JPH0220547A - Sealing resin composition - Google Patents
Sealing resin compositionInfo
- Publication number
- JPH0220547A JPH0220547A JP16932688A JP16932688A JPH0220547A JP H0220547 A JPH0220547 A JP H0220547A JP 16932688 A JP16932688 A JP 16932688A JP 16932688 A JP16932688 A JP 16932688A JP H0220547 A JPH0220547 A JP H0220547A
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- sealing resin
- moldability
- resin
- aluminum oxide
- 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
- 239000011342 resin composition Substances 0.000 title claims abstract description 19
- 238000007789 sealing Methods 0.000 title claims abstract description 16
- 239000000843 powder Substances 0.000 claims abstract description 25
- 239000003822 epoxy resin Substances 0.000 claims abstract description 16
- 229920003986 novolac Polymers 0.000 claims abstract description 16
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 16
- 239000005011 phenolic resin Substances 0.000 claims abstract description 14
- 239000002245 particle Substances 0.000 claims abstract description 5
- 229910001413 alkali metal ion Inorganic materials 0.000 claims abstract description 4
- -1 halide ions Chemical class 0.000 claims abstract description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 abstract description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 3
- 229910052593 corundum Inorganic materials 0.000 abstract 3
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 3
- 229910001508 alkali metal halide Inorganic materials 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 239000012778 molding material Substances 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 238000002156 mixing Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000004065 semiconductor Substances 0.000 description 6
- 230000017525 heat dissipation Effects 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 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 4
- 238000001721 transfer moulding Methods 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229910002026 crystalline silica Inorganic materials 0.000 description 3
- 239000006082 mold release agent Chemical class 0.000 description 3
- 239000010680 novolac-type phenolic resin Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 239000005350 fused silica glass Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- QSSXJPIWXQTSIX-UHFFFAOYSA-N 1-bromo-2-methylbenzene Chemical compound CC1=CC=CC=C1Br QSSXJPIWXQTSIX-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 125000000113 cyclohexyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- CAYGQBVSOZLICD-UHFFFAOYSA-N hexabromobenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1Br CAYGQBVSOZLICD-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000004843 novolac epoxy resin Substances 0.000 description 1
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 125000005480 straight-chain fatty acid group Chemical class 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
Abstract
Description
【発明の詳細な説明】
[発明の目的]
(産業上の利用分野)
本発明は、熱膨張係数が小さく、熱伝導率が大きく、し
かも成形性・耐湿性に優れた特性バランスのよい封止用
樹脂組成物に関する。[Detailed Description of the Invention] [Objective of the Invention] (Industrial Application Field) The present invention provides a well-balanced seal with a low coefficient of thermal expansion, high thermal conductivity, and excellent moldability and moisture resistance. The present invention relates to a resin composition for use.
(従来の技術)
従来から、ダイオード、トランジスタ、集積回路等の電
子部品を熱硬化性樹脂を用いて樹脂封止する方法が行わ
れてきた。 この樹脂封止は、ガラス、金属、セラミッ
クを用いたハーメチックシール方式に比較して経済的に
有利なため、広く実用化されている。 封止用樹脂とし
ては、熱硬化性樹脂の中でも信頼性および価格の点から
エポキシ樹脂が最も一般的に用いられている。 エポキ
シ樹脂には、酸無水物、芳香族アミン、ノボラック型フ
ェノール樹脂等の硬化剤が用いられている。(Prior Art) Conventionally, methods have been used to resin-seal electronic components such as diodes, transistors, and integrated circuits using thermosetting resins. This resin sealing is economically advantageous compared to hermetic sealing methods using glass, metal, or ceramic, and is therefore widely put into practical use. Among thermosetting resins, epoxy resin is most commonly used as the sealing resin in terms of reliability and cost. For epoxy resins, curing agents such as acid anhydrides, aromatic amines, and novolac-type phenolic resins are used.
これらの中でもノボラック型フェノール樹脂を硬化剤と
したエポキシ樹脂は、他の硬化剤を使用したものに比べ
て成形性、耐湿性に優れ、毒性がなく、かつ安価である
ため半導体封止用樹脂として広く使用されている。 ま
た充填剤としては、溶融シリカ粉末や結晶性シリカ粉末
が前記の硬化剤と共に最も一般的に使用されている。
近年、半導体部品の高密度化、大電力化に伴い熱放散性
の良い半導体封止用樹脂が要望されてきた。Among these, epoxy resins that use novolak type phenolic resin as a curing agent are preferred as resins for semiconductor encapsulation because they have superior moldability and moisture resistance, are nontoxic, and are inexpensive compared to those that use other curing agents. Widely used. As the filler, fused silica powder and crystalline silica powder are most commonly used together with the above-mentioned curing agent.
In recent years, with the increasing density and power consumption of semiconductor components, there has been a demand for semiconductor encapsulation resins with good heat dissipation properties.
(発明が解決しようとする課題)
しかしながら、ノボラック型フェノール樹脂を硬化剤と
したエポキシ樹脂と溶融シリカ粉末からなる樹脂組成物
は、熱膨脂係数が小さく、耐湿性がよく、従って温寒サ
イクル試験によるボンディングワイヤのオープン、樹脂
クラック、ベレットクラック等に優れているという特徴
を有するものの、熱伝導率が小さいなめ熱放散が悪く、
消費電力の大きいパワー半導体ではその機能が果せなく
なる欠点がある。 一方、ノボラック型フェノール樹脂
を硬化剤としたエポキシ樹脂と、結晶性シリカ粉末とか
らなる樹脂組成物は、結晶性シリカ粉末の配合割合を上
げると熱伝導率が大きくなっで、熱放散も良好となるが
、熱膨脂係数が大きく、また耐湿性に対する信頼性も悪
くなる欠点がある。(Problem to be Solved by the Invention) However, a resin composition consisting of an epoxy resin using a novolak type phenol resin as a curing agent and fused silica powder has a small coefficient of thermal expansion and good moisture resistance, and therefore has a low coefficient of thermal expansion and good moisture resistance. Although it has the characteristics of being excellent in preventing bonding wire opens, resin cracks, bullet cracks, etc., it has low thermal conductivity and poor heat dissipation.
Power semiconductors with high power consumption have the disadvantage that they cannot perform their functions. On the other hand, in a resin composition consisting of an epoxy resin using a novolak type phenol resin as a curing agent and crystalline silica powder, increasing the blending ratio of crystalline silica powder increases the thermal conductivity and improves heat dissipation. However, it has the drawbacks of a large coefficient of thermal expansion and poor reliability in moisture resistance.
更に、この樹脂組成物から得られる成形品は、機械的特
性や成形性が低下する傾向がある。 従ってシリカ粉末
を用いる封止用樹脂組成物の高熱伝導化にはおのずから
限界があった。Furthermore, molded articles obtained from this resin composition tend to have poor mechanical properties and moldability. Therefore, there is a natural limit to the ability to increase the thermal conductivity of a sealing resin composition using silica powder.
本発明は、上記の欠点を解消するためになされたもので
、熱伝導率が大きく、熱膨脂係数が小さく、熱放散性、
成形性に優れた、耐湿性に対する信頼性の高い、特性バ
ランスのよい封止用樹脂組成物を提供しようとするもの
である。The present invention was made to eliminate the above-mentioned drawbacks, and has high thermal conductivity, low thermal expansion coefficient, heat dissipation,
The present invention aims to provide a sealing resin composition with excellent moldability, high reliability in moisture resistance, and well-balanced properties.
[発明の構成]
(課題を解決するための手段)
本発明者らは、上記の目的を達成すべく鋭意研究を重ね
た結果、特定の酸化アルミニウム粉末を配合すると熱膨
脂係数が小さく、熱伝導率が大きく、耐湿性、成形性に
優れるなど上記目的を達成することができることを見い
だし、本発明を完成したものである。[Structure of the Invention] (Means for Solving the Problems) As a result of intensive research to achieve the above object, the inventors of the present invention have found that when a specific aluminum oxide powder is blended, the coefficient of thermal expansion is small, and the coefficient of thermal expansion is low. The present invention was completed based on the discovery that the above objects can be achieved by having high conductivity, excellent moisture resistance, and moldability.
すなわち、本発明は、
(A)エポキシ樹脂
(B)ノボラック型フェノール樹脂
(C)酸化アルミニウム粉末
を必須成分とし、前記(C)酸化アルミニウム粉末は、
その平均粒子径が250μl以下の細径で、その長短径
比が1.0〜1.4の球状体で、121℃。That is, the present invention includes (A) an epoxy resin, (B) a novolak type phenol resin, and (C) an aluminum oxide powder as an essential component, and the (C) aluminum oxide powder has the following components:
A spherical body with an average particle size of 250 μl or less and a ratio of major to minor axis of 1.0 to 1.4, at 121°C.
2気圧、100%RH下で抽出されるアルカリ金属イオ
ン及びハロゲンイオン含有量が10ppm以下のもので
あり、またその配合量が全体の樹脂組成物に対して25
〜90重量%の割合であることを特徴とする封止用樹脂
組成物である。The content of alkali metal ions and halogen ions extracted under 2 atmospheres and 100% RH is 10 ppm or less, and the blending amount is 25 ppm or less with respect to the entire resin composition.
This is a sealing resin composition characterized in that the proportion is 90% by weight.
本発明に用いる(A)エポキシ樹脂は、その分子中にエ
ポキシ基を少なくとも2個有する化合物であるかぎり、
分子構造、分子量等に特に制限はなく、一般に使用され
ているものを広く包含することができる。 例えばビス
フェノール型の芳香族、シクロヘキサン誘導体等の脂環
族系、さらに次の一般式で示されるエポキシノボラック
系等のエポキシ樹脂が挙げられる。As long as the epoxy resin (A) used in the present invention is a compound having at least two epoxy groups in its molecule,
There are no particular limitations on the molecular structure, molecular weight, etc., and a wide range of commonly used ones can be included. Examples include aromatic resins such as bisphenol, alicyclic resins such as cyclohexane derivatives, and epoxy resins such as epoxy novolac resins represented by the following general formula.
(但し、式中R1は水素原子、ハロゲン原子又はアルキ
ル基を、R2は水素原子又はアルキル基を、口は1以上
の整数を表す)これらのエポキシ樹脂は単独又は2種以
上混合して用いることができる。(However, in the formula, R1 represents a hydrogen atom, a halogen atom, or an alkyl group, R2 represents a hydrogen atom or an alkyl group, and the number represents an integer of 1 or more.) These epoxy resins may be used alone or in a mixture of two or more. I can do it.
本発明に用いる(B)ノボラック型フェノール樹脂とし
ては、フェノール、アルキルフェノール等のフェノール
類とホルムアルデヒドあるいはパラホルムアルデヒドを
反応させて得られるノボラック型フェノール樹脂および
これらの変性樹脂、例えばエポキシ化もしくはブチル化
ノボラック型フェノール樹脂等が挙げられ、これらは単
独又は2種以上混合して使用する。 ノボラック型フェ
ノール樹脂の配合割合は、前述したエポキシ樹脂のエポ
キシ基(a )とノボラック型フェノール樹脂のフェノ
ール性水酸基(b )とのモル比[(a)/(b)]が
0.1〜10の範囲内であることが望ましい、 モル比
が0゜1未満もしくは10を超えると耐湿性、成形作業
性および硬化物の電気特性が悪くなりいずれの場合も好
ましくない。The (B) novolak type phenolic resin used in the present invention includes novolak type phenol resins obtained by reacting phenols such as phenol and alkylphenols with formaldehyde or paraformaldehyde, and modified resins thereof, such as epoxidized or butylated novolak types. Examples include phenol resins, which may be used alone or in combination of two or more. The blending ratio of the novolac type phenolic resin is such that the molar ratio [(a)/(b)] between the epoxy group (a) of the epoxy resin described above and the phenolic hydroxyl group (b) of the novolac type phenol resin is 0.1 to 10. If the molar ratio is less than 0.1 or more than 10, the moisture resistance, molding workability, and electrical properties of the cured product will deteriorate, which is undesirable.
本発明に用いる(C)酸化アルミニウム粉末としては、
次の条件をもっているものであれば特に制限はなく広く
使用できる。 まず、酸化アルミニウム粉末の平均粒子
径は250μm以下の細径で、長短径比が1,0〜1,
4の球状体であることが好ましい、 平均粒子径が25
0μlを超えて粗い場合は成形時にゲート詰まりやワイ
ヤー流れが生じて好ましくない。 また長短径比が1.
4を超えると流動特性が低下し、また金型摩耗等が生じ
て好ましくない、 第二に、酸化アルミニウム粉末は、
121℃、2気圧、100%RH下で抽出されるアルカ
リ金属イオン及びハロゲンイオンの含量が該粉末絶乾重
量に対して10 fil)TI以下であることが好まし
い。 10ppn+を超えると半導体素子の信頼性を低
下させ好ましくない、 かかる酸化アルミニウム粉末と
しで、例えばAs−20、As−40(昭和電工社製、
商品名)等が挙げ゛られ、これらは晒独又は2種以上混
合して使用することができる。 酸化アルミニウム粉末
の配合割合は、全体の樹脂組成物に対して25〜90重
1%含有することが好ましい。 配合割合が25重量%
未満では熱膨脂係数が大きく、熱伝導率が小さく、好ま
しくない、 また90重量%を超えるとがさばりが大き
く、成形性も悪く実用に適さない、 従ってこの範囲に
限定される。As the aluminum oxide powder (C) used in the present invention,
It can be widely used without any particular restrictions as long as it meets the following conditions. First, the average particle diameter of the aluminum oxide powder is 250 μm or less, and the length ratio is 1.0 to 1.
Preferably, it is a spherical body with an average particle diameter of 25.
If it exceeds 0 μl and is coarse, gate clogging or wire flow may occur during molding, which is undesirable. Also, the length/breadth axis ratio is 1.
If it exceeds 4, the flow characteristics will deteriorate and mold wear will occur, which is undesirable.Secondly, aluminum oxide powder is
It is preferable that the content of alkali metal ions and halogen ions extracted under 121° C., 2 atm, and 100% RH is 10 fil)TI or less based on the bone dry weight of the powder. Exceeding 10 ppn+ is undesirable because it reduces the reliability of semiconductor devices. Examples of such aluminum oxide powder include As-20, As-40 (manufactured by Showa Denko Co., Ltd.,
(trade name), etc., and these can be used alone or in combination of two or more kinds. The blending ratio of aluminum oxide powder is preferably 25 to 90% by weight based on the entire resin composition. Blending ratio is 25% by weight
If it is less than 90% by weight, the coefficient of thermal expansion will be large and the thermal conductivity will be low, which is undesirable. If it exceeds 90% by weight, it will be bulky and have poor moldability, making it unsuitable for practical use. Therefore, it is limited to this range.
本発明の封止用樹脂組成物は、エポキシ樹脂、ノボラッ
ク型フェノール樹脂、酸化アルミニウム粉末を必須成分
とするが、本発明の目的に反しない限度においで、必要
に応じで、例えば天然ワックス類、合成ワックス類、直
鎖脂肪酸の金属塩、酸アミド類、エステル類、パラフィ
ン類等の離型剤、塩素化パラヒイン、ブロムトルエン、
ヘキサブロムベンゼン、三酸化アンチモン等の難燃剤、
カーボンブラック、ベンガラ等の着色剤、カップリング
剤、種々の硬化促進剤などを適宜添加配合することがで
きる。The sealing resin composition of the present invention contains an epoxy resin, a novolac type phenol resin, and an aluminum oxide powder as essential components, but may optionally contain natural waxes, for example, as long as it does not contradict the purpose of the present invention. Synthetic waxes, metal salts of straight chain fatty acids, acid amides, esters, mold release agents such as paraffins, chlorinated parahynes, bromotoluene,
Flame retardants such as hexabromobenzene and antimony trioxide,
Coloring agents such as carbon black and red iron oxide, coupling agents, various curing accelerators, and the like can be appropriately added and blended.
本発明の封止用樹脂組成物を成形材料として製造する場
合の一般的な方法としては、エポキシ樹脂、ノボラック
型フェノール樹脂、酸化アルミニウム粉末、その他を所
定の組成比に選択した原料組成分をミキサー等によって
十分均一に混合した後、更に熱ロールによる溶融混合処
理、又はニーダ等による混合処理を行い、次いで冷却固
化させ、適当な大きさに粉砕して成形材料とすることが
できる。 こうして得た成形材料は、電子部品或いは電
気部品の封止用としで、また被覆、絶縁等に適用すれば
優れた特性と信頼性を付与することができる。A general method for manufacturing the sealing resin composition of the present invention as a molding material is to mix raw materials selected at predetermined composition ratios, such as epoxy resin, novolac type phenolic resin, aluminum oxide powder, etc. After sufficiently uniformly mixing the mixture using a heating roller or the like, the mixture can be further melt-mixed using a hot roll or mixed using a kneader, etc., and then cooled to solidify and pulverized to an appropriate size to form a molding material. The molding material thus obtained can be used for sealing electronic or electrical parts, and can provide excellent properties and reliability when applied to coatings, insulation, etc.
(実施例)
次に、本発明を実施例によって具体的に説明するが、本
発明はこれらの実施例によって限定されるものではない
。 以下の実施例および比較例において「%」とあるの
は「重量%」を意味する。(Examples) Next, the present invention will be specifically explained by examples, but the present invention is not limited by these examples. In the following Examples and Comparative Examples, "%" means "% by weight".
実施例 1
クレゾールノボラックエポキシ樹脂(エポキシ当J12
15) 18%にノボラック型フェノール樹脂(フェノ
ール当量104) 9%、第1表の特性の酸化アルミ
ニウム70%、離型剤等3%を常温で混合し、更に90
〜95℃で混練してこれを冷却後粉砕し、成形材料を製
造した。Example 1 Cresol novolak epoxy resin (epoxy J12
15) Mix 18% with 9% novolac type phenol resin (phenol equivalent: 104), 70% aluminum oxide with the properties shown in Table 1, and 3% mold release agent, etc. at room temperature, and then add 90%
The mixture was kneaded at ~95°C, cooled, and then pulverized to produce a molding material.
実施例 2
クレゾールノボラックエポキシ樹脂(エポキシ当量21
5) 10%に、ノボラック型フェノール樹脂(フェノ
ール当量104) 5%、第1表の特性の酸化アルミ
ニウム粉末82%、離型剤等3%を実施例1と同様にし
て成形材料を製造した。Example 2 Cresol novolac epoxy resin (epoxy equivalent weight 21
5) A molding material was produced in the same manner as in Example 1, adding 10%, 5% novolac type phenol resin (phenol equivalent: 104), 82% aluminum oxide powder having the characteristics shown in Table 1, and 3% mold release agent.
比較例 1
実施例1においで、第1表に示した酸化アルミニウム粉
末を用いた以外はすべて実施例1と同一にして成形材料
を製造した。Comparative Example 1 A molding material was produced in the same manner as in Example 1 except that the aluminum oxide powder shown in Table 1 was used.
比較例 2
実施例2においで、第1表に示した酸化アルミニウム粉
末を用いた以外はすべて実施例1と同一にして成形材料
を製造した。Comparative Example 2 A molding material was produced in the same manner as in Example 1 except that the aluminum oxide powder shown in Table 1 was used.
実施例1〜2および比較例1〜2において製造した成形
材料をタブレット化し、予熱しで、トランスファー成形
により 170’Cに加熱した金型内に注入し硬化させ
で、封止した成形品を得た。 得られた成形品について
熱伝導率、耐湿性を試験し、また成形材料について成形
性、金型摩耗の試験を行い、結果を得たので第1表に示
したが、本発明の効果が確認された。The molding materials produced in Examples 1 and 2 and Comparative Examples 1 and 2 were tabletted, preheated, and injected into a mold heated to 170°C by transfer molding and cured to obtain a sealed molded product. Ta. The obtained molded product was tested for thermal conductivity and moisture resistance, and the molding material was tested for moldability and mold wear.The results are shown in Table 1 and confirm the effectiveness of the present invention. It was done.
*1 :成形品を迅速熱伝導計(昭和電工社製、商品名
QTM−MD)を用いて室温下で測定した。*1: The molded product was measured at room temperature using a rapid thermal conductivity meter (manufactured by Showa Denko, trade name QTM-MD).
ネ2:成形材料を用いて2本のアルミニウム配線を有す
る電気部品を170℃で3分間トランスファー成形し、
その後180℃で8時間後硬化させた。 こうして得た
成形品(封止品)100個についで、120℃の高圧水
蒸気中で耐湿試験を行い、アルミニウム腐食による50
%個数の断線(不良発生)の起る時間を評価した。Ne2: Transfer molding an electrical component with two aluminum wirings at 170°C for 3 minutes using the molding material,
Thereafter, it was post-cured at 180°C for 8 hours. 100 molded products (sealed products) obtained in this way were subjected to a moisture resistance test in high-pressure steam at 120°C.
The time required for wire breakage (occurrence of defects) in % number was evaluated.
*3:入れ子をA1入れ子に置換した金型を用いて 1
70℃でトランスファー成形し、100シヨツト後のA
1の入れ子の摩耗量を測定した。*3: Using a mold in which the nest was replaced with an A1 nest 1
A after transfer molding at 70℃ and 100 shots
The amount of wear on the insert No. 1 was measured.
*4:120−1(ヤビティ取り16ピンDIP金型を
用いで、170℃で3分間トランスファー成形しその充
填性を評価した。 O印は良好。*4: 120-1 (transfer molding was performed at 170° C. for 3 minutes using a 16-pin DIP mold with a groove and the filling property was evaluated. O mark indicates good quality.
X印は不良
U発明の効果]
以上の説明および第1表から明らかなように、本発明の
封止用樹脂組成物は、熱伝導率が大きく、熱膨脂係数が
小さく、熱放散性がよいため消費電力の大きい等のパワ
ー半導体機器に使用して特に効果がある。 また、耐湿
性に優れているため、温寒サイクル試験のボンディング
ワイヤのオープン、樹脂クラック、ペレットクラック等
がなく、成形性に優れている等特性バランスが良く、電
子・電気部品の封止用に用いると十分な信頼性を付与す
ることができる。As is clear from the above explanation and Table 1, the sealing resin composition of the present invention has a high thermal conductivity, a low coefficient of thermal expansion, and a low heat dissipation property. Therefore, it is particularly effective when used in power semiconductor equipment that consumes a large amount of power. In addition, due to its excellent moisture resistance, there are no open bonding wires, resin cracks, pellet cracks, etc. in hot and cold cycle tests, and it has a good balance of properties such as excellent moldability, making it suitable for sealing electronic and electrical parts. If used, sufficient reliability can be imparted.
Claims (1)
その平均粒子径が250μm以下の細径で、その長短径
比が1.0〜1.4の球状体で、121℃、2気圧、1
00%RH下で抽出されるアルカリ金属イオン及びハロ
ゲンイオンの含有量が10ppm以下のものであり、ま
たその配合量が全体の樹脂組成物に対して25〜90重
量%の割合であることを特徴とする封止用樹脂組成物。[Scope of Claims] 1 (A) an epoxy resin, (B) a novolak type phenol resin, and (C) an aluminum oxide powder as essential components, the aluminum oxide powder (C) comprising:
It is a spherical body with an average particle size of 250 μm or less and a ratio of major to minor axis of 1.0 to 1.4.
The content of alkali metal ions and halogen ions extracted under 00% RH is 10 ppm or less, and the amount thereof is 25 to 90% by weight based on the entire resin composition. A sealing resin composition.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16932688A JPH0220547A (en) | 1988-07-07 | 1988-07-07 | Sealing resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16932688A JPH0220547A (en) | 1988-07-07 | 1988-07-07 | Sealing resin composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0220547A true JPH0220547A (en) | 1990-01-24 |
Family
ID=15884474
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16932688A Pending JPH0220547A (en) | 1988-07-07 | 1988-07-07 | Sealing resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0220547A (en) |
-
1988
- 1988-07-07 JP JP16932688A patent/JPH0220547A/en active Pending
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