Moisture curable compositions
US-2024400829-A1 · Dec 5, 2024 · US
US9464211B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9464211-B2 |
| Application number | US-201314426524-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 6, 2013 |
| Priority date | Sep 7, 2012 |
| Publication date | Oct 11, 2016 |
| Grant date | Oct 11, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention relates to a curable silicone composition which is a hydrosilylation reaction curable silicone composition for sealing, coating, or adhering of an optical semiconductor element, and includes at least one type of compound selected from triazole-based compounds with the exception of benzotriazole. The curable silicone composition, for example, includes (A) an organopolysiloxane having at least 2 aliphatic unsaturated hydrocarbon groups per molecule, (B) an organopolysiloxane having at least two silicon-bonded hydrogen atoms per molecule, (C) at least one type of compound selected from among triazole-based compounds with the exception of non-substituted benzotriazole, and (D) a hydrosilylation reaction catalyst. The curable silicone composition forms a cured product having excellent transparency and thermal shock resistance, and the optical semiconductor device utilizing the composition has excellent reliability.
Opening claim text (preview).
The invention claimed is: 1. A hydrosilylation reaction curable silicone composition for sealing, coating, or adhering of an optical semiconductor element; the hydrosilylation reaction curable silicone composition comprising at least one compound selected from the group consisting of triazole-based compounds with the exception of non-substituted benzotriazole, wherein the triazole-based compound is selected from the group consisting of N-alkyl substituted triazoles, N-alkylaminoalkyl substituted triazoles, alkyl substituted benzotriazoles, carboxy substituted benzotriazoles, and nitro substituted benzotriazoles. 2. The hydrosilylation reaction curable silicone composition according to claim 1 ; wherein the hydrosilylation reaction curable silicone composition comprises: (A) an organopolysiloxane having at least two aliphatic unsaturated hydrocarbon groups per molecule; (B) an organohydrogenpolysiloxane having at least two silicon-bonded hydrogen atoms per molecule; (C) at least one type of compound selected from the group consisting of triazole-based compounds with the exception of non-substituted benzotriazole; and (D) a hydrosilylation reaction catalyst. 3. The hydrosilylation reaction curable silicone composition according to claim 2 ; wherein component (A) is an organopolysiloxane represented by the following average composition formula: (R 1 SiO 3/2 ) a (R 2 R 3 SiO 2/2 ) b (R 4 R 5 R 6 SiO 1/2 ) c (SiO 4/2 ) d wherein, R 1 to R 6 may be identical or different monovalent hydrocarbon groups, from 0.01 to 50 mol % of all monovalent hydrocarbon groups are aliphatic unsaturated hydrocarbon groups; a, b, c, and d represent mole ratios of the respective siloxane units and are numbers that respectively satisfy: a+b+c+d=1.0, 0≦a≦1.0, 0≦b≦1.0, 0≦c<0.83, and 0≦d<0.50. 4. The hydrosilylation reaction curable silicone composition according to claim 3 ; wherein component (B) is an organohydrogenpolysiloxane represented by the following average composition formula: R 7 e H f SiO [(4-e-f)/2] wherein, R 7 is a substituted or non-substituted monovalent hydrocarbon group with the exception of aliphatic unsaturated hydrocarbon groups; and e and f are numbers that respectively satisfy: 1.0≦e≦2.0, 0.1<f<1.0, and 1.5≦e+f<2.7. 5. The hydrosilylation reaction curable silicone composition according to claim 2 ; wherein component (B) is an organohydrogenpolysiloxane represented by the following average composition formula: R 7 e H f SiO [(4-e-f)/2] wherein, R 7 is a substituted or non-substituted monovalent hydrocarbon group with the exception of aliphatic unsaturated hydrocarbon groups; and e and f are numbers that respectively satisfy: 1.0≦e≦2.0, 0.1<f<1.0, and 1.5≦e+f<2.7. 6. An optical semiconductor device fabricated by using the hydrosilylation reaction curable silicone composition described in claim 1 for sealing, coating, or adhering an optical semiconductor element. 7. The optical semiconductor device according to claim 6 , wherein the optical semiconductor element is a light emitting diode. 8. The hydrosilylation reaction curable silicone composition according to claim 1 ; wherein the triazole-based compound is selected from the group consisting of N,N-bis(2-ethylhexyl)-[(1,2,4-triazol-1-yl)methyl]amine, tolyl triazole, carboxybenzotriazole, and nitrobenzotriazole. 9. The hydrosilylation reaction curable silicone composition according to any claim 1 ; wherein a content of the triazole-based compound in the hydrosilylation reaction curable silicone composition is 0.01 ppm to 3% by mass.
Die-attach connectors and bond wires · CPC title
between a chip and a stacked lead frame, conducting package substrate or heat sink · CPC title
between a chip and a stacked lead frame, conducting package substrate or heat sink · CPC title
Solid or gel fillings · CPC title
Organic materials comprising silicon · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.