IP Library Granted Patent US 7,094,859
Granted Patent B2
US 7,094,859 · App. 10/501,214 · Granted Aug 22, 2006

Cross-linkable polymer blends containing alkoxysilane-terminated polymers

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Quick Facts
Patent No.
US 7,094,859
App. No.
10/501,214
Granted
Aug 22, 2006
Kind
B2
Abstract

Alkoxysilane-terminated polymers prepared by reacting an isocyanatoalkoxysilane, preferably an isocyanatodialkyalkoxysilane, with an isocyanate-reactive prepolymer, can provide chain extension even when a monoalkoxy-functional silane, while retaining suitable reactivity profiles. The products are useful in sealants, caulks, coatings, and moldings.

Claims (33)

1. A crosslinkable polymer blend, comprising at least one polymer A having endgroups of the formula (1)

-L-CH 2 —SiR 1 a (OR 2 ) 3-a   (1)

wherein

L is a divalent linking group selected from —O—CO—NH—, —N(R 3 )—CO—NH—, —S—CO—NH—,

R 1 is an optionally halogen-substituted alkyl, cycloalkyl, alkenyl or aryl radical having 1–10 carbon atoms,

R 2 is an alkyl radical having 1–6 carbon atoms or an ω-oxyalkylalkyl radical having a total of 2–10 carbon atoms,

R 3 is hydrogen, an optionally halogen-substituted cyclic, linear or branched C 1 to C 18 alkyl or alkenyl radical or a C 6 to C 18 aryl radical, and

a is an integer from 0 to 2,

with the proviso that the fraction of the endgroups of the general formula (1) where a=2, relative to all the endgroups of the polymers present in the mixture which have alkoxysilane endgroups, is from 5% to 100%.

2. The polymer blend of claim 1 , wherein the fraction of the endgroups of the general formula (1) where a=2, relative to all the endgroups of the polymers present in the polymer mixture which have alkoxysilane endgroups, is at least 50%.

3. The polymer blend of claim 1 , wherein the radicals R 1 are independently methyl, ethyl or phenyl radicals.

4. The polymer blend of claim 2 , wherein the radicals R 1 are independently methyl, ethyl or phenyl radicals.

5. The polymer blend of claim 1 , wherein the radicals R 2 are independently methyl or ethyl radicals.

6. The polymer blend of claim 2 , wherein the radicals R 2 are independently methyl or ethyl radicals.

7. The polymer blend of claim 3 , wherein the radicals R 2 are independently methyl or ethyl radicals.

8. The polymer blend of claim 1 , further comprising at least one organic amino compound as a basic catalyst (B).

9. The polymer blend of claim 3 , further comprising at least one organic amino compound as a basic catalyst (B).

10. The polymer blend of claim 5 , further comprising at least one organic amino compound as a basic catalyst (B).

11. In an adhesive, sealant, coating, or moldable elastomer which is moisture curable and which contains a blend of one or more alkoxysilane-functional polymers, the improvement comprising selecting as said blend, a crosslinkable polymer blend of claim 1 .

12. In an adhesive, sealant, coating, or moldable elastomer which is moisture curable and which contains a blend of one or more alkoxysilane-functional polymers, the improvement comprising selecting as said blend, a crosslinkable polymer blend of claim 2 .

13. In an adhesive, sealant, coating, or moldable elastomer which is moisture curable and which contains a blend of one or more alkoxysilane-functional polymers, the improvement comprising selecting as said blend, a crosslinkable polymer blend of claim 3 .

14. In an adhesive, sealant, coating, or moldable elastomer which is moisture curable and which contains a blend of one or more alkoxysilane-functional polymers, the improvement comprising selecting as said blend, a crosslinkable polymer blend of claim 5 .

15. In an adhesive, sealant, coating, or moldable elastomer which is moisture curable and which contains a blend of one or more alkoxysilane-functional polymers, the improvement comprising selecting as said blend, a crosslinkable polymer blend of claim 8 .

16. A process for the preparation of an alkoxysilane-functional polymer suitable for use in the crosslinkable polymer blend of claim 1 , said process comprising reacting at least one isocyanatosilane of the formula (2)

OCN—CH 2 —SiR 1 a (OR 2 ) 3-a   (2)

with one or more prepolymers having at least one terminal isocyanate-reactive end group selected from the group consisting of OH, HNR 3, and HS,

wherein

R 1 is an alkyl radical having 1 to 6 carbon atoms or an ω-oxyalkyl radical having a total of 2 to 10 carbon atoms; and

a is an integer from 0 to 2,

with the proviso that the fraction of the isocyanatosilanes of the formula (2) where a=2 relative to all isocyanatosilanes which bear SiR 1 a (OR 2 ) 3-a groups is from 5% to 100%.

17. The process of claim 16 wherein said prepolymer is a linear polymer selected from the group consisting of polysiloxanes, polysiloxane-urea/urethane copolymers, polyurethanes, polyureas, polyethers, polyesters, poly(meth)acrylates, polycarbonates, polystyrenes, polyamindes, polyvinyl esters, styrene/butadiene copolymers, and polyolefins.

18. The process of claim 17 wherein said prepolymer is α, ω-bis-terminated with a single type of isocyanate reactive end group.

19. A crosslinkable blend comprising at least one alkoxysilane-functional polymer prepared by the process of claim 16 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2007
From: CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIES GMBH
To: WACKER CHEMIE AG
Reel/Frame 019725/0609 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2004
From: SCHINDLER, WOLFRAM; SCHEIM, UWE; PACHALY, BERND
To: CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH
Reel/Frame 016266/0455 →