JPS63219145A - Pps sealed electronic component - Google Patents
Pps sealed electronic componentInfo
- Publication number
- JPS63219145A JPS63219145A JP5196987A JP5196987A JPS63219145A JP S63219145 A JPS63219145 A JP S63219145A JP 5196987 A JP5196987 A JP 5196987A JP 5196987 A JP5196987 A JP 5196987A JP S63219145 A JPS63219145 A JP S63219145A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- sealed
- silicon oil
- pps
- polyphenylene sulfide
- 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
- 239000004734 Polyphenylene sulfide Substances 0.000 claims abstract description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229920000069 polyphenylene sulfide Polymers 0.000 claims abstract description 16
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 8
- 239000003365 glass fiber Substances 0.000 claims abstract description 7
- 229920002545 silicone oil Polymers 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 9
- 239000000155 melt Substances 0.000 claims description 2
- 229920005989 resin Polymers 0.000 abstract description 13
- 239000011347 resin Substances 0.000 abstract description 13
- 239000003921 oil Substances 0.000 abstract description 6
- 238000007789 sealing Methods 0.000 abstract description 6
- 238000000034 method Methods 0.000 abstract description 5
- 239000011342 resin composition Substances 0.000 abstract description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 4
- 229910052710 silicon Inorganic materials 0.000 abstract 4
- 239000010703 silicon Substances 0.000 abstract 4
- 230000003190 augmentative effect Effects 0.000 abstract 1
- 238000002844 melting Methods 0.000 abstract 1
- 230000008018 melting Effects 0.000 abstract 1
- 238000005382 thermal cycling Methods 0.000 abstract 1
- 238000001746 injection moulding Methods 0.000 description 4
- 229920005992 thermoplastic resin Polymers 0.000 description 4
- 229920001187 thermosetting polymer Polymers 0.000 description 4
- 239000007788 liquid Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- -1 polydimethylsiloxane Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 241000251730 Chondrichthyes Species 0.000 description 1
- 208000015943 Coeliac disease Diseases 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Insulating Materials (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Details Of Resistors (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は未変性シリコーンオイル及び変性シリコーンオ
イルを含有するポリフェニレンサルファイド組成物、特
に耐湿性及びサーマルサイクル特性の優れた電子部品封
止用樹脂組成物に関するものである。Detailed Description of the Invention [Industrial Application Field] The present invention provides a polyphenylene sulfide composition containing an unmodified silicone oil and a modified silicone oil, particularly a resin composition for encapsulating electronic components with excellent moisture resistance and thermal cycle characteristics. It is about things.
従来の樹脂封止はエポキシ樹脂、ソリコーン樹脂等の熱
硬化性樹脂を用いてトランスファー成形により行なうの
が普通であったが、熱硬化性樹脂を用いるため、成形時
間が長くなること、長時間のポストキュアーが必要であ
る。成形ショツト数が増えるに従い金型よごれを生じる
等の欠点があった。Conventional resin encapsulation was usually performed by transfer molding using thermosetting resins such as epoxy resins and soricone resins, but since thermosetting resins are used, the molding time is long and the process requires a long time. Post cure is required. As the number of molding shots increases, there are drawbacks such as mold staining.
前述の様な欠点をもつ熱硬化性樹脂に替えるものとして
、熱可塑性樹脂のポリフェニレンサルファイドを用いる
ことが試みられている。ポリフェニレンサルファイドは
耐熱性、電気特性、難燃性が良好である等、電子部品の
封止に好適な性質を有しており、かつ熱可塑性樹脂であ
るため、スプルー、ランナー等のスクラップの再利用が
可能であり、封止の際の成形サイクルも射出成形により
短縮できる、など熱硬化性樹脂よりすぐれた点も多いが
、このポリフェニレンサルファイドを用いて封止した電
子部品は、熱硬化性樹脂を用いて封止した電子部品に比
べて、耐湿特性及びサーマルサイクル特性が大巾に劣る
という欠点を有している。Attempts have been made to use polyphenylene sulfide, a thermoplastic resin, as a substitute for thermosetting resins, which have the drawbacks mentioned above. Polyphenylene sulfide has properties suitable for sealing electronic components, such as good heat resistance, electrical properties, and flame retardancy, and because it is a thermoplastic resin, it can be used to reuse scraps such as sprues and runners. Although it has many advantages over thermosetting resins, such as being able to shorten the molding cycle for sealing by injection molding, electronic components sealed using polyphenylene sulfide are Compared to electronic components sealed using this method, it has the disadvantage that its moisture resistance and thermal cycle characteristics are significantly inferior.
すなわちポリフェニレンサルファイド樹脂は、エポキシ
樹脂、シリコーン樹脂と比較して電子部品のリードフレ
ームあるいはICのボンディングワイヤーとの密着性に
劣り又機械強度も弱いため、これを用いて封止した電子
部品を高温・高湿度雰囲気においた場合誤封正樹脂と、
リードフレームあるいはポンディングワイヤーの界面か
ら容易に水が侵入し、このため、電気絶縁性の低下やア
ル木発明者らはこのような欠点を改良するために検討を
重ねた結果、未変性シリコーンオイル及び変性シリコー
ンオイルを併用することにより、封止樹脂とリードフレ
ームあるいはポンディングワイヤーとの密着性が大11
に向上し、封止電子部品の耐湿性及びザーマルザイクル
特性が大中に改善されることを見出した。In other words, polyphenylene sulfide resin has poor adhesion to lead frames of electronic components or bonding wires of ICs, and has weak mechanical strength, compared to epoxy resins and silicone resins. If placed in a high humidity atmosphere, the resin may be sealed incorrectly.
Water easily enters through the interface of the lead frame or the bonding wire, resulting in a decrease in electrical insulation.The inventors of Alki conducted repeated studies to improve these defects, and the inventors developed an unmodified silicone oil. By using together with modified silicone oil, the adhesion between the sealing resin and the lead frame or bonding wire is greatly improved.
It has been found that the moisture resistance and thermal cycle characteristics of sealed electronic components are significantly improved.
本発明は、ポリフェニレンサルファイド(PPS)と未
変性シリコーンオイル及び変性シリコーンオイルの併用
、シリカ及びガラス繊維からなる溶融粘度の低い電子部
品封止樹脂組成物を提供するものである。The present invention provides an electronic component sealing resin composition with a low melt viscosity, which is composed of a combination of polyphenylene sulfide (PPS), unmodified silicone oil, and modified silicone oil, silica, and glass fiber.
本発明において用いられるポリフェニレンサルファイド
樹脂(以下PPSと略す)は、〔−◎−8′l−7の一
般式を有する熱可塑性樹脂で架橋度の違いによりいくつ
かのタイプがありいずれのタイプを用いてもさしつかえ
ないが、本発明MR−11グレード)を用いるのが望ま
しい。The polyphenylene sulfide resin (hereinafter abbreviated as PPS) used in the present invention is a thermoplastic resin having the general formula [-◎-8'l-7.There are several types depending on the degree of crosslinking, and which type is used. However, it is preferable to use the MR-11 grade of the present invention.
本発明で用いられる未変性シリコーンオイルはポリジメ
チルシロギサンオイルであり、変性シリコーンオイルは
ポリジメチルシロキザンオイルの側鎖メチル基の一部に
エポキシ基、カルボキシル基、アミノ基、水酸基などの
反応性置換基をW人したもので、全組成物中の合計の割
合が0.1〜10重量%特に2〜10重量%が好ましい
。シリコーンオイルの割合が2重量%以下では封止IC
の耐湿性及びサーマルサイクル性の改良効果がほとんど
みられない。また10重量%以上使用しても顕著な耐湿
性及びサーマルサイクル性の改良効果がみられないだけ
でなく封止品の機械的強度の低下をもたらす。The unmodified silicone oil used in the present invention is polydimethylsiloxane oil, and the modified silicone oil has reactive properties such as epoxy groups, carboxyl groups, amino groups, and hydroxyl groups in some of the side chain methyl groups of polydimethylsiloxane oil. The total proportion of the substituents in the entire composition is preferably 0.1 to 10% by weight, particularly 2 to 10% by weight. If the proportion of silicone oil is less than 2% by weight, the sealed IC
Almost no improvement effect on moisture resistance and thermal cyclability was observed. Furthermore, even if it is used in an amount of 10% by weight or more, not only is no significant effect of improving moisture resistance and thermal cyclability observed, but also the mechanical strength of the sealed product is reduced.
シリカは、機械的強度の向上、線膨張係数の減少、熱伝
導率の増大のため必要であり、本発明においては平均粒
径30μ以下のものを使用し、ガラス繊維は溶融粘度と
機械的強度、線膨張係数、及シリカとガラス繊維の割合
は合計で20〜80重量%、好ましくは30〜80重量
%であることがよい。Silica is necessary to improve mechanical strength, reduce linear expansion coefficient, and increase thermal conductivity. In the present invention, silica is used with an average particle size of 30μ or less, and glass fiber is used to improve melt viscosity and mechanical strength. , the coefficient of linear expansion, and the ratio of silica and glass fiber in total are preferably 20 to 80% by weight, preferably 30 to 80% by weight.
20重量%以下では機械的強度が低く熱伝導率も小さい
。80重量%をこえると組成物の溶融粘度が高すぎて、
封止特電子部品のボンディングワイヤーの損傷をもたら
す。If it is less than 20% by weight, the mechanical strength is low and the thermal conductivity is also low. If it exceeds 80% by weight, the melt viscosity of the composition will be too high,
This will cause damage to the bonding wires of the encapsulated special electronic components.
またシリカ及びガラス繊維をシランカップリング剤など
で表面処理することは成形品の機械的強度の向−に、耐
湿性の向上の面で好ましい。Furthermore, it is preferable to surface-treat the silica and glass fibers with a silane coupling agent or the like in order to improve the mechanical strength and moisture resistance of the molded product.
本発明の樹脂組成物は、ASTM−1703の方法でダ
イス1.0φ璽1×10βIN %温度300℃、押出
圧力IQkg/cutで測定して1000ポイズ以下で
あることが電子部品のワイヤーを損傷しないために好ま
しい。The resin composition of the present invention has an extrusion pressure of 1,000 poise or less when measured using a die of 1.0φ, 1×10βIN% temperature, 300°C, and an extrusion pressure of IQ kg/cut according to the method of ASTM-1703, so that it will not damage the wires of electronic components. preferred for.
本発明の目的を逸脱しない範囲において、PPS樹脂の
混合及び又は他の熱可塑性樹脂をブレンドすることも可
能であるし、必要に応じて着色剤、離型剤等を添加する
ことは何らさしつかえない。It is also possible to mix PPS resin and/or blend other thermoplastic resins without departing from the purpose of the present invention, and there is no problem in adding colorants, mold release agents, etc. as necessary. .
pps <ライドンMR−11) 、未変性シリコーン
オイル及び変性シリコーンオイルの併用、シリカ及び平
均アスペクト比10以」二のガラス繊維を第1表に示す
配合割合(値は重量%)でヘンシェルミキサーを用いて
均一に混合したのちスクリュー径30.1φの2軸押用
機にてシリンダ一温度290〜320 °Cスクリュー
回転数1100rpで押出しコンパウンド化した。この
コンパウンドを射出成形機を用いてシリンダ一温度30
0〜320’C1金型温度150〜200 ’C1射出
圧力50〜100 kg / cnlで16pinDI
PのIC空フレームをインサートした金型にて射出成形
した。得られた封止品を螢光液(スーパーグローOD=
、280(M 特殊塗料■製)に20時間室温で浸漬
したのちフレームと封止樹脂の界面からの螢光液の侵入
状態を調べ表1に示した。pps <Rydon MR-11), a combination of unmodified silicone oil and modified silicone oil, silica and glass fibers with an average aspect ratio of 10 or more using a Henschel mixer at the blending ratios (values are weight %) shown in Table 1. After uniformly mixing the mixture, it was extruded into a compound using a twin-screw extruder with a screw diameter of 30.1φ at a cylinder temperature of 290 to 320°C and a screw rotation speed of 1100 rpm. This compound was molded into a cylinder at a temperature of 30°C using an injection molding machine.
16pinDI at 0~320'C1 mold temperature 150~200'C1 injection pressure 50~100 kg/cnl
Injection molding was performed using a mold into which an empty IC frame of P was inserted. The obtained sealed product was treated with fluorescent liquid (Super Glow OD=
, 280 (manufactured by M Special Paints ■) at room temperature for 20 hours, the state of penetration of the fluorescent liquid from the interface between the frame and the sealing resin was investigated and shown in Table 1.
この測定は第1図に示すような判定基準を設けて、螢光
液の侵入位置(1〜6)を示した。In this measurement, the criteria as shown in FIG. 1 were set, and the penetration positions (1 to 6) of the fluorescent liquid were indicated.
DIPフレームをインサートした金型にて射出成形した
。この組成物の溶融粘度、曲げ強度、線膨張係数、サー
マルサイクル試験(−65℃ (30分)−150℃
(15分):1サイクル)及びプレソシャーク、カー試
験結果を第2表に示した。Injection molding was performed using a mold with a DIP frame inserted. Melt viscosity, bending strength, linear expansion coefficient, thermal cycle test (-65°C (30 minutes) -150°C) of this composition
(15 minutes): 1 cycle) and the Presso Shark and Kerr test results are shown in Table 2.
第1図は本発明の組成物及び比較品でIC空フレームを
封止した状態のアイランド部分を示す概略図である。
特許出願人 住友ヘークライト株式会社第1図FIG. 1 is a schematic diagram showing an island portion of an IC empty frame sealed with the composition of the present invention and a comparative product. Patent applicant: Sumitomo Heckleite Co., Ltd. Figure 1
Claims (1)
量%、未変性シリコーンオイル及び変性シリコーンオイ
ルの併用で0.1〜10重量%、シリカ及び平均アスペ
クト比10以上のガラス繊維の合計が20〜80重量%
からなり、溶融粘度が1000ポイズ以下であることを
特徴とするPPS組成物を用いて封止したことを特徴と
する電子部品。Polyphenylene sulfide (PPS) 20-80% by weight, a combination of unmodified silicone oil and modified silicone oil 0.1-10% by weight, silica and glass fibers with an average aspect ratio of 10 or more total 20-80% by weight
An electronic component sealed using a PPS composition comprising: a PPS composition having a melt viscosity of 1000 poise or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5196987A JPS63219145A (en) | 1987-03-09 | 1987-03-09 | Pps sealed electronic component |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5196987A JPS63219145A (en) | 1987-03-09 | 1987-03-09 | Pps sealed electronic component |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63219145A true JPS63219145A (en) | 1988-09-12 |
Family
ID=12901698
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5196987A Pending JPS63219145A (en) | 1987-03-09 | 1987-03-09 | Pps sealed electronic component |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63219145A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5223557A (en) * | 1989-12-28 | 1993-06-29 | Kureha Kagaku Kogyo K.K. | Electronic device sealing resin compositions and sealed electronic devices |
EP0601781A2 (en) * | 1992-12-02 | 1994-06-15 | General Electric Company | Polyarylene sulfide and epoxy-functionalized siloxane blends |
US5332770A (en) * | 1988-11-12 | 1994-07-26 | Kureha Kagaku Kogyo K.K. | Electronic device sealing resin compositions and sealed electronic devices |
EP0749159A3 (en) * | 1993-01-13 | 1997-04-02 | Fuji Electric Co Ltd | Resin-sealed semiconductor device |
JPH10330617A (en) * | 1997-06-03 | 1998-12-15 | Jsr Corp | Thermoplastic resin composition |
JP2002012763A (en) * | 2000-06-29 | 2002-01-15 | Idemitsu Petrochem Co Ltd | Polyarylene sulfide resin composition |
JP2015513000A (en) * | 2012-04-13 | 2015-04-30 | ティコナ・エルエルシー | Polyarylene sulfide composition comprising a functionalized siloxane polymer and a non-aromatic impact modifier |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5717153A (en) * | 1980-07-04 | 1982-01-28 | Asahi Glass Co Ltd | Sealing method of electronic parts |
JPS5721844A (en) * | 1980-07-16 | 1982-02-04 | Shin Etsu Chem Co Ltd | Resin composition for sealing electronic parts |
JPS5920911A (en) * | 1982-07-28 | 1984-02-02 | 住友ベークライト株式会社 | Pps composition and sealed electronic part |
-
1987
- 1987-03-09 JP JP5196987A patent/JPS63219145A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5717153A (en) * | 1980-07-04 | 1982-01-28 | Asahi Glass Co Ltd | Sealing method of electronic parts |
JPS5721844A (en) * | 1980-07-16 | 1982-02-04 | Shin Etsu Chem Co Ltd | Resin composition for sealing electronic parts |
JPS5920911A (en) * | 1982-07-28 | 1984-02-02 | 住友ベークライト株式会社 | Pps composition and sealed electronic part |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5332770A (en) * | 1988-11-12 | 1994-07-26 | Kureha Kagaku Kogyo K.K. | Electronic device sealing resin compositions and sealed electronic devices |
US5474828A (en) * | 1988-11-12 | 1995-12-12 | Kureha Kagaku Kogyo K.K. | Electronic device sealing resin compositions and sealed electronic devices |
US5223557A (en) * | 1989-12-28 | 1993-06-29 | Kureha Kagaku Kogyo K.K. | Electronic device sealing resin compositions and sealed electronic devices |
EP0601781A2 (en) * | 1992-12-02 | 1994-06-15 | General Electric Company | Polyarylene sulfide and epoxy-functionalized siloxane blends |
EP0601781A3 (en) * | 1992-12-02 | 1994-09-07 | Gen Electric | Polyarylene sulfide and epoxy-functionalized siloxane blends. |
EP0749159A3 (en) * | 1993-01-13 | 1997-04-02 | Fuji Electric Co Ltd | Resin-sealed semiconductor device |
JPH10330617A (en) * | 1997-06-03 | 1998-12-15 | Jsr Corp | Thermoplastic resin composition |
JP2002012763A (en) * | 2000-06-29 | 2002-01-15 | Idemitsu Petrochem Co Ltd | Polyarylene sulfide resin composition |
JP2015513000A (en) * | 2012-04-13 | 2015-04-30 | ティコナ・エルエルシー | Polyarylene sulfide composition comprising a functionalized siloxane polymer and a non-aromatic impact modifier |
JP2017214586A (en) * | 2012-04-13 | 2017-12-07 | ティコナ・エルエルシー | Polyarylene sulfide composition including functionalized siloxane polymer and non-aromatic impact modifier |
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