TWI270558B - Latent hardener, manufacturing method for latent hardener, and adhesive - Google Patents

Latent hardener, manufacturing method for latent hardener, and adhesive Download PDF

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Publication number
TWI270558B
TWI270558B TW91134974A TW91134974A TWI270558B TW I270558 B TWI270558 B TW I270558B TW 91134974 A TW91134974 A TW 91134974A TW 91134974 A TW91134974 A TW 91134974A TW I270558 B TWI270558 B TW I270558B
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Taiwan
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hardener
particles
adhesive
capsule
resin
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TW91134974A
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Chinese (zh)
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TW200409785A (en
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Takayuki Matsushima
Masao Saito
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Sony Chemicals Corp
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/01Chemical elements
    • H01L2924/01013Aluminum [Al]

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  • Adhesives Or Adhesive Processes (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)

Abstract

This invention is to obtain an adhesive which is curable under conditions of low temperature and short time and has high shelf life. The adhesive has a silane coupling agent, an epoxy resin and a latent curing agent in which curing agent particles composed of a metal chelate are covered with a capsule. Since these curing agent particles are covered with the capsule at ordinary temperature, polymerization reaction of the epoxy resin does not occur, but when the adhesive is heated, the capsule is broken and the metal chelate constituting the curing agent particles reacts with the silane coupling agent to produce a cation, and the epoxy resin is polymerized by the cation (cation polymerization) to cure the adhesive. Since the reaction with which the cation is produced occurs at a lower temperature than a temperature at which conventional adhesive is thermally cured, the adhesive of the present invention is cured at a lower temperature and in a shorter time. As a result, the adhesive of the present invention is low-temperature curing type and has high shelf life.

Description

12705581270558

File:TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 玫x發明說明 (發明說明應敘明:發明所屬之技術領域、先前技術、內容、實施方式及圖式簡 單說明) 【發明所屬之技術領域】 本發明係有關接著劑,尤其是與半導體晶片與TCP 利用熱壓著方式連接時所使用之接著劑的潛在性硬化劑 有關。 【先前技術】File: TW1009 (060314) CRF.doc SUNDIAL CONFIDENTIAL (Description of the invention should be described: the technical field, prior art, content, embodiment and schematic description of the invention) It is related to the adhesive, especially the latent hardener used in the semiconductor wafer and TCP when it is joined by heat pressing. [Prior Art]

過去,在基板上要接著半導體晶片時,或是TCP (Tape Carrier Package)與 LCD (Liquid Crystal Display)在 接著製造電氣設備時,都是採用含熱硬化性樹脂環氧樹脂 的接著劑。 如第7 (a)圖的符號111所顯示的LCD,LCD111包 含玻璃基板112、配置在玻璃基板112上的ITO電極 (Indium tinoxide)113cLCDlll 在與後述的 TCP 接著時, 首先要在LCD111的ITO電極113所要配置的面上塗上接 著劑。第7 (b)圖的符號125是LCD111上塗抹了接著劑 後的情形。 第7(c)圖的符號115所示為TCP,TCP115包括了 基座膠膜(base film) 116、配置在基座膠膜116表面上 的金屬配線117。TCP115的金屬配線117在所配置的面, 是朝著LCD111上的接著劑125配置,在對準位置後, 1270558In the past, when a semiconductor wafer was to be mounted on a substrate, or a TCP (Tape Carrier Package) and an LCD (Liquid Crystal Display) were used to manufacture an electrical device, an adhesive containing a thermosetting resin epoxy resin was used. As shown in the symbol 111 of Fig. 7(a), the LCD 111 includes a glass substrate 112, and an ITO electrode (Indium tin oxide) 113cLCDl disposed on the glass substrate 112. Next, when the TCP is described later, the ITO electrode of the LCD 111 is first used. The surface to be placed on the 113 is coated with an adhesive. The symbol 125 in Fig. 7(b) is the case where the adhesive is applied to the LCD 111. Reference numeral 115 in Fig. 7(c) shows TCP, and TCP 115 includes a base film 116 and a metal wiring 117 disposed on the surface of the susceptor film 116. The metal wiring 117 of the TCP 115 is disposed toward the adhesive 125 on the LCD 111 on the configured side, after the alignment position, 1270558

File:TW1009(060314)CRF.docFile:TW1009(060314)CRF.doc

SUNDIAL CONFIDENTIAL TCP115的金屬配、線117的配置面會被按向接著劑i25。 在這個狀態下壓住加熱的話,接㈣125會軟化, 金屬配、線117會將軟化了的接著齊U25按往後退,接觸到 ITO電極113的表面。 在上述的接著劑上’—般都添加了加熱後會與環氧 樹脂重合、像imidazol類的硬化劑,當金屬配線工17與ιτ〇 電極113在黏接狀態下繼續加熱的話,由於硬化劑的觸媒 作用,會使環氧樹脂重合,讓接著劑125硬化。 第7 (c)圖的符號ι〇1所示的是接著劑125在硬化後 狀態下的電氣設備。該電氣設備1〇1在金屬配線117與1丁〇 電極113相接的狀態下,透過硬化了的接著劑125將 TCP115與LCD111固定住。因此Tcpn5與LCDU1在電 力上、機械上都相連接在一起了。 但是,上述的接著劑在使其硬化時,須以18〇t以上 兩溫將接著劑加熱,當金屬配線117的電路非常細微時, 加熱時會造成TCP115發生伸長或縮短等變形的情形。這 個問題可以藉由降低加熱溫度來解決,但是就會延長加熱 處理所需的時間,降低生產性。 低溫下硬化性也很優異的接著劑在近年來開發出了 Acrylate 之類自由基聚合(一radically polymerizable)性樹脂 1270558The arrangement surface of the metal fitting and line 117 of the SUNDIAL CONFIDENTIAL TCP 115 is pressed to the adhesive i25. When the heating is pressed in this state, the (four) 125 will soften, and the metal distribution and the line 117 will soften the subsequent U25 to retreat to contact the surface of the ITO electrode 113. On the above-mentioned adhesive, a curing agent which is superposed on the epoxy resin and is like an imidazol type is added, and when the metal wiring worker 17 and the ιτ〇 electrode 113 are heated in the bonded state, the hardener is added. The catalytic action causes the epoxy to overlap and the adhesive 125 to harden. The symbol ι 〇 1 of Fig. 7 (c) shows the electrical equipment of the adhesive 125 in the post-hardened state. The electric device 1〇1 fixes the TCP 115 and the LCD 111 through the cured adhesive 125 in a state where the metal wiring 117 is in contact with the butadiene electrode 113. Therefore, Tcpn5 is electrically and mechanically connected to LCDU1. However, when the above-mentioned adhesive is hardened, it is necessary to heat the adhesive at a temperature of 18 Torr or more. When the circuit of the metal wiring 117 is very fine, the TCP 115 may be deformed by elongation or shortening during heating. This problem can be solved by lowering the heating temperature, but it prolongs the time required for the heat treatment and reduces productivity. An adhesive which is excellent in hardenability at low temperature has developed a radically polymerizable resin such as Acrylate in recent years.

File:TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 以及含有自由基聚合開始劑的接著劑。但是這類接著劑和 使用環氧樹脂相較之下,硬化狀態下的電氣特性與耐熱性 都較差。 【發明内容】 •本發明乃是為了解決上述舊有技術的問題所創作 的,其目的是為了提供一種能在低溫、短時間的條件下硬 化,同時具有優秀保存性的接著劑。 本發明的發明者等,不採用一般所使甩的硬化劑, 而著眼於使環氧樹脂做陽離子重合的手法上。經過反覆研 究,找出了以下方法:在構造中至少將一個烷氧基、構造 中含有石夕烧化合物(石夕烧偶合劑(Silane Coupling))以及 金屬螯合物(或是金屬Alcoholate)添加到接著劑中,利 用金屬螯合物與石夕院偶合(Silane Coupling)劑反應時所產 生的陽離子讓環氧樹脂重合(陽離子重合)。 添加了金屬螯合物與石夕烧偶合(Silane Coupling)劑的 接著劑,讓環氧樹脂硬化的硬化工程以下列反應式(1)〜(4) 來說明如下。 1270558File: TW1009 (060314) CRF.doc SUNDIAL CONFIDENTIAL and an adhesive containing a radical polymerization initiator. However, such an adhesive is inferior in electrical properties and heat resistance in a hardened state as compared with the use of an epoxy resin. SUMMARY OF THE INVENTION The present invention has been made to solve the above problems of the prior art, and an object thereof is to provide an adhesive which can be hardened under low temperature and short-time conditions while having excellent preservability. The inventors of the present invention have not focused on a hardener which is generally used for bismuth, but have focused on a method in which an epoxy resin is used as a cation. After repeated research, we found the following method: at least one alkoxy group in the structure, the structure containing the Si Xizhuo compound (Silane Coupling) and the metal chelate (or metal Alcoholate) added In the adhesive, the cation generated by the reaction of the metal chelate with the Silane Coupling agent causes the epoxy resin to overlap (cation overlap). A hardening process in which a metal chelate compound and a Silane Coupling agent are added and the epoxy resin is hardened is explained below by the following reaction formulas (1) to (4). 1270558

SUNDIAL CONFIDENTIALSUNDIAL CONFIDENTIAL

File:TW1009(060314)CRF.doc 【化1】 X-Si-0R+H20—X-Si-OH+R-OH 反應式(1) A1 + OH-Si-X^ XAl-0-Si-X+RH 反應式(2)File:TW1009(060314)CRF.doc [Chemical 1] X-Si-0R+H20-X-Si-OH+R-OH Reaction formula (1) A1 + OH-Si-X^ XAl-0-Si-X +RH reaction formula (2)

R 、Al-0-Si-X+X-Si-OH—X-Si-〇 -H+ ;Al-〇-Si-X 反應式(3) R-CH-CH2-^R-CH-CH2 + -> R-CH-CH2+R, Al-0-Si-X+X-Si-OH-X-Si-〇-H+ ; Al-〇-Si-X Reaction formula (3) R-CH-CH2-^R-CH-CH2 + - > R-CH-CH2+

\ I I I\ I I I

Ο H+ OH' R-CH-CH2 O \〇’ R-CH-CH2 ΟΗΓ 反應式(4) 至少擁有一個烧氧的石夕烧化合物,如反應式(1)所 示,與接著劑中的水反應,烧氧基就會加水分解,成為石夕 烷醇(Silanol)基。 將接著劑加熱,石夕烧醇基會與像铭螯合物這類的金 屬螯合物產生反應,矽烷化合物會與鋁螯合物結合。(反 應式(2)) 然後如反應式(3)所示,矽烷醇基與結合了的鋁螯合 物因為平衡反應,接著劑中殘留的其他矽烷醇基會配位, 1270558Ο H+ OH' R-CH-CH2 O \〇' R-CH-CH2 ΟΗΓ Reaction formula (4) At least one oxygen-burning compound, as shown in reaction formula (1), with water in the adhesive In the reaction, the alkoxy group is hydrolyzed to form a Silanol group. When the adhesive is heated, the sulphuric acid group reacts with a metal chelate such as a chelate compound, and the decane compound binds to the aluminum chelate compound. (Reaction formula (2)) Then, as shown in the reaction formula (3), the decyl alcohol group and the combined aluminum chelate are coordinated by the equilibrium reaction, and other stanol groups remaining in the binder are coordinated, 1270558

File:TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 產生Branstade酸點,如反應式(4)所示,因為活性化了的 質子的關係,位於環氧樹脂末端的環氧環就會打開環,與 其他的環氧樹脂的環氧環相重合(陽離子重合)。因此, 將石夕烧偶合劑(Silane Coupling)與金屬螯合劑添加到接著 劑中時,像環氧樹脂這類的熱硬化樹脂就會發生陽離子重 合。反應式(2)〜(4)所示的反應,是在比舊有接著劑硬化 的溫度(180°C以上)還低的溫度下進行的,因此前述的 接著劑比起舊有的接著劑,可在較低溫、短時間内硬化。 但是,金屬螯合物與金屬Alcoholate如與石夕烧偶合 (Silane Coupling)劑一起直接添加到接著劑中時,就會在 常溫下也能進行環氧樹脂的重合反應,造成接著劑黏度變 高。 因此,本發明者等人,在常溫下不會與環氧樹脂發 生反應的樹脂成份所構成的膠囊中,封入上述的金屬螯合 物,找出了潛在性硬化劑添加在接著劑的方法。 本發明即是基於上述創見所創作,申請專利範圍第1 項所記載的發明,為一種潛在性硬化劑,具有硬化劑粒子 以及包覆前述硬化劑粒子表面的膠囊,前述硬化劑粒子是 以金屬螯合物或是金屬Alcoholate之其中一者,或兩者為 主要成份。其前述膠囊,是以氟化樹脂為主成份之潛在性 1270558File:TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL Produces Branstade acid point. As shown in reaction formula (4), the epoxy ring at the end of the epoxy resin opens the ring due to the activated proton relationship. The epoxy ring of the epoxy resin is coincident (cationic overlap). Therefore, when a Silane Coupling and a metal chelating agent are added to the adhesive, a thermosetting resin such as an epoxy resin undergoes cation overlap. The reaction represented by the reaction formulas (2) to (4) is carried out at a temperature lower than the temperature at which the old adhesive is cured (180 ° C or higher), so that the above-mentioned adhesive is superior to the conventional adhesive. It can be hardened at a lower temperature and in a shorter time. However, when the metal chelate compound and the metal Alcoholate are directly added to the adhesive together with the Silane Coupling agent, the epoxy resin can be recombined at room temperature, resulting in high adhesive viscosity. . Therefore, the inventors of the present invention have sealed a metal chelating agent in a capsule composed of a resin component which does not react with an epoxy resin at a normal temperature, and have found a method in which a latent curing agent is added to an adhesive. The present invention is based on the above-mentioned invention, and the invention described in claim 1 is a latent curing agent having a hardener particle and a capsule covering the surface of the hardener particle, wherein the hardener particle is a metal. One of the chelate or metal Alcoholate, or both, is the main component. The aforementioned capsule is the potential of fluorinated resin as the main component 1270558

FileiTWl 009(060314)CRF.doc SUNDIAL CONFIDENTIAL 硬化劑。 申請專利範圍第2項所記載的發明,是如申請專利範 圍第1項所記載之潛在性硬化劑,其前述的金屬螯合物是 以紹螯合物為主成份之潛在性硬化劑。 申請專利範圍第3項所記載之發明,是如申請專利 範圍第1項所記載之潛在性硬化劑,其前述的金屬 Alcoholate是以銘Alcoholate為主成份之潛在性硬化劑。 申請專利範圍第4項所記載之發明,是一種如申請 專利範圍第1項到申請專利範圍第4項之任何一項記載之 潛在性硬化劑。前述膠囊為平均粒徑比硬化劑粒子的平均 粒徑還小的樹脂粒子,該樹脂粒子會附著於前述硬化劑表 面,經熔解形成如前述申請專利範圍第1項〜第3項中所 記載之任何一種潛在性硬化劑。 申請專利範圍第5項所記載之發明,如申請專利範 圍第4項所記載之潛在性硬化劑,其前述的樹脂粒子熔點 在30°C以上350°C以下。 申請專利範圍第6項所記載之發明,如申請專利範 圍第4項所記載之潛在性硬化劑,其前述的樹脂粒子的熱 分解温度在50°C以上500°C以下。 申請專利範圍第7項所記載之發明,如申請專利範 11 1270558FileiTWl 009 (060314) CRF.doc SUNDIAL CONFIDENTIAL Hardener. The invention described in claim 2 is the latent curing agent according to the first aspect of the invention, wherein the metal chelate compound is a latent curing agent containing a chelating chelate as a main component. The invention described in claim 3 is the latent curing agent according to the first aspect of the patent application, wherein the metal Alcoholate is a latent curing agent containing Alcoholate as a main component. The invention described in claim 4 is a latent sclerosing agent as described in any one of claims 1 to 4 of the patent application. The capsule is a resin particle having an average particle diameter smaller than an average particle diameter of the curing agent particles, and the resin particles adhere to the surface of the curing agent and are melted to form the first to third items as recited in the aforementioned patent scope. Any kind of latent hardener. The invention described in claim 5, wherein the resin particles have a melting point of 30 ° C or more and 350 ° C or less as described in the fourth aspect of the invention. The invention described in claim 6 is the latent hardener according to the fourth aspect of the invention, wherein the resin particles have a thermal decomposition temperature of 50 ° C or more and 500 ° C or less. Applying for the invention described in item 7 of the patent scope, such as applying for a patent model 11 1270558

File:TW1009(060314)CRF.doc οτFile:TW1009(060314)CRF.doc οτ

SUNDIAL CONFIDENTIAL 圍第4項戶斤記載之潛在性硬化劑,其前述的樹脂粒子的軟 化溫度在〇°C以上300°C以下。 申請專利範圍第8項所記載之發明,如申請專利範 圍第4項所記載之潛在性硬化劑,其前述的樹脂粒子的玻 璃移轉溫度在—40°C以上300°C以下。 申請專利範圍第9項所記載之發明,是—種潛在性 硬化劑的製造方法,該方法包括硬化劑粒子、前述包覆在 硬化劑粒子表面的膝囊,以及製造前述硬化劑粒子的工 程,其前述膠囊,是以敦化樹脂為主成份之潛在性硬化 劑’同時是-種潛在性硬化劑的製造方法,該方法包含了 以則述樹脂成份為主要成份,以平均粒徑較前述硬化劑粒 子還小的粉體狀樹脂粒子附著在前述硬化劑粒子的表面 上’讓附著在前述硬化劑粒子表面的前述樹脂粒子溶解, 形成4述膠囊的膠囊化工程。 申請專利範圍第1G項所記載之發明,如巾請專利範 圍第9項所3己載的潛在性硬化劑的製造方法中,具有2種 工程。1是前述的膠囊化工程,是將前述硬化劑粒子與前 述膠囊材料混合,讓前述硬化劑粒子表面沾附前述的膠囊 材料的此合工程。1是在前述硬化劑粒子沾附了前述膠囊 ;斗的狀U進^Γ擾拌,讓前述膠囊材料熔解的擾样工 12 1270558SUNDIAL CONFIDENTIAL The latent hardener described in the fourth item, wherein the resin particles have a softening temperature of 〇 ° C or more and 300 ° C or less. The invention described in claim 8 is the latent curing agent according to the fourth aspect of the invention, wherein the resin particles have a glass transition temperature of from -40 ° C to 300 ° C. The invention described in claim 9 is a method for producing a latent curing agent, which comprises a hardener particle, a knee capsule coated on the surface of the hardener particle, and a process for producing the hardener particle. The capsule is a latent hardener which is a main component of Dunhua resin, and is a method for producing a latent hardener. The method comprises the above-mentioned resin component as a main component and an average particle diameter of the hardener. The powdery resin particles having small particles adhere to the surface of the hardener particles, and the resin particles adhering to the surface of the hardener particles are dissolved to form an encapsulation process of the capsules. The invention described in the Patent Application No. 1G has two types of work in the method for producing a latent curing agent contained in the third paragraph of the Patent Application No. 9. 1 is the above-described encapsulation process in which the above-mentioned hardener particles are mixed with the above-mentioned capsule material, and the above-mentioned capsule material is adhered to the surface of the above-mentioned hardener particles. 1 is a scrambler in which the aforementioned hardener particles are adhered to the capsule; the shape of the bucket is disturbed, and the capsule material is melted. 12 1270558

File:TW1009(060314)CRF.docFile:TW1009(060314)CRF.doc

SUNDIAL CONFIDENTIAL 程0 申請專利範圍第1 1 圍第9項以及申請項目第 性硬化劑的製造方法中, 述膠囊材料的平均粒徑的 項所記載之發明,如申請專利範 10項之任何一項所記載的潛在 鈾述硬化劑粒子的平均粒徑對前 比為 100 : 80。 申請專利範圍第12項所印截夕菰0日L ^ 、汴。己戟之卷明,如申請專利範 圍第9項以及申請專利範圍筮 月斧〜乾固弟10項之任何一項所記載的 潛在性硬化劑的製造方法Φ 乂 安中則述硬化劑粒子的平均粒徑 對前述膠囊材料的平均粒徑的比為100:50。 申請專利範圍第13項所記載之發明,含有熱硬化性 樹脂、石夕炫偶合劑(silane coupling)以及如申請專利範圍 第1項至中ef專利*圍第8項之任何—項所記載的潛在性 硬化劑之接著劑。 本發明的構成如上,將粉體狀的膠囊材料與硬化劑 粒子混合攪拌後,膠囊材料就會因為靜電效果附著在硬化 劑粒子表面。在這個狀態下,以高速攪拌硬化劑粒子的 話,硬化劑粒子表面上因為靜電附著的樹脂粒子就會與攪 拌裝置内的攪拌器、内壁以及其他的硬化劑粒子表面的樹 脂粒子等撞及,因為這種物理性的撞擊所產生的能量黑樹 脂粒子溶解,或是打入芯物質(硬化劑粒子)。溶解了的 13 1270558SUNDIAL CONFIDENTIAL Process 0 Patent Application No. 9 of the Patent Application No. 9 and the manufacturing method of the first-part hardening agent of the application item, the invention described in the item of the average particle diameter of the capsule material, such as any one of the application patents No. 10 The average granule size of the potential uranium hardener particles described is 100:80. The date of application for the patent application is 12th, 菰 0, L ^, 汴. The method of manufacturing the latent hardener described in item 9 of the scope of patent application and the scope of application of the patent, 筮月Axe~ dry solid 10, Φ 乂The ratio of the average particle diameter to the average particle diameter of the aforementioned capsule material was 100:50. The invention described in claim 13 contains a thermosetting resin, a silane coupling, and any one of items 8 to 8 of the patent application scope 1 to ef patent*. An adhesive for latent hardeners. According to the configuration of the present invention, after the powdery capsule material and the hardener particles are mixed and stirred, the capsule material adheres to the surface of the hardener particles due to the electrostatic effect. In this state, when the hardener particles are agitated at a high speed, the resin particles adhering to the surface of the hardener particles due to static electricity collide with the agitator, the inner wall, and other resin particles on the surface of the hardener particles in the stirring device because The energy generated by this physical impact dissolves the black resin particles or breaks into the core material (hardener particles). Dissolved 13 1270558

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SUNDIAL CONFIDENTIAL 樹脂粒子會融合為-體,形成包覆硬化劑粒子表面的膠 囊。 以上述以潛在性硬化劑與矽烷偶合(su⑽㊁叩) 劑以及環氧樹脂混合製成接著劑時,在常溫下硬化劑粒子 表面王邛被膠囊所包覆,不會與環氧樹脂發生重合反應, 因此接著記得保存性很高,但是當接著劑被加熱時,勝囊 會軟化或熔解,膠囊的機械性強度會明顯降低。所以當接 著劑被加熱時,硬化劑粒子會因為熱膨脹與熱壓著時的加 壓等物理性衝擊讓膠囊輕易遭到破壞,硬化劑粒子就會被 釋放到接著劑中。 這個狀態要是持續加熱,硬化劑粒子的主成份__ 金屬螯合物與接著劑中的矽烷偶合(Silane c〇upHng)劑就 會產生反應,生成陽離子,因為陽離子而與環氧樹脂重合 (陽離子重合),接著劑就會硬化。 硬化劑粒子與石夕烧偶合(Silane Coupling)劑的反應, 比統的接著劑發生熱硬化的溫度以上)還低溫, 因此本發明之接著劑能以更低溫、更短時間内硬化。 為了加大與環氧樹脂接觸的面積,硬化劑粒子的平 均粒控最好小一些,但是當硬化劑粒子的平均粒徑變得太 小時’與樹脂粒子的粒徑差就變小,很難形成膠囊,所以 14 1270558SUNDIAL CONFIDENTIAL Resin particles are fused into a body to form a capsule covering the surface of the hardener particles. When the above-mentioned latent curing agent is mixed with a decane coupling (su(10) diterpenal) agent and an epoxy resin to form an adhesive, the surface of the hardener particles is coated with a capsule at room temperature, and does not overlap with the epoxy resin. Therefore, it is then remembered that the preservative is very high, but when the adhesive is heated, the winning capsule will soften or melt, and the mechanical strength of the capsule will be significantly lowered. Therefore, when the binder is heated, the hardener particles are easily damaged by physical shocks such as thermal expansion and compression at the time of hot pressing, and the hardener particles are released into the adhesive. In this state, if the heating is continued, the main component of the hardener particles, the metal chelate, reacts with the decane coupling (Silane c〇upHng) in the adhesive to form a cation, which is superposed with the epoxy resin due to the cation (cation Coincidence), the adhesive will harden. The reaction of the hardener particles with the Silane Coupling agent at a temperature higher than the temperature at which the adhesive is thermally cured is also low, so that the adhesive of the present invention can be hardened at a lower temperature and in a shorter time. In order to increase the area in contact with the epoxy resin, the average particle size of the hardener particles is preferably smaller, but when the average particle diameter of the hardener particles becomes too small, the difference in particle size from the resin particles becomes small, which is difficult. Forming a capsule, so 14 1270558

File:TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 硬化劑粒子的平均粒徑最好在〇. 5 // m以上5 0 // m以下。 此外,如上所數,樹脂粒子與硬化劑粒子的混合需 要經攪拌來製造潛在性硬化劑時,可採用混合攪拌裝置 (例如奈良機械製作所(株)公司製造的「NHS-0」)。這 裡的硬化劑粒子與膠囊材料的添加比率,以下列式子(1) 來計算。 式(1)……M/m=D X F/(4xdxf) 上列式子(1)中,Μ為硬化劑粒子的添加量(g),m為膠 囊材料的添加量(g),D為粉體狀硬化劑粒子的平均粒徑 (/zm),d為膠囊材料的平均粒徑(/zm),F為硬化劑粒 子的比重,f為膠囊材料的比重。此外,比重是指標準物 質在4 °C時,對水的密度各物質的密度比。但是,上述式 (1)為理論式子,硬化劑粒子與膠囊材料的最佳添加比率還 是要看狀況來決定。 此外,接著劑中如添加熱可塑性樹脂的話,熱可塑 性樹脂的性質會增加凝聚力,接著劑的黏著性會更高。如 果採用極性極高的熱可塑性樹脂,熱可塑性樹脂不僅會加 入環氧樹脂的硬化反應,透過$夕烧偶合(Silane Coupling) 劑也會與無機材料結合。因此不僅會讓接著劑的硬化性更 高,與無機材料類的被包覆體的親和性也會提高。 為讓本發明之上述目的、特徵、和優點能更明顯易 懂,下文特舉一較佳實施例,並配合所附圖式,作詳細說 15 1270558File: TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL The average particle size of the hardener particles is preferably 〇. 5 // m or more and 5 0 // m or less. In addition, when the mixing of the resin particles and the hardener particles is required to produce a latent curing agent, a mixing and agitating device (for example, "NHS-0" manufactured by Nara Machinery Co., Ltd.) can be used. The ratio of addition of the hardener particles to the capsule material herein is calculated by the following formula (1). Formula (1)...M/m=DXF/(4xdxf) In the above formula (1), Μ is the amount of addition of the hardener particles (g), m is the amount of addition of the capsule material (g), and D is powder. The average particle diameter (/zm) of the bulk hardener particles, d is the average particle diameter (/zm) of the capsule material, F is the specific gravity of the hardener particles, and f is the specific gravity of the capsule material. In addition, the specific gravity refers to the density ratio of each substance to the density of water at a standard substance at 4 °C. However, the above formula (1) is a theoretical formula, and the optimum addition ratio of the hardener particles to the capsule material is determined depending on the condition. Further, if a thermoplastic resin is added to the adhesive, the properties of the thermoplastic resin increase the cohesive force, and the adhesion of the adhesive is higher. If a highly polar thermoplastic resin is used, the thermoplastic resin will not only be added to the hardening reaction of the epoxy resin, but also the inorganic material will be bonded through the Silane Coupling agent. Therefore, not only the curability of the adhesive is increased, but also the affinity with the coated body of the inorganic material is improved. The above described objects, features, and advantages of the present invention will become more apparent and understood.

File:TWl009(060314)CRF.docFile:TWl009(060314)CRF.doc

SUNDIAL CONFIDENTIAL 明如下: 【實施方式】 以下說明製造本發明之潛在性硬化劑的工程。 首先,將金屬螯合物一一鋁螯合物溶解在有機溶劑 中,製成金屬螯合物溶解劑後,以噴霧乾燥裝置將上述金 屬折合物溶液喷霧乾燥,得到硬化劑粒子(噴霧乾燥Spray dryer法)。第1(a)圖的符號31所示為硬化性粒子。 然後準備熔點在3(TC以上35CTC以下,熱分解溫度 在5(TC以上500它以下,軟化溫度在0它以上3〇(rc以下, 玻璃移轉溫度在-40°C以上300°C以下等各項條件之粉體 狀樹脂(樹脂粒子)。樹脂粒子的平均粒徑對上述硬化劑 粒子材料的平均粒徑比為丨〇〇 : 80以上。 接著,將硬化性粒子31與樹脂粒子依照規定的添加 比率混合,放在混合裝置内攪拌後,平均粒徑比硬化劑粒 子31還小的樹脂粒子就會因為靜電性附著包覆在硬化劑 粒子31的表面上(混合工程)。第1(b)圖的符號32所示 為在此狀態下的膠囊材料,1個硬化劑粒子31的表面上 包覆著許多個樹脂粒子32。 將表面上有靜電性附著樹脂粒子32的硬化劑粒子31 杈入攪拌裝置硬化劑粒子3丨表面的樹脂粒子32就會因為 1270558SUNDIAL CONFIDENTIAL is as follows: [Embodiment] The following is a description of the process for producing the latent hardener of the present invention. First, the metal chelate compound-aluminum chelate compound is dissolved in an organic solvent to prepare a metal chelate dissolving agent, and then the metal compound solution is spray-dried by a spray drying device to obtain a hardener particle (spray drying). Spray dryer method). Symbol 31 in the first (a) diagram shows curable particles. Then, the melting point is 3 (TC or more and 35 CTC or less, the thermal decomposition temperature is 5 (TC or more and 500 or less, and the softening temperature is 0 or more and 3 〇 (rc or less, glass transition temperature is -40 ° C or higher and 300 ° C or lower, etc.) Powder-like resin (resin particle) of various conditions. The average particle diameter of the resin particle to the hardener particle material has an average particle diameter ratio of 丨〇〇: 80 or more. Next, the curable particle 31 and the resin particle are regulated. After the addition ratio is mixed and stirred in the mixing device, the resin particles having an average particle diameter smaller than the hardener particles 31 are coated on the surface of the hardener particles 31 by electrostatic adhesion (mixing process). b) The capsule material in this state is shown in the figure 32. The surface of one hardener particle 31 is covered with a plurality of resin particles 32. The hardener particles 31 having electrostatically attached resin particles 32 on the surface are provided. Pour the resin particles 32 on the surface of the hardener particles 3 of the stirring device because 1270558

File:TW1009(060314)CRP.doc SUNDIAL CONFIDENTIAL 與其他硬化性粒子31表面的樹脂粒子32,或是攪拌裝置 的迴轉扇葉、内壁等碰撞,或是摩擦生熱,而讓樹脂粒子 32熔解,熔解了的樹脂粒子32之間就會變成一體(攪拌 工程)。 第1 ( C)圖的符號33所示就是樹脂粒子32合成一 體後所形成的膠囊。膠囊33會包覆住整個硬化劑粒子31 的表面,硬化劑粒子31與膠囊33就構成了潛在性硬化劑 30 ° 接著要說明使用上述潛在性硬化劑30製成的本發明 接著劑以及使用本發明之接著劑所製成的電氣設備的製 造工程。將屬熱硬化性樹脂的環氧樹脂、熱可塑性樹脂、 石夕烧偶合(Silane Coupling)劑、上述的潛在性硬化劑30、 導電性粒子、溶劑分別依規定的添加比率混合攪拌,做成 接著劑。在這個狀態時,接著劑為糨糊狀。 第2(a)圖的符號21所顯示的是剝離膠膜。將上述 接著劑以一定量塗抹於此剝離膠膜21表面,乾燥後接著 劑中的溶劑會揮發掉,形成接著劑的塗佈層(第2(b)圖)。 第2(b)圖的符號20顯示的是形成了塗佈層25狀態 '的接著膜。該圖的符號27所示為隨著潛在性硬化劑30 — 起分散到接著劑中的導電性粒子。在這個狀態下,潛在性 17 1270558File: TW1009 (060314) CRP.doc SUNDIAL CONFIDENTIAL Collisions with the resin particles 32 on the surface of the other hardenable particles 31, or the rotating blades, inner walls, etc. of the stirring device, or frictional heat generation, and the resin particles 32 are melted and melted. The resin particles 32 become integrated (stirring process). The symbol 33 of the first (C) diagram shows a capsule formed by combining the resin particles 32. The capsule 33 covers the entire surface of the hardener particles 31, and the hardener particles 31 and the capsule 33 constitute a latent curing agent 30°. Next, the adhesive of the present invention prepared using the above-mentioned latent curing agent 30 and the use of the present invention will be described. Manufacturing work of electrical equipment made by the adhesive of the invention. The epoxy resin, the thermoplastic resin, the Silane Coupling agent, the above-mentioned latent curing agent 30, the conductive particles, and the solvent which are thermosetting resins are mixed and stirred at a predetermined addition ratio, respectively Agent. In this state, the adhesive is paste-like. The symbol 21 of the second (a) figure shows a peeling film. The above-mentioned subsequent agent is applied to the surface of the release film 21 in a predetermined amount, and after drying, the solvent in the adhesive is volatilized to form a coating layer of the adhesive (Fig. 2(b)). Reference numeral 20 in Fig. 2(b) shows an adhesive film in which the state of the coating layer 25 is formed. Symbol 27 of the figure shows conductive particles dispersed in the adhesive together with the latent curing agent 30. In this state, the potential 17 1270558

File:TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 硬化劑30的硬化性粒子31被封入到膠囊33内,硬化性 粒子30不會和構成圖塗佈層25之接著劑中的矽烷偶合 (Silane Coupling)劑接觸,在常溫下不會和塗佈層25發生 硬化反應。 第3(a)圖的符號11所示為LCD,LCD11在玻璃基 板12、玻璃基板12的一面上形成狹窄、多支的ITO電極 13 ( Indium tin oxide )。此圖所示為5條的ITO電極13。 在LCD11形成ITO電極13的面上,連接後述的TCP 部份對準第2(b)圖所示支接著膜20的塗佈層25(第3(b) 圖)。剝離膜21與塗佈層25的接著力,由於比塗佈層25 與ITO電極13之間的還小,因此當剝離膜21剝離後,塗 佈層25就留在LCD11上(第3(c)圖)。 第5圖符號15所示為TCP。TCP15有長形的基礎膜 16,在基礎膜16的一面上,狹窄的金屬配線17沿著基礎 膜16的長度方向配置(在此的圖示為5條的金屬配線) 了好幾條。金屬配線17在長度方向的末端分別位於基礎 膜16的長度方向的末端。 第3(d)圖所示為第5圖中A-A線截面圖,在配置有 TCP15金屬配線17那一側的面上,朝向配置有LCD11ITO 電極13,TCP15的一端與ITO電極13的塗佈層25相對, 18 1270558File: TW1009 (060314) CRF.doc SUNDIAL CONFIDENTIAL The curable particles 31 of the curing agent 30 are enclosed in the capsule 33, and the curable particles 30 are not coupled to the decane in the adhesive constituting the coating layer 25 (Silane Coupling). When the agent is in contact, it does not undergo a hardening reaction with the coating layer 25 at normal temperature. The reference numeral 11 in Fig. 3(a) shows an LCD, and the LCD 11 forms a narrow and a plurality of ITO electrodes 13 (Indium tin oxide) on one surface of the glass substrate 12 and the glass substrate 12. This figure shows five ITO electrodes 13. On the surface of the LCD 11 on which the ITO electrode 13 is formed, a TCP portion to be described later is connected to the coating layer 25 of the support film 20 shown in Fig. 2(b) (Fig. 3(b)). Since the adhesion between the release film 21 and the coating layer 25 is smaller than that between the coating layer 25 and the ITO electrode 13, the coating layer 25 remains on the LCD 11 after the release film 21 is peeled off (3 (c )))). The symbol 15 in Fig. 5 shows TCP. The TCP 15 has an elongated base film 16. On one surface of the base film 16, a narrow metal wiring 17 is disposed along the longitudinal direction of the base film 16 (here, five metal wirings are shown here). The ends of the metal wires 17 in the longitudinal direction are respectively located at the ends in the longitudinal direction of the base film 16. 3(d) is a cross-sectional view taken along line AA of FIG. 5, and a coating layer on which the LCD11 ITO electrode 13, the one end of the TCP 15 and the ITO electrode 13 are disposed is disposed on the surface on the side where the TCP15 metal wiring 17 is disposed. 25 relative, 18 1270558

File:TW1009(060314)CRP.doc LCD11 的 ITO 電極 13 與 TCP15 SUNDIAL CONFIDENTIAL 的金屬配線17相互相對。 在此狀態下,將TCP15的金屬配線17所配置的面按 壓向塗佈層25 ’將TCP15與LCD 11相重疊的部份按壓在 一起,然後整體作加熱,這麼一來塗佈層25就會軟化, 因為按壓金屬配線17會將軟化了的塗佈層25按壓後退, 殘留的塗佈層25中的導電性粒子27就會被夾在金屬配線 17與ITO電極13之間(第4(e)圖)。 在這個狀態下如果繼續加熱按壓,加熱會使膠囊33 熔解或軟化,膠囊33的機械強度就會明顯變弱。這時, 因為加熱硬化劑粒子會發生熱膨脹,因為加熱而使機械性 強度減弱的膠囊33就會破裂,硬化劑粒子31就會與塗布 層25中的環氧樹脂以及矽烷偶合(Silane c〇upling)劑混 合。 當硬化劑粒子31就會與塗布層25中的環氧樹脂以 及矽烷偶合(Silane Coupling)劑混合,構成硬化劑粒子31 的銘螯合物就會與矽烷偶合(Silane coupling)劑反應,塗 佈層25中的陽離子就會被釋放出來。該陽離子會使環氧 進行(陽離子重合),金屬配線17與ΓΓΟ電極13就會在 包夾住導電性粒子27 ,在此狀態下塗佈層25就會硬化。 (第4(f)圖) 19 1270558File: TW1009 (060314) CRP.doc The ITO electrode 13 of the LCD11 and the metal wiring 17 of the TCP15 SUNDIAL CONFIDENTIAL are opposed to each other. In this state, the surface on which the metal wiring 17 of the TCP 15 is placed is pressed against the coating layer 25' to press the portion where the TCP 15 and the LCD 11 overlap, and then the whole is heated, so that the coating layer 25 is applied. Softening, since pressing the metal wiring 17 presses and retreats the softened coating layer 25, and the conductive particles 27 in the remaining coating layer 25 are sandwiched between the metal wiring 17 and the ITO electrode 13 (4th (e )))). In this state, if the heating and pressing are continued, the heating causes the capsule 33 to melt or soften, and the mechanical strength of the capsule 33 is remarkably weakened. At this time, since the heat hardener particles are thermally expanded, the capsule 33 which is weakened by mechanical strength is broken, and the hardener particles 31 are coupled with the epoxy resin and the decane in the coating layer 25 (Silane c〇upling). Mix the agents. When the hardener particles 31 are mixed with the epoxy resin and the silane coupling agent in the coating layer 25, the chelating compound constituting the hardener particles 31 is reacted with a silane coupling agent, and coated. The cations in layer 25 will be released. The cation causes the epoxy to proceed (cation overlap), and the metal wiring 17 and the ruthenium electrode 13 sandwich the conductive particles 27, and the coating layer 25 is hardened in this state. (Fig. 4(f)) 19 1270558

File:TW1009(060314)CRF,doc SUNDIAL CONFIDENTIAL 第4(f)圖的符號10所示為塗佈層25在硬化狀態下 的電氣設備。該電氣設備1〇不僅其金屬配線17與It〇電 極13透過導電性粒子27電子得以繼續連接,LCD11與 TCP15也會硬化了的塗佈層25而產生機械性的連接,如 第5圖所示。 這麼一來,本發明之接著劑不僅擁有優秀的保存 性,還因為陽離子的重合而使環氧樹脂硬化,比過去的硬 化劑更能在低溫、短時間下讓接著劑硬化。 【實施例】 使用鋁螯合物(川研精練化學(株)公司製造的 Alumiun Tris acetactate )(商品名稱「I呂螯合物A(W)」以 及銘Alcoholate(川研精練化學(株)公司製造的Alumium Isopropylate (商品名稱「AIPD」)),將之分別分散到溶劑 曱基乙基甲酮(Methyl ethyl ketone ),分別製成含銘螯合 物10重量%的金屬螯合物溶液,含鋁Alcoholate 10重量 %的金屬Alcoholate溶液。 接著使用喷霧乾燥裝置(Yamato Lapochic (株)公 司製造商品名稱為「GC-31」),以噴霧入口溫度80。(:,噴 霧出口溫度60°C、喷霧壓力lkg/c πί,乾燥氮氣的流入量 20 1270558File: TW1009 (060314) CRF, doc SUNDIAL CONFIDENTIAL The symbol 10 of Fig. 4(f) shows the electrical equipment of the coating layer 25 in a hardened state. In the electrical device 1A, not only the metal wiring 17 and the It〇 electrode 13 are continuously connected to the electrons of the conductive particles 27, but the LCD layer 11 and the TCP 15 are also hardened by the coating layer 25 to form a mechanical connection, as shown in FIG. . As a result, the adhesive of the present invention not only has excellent preservability, but also hardens the epoxy resin because of the overlapping of the cations, and hardens the adhesive at a low temperature and a short time more than the conventional hardener. [Examples] An aluminum chelate compound (Alumiun Tris acetactate manufactured by Kawasaki Seiko Chemical Co., Ltd.) (trade name "I Lu Chelate A (W)" and Ming Alcoholate (manufactured by Kasei Seiko Chemical Co., Ltd.) were used. Alumium Isopropylate (trade name "AIPD"), which is separately dispersed in the solvent Methyl ethyl ketone to form a 10 chel % metal chelate solution containing the chelating compound, containing aluminum Alcoholate 10% by weight of a metal Alcoholate solution. Next, a spray drying apparatus (manufactured by Yamato Lapochic Co., Ltd., trade name "GC-31") was used to spray the inlet temperature of 80. (:, spray outlet temperature: 60 ° C, spray Pressure lkg/c πί, inflow of dry nitrogen 20 1270558

File:TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 0.5m3/分的條件,將金屬螯合物溶液與金屬Alcoholate溶 液分別喷霧、乾燥,製成2種粉體狀硬化劑(硬化劑粒子) (喷霧乾燥法)。另外,再準備樹脂粒子32——粉體狀的 氟化樹脂(Daikin工業(株)公司製造,商品名稱「Lupron L-5」,一次粒子直徑0.2/zm,熔點327°C )。 使用奈良機械製作所(株)公司製造、商品名稱為 「Hybridaizer-NHS-O」,以上述的第1(a),(b)圖之工程, 將上述硬化劑粒子31以20重量部以及上述樹脂粒子32 以3重量部混合,將樹脂粒子32靜電附著於硬化劑表面 後(混合工程),以周速l〇〇m/秒,處理時間5分鐘的運 轉條件進行攪拌(攪拌工程),形成膠囊33,獲得2種的 潛在性硬化劑30。 以對熱可塑性樹脂雙盼(bis phenol ) A型環氧樹脂 (油化Shell Epoxy (株)公司製造,商品名稱[「EP828」 50重量部添加熱可塑性樹脂酚鹽(phenoxy)樹脂(東都 化成(株)製造,商品名稱「YP50」)50重量部,矽烷偶 合(Silane Coupling)劑(曰本Unica (株)公司製造,商品 名稱「A-187」)1重量部、導電性粒子2.5重量部、各潛 在性硬化劑10重量部,以及有機溶劑,然後分散製成糨 糊狀的接著劑,以這些接著劑在上第2(a),(b)圖的工程 21 1270558File: TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 0.5m3/min, spray and dry the metal chelate solution and the metal Alcoholate solution to prepare two powdery hardeners (hardener particles) Fog drying method). In addition, resin particles 32, a powdery fluorinated resin (manufactured by Daikin Industrial Co., Ltd., trade name "Lupron L-5", primary particle diameter 0.2/zm, melting point 327 ° C) were prepared. The product of the first (a) and (b) above is manufactured by the Nara Machinery Co., Ltd. product under the trade name "Hybridaizer-NHS-O", and the above-mentioned hardener particles 31 are 20 parts by weight and the above resin. The particles 32 were mixed at a weight of 3 parts, and the resin particles 32 were electrostatically adhered to the surface of the curing agent (mixing process), and stirred at a peripheral speed of 1 〇〇 m / sec and a treatment time of 5 minutes (stirring process) to form a capsule. 33. Two types of latent hardeners 30 are obtained. Adding a thermoplastic resin phenate resin to the 50-weight portion of the thermoplastic resin bis phenol type A epoxy resin (manufactured by Oily Shell Epoxy Co., Ltd., trade name [EP828] (Dongdu Huacheng ( (manufactured by the company, "YP50"), a weight of 50 parts, a sane coupling (Silane Coupling) (manufactured by Uni本Unica Co., Ltd., trade name "A-187"), 1 part by weight, 2.5 parts by weight of conductive particles, 10 parts by weight of each latent hardener, and an organic solvent, and then dispersed to form a paste-like adhesive, with these adhesives in the second (a), (b) drawings of the work 21 1270558

File:TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 中,製成了實施例卜2的接著膜20。使用這些實施例1、 2的接著膜20分別進行下述的「室溫保存試驗」、「40°C 保存試驗」。 〔室溫保存試驗〕 利用這些實施例1、2與比較例1、2的接著膜20, 在上述第3(a)〜3(d)圖、第4 (e)、4(f)圖的工程,在TCP15 與LCD11連接後,測定LCD11上TCP15剝離時的剝離強 度(初期剝離強度)。 另外,利用這些實施例1、2與比較例1、2的接著 膜20,在室溫(25°C )下分別保存1日、3日、7曰, 使用保存過後的各接著膜20以上述相同的工程,分別連 接TCP15與LCD11之後,測定LCD11上TCP15剝離時 的剝離強度(保存後剝離強度)。 〔40°C保存試驗〕 這個試驗除了將接著膜20的保存溫度從室溫調整到 40°C之外,以前述的「室溫保存試驗」中相同條件保存接 著膜20,待TCP15與LCD11連接後,測定保存後剝離強 22 1270558File: TW1009 (060314) CRF.doc SUNDIAL CONFIDENTIAL The adhesive film 20 of Example 2 was produced. Using the adhesive film 20 of each of Examples 1 and 2, the following "room temperature storage test" and "40 ° C storage test" were carried out, respectively. [Room-temperature storage test] Using the adhesive films 20 of Examples 1 and 2 and Comparative Examples 1 and 2, the above-mentioned 3(a) to 3(d), 4(e), 4(f) In the project, after the TCP 15 was connected to the LCD 11, the peel strength (initial peel strength) at the time of peeling off the TCP 15 on the LCD 11 was measured. Further, the adhesive films 20 of the first and second embodiments and the comparative examples 1 and 2 were stored at room temperature (25 ° C) for 1 day, 3 days, and 7 weeks, respectively, and the respective adhesive films 20 after storage were used. In the same procedure, after connecting the TCP 15 and the LCD 11 respectively, the peel strength (peeling strength after storage) at the time of peeling off the TCP 15 on the LCD 11 was measured. [40 ° C storage test] In this test, except that the storage temperature of the adhesive film 20 was adjusted from room temperature to 40 ° C, the film 20 was stored under the same conditions as in the above-mentioned "room temperature storage test", and the TCP 15 was connected to the LCD 11 After the measurement, the peeling after the preservation is strong 22 1270558

File:TW1009F-IP〇.doc SUNDIAL CONFIDENTIAL 度。 在上述的「室溫保存試驗」與「4〇°C保存試驗」中, 保存後剝離強度如達初期剝離強度的90%以上則畫 「◎」,80%以上90%以下晝「〇」,70%以上80%以下畫 「△」,70%以下晝「X」以資評估,其評價結果如下表2 所記載。 【表1】 表1 :評價試驗的結果File:TW1009F-IP〇.doc SUNDIAL CONFIDENTIAL Degree. In the above-mentioned "room temperature storage test" and "4 〇 ° C storage test", if the peel strength after storage is 90% or more of the initial peel strength, "◎" is drawn, and 80% or more and 90% or less are "〇". 70% or more and 80% or less are drawn as "△", and 70% or less is evaluated as "X". The evaluation results are shown in Table 2 below. [Table 1] Table 1: Results of the evaluation test

室溫保存 40t保存 3曰 7曰 3曰 7曰 實施例1 ◎ ◎ ◎ 〇 實施例2 ◎ ◎ ◎ 〇 比較例1 X X X X 比較例2 X X Γ X X 上表1的比較例1、2是將實施例1、2所使用的 2種硬化劑粒子,不形成膠囊就直接添加到接著劑中。 此外,TCP15是以25/z m的金屬配線以25 # m的間 隔配置,LCD 11是表面積每Icm2的電阻是由10〇的IT〇 電極13所形成,在TCP15與LCD11相重疊的部份加上了 3Mpa的荷重,做10秒鐘加熱,讓塗佈層25的溫度升高 1270558Storage at room temperature 40 Torr storage 3 曰 7 曰 3 曰 7 曰 Example 1 ◎ ◎ ◎ 〇 Example 2 ◎ ◎ ◎ 〇 Comparative Example 1 XXXX Comparative Example 2 XX Γ XX Comparative Examples 1 and 2 of Table 1 above are examples The two types of hardener particles used in 1, 2 are directly added to the adhesive without forming a capsule. Further, the TCP 15 is arranged at 25 #m intervals with 25/zm metal wiring, and the LCD 11 has a surface area per Icm2. The resistance is formed by a 10 〇 IT 〇 electrode 13, which is overlapped between the TCP 15 and the LCD 11 The load of 3Mpa is heated for 10 seconds to increase the temperature of the coating layer 25 by 1270558.

File:TW1009F-IPO.doc 0File:TW1009F-IPO.doc 0

SUNDIAL CONFIDENTIAL 到130°C後相連接。 k上述表1、2中可看出,在使用將硬化劑粒子3 i 封入膠囊33中的實施例1、2當中,「室溫保存試驗」與 「4(TC保存試驗」的評價結果都良好。另一方面,未形成 膠囊’直接僵硬化劑添加到接著劑中的比較例丄、2,則 再各保存試驗的結果都很差。從這些結果來看,確認了使 用本發明之潛在性硬化劑的接著劑具有優秀的保存性。 以上說明了使用接著劑製造接著膜的情形,但是本 發明的用途不僅限於此,例如接著劑也可以直接以糨糊狀 來使用。 第6(a)圖的符號11所示與第3(a)圖所示相同,為 LCD,該LCD11在與TCpi^連接時,首先要在[cm 的ITO電極13表面上,在與TCP15相連接的部份塗抹接 著劑’形成接著劑的塗佈層45(第6(b)圖 然後在上第3(d)圖的工程中進行Tcpi5的對準位子 後,在上述第4(e)、4(f)圖的工程中,將TCpi5與LCmi 相連接,就可得到電氣設備4〇 (第6(c)圖)。 以上說明了使用接著劑連接TCP15與LCD11的情 形仁疋本發明之用途也不限於此,在基板與半導體晶片 的連接上,各種電氣設備的製造上都可使用。 24 1270558SUNDIAL CONFIDENTIAL is connected to 130 °C. k In the above Tables 1 and 2, in the examples 1 and 2 in which the hardener particles 3 i were enclosed in the capsule 33, the evaluation results of the "room storage test" and the "4 (TC storage test) were good. On the other hand, in the comparative example 丄 and 2 in which the capsule rigid hardener was not added to the adhesive, the results of the respective storage tests were poor. From these results, the potential of using the present invention was confirmed. The adhesive of the hardener has excellent storage stability. The above description has been made on the case of using an adhesive to produce a film, but the use of the present invention is not limited thereto, and for example, the adhesive may be used directly in the form of a paste. Fig. 6(a) The symbol 11 is the same as that shown in Fig. 3(a), and is an LCD. When the LCD 11 is connected to the TCpi, it is first applied on the surface of the [cm ITO electrode 13 and connected to the TCP 15 The agent 'forms the coating layer 45 of the adhesive (Fig. 6(b) and then performs the aligned position of Tcpi5 in the work of the above figure (d), in the above 4(e), 4(f) In the engineering, the TCpi5 is connected to the LCmi, and the electrical equipment is obtained (Fig. 6(c)). Illustrates the use of the adhesive connection TCP15 shaped kernel Cloth LCD11 situation of use of the present invention is not limited to this, on a connection substrate of the semiconductor wafer, can be used to manufacture a variety of electrical equipment. 241270558

File:TW1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 以上是指將導電性粒子分散到接著劑中的情形來作 說明,但本發明之用途也不限於此,例如不含導電性粒子 的接著劑也包含在本發明之範圍内。 金屬螯合物可以使用锆螯合物、鈦螯合物、鋁螯合 物等各種金屬螯合物,其中,最好採用反應性最高的鋁螯 合物。此外,以上也說明了喷霧乾燥法的硬化劑粒子製造 方法,但本發明不僅限於此。 以上說明了採用熔點327°C的氟化樹脂的情形,但本 發明的使用範圍不僅限於此,只要符合熔點在30°C以上 3 50°C以下,熱分解溫度在50°C以上500°C以下,軟化溫 度在0°C以上300°C以下,玻璃移轉溫度在-40°C以上300 °C以下等之一項條件,也可使用熱可塑性樹脂、架橋樹 脂、膠狀樹脂。 上述的樹脂,可使用例如較瞧壓克力樹脂(日本塗 料(株)公司製,商品名「Micro Gel」)、Poly-methyl methacrylate樹脂(綜研化學(株)公司製的「MP系列」)、 苯併二氨基三秦(Benzoguanamine )樹脂(日本觸媒(株) 公司製,商品名「Eposter」)、矽利康樹脂(GE東芝矽利 康(株)公司製,商品名「Tospar」)等。 具有上述特性之樹脂粒子溶解形成的膠囊,在膠囊 25 1270558File: TW1009 (060314) CRF.doc SUNDIAL CONFIDENTIAL The above description is for the case where the conductive particles are dispersed in the adhesive. However, the use of the present invention is not limited thereto, and for example, an adhesive containing no conductive particles is also included. It is within the scope of the invention. As the metal chelate compound, various metal chelate compounds such as a zirconium chelate compound, a titanium chelate compound, and an aluminum chelate compound can be used. Among them, the most reactive aluminum chelate compound is preferably used. Further, the method of producing the hardener particles by the spray drying method has also been described above, but the present invention is not limited thereto. Although the case of using a fluorinated resin having a melting point of 327 ° C has been described above, the scope of use of the present invention is not limited thereto, as long as the melting point is 30 ° C or more and 3 50 ° C or less, and the thermal decomposition temperature is 50 ° C or more and 500 ° C. Hereinafter, a softening temperature of 0 ° C or more and 300 ° C or less, and a glass transition temperature of -40 ° C or more and 300 ° C or less may be used, and a thermoplastic resin, a bridging resin, or a gel resin may be used. For the above-mentioned resin, for example, acryl resin (manufactured by Nippon Paint Co., Ltd., trade name "Micro Gel"), Poly-methyl methacrylate resin ("MP series" manufactured by Soken Chemical Co., Ltd.), Benzoguanamine resin (trade name "Eposter", manufactured by Nippon Shokubai Co., Ltd.), and Philippene resin (trade name "Tospar", manufactured by Toshiba Co., Ltd., GE Toshiba Co., Ltd.). A capsule having the above characteristics is dissolved in a capsule formed in a capsule 25 1270558

File:TWl009(060314)CRF.doc SUNDIAL CONFIDENTIAL 話工程中,構成樹脂粒子的樹脂有時會產生化學性變質, 這個情形可能是因為膠囊的熔點、熱分解溫度、軟化溫 度、玻璃移轉溫度分別超過前樹脂溫度範圍。File:TWl009(060314)CRF.doc SUNDIAL CONFIDENTIAL In the case of engineering, the resin constituting the resin particles sometimes undergoes chemical deterioration. This may be because the melting point, thermal decomposition temperature, softening temperature, and glass transition temperature of the capsule exceed Pre-resin temperature range.

以上的熱硬化性樹脂以環氧樹脂為例進行說明,但 本發明的用途不限於此。如果是陽離子重合樹脂,例如尿 素樹脂、三聚氰氨(melamin)樹脂、紛藤樹脂、乙烯醚 (vinyle ether )樹脂、Oxetane樹脂等等各種樹脂,但是 如考慮到硬化後的接著劑強度等,最好還是採用環氧樹 脂0 另外,本發明所採用的石夕烧偶合(Silane Coupling) 劑,最好能採用下列式子(6)所示的物質。 【化2】 X1—-Si——X3 ……一般式(5) (上列一般式子(5)裡,在置換基X1〜X4中至少有一 個置換基是烷氧基(alkoxy)。該烷氧基最好為甲氧基 (Methoxy )或乙氧基(Ethoxy )。此外,在烧氧基之外的 置換基X1〜X4當中,最好至少有一個置換基是環氧或乙 烯基,尤其最好是具有環氧置換基之Glycidil基。擁有乙 26 1270558The above thermosetting resin is exemplified by an epoxy resin, but the use of the present invention is not limited thereto. In the case of a cationically-carrying resin, for example, a urea resin, a melamin resin, a rattan resin, a vinyle ether resin, an Oxetane resin, or the like, but considering the strength of the adhesive after hardening, etc. It is preferable to use an epoxy resin. Further, in the case of the Silane Coupling agent used in the present invention, it is preferable to use the substance represented by the following formula (6). X1—-Si—X3 ...... General Formula (5) (In the above general formula (5), at least one of the substituents in the substituents X1 to X4 is an alkoxy. The alkoxy group is preferably a methoxy group (Methoxy) or an ethoxy group (Ethoxy). Further, among the substituents X1 to X4 other than the alkoxy group, at least one of the substituents is preferably an epoxy group or a vinyl group. Particularly preferred is a Glycidil group having an epoxy substituent. Having B 26 1270558

File:TW 1009(060314)CRF.doc SUNDIAL CONFIDENTIAL 稀基的有例如Metacryloxipropil基。此外置換基XI〜X4 全部都由Alchoxy基,即所謂的石夕酸鹽(Silicate )也可。) 熱可塑性樹脂除Phenoxy樹脂外,例如聚乙烯樹脂、 尿烧樹脂、聚醏酸乙烯_ (Polyvinyl acetate)、錯酸乙烯酉旨 (Ethylene Vinyle Acetate)、聚 丁二烯(Polybutadiene)橡膝 等橡膠類也可以使用。File: TW 1009 (060314) CRF.doc SUNDIAL CONFIDENTIAL There are, for example, Metacryloxipropil groups. Further, all of the substituents XI to X4 are derived from an Alchoxy group, a so-called Silicate. In addition to Phenoxy resin, thermoplastic resin, such as polyethylene resin, urinary resin, polyvinyl acetate, Ethylene Vinyle Acetate, Polybutadiene, rubber, rubber, etc. Classes can also be used.

此外,本發明之接著記也可添加老化防止劑、填充 劑、著色劑等等添加劑。 本發明之接著劑中,由於金屬螯合物所構成之硬化 劑粒子上包覆著膠囊,因此在常溫下不會發生環氧樹脂的 重合反應,接著劑的保存性很高。而且,本發明之接著劑, 會因為環氧樹脂的陽離子重合反應而硬化。陽離子的重合 反應比過去舊有的硬化劑重合反應發生的溫度還低,因 此,本發明之接著劑與過去的接著劑比較下,能在低溫、 短時間内硬化。 綜上所述,雖然本發明已以一較佳實施例揭露如 上,然其並非用以限定本發明,任何熟習此技藝者,在不 脫離本發明之精神和範圍内,當可作各種之更動與潤飾, 因此本發明之保護範圍當視後附之申請專利範圍所界定 者為準。 27 1270558Further, an additive such as an anti-aging agent, a filler, a coloring agent or the like may be added to the following in the present invention. In the adhesive of the present invention, since the hardener particles composed of the metal chelate compound are coated with the capsule, the superposition reaction of the epoxy resin does not occur at normal temperature, and the storage property of the adhesive is high. Further, the adhesive of the present invention is hardened by the cationic overlapping reaction of the epoxy resin. The superposition reaction of the cations is lower than the temperature at which the conventional hardener superposition reaction occurs in the past, and therefore, the adhesive of the present invention can be hardened at a low temperature and in a short time as compared with the conventional adhesive. In view of the above, the present invention has been described above in terms of a preferred embodiment, and is not intended to limit the invention, and various modifications may be made without departing from the spirit and scope of the invention. And the scope of the present invention is defined by the scope of the appended claims. 27 1270558

File:TW1009F-IPO.doc SUNDIAL CONFIDENTIAL 【圖式簡單說明】 第1(a)〜1(c)圖係為本發明一潛在性硬化劑製造工 程之一例的說明用圖面。 第2(a)、2(b)圖係為使用本發明之接著劑製造接著膜 的一工程例說明用圖面。 第3(a)〜3(d)圖係為使用本發明之接著劑黏接LCD 與TCP的前半段工程說明用圖面。 第4(e)、4(f)圖係為TCP與LCD黏接之後半工程的 說明用圖面。 第5圖係說明TCP與LCD在對準位置狀態下的平面 圖。 第6(a)〜6(c)圖係為其他使用本發明之接著劑之黏接 工程例的說明圖。 第7(a)〜7(c)圖係為使用傳統技術之接著劑,黏接 LCD與TCP之工程的說明圖。 圖式標號說明 20, 45 :接著劑(塗布層) 3 0 :潛在性硬化劑 31 :硬化劑粒子 32 :膠囊材料 28 1270558File: TW1009F-IPO.doc SUNDIAL CONFIDENTIAL [Simplified Schematic Description] Figs. 1(a) to 1(c) are diagrams for explaining an example of a latent hardener manufacturing process of the present invention. Figs. 2(a) and 2(b) are drawings for explaining an example of the construction of the adhesive film using the adhesive of the present invention. Figures 3(a) to 3(d) are drawings for the first half of the description of the bonding of the LCD and the TCP using the adhesive of the present invention. Figures 4(e) and 4(f) are diagrams for the half-engineering of TCP and LCD. Figure 5 is a plan view showing the state of the TCP and LCD in an aligned position. Figs. 6(a) to 6(c) are explanatory views of other examples of bonding work using the adhesive of the present invention. Figures 7(a) to 7(c) are explanatory diagrams of the process of bonding LCD and TCP using an adhesive of a conventional technique. DESCRIPTION OF SYMBOLS 20, 45 : Adhesive (coating layer) 3 0 : latent hardener 31 : hardener particle 32 : capsule material 28 1270558

File:TW1009F-IPO.doc SUNDIAL CONFIDENTIAL 33 :膠囊 29File:TW1009F-IPO.doc SUNDIAL CONFIDENTIAL 33 :Capsule 29

Claims (1)

1270558 File:TWl009(060314)CRP.doc SUNDIAL CONFIDENTIAL 申請專利範圍, 1. 一種潛在性硬化劑,包括一硬化劑粒子以及一包覆該 硬化劑粒子之表面的膠囊, 該硬化劑粒子具有一金屬螯合物及一金屬醇鹽 (Alcoholate)之其中一者或兩者,其中該膠囊成份的主 成份為氟化樹脂。 2. 如申請專利範圍第1項所述之潛在性硬化劑,其中該 金屬螯合物的主成份為铭螯合物。 3. 如申請專利範圍第1項所述之潛在性硬化劑,其中該 金屬Alcoholate的主成份為I呂Alcoholate。 4. 如申請專利範圍第1項所述之潛在性硬化劑,其中該 膠囊具有一平均粒徑比硬化劑粒子的平均粒徑還小的樹 脂粒子,該樹脂粒子會附著於該硬化劑粒子之表面,經熔 解形成如前述申請專利範圍第1〜3項中所記載之任何一 種膠囊。 5. 如申請專利範圍第4項所述之潛在性硬化劑,其中該 樹脂粒子熔點在30°C以上350°C以下。 6. 如申請專利範圍第4項所述之潛在性硬化劑,其中該 樹脂粒子的熱分解溫度在50°C以上500°C以下。 7.如申請專利範圍第4項所述之潛在性硬化劑,其中該 1270558 File:TWl 009(060314)CRF doc SUNDIAL CONFIDENTIAL 樹脂粒子的軟化溫度在以上30(TC以下。 &如中明專利_第4項所述之潛在性硬化劑,其中該 樹脂粒子的玻璃移轉溫度在書C以上30(TC以下。 9· -種潛在性硬化劑的製造方法,該潛在性硬化劑 更化W]粒子、一包覆在該硬化劑粒子之表面的膠 囊’该方法包括: 裝備該硬化劑粒子,該硬化劑粒子具有-金屬螯合物 及—金屬版相咖之其中—者或兩者; 附著—平均粒役較該硬化劑粒子還小的膠囊材料在 該硬化劑粒子的表面上’該膠囊材料具有一氟化樹脂,且 為粉體狀;以及 熔解附著在該硬化劑粒子之表面的該膠囊材料熔 解’以形成該膠囊。 10.如申凊專利範圍第9項所述之潛在性硬化劑的製造方 法,其中該形成該膠囊之步驟包括: 混合該硬化劑粒子與_囊材料,讓該硬化劑粒子 之表面沾附該膠囊材料;以及 攪 在該硬化劑粒子沾附了該膠囊材料的狀態下進行 拌’讓該膠囊材料熔解。 項其中之一所述之潛在性 U.如申請專利範圍第9與1〇 31 * 1270558 File.TWl〇〇9(〇6〇314)CRF.doc SUNDIAL CONFIDENTIAL 硬化劑的製造方法,其中該硬化劑粒子的平均粒徑對該膠 囊材料的平均粒徑的比為1⑽· 8〇。 12·如申請專利範圍第9與1〇項其中之一所述之潛在性 硬化劑的製造方法,其中該硬化劑粒子的平均粒徑對該膠 •囊材料的平均粒徑的比為1〇〇 : 50。 13. 一種接著劑,包括—熱硬化性樹脂、一石夕烧偶合⑽継 Couphng)劑以及一如申請專利範圍第i至8項之任何一項 所記載的潛在性硬化劑。 321270558 File: TWl009 (060314) CRP.doc SUNDIAL CONFIDENTIAL Patent application scope, 1. A latent hardener comprising a hardener particle and a capsule covering the surface of the hardener particle, the hardener particle having a metal chelate And one or both of the metal alkoxides, wherein the main component of the capsule component is a fluorinated resin. 2. The latent hardener according to claim 1, wherein the main component of the metal chelate is a chelate. 3. The latent hardener according to claim 1, wherein the metal Alcoholate has a main component of Ilu Alcoholate. 4. The latent hardener according to claim 1, wherein the capsule has resin particles having an average particle diameter smaller than an average particle diameter of the hardener particles, and the resin particles are attached to the hardener particles. The surface is melted to form any one of the capsules described in the first to third aspects of the above-mentioned patent application. 5. The latent hardener according to claim 4, wherein the resin particles have a melting point of from 30 ° C to 350 ° C. 6. The latent curing agent according to claim 4, wherein the resin particles have a thermal decomposition temperature of from 50 ° C to 500 ° C. 7. The latent hardener according to claim 4, wherein the softening temperature of the 1270558 File: TWl 009 (060314) CRF doc SUNDIAL CONFIDENTIAL resin particles is above 30 (TC or less. & The latent hardener according to Item 4, wherein the glass transition temperature of the resin particles is 30 or more in the book C (TC or less. 9. The method for producing a latent hardener, the latent hardener is further changed W] a particle, a capsule coated on the surface of the hardener particle, the method comprising: equipping the hardener particle, the hardener particle having a metal chelate and a metal plate, or both; - a capsule material having a smaller average particle size than the hardener particles on the surface of the hardener particles - the capsule material having a fluorinated resin and being in the form of a powder; and melting the surface attached to the surface of the hardener particle The capsule material is melted to form the capsule. The method for producing a latent hardener according to claim 9, wherein the step of forming the capsule comprises: mixing the hardener particles with _ a material, the surface of the hardener particles is adhered to the capsule material; and the mixture is stirred in a state in which the hardener particles are adhered to the capsule material, and the capsule material is melted. The potential U is one of the items. Patent Application No. 9 and 1 〇 31 * 1270558 File.TWl〇〇9(〇6〇314) CRF.doc SUNDIAL CONFIDENTIAL A method for producing a hardener, wherein an average particle diameter of the hardener particles is for the capsule material The ratio of the average particle diameter is 1 (10)·8 〇. The method for producing a latent hardener according to any one of claims 9 to 1 wherein the average particle size of the hardener particles is to the gel. The ratio of the average particle diameter of the capsule material is 1 〇〇: 50. 13. An adhesive comprising - a thermosetting resin, a singly coupled (10) 継 Couphng agent, and any of the items i to 8 of the patent application scope A potential hardener described. 32
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3565797B2 (en) * 2001-06-06 2004-09-15 ソニーケミカル株式会社 Latent curing agent, method for producing latent curing agent, and adhesive
JP4148685B2 (en) * 2002-02-18 2008-09-10 ソニーケミカル&インフォメーションデバイス株式会社 Latent curing agent, method for producing latent curing agent, and adhesive
JP4381255B2 (en) * 2003-09-08 2009-12-09 ソニーケミカル&インフォメーションデバイス株式会社 Latent curing agent
JP5417982B2 (en) * 2003-09-08 2014-02-19 デクセリアルズ株式会社 Latent curing agent
JP4811555B2 (en) 2005-01-12 2011-11-09 ソニーケミカル&インフォメーションデバイス株式会社 Latent curing agent
WO2006109831A1 (en) * 2005-04-12 2006-10-19 Sony Chemical & Information Device Corporation Processes for production of adhesives
JP5285841B2 (en) * 2005-04-12 2013-09-11 デクセリアルズ株式会社 Method for producing film adhesive
US7557230B2 (en) 2005-06-06 2009-07-07 Sony Corporation Latent curing agent
JP5057011B2 (en) * 2005-06-06 2012-10-24 ソニーケミカル&インフォメーションデバイス株式会社 Latent curing agent
WO2007007725A1 (en) * 2005-07-11 2007-01-18 Sony Chemical & Information Device Corporation Thermosetting epoxy resin composition
JPWO2007129662A1 (en) * 2006-05-08 2009-09-17 積水化学工業株式会社 Insulating material, method of manufacturing electronic component device, and electronic component device
JP4899095B2 (en) * 2006-12-04 2012-03-21 富士通株式会社 Manufacturing method of semiconductor device and adhesive used in the method
WO2008090719A1 (en) 2007-01-24 2008-07-31 Sony Chemical & Information Device Corporation Latent curing agent
JP5146645B2 (en) 2007-08-28 2013-02-20 デクセリアルズ株式会社 Microcapsule type latent curing agent
JP5469956B2 (en) * 2008-08-27 2014-04-16 デクセリアルズ株式会社 Magnetic sheet composition, magnetic sheet, and method for producing magnetic sheet
JP5832740B2 (en) 2010-11-30 2015-12-16 株式会社ダイセル Curable epoxy resin composition
JP7097665B2 (en) * 2015-12-11 2022-07-08 デクセリアルズ株式会社 Method for Producing Aluminum Chelate Latent Curing Agent and Thermosetting Epoxy Resin Composition

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