JP2001151867A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2001151867A5 JP2001151867A5 JP1999339933A JP33993399A JP2001151867A5 JP 2001151867 A5 JP2001151867 A5 JP 2001151867A5 JP 1999339933 A JP1999339933 A JP 1999339933A JP 33993399 A JP33993399 A JP 33993399A JP 2001151867 A5 JP2001151867 A5 JP 2001151867A5
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- molding material
- resin molding
- sealing
- following general
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Description
【0005】
すなわち、本発明は、
(1) (A)エポキシ樹脂、(B)硬化剤、(C)下記一般式(I)で示される環状ホスファゼン化合物、及び(D)無機充填剤を必須成分とし、(C)成分の配合量は無機充填剤(D)を除く配合成分の合計量に対して燐原子の量が0.5〜5重量%となる量で、(D)成分の配合量が封止用エポキシ樹脂成形材料に対して70重量%以上である封止用エポキシ樹脂成形材料、及び
【化3】
(ここで、X1〜X6のいずれか1又は2は水酸基でそれ以外は水素原子である。)
(2) (C)成分が下記一般式(II)〜(V)で示される環状ホスファゼン化合物から選ばれる少なくとも一種である上記(1)記載の封止用エポキシ樹脂成形材料、並びに
【化4】
(3) (A)エポキシ樹脂として、下記一般式( VI )で示されるビフェニル型エポキシ樹脂を含む上記(1)または(2)記載の封止用エポキシ樹脂成形材料、
【化16】
(ここで、R 1 〜R 4 は水素原子及び炭素数1〜10の置換又は非置換の一価の炭化水素基から選ばれ、全てが同一でも異なっていてもよい。nは0〜3の整数を示す。)
(4) (B)硬化剤として、下記一般式( VII )で示されるフェノール・アラルキル樹脂を含む上記(1)〜(3)いずれか記載の封止用エポキシ樹脂成形材料、
【化17】
(ここで、Rは水素原子及び炭素数1〜10の置換又は非置換の一価の炭化水素基から選ばれ、nは0〜10の整数を示す。)
(5) さらに応力緩和剤を含む上記(1)〜(4)いずれか記載の封止用エポキシ樹脂成形材料、
(6) さらにカップリング剤を含む上記(1)〜(5)いずれか記載の封止用エポキシ樹脂成形材料、
(7) 上記(1)〜(6)いずれか記載の封止用エポキシ樹脂成形材料により封止された素子を備えた電子部品装置、
に関する。[0005]
That is, the present invention
(1) (A) epoxy resin, (B) curing agent, (C) cyclic phosphazene compound represented by the following general formula (I), and (D) inorganic filler as essential components, blending amount of (C) component The amount of the phosphorus atom is 0.5 to 5% by weight based on the total amount of the compounding components excluding the inorganic filler (D), and the compounding amount of the component (D) is an epoxy resin molding material for sealing And an epoxy resin molding material for sealing which is 70% by weight or more, and
(Here, any one or two of X 1 to X 6 are a hydroxyl group and the others are hydrogen atoms.)
(2) The epoxy resin molding material for sealing according to the above (1), wherein the component (C) is at least one selected from cyclic phosphazene compounds represented by the following general formulas (II) to (V), and
(3) The epoxy resin molding material for sealing according to the above (1) or (2), which comprises a biphenyl type epoxy resin represented by the following general formula ( VI ) as (A) epoxy resin
Embedded image
(Here, R 1 to R 4 are selected from a hydrogen atom and a substituted or unsubstituted monovalent hydrocarbon group having 1 to 10 carbon atoms, and all may be the same or different. N is 0 to 3) Indicates an integer.)
(4) The epoxy resin molding material for sealing according to any one of the above (1) to (3), which comprises a phenol / aralkyl resin represented by the following general formula ( VII ) as the curing agent (B)
[Image 17]
(Here, R is selected from a hydrogen atom and a substituted or unsubstituted monovalent hydrocarbon group having 1 to 10 carbon atoms, and n is an integer of 0 to 10).
(5) The epoxy resin molding material for sealing according to any one of the above (1) to (4 ), further comprising a stress relaxation agent,
(6) The epoxy resin molding material for sealing according to any one of the above (1) to (5 ), further containing a coupling agent,
(7) An electronic component device comprising an element sealed by the sealing epoxy resin molding material according to any one of the above (1) to (6) ,
About.
【0007】
中でも接着性、低吸湿性の観点からは、下記一般式(VI)で示されるビフェニル型エポキシ樹脂が好ましい。
【化5】
(ここで、R1〜R4は水素原子及び炭素数1〜10の置換又は非置換の一価の炭化水素基から選ばれ、全てが同一でも異なっていてもよい。nは0〜3の整数を示す。)
上記一般式( VI )で示されるビフェニル型エポキシ樹脂としては、例えば、4,4’−ビス(2,3−エポキシプロポキシ)ビフェニル又は4,4’−ビス(2,3−エポキシプロポキシ)−3,3’,5,5’−テトラメチルビフェニルを主成分とするエポキシ樹脂、エピクロルヒドリンと4,4’−ビフェノール又は4,4’−(3,3’,5,5’−テトラメチル)ビフェノールとを反応させて得られるエポキシ樹脂等が挙げられる。中でも4,4’−ビス(2,3−エポキシプロポキシ)−3,3’,5,5’−テトラメチルビフェニルを主成分とするエポキシ樹脂が好ましい。このビフェニル型エポキシ樹脂を使用する場合、その配合量は、その性能を発揮するためにエポキシ樹脂全量に対して30重量%以上とすることが好ましく、50重量%以上がより好ましく、60重量%以上がさらに好ましい。[0007]
Among them, a biphenyl type epoxy resin represented by the following general formula (VI) is preferable from the viewpoint of adhesiveness and low hygroscopicity.
[Chemical formula 5]
(Here, R 1 to R 4 are selected from a hydrogen atom and a substituted or unsubstituted monovalent hydrocarbon group having 1 to 10 carbon atoms, and all may be the same or different. N is 0 to 3) Indicates an integer.)
Examples of the biphenyl type epoxy resin represented by the above general formula ( VI ) include 4,4′-bis (2,3-epoxypropoxy) biphenyl or 4,4′-bis (2,3-epoxypropoxy) -3. Epoxy resin containing epichlorohydrin and 4,4'-biphenol or 4,4 '-(3,3', 5,5'-tetramethyl) biphenol The epoxy resin etc. which are obtained by making it react are mentioned. Among them, an epoxy resin containing 4,4'-bis (2,3-epoxypropoxy) -3,3 ', 5,5'-tetramethylbiphenyl as a main component is preferable. When using this biphenyl type epoxy resin, it is preferable to make the compounding quantity into 30 weight% or more with respect to the epoxy resin whole quantity, in order to exhibit the performance, 50 weight% or more is more preferable, 60 weight% or more Is more preferred.
【0030】
【表1】
[0030]
[Table 1]
【0031】
【表2】
[0031]
【Table 2】
Claims (7)
【化14】
(ここで、R 1 〜R 4 は水素原子及び炭素数1〜10の置換又は非置換の一価の炭化水素基から選ばれ、全てが同一でも異なっていてもよい。nは0〜3の整数を示す。) The epoxy resin molding material for sealing according to claim 1 or 2, wherein a biphenyl type epoxy resin represented by the following general formula ( VI ) is contained as the epoxy resin (A) .
[Image 14]
(Here, R 1 to R 4 are selected from a hydrogen atom and a substituted or unsubstituted monovalent hydrocarbon group having 1 to 10 carbon atoms, and all may be the same or different. N is 0 to 3) Indicates an integer.)
【化15】
(ここで、Rは水素原子及び炭素数1〜10の置換又は非置換の一価の炭化水素基から選ばれ、nは0〜10の整数を示す。) The epoxy resin molding material for sealing according to any one of claims 1 to 3, containing a phenol-aralkyl resin represented by the following general formula ( VII ) as the curing agent (B) .
[Image 15]
(Here, R is selected from a hydrogen atom and a substituted or unsubstituted monovalent hydrocarbon group having 1 to 10 carbon atoms, and n is an integer of 0 to 10).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33993399A JP2001151867A (en) | 1999-11-30 | 1999-11-30 | Epoxy resin molding material for sealing and electronic component device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33993399A JP2001151867A (en) | 1999-11-30 | 1999-11-30 | Epoxy resin molding material for sealing and electronic component device |
Related Child Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004028111A Division JP2004143465A (en) | 2004-02-04 | 2004-02-04 | Epoxy resin molding compound for sealing and electronic component device |
JP2004028138A Division JP2004143466A (en) | 2004-02-04 | 2004-02-04 | Epoxy resin molding compound for sealing and electronic component device |
JP2006013632A Division JP2006161055A (en) | 2006-01-23 | 2006-01-23 | Epoxy resin molding material for sealing and electronic component device |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2001151867A JP2001151867A (en) | 2001-06-05 |
JP2001151867A5 true JP2001151867A5 (en) | 2005-01-06 |
Family
ID=18332141
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP33993399A Pending JP2001151867A (en) | 1999-11-30 | 1999-11-30 | Epoxy resin molding material for sealing and electronic component device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2001151867A (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001316565A (en) * | 2000-05-10 | 2001-11-16 | Sumitomo Bakelite Co Ltd | Epoxy resin composition and semiconductor device |
JP2001354839A (en) * | 2000-06-15 | 2001-12-25 | Sumitomo Bakelite Co Ltd | Epoxy resin composition and semiconductor device |
JP2002012741A (en) * | 2000-06-27 | 2002-01-15 | Sumitomo Bakelite Co Ltd | Epoxy resin composition and semiconductor device |
JP2003012897A (en) * | 2001-06-27 | 2003-01-15 | Hitachi Chem Co Ltd | Resin composition for friction material |
JP2003012890A (en) * | 2001-07-03 | 2003-01-15 | Kyocera Chemical Corp | Resin composition for sealing and electronic parts sealed device |
KR100600597B1 (en) * | 2001-12-28 | 2006-07-13 | 제일모직주식회사 | Epoxy Resin Compositions for Semiconductor Encapsulant |
KR100679491B1 (en) | 2005-02-03 | 2007-02-06 | 주식회사 케이씨씨 | Eco-friendly epoxy resin composition for semiconductor device encapsulation |
US20090023351A1 (en) * | 2006-02-21 | 2009-01-22 | Keiko Kashihara | Flame-retardant resin composition, prepreg, resin sheet, and molding |
JP6095150B2 (en) * | 2010-10-12 | 2017-03-15 | 株式会社伏見製薬所 | Resin composition |
CN105153234B (en) * | 2014-06-13 | 2018-01-30 | 广东生益科技股份有限公司 | A kind of phenoxy cyclotriphosphazene active ester, halogen-free resin composition and application thereof |
US20160244471A1 (en) * | 2014-06-13 | 2016-08-25 | Shengyi Technology Co., Ltd. | Phenoxycyclotriphosphazene active ester, halogen-free resin composition and uses thereof |
-
1999
- 1999-11-30 JP JP33993399A patent/JP2001151867A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2570002B2 (en) | Flip chip sealing material and semiconductor device | |
US8309652B2 (en) | Curable silicone composition and cured product therefrom | |
EP2061839B1 (en) | Curable silicone composition and electronic component | |
JP2001151867A5 (en) | ||
JP2000103939A5 (en) | ||
DE60200272T2 (en) | Room temperature cure silicone rubber composition | |
EP1191066B1 (en) | Room temperature-curing organopolysiloxane composition | |
KR20110053441A (en) | Thermally Conductive Silicone Compositions and Semiconductor Devices | |
TW412565B (en) | Epoxy resin composition | |
EP1045005B1 (en) | Silicone gel composition | |
JPS61271319A (en) | Epoxy resin composition for semiconductor sealing | |
JPH05112722A (en) | Highly damping silicone composition and cured article prepared therefrom | |
JP2864944B2 (en) | Flame retardant silicone composition | |
JPS6123942B2 (en) | ||
JP2003012927A (en) | Room temperature-curable organopolysiloxane composition | |
JP4522816B2 (en) | Adhesive polyorganosiloxane composition having flame retardancy | |
JP4811562B2 (en) | Room temperature curable organopolysiloxane composition | |
JP3253981B2 (en) | Curable organopolysiloxane gel composition | |
JP4535214B2 (en) | Flame retardant liquid epoxy resin composition | |
KR20230008080A (en) | Room temperature curable organopolysiloxane compositions and articles | |
EP0953588A3 (en) | An epoxy-resin composition and use thereof | |
EP0869140A3 (en) | Epoxy resin composition and resin-encapsulated semiconductor device | |
JP2005179533A (en) | Silicone gel composition | |
JPH0686572B2 (en) | Room temperature curable organopolysiloxane composition | |
JPH08104815A (en) | One pack type room temperature curable silicone elastomer compositon |