JPS63132435A - Semiconductor element - Google Patents
Semiconductor elementInfo
- Publication number
- JPS63132435A JPS63132435A JP27785786A JP27785786A JPS63132435A JP S63132435 A JPS63132435 A JP S63132435A JP 27785786 A JP27785786 A JP 27785786A JP 27785786 A JP27785786 A JP 27785786A JP S63132435 A JPS63132435 A JP S63132435A
- Authority
- JP
- Japan
- Prior art keywords
- chips
- group
- semiconductor element
- tetraglycidylamine
- represented
- 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.)
- Granted
Links
- 239000004065 semiconductor Substances 0.000 title claims abstract description 22
- 239000000843 powder Substances 0.000 claims abstract description 10
- 239000000853 adhesive Substances 0.000 claims description 21
- 230000001070 adhesive effect Effects 0.000 claims description 21
- 239000003822 epoxy resin Substances 0.000 claims description 12
- 229920000647 polyepoxide Polymers 0.000 claims description 12
- 125000002723 alicyclic group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims 2
- 230000002950 deficient Effects 0.000 abstract description 11
- 238000000034 method Methods 0.000 abstract description 2
- 239000007767 bonding agent Substances 0.000 abstract 3
- 238000001723 curing Methods 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000003990 capacitor Substances 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 4
- 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 3
- 230000000694 effects Effects 0.000 description 3
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 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
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- UALAKBZSBJIXBP-UHFFFAOYSA-N 1-phenylethane-1,1,2,2-tetrol Chemical compound OC(O)C(O)(O)C1=CC=CC=C1 UALAKBZSBJIXBP-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- OECTYKWYRCHAKR-UHFFFAOYSA-N 4-vinylcyclohexene dioxide Chemical compound C1OC1C1CC2OC2CC1 OECTYKWYRCHAKR-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 101100289792 Squirrel monkey polyomavirus large T gene Proteins 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
- 238000012937 correction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- VQCBHWLJZDBHOS-UHFFFAOYSA-N erbium(III) oxide Inorganic materials O=[Er]O[Er]=O VQCBHWLJZDBHOS-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L24/00—Arrangements for connecting or disconnecting semiconductor or solid-state bodies; Methods or apparatus related thereto
- H01L24/01—Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
- H01L24/26—Layer connectors, e.g. plate connectors, solder or adhesive layers; Manufacturing methods related thereto
- H01L24/28—Structure, shape, material or disposition of the layer connectors prior to the connecting process
- H01L24/29—Structure, shape, material or disposition of the layer connectors prior to the connecting process of an individual layer connector
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/30—Assembling printed circuits with electric components, e.g. with resistor
- H05K3/32—Assembling printed circuits with electric components, e.g. with resistor electrically connecting electric components or wires to printed circuits
- H05K3/321—Assembling printed circuits with electric components, e.g. with resistor electrically connecting electric components or wires to printed circuits by conductive adhesives
Landscapes
- Engineering & Computer Science (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Die Bonding (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、ハイブリッドIC等、コンデンサチップが接
看されている半導体素子であって、不良となったチップ
等を250℃程度の熱で簡11に取りはずし、良品チッ
プと交換することが可能な半導体素子に関する。Detailed Description of the Invention [Objective of the Invention] (Industrial Field of Application) The present invention relates to a semiconductor device such as a hybrid IC in which a capacitor chip is in contact with the semiconductor device, and a defective chip etc. is heated to 250°C. The present invention relates to a semiconductor element that can be easily removed with a moderate amount of heat and replaced with a non-defective chip.
(従来の技術)
ハイブリッドICは、1枚の基板上にIGチップやコン
デンサチップ等が、数個から多いもので数十個搭載され
ており、これらチップのうち1個でも不良になると、基
板そのものを不良としなければならず、大変に不軽済で
あった。 不良チップのみを交換し、基板不良をなくす
ことが必要となっている。(Prior art) A hybrid IC is equipped with several to dozens of IG chips, capacitor chips, etc. on one board, and if even one of these chips becomes defective, the board itself will be destroyed. had to be declared defective, which was extremely inconvenient. It is now necessary to replace only defective chips and eliminate board defects.
従来のハイブリッドIcでチップを接着するに用いられ
ているIC/LSIダイボンディング用の導電性接着剤
は、ボンディング温度を250〜350℃に設計してい
るため、一度チツブを接着固定すると、不良チップとな
ったチップをi++度加熱加熱除去ことが困難であった
。 また、1個の不良チップを除去するために基板全体
を300°C程度に加熱長時間さらずことは、他の半導
体素子等の信頼性に少なからず影響を与えるので問題と
なっていた。The conductive adhesive for IC/LSI die bonding that is used to bond chips with conventional hybrid ICs is designed to have a bonding temperature of 250 to 350°C, so once the chip is bonded and fixed, it may cause defective chips. It was difficult to remove the chip by heating it to i++ degrees. In addition, it has been a problem that the entire substrate is not heated to about 300° C. for a long period of time in order to remove one defective chip because it has a considerable effect on the reliability of other semiconductor elements.
(発明が解決しようとする問題点)
本発明は、上記の問題点を解決するためになされたしの
で、ICチップやコンデンサチップを低温、かつ短時間
に接着・固定ができ、200℃のボンディングに耐える
接着強度を有し、また接着したデツプが不良であるとわ
かった場合に250℃程度の加熱で簡(Iiに不良チッ
プを除去することが可能な半導体素子をfjP供しよう
とするものである。(Problems to be Solved by the Invention) The present invention was made in order to solve the above problems. The aim is to provide fjP with semiconductor elements that have adhesive strength that can withstand the be.
し発明の構成]
(問題tAを解決するための手段)
本発明者らは、上記の目的をj構成しようと鋭意rtl
l究を重ねた結果、後jホづ゛る組成の導電性接着剤を
使用すれば、ICチップやコンデサチップの接着固定が
低温、短時間で簡単にでき、かつ接着したチップを容易
に除去することが可能であることを見いだし、本5N明
を完成させたものである。[Structure of the Invention] (Means for Solving Problem tA) The present inventors have worked hard to achieve the above object.
As a result of repeated research, we have found that by using a conductive adhesive with the composition described below, IC chips and capacitor chips can be easily bonded and fixed at low temperatures in a short time, and the adhered chips can be easily removed. He discovered that it was possible to do this, and completed this book 5N Ming.
すなわら、本発明は、
(△)次の一般式で示されるテトラグリシジルアミン
(但し、式中Rは2価の脂肪族基、芳香a基、脂環族基
を表す)
(B)導電性粉末、又は必要により(C)エポキシ樹脂
を含む導電性接着剤を用いてなる半導体素子である。That is, the present invention provides: (△) Tetraglycidylamine represented by the following general formula (wherein R represents a divalent aliphatic group, aromatic a group, or alicyclic group) (B) Conductive This is a semiconductor element using a conductive adhesive containing a conductive powder or (C) an epoxy resin if necessary.
本弁明に用いる(A>テトラグリシジルアミンは、次の
一般式、
(但し、式中Rは2illbの脂肪1+X基、芳香族基
、脂環族基を表す)
で示されるものであればよく、耐熱性や作業性等導電性
接着剤の要求特性の必廿に応じてRは種々のものが使用
できる。 具体的な化合物としては、例えば、TETR
AD−C,TETRAD−D。The (A>tetraglycidylamine used in the present defense) may be one represented by the following general formula (wherein R represents a 2illb fatty 1+X group, an aromatic group, or an alicyclic group), Various types of R can be used depending on the required properties of the conductive adhesive, such as heat resistance and workability.Specific compounds include, for example, TETR.
AD-C, TETRAD-D.
丁El RAD−X、TETRAD−Y (三菱化成社
製、商品名)、Er2O3(油化シェルエポキシ社製、
商品名)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。Ding El RAD-X, TETRAD-Y (manufactured by Mitsubishi Kasei Co., Ltd., product name), Er2O3 (manufactured by Yuka Shell Epoxy Co., Ltd.,
(trade name), and these may be used alone or in combination of two or more.
本発明に用いる(C)エポキシ樹脂としては、すべての
種類のエポキシ樹脂を使用することが可能であるが、そ
の主体は、1分子中に2個以上のエポキシ基を有するポ
リエポキシ樹脂である。Although all types of epoxy resins can be used as the epoxy resin (C) used in the present invention, the main epoxy resins are polyepoxy resins having two or more epoxy groups in one molecule.
具体的にはビスフェノールA型、ハロゲン化ビスフェノ
ール型、レゾルシン型、ビスフェノールF型、ポリアル
コール・ポリグリコール型、ノボラック型、テトラヒド
ロキシフェニルエタン型、グリセリントリエーテル型、
ポリオレフィン型、エポキシ化大豆油、ジシクロペンタ
ジェンオキシド、ビニルシクロヘキセンジオキシド等が
挙げられ、これらは単独又は2種以上混合して用いる。Specifically, bisphenol A type, halogenated bisphenol type, resorcin type, bisphenol F type, polyalcohol/polyglycol type, novolak type, tetrahydroxyphenylethane type, glycerin triether type,
Examples include polyolefin type, epoxidized soybean oil, dicyclopentadiene oxide, vinylcyclohexene dioxide, etc., and these can be used alone or in combination of two or more.
本発明に用いる接着剤では、(Δ)のテトラグリシジル
アミン(第一発明)、又は(A)テトラグリシジルアミ
ンと(C)エポキシ樹脂(第二発明)をもって結合剤と
する。 通常の場合には(△)のテトラグリシジルアミ
ンのみで十分であるが、必要によって例えば導電性接着
剤としてそれほど耐熱性を要求されない場合には(A)
テトラグリシジルアミンに(C)エポキシ樹脂を配合し
て結合剤とする。 (A)テトラグリシジルアミンと
(C)エポキシ樹脂との配合ハ1合[(A):(C)コ
は、重量比で90:10〜10:90の範囲が好ましく
、より好ましくは70 : 30〜40:60の範囲内
である。 テトラグリシジルアミンの配合割合が10重
1a部未満では十分な熱時接希強度J3よび耐熱性が得
られず好ましくなく、また90重組部を超えると余りに
も反応が進み過ぎ、硬くてbろ(なる場合がある。 よ
って上記の範囲内に限定するのがよい。In the adhesive used in the present invention, (Δ) tetraglycidylamine (first invention) or (A) tetraglycidylamine and (C) epoxy resin (second invention) are used as a binder. In normal cases, only tetraglycidylamine (△) is sufficient, but if necessary, for example, when high heat resistance is not required as a conductive adhesive, (A)
Epoxy resin (C) is blended with tetraglycidylamine to form a binder. (A) Tetraglycidylamine and (C) epoxy resin are mixed together [(A):(C) is preferably in a weight ratio of 90:10 to 10:90, more preferably 70:30. ~40:60. If the blending ratio of tetraglycidylamine is less than 10 parts by weight and 1a parts, sufficient heat welding strength J3 and heat resistance cannot be obtained, which is undesirable.If it exceeds 90 parts by weight, the reaction proceeds too much and the product becomes hard and brittle. Therefore, it is better to limit it within the above range.
本発明に用いる(B)導電性粉末としては、フレーク状
、鱗片状などのものち使用されるが、特に球状あるいは
樹脂被覆された平均粒径10μm以下の銀、銅、ニッケ
ル等の金属粉末が好ましく使用される。 導電性粉末の
配合割合は、(A)テトラグリシジルアミン、又は(A
)テトラグリシジルアミンと(C)エポキシ樹脂とから
なる結合剤どの比で決められる。 導電性粉末と結合剤
の割合は、重量比で70 + 30〜90:10の範囲
内であることが好ましい。 導電性粉末が70未満では
十分な導電性が得られず、また90を超えると作業性や
接着強度が低下し、いずれの場合も好ましくない。The conductive powder (B) used in the present invention may be in the form of flakes or scales, but in particular, spherical or resin-coated metal powders such as silver, copper, and nickel with an average particle size of 10 μm or less are used. Preferably used. The blending ratio of the conductive powder is (A) tetraglycidylamine or (A)
) The ratio of the binder consisting of tetraglycidylamine and (C) epoxy resin is determined. The ratio of the conductive powder to the binder is preferably in the range of 70+30 to 90:10 by weight. When the conductive powder is less than 70, sufficient conductivity cannot be obtained, and when it exceeds 90, workability and adhesive strength are reduced, and both cases are unfavorable.
本発明に用いる導電性接着剤には、硬化触媒として、通
常の−a型エポキシ樹脂接着剤に用いるものをそのまま
使用することができ、例えばイミダゾール系、ジシアン
ジアミドーイミダゾール系等の触媒が使用される。In the conductive adhesive used in the present invention, as a curing catalyst, those used for ordinary -a type epoxy resin adhesives can be used as they are, for example, imidazole-based, dicyandiamide-imidazole-based, etc. catalysts are used. .
また粘度調整用として各種の溶剤を使用覆ることができ
、例えばブチルセロソルブ、エチルセロソルブ、ブブル
廿ロソルブアセテート、エチルセロソルブアセテ−1−
、ブチルカルピトールアビテートは2種以上混合して使
用する。 また無溶剤型にするには、液状低粘度のエポ
キシ樹脂を使用するか或いはエポキシモノマーを使用す
ることができる。In addition, various solvents can be used to adjust the viscosity, such as butyl cellosolve, ethyl cellosolve, bubyl cellosolve acetate, and ethyl cellosolve acetate.
, butyl carpitol abitate is used in combination of two or more types. In order to make it solvent-free, a liquid low-viscosity epoxy resin or an epoxy monomer can be used.
本発明に用いる導電性接着剤は、以上の各成分を配合し
、それを3本ロール等により均一に混練して容易に製)
古することができる。 こうして背られた導電性接着剤
を所定の場所にディスペンサー、スクリーン印刷、ビン
転写法等によって塗布した後、数秒から数時間後、コン
デンサチップ等を載せ、加熱硬化させて半導体素子をつ
くることができる。 この導電性接着剤は種々の硬化条
件で硬化させることが可能であるが、 150℃で30
分間あるいは120℃で90分間のA゛−ブン硬化、又
は200℃以上で数十秒のヒータブ[コック硬化が好ま
しい。The conductive adhesive used in the present invention can be easily produced by blending the above components and kneading them uniformly using three rolls, etc.)
It can be old. After applying the conductive adhesive to a predetermined location using a dispenser, screen printing, bottle transfer method, etc., a capacitor chip, etc. is placed on it after a few seconds to several hours, and it is heated and cured to create a semiconductor element. . This conductive adhesive can be cured under various curing conditions;
or oven curing for 90 minutes at 120°C, or heat tub curing for several tens of seconds at 200°C or higher (cock curing is preferred).
(実施例)
次に本発明゛を実施例によって説明するが、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。(Examples) Next, the present invention will be explained by examples, but the present invention is not limited by the following examples.
実施例 1〜5
第1表に示した各成分を3本ロールにより3回混練して
導電性接着剤を得た。 iqられた導電性接着剤を、ア
ルミニウム基板上に金メッキされたパッド部にディスペ
ンス塗布した後、4.5X 6.5mmのICチップ
と 1,8x 1,9m111のコンデンサチップを
マウン]へし、150°Cの温度で30分間加熱硬化さ
けて半導体素子を製造した。 この半導体素子に関して
ボンディングテスト、250℃でのチップ剥離性、接着
強度、耐湿性についてについて試験し、その結果を第1
表に示したが、いずれも本発明の題名な効果が認められ
た。Examples 1 to 5 Each component shown in Table 1 was kneaded three times using three rolls to obtain a conductive adhesive. After dispensing and applying the iq conductive adhesive to the gold-plated pads on the aluminum substrate, a 4.5 x 6.5 mm IC chip and a 1.8 x 1.9 m capacitor chip were mounted on the board. A semiconductor device was manufactured by heat curing at a temperature of °C for 30 minutes. This semiconductor device was tested for bonding, chip peelability at 250°C, adhesive strength, and moisture resistance, and the results were presented in the first
As shown in the table, the title effect of the present invention was observed in all cases.
比較例 1
実施例2において、テトラグリシジルアミン(TETR
AD−C)を除いた以外は、すべて実施例2と同一にし
て導電性接着剤、半導体素子を得て、実施例と同様な試
験を行ったので、その結果を第1表に示した。Comparative Example 1 In Example 2, tetraglycidylamine (TETR
A conductive adhesive and a semiconductor element were obtained in the same manner as in Example 2, except that AD-C) was removed, and the same tests as in Example were conducted, and the results are shown in Table 1.
比較例 2
市販のIC/LSIダイボンディング用導電性接着剤を
用いて実施例と同様な試験を行ったので、その結果を第
1表に示した。Comparative Example 2 A test similar to that of the example was conducted using a commercially available conductive adhesive for IC/LSI die bonding, and the results are shown in Table 1.
*1 :油化シエルエポギシ社製、商品名;に2 :三
菱化成社製、商品名
:l:3H油化シ1ル工ボキシ社製、商品名*4 :
200℃におけるICチップ300個のボンディン
グテストでチップハガレを起こしたチップの個数
*!i : 250℃のヒート盤上で20秒間敢′
?i後、4日/ C1112の力でチップが剥離できる
かを試験した。(チップスサイズは4゜5X6,511
m>#i 6: 4,5x 6,5mm1 Cチップ
の側面をプッシュプルゲージで水平に押した時の9つ断
強度を測定した〈実施例1〜5.比較例の硬化条Vトは
150℃×30分間、比較例2の硬化条件は200℃×
60分間である)。*1: Manufactured by Yuka Ciel Epogishi Co., Ltd., product name; Ni2: Manufactured by Mitsubishi Kasei Co., Ltd., product name: l: 3H Manufactured by Yuka Ciel Epogishi Co., Ltd., product name *4:
Number of chips that suffered chip peeling in a bonding test of 300 IC chips at 200℃*! i: Heat for 20 seconds on a heat board at 250℃
? After 4 days, a test was conducted to see if the chip could be peeled off with a force of C1112. (Chips size is 4゜5X6,511
m>#i 6: 4,5x 6,5mm1 The nine-piece breaking strength was measured when the side surface of the C chip was pushed horizontally with a push-pull gauge (Examples 1 to 5). The curing condition of Comparative Example was 150°C for 30 minutes, and the curing condition of Comparative Example 2 was 200°C.
(60 minutes).
:lニア;温度121℃、圧力2気圧の水熱気中におけ
る耐湿試験(PCT)、および温度120℃。: l Near; Humidity test (PCT) in hot water at a temperature of 121°C and a pressure of 2 atmospheres, and a temperature of 120°C.
圧力2気圧の水蒸気中で印加電圧直流15vを通電して
の耐湿試験(バイアス−PCT)を各半導体素子につい
て行い、評価した。A moisture resistance test (bias-PCT) was performed on each semiconductor element by applying an applied voltage of 15 V DC in water vapor at a pressure of 2 atmospheres, and the semiconductor elements were evaluated.
この試験に供した半導体素子数は、各々60個である。The number of semiconductor elements subjected to this test was 60 each.
評価の方法は、半導体素子を構成するアルミニウム電
極の腐蝕によるA−ブン、又はリークTi流が訂容伯の
50%以上への上置をもって、不良と判定した。As for the evaluation method, if the A-bun due to corrosion of the aluminum electrode constituting the semiconductor element or the leakage Ti flow exceeds 50% of the correction value, it is determined to be defective.
[ブを明の効果]
以上の説明および第1表の結果からも明らかなように、
本発明の半導体素子によれば、ICチップやコンデン争
ナチツブを低温、層時間ぐ筒中に接着でき、接着された
チップは200℃のワイヤボンディングに耐える接着強
tgを有し、一方不良チツブの交換時には250°C程
度の熱で容易に不良チップを除去できるものであるので
、半導体素子の歩留りa3」;びイ8頼性も高く、本発
明はT集的1lIll値の大きいものである。[Effect of bright light] As is clear from the above explanation and the results in Table 1,
According to the semiconductor device of the present invention, IC chips and capacitor chips can be bonded in a cylinder at low temperature and layer time, and the bonded chips have an adhesive strength tg that can withstand wire bonding at 200°C, while defective chips can be replaced. In some cases, defective chips can be easily removed with heat of about 250° C., so the yield rate and reliability of semiconductor devices are high, and the present invention has a large T aggregate value.
Claims (1)
、および ▲数式、化学式、表等があります▼ (但し、式中Rは2価の脂肪族基、芳香族基、脂環族基
を表す) (B)導電性粉末 を含む導電性接着剤を用いてなる半導体素子。 2(A)次の一般式で示されるテトラグリシジルアミン
及び ▲数式、化学式、表等があります▼ (但し、式中Rは2価の脂肪族基、 芳香族基、脂環族基を表す) (B)導電性粉末、および (C)エポキシ樹脂 を含む導電性接着剤を用いてなる半導体素子。 3(A)テトラグリシジルアミンと(C)エポキシ樹脂
との配合割合[(A)/(C)]が、重量比で90/1
0〜10/90の範囲内である特許請求の範囲第2項記
載の半導体素子。[Claims] 1(A) Tetraglycidylamine represented by the following general formula, and ▲numerical formulas, chemical formulas, tables, etc.▼ (However, in the formula, R is a divalent aliphatic group, an aromatic group, represents an alicyclic group) (B) A semiconductor element using a conductive adhesive containing conductive powder. 2(A) Tetraglycidylamine represented by the following general formula and ▲ Numerical formulas, chemical formulas, tables, etc. ▼ (However, in the formula, R represents a divalent aliphatic group, aromatic group, or alicyclic group) A semiconductor element using (B) a conductive powder and (C) a conductive adhesive containing an epoxy resin. 3. The blending ratio [(A)/(C)] of (A) tetraglycidylamine and (C) epoxy resin is 90/1 by weight.
3. The semiconductor device according to claim 2, wherein the semiconductor element is within the range of 0 to 10/90.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27785786A JPH0793331B2 (en) | 1986-11-22 | 1986-11-22 | Semiconductor element |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27785786A JPH0793331B2 (en) | 1986-11-22 | 1986-11-22 | Semiconductor element |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63132435A true JPS63132435A (en) | 1988-06-04 |
JPH0793331B2 JPH0793331B2 (en) | 1995-10-09 |
Family
ID=17589246
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27785786A Expired - Fee Related JPH0793331B2 (en) | 1986-11-22 | 1986-11-22 | Semiconductor element |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0793331B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04501635A (en) * | 1989-09-05 | 1992-03-19 | ヒューズ・エアクラフト・カンパニー | Remanufactured Repairable Epoxy Die Mount Adhesive |
JP2011237645A (en) * | 2010-05-11 | 2011-11-24 | Nitto Denko Corp | Resin composition for optical waveguide formation and optical waveguide using the same |
JP2016017148A (en) * | 2014-07-09 | 2016-02-01 | 三菱化学株式会社 | Epoxy compound, epoxy compound-containing composition and cured product |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060116865A1 (en) | 1999-09-17 | 2006-06-01 | Www.Uniscape.Com | E-services translation utilizing machine translation and translation memory |
US7983896B2 (en) | 2004-03-05 | 2011-07-19 | SDL Language Technology | In-context exact (ICE) matching |
US8521506B2 (en) | 2006-09-21 | 2013-08-27 | Sdl Plc | Computer-implemented method, computer software and apparatus for use in a translation system |
US9262403B2 (en) | 2009-03-02 | 2016-02-16 | Sdl Plc | Dynamic generation of auto-suggest dictionary for natural language translation |
GB2468278A (en) | 2009-03-02 | 2010-09-08 | Sdl Plc | Computer assisted natural language translation outputs selectable target text associated in bilingual corpus with input target text from partial translation |
US9128929B2 (en) | 2011-01-14 | 2015-09-08 | Sdl Language Technologies | Systems and methods for automatically estimating a translation time including preparation time in addition to the translation itself |
-
1986
- 1986-11-22 JP JP27785786A patent/JPH0793331B2/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04501635A (en) * | 1989-09-05 | 1992-03-19 | ヒューズ・エアクラフト・カンパニー | Remanufactured Repairable Epoxy Die Mount Adhesive |
JP2011237645A (en) * | 2010-05-11 | 2011-11-24 | Nitto Denko Corp | Resin composition for optical waveguide formation and optical waveguide using the same |
JP2016017148A (en) * | 2014-07-09 | 2016-02-01 | 三菱化学株式会社 | Epoxy compound, epoxy compound-containing composition and cured product |
Also Published As
Publication number | Publication date |
---|---|
JPH0793331B2 (en) | 1995-10-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TWI485218B (en) | Anisotropic conductive film, and semiconductor device | |
JP4994743B2 (en) | Film adhesive and method of manufacturing semiconductor package using the same | |
JPS63132435A (en) | Semiconductor element | |
EP1657725A1 (en) | Insulation-coated electroconductive particles | |
JP3506185B2 (en) | Adhesive and semiconductor device | |
JPH0726235A (en) | Conductive paste | |
JPH03192178A (en) | Adhesive sheet for die bonding | |
JPS58153338A (en) | Semiconductor element | |
JPS5966129A (en) | Semiconductor element | |
JPS63161014A (en) | Electrically conductive resin paste | |
JPS6261336A (en) | Semiconductor element | |
JPS61237436A (en) | Manufacture of semiconductor element | |
JPH0860103A (en) | Sheet type adhesive | |
JP2003206469A (en) | Adhesive composition and semiconductor device using the same | |
JPS6140371A (en) | Joining varnish | |
JPH05342910A (en) | Conductive paste | |
JPS62218413A (en) | Paste | |
JPS63120432A (en) | Semiconductor element | |
JPH08245765A (en) | Compound semiconductor device | |
JPH03145740A (en) | Semiconductor device | |
JPS63196619A (en) | Electroconductive resin composition | |
JPH0212509B2 (en) | ||
JPS58131740A (en) | Manufacture of semiconductor device | |
JPH04332143A (en) | Semiconductor device | |
JPH0465012A (en) | Conductive paste |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |