane-siloxane copolymer).

9. A polymerizable composition according to claim 1 , wherein the ratio of silicon hydride functional groups to reactive heterocycloalkyl functional groups in the composition is within the range of 1:1.5 to 1.5:1.

10. A polymerizable composition according to claim 1 , wherein the ratio of hydrosilylatable ethylenic unsaturations to silicon hydride functional groups is less than 0.05.

11. A polymerizable composition according to claim 1 , wherein the borane catalyst comprises a compound of the formula B(R C ) q (R D ) f

wherein:

each R C is independently C 6 -C 14 aryl, optionally substituted with one or more groups that are independently C 1 -C 3 fluoroalkyl, halogen, nitro, or CN;

each R D is independently halogen;

q is 1-3;

r is 0-2; and

the sum of q and r is 3.

12. A polymerizable composition according to claim 1 , wherein the borane catalyst is present in an amount in the range of about 0.1 wt % to about 5 wt %.

13. A polymerizable composition according to claim 1 , wherein the total amount of first and second organosiloxanes, any third organosiloxanes if present, adhesion promoters, fillers, and borane catalyst is at least about 70 wt % of the composition.

14. A solvent-borne coating composition, comprising a polymerizable composition according to claim 1 , dispersed in a solvent.

15. A method for preparing a cross-linked silicone material, the method comprising

providing a polymerizable composition comprising

one or more organosiloxanes or organosilanes, the one or more organosiloxanes or organosilanes comprising one or more of

one or more first organosiloxanes or organosilanes, each comprising a plurality of silicon hydride functional groups but lacking reactive heterocycloalkyl functional groups, present in an amount within the range of about 0.05 wt % to about 99.95 wt %;

one or more second organosiloxanes or organosilane, each comprising a plurality of reactive heterocycloalkyl functional groups but lacking reactive silicon hydride functional groups, present in an amount within the range of about 0.05 wt % to about 99.95 wt %; and

one or more third organosiloxanes or organosilanes, each comprising at least about one silicon hydride functional group and at least about one reactive heterocycloalkyl functional group, present in an amount within the range of about 0.05 wt % to about 99.9999 wt %,

wherein if the one or more third organosiloxanes or organosilanes is absent, then both one or more first organosiloxanes or organosilanes and one or more second organosiloxanes or organosilanes are present in the polymerizable composition, and

an effective amount of a borane catalyst, present in an amount within the range of 0.0005 wt % to about 10 wt %,

wherein the ratio of reactive heterocycloalkyl functional groups to reactive silicon hydride functional groups in the composition is in the range of 1:5 to 5:1, and

polymerizing the polymerizable composition under conditions sufficient to cause silicon hydrides to hydrosilylate reactive heterocycloalkyl groups with ring opening to form silyl ethers, thereby providing crosslinks to the crosslinked silicone material.

16. A polymerized composition that is the polymerization product of a polymerizable composition comprising

one or more organosiloxanes or organosilanes, the one or more organosiloxanes or organosilanes comprising one or more of

one or more first organosiloxanes or organosilanes, each comprising a plurality of silicon hydride functional groups but lacking reactive heterocycloalkyl functional groups, present in an amount within the range of about 0.05 wt % to about 99.95 wt %;

one or more second organosiloxanes or organosilane, each comprising a plurality of reactive heterocycloalkyl functional groups but lacking reactive silicon hydride functional groups, present in an amount within the range of about 0.05 wt % to about 99.95 wt %; and

one or more third organosiloxanes or organosilanes, each comprising at least about one silicon hydride functional group and at least about one reactive heterocycloalkyl functional group, present in an amount within the range of about 0.05 wt % to about 99.9999 wt %,

wherein if the one or more third organosiloxanes or organosilanes is absent, then both one or more first organosiloxanes or organosilanes and one or more second organosiloxanes or organosilanes are present in the polymerizable composition, and

an effective amount of a borane catalyst, present in an amount within the range of 0.0005 wt % to about 10 wt %,

wherein the ratio of reactive heterocycloalkyl functional groups to reactive silicon hydride functional groups in the composition is in the range of 1:5 to 5:1, and

wherein the polymerization causes silicon hydrides to hydrosilylate reactive heterocycloalkyl groups with ring opening to form silyl ethers, thereby providing crosslinks to the crosslinked silicone material.

17. A polymerized composition according to claim 16 , wherein the one or more first organosiloxanes or organosilanes is present in the polymerizable composition in an amount within the range of about 0.05 wt % to about 90 wt %, the one or more second organosiloxanes or organosilanes is present in the polymerizable composition in an amount within the range of about 0.05 wt % to about 90 wt %, and the polymerizable composition further comprises one or more tackifiers, present in an amount within the range of about 10 wt % to about 99.95 wt %.

18. An article comprising:

a substrate; and

a pressure-sensitive adhesive disposed on the substrate, wherein the pressure-sensitive adhesive is a polymerized product of a composition according to claim 16 .

19. A polymerized composition according to claim 16 , having a release force of no more than 200 gf/inch as measured by the PSTC 4 test procedure.

20. A polymerizable composition according to claim 1 , having less than 1 wt % of one or more third organosiloxanes, each comprising at least about one silicon hydride functional group and at least about one reactive heterocycloalkyl functional group.

21. A polymerizable composition according to claim 1 , having in the range of about 0.05 wt % to about 90 wt % of one or more third organosiloxanes, each comprising at least about one silicon hydride functional group and at least about one reactive heterocycloalkyl functional group.

22. A polymerized composition according to claim 16 , wherein the one or more third organosiloxanes or organosilanes are present in the polymerizable composition in a total amount of about 25 wt % to about 99.5 wt %.

23. A polymerized composition according to claim 16 , wherein at least one of the third organosiloxanes or organosilanes is a compound of Formula III-A:

wherein:

each of R 41 , R 42 , R 43 , R 47 , and R 50 is independently C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon, hydrogen, R A or R B ;

R A is

in which

each of Q 1 and T 1 is independently O, or S;

R C is C 1 -C 20 hydrocarbonylene;

each of R D and R E is independently C 1 -C 6 hydrocarbonylene or a covalent bond;

r is 0 or 1; and

R F is C 1 -C 6 hydrocarbonylene;

R B is

in which

each of Q 2 and T 2 is independently O, or S;

R G is C 1 -C 20 hydrocarbonylene;

each of R H and R J is independently C 1 -C 5 hydrocarbonylene;

r is 0 or 1;

R K is C 1 -C 6 hydrocarbonylene if r is 1; and

R K is C 1 -C 6 hydrocarbonylene or a covalent bond if r is 0;

each of R 44 , R 45 , and R 46 is independently C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

each of R 49 and R 52 is independently C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

R 48 is O, or C 1 -C 60 hydrocarbon;

R 51 is a covalent bond to R 48 if R 48 is O, or is otherwise C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

each of D, E, and F is independently 0-20,000, provided that at least one of D, E and F is not zero, provided that the molecule bears at least one reactive silicon hydride and at least one reactive heterocycloalkyl group.

24. A polymerized composition according to claim 16 , wherein each heterocycloalkyl functional group is an epoxide.

25. A polymerized composition according to claim 16 , wherein at least one of the first organosiloxanes or organosilanes is a compound of Formula I-A:

wherein:

each of R 1 , R 2 , and R 3 is independently hydrogen, C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

each of R 4 , R 5 , and R 6 is independently C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

each of R 7 , R 9 , R 10 , and R 12 is independently hydrogen or C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

R 8 is hydrogen, O, or C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

R 11 is a covalent bond to R 8 if R 8 is O and is otherwise hydrogen or C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon; and

each of X, Y, and Z is independently 0-20,000, provided that at least one of X, Y and Z is not zero, and that the molecule bears at least two reactive silicon hydride groups.

26. A polymerized composition according to claim 16 , wherein the one or more first organosiloxanes or organosilanes-comprise one or more of hydride-terminated PDMS; methylhydrosiloxane-dimethylsiloxane copolymer; polymethylhydrosiloxanes; and methylhydrogen silicone fluid (side chain type); 2,4,6,8-tetramethylcyclotetrasiloxane; and methylhydrosiloxane-phenylmethylsiloxane copolymer.

27. A polymerized composition according to claim 16 , wherein at least one of the second organosiloxanes or organosilanes is a compound of Formula II-A:

wherein:

each of R 21 , R 22 , R 23 , R 27 , and R 30 is independently C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon, R A or R B ;

R A is

in which

each of Q 1 and T 1 is independently O, or S;

R C is C 1 -C 20 hydrocarbonylene;

each of R D and R E is independently C 1 -C 6 hydrocarbonylene or a covalent bond;

r is 0 or 1; and

R F is C 1 -C 6 hydrocarbonylene;

R B is

in which

each of Q 2 and T 2 is independently O, or S;

R G is C 1 -C 20 hydrocarbonylene;

each of R H and R J is independently C 1 -C 5 hydrocarbonylene;

r is 0 or 1;

R K is C 1 -C 6 hydrocarbonylene if r is 1; and

R K is C 1 -C 6 hydrocarbonylene or a covalent bond if r is 0;

each of R 24 , R 25 , and R 26 is independently C 1 -C 60 (e.g., C 1 -C 8 or C 1 -C 3 ) hydrocarbon;

each of R 29 and R 32 is independently hydrogen or C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

R 28 is O, or C 1 -C 60 hydrocarbon;

R 31 is a covalent bond to R 28 if R 28 is O, or is otherwise C 1 -C 60 (e.g., C 1 -C 6 or C 1 -C 3 ) hydrocarbon;

each of A, B, and C is independently 0-20,000, provided that at least one of A, B and C is not zero, and that the molecule bears at least two reactive heterocycloalkyl groups.

28. A polymerized composition according to claim 16 , wherein the one or more second organosiloxanes or organosilanes comprise one or more of epoxide-terminated polysiloxanes; epoxycyclohexylethylmethylsiloxane-dimethylsiloxane copolymer; 2,4,6,8-tetramethyl-2,4,6,8-tetrakis(propyl glycidyl ether)cyclotetrasiloxane; and epoxy-modified side-chain type silicone fluids (e.g., epoxypropoxypropyl)methylsiloxanesiloxane copolymer).

29. A polymerized composition according to claim 16 , wherein the ratio of silicon hydride functional groups to reactive heterocycloalkyl functional groups in the polymerizable composition is within the range of 1:1.5 to 1.5:1.

30. A polymerized composition according to claim 16 , wherein the ratio of hydrosilylatable ethylenic unsaturations to silicon hydride functional groups in the polymerizable composition is less than 0.05.

Assignments (1)
NUNC PRO TUNC ASSIGNMENT Recorded May 14, 2020
From: ZHANG, JIANFENG; TZIVANIS, MICHAEL J.; LIU, XIPENG; DING, JIAN L.
To: SAINT-GOBAIN PERFORMANCE PLASTICS CORPORATION
Reel/Frame 052657/0565 →
Continuity (5)
Provisional Application 62565870 · Sep 29, 2017
Provisional Application 62612336 · Dec 30, 2017
Provisional Application 62612337 · Dec 30, 2017
Provisional Application 62612338 · Dec 30, 2017
Related Publication 20190031932A1 · Jan 31, 2019