Sealing epoxy resin composition, hardened product, and semiconductor device
US-9633922-B2 · Apr 25, 2017 · US
US10385161B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10385161-B2 |
| Application number | US-201615523501-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 22, 2016 |
| Priority date | Apr 15, 2015 |
| Publication date | Aug 20, 2019 |
| Grant date | Aug 20, 2019 |
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 phosphonium-based compound represented by chemical formula 1, an epoxy resin composition containing the same, and a semiconductor device manufactured by using the same.
Opening claim text (preview).
The invention claimed is: 1. A phosphonium compound, wherein the phosphonium compound is any one of compounds represented by Formulae 1a to 1f: 2. An epoxy resin composition, comprising: an epoxy resin, a curing agent, an inorganic filler, and a curing catalyst, the curing catalyst including the phosphonium compound according to claim 1 . 3. The epoxy resin composition according to claim 2 , wherein the epoxy resin includes one or more of a bisphenol A type epoxy resin, a bisphenol F type epoxy resin, a phenol novolac type epoxy resin, a tert-butyl catechol type epoxy resin, a naphthalene type epoxy resin, a glycidyl amine type epoxy resin, a cresol novolac type epoxy resin, a biphenyl type epoxy resin, a linear aliphatic epoxy resin, a cycloaliphatic epoxy resin, a heterocyclic epoxy resin, a spiro ring-containing epoxy resin, a cyclohexane dimethanol type epoxy resin, a trimethylol type epoxy resin, or a halogenated epoxy resin. 4. The epoxy resin composition according to claim 2 , wherein the curing agent includes a phenol resin. 5. The epoxy resin composition according to claim 2 , wherein the curing agent includes one or more of a phenolaralkyl type phenol resin, a phenol novolac type phenol resin, a xyloc type phenol resin, a cresol novolac type phenol resin, a naphthol type phenol resin, a terpene type phenol resin, a multifunctional phenol resin, a dicyclopentadiene-based phenol resin, a novolac type phenol resin synthesized from bisphenol A and resol, a polyhydric phenol compound, an acid anhydride, or an aromatic amine. 6. The epoxy resin composition according to claim 2 , wherein the curing catalyst is present in an amount of 0.01 wt % to 5 wt % in the epoxy resin composition. 7. The epoxy resin composition according to claim 2 , wherein the phosphonium compound is present in an amount of 10 wt % to 100 wt % in the curing catalyst. 8. The epoxy resin composition according to claim 2 , wherein the epoxy resin composition has a curing shrinkage of not more than 0.4%, as calculated according to Equation 1: Curing shrinkage=| C−D|/C× 100 <Equation 1> wherein C is the length of a specimen obtained by transfer molding of the epoxy resin composition at 175° C. and 70 kgf/cm 2 , and D is the length of the specimen after post-curing the specimen at 170° C. to 180° C. for 4 hours and cooling. 9. The epoxy resin composition according to claim 2 , wherein the epoxy resin composition has a storage stability of about 80% or more, as calculated according to Equation 2: Storage stability=( F 1− F 0)/ F 0×100 <Equation 2> wherein F 1 is the flow length (inches) of the epoxy resin composition measured after storing the composition at 25° C./50% RH for 72 hours using a transfer molding press at 175° C. and 70 kgf/cm 2 in accordance with EMMI-1-66, and F0 is the initial flow length (inches) of the epoxy resin composition. 10. A semiconductor device encapsulated with the epoxy resin composition according to claim 2 .
between a chip and a stacked insulating package substrate, interposer or RDL · CPC title
the encapsulations exposing the passive side of the semiconductor body · CPC title
on active surfaces of flip-chip devices, e.g. underfills · CPC title
the semiconductor body being completely enclosed · CPC title
comprising organic materials, e.g. plastics or resins · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.