Silicone resin composition for optical semiconductors
US-2016194452-A1 · Jul 7, 2016 · US
US10655014B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10655014-B2 |
| Application number | US-201616063411-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 7, 2016 |
| Priority date | Dec 18, 2015 |
| Publication date | May 19, 2020 |
| Grant date | May 19, 2020 |
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Addition curable silicone resin compositions have excellent processing characteristics, and can be used to encapsulate electrical and electronic devices.
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The invention claimed is: 1. A compositions comprising: (A) at least one organopolysiloxane comprising at least 3 units of the formula R 1 a R 2 b R 3 c H d (RO) e SiO (4-a-b-c-d-e)/2 (I), where R 1 each independently are monovalent, SiC-bonded, optionally halogen- or cyano-substituted hydrocarbyl moieties with aliphatic carbon-carbon multiple bonding, R 2 each independently are monovalent, SiC-bonded, optionally halogen- or cyano-substituted, saturated hydrocarbyl moieties, R 3 each independently are monovalent SiC-bonded aromatic moieties, R each independently are hydrogen or monovalent, optionally substituted hydrocarbyl moieties which are optionally interrupted by heteroatoms, a is 0, 1, 2 or 3, b is 0, 1, 2 or 3, c is 0, 1, 2 or 3, d is 0, 1 or 2, and e is 0, 1 or 2, with the proviso that the a+b+c+d+e sum is not more than 3, the sum total of Si-bonded hydrogen atoms and R 1 moieties per molecule is at least 3, the a+b+c+d sum is equal to 0 or 1 in at least 10 mol % of the units of formula (I), c is other than 0 in at least one unit, and the ratio of Si-bonded hydrogen atoms to Si-bonded R 1 moieties in the siloxane (A) is from 0.1 to 9, optionally (B) organopolysiloxanes comprising units of the formula R 4 f R 5 g R 6 h (R 7 O) t SiO (4-f-g-h-i)/2 (VI), where R 4 each independently are monovalent, SiC-bonded, optionally halogen- or cyano-substituted, hydrocarbyl moieties with aliphatic carbon-carbon multiple bonding, R 5 each independently are monovalent, SiC-bonded, optionally halogen- or cyano-substituted, saturated hydrocarbyl moieties, R 6 each independently are monovalent SiC-bonded aromatic moieties, R 7 each independently are hydrogen or monovalent, optionally substituted hydrocarbyl moieties, which are optionally interrupted by heteroatoms, f is 0, 1, 2 or 3, g is 0, 1, 2 or 3, h is 0, 1 or 2, i is 0 or 1, with the proviso that the f+g+h+i sum is not more than 3, siloxanes (B) have at least two R 4 moieties per molecule, the f+g+h+i sum is equal to 0 or 1 in not more than 20 mol % of the units of formula (VI) and h is other than 0 in at least one unit of formula (VI), (C) at least one organopolysiloxane comprising units of the formula R 8 k R 9 l R 10 m (R 11 O) n SiO (4-k-l-m-n)/2 (X), where R 8 each independently are monovalent, SiC-bonded, optionally halogen- or cyano-substituted, hydrocarbyl moieties with aliphatic carbon-carbon multiple bonding, R 9 each independently are monovalent, SiC-bonded, optionally halogen- or cyano-substituted, saturated hydrocarbyl moieties, R 10 each independently are monovalent SiC-bonded aromatic moieties, R 11 each independently are hydrogen or monovalent, optionally substituted hydrocarbyl moieties, which are optionally interrupted by heteroatoms, k is 0, 1, 2 or 3, l is 0, 1, 2 or 3, m is 0, 1 or 2, and n is 0 or 1, with the proviso that the k+l+m+n sum is not more than 3, siloxanes (C) have at least two R 8 moieties per molecule, the k+l+m+n sum is equal to 0 or 1 in at least 10 mol % of the units of formula (X) and m is other than 0 in at least one unit of formula (X), and optionally, (D) a catalyst which promotes the addition of Si-bonded hydrogen onto aliphatic carbon-carbon multiple bonds. 2. The composition of claim 1 , wherein siloxane(s) (A) comprise siloxanes having at least 3 units selected from the group consisting of the formulae R 1 a R 2 b R 3 c H d (RO) e SiO 1/2 where ( a+b+c+d+e )=3 (II), R 2 b R 3 c (RO)SiO 2/2 where ( b+c )=1 (IIIa), R 2 b R 3 c SiO 2/2 where ( b+c )=2 (IIIb), R 2 b R 3 c (RO) e SiO 3/2 where ( b+c+e )=1 (IV), and SiO 4/2 (V), where R, R 1 , R 2 , R 3 , a, b, c, d and e are each as defined above, with the proviso that not more than 25 mol % of the units in the siloxanes (A) are of formula (IIIb), the sum total of Si-bonded hydrogen atoms and R 1 moieties per molecule is at least 3, at least one R 3 moiety is present per molecule, and at least one unit of formula (IV) and/or (V) is present. 3. The composition of claim 1 , wherein component (C) comprises siloxanes consisting of units selected from the group consisting of: R 8 k R 9 l R 10 m (R 11 O) n SiO 1/2 where ( k+l+m+n )=3 (XI), R 9 l R 10 m (R 11 O)SiO 2/2 where ( l+m )=1 (XIIa), R 9 l R 10 m SiO 2/2 where ( l+m )=2 (XIIb), R 9 l R 10 m (R 11 O) n SiO 3/2 where ( l+m+n )=1 (XIII), and SiO 4/2 (V) where R 8 , R 9 , R 10 , R 11 , k, l, m and n are each as defined above, with the proviso that siloxanes (C) have at least two R 8 moieties per molecule, at least one R 10 moiety is present per molecule, and at least one unit of formula (XIII) and/or (V) is present. 4. The composition of claim 2 , wherein component (C) comprises siloxanes consisting of units selected from the group consisting of: R 8 k R 9 l R 10 m (R 11 O) n SiO 1/2 where ( k+l+m+n )=3 (XI), R 9 l R 10 m (R 11 O)SiO 2/2 where ( l+m )=1 (XIIa), R 9 l R 10 m SiO 2/2 where ( l+m )=2 (XIIb), R 9 l R 10 m (R 11 O) n SiO 3/2 where ( l+m+n )=1 (XIII), and SiO 4/2 (V) where R 8 , R 9 , R 10 , R 11 , k, l, m and n are each as defined above, with the proviso that siloxanes (C) have at least two R 8 moieties per molecule, at least one R 10 moiety is present per molecule, and at least one unit of formula (XIII) and/or (V) is present. 5. The composition of claim 1 , comprising from 1 to 200 parts by weight of siloxane (C), based on 100 parts by weight of component (A). 6. The composition of claim 2 , comprising from 1 to 200 parts by weight of siloxane (C), based on 100 parts by weight of component (A). 7. The composition of claim 3 , comprising from 1 to 200 parts by weight of siloxane (C), based on 100 parts by weight of component (A). 8. The composition of claim 1 , comprising: (A) siloxanes comprising units of formula (I), optionally (B) siloxanes comprising units of formula (VI), (C) siloxanes comprising units of formula (X), (D) a catalyst which promotes the addition of Si-bonded hydrogen onto aliphatic carbon-carbon multiple bonds, optionally (E) fillers, optionally (F) adhesion promoters, optionally (G) inhibitors, optionally (H) plasticizers, optionally (K) additives, and optionally (L) solvents. 9. The composition of claim 1 , comprising: (A) siloxanes comprising units of formula (I), optionally (B) siloxanes comprising units of formula (VI), (C) siloxanes comprising units of formula (X), (D) a catalyst which promotes the addition of Si-bonded hydrogen onto aliphatic carbon-carbon multiple bonds, optionally (E) fillers, (F) adhesion promoters, optionally (G) inhibitors, optionally (H) plasticizers, optionally (K) additives, and optionally (L) solvents. 10. A process for producing a composition of claim 1 , comprising mixing the individual components in arbitrary order. 11. A shaped article obtained by crosslinking a composition of claim 1 . 12. The shaped article of claim 11 , which is a coating, encapsulation, or lens. 13. In a process for encapsulation of electrical or electronic components, the improvement comprising encapsulating with a composition of claim 1 . 14. In a process for the manufacture of devices containing LEDs, the improvement comprising encapsulating at least one LED with a composition of claim 1 .
to alkoxy or aryloxy groups · CPC title
containing silicon bound to hydrogen · CPC title
Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers · CPC title
Polysiloxanes · CPC title
Siloxanes having aromatic substituents, e.g. phenyl side groups · CPC title
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