Curable composition

US9243143B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9243143-B2
Application numberUS-201414459184-A
CountryUS
Kind codeB2
Filing dateAug 13, 2014
Priority dateApr 4, 2013
Publication dateJan 26, 2016
Grant dateJan 26, 2016

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Provided are a curable composition and its use. The curable composition may provide a cured product having excellent processability and workability, no whitening and surface stickiness, and an excellent adhesive property. Since the curable composition has excellent thermal resistance, gas barrier-ability, and crack resistance, even when a semiconductor device to which the composition is applied is used at a high temperature for a long time, performance of the device may be stably maintained. Specifically the curable composition is a blend of three different polyorganosiloxanes having aliphatic unsaturated groups and specific Ar/Si ratios and a polyorganosiloxane having SiH groups.

First claim

Opening claim text (preview).

What is claimed is: 1. A curable composition, comprising: (A) a linear or partially-crosslinked polyorganosiloxane having an aliphatic unsaturated bond; (B) a mixture of a first crosslinked polyorganosiloxane having an aliphatic unsaturated bond and a molar ratio (Ar/Si) of aryl (Ar) groups to total silicon (Si) atoms of 0.3 or less and having an average empirical formula of Formula 1, and a second crosslinked polyorganosiloxane having an aliphatic unsaturated bond and a molar ratio (Ar/Si) of aryl (Ar) groups to total silicon (Si) atoms of 0.3 or more, which is different from that of the first crosslinked polyorganosiloxane; and (C) a polyorganosiloxane including a hydrogen atom and an aryl group, which bind to a silicon atom, having a molar ratio of aryl (Ar) groups to silicon (Si) atoms of 0.3 or more, and including 3 to 10 silicon atoms: (R 1 3 SiO 1/2 ) a (R 2 2 SiO 2/2 ) b (R 3 SiO 3/2 ) c (SiO 4/2 ) d (OR) e   [Formula 1] where R 1 to R 3 are each independently an alkyl group, an alkenyl group, an alkynyl group or an aryl group, at least one of R 1 to R 3 is an alkenyl group, R is hydrogen, an alkyl group, an alkenyl group or an alkynyl group, a, b, c and e are each independently 0 or a positive number, d is a positive number, d/(c+d) is 0.3 or more, and e/(c+d) is 0.2 or less. 2. The curable composition according to claim 1 , wherein the second crosslinked polyorganosiloxane has an average empirical formula of Formula 2: (R 4 3 SiO 1/2 ) f (R 5 2 SiO 2/2 ) g (R 6 SiO 3/2 ) h (SiO 4/2 ) i (OR) j   [Formula 2] where R, R 4 , and R 5 are each independently an epoxy group or a monovalent hydrocarbon group, at least one of R 4 and R 5 is an alkenyl group, at least one of R 4 and R 5 is an aryl group, R is hydrogen or a monovalent hydrocarbon group, f, g, and i are each independently 0 or a positive number, h is a positive number, h/(h+i) is 0.7 or more, and j/(h+i) is 0.2 or less. 3. The curable composition according to claim 1 , wherein the second crosslinked polyorganosiloxane is included at 5 to 100 parts by weight with respect to 100 parts by weight of the first crosslinked polyorganosiloxane. 4. The curable composition according to claim 1 , wherein a ratio (H/Si) of a number of moles of hydrogen (H) atoms to a number of moles of total silicon (Si) atoms of the polyorganosiloxane (C) is 0.2 to 0.8. 5. The curable composition according to claim 1 , wherein the polyorganosiloxane (C) has a viscosity at 25° C. of 300 mPa·s or less. 6. The curable composition according to claim 1 , wherein the polyorganosiloxane (C) has a molecular weight of less than 1,000. 7. The curable composition according to claim 1 , wherein the polyorganosiloxane (C) is a compound of Formula 3 or 4: where R, R 1 , and R 2 are each independently hydrogen, an epoxy group, or a monovalent hydrocarbon group, at least one R is an aryl group, at least one of R 1 and R 2 is an aryl group, and n is a number from 1 to 10. 8. The curable composition according to claim 1 , wherein the polyorganosiloxane (C) is included in such a range that a molar ratio (H/Ak) of hydrogen (H) atoms binding to a silicon atom to total alkenyl (Ak) groups included in the curable composition is 0.5 to 3.0. 9. The curable composition according to claim 1 , further comprising a polyorganosiloxane including a hydrogen atom binding to a silicon atom, having a molar ratio of aryl (Ar) groups to silicon (Si) atoms of 0.3 or less, and including 10 to 50 silicon atoms. 10. The curable composition according to claim 1 , further comprising a compound of an average empirical formula of Formula 5: (HR 2 SiO 1/2 ) a (RSiO 3/2 ) b (R 2 SiO 2/2 ) c   [Formula 5] where each R is independently a monovalent hydrocarbon group, at least one R is an aryl group, and when the sum (a+b+c) of a, b, and c is 1, a is 0.3 to 0.8, b is 0.2 to 0.7, and c is 0 to 0.5. 11. The curable composition according to claim 1 , further comprising a compound of Formula 6: R 3 SiO(HRSiO) r (R 2 SiO) s OSiR 3   [Formula 6] where each R is independently hydrogen, an epoxy group, or a monovalent hydrocarbon group, r is a number from 5 to 100, and s is a number from 0 to 100. 12. The curable composition according to claim 1 , wherein the linear or partially-crosslinked polyorganosiloxane has a molar ratio (Ar/Si) of aryl (Ar) groups to total silicon (Si) atoms of 0.2 or less. 13. The curable composition according to claim 1 , wherein the linear or partially-crosslinked polyorganosiloxane has a molar ratio (Ar/Si) of aryl (Ar) groups to total silicon (Si) atoms of 0.3 or more. 14. The curable composition according to claim 1 , further comprising a polyorganosiloxane including an alkenyl group and an epoxy group, which bind to a silicon atom, and having a molar ratio (Ak/Si) of alkenyl (Ak) groups to total silicon (Si) atoms of 0.02 to 0.5, a molar ratio (Ar/Si) of aryl (Ar) groups to total silicon (Si) atoms of 0.9 or less, and a molar ratio (Ep/Si) of epoxy (Ep) groups to total silicon (Si) atoms of 0.01 to 0.5. 15. A semiconductor device encapsulated with an encapsulant including a cured product of the curable composition of claim 1 . 16. An optical semiconductor device encapsulated with an encapsulant including a cured product of the curable composition of claim 1 . 17. A liquid crystal display device comprising the optical semiconductor device of claim 16 . 18. A lighting apparatus comprising the optical semiconductor device of claim 16 .

Assignees

Inventors

Classifications

  • Organic materials comprising silicon · CPC title

  • containing silicon bound to oxygen-containing groups · CPC title

  • Siloxanes having aromatic substituents, e.g. phenyl side groups · CPC title

  • C08L83/04Primary

    Polysiloxanes · CPC title

  • use in coating or encapsulating of electronic parts · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9243143B2 cover?
Provided are a curable composition and its use. The curable composition may provide a cured product having excellent processability and workability, no whitening and surface stickiness, and an excellent adhesive property. Since the curable composition has excellent thermal resistance, gas barrier-ability, and crack resistance, even when a semiconductor device to which the composition is applied…
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C08L83/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).