IP Library Granted Patent US 8,686,094
Granted Patent B2
US 8,686,094 · App. 13/111,236 · Granted Apr 1, 2014

Storage-stable two-component silicone adhesives and sealants with extended mixer open time

Inventors: Alexander Djurdjevic (Zürich, CH); Christin Hamann (Widen, CH); Michael Böttiger (Rudolfstetten, CH)
Assignee: Sika Technology AG
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Quick Facts
Patent No.
US 8,686,094
App. No.
13/111,236
Granted
Apr 1, 2014
Kind
B2
Abstract

A two-component silicone composition that includes a component A that includes i) at least one hydroxyl-group-terminated polydiorganosiloxane P; ii) at least one catalyst K for the cross-linking of polydiorganosiloxanes; and a component B that includes i′) at least one cross-linking agent for polydiorganosiloxanes. Compositions can be used as adhesives, sealants, coatings or as casting compounds and can be distinguished by a very long shelf life.

Claims (32)

1. A two-component silicone composition, comprising:

a component A that comprises

i) at least one hydroxyl-group-terminated polydiorganosiloxane P;

ii) at least one catalyst K for the cross-linking of polydiorganosiloxanes; and

a component B that comprises

i′) at least one cross-linking agent for polydiorganosiloxanes,

wherein the weight ratio of component A to component B is 3:1 to 15:1.

2. The two-component silicone composition according to claim 1 , wherein the hydroxyl-group-terminated polydiorganosiloxane P is a polydiorganosiloxane P′ of Formula (I):

wherein, in the Formula (I),

each of radicals R 1 and R 2 , independently of one another, represents a linear or branched, monovalent hydrocarbon radical comprising 1 to 12 C atoms, which optionally comprises one or more heteroatoms and optionally one or more C—C multiple bonds and/or optionally cycloaliphatic and/or aromatic portions; and

n is selected in such a way that a weight mean of the molecular weight M w of the polydiorganosiloxane P′ relative to polystyrene is 500 to 250,000 g/mol.

3. The two-component silicone composition according to claim 2 , wherein the hydroxyl-group-terminated polydiorganosiloxane P′ is a polydiorganosiloxane P1 of Formula (I), wherein n is selected in such a way that the weight mean of the molecular weight M w of the polydiorganosiloxane P1 relative to polystyrene is 30,000 to 80,000 g/mol; or in such a way that a mixture of

i″) at least one hydroxyl-group-terminated polydiorganosiloxane P2 of Formula (I), wherein n is selected in such a way that the weight mean of the molecular weight M w of the polydiorganosiloxane P2 relative to polystyrene is >80,000 to 250,000 g/mol; and

ii″) at least one hydroxyl-group-terminated polydiorganosiloxane P3 of Formula (I), wherein n is selected in such a way that the weight mean of the molecular weight M w of the polydiorganosiloxane P3 relative to polystyrene is 500 to ≦80,000 g/mol, is used as polydiorganosiloxane P′.

4. The two-component silicone composition according to claim 3 , wherein the radicals R 1 and R 2 represent alkyl radicals with 1 to 5 C atoms.

5. The two-component silicone composition according to claim 1 , wherein the cross-linking agent for polydiorganosiloxanes is a silane of Formula (II):

wherein the radical R 3 , independently of one another, represents a linear or branched, monovalent hydrocarbon radical with 1 to 12 C atoms, which optionally has one or more heteroatoms and optionally one or more C—C multiple bonds and/or optionally cycloaliphatic and/or aromatic portions;

the radical R 4 , independently of one another, represents a hydrogen atom, or an alkyl radical with 1 to 12 C atoms, or an oxime radical with 1 to 12 C atoms, or an acyl radical with 1 to 12 C atoms; and

p represents a value of 0 to 4, provided that if p represents a value of 3 or 4, at least p−2 radicals R 3 in each case have at least one group that can be condensed and is reactive with the hydroxyl groups of the polydiorganosiloxane P.

6. The two-component silicone composition according to claim 5 , wherein p represents a value of 0.

7. The two-component silicone composition according to claim 6 , wherein the radical R 4 represents an alkyl radical with 1 to 5 C atoms.

8. The two-component silicone composition according to claim 1 , wherein the component B does not contain any polymerizable polydiorganosiloxanes.

9. The two-component silicone composition according to claim 1 , wherein the catalyst K is an organotin compound or a titanate.

10. The two-component silicone composition according to claim 1 , further comprising at least one adhesion promoter.

11. A method of forming a cured silicone composition from the two-component silicone composition according to claim 1 , comprising mixing component A with component B.

12. A method for extending the mixer open time with a uniform pot life or a simultaneous shortening of the pot life of a two-component silicone composition, comprising providing the two-component silicone composition of claim 1 , and mixing component A with component B.

13. The two-component silicone composition according to claim 4 , wherein the radicals R 1 and R 2 represent alkyl radicals with 1 to 3 C atoms.

14. The two-component silicone composition according to claim 4 , wherein the radicals R 1 and R 2 represent methyl groups.

15. The two-component silicone composition according to claim 7 , wherein the radical R 4 represents an alkyl radical with 1 to 3 C atoms.

16. The two-component silicone composition according to claim 7 , wherein the radical R 4 represents a methyl group or an ethyl group.

17. The two-component silicone composition according to claim 1 , wherein the weight ratio of component A to component B is 10:1 to 13:1.

18. The two-component silicone composition according to claim 10 , wherein the at least one adhesion promoter comprises an organoalkoxysilane that has amino groups.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2011
From: DJURDJEVIC, ALEXANDER; HAMANN, CHRISTIN; BOTTIGER, MICHAEL
To: SIKA TECHNOLOGY AG
Reel/Frame 027025/0956 →
Priority Claims (1)
EP 08169676 · Nov 21, 2008 · regional
Continuity (2)
Continuation PCTEP2009065517 · Nov 20, 2009
Related Publication 20120022209A1 · Jan 26, 2012