Stable thermal radical curable silicone adhesive compositions

Patent metadata

Field	Value
Publication number	US-9670392-B2
Application number	US-201414766770-A
Country	US
Kind code	B2
Filing date	Feb 10, 2014
Priority date	Feb 11, 2013
Publication date	Jun 6, 2017
Grant date	Jun 6, 2017

Abstract

A stable thermal radical curable silicone composition is provided that comprises (I) a clustered functional polyorganopolysiloxane having one or more radical curable groups selected from an acrylate group and a methacrylate group; (II) a reactive resin and polymer; (III) a radical initiator; (IV) a moisture cure initiator; and (V) a crosslinker. The reactive resin and polymer includes (a) an organopolysiloxane polymer and (b) an alkoxy-functional organopolysiloxane resin. The alkoxy-functional organopolysiloxane resin comprises the reaction product of a reaction of (i) an alkenyl-functional siloxane resin, (ii) an alkoxysilane-functional organosiloxane, and (iii) an endcapper in the presence of (iv) hydrosilylation catalyst. The stable thermal radical curable silicone composition can be utilized for electronics applications.

First claim

The invention claimed is:

1. A stable thermal radical curable silicone adhesive composition comprising:
(I) a clustered functional polyorganosiloxane having at least one radical curable group selected from an acrylate group and a methacrylate group;
(II) a reactive resin and polymer comprising:
(a) an organopolysiloxane polymer of the formula (R 7 O) 3-z R 6 z Si-Q-(R 25 2 SiO 2/2 ) y -Q-SiR 6 z (OR 7 ) 3-z ,
wherein each R 25 is independently a monovalent hydrocarbon radical having 1 to 6 carbon atoms, each R 6 independently is a monovalent hydrocarbon radical having 1 to 6 carbon atoms, each R 7 independently is selected from the group consisting of an alkyl radical and alkoxyalkyl radical, Q is a divalent linking radical, the subscript z has a value of 0, 1 or 2, and the subscript y has a value of 60 to 1000; and

(b) an alkoxy-functional organopolysiloxane resin comprising the reaction product of a reaction of:
(i) an alkenyl-functional siloxane resin comprising R 26 3 SiO 1/2 units and SiO 4/2 units,
wherein each R 26 is independently a monovalent hydrocarbon radical having 1 to 6 carbon atoms with the proviso that at least one R 26 is an alkenyl radical,
wherein the molar ratio of the R 26 3 SiO 1/2 units to SiO 4/2 units has a value of from 0.5/1 to 1.5/1;
(ii) an alkoxysilane-functional organosiloxane compound having at least one silicon-bonded hydrogen atom at a molecular terminal; and
(iii) an endcapper of the formula R 17 3 SiO—(R 17 2 SiO) s —SiR 17 2 H or R 18 3 SiO—(R 18 2 SiO) t —(HR 18 SiO)—SiR 18 3 or combinations thereof, wherein each R 17 and R 18 are independently a monovalent hydrocarbon group and wherein subscripts s and t independently have a value ranging from 0 to 10;
in the presence of (iv) a hydrosilylation catalyst;

(III) a radical initiator;
(IV) a moisture cure initiator; and
(V) a crosslinker.

2. The adhesive composition according to claim 1 , wherein the clustered functional polyorganosiloxane (I) comprises the reaction product of:
a) a polyorganosiloxane having an average, per molecule, of at least 2 aliphatically unsaturated organic groups,
b) a polyorganohydrogensiloxane having an average, per molecule, of 4 to 15 silicon atoms and at least 4 silicon bonded hydrogen atoms per aliphatically unsaturated organic group in component a), and
c) a reactive species having, per molecule, at least one aliphatically unsaturated organic group and one or more curable groups selected from acrylate groups and methacrylate groups,
in the presence of d) a hydrosilylation catalyst and e) an isomer reducing agent.

3. The adhesive composition according to claim 1 , wherein the clustered functional polyorganosiloxane (I) comprises a reaction product of a reaction of:
a) a polyorganosiloxane having an average, per molecule, of at least 2 aliphatically unsaturated organic groups,
b) a polyorganohydrogensiloxane having an average, per molecule, of 4 to 15 silicon atoms and at least 4 silicon bonded hydrogen atoms per aliphatically unsaturated organic group in component a), and
c) a reactive species having, per molecule, at least one aliphatically unsaturated organic group and one or more curable groups selected from acrylate groups and methacrylate groups,
in the presence of d) a hydrosilylation catalyst.

4. The adhesive composition according to claim 2 , wherein a weight percent of silicon bonded hydrogen atoms in the polyorganohydrogensiloxane b) divided by a weight percent of aliphatically unsaturated organic groups in the polyorganosiloxane a) (the SiH b /Vi a ratio) ranges from 4/1 to 20/1 and the clustered functional polyorganosiloxane (I) prepared by the process has more than one curable group at each molecular terminal of the polyorganosiloxane of component a).

5. The adhesive composition according to claim 1 , wherein a weight ratio of the organopolysiloxane polymer (a) to the alkoxy-functional organopolysiloxane resin (b) varies from 75/25 to 35/65.

6. The adhesive composition according to claim 1 , wherein Q is a divalent linking radical selected from a divalent hydrocarbon radical, a divalent siloxane radical, and combinations thereof, wherein the number of carbon atoms in the hydrocarbon radical ranges from 2 to 12 and wherein the number of siloxane repeat units in the siloxane radical ranges from 0 to 20.

7. The adhesive composition according to claim 1 , wherein the endcapper (iii) comprises Me 3 Si—O—Si(Me)H—OSiMe 3 or Me 3 Si—O—Si(Me) 2 —OSiHMe 2 , wherein Me denotes methyl.

8. The adhesive composition according to claim 1 , wherein the alkoxysilane-functional organosiloxane compound (ii) is of the formula HSi(R 27 ) 2 OSi(R 27 ) 2 CH 2 CH 2 SiR 27 zz (OR 27 ) 3-zz wherein each R 27 is independently a monovalent hydrocarbon having 1 to 6 carbon atoms and wherein the subscript zz is 0 or 1.

9. The adhesive composition according to claim 1 , wherein the reactive resin and polymer (II) comprises from 5 to 50 weight percent of the total weight of the adhesive composition.

10. The adhesive composition according to claim 1 , wherein alkenyl-functional siloxane resin (i) includes from 0.5 to 4 weight percent alkenyl functionality, based on the total weight of the alkenyl-functional siloxane resin (i).

11. The adhesive composition according to claim 1 , wherein the radical initiator (III) comprises from 0.01 to 15 weight percent of the total weight of the adhesive composition.

12. The adhesive composition according to claim 1 , wherein the moisture cure catalyst (IV) comprises from 0.001 to 5 weight percent of the total weight of the reactive resin and polymer (II).

13. The adhesive composition according to claim 1 , wherein the crosslinker (V) is a condensation reaction crosslinker selected from the group consisting of trialkoxysilanes, acetoxysilanes, ketoximinosilanes, alkyl orthosilicates, methylvinyl bis(n-methylacetamido) silane, and combinations thereof.

14. The adhesive composition according to claim 1 further comprising an iron oxide pigment.

15. A method for forming a cured silicone adhesive composition on a substrate, the method comprising:
(a) forming a stable thermal radical curable silicone adhesive composition comprising:
(I) a clustered functional polyorganosiloxane having at least one radical curable group selected from an acrylate group and a methacrylate group;
(II) a reactive resin and polymer comprising:
(a) an organopolysiloxane polymer of the formula (OR 7 ) 3-z R 6 z Si-Q-(R 25 2 SiO 2/2 ) y -Q-SiR 6 z (OR 7 ) 3-z ,
wherein each R 25 is independently a monovalent hydrocarbon radical having 1 to 6 carbon atoms, each R 6 independently is a monovalent hydrocarbon radical having 1 to 6 carbon atoms, each R 7 independently is selected from the group consisting of an alkyl radical and alkoxyalkyl radical, Q is a divalent linking radical, the subscript z has a value of 0, 1 or 2, and the subscript y has a value of 60 to 1000, and
(b) an alkoxy-functional organopolysiloxane resin comprising the reaction product of a reaction of:

(i) an alkenyl-functional siloxane resin comprising R 26 3 SiO 1/2 units and SiO 4/2 units,
wherein each R 26 is independently a monovalent hydrocarbon radical having 1 to 6 carbon atoms with the proviso that at least one R 26 is an alkenyl radical,
wherein the molar ratio of the R 26 3 SiO 1/2 units to SiO 4/2 units has a value of from 0.5/1 to 1.5/1;
(ii) an alkoxysilane-functional organosiloxane compound having at least one silicon-bonded hydrogen atom at a molecular terminal; and
(iii) an endcapper of the formula R 17 3 SiO—(R 17 2 SiO) s —SiR 17 2 H

Assignees

• Dow Corning

Inventors

• Larson Kent
• Steinbrecher Kristen
• Tonge James
• Zarisfi Afrooz

Classifications

• C09J183/06 Primary

  containing silicon bound to oxygen-containing groups (C09J183/12 takes precedence) · CPC title

• C09J183/14

  in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms (C09J183/10 takes precedence) · CPC title

• C08G77/20

  containing silicon bound to unsaturated aliphatic groups · CPC title

• C08G77/12

  containing silicon bound to hydrogen · CPC title

• C08G77/14

  containing silicon bound to oxygen-containing groups · CPC title