JPH0214237A - Resin composition for sealing - Google Patents
Resin composition for sealingInfo
- Publication number
- JPH0214237A JPH0214237A JP16328588A JP16328588A JPH0214237A JP H0214237 A JPH0214237 A JP H0214237A JP 16328588 A JP16328588 A JP 16328588A JP 16328588 A JP16328588 A JP 16328588A JP H0214237 A JPH0214237 A JP H0214237A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- sealing
- epoxy
- resin composition
- thermoplastic elastomer
- 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 18
- 239000003822 epoxy resin Substances 0.000 claims abstract description 17
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 17
- 229920003986 novolac Polymers 0.000 claims abstract description 14
- 239000005011 phenolic resin Substances 0.000 claims abstract description 12
- 229920003187 saturated thermoplastic elastomer Polymers 0.000 claims abstract description 11
- 239000011256 inorganic filler Substances 0.000 claims abstract description 10
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229920001568 phenolic resin Polymers 0.000 claims abstract description 7
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000003700 epoxy group Chemical group 0.000 claims abstract description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 229920005989 resin Polymers 0.000 abstract description 17
- 239000011347 resin Substances 0.000 abstract description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 11
- 239000000203 mixture Substances 0.000 abstract description 9
- 238000002156 mixing Methods 0.000 abstract description 7
- 239000000843 powder Substances 0.000 abstract description 6
- 239000000377 silicon dioxide Substances 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 3
- 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 abstract description 2
- 229930003836 cresol Natural products 0.000 abstract description 2
- 238000001816 cooling Methods 0.000 abstract 1
- 239000008240 homogeneous mixture Substances 0.000 abstract 1
- 238000002844 melting Methods 0.000 abstract 1
- 230000008018 melting Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 239000012778 molding material Substances 0.000 description 8
- 239000010680 novolac-type phenolic resin Substances 0.000 description 6
- 239000001993 wax Substances 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- 239000006087 Silane Coupling Agent Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000694 effects 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
- 239000004065 semiconductor Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- QEZIKGQWAWNWIR-UHFFFAOYSA-N antimony(3+) antimony(5+) oxygen(2-) Chemical compound [O--].[O--].[O--].[O--].[Sb+3].[Sb+5] QEZIKGQWAWNWIR-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000002148 esters Chemical class 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
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- QSSXJPIWXQTSIX-UHFFFAOYSA-N 1-bromo-2-methylbenzene Chemical compound CC1=CC=CC=C1Br QSSXJPIWXQTSIX-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 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
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 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
- 238000005538 encapsulation Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 125000005843 halogen group Chemical group 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
- 230000010354 integration Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 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
- 150000002989 phenols Chemical class 0.000 description 1
- 230000008092 positive effect Effects 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
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 125000005480 straight-chain fatty acid group Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Sealing Material Composition (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、低応力で耐クラツク性に優れた電子・電気部
品の封止等に用いる封止用樹脂組成物に関する。DETAILED DESCRIPTION OF THE INVENTION OBJECTS OF THE INVENTION (Industrial Field of Application) The present invention relates to a sealing resin composition that is low stress and has excellent crack resistance and is used for sealing electronic and electrical components.
(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
であるため、広く実用化されている。 封止用樹脂とし
て使用される熱硬化性樹脂の中でも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。 これらの硬化剤の中でもノボラ
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、半導体封止材
料として広く用いられている。(Prior Art) Conventionally, methods have been used to 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 used as sealing resins, epoxy resins are most commonly used. Hardening agents such as acid anhydrides, aromatic amines, and novolak-type phenolic resins are used in epoxy resins. Among these hardening agents, epoxy resins using novolac type phenolic resin as hardening agents are
Compared to materials using other curing agents, it has excellent moldability and moisture resistance, is non-toxic, and is inexpensive, so it is widely used as a semiconductor encapsulation material.
(発明が解決しようとする問題点)
近年、半導体、集積回路の分野において、素−tの高集
積化、ペレットの大形化が進んでおり、これまでのノボ
ラyり型フェノール樹脂を硬化剤としたエポキシ樹脂で
は、成形峻化時に収縮して半導体素子に応力がかかり、
信頼性に劣るという欠点がある。 こうした樹脂を使用
した成形品(封止品)の温寒サイクルテストを行うと、
ボンディングワイヤのオープン、樹脂クラック、ベレッ
トクラックが発生し、電子・電気部品としてのRe5が
果せなくなるという欠点があった。(Problems to be Solved by the Invention) In recent years, in the fields of semiconductors and integrated circuits, there has been an increase in the degree of integration of elements and the increase in the size of pellets. The epoxy resin used for this purpose shrinks during molding and puts stress on the semiconductor element.
The drawback is that it is less reliable. When performing hot and cold cycle tests on molded products (sealed products) using these resins,
There was a drawback that open bonding wires, resin cracks, and pellet cracks occurred, making it impossible to achieve Re5 as an electronic/electrical component.
本発明は、これらの欠点を解消するためになされたもの
で、低応力で耐クラツク性に優れたもので、半導体素子
等に応力がかからず、ワイヤーオープンやクラック発生
のない「コ頼性の高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 these drawbacks, and is low stress and has excellent crack resistance.It does not apply stress to semiconductor elements, etc., and has "reliability" that does not cause wire opens or cracks. The purpose of the present invention is to provide a sealing resin composition with a high
[発明の構成]
(問題点を解決するための手段)
本発明者らは、上記の目的を達成しようと鋭意研究を重
ねた結果、飽和型熱可塑性エラストマーを導入すること
により、成形硬化時の収縮が小さく、低応力で耐クラツ
ク性に優れた樹脂組成物が得られることを見いだし、本
発明を完成したものである。 即ち、本発明は、
(A>エポキシ樹脂、
([3)ノボラック型フェノール樹脂、(C)飽和型熱
可塑性エラストマーおよび(D)無機質充填剤
を必須成分とし、全体の樹脂組成物に対して、前記(C
)の飽和型熱可塑性エラストマーを0.1−5重I%、
また、前記(D)の無機質充填剤を25〜90@量%含
有することを特徴とする封止用樹脂組成物である。 そ
して、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エフェノール性水酸基(b)との当
量比[(a)/(b)]が0.1〜10の範囲内にある
封止用樹脂組成物である。[Structure of the Invention] (Means for Solving the Problems) As a result of intensive research aimed at achieving the above object, the present inventors have discovered that by introducing a saturated thermoplastic elastomer, the The present invention was completed based on the discovery that a resin composition with low shrinkage, low stress, and excellent crack resistance can be obtained. That is, the present invention includes (A>epoxy resin, ([3) novolak phenol resin, (C) saturated thermoplastic elastomer, and (D) inorganic filler] as essential components, and with respect to the entire resin composition, Said (C
) 0.1-5% by weight of saturated thermoplastic elastomer,
Moreover, it is a resin composition for sealing characterized by containing 25 to 90@% of the inorganic filler of the above (D). For sealing, the equivalent ratio [(a)/(b)] between the epoxy group (a) of the epoxy resin and the phephenolic hydroxyl group (b) of the novolac type phenolic resin is within the range of 0.1 to 10. It is a resin composition.
本発明に用いる(A)エポキシ樹脂としては、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限
り、分?梢逍、分子量など特に制限はなく、一般に封止
材料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系、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樹脂が挙げられる。As long as the epoxy resin (A) used in the present invention is a compound that has at least two epoxy groups in its molecule, There are no particular restrictions on the composition or molecular weight, and a wide range of materials commonly used for sealing materials can be included. Examples include aromatic resins such as bisphenol type, alicyclic resins such as cyclohexane derivatives, and epoxy novolak 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、nは1以上
の整数を表す)、 これらのエポキシ樹脂は、単独もし
くは2種以上混合して使用する。(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 n represents an integer of 1 or more.) These epoxy resins may be used alone or in combination of two or more. use.
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バ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グチル
化ノボラツクヤフェノール樹脂等が挙げられる。 そし
てこれらの樹脂は単独もしくは2種以上混合して使用す
る。The novolak phenol resin (B) used in the present invention includes novolak phenol resins obtained by reacting phenols such as phenol and alkylphenols with formaldehyde or paraformaldehyde, and modified resins thereof, such as epoxidized or gtylated resins. Examples include boratsuya phenol resin. These resins may be used alone or in combination of two or more.
ノボラック型フェノール樹脂の配合割合は、前記<A>
エポキシ樹脂のエポキシ%(a)と(13)ノボラック
型フェノール樹脂のフェノール性水酸基(b)との当量
比[(a)/(b)]が0.1〜10の範囲内にあるこ
とが望ましい、 この当量比が0.1未満又は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。 従って、上
記の範囲内に限定される。The blending ratio of the novolac type phenolic resin is as described above in <A>.
It is desirable that the equivalent ratio [(a)/(b)] between the epoxy % (a) of the epoxy resin and the phenolic hydroxyl group (b) of the (13) novolac type phenolic resin is within the range of 0.1 to 10. If this equivalent ratio is less than 0.1 or more than 10, the moisture resistance, molding workability, and electrical properties of the cured product will deteriorate, and either case is unfavorable. Therefore, it is limited within the above range.
本発明に用いる(C)飽和型熱可塑性エラストマーとし
ては、例えばタフデヅク(旭化成工業社製、商品名)等
が挙げられ、これらは単独もしくは2種以上混合して使
用する。 飽和型熱可塑性エラストマーの配合割合は、
全体の樹脂組成物に対して、0.1〜10重量%含有す
ることが好ましい。Examples of the saturated thermoplastic elastomer (C) used in the present invention include Tafdzuku (manufactured by Asahi Kasei Kogyo Co., Ltd., trade name), which may be used alone or in combination of two or more. The blending ratio of saturated thermoplastic elastomer is
The content is preferably 0.1 to 10% by weight based on the entire resin composition.
その割合が0.1重量%未満では低応力化に効果なく、
また10重1%を超えると増粘効果が著しくなり実用に
適さず好ましくない。If the proportion is less than 0.1% by weight, it will not be effective in reducing stress;
Moreover, if it exceeds 10% by weight, the thickening effect becomes significant, making it unsuitable for practical use.
本発明に用いる(DJ無機質充填剤としては、シリカ粉
末、アルミナ、二酸化アンチモン、タルク、炭酸カルシ
ウム、チタンホワイト、クレーマイカ、ベンガラ、ガラ
ス繊維、炭素繊維等が挙げられ、これらは単独又は2種
以上混合して使用する。 中でもシリカ粉末やアルミナ
が好ましく用いられる。 無機質充填剤の配合割合は、
全体の樹脂組成物に対して25〜90f!量%含有する
ことが望ましい、 その割合が25重凰%未満では、耐
湿性、INI熱性、機械的特性および成形性に効果なく
、また90重量%を超えるとカサバリが大きくなり成形
性か悪く実用に適さない。Examples of the DJ inorganic filler used in the present invention include silica powder, alumina, antimony dioxide, talc, calcium carbonate, titanium white, clay mica, red iron oxide, glass fiber, and carbon fiber, which may be used alone or in combination of two or more. Among them, silica powder and alumina are preferably used.The blending ratio of the inorganic filler is as follows:
25-90 f for the entire resin composition! If the proportion is less than 25% by weight, it will have no effect on moisture resistance, INI heat resistance, mechanical properties, and formability, and if it exceeds 90% by weight, the bulk will be large and the formability will be poor, making it impractical for practical use. Not suitable for
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、飽和型熱可塑性エラストマーおよ
び無機質充填剤を必須成分とするか、本発明の目的を損
なわない限り、必要に応じて、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、ニス
デル類、パラフィン類などの静型刑、塩素化パラフィン
、ブロムトルエン、ヘキサブロムベンゼン、二酸化アン
チモン等の難燃剤、カーボンブラック、ペン力う、など
の着色剤、シランカップリング剤、種々の硬化促進剤等
を適宜添加配合することができる。The sealing resin composition of the present invention may contain an epoxy resin, a novolak phenolic resin, a saturated thermoplastic elastomer, and an inorganic filler as essential components, or may contain, as necessary, e.g. natural waxes,
Static waxes such as synthetic waxes, metal salts of straight chain fatty acids, acid amides, Nisdels, paraffins, flame retardants such as chlorinated paraffins, bromotoluene, hexabromobenzene, antimony dioxide, carbon black, pen strength, Coloring agents such as, silane coupling agents, various curing accelerators, etc. can be added and blended as appropriate.
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
合の一般的方法は、エポキシ樹脂、)fcラック型ラフ
エノール樹脂飽和型熱可塑性エラストマー、無機質充填
剤その他所定の組成比に選択した原料成分をミキサー等
によってF分向−に混合した後、更に熱ロールによる溶
融混合処理、また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。 こうして得られた成形材料は電子部品あるいは
電気部品の封止、被覆、絶縁等に適用することができる
。A general method for producing the sealing resin composition of the present invention as a molding material consists of epoxy resin, FC lac type rough henol resin saturated thermoplastic elastomer, inorganic filler, and other raw materials selected in a predetermined composition ratio. After mixing in the F direction using a mixer or the like, the mixture is further melt-mixed using hot rolls or mixed using a kneader or the like, then cooled and solidified, and pulverized to an appropriate size to form a molding material. The molding material thus obtained can be applied to sealing, covering, insulating, etc. electronic or electrical components.
(作用)
本発明の封止用樹脂組成物において、飽和■1熱可塑性
エラストマーを配合することによって、樹脂組成物に柔
軟性を付与し、応力を緩和させて低応力をりえることが
できる。(Function) In the sealing resin composition of the present invention, by blending the saturated (1) thermoplastic elastomer, flexibility can be imparted to the resin composition and stress can be relaxed to reduce stress.
(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
明は以下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1%」とは1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 the following examples.
In the following Examples and Comparative Examples, "1%" means 1% by weight.
” means.
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t21
5) 18%に、ノボラック型フェノール樹脂(フェノ
ール当41107) 9%、タフチック111041
(旭化成工業社製、商品名)3%、溶融シリカ粉末69
%、硬化促進剤0.3%、エステル系ワックス0.3%
およびシランカップリング剤O14%を常温で混合し、
更に90〜95℃で混練して冷却した後、粉砕して成形
材料とした。 この成形材料を170℃に加熱した金型
内にトランスファー注入し、硬化させて成形品(封止品
)をつくった。Example 1 Cresol novolak epoxy resin (epoxy t21
5) 18%, novolac type phenolic resin (phenol 41107), 9%, Toughtic 111041
(manufactured by Asahi Kasei Industries, trade name) 3%, fused silica powder 69
%, curing accelerator 0.3%, ester wax 0.3%
and 14% silane coupling agent O are mixed at room temperature,
The mixture was further kneaded at 90 to 95°C, cooled, and then ground to obtain a molding material. This molding material was transfer-injected into a mold heated to 170° C. and cured to produce a molded product (sealed product).
この成形品について耐湿性、応力等に関連する緒特性を
試験し、その結果を第1表に示した。 本発明のHff
な効果が認められた。This molded article was tested for properties related to moisture resistance, stress, etc., and the results are shown in Table 1. Hff of the present invention
A positive effect was observed.
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) 18%、ノボラック型フェノール樹脂(フェノー
ル当11107) 9%、タフチックH1041旭化
成工業社製、商品名)1.5%、シリカ粉末69%、硬
化促進剤0.3%、ニスデル系ワックス0.3%および
シラン系カップリング剤0.4%を実施例1と同様に混
合、混練、粉砕して成形材料とした。 また同様にして
成形品を得て、成形品について実施例1と同様にして耐
湿性、応力等に関連する緒特性を試験し、その結果を第
1表に示した。 本発明の2Wな効果が認められた。Example 2 Cresol novolac epoxy resin (epoxy equivalent weight 21
5) 18%, novolac type phenol resin (phenol 11107) 9%, Toughtic H1041 manufactured by Asahi Kasei Kogyo Co., Ltd. (trade name) 1.5%, silica powder 69%, curing accelerator 0.3%, Nisdel wax 0. 3% of the silane coupling agent and 0.4% of the silane coupling agent were mixed, kneaded, and pulverized in the same manner as in Example 1 to obtain a molding material. A molded article was also obtained in the same manner, and the molded article was tested for moisture resistance, stress, and other related properties in the same manner as in Example 1, and the results are shown in Table 1. The 2W effect of the present invention was observed.
比較例
タレゾールノボラックエポキシ樹脂(エポキシ当量21
5) 20%に、ノボラック型フェノール樹脂(フェノ
ール当ji 107) 10%、シリカ粉末69%、硬
化促進剤0.3%、エステル系ワックス0.3%および
シラン系カップリング剤0,4%を実施例1と同様に混
合、混練、粉砕して成形材料とした。Comparative example Talesol novolak epoxy resin (epoxy equivalent: 21
5) To 20%, add 10% novolac type phenolic resin (phenol 107), 69% silica powder, 0.3% curing accelerator, 0.3% ester wax and 0.4% silane coupling agent. The mixture was mixed, kneaded, and crushed in the same manner as in Example 1 to obtain a molding material.
この成形材料を用いて成形品とし、成形品の緒特性につ
いて実施例1と同様に試験したので、その結果を第1表
に示した。This molding material was used to make a molded article, and the properties of the molded article were tested in the same manner as in Example 1. The results are shown in Table 1.
第
表
(単位)
クラック数は30X 25X 5111の成形品の底面
に25x 25x 31覆の銅板を埋め込み、−40℃
とモ200℃の恒温槽に各30分間ずつ入れ、15サイ
クル繰り返した後の樹脂クラックを調査した。Table (Units) The number of cracks is 30x 25x A copper plate of 25x 25x 31 is embedded in the bottom of a 5111 molded product, and the temperature is -40℃.
The resin was placed in a constant temperature bath at 200° C. for 30 minutes each, and cracks in the resin were investigated after 15 cycles were repeated.
*2 :1)IP16ピンリードフレームのアイランド
部に市販のストレインゲージを接着し、180℃で、8
時間硬化させた後の歪を測定しな。*2:1) Glue a commercially available strain gauge to the island part of the IP16-pin lead frame, and
Measure the strain after time curing.
[発明の効果1
以上の説明および第1表からも明らかなように、本発明
の封止用樹脂組成物は、低応力で耐クラツク性に優れて
いるため、ボンディングワイヤーのオープンや樹脂クラ
ック、ペレットクラックの発生がなく、かつ硬化時の収
縮による応力が低い。[Effect of the invention 1] As is clear from the above explanation and Table 1, the sealing resin composition of the present invention has low stress and excellent crack resistance, so it does not cause open bonding wires, resin cracks, No pellet cracks occur, and stress caused by shrinkage during curing is low.
従ってこの樹脂組成物を使用することによって信顆性の
高い、電子・電気部品を得ることができる。Therefore, by using this resin composition, electronic/electrical parts with high reliability can be obtained.
Claims (1)
の飽和型熱可塑性エラストマーを0.1〜5重量%、ま
た前記(D)の無機質充填剤を25〜90重量%含有す
ることを特徴とする封止用樹脂組成物。 2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)との当量比[(
a)/(b)]が0.1〜10の範囲内にある特許請求
の範囲第1項記載の封止用樹脂組成物。[Scope of Claims] 1 (A) an epoxy resin, (B) a novolak type phenolic resin, (C) a saturated thermoplastic elastomer, and (D) an inorganic filler are essential components, and the above-mentioned components are added to the entire resin composition. (C)
A sealing resin composition comprising 0.1 to 5% by weight of the saturated thermoplastic elastomer and 25 to 90% by weight of the inorganic filler (D). 2 Equivalent ratio of the epoxy group (a) of the epoxy resin to the phenolic hydroxyl group (b) of the novolak type phenolic resin [(
a)/(b)] is within the range of 0.1 to 10.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16328588A JPH0214237A (en) | 1988-06-30 | 1988-06-30 | Resin composition for sealing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16328588A JPH0214237A (en) | 1988-06-30 | 1988-06-30 | Resin composition for sealing |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0214237A true JPH0214237A (en) | 1990-01-18 |
Family
ID=15770913
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16328588A Pending JPH0214237A (en) | 1988-06-30 | 1988-06-30 | Resin composition for sealing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0214237A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7647682B2 (en) * | 2004-06-17 | 2010-01-19 | Adams Marve D | Motor mount repair system and methods therefor |
-
1988
- 1988-06-30 JP JP16328588A patent/JPH0214237A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7647682B2 (en) * | 2004-06-17 | 2010-01-19 | Adams Marve D | Motor mount repair system and methods therefor |
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