Curable silicone composition, curable hot-melt silicone, and optical device

Patent metadata

Field	Value
Publication number	US-10208164-B2
Application number	US-201515506834-A
Country	US
Kind code	B2
Filing date	Aug 26, 2015
Priority date	Sep 1, 2014
Publication date	Feb 19, 2019
Grant date	Feb 19, 2019

Abstract

A curable silicone composition comprises: (A) an organopolysiloxane represented by a specific average unit formula; optionally, (B) an organopolysiloxane represented by a specific average unit formula; (C) an organohydrogenpolysiloxane represented by a specific average composition formula; and (D) a hydrosilylation catalyst. A curable hot-melt silicone is obtained by subjecting the curable silicone composition to a hydrosilylation reaction to a degree that does not form a cured product. The curable hot-melt silicone is non-flowable at 25° C. and has a melt viscosity at 100° C. of 5000 Pa·s or less. The curable silicone composition provides a cured product having excellent heat resistance and light resistance after being cured. The curable hot-melt silicone is non-flowable at room temperature, has low surface stickiness, and is readily melted by heating.

First claim

The invention claimed is:

1. A curable silicone composition comprising:
(A) 100 parts by mass of an organopolysiloxane represented by the average unit formula:
(R 1 3 SiO 1/2 ) a (R 2 2 SiO 2/2 ) b (R 3 SiO 3/2 ) c (SiO 4/2 ) d (R 4 O 1/2 ) e

wherein,
R 1 , R 2 , and R 3 are the same or different and are each a phenyl group, an alkyl group having from 1 to 6 carbons, or an alkenyl group having from 2 to 6 carbons;
provided that, 40 mol % or less of R 1 , 30 mol % or greater of R 2 , and 10 mol % or less of R 3 are alkenyl groups, and 30 to 60 mol % of the total of R 1 , R 2 , and R 3 are phenyl groups;
R 4 is a hydrogen atom or an alkyl group having from 1 to 6 carbons; and
“a” is a number of 0 to 0.2, “b” is a number of 0.2 to 0.5, “c” is a number of 0.3 to 0.8, “d” is a number of 0 to 0.5, “e” is a number of 0 to 0.1, “c+d” is a number of 0.3 to 0.8, and “a+b+c+d” is 1;

(B) from 0 to 150 parts by mass of an organopolysiloxane represented by the average unit formula:
(R 5 3 SiO 1/2 ) f (R 5 2 SiO 2/2 ) g (R 5 SiO 3/2 ) h (SiO 4/2 ) i (R 6 O 1/2 ) j

wherein,
R 5 are the same or different and are each a phenyl group, an alkyl group having from 1 to 6 carbons, or an alkenyl group having from 2 to 6 carbons;
provided that, 10 to 70 mol % of all R 5 are phenyl groups, and at least one of all R 5 is an alkenyl group;
R 6 is a hydrogen atom or an alkyl group having from 1 to 6 carbons; and
“f” is a number of 0.01 to 0.3, “g” is a number of 0.4 to 0.99, “h” is a number of 0 to 0.2, “i” is a number of 0 to 0.2, “j” is a number of 0 to 0.1, “h+i” is a number of 0 to 0.2, and “f+g+h+i” is 1;

(C) an organohydrogenpolysiloxane represented by the average composition formula:
R 7 k H l SiO (4-k-l)/2

wherein,
R 7 is a phenyl group or an alkyl group having from 1 to 6 carbons;
provided that, 10 to 70 mol % of all R 7 are phenyl groups; and
“k” is a number of 1.0 to 2.5, “l” is a number of 0.01 to 0.9, and “k+l” is a number of 1.5 to 3.0; and

wherein component (C) is present in an amount such that silicon atom-bonded hydrogen atoms in component (C) is from 0.5 to 2.0 mol per 1 mol of the total alkenyl groups in components (A) and (B); and
(D) a hydrosilylation catalyst in an amount sufficient to accelerate hydrosilylation reaction of the composition.

2. The curable silicone composition according to claim 1 , further comprising (E) from 0.0001 to 5 parts by mass of a reaction inhibitor per 100 parts by mass of the total amount of components (A) to (D).

3. An optical device comprising an optical semiconductor element that is encapsulated, protected, or covered with a cured product of the curable silicone composition according to claim 1 .

4. The curable silicone composition according to claim 1 , wherein component (B) is present in the composition.

5. The curable silicone composition according to claim 1 , wherein component (A) is an organopolysiloxane in which 35 to 55 mol % of the total of R 1 , R 2 , and R 3 are phenyl groups.

6. A curable hot-melt silicone that is non-flowable at 25° C. and that has a melt viscosity at 100° C. of 5000 Pa·s or less, wherein the curable hot melt silicon is formed by subjecting a curable silicone composition to a hydrosilylation reaction to a degree that does not form a cured product, and wherein the curable silicone composition comprises:
(A) 100 parts by mass of an organopolysiloxane represented by the average unit formula:
(R 1 3 SiO 1/2 ) a (R 2 2 SiO 2/2 ) b (R 3 SiO 3/2 ) c (SiO 4/2 ) d (R 4 O 1/2 ) e

wherein,
R 1 , R 2 , and R 3 are the same or different and are each a phenyl group, an alkyl group having from 1 to 6 carbons, or an alkenyl group having from 2 to 6 carbons;
provided that, 40 mol % or less of R 1 , 30 mol % or greater of R 2 , and 10 mol % or less of R 3 are alkenyl groups, and 30 to 60 mol % of the total of R 1 , R 2 , and R 3 are phenyl groups;
R 4 is a hydrogen atom or an alkyl group having from 1 to 6 carbons; and
“a” is a number of 0 to 0.2, “b” is a number of 0.2 to 0.5, “c” is a number of 0 to 0.8, “d” is a number of 0 to 0.5, “e” is a number of 0 to 0.1, “c +d” is a number of 0.3 to 0.8, and “a+b+c+d” is 1;

(B) from 0 to 40 parts by mass of an organopolysiloxane represented by the average unit formula:
(R 5 3 SiO 1/2 ) f (R 5 2 SiO 2/2 ) g (R 5 SiO 3/2 ) h (SiO 4/2 ) i (R 6 O 1/2 ) j

wherein,
R 5 are the same or different and are each a phenyl group, an alkyl group having from 1 to 6 carbons, or an alkenyl group having from 2 to 6 carbons;
provided that, 10 to 70 mol % of all R 5 are phenyl groups, and at least one of all R 5 is an alkenyl group;
R 6 is a hydrogen atom or an alkyl group having from 1 to 6 carbons; and
“f” is a number of 0.01 to 0.3, “g” is a number of 0.4 to 0.99, “h” is a number of 0 to 0.2, “i” is a number of 0 to 0.2, “j” is a number of 0 to 0.1, “h+i” is a number of 0 to 0.2, and “f+g+h+i” is 1;

(C) an organohydrogenpolysiloxane represented by the average composition formula:
R 7 k H l SiO (4-k-l)/2

wherein,
R 7 is a phenyl group or an alkyl group having from 1 to 6 carbons;
provided that, 10 to 70 mol % of all R 7 are phenyl groups;
“k” is a number of 1.0 to 2.5, “l” is a number of 0.01 to 0.9, and “k+l” is a number of 1.5 to 3.0; and

wherein component (C) is present in an amount such that silicon atom-bonded hydrogen atoms in component (C) is from 0.5 to 2.0 mol per 1 mol of the total alkenyl groups in components (A) and (B); and
(D) a hydrosilylation catalyst in an amount sufficient to accelerate hydrosilylation reaction of the composition.

7. The curable hot-melt silicone according to claim 6 , wherein the curable silicone composition further comprises (E) from 0.0001 to 5 parts by mass of a reaction inhibitor per 100 parts by mass of the total amount of components (A) to (D).

8. The curable hot-melt silicone according to claim 7 , wherein the degree of conversion in the hydrosilylation reaction is from 50% to 90%.

9. The curable hot-melt silicone according to claim 7 , in the form of a sheet, powder, or tablet.

10. The curable hot-melt silicone according to claim 6 , in the form of a sheet, powder, or tablet.

11. The curable hot-melt silicone according to claim 6 , wherein component (B) is present in the composition.

12. The curable hot-melt silicone according to claim 6 , wherein the degree of conversion in the hydrosilylation reaction is from 50% to 90%.

13. An optical device comprising an optical semiconductor element that is encapsulated, protected, or covered with the curable hot-melt silicone according to claim 6 .

14. The curable hot-melt silicone according to claim 6 , wherein component (A) is an organopolysiloxane in which 35 to 55 mol % of the total of R 1 , R 2 , and R 3 are phenyl groups.

Assignees

• Dow Corning Toray Co Ltd

Inventors

• Dogen Ryota
• Yamazaki Haruna
• Yoshitake Makoto

Classifications

• H10W74/40

  characterised by their materials · CPC title

• H10W74/10

  characterised by their shape or disposition · CPC title

• C09D183/04

  Polysiloxanes · CPC title

• C08L83/04

  Polysiloxanes · CPC title

• C08G77/20

  containing silicon bound to unsaturated aliphatic groups · CPC title