JP2008038111A - Film-shaped adhesive and method for producing semiconductor package using the same - Google Patents
Film-shaped adhesive and method for producing semiconductor package using the same Download PDFInfo
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- JP2008038111A JP2008038111A JP2006218241A JP2006218241A JP2008038111A JP 2008038111 A JP2008038111 A JP 2008038111A JP 2006218241 A JP2006218241 A JP 2006218241A JP 2006218241 A JP2006218241 A JP 2006218241A JP 2008038111 A JP2008038111 A JP 2008038111A
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- 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
- H01L24/27—Manufacturing methods
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- 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
- H01L24/80—Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected
- H01L24/83—Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected using a layer connector
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/01—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
- H01L2224/42—Wire connectors; Manufacturing methods related thereto
- H01L2224/47—Structure, shape, material or disposition of the wire connectors after the connecting process
- H01L2224/48—Structure, shape, material or disposition of the wire connectors after the connecting process of an individual wire connector
- H01L2224/4805—Shape
- H01L2224/4809—Loop shape
- H01L2224/48091—Arched
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/73—Means for bonding being of different types provided for in two or more of groups H01L2224/10, H01L2224/18, H01L2224/26, H01L2224/34, H01L2224/42, H01L2224/50, H01L2224/63, H01L2224/71
- H01L2224/732—Location after the connecting process
- H01L2224/73251—Location after the connecting process on different surfaces
- H01L2224/73265—Layer and wire connectors
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/80—Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected
- H01L2224/83—Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected using a layer connector
- H01L2224/8319—Arrangement of the layer connectors prior to mounting
- H01L2224/83191—Arrangement of the layer connectors prior to mounting wherein the layer connectors are disposed only on the semiconductor or solid-state body
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/80—Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected
- H01L2224/83—Methods for connecting semiconductor or other solid state bodies using means for bonding being attached to, or being formed on, the surface to be connected using a layer connector
- H01L2224/8319—Arrangement of the layer connectors prior to mounting
- H01L2224/83192—Arrangement of the layer connectors prior to mounting wherein the layer connectors are disposed only on another item or body to be connected to the semiconductor or solid-state body
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/10—Details of semiconductor or other solid state devices to be connected
- H01L2924/102—Material of the semiconductor or solid state bodies
- H01L2924/1025—Semiconducting materials
- H01L2924/10251—Elemental semiconductors, i.e. Group IV
- H01L2924/10253—Silicon [Si]
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- Manufacturing & Machinery (AREA)
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Abstract
Description
本発明は、フィルム状接着剤、それを使用する半導体パッケージの製造方法及びそれにより得られた半導体パッケージに関するものである。詳しくは、半導体パッケージ内の半導体素子とインターポーザ基板を接合するに適した絶縁性フィルム状接着剤に関するものである。 The present invention relates to a film adhesive, a method for manufacturing a semiconductor package using the same, and a semiconductor package obtained thereby. Specifically, the present invention relates to an insulating film adhesive suitable for bonding a semiconductor element in a semiconductor package and an interposer substrate.
近年、電子機器の小型化及び高機能化が進む中で、内部に搭載される半導体パッケージ構造は限られた実装領域の中で実装効率をより高めることが求められている。例えば、周辺端子配列のクワッドフラットパッケージ(以下、QFP)に代わり、面端子配列のチップサイズパッケージ(以下、CSP)やボールグリッドアレイ(BGA)が増えてきたり、また単一パッケージ内に複数個の半導体素子を搭載することにより、携帯機器等に搭載されるメモリへ付加価値を付与したり、メモリ容量を増大させたりすることを狙ったスタックドパッケージ等の登場が代表的な例である。 In recent years, with the progress of downsizing and higher functionality of electronic devices, the semiconductor package structure mounted inside is required to further improve the mounting efficiency within a limited mounting area. For example, chip size packages (hereinafter CSP) and ball grid arrays (BGA) with planar terminal arrangements are increasing instead of quad flat packages (hereinafter QFP) with peripheral terminal arrangements, and multiple packages within a single package. A typical example is the appearance of a stacked package aiming to add value to a memory mounted on a portable device or the like or increase a memory capacity by mounting a semiconductor element.
このような高密度実装化の要求に対し、半導体パッケージ内部に使用される部材は薄型化されている。スタックドパッケージにおいては、同じパッケージサイズの中でより多くの半導体素子を積層させるために、半導体素子、インターポーザ基板、封止樹脂、半導体素子とインターポーザ基板を接着するダイアタッチ材料等の各種部材が薄型化している。 In response to such a demand for high-density mounting, members used in the semiconductor package are made thinner. In stacked packages, in order to stack more semiconductor elements within the same package size, various members such as semiconductor elements, interposer substrates, sealing resins, die attach materials for bonding semiconductor elements and interposer substrates are thin. It has become.
インターポーザ基板が薄型化すると、半導体素子をインターポーザ基板に搭載するダイアタッチ工程において、熱による基板反りが発生しやすくなる。例えば、代表的なインターポーザ基板材料であるビスマレイミド・トリアジン(BT)基板においては、基板厚みが薄くなると、100℃以上で基板反りが発生する。この基板反りにより、ダイアタッチ工程において半導体素子とインターポーザ基板の間に接着不具合を発生させる(図3参照)。従来のフィルム状のダイアタッチ材料(以下、ダイアタッチフィルム)には基板反りを発生させる100℃以上の高温搭載条件が必要であった(特許文献1参照)。 When the interposer substrate is thinned, substrate warpage due to heat tends to occur in a die attach process for mounting a semiconductor element on the interposer substrate. For example, in a bismaleimide triazine (BT) substrate, which is a typical interposer substrate material, when the substrate thickness is reduced, substrate warpage occurs at 100 ° C. or higher. This substrate warpage causes a bonding failure between the semiconductor element and the interposer substrate in the die attach process (see FIG. 3). Conventional film-like die attach materials (hereinafter referred to as die attach films) require high-temperature mounting conditions of 100 ° C. or higher that cause substrate warpage (see Patent Document 1).
また、インターポーザ基板表面は必ずしも平滑な面状態ではないため、ダイアタッチ工程において被着体との界面に空気を巻き込むことがある。巻き込まれた空気は加熱硬化後の接着力を低下させるだけでなく、パッケージクラックの原因ともなる。ダイアタッチフィルムが凹凸のあるインターポーザ基板の面によく追従するには、搭載温度における粘度が低いことが必要である。従って、基板反りのない低温領域で搭載可能なダイアタッチフィルム材料特性には、常温ではフィルム性を保持するための高粘度を保ちつつ、60℃〜90℃の温度領域で低粘度領域に到達できることが必要となる。 Further, since the surface of the interposer substrate is not necessarily a smooth surface state, air may be caught in the interface with the adherend in the die attach process. The entrained air not only lowers the adhesive strength after heat curing, but also causes package cracks. In order for the die attach film to follow the surface of the uneven interposer substrate well, it is necessary that the viscosity at the mounting temperature is low. Therefore, the die attach film material characteristics that can be mounted in the low temperature region without substrate warpage can reach the low viscosity region in the temperature range of 60 ° C to 90 ° C while maintaining high viscosity to maintain film properties at room temperature. Is required.
このような低溶融粘度特性を持たせるためには、常温では固形であり軟化点が低温領域に存在する樹脂を多く配合することが容易である。しかし、一般的に使用されるエポキシ樹脂、ポリイミド樹脂、アクリル系樹脂などの樹脂骨格にはヘテロ原子(酸素、窒素など)を含有するものが多く、水素結合により水分子を吸収しやすいものが殆どである。そのため、樹脂配合量の増加とともに吸水率が上昇し、吸水された水分が気化膨張し半導体パッケージクラックを発生し易くする。 In order to have such a low melt viscosity characteristic, it is easy to blend a large amount of a resin that is solid at room temperature and has a softening point in a low temperature region. However, many commonly used resin skeletons such as epoxy resins, polyimide resins, and acrylic resins contain heteroatoms (oxygen, nitrogen, etc.), and most of them easily absorb water molecules by hydrogen bonds. It is. For this reason, the water absorption rate increases with an increase in the resin compounding amount, and the absorbed water vaporizes and expands, so that semiconductor package cracks are easily generated.
熱硬化型接着剤には一般的にエポキシ樹脂が使用されるが、樹脂硬化物の吸水率を低減するために、ジシクロペンタジエン型エポキシ樹脂を使用することは公知の技術である。例えば、アクリル系粘着成分にジシクロペンタジエン型エポキシ樹脂をブレンドしたことで、組成物の低吸水化を発現した例がある(特許文献2、3参照)。しかし、この場合、アクリル系粘着成分の吸水率が高く、またシリカ等の無機フィラーも混在しないため、更なる耐湿信頼性付与には限界がある。 An epoxy resin is generally used for the thermosetting adhesive, but it is a known technique to use a dicyclopentadiene type epoxy resin in order to reduce the water absorption of the cured resin. For example, there is an example in which the water absorption of the composition is reduced by blending an acrylic adhesive component with a dicyclopentadiene type epoxy resin (see Patent Documents 2 and 3). However, in this case, since the water-absorbing rate of the acrylic adhesive component is high and inorganic fillers such as silica are not mixed, there is a limit to further imparting moisture resistance reliability.
本発明の目的は、上記のような基板反りの発生しない100℃以下の低温領域で半導体素子を配線基板へ搭載可能にし、耐湿信頼性がより高い絶縁性フィルム状接着剤を提供することにある。また、ダイアタッチフィルムとして優れるフィルム状接着剤を提供することにある。 An object of the present invention is to provide an insulating film adhesive having a higher moisture resistance reliability, which enables a semiconductor element to be mounted on a wiring board in a low temperature region of 100 ° C. or lower where substrate warpage does not occur. . Another object of the present invention is to provide a film adhesive excellent as a die attach film.
すなわち本発明は、(A)ジシクロペンタジエン骨格含有エポキシ樹脂、(B)平均粒径3〜20μmであり、体積平均粒子径/個数平均粒子径の比が3以下である球状シリカ、(C)フェノキシ樹脂、及び(D)エポキシ樹脂硬化剤を必須成分とし、組成物中の(B)球状シリカ含有量が30〜80重量%であるフィルム状接着剤である。 That is, the present invention includes (A) a dicyclopentadiene skeleton-containing epoxy resin, (B) a spherical silica having an average particle diameter of 3 to 20 μm and a volume average particle diameter / number average particle diameter ratio of 3 or less, (C) A film-like adhesive comprising a phenoxy resin and (D) an epoxy resin curing agent as essential components, and (B) a spherical silica content in the composition of 30 to 80% by weight.
また、本発明は、(A)ジシクロペンタジエン骨格含有エポキシ樹脂が、式(1)
また、本発明は、多数の半導体素子が形成されたウェハ裏面に上記のフィルム状接着剤層を設ける工程、ダイシングテープをフィルム状接着剤層側に貼り合せる工程、フィルム状接着剤層とウェハを同時にダイシングして、フィルム状接着剤付き半導体素子とする工程、フィルム状接着剤付き半導体素子をダイシングテープから剥がし、被着体のインターポーザー基板とダイアタッチする工程を含む半導体パッケージの製造方法及びこの製造方法により製造された半導体パッケージである。 The present invention also includes a step of providing the film-like adhesive layer on the wafer back surface on which a large number of semiconductor elements are formed, a step of bonding a dicing tape to the film-like adhesive layer side, a film-like adhesive layer and a wafer. A semiconductor package manufacturing method including a step of dicing simultaneously to form a semiconductor element with a film adhesive, a step of peeling the semiconductor element with a film adhesive from a dicing tape, and die attaching to an interposer substrate of an adherend, and this A semiconductor package manufactured by a manufacturing method.
半導体素子を、基板反りの発生しない100℃以下の低温条件でインターポーザ基板に搭載することが可能であり、また、組成物硬化物の吸水率が低いためリフロー時のパッケージクラックを防止できるフィルム状接着剤が提供される。 It is possible to mount a semiconductor element on an interposer substrate under a low temperature condition of 100 ° C. or less where no substrate warpage occurs, and film adhesive that prevents package cracking during reflow due to the low water absorption rate of the cured composition An agent is provided.
本発明のフィルム状接着剤は、(A)ジシクロペンタジエン骨格含有エポキシ樹脂、(B)球状シリカ、(C)フェノキシ樹脂、及び(D)エポキシ樹脂硬化剤を必須成分とする組成物をフィルム状に形成してなる。 The film-like adhesive of the present invention is a film-like composition comprising (A) a dicyclopentadiene skeleton-containing epoxy resin, (B) spherical silica, (C) a phenoxy resin, and (D) an epoxy resin curing agent. Formed.
(A)ジシクロペンタジエン骨格含有エポキシ樹脂(以下、DCP型エポキシ樹脂ともいう)は、分子内にジシクロペンタジエン骨格と、反応性のエポキシ基を有する樹脂であり、通常は、常温で固形であり、軟化点は好ましくは50℃〜100℃、更に好ましくは60℃〜80℃程度である。これは、常温ではフィルム性を保持するための高粘度を保ちつつ、60℃〜100℃の温度領域で低粘度領域に到達できることが必要だからである。また、分子量は好ましくは430〜2000、更に好ましくは600〜1200である。更に、エポキシ当量は、好ましくは 200〜300g/eq、特に好ましくは240〜280g/eqである。 (A) A dicyclopentadiene skeleton-containing epoxy resin (hereinafter also referred to as a DCP type epoxy resin) is a resin having a dicyclopentadiene skeleton and a reactive epoxy group in the molecule, and is usually solid at room temperature. The softening point is preferably about 50 ° C to 100 ° C, more preferably about 60 ° C to 80 ° C. This is because it is necessary to reach a low viscosity region in a temperature range of 60 ° C. to 100 ° C. while maintaining a high viscosity for maintaining film properties at room temperature. The molecular weight is preferably 430 to 2000, more preferably 600 to 1200. Furthermore, the epoxy equivalent is preferably 200 to 300 g / eq, particularly preferably 240 to 280 g / eq.
このようなDCP型エポキシ樹脂としては、上記式(1)で示されるエポキシ樹脂が好ましく使用される。式(1)において、nは0〜10、好ましくは0〜5の整数である。DCP型エポキシ樹脂としては、nが0〜10の混合物として供給されており、具体的にはXD-1000(商品名:日本化薬社製)、HP-7200H(商品名:大日本インキ化学工業社製)等が挙げられる。 As such a DCP type epoxy resin, an epoxy resin represented by the above formula (1) is preferably used. In Formula (1), n is an integer of 0 to 0, preferably 0 to 5. As a DCP type epoxy resin, n is supplied as a mixture of 0 to 0. Specifically, XD-1000 (trade name: manufactured by Nippon Kayaku Co., Ltd.), HP-7200H (trade name: Dainippon Ink & Chemicals, Inc.) Etc.).
また、DCP型エポキシ樹脂と汎用の他のエポキシ樹脂を併用してもよい。特に軟化点の高いDCP型エポキシ樹脂を用いた場合には、組成物の粘度が上昇し、フィルムとしたときに脆くなるため、分子量300〜500の常温液状のエポキシ樹脂をブレンドして用いるのが好ましい。この場合、DCP型エポキシ樹脂100重量部に対し、他のエポキシ樹脂5〜70重量部、更に好ましくは30〜60重量部の割合で用いられる。 Moreover, you may use together a DCP type epoxy resin and the other general purpose epoxy resin. In particular, when a DCP type epoxy resin having a high softening point is used, the viscosity of the composition increases and the film becomes brittle when used as a film. Therefore, it is necessary to blend a room temperature liquid epoxy resin having a molecular weight of 300 to 500. preferable. In this case, another epoxy resin is used in an amount of 5 to 70 parts by weight, more preferably 30 to 60 parts by weight with respect to 100 parts by weight of the DCP type epoxy resin.
(B)球状シリカ(以下、球状シリカという)は、組成物の低吸水化、線膨張係数の低減に貢献する。線膨張率の値が高いと配線基板との線膨張率の差が大きくなるため、これら被接着物との応力を抑制する効果が低く、パッケージクラックを発生させることにつながり好ましくない。 (B) Spherical silica (hereinafter referred to as spherical silica) contributes to reducing the water absorption of the composition and reducing the linear expansion coefficient. If the value of the coefficient of linear expansion is high, the difference in coefficient of linear expansion from the wiring board becomes large, so that the effect of suppressing stress with these adherends is low, which leads to generation of package cracks.
球状シリカは高充填化、流動性の観点から優れる。球状シリカの平均粒径は3〜20μmであり、体積平均粒子径/個数平均粒子径の比(以下、粒子径の比ともいう)が3以下である。平均粒径が3μmより小さいとフィラーが凝集しやすくなるため樹脂バインダー中に分散しにくくなり、また比表面積が大きくなるため樹脂との接触面積を大きくし溶融粘度を上昇させてしまう。粒径が20μmより大きいとロールナイフコーター等の塗工機で薄型のフィルムを作製する際に、フィラーがきっかけとなりフィルム表面にスジを発生しやすくなる。 Spherical silica is excellent in terms of high packing and fluidity. The average particle diameter of the spherical silica is 3 to 20 μm, and the volume average particle diameter / number average particle diameter ratio (hereinafter also referred to as the particle diameter ratio) is 3 or less. If the average particle size is less than 3 μm, the filler tends to aggregate, making it difficult to disperse in the resin binder, and since the specific surface area becomes large, the contact area with the resin is increased and the melt viscosity is increased. When the particle size is larger than 20 μm, when a thin film is produced with a coating machine such as a roll knife coater, the filler becomes a trigger, and it becomes easy to generate streaks on the film surface.
上記粒子径の比は粒子径分布を表す指標として用いられるものであって、一般に体積平均粒子径/個数平均粒子径≧1であり、この値が小さいほど粒子径分布がシャープであり、この値が大きいほど粒子径分布がブロードであることを表す。この粒子径の比が3を超えると、組成物において、粒径の大きなフィラーの隙間に粒径の小さなフィラーが存在し樹脂中にフィラーが密に充填される構造をとり、樹脂とフィラーとの接触面積がより大きくなる。そのため、ダイアタッチ工程において、フィルム状接着剤が熱により溶融しにくくなり(図1参照)、インターポーザ基板と接着層の間に空気を巻き込みやすくする。 The particle size ratio is used as an index representing the particle size distribution, and is generally volume average particle size / number average particle size ≧ 1, and the smaller this value, the sharper the particle size distribution. The larger the value, the broader the particle size distribution. When the ratio of the particle diameters exceeds 3, the composition has a structure in which fillers with small particle diameters exist in the gaps between the fillers with large particle diameters, and the filler is densely filled in the resin. The contact area becomes larger. Therefore, in the die attach process, the film-like adhesive is not easily melted by heat (see FIG. 1), and air is easily caught between the interposer substrate and the adhesive layer.
組成物中(接着剤中)の球状シリカの配合割合は30〜80重量%である。配合量が80重量%を超えると、バインダーとして働く樹脂成分の不足により組成物の粘度が上昇し、フィルムとしたときに脆くなる、30重量%未満ではフィルム表面タック性が生じハンドリング性が著しく悪化する。 The blending ratio of the spherical silica in the composition (in the adhesive) is 30 to 80% by weight. If the blending amount exceeds 80% by weight, the viscosity of the composition increases due to the lack of the resin component that acts as a binder and becomes brittle when made into a film, and if it is less than 30% by weight, the film surface tackiness occurs and handling properties are significantly deteriorated. To do.
(C)フェノキシ樹脂(以下、フェノキシ樹脂という)は、公知のフェノキシ樹脂を用いることができる。フェノキシ樹脂は、例えば、ビスフェノールAのようなビスフェノールとエピクロロヒドリンとから得られる通常、分子量が10000以上の熱可塑性樹脂である。このフェノキシ樹脂は、エポキシ樹脂と構造が類似していることから相溶性がよく、樹脂溶融粘度も低く、接着性もよいという特長を示す。好ましいフェノキシ樹脂は、主骨格がビスフェノールA型であるYP-50S(商品名:東都化成社製)があるが、その他に優れた溶融粘度特性を示すビスフェノールF型であるFX-316(商品名:東都化成社製)、高耐熱性を有したFX-280S(商品名:東都化成社製)などが挙げられる。フェノキシ樹脂の配合割合はDCP型エポキシ樹脂100重量部に対し10〜200重量部、好ましくは30〜70重量部の割合とすることがよい。10重量部未満の場合、フィルム表面タック性が生じハンドリング性が著しく悪化し、200重量部を超えるとフィルムが硬くなり、フィルム単独では割れやすくなる。 As the (C) phenoxy resin (hereinafter referred to as phenoxy resin), a known phenoxy resin can be used. The phenoxy resin is usually a thermoplastic resin having a molecular weight of 10,000 or more obtained from bisphenol such as bisphenol A and epichlorohydrin. Since this phenoxy resin has a similar structure to the epoxy resin, it has good compatibility, low resin melt viscosity, and good adhesion. A preferred phenoxy resin is YP-50S (trade name: manufactured by Toto Kasei Co., Ltd.) whose main skeleton is bisphenol A type, but FX-316 (trade name: product name: bisphenol F type which exhibits excellent melt viscosity properties). FX-280S (trade name: manufactured by Toto Kasei Co., Ltd.) having high heat resistance. The blending ratio of the phenoxy resin is 10 to 200 parts by weight, preferably 30 to 70 parts by weight with respect to 100 parts by weight of the DCP type epoxy resin. When the amount is less than 10 parts by weight, the film surface tackiness is caused and the handling property is remarkably deteriorated. When the amount exceeds 200 parts by weight, the film becomes hard and the film alone is easily broken.
本発明に用いる(D)エポキシ樹脂硬化剤(以下、硬化剤ともいう)には、アミン類、酸無水物類、多価フェノール類等の公知の硬化剤を用いることができるが、好ましくは常温以上の所定の温度、例えば樹脂成分が必要な粘着性を示す温度以上で硬化性を発揮し、しかも速硬化性を発揮する潜在性硬化剤である。潜在性硬化剤には、ジシアンジアミド、イミダゾール類、ヒドラジド類、三弗化ホウ素−アミン錯体、アミンイミド、ポリアミン塩及びこれらの変性物、更にマイクロカプセル型のものも使用可能である。これらは、単独あるいは2種以上混ぜて使用できる。潜在性硬化剤を使用することで室温での長期保存も可能な保存安定性の高いフィルム接着剤を提供できる。エポキシ樹脂硬化剤の使用量は、通常、エポキシ樹脂に対して0.5〜50wt%の範囲である。 As the (D) epoxy resin curing agent (hereinafter also referred to as curing agent) used in the present invention, known curing agents such as amines, acid anhydrides and polyhydric phenols can be used, but preferably at room temperature. It is a latent curing agent that exhibits curability at the above predetermined temperature, for example, at or above the temperature at which the resin component exhibits the necessary tackiness, and also exhibits fast curability. As the latent curing agent, dicyandiamide, imidazoles, hydrazides, boron trifluoride-amine complexes, amine imides, polyamine salts and modified products thereof, and microcapsules can also be used. These can be used alone or in admixture of two or more. By using a latent curing agent, it is possible to provide a film adhesive with high storage stability that can be stored for a long period of time at room temperature. The usage-amount of an epoxy resin hardening | curing agent is the range of 0.5-50 wt% normally with respect to an epoxy resin.
上記(A)〜(D)を必須成分とする接着剤形成用の組成物中には、他の添加剤として、例えばカップリング剤、酸化防止剤、難燃剤、着色剤、応力緩和剤としてブタジエン系ゴムやシリコーンゴム等を含有することも可能である。 In the composition for forming an adhesive comprising the above (A) to (D) as essential components, other additives such as a coupling agent, an antioxidant, a flame retardant, a colorant, and a butadiene as a stress relaxation agent. It is also possible to contain a system rubber or a silicone rubber.
カップリング剤は、シリカとの界面を補強し高い破壊強度を発現させるとともに接着力向上の目的から好ましい。カップリング剤としては、アミノ基、エポキシ基を含有したものが好ましい。 The coupling agent is preferable for the purpose of reinforcing the interface with silica and exhibiting high breaking strength and improving the adhesive strength. As the coupling agent, those containing an amino group or an epoxy group are preferable.
本発明のフィルム状接着剤は、例えばトルエン、キシレン等の芳香族炭化水素、MIBKやMEK等のケトン系、モノグライム、ジグライム等のエーテル系の単独又は混合系の溶媒に上記(A)〜(D)を必須成分とする組成物を溶解させたワニスを、離型処理されたPP、PE、PET等の基材(保護フィルム)にロールナイフコーター、グラビアコーター、ダイコーター、リバースコーターなど一般的に公知の方法に従って塗工し、樹脂混合物の硬化開始温度以下の熱処理を施し、乾燥することで得られる。本発明のフィルム状接着剤の厚みは、10〜150μmの範囲であることが好ましい。 The film-like adhesive of the present invention is, for example, an aromatic hydrocarbon such as toluene or xylene, a ketone solvent such as MIBK or MEK, an ether solvent such as monoglyme or diglyme, or a mixture of the above (A) to (D ) Varnish in which a composition containing essential components is dissolved is applied to a base material (protective film) such as PP, PE, PET, etc., which has been subjected to mold release treatment, such as a roll knife coater, gravure coater, die coater, reverse coater It is obtained by coating according to a known method, applying a heat treatment not higher than the curing start temperature of the resin mixture, and drying. The thickness of the film adhesive of the present invention is preferably in the range of 10 to 150 μm.
本発明のフィルム状接着剤又はその組成物の粘度は、常温では10000Pas以上の高粘度を有し、基板反りが発生しない60℃〜90℃の温度領域で900Pas以下に達することが好ましい。常温の粘度が10000Pas未満だとフィルム表面タック性が生じハンドリング性が著しく悪化する、60℃〜100℃における粘度の値が900Pasより高いと、ダイアタッチ工程において被着体との界面に空気を巻き込みやすくなる。 The viscosity of the film adhesive of the present invention or the composition thereof preferably has a high viscosity of 10000 Pas or more at room temperature and reaches 900 Pas or less in a temperature range of 60 ° C. to 90 ° C. at which no substrate warpage occurs. If the viscosity at room temperature is less than 10000 Pas, the film surface tackiness will be significantly deteriorated, and the handling properties will be significantly deteriorated. It becomes easy.
また、フィルム状接着剤は加熱等により硬化するが、その硬化物の吸水率(85℃、85%RH、100時間)は、1.5重量%以下が好ましい。吸水率が高いと、リフロー時に高温に曝されると、水分の揮発が多くなるので、パッケージクラックが発生し易くなる。DCP型エポキシ樹脂は低吸水性を特長としており、耐湿信頼性を付与するには適した樹脂である。 The film adhesive is cured by heating or the like, and the water absorption rate (85 ° C., 85% RH, 100 hours) of the cured product is preferably 1.5% by weight or less. When the water absorption rate is high, when exposed to a high temperature during reflow, the volatilization of moisture increases, and package cracks are likely to occur. The DCP type epoxy resin is characterized by low water absorption, and is a resin suitable for imparting moisture resistance reliability.
本発明のフィルム状接着剤をダイアタッチフィルムとして使用する場合について、図面を参照して説明する。図2は、半導体素子とインターポーザ基板とを熱圧着する工程を示す。 The case where the film adhesive of this invention is used as a die attach film is demonstrated with reference to drawings. FIG. 2 shows a process of thermocompression bonding the semiconductor element and the interposer substrate.
先ずシリコンウエハ5の一方の面にフィルム状接着剤(ダイアタッチフィルム)6を貼り付けた後、ダイシングテープ7を下地にしてシリコンウエハとフィルム状接着剤を切断して、フィルム状接着剤付き半導体素子1を得る。次いで、接着剤付き半導体素子1をダイシングテープ7から剥がし、インターポーザー基板2に反りの発生しない100℃以下の加温条件でインターポーザ基板に搭載し、加熱することにより接着剤中のエポキシ樹脂を硬化させ、半導体素子とインターポーザ基板とを熱圧着を行う。この場合の加熱温度は通常は80℃〜180℃であり、加熱時間は1分〜180分間である。この様な加熱により、エポキシ樹脂が硬化し、半導体素子とインターポーザ基板とを強固に接着できる。接着して得られる半導体素子接着基板8は、その後、半導体素子とインターポーザ基板とをワイヤー9で接続され、モールド工程で封止材10により封止される。
First, a film-like adhesive (die attach film) 6 is attached to one surface of a silicon wafer 5, and then the silicon wafer and the film-like adhesive are cut using a
図3は、ダイアタッチフィルムを貼り付けた半導体素子1をインターポーザー基板2にダイアタッチする従来の工程を模式的に示す。ヒートステージ3で加熱されたインターポーザー基板がBT基板である場合、BT基板は100℃を超える加熱により反りが生じる。そこで、ダイアタッチフィルムを貼り付けた半導体素子のダイアタッチフィルム面とBT基板の接着面に非接触面4が生じ、接着力が低下することになる。
FIG. 3 schematically shows a conventional process for die-attaching the
以下本発明を実施例により説明するが、本発明はこれら実施例に限定されるものではない。なお、以下の実施例及び比較例において、「溶融粘度」、「吸水率」、「表面タック性」は次のように評価した。 EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited to these examples. In the following Examples and Comparative Examples, “melt viscosity”, “water absorption”, and “surface tack” were evaluated as follows.
「溶融粘度」 熱硬化前のフィルムを約10g切り取り、簡易プレス機を用いて高さ約4cmの棒状に加工する。このサンプルを島津製作所製高化式フローテスター(CFT-500A)を用いて、各測定温度で測定した。 “Melting viscosity” About 10g of the film before thermosetting is cut out and processed into a 4cm high bar using a simple press. This sample was measured at each measurement temperature using a high-pressure flow tester (CFT-500A) manufactured by Shimadzu Corporation.
「吸水率」 熱硬化前のフィルムを約10g切り取り、一定寸法金型に入れ熱板上で溶融させ成型する。成型後サンプルを室温下で冷却し、180℃/1時間熱処理を行う。このサンプルを、85℃、相対湿度85%で、168時間放置後の重量増加から吸水率を求めた。 "Water absorption rate" Cut about 10g of the film before thermosetting, put it in a fixed dimension mold and melt it on a hot plate. After molding, the sample is cooled at room temperature and heat-treated at 180 ° C for 1 hour. The water absorption was determined from the weight increase of this sample after standing for 168 hours at 85 ° C. and 85% relative humidity.
「表面タック性」 熱硬化前のフィルムの触感、離型処理PETフィルムからの剥離性を観察し、◎(良好)、○(ほぼ良好)、△(やや悪い)、×(悪い)の4段階で評価した。 "Surface tackiness" Tactile sensation of film before thermosetting and peelability from release-treated PET film were observed. ◎ (good), ○ (nearly good), △ (slightly bad), x (bad) It was evaluated with.
実施例1
XD-1000(ジシクロペンタジエン型エポキシ樹脂、軟化点 約70℃、日本化薬社製)60g、YP-50S(フェノキシ樹脂、Tg約100℃、東都化成社製)20g、エピコート828(ビスフェノールA型エポキシ樹脂、東都化成社製) 44gを秤量し、70gのMIBKを溶剤として500mlのセパラブルフラスコ中、110℃で2時間加熱攪拌して樹脂ワニスを得た。この溶液187gを800mlのプラネタリーミキサーに秤量し、FB-3SDX(球状シリカ、平均粒径 3μm 、粒子径の比=2.4、デンカ社製) 72gを加えて混合したものを3本ロールで混練した。この混合物に、AH-150(ジシアンジアミド、味の素社製) 6g、HX-3722 (マイクロカプセル型イミダゾール系潜在性硬化剤、旭化成エポキシ社製) 2gを加えてプラネタリーミキサーで攪拌混合後、真空脱泡して混合ワニスを得た。上記ワニスを厚さ50μmの離型処理されたPETフィルム上に塗布後、80℃/10min、150℃/1minで熱風乾燥させ、30μmの接着シート、すなわちフィルム状接着剤を得た。
Example 1
XD-1000 (dicyclopentadiene type epoxy resin, softening point approx. 70 ° C, Nippon Kayaku Co., Ltd.) 60g, YP-50S (phenoxy resin, Tg approx. 100 ° C, Toto Kasei Co., Ltd.) 20g, Epicoat 828 (bisphenol A type) 44 g of epoxy resin (manufactured by Toto Kasei Co., Ltd.) was weighed and heated and stirred at 110 ° C. for 2 hours in a 500 ml separable flask using 70 g of MIBK as a solvent to obtain a resin varnish. 187 g of this solution was weighed in an 800 ml planetary mixer, and 72 g of FB-3SDX (spherical silica, average particle size 3 μm, particle size ratio = 2.4, manufactured by Denka) was added and mixed with three rolls. . Add 6g of AH-150 (Dicyandiamide, Ajinomoto Co., Inc.) and 2g of HX-3722 (Microcapsule type imidazole latent curing agent, Asahi Kasei Epoxy Co., Ltd.) to this mixture. To obtain a mixed varnish. The varnish was applied onto a 50 μm thick PET film which had been subjected to a release treatment, and then dried with hot air at 80 ° C./10 min and 150 ° C./1 min to obtain a 30 μm adhesive sheet, that is, a film adhesive.
実施例2
ジシクロペンタジエン型エポキシ樹脂として、HP-7200H(ジシクロペンタジエン型エポキシ樹脂、軟化点約80℃、大日本インキ化学工業製)60g を使用した他は、実施例1と同様にして接着シートを製造し、評価した。
Example 2
An adhesive sheet was produced in the same manner as in Example 1 except that 60 g of HP-7200H (dicyclopentadiene type epoxy resin, softening point of about 80 ° C., manufactured by Dainippon Ink and Chemicals) was used as the dicyclopentadiene type epoxy resin. And evaluated.
実施例3
球状シリカとして、FB-3SDXを134g 使用した他は、実施例1と同様にして接着シートを製造し、評価した。
Example 3
An adhesive sheet was produced and evaluated in the same manner as in Example 1 except that 134 g of FB-3SDX was used as the spherical silica.
実施例4
球状シリカとして、FB-3SDXを314g使用した他は、実施例1と同様にして接着シートを製造し、評価した。
Example 4
An adhesive sheet was produced and evaluated in the same manner as in Example 1 except that 314 g of FB-3SDX was used as the spherical silica.
比較例1
球状シリカとして、FB-3SDXを58g、SO-25R(龍森社製、微粒子球状シリカ、平均粒径0.5μm、粒子径の比=4.3)を14g使用した他は、実施例1と同様にして接着シートを製造し、評価した。
Comparative Example 1
Except that 58 g of FB-3SDX and 14 g of SO-25R (manufactured by Tatsumori Co., Ltd., fine spherical silica, average particle size 0.5 μm, particle size ratio = 4.3) were used as the spherical silica, the same as in Example 1. An adhesive sheet was manufactured and evaluated.
比較例2
エポキシ樹脂として、YDCN-702H(クレゾールノボラック型エポキシ樹脂、軟化点約75℃、東都化成社製) を60g 使用した他は、実施例1と同様にして接着シートを製造し、評価した。
Comparative Example 2
An adhesive sheet was produced and evaluated in the same manner as in Example 1 except that 60 g of YDCN-702H (cresol novolac type epoxy resin, softening point: about 75 ° C., manufactured by Tohto Kasei Co., Ltd.) was used as the epoxy resin.
比較例3
エポキシ樹脂として、EPPN-501H(トリフェニルメタン型エポキシ樹脂、軟化点約55℃、日本化薬社製)を60g使用した他は、実施例1と同様にして接着シートを製造し、評価した。
Comparative Example 3
An adhesive sheet was produced and evaluated in the same manner as in Example 1 except that 60 g of EPPN-501H (triphenylmethane type epoxy resin, softening point: about 55 ° C., manufactured by Nippon Kayaku Co., Ltd.) was used as the epoxy resin.
比較例4
球状シリカを配合しない他は、実施例1と同様にして接着シートを製造し、評価した。
実施例1〜4、比較例1〜4の組成及び評価結果をまとめて表1に示す。
Comparative Example 4
An adhesive sheet was produced and evaluated in the same manner as in Example 1 except that spherical silica was not blended.
Table 1 summarizes the compositions and evaluation results of Examples 1 to 4 and Comparative Examples 1 to 4.
実施例5
XD-1000(ジシクロペンタジエン型エポキシ樹脂)60g、YP-50S(フェノキシ樹脂)20g、エピコート828(ビスフェノールA型エポキシ樹脂) 44gを秤量し、70gのMIBKを溶剤として500mlのセパラブルフラスコ中、110℃で2時間加熱攪拌して樹脂ワニスを得た。この溶液187gを800mlのプラネタリーミキサーに秤量し、FB-3SDX(球状シリカ) 72gを加えて混合したものを真空脱泡して混合ワニスを得た。上記ワニスを厚さ50μmの離型処理されたPETフィルム上に塗布後、80℃/10min、150℃/1minで熱風乾燥させ、30μmの接着シート、すなわちフィルム状接着剤を得た。このフィルムの硬化前の溶融粘度を測定した(図1参照)。なお、本実施例においては未硬化状態における溶融粘度を測定するため、エポキシ樹脂硬化剤は配合していない。
Example 5
XD-1000 (dicyclopentadiene type epoxy resin) 60g, YP-50S (phenoxy resin) 20g, Epicoat 828 (bisphenol A type epoxy resin) 44g, weighed 110g in a 500ml separable flask using 70g MIBK as solvent. The resin varnish was obtained by heating and stirring at 2 ° C. for 2 hours. 187 g of this solution was weighed in an 800 ml planetary mixer, and 72 g of FB-3SDX (spherical silica) was added and mixed to obtain a mixed varnish by vacuum degassing. The varnish was applied onto a 50 μm thick PET film which had been subjected to a release treatment, and then dried with hot air at 80 ° C./10 min and 150 ° C./1 min to obtain a 30 μm adhesive sheet, that is, a film adhesive. The melt viscosity before curing of this film was measured (see FIG. 1). In this example, an epoxy resin curing agent is not blended in order to measure the melt viscosity in an uncured state.
比較例5
球状シリカとして、FB-3SDXを36g、SO-25Rを36g使用した他は、実施例5と同様にして接着シートを製造し、このフィルムの溶融粘度を測定した(図1参照)。
Comparative Example 5
An adhesive sheet was produced in the same manner as in Example 5 except that 36 g of FB-3SDX and 36 g of SO-25R were used as spherical silica, and the melt viscosity of this film was measured (see FIG. 1).
比較例6
球状シリカとして、SO-25Rを72g使用した他は、実施例5と同様にして接着シートを製造し、このフィルムの硬化前の溶融粘度を測定した(図1参照)。
Comparative Example 6
An adhesive sheet was produced in the same manner as in Example 5 except that 72 g of SO-25R was used as the spherical silica, and the melt viscosity before curing of this film was measured (see FIG. 1).
実施例5、比較例5〜6の組成及び溶融粘度結果を表2及び図1に示す。表2に示す粒子径の比の値は単一フィラー配合系では、そのフィラー種の値を記載し、混合配合系では、以下の式により混合系の粒子径の比の値を計算した。
混合配合系の粒子径の比=(フィラーAの配合割合×フィラーAの[体積平均粒子径]/[個数平均粒子径])+(フィラーBの配合割合×フィラーBの[体積平均粒子径]/[個数平均粒子径])
The compositions and melt viscosity results of Example 5 and Comparative Examples 5 to 6 are shown in Table 2 and FIG. The particle size ratio values shown in Table 2 describe the value of the filler type in the case of a single filler compounding system, and in the mixed compounding system, the value of the particle size ratio of the mixed system was calculated by the following formula.
Ratio of particle diameter of mixed blending system = (blending ratio of filler A × [volume average particle diameter] of filler A / [number average particle diameter]) + (blending ratio of filler B × [volume average particle diameter] of filler B) / [Number average particle size])
1:接着剤付き半導体素子、2:インターポーザー基板、3:ヒートステージ、4:非接触面、5:シリコンウエハ、6:フィルム状接着剤、7:ダイシングテープ、8:半導体素子接着基板、9:ワイヤー、10:封止材 1: Semiconductor element with adhesive, 2: Interposer substrate, 3: Heat stage, 4: Non-contact surface, 5: Silicon wafer, 6: Film adhesive, 7: Dicing tape, 8: Semiconductor element adhesive substrate, 9 : Wire, 10: Sealing material
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JP2009149727A (en) * | 2007-12-19 | 2009-07-09 | Nippon Steel Chem Co Ltd | Film-like adhesive, semiconductor package using it, and its manufacturing method |
JP2010070653A (en) * | 2008-09-18 | 2010-04-02 | Sekisui Chem Co Ltd | Insulating sheet and laminated structure |
WO2010038733A1 (en) * | 2008-09-30 | 2010-04-08 | 東洋紡績株式会社 | Resin composition for adhesive agent, adhesive agent and adhesive sheet each comprising same, and laminate for print circuit board adhered by using same |
JP2010116453A (en) * | 2008-11-12 | 2010-05-27 | Nippon Steel Chem Co Ltd | Film adhesive, semiconductor package using the same, and method for producing semiconductor package |
JP2010225624A (en) * | 2009-03-19 | 2010-10-07 | Sekisui Chem Co Ltd | Adhesive sheet and dicing-die bonding tape |
JP2011159793A (en) * | 2010-02-01 | 2011-08-18 | Murata Mfg Co Ltd | Winding coil component manufacturing method |
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JP2016058457A (en) * | 2014-09-05 | 2016-04-21 | 古河電気工業株式会社 | Film-shaped adhesive, semiconductor package arranged by use of film-shaped adhesive and method for manufacturing the same |
CN111039255A (en) * | 2019-12-06 | 2020-04-21 | 上海航天控制技术研究所 | Method for reducing packaging stress of MEMS (micro-electromechanical system) inertial device and MEMS device |
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