TW200409785A - Latent hardener, manufacturing method for latent hardener, and adhesive - Google Patents
Latent hardener, manufacturing method for latent hardener, and adhesive Download PDFInfo
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- TW200409785A TW200409785A TW91134974A TW91134974A TW200409785A TW 200409785 A TW200409785 A TW 200409785A TW 91134974 A TW91134974 A TW 91134974A TW 91134974 A TW91134974 A TW 91134974A TW 200409785 A TW200409785 A TW 200409785A
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- 239000000853 adhesive Substances 0.000 title claims abstract description 83
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 81
- 239000004849 latent hardener Substances 0.000 title claims description 35
- 238000004519 manufacturing process Methods 0.000 title claims description 18
- 239000002245 particle Substances 0.000 claims abstract description 141
- 239000002775 capsule Substances 0.000 claims abstract description 54
- 229910052751 metal Inorganic materials 0.000 claims abstract description 44
- 239000002184 metal Substances 0.000 claims abstract description 44
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 15
- 239000004848 polyfunctional curative Substances 0.000 claims description 91
- 229920005989 resin Polymers 0.000 claims description 59
- 239000011347 resin Substances 0.000 claims description 59
- 238000000034 method Methods 0.000 claims description 38
- 241001247287 Pentalinon luteum Species 0.000 claims description 27
- 230000008569 process Effects 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 22
- 229910000077 silane Inorganic materials 0.000 claims description 19
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 17
- 230000008878 coupling Effects 0.000 claims description 16
- 238000010168 coupling process Methods 0.000 claims description 16
- 238000005859 coupling reaction Methods 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 8
- 230000008018 melting Effects 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 7
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 230000009477 glass transition Effects 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- 238000005538 encapsulation Methods 0.000 claims description 4
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 4
- 230000008859 change Effects 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 2
- 150000002739 metals Chemical class 0.000 claims 1
- 239000003822 epoxy resin Substances 0.000 abstract description 25
- 229920000647 polyepoxide Polymers 0.000 abstract description 25
- 238000006243 chemical reaction Methods 0.000 abstract description 20
- 150000001768 cations Chemical class 0.000 abstract description 14
- 239000003795 chemical substances by application Substances 0.000 abstract description 11
- 238000001723 curing Methods 0.000 abstract description 5
- 239000013522 chelant Substances 0.000 abstract 2
- 238000010538 cationic polymerization reaction Methods 0.000 abstract 1
- 238000013035 low temperature curing Methods 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 239000011247 coating layer Substances 0.000 description 22
- 238000003860 storage Methods 0.000 description 18
- 101100206181 Arabidopsis thaliana TCP15 gene Proteins 0.000 description 13
- 238000012360 testing method Methods 0.000 description 12
- 239000002313 adhesive film Substances 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 10
- 229920005992 thermoplastic resin Polymers 0.000 description 9
- -1 silane compound Chemical class 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 150000002736 metal compounds Chemical class 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 238000001694 spray drying Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000007822 coupling agent Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 125000005372 silanol group Chemical group 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 235000012431 wafers Nutrition 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 239000013034 phenoxy resin Substances 0.000 description 2
- 229920006287 phenoxy resin Polymers 0.000 description 2
- 238000004321 preservation Methods 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- OMOYYCNTSLVTOE-SYXWNFKLSA-N 2-[[(e)-3-(carboxymethylimino)prop-1-enyl]amino]acetic acid Chemical compound OC(=O)CN\C=C\C=NCC(O)=O OMOYYCNTSLVTOE-SYXWNFKLSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 102100035353 Cyclin-dependent kinase 2-associated protein 1 Human genes 0.000 description 1
- 101000666730 Homo sapiens T-complex protein 1 subunit alpha Proteins 0.000 description 1
- 108010000817 Leuprolide Proteins 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 101100067759 Mus musculus Gast gene Proteins 0.000 description 1
- 229910018557 Si O Inorganic materials 0.000 description 1
- 229910008051 Si-OH Inorganic materials 0.000 description 1
- 229910006358 Si—OH Inorganic materials 0.000 description 1
- 102100038410 T-complex protein 1 subunit alpha Human genes 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- RGLRXNKKBLIBQS-XNHQSDQCSA-N leuprolide acetate Chemical compound CC(O)=O.CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H]1NC(=O)CC1)CC1=CC=C(O)C=C1 RGLRXNKKBLIBQS-XNHQSDQCSA-N 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229940087857 lupron Drugs 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- LMHHRCOWPQNFTF-UHFFFAOYSA-N s-propan-2-yl azepane-1-carbothioate Chemical compound CC(C)SC(=O)N1CCCCCC1 LMHHRCOWPQNFTF-UHFFFAOYSA-N 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 description 1
- 230000002485 urinary effect Effects 0.000 description 1
Classifications
-
- 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
- H01L2924/01—Chemical elements
- H01L2924/01013—Aluminum [Al]
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Abstract
Description
200409785200409785
File:TW 1009F-IPO.doc SUNDIAL CONFIDENTIAL 玖、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】 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)113°LCDlll 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, 200409785File: TW 1009F-IPO.doc SUNDIAL CONFIDENTIAL 玖, description of the invention (the description of the invention should state: the technical field to which the invention belongs, the prior art, the content, the embodiments, and the drawings are briefly explained) [the technical field to which the invention belongs] The present invention is The adhesive is particularly related to a latent hardener of the adhesive used when the semiconductor wafer and the TCP are connected by thermocompression. [Previous technology] In the past, when a semiconductor wafer was bonded to a substrate, or when TCP (Tape Carrier Package) and LCD (Liquid Crystal Display) were used to manufacture electrical equipment, they were bonded with a thermosetting resin epoxy resin. Agent. As shown by the symbol 111 in FIG. 7 (a), the LCD 111 includes a glass substrate 112, and an ITO electrode (Indium tinoxide) 113 ° LCD 111 disposed on the glass substrate 112. When following the TCP described below, the LCD 111 The surface on which the ITO electrode 113 is to be arranged is coated with an adhesive. Reference numeral 125 in FIG. 7 (b) indicates a state where the adhesive is applied to the LCD 111. Reference numeral 115 in FIG. 7 (C) indicates TCP. The TCP 115 includes a base film 116 and a metal wiring 117 disposed on the surface of the base film 116. The metal wiring 117 of the TCP115 is arranged on the arranged surface toward the adhesive 125 on the LCD111. After the alignment position, 200409785
File:T W1009F-IPO.doc , * SUNDIAL CONFIDENTIAt TCP 115的金屬配線117的配置面會被按向接著劑}25。 在這個狀態下壓住加熱的話,接著劑125會軟化, 金屬配線117會將軟化了的接著劑125按往後退,接觸到 ITO電極113的表面。 在上述的接著劑上,一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117與IT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,讓接著劑丨25硬化。 第7 (C)圖的符號1〇1所示的是接著劑ι25在硬化 後狀怨下的電氣設備。該電氣設備丨〇丨在金屬配線丨丨7與 IT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TCP115與LCD111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i 8〇。〇以上 回溫將接著劑加熱,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之類邏輯重合性樹脂以及含有邏輯重合開始劑的 200409785File: T W1009F-IPO.doc, * SUNDIAL CONFIDENTIAt The layout of the metal wiring 117 of the TCP 115 will be pressed to the adhesive} 25. When the heating is held in this state, the adhesive 125 is softened, and the metal wiring 117 pushes the softened adhesive 125 backward and contacts the surface of the ITO electrode 113. Generally, a hardening agent such as imidazol is added to the above-mentioned adhesive after heating, and when the metal wiring 117 and the IT0 electrode 113 continue to be heated under the bonding state, the contact of the hardening agent is added. The effect of the medium will make the epoxy resin coincide and let the adhesive 25 harden. The reference numeral 101 in Fig. 7 (C) shows the electrical equipment in which the adhesive 25 is cured after being cured. This electrical equipment 丨 〇 丨 is in a state where the metal wiring 丨 丨 7 is in contact with the IT〇 electrode 113, and the TCP 115 and the LCD 111 are fixed by the hardened adhesive 125. Therefore, TCP115 and LCD111 are connected electrically and mechanically. However, when the above-mentioned adhesive is allowed to harden, it must be i 80. 〇 Above the temperature, the adhesive is heated. When the circuit of the metal wiring 117 is very fine, the TCP 115 may be deformed such as elongation or contraction during heating. This problem can be solved by lowering the heating temperature, but it will increase the time required for heat treatment and reduce productivity. Adhesives that are also excellent in hardening properties at low temperatures. In recent years, logically coincident resins such as Acrylate and logically coincident starters have been developed. 200409785
FiIe:TW1009F-IPO.doc ·FiIe: TW1009F-IPO.doc
SUNDIAL CONFIDENTIAL 接著劑。但是這類接著劍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-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,不採用一般所使用的硬化劑, 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 中含有矽烷化合物(硅烷偶合劑(SilaneC〇upHng))以及 金屬蜇合物(或是金屬Alcolart)添加到接著劑中,利用 金屬差a物與磋烧偶合劑(Silane C〇Upiing)反應時所產生 的陽離子讓環氧樹脂重合(陽離子重合)。 添加了金屬蜇合物與硅烷偶合劑(Silane c〇upling)的 接著9丨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。 200409785 * tSUNDIAL CONFIDENTIAL. However, compared with the use of epoxy resins, the electrical properties and heat resistance in the hardened state are poor. [Summary of the Invention] The present invention was created to solve the above-mentioned problems of the prior art, and its purpose is to provide an adhesive which can be hardened under low temperature and short time conditions and has excellent preservation properties. The inventors of the present invention, instead of using a commonly used hardener, have focused on a method of superposing epoxy resin into cations. After repeated research, the following methods were found: at least one alkoxy group in the structure, a silane compound (Silane Couphng) and a metal adduct (or metal Alcolart) were added to the adhesive in the structure In the method, the epoxy resin is superposed (cation superposition) by using a cation generated when the metal difference a reacts with a sintering coupling agent (Silane Coupling). The hardening process in which a metal adduct and a silane coupling agent (Silane coupling) are added is then described in the following reaction formulas (1) to (4). 200409785 * t
II
File:TW1009F-IPO.doc SUNDIAL CONFIDENTIAL 【化1】 X-Si-OR+H2O^X-Si-OH+R-OH 反應式(1) A1 + OH-Si-X 厶File: TW1009F-IPO.doc SUNDIAL CONFIDENTIAL [Chem. 1] X-Si-OR + H2O ^ X-Si-OH + R-OH Reaction formula (1) A1 + OH-Si-X 厶
Al-O-Si-X+RHAl-O-Si-X + RH
反應式(2)Reaction Formula (2)
^Al-O-Si-X+X-Si-OH-^X-Si-O -Hh \1/^ Al-O-Si-X + X-Si-OH- ^ X-Si-O -Hh \ 1 /
;Al-〇-Si-X 反應式(3) r-ch-ch2-^r-ch-ch2 + -> r-ch-ch2+; Al-〇-Si-X Reaction Formula (3) r-ch-ch2- ^ r-ch-ch2 +-> r-ch-ch2 +
\ / I I\ / I I
Ο H+ OH' R-CH-CH2 O V 1 '〇 r-ch_ch2 OH* 反應式(4) 至少擁有一個烷氧的矽烷化合物,如反應式(1)所 示,與接著劑中的水反應,院氧基就會加水分解,成為石圭 烧醇(Silanol)基。 將接著劑加熱,破院醇基會與像铭蜇合物這類的金 屬蜇合物產生反應,石夕院化合物會與铭蜇合物結合。(反 應式(2)) 然後如反應式(3)所示,硅烷醇基與結合了的鋁蜇合 物因為平衡反應,接著劑中殘留的其他硅烷醇基會配位, 200409785〇 H + OH 'R-CH-CH2 OV 1' 〇r-ch_ch2 OH * Reaction formula (4) A silane compound having at least one alkoxy group, as shown in reaction formula (1), reacts with water in the adhesive. Oxygen will be hydrolyzed to become a silanol group. When the adhesive is heated, the broken alcohol group will react with metal compounds such as Ming compound, and Shixiyuan compound will bind with Ming compound. (Reaction formula (2)) Then, as shown in reaction formula (3), due to the equilibrium reaction between the silanol group and the bonded aluminum compound, other silanol groups remaining in the adhesive will coordinate, 200409785
File:TW1009F-IPO.doc 、,File: TW1009F-IPO.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, 將硅烷偶合劑(Silane Coupling)與金屬蜇合劑添加到接著 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⑺〜⑷所示的反應,是在比舊有接著劑硬化 的溫度(180。。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,金屬蜇合物與金屬Alc〇丨art如與硅烷偶合劑 (Silane Coupling)—起直接添加到接著劑中時,就會在常 溫下也能進行環旨的重合反應,造成接著劑黏度變 高。 因此’本發明者等人,纟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,封入上述的金屬蜇合 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,申請專利範圍第工 項所記載的發明’為-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 以金屬蜇合物或是金屬Alc〇lart之其中一者,或兩者為主 要成份。 10 200409785SUNDIAL CONFIDENTIAL generates the Branstade acid point, as shown in reaction formula (4). 'Because of the activated proton, the epoxy ring at the end of the epoxy resin will open the ring, and it will be in phase with the epoxy ring of other epoxy resins. Coincidence (cationic coincidence). Therefore, when a silane coupling agent (Silane Coupling) and a metal coupler are added to the adhesive, a thermosetting resin such as an epoxy resin is cationically overlapped. The reactions shown in the reaction formulas ⑺ to ⑷ are performed at a temperature lower than the temperature at which the old adhesive hardens (180 ° or more). Therefore, the aforementioned adhesive can be used at a lower temperature than the old adhesive. Low temperature and short time hardening. However, when the metal adduct and the metal Alc〇art are added directly to the adhesive together with the silane coupling agent (Silane Coupling), the ring-like superposition reaction can also be performed at normal temperature, causing the adhesive viscosity to change. high. Therefore, the present inventors et al. Found a method of adding a latent hardener to an adhesive in a capsule made of a resin component that does not react with epoxy resin at ordinary temperature, and the above-mentioned metal compound was sealed. The present invention is based on the above-mentioned Transcendence, and the invention described in the item of the scope of patent application is a potential hardener, which has hardener particles and a capsule covering the surface of the hardener particles. The hardener particles are One of the metal adducts or the metal Alcolart, or both are the main components. 10 200409785
File.TW 1009F-IPO.doc , sundial confidentiai 申請專利範@第2項所記載的發明,是如中請專利範 圍第1項所記载之潛在性硬化劑,其前述的金屬哲合物是 以铭蜇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 Aleolamx AleGlan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,是如中請專利 範圍第1項〜第3項所記載之潛在性硬化劑,其前述膠 囊’是以氟化樹脂為主成份之潛在性硬化劑。 申請專利範圍第5項所記載之發明,是—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。前述膠囊為平均粒子直徑比硬化劑粒子的 平均粒徑還小的樹脂粒子,該樹脂粒子㈣著於前述硬化 劑表面’經炼解形成如前述申請專利範圍第i項〜第々項 中所記載之任何一種潛在性硬化劑。 申請專利範圍第6項所記狀發明,如申請專利範 圍第5項所記載之潛在性硬化劑,其前述的樹脂粒子炼點 在30 C以上350°C以下。 申"月專利|巳圍第7項所記載之發明,如申請專利範 圍第5項所記載之潛在性硬化劑,其前述的樹脂粒子的熱 200409785File.TW 1009F-IPO.doc, sundial confidentiai The invention described in the patent application @ item 2 is a potential hardener as described in item 1 of the patent scope, and the aforementioned metal philate is based on Latent compound is a potential hardener for the main ingredient. The invention described in item 3 of the scope of patent application is a potential hardener as described in item 1 of the scope of patent application, and the aforementioned metal Aleolamx AleGlan is a potential hardener. The invention described in item 4 of the scope of patent application is a latent hardener as described in items 1 to 3 of the patent scope. The aforementioned capsule ′ is a latent hardener of fluorinated resin as the main component. The invention described in the scope of patent application No. 5 is a potential hardener as described in any one of the scope of patent application No. 1 to the scope of patent application No. 4. The capsule is a resin particle having an average particle diameter smaller than the average particle diameter of the hardener particles, and the resin particles are stuck on the surface of the hardener, and are formed by refining as described in items i to ii of the aforementioned patent application range. Any of the potential hardeners. The invention described in item 6 of the scope of patent application, and the latent hardener described in item 5 of the scope of patent application, has a resin particle melting point of 30 ° C to 350 ° C. Apply for the monthly patent | The invention described in item 7 and the potential hardener described in item 5 of the patent application range, the heat of the resin particles mentioned above 200409785
FilerTWl 009F-IPO.doc 'FilerTWl 009F-IPO.doc ''
SUNDIAL CONFIDENTIAL 分解溫度在50°C以上500°C以下。 申請專利範IS第8項所記載之發明,如中請專利範 圍第5項所記載之潛在性硬化劑,其前述的樹月旨粒子的軟 化溫度在〇°C以上300°C以下。 中請專利範圍第9項所記載之發明,如中請專利範 圍第5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1〇項所記載之發明,是一種潛在性 硬化劑的製造方法,該方法包括硬化劑粒子、前述包覆在 硬化劑粒子表面的膠囊,以及製造前述硬化劑粒子的工 程,同時是-種潛在性硬化劑的製造方法,該方法包含了 以前述樹脂成份為主要成份,以平均例徑較前述硬化劑粒 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, 形成前述膠囊的膠囊化工程。 申請專利範圍帛11項所記載之發明,#申請專利範 圍第10項所記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 囊材料的混合工程。丄是在前述硬化劑粒子沾附了前述膠 12 200409785SUNDIAL CONFIDENTIAL The decomposition temperature is above 50 ° C and below 500 ° C. For the invention described in item 8 of the patent application IS, and the latent hardener described in item 5 of the patent application, the softening temperature of the aforementioned tree-moon particles is 0 ° C to 300 ° C. For the invention described in item 9 of the patent application, and the potential hardener described in item 5 of the patent application, the glass transition temperature of the aforementioned resin particles is -40 ° C to 300 ° C. The invention described in claim 10 of the scope of the patent application is a method for manufacturing a latent hardener. The method includes a hardener particle, the capsule coated on the surface of the hardener particle, and a process for manufacturing the hardener particle. Yes-A method for producing a latent hardener, the method includes the aforementioned resin component as a main component, and powder-like resin particles having an average diameter smaller than that of the hardener particles are attached to the surface of the hardener particles. The resin particles adhered to the surface of the hardener particles are dissolved to form a capsule encapsulation process. The invention described in the scope of patent application 帛 11, and the method of manufacturing the latent hardener described in scope of patent application # 10, have two processes. 1 is the aforementioned encapsulation process, which is a mixing process of mixing the hardener particles and the capsule material, and allowing the surface of the hardener particles to adhere to the capsule material.丄 The glue is attached to the hardener particles 12 200409785
File.TW 1009F-IPO.doc SUNDIAL CONFIDENTIAL 讓别述膠囊材料熔解的攪拌工 囊材料的狀態下進行授拌 程。 申請專利範圍第12項所記載之發明,如中請專利襄 圍第1〇項以及中請項目第11項之任何—項所記載的潛在 性硬化劑的製造方法中,前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1〇〇 : 8〇。File.TW 1009F-IPO.doc SUNDIAL CONFIDENTIAL The mixing process is performed while the capsule material is melted apart from other capsule materials. In the invention described in item 12 of the scope of patent application, as in the method of manufacturing a latent hardener described in any of the items in item 10 of the patent application and item 11 of the application, the average of the hardener particles is The ratio of the particle diameter to the average particle diameter of the aforementioned capsule material was 100: 80.
申請專利範圍第13項所記載之發明,如中請專利範 圍第1〇項以及中請專利範圍第u項之任何-項所記載的 潛在性硬化劑的製造方法中,前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1〇〇: 5〇。 申請專利範圍第14項所記載之發明,含有熱硬化性 樹脂、石圭烧偶合劑(SilaneCoupling)以及如申請專利範圍 第1項至中請專利範圍第9項之任何—項所記載的潛在性 硬化劑之接著劑。In the invention described in claim 13 in the scope of patent application, as in the method for manufacturing a latent hardener described in claim 10 of the scope of patent claims and any one of the paragraph u of the scope of patent claims, the average of the aforementioned hardener particles is The ratio of the particle diameter to the average particle diameter of the aforementioned capsule material was 100: 50. The invention described in item 14 of the scope of patent application contains a thermosetting resin, a silicon coupling agent (Silane Coupling), and the potential as described in any one of the items in the scope of patent application 1 to 9 of the patent scope Adhesive for hardener.
本lx月的構成如上,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 Μ粒子表面。在這個狀態下,以高速授拌硬化劑粒子的 活,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 月曰粒子等彳里及,因為這種物理性的撞擊所產生的能量黑樹 13The structure of this month is as above. After the powdered capsule material is mixed with the hardener particles, the capsule material will adhere to the surface of the hardened M particles due to the electrostatic effect. In this state, the hardener particles are mixed at a high speed, and the resin particles adhered to the surface of the hardener particles due to static electricity will be mixed with the agitator, the inner wall of the stirring device, and the other tree hardener particles on the surface of the hardener particles. Time lapse, because of the energy generated by this physical impact Black Tree 13
Fiie:TW 1009F-IPO.docFiie: TW 1009F-IPO.doc
Fiie:TW 1009F-IPO.doc 脂粒子溶解,或是打 樹脂粒子會融合為_ 囊0 SUNDIAL CONFIDENtlAL· 入4物質(硬化劑粒子)。溶解了的 體’形成包覆硬化劑粒子表面的膠 以上述以潛在性硬化劑與娃院偶合劑(Silane 〜咖㈣)以及環氧樹脂混合製成接著劑時,在常溫下硬 化劑粒子表面全部被膠囊所包覆,不t與環氧樹脂發生重 口反應’因此接著記得保存性很高,但是當接著劑被加熱 時,膠囊會軟化或轉,膠囊的機械性強度會明顯降低。 所以當接著劑被加熱時,硬化劑粒子會目為熱膨脹與熱壓 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。 這個狀怨要是持續加熱,硬化劑粒子的煮成份__ 金屬蜇合物與接著劑中的硅烷偶合劑(Silane c〇upling)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。 硬化劑粒子與硅烷偶合劑(Silane Coupling)的反應, 比統的接著劑發生熱硬化的溫度(18〇°c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 均粒徑最好小一些,但是當硬化劑粒子的平均粒徑變得太 14Fiie: TW 1009F-IPO.doc Lipid particles dissolve, or resin particles will fuse into sac 0 SUNDIAL CONFIDENtlAL · 4 substances (hardener particles). When the melted body forms the glue that coats the surface of the hardener particles, the latent hardener is combined with a silicon coupling agent (Silane ~ coffee) and an epoxy resin to make an adhesive, and the surface of the hardener particles is at room temperature. It is completely covered by the capsule, and does not react with the epoxy resin. Therefore, it is remembered that the preservation is very high, but when the adhesive is heated, the capsule will soften or turn, and the mechanical strength of the capsule will be significantly reduced. Therefore, when the adhesive is heated, the hardener particles will be subject to physical shock such as thermal expansion and pressure during thermal compression, which will easily damage the capsule, and the hardener particles will be released into the adhesive. If this kind of complaint is continuously heated, the cooking component of the hardener particles __ The metal admixture and the silane coupling agent (Silane coupling) in the adhesive will react to generate cations, which are overlapped with the epoxy resin because of the cations ( Cation overlap), and the adhesive will harden. The reaction between the hardener particles and the silane coupling agent (Silane Coupling) is lower than the temperature at which the conventional adhesives are thermally cured (above 180 ° C). Therefore, the adhesive of the present invention can be cured at a lower temperature and in a shorter time. . In order to increase the area in contact with the epoxy resin, the average particle diameter of the hardener particles is preferably smaller, but when the average particle diameter of the hardener particles becomes too large, 14
FilerTWl009F-IPO.docFilerTWl009F-IPO.doc
FilerTWl009F-IPO.doc SUNDIAL CONFIDENTIAL ’很難形成膠囊,所以 m以上50 // m以下。 硬化劑粒子的混合需 小時,與樹脂粒子的粒徑差就變小 硬化劑粒子的平均粒徑最好在0.5以 此外,如上所數,樹脂粒子與 要經㈣來製造潛在性硬化劑時,可採用混合刪置 (例如奈良機械製作所(株)公司製造的「NHS_0」)。這 裡的硬化齡子與膠囊材料的添加比率,町列式子⑴ 來計算。 式(1)......M/m=D X F/(4xdxf) 上列式子⑴中,Μ為硬化劑粒子的添加量(g),m為勝 囊材料的添加量(g),D為粉體狀硬化劑粒子的平均粒徑 (# m ) ’ d為膠囊材料的平均粒徑(# m ),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,透過硅烷偶合劑(Silane Coupling) 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。 15 200409785FilerTWl009F-IPO.doc SUNDIAL CONFIDENTIAL ′ It is difficult to form capsules, so m is more than 50 // m is less than. It takes hours to mix the hardener particles. The difference between the particle size of the hardener particles and the smaller the average particle size of the hardener particles is preferably 0.5 or more. As mentioned above, when the resin particles and latent hardeners are processed through the process, Hybrid deletion (for example, "NHS_0" manufactured by Nara Machinery Co., Ltd.) can be used. The ratio of the hardening age to the capsule material is calculated by the formula. Formula (1) ... M / m = DXF / (4xdxf) In the above formula ⑴, M is the amount of hardener particles added (g), m is the amount of sacrifice material added (g), D is the average particle diameter (#m) of the powdery hardener particles; d is the average particle diameter (#m) 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 when the standard substance is at 4 ° C. However, the above formula (1) is a theoretical formula, and the optimum addition ratio of the hardener particles and the capsule material is determined depending on the situation. In addition, if a thermoplastic resin is added to the adhesive, the properties of the thermoplastic resin will increase cohesion and the adhesiveness of the adhesive will be higher. If a highly polar thermoplastic resin is used, the thermoplastic resin not only adds to the hardening reaction of the epoxy resin, but also combines with the inorganic material through the silane coupling agent (Silane Coupling). Therefore, not only does the adhesive harden more, it also improves the affinity with the coating of inorganic materials. 15 200409785
File:TW 1009F-lPO.doc 1 SUNDIAL CONFIEiENTlAl: ▲為讓本發明之上述㈣、特禮支、和優點能更明顯易 懂’下文特舉-較佳實施例,並配合所附圖式,作詳細說 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,將金屬蜇合物一一鋁蜇合物溶解在有機溶劑 中,製成金屬蜇合物溶解劑後,以喷霧乾燥裝置將上述金 屬折合物溶液噴霧乾燥,得到硬化_子(喷霧乾燥 dryer法)。第1(a)圖的符號31所示為硬化性粒子。 然後準備溶點在30°C以上35(rc以下,熱分解溫度 在50°C以上500t:以下,軟化溫度在〇t:以上3〇(Γ(:以下, 玻璃移轉溫度在-40°C以上30(TC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100 ·· 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/% σ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)。第丨化)圖的符號所示 為在此狀恶下的膠囊材料,丄個硬化劑粒子3丨的表面上 包覆著許多個樹脂粒子32。 16 200409785File: TW 1009F-lPO.doc 1 SUNDIAL CONFIEiENTlAl: ▲ In order to make the above-mentioned inventions, special gifts, and advantages of the present invention more obvious and understandable, the following exemplified-the preferred embodiment, and with the accompanying drawings, make The detailed description is as follows: [Embodiment] The process for manufacturing the latent hardener of the present invention is described below. First, the metal adduct-aluminum adduct is dissolved in an organic solvent to prepare a metal adduct dissolving agent, and then the above metal fold compound solution is spray-dried by a spray-drying device to obtain a hardened product (spray Dryer method). Numeral 31 in FIG. 1 (a) indicates hardenable particles. Then prepare a melting point above 30 ° C, below 35 ° (rc, thermal decomposition temperature above 50 ° C, 500t: below, softening temperature above 0t: above 3 ° (Γ (: below, glass transition temperature at -40 ° C) Powder resin (resin particles) of various conditions above 30 (TC and below). The ratio of the average particle diameter of the resin particles to the average particle diameter of the hardener particle material is 100 or more. 80. Next, the hardenable particles are 31. After mixing with the resin particles in a predetermined addition ratio /% σ and mixing in the mixing device, the resin particles having an average particle size smaller than the hardener particles 31 will be electrostatically adhered and coated on the surface of the hardener particles 31 (mixed Engineering). The symbol in the figure shows the capsule material in this state. The surface of each hardener particle 3 is covered with many resin particles 32. 16 200409785
File:TW 1009F-IPO.docFile: TW 1009F-IPO.doc
SUNDIAL CONFIDENTIAL 將表面上有靜電性附著樹脂粒子32的硬化劑粒子3】 投入攪拌裝置硬化劑粒子3 1表面的樹脂粒子32就會因為 與其他硬化性粒子3 1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炼解’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3 3會包覆住整個硬化劑粒子3 1 的表面,硬化劑粒子31與膠囊33就構成了潛在性硬化劑 30 〇 接著要說明使用上述潛在性硬化劑3〇製成的本發明 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、 石土燒偶合劑(Silane Coupling)、上述的潛在性硬化劑3〇、 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)圖的符说2G顯示的是形成了塗佈層25狀態SUNDIAL CONFIDENTIAL Put the hardener particles 3 with electrostatically attached resin particles 32 on the surface.] Put them into the hardener particle 3 of the stirring device. The resin particles 32 on the surface will be mixed with the resin particles 32 on the surface of other hardening particles 31, or they will be stirred. The rotating fan blades, inner walls, etc. of the device collide, or friction generates heat, and the resin particles 32 are melted. The melted resin particles 32 become one body (stirring process). Reference numeral 33 in FIG. 1 (C) shows a capsule formed by the resin particles 32 as a whole. The capsule 3 3 covers the entire surface of the hardener particles 31, and the hardener particles 31 and the capsule 33 constitute a latent hardener 30. Next, the adhesive of the present invention made using the latent hardener 3 will be described. And the manufacturing process of electrical equipment using the adhesive of the present invention. The epoxy resin, the thermoplastic resin, the Silane Coupling, which is a thermosetting resin, the above-mentioned latent hardener 30, the conductive particles, and the solvent are mixed and stirred according to a predetermined addition ratio, respectively. Then agent. In this state, the adhesive is paste-like. Reference numeral 21 in FIG. 2 (a) shows a release film. A certain amount of the above-mentioned adhesive is applied to the surface of the release adhesive film 21, and the solvent in the adhesive will evaporate after drying to form a coating layer of the adhesive (Fig. 2 (b)). The symbol 2G in Figure 2 (b) shows the state where the coating layer 25 is formed.
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SUNDIAL CONFIDENTIAL 的接著膜。該圖的符號27所示為隨著潛在性硬化劑3〇一 起分散到接著劑中的導電性粒子。在這個狀態下,潛在性 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之接著劑中的硅烷偶合劑 (Sdane Coupling)接觸,在常溫下不會和塗佈層乃發生硬 化反應。 第3(a)圖的符號11所示為LCD,LCDU在玻璃基 板12、玻璃基板12的一面上形成狹窄、多支的IT〇電極 13 (Indium tin oxide)。此圖所示為5條的ιτ〇電極13。 在LCD11形成ΙΤΟ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2〇的塗佈層25(第3(b) 圖)。剝離膜21與塗佈層25的接著力,由於比塗佈層乃 /、ITO電極13之間的還小,因此當剝離膜2丨剝離後,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 6在基礎膜16的一面上,狹窄的金屬配線丨7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 膜丨6的長度方向的末端。 第3(d)圖所不為第5圖中A-A線截面圖,在配置有 200409785Adhesive film for SUNDIAL CONFIDENTIAL. Reference numeral 27 in the figure shows conductive particles dispersed in the adhesive as the latent hardener 30. In this state, the hardenable particles 31 of the latent hardener 30 are enclosed in the capsule 33 and the hardenable particles 30 do not contact the silane coupling agent (Sdane Coupling) in the adhesive constituting the coating layer 25 of the figure. Hardening reaction does not occur with the coating layer. Reference numeral 11 in FIG. 3 (a) shows an LCD, and the LCDU forms a narrow, multi-branch IT0 electrode 13 (Indium tin oxide) on one side of the glass substrate 12 and the glass substrate 12. This figure shows five ιτ〇 electrodes 13. On the surface of the LCD 11 where the ITO electrode 13 is formed, a Tcp portion, which will be described later, is connected to the coating layer 25 (FIG. 3 (b)) supporting the adhesive film 20 shown in FIG. 2 (b). Since the adhesive force between the release film 21 and the coating layer 25 is smaller than that between the coating layer and the ITO electrode 13, when the release film 2 is peeled off, the coating layer 25 remains on the LCD 11 (No. 3 (c) Figure). Reference numeral 15 in FIG. 5 indicates TCP. TCP15 has a long base film 6 On one side of the base film 16, narrow metal wirings 7 are arranged along the length direction of the base film 16 (the figure here shows five metal wirings). The ends of the metal wiring 17 in the longitudinal direction are located at the ends of the base film 6 in the longitudinal direction, respectively. Figure 3 (d) is not a cross-sectional view taken along line A-A in Figure 5.
File:TW1009F-IPO.doc SUNDIAL CONFIDENTIAL 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, LCD11的IT0電極13與TCPI5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LCD11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 炼解或軟化,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中的環氧樹脂以及硅烷偶合劑(Silane c〇upling)混 合0 當硬化劑粒子3 1就會與塗布層25中的環氧樹脂以 及硅烷偶合劑(Silane Coupling)混合,構成硬化劑粒子31 的銘蜇合物就會與硅烷偶合 劑(Silane Coupling)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Π與Ito電極13就會在包 19 * 1 200409785File: TW1009F-IPO.doc SUNDIAL CONFIDENTIAL The surface of the metal wiring 17 on the side of the TCP15 is facing the LCD11ITO electrode 13, the end of the TCP15 is opposite the coating layer 25 of the ITO electrode 13, the IT0 electrode 13 of the LCD11 and the metal of TCPI5 The wirings 17 are opposed to each other. In this state, the surface on which the metal wiring 17 of TCP15 is arranged is pressed against the coating layer 25, and the overlapping portion of TCP15 and LCD11 is pressed together, and then the whole is heated, so that the coating layer 25 is softened. Because pressing the metal wiring 17 will push the softened coating layer 25 back, the conductive particles 27 in the remaining coating layer 25 will be sandwiched between the metal wiring 17 and the ITO electrode 13 (Section 4 (e) Figure). If heating and pressing are continued in this state, heating will cause the capsule 33 to deflate or soften, and the mechanical strength of the capsule 33 will be significantly weakened. At this time, because the hardener particles are thermally expanded due to heating, the capsule 33 that is weakened in mechanical strength due to heating is broken, and the hardener particles 31 and the epoxy resin and the silane coupling agent (Silane Coupling) in the coating layer 25 are broken. ) Mix 0 When the hardener particles 31 are mixed with the epoxy resin and the silane coupling agent (Silane Coupling) in the coating layer 25, the compound containing the hardener particles 31 will be mixed with the silane coupling agent (Silane Coupling). As a result, the cations in the coating layer 25 are released. This cation causes the epoxy to proceed (cation overlap), and the metal wiring Π and the Ito electrode 13 will be in the package 19 * 1 200409785
File:TWl〇〇9F-IPO.doc SUNDIAL CONFIDENTIAL· 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) 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10不僅其金屬配線Π與Ito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。 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】 使用鋁蜇合物(川研精練化學(株)公司製造的 Alumiun Tris acetactate )(商品名稱「I呂蜇合物A(W)」以 及銘Alcolrat (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 曱基乙基甲蒙I ( Methyl ethyl ketone ),分別製成含銘蜇合 物10重量%的金屬蜇合物溶液,含铭Alcolart 10重量% 的金屬Alcolart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」),以喷霧入口溫度80°C,噴 20 200409785File: TW1009F-IPO.doc SUNDIAL CONFIDENTIAL · The conductive layer 27 is sandwiched, and the coating layer 25 is hardened in this state. (Fig. 4 (f)) The numeral 10 in Fig. 4 (f) shows the electrical equipment in which the coating layer 25 is hardened. In this electrical device 10, not only the metal wiring Π and the Ito electrode 13 can continue to be connected through the conductive particles 27, but also the LCD 11 and the TCP 15 are hardened and the coating layer 25 is mechanically connected. In this way, the adhesive of the present invention not only has excellent storage properties, but also hardens the epoxy resin due to the superposition of cations. The adhesive can harden the adhesive at a lower temperature and in a shorter time than conventional hardeners. [Example] An aluminum compound (Alumiun Tris acetactate manufactured by Kawaken Seika Chemical Co., Ltd.) (trade name "I Lukate A (W)" and an inscription Alcolrat (Kawaken Seiko Chemical Co., Ltd.) were used. Manufactured Alumium Isopropylate (trade name "AIPD")), disperse them separately in the solvent methethyl ethyl ketone I (Methyl ethyl ketone), respectively, to make a metal admixture solution containing 10% by weight of the adduct, A metal Alcolart solution containing 10% by weight of Alcolart. Next, using a spray drying device (trade name "GC-31" manufactured by Yamato Lapochic Co., Ltd.), spray 20 200409785 at a spray inlet temperature of 80 ° C.
File:TW 1009F-lPO.doc SUNDIAL CONFIDENTIAL 乾鼠氣的流入量 霧出口溫度60°C、喷霧壓力lkg/c m2 MW分的條件,將金屬蜇合物溶液與金屬偏奶溶液 分別喷霧、乾燥,製成2種粉體狀硬化劑(硬化劑粒子) (噴霧乾燥法)。另外,再準備樹餘子32——粉體狀的 氟化樹脂(Daikin 工業(株)公司製造,商品名稱「Lupr〇n L-5」’ 一次粒子直徑0.2 v m,熔點327。〇)。 使用奈良機械製作所(株)公司製造、商品名稱為 「Hybndaize卜NHS-0」,以上述的第i⑷,⑻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1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1 〇〇111/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3 0。 以對熱可塑性樹脂雙酚(bis phenol ) A型環氧樹脂 (油化Shell Epoxy (株)公司製造,商品名稱[r EP828」 5〇重量部添加熱可塑性樹脂酚鹽(phen〇xy)樹脂(東都 化成(株)製造,商品名稱「YP50」)50重量部,硅烷偶 合劑(Silane Coupling)(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1 〇重量部,以及有機溶劑,然後分散製成糨 14〇 200409785File: TW 1009F-lPO.doc SUNDIAL CONFIDENTIAL Dry mouse gas inflow Mist outlet temperature of 60 ° C, spray pressure of 1kg / c m2 MW minutes, spray the metal admixture solution and metal partial milk solution separately, It is dried and made into 2 kinds of powdery hardeners (hardener particles) (spray drying method). In addition, Shuyuko 32, a powdery fluorinated resin (manufactured by Daikin Industry Co., Ltd., with a trade name of "Lupron L-5", having a primary particle diameter of 0.2 v m and a melting point of 327.0) was prepared. Using the product manufactured by Nara Machinery Manufacturing Co., Ltd. under the trade name "Hybndaize BU NHS-0", the hardener particles 31 to 20 parts by weight and the resin particles 32 to 3 parts are used in the process described in item i) above. After mixing, the resin particles 32 are electrostatically adhered to the surface of the hardener (mixing process), and are stirred at a running speed of 100111 / sec and a processing time of 5 minutes (stirring process) to form capsules 33 to obtain 2 types Of potential hardener 30. Thermoplastic resin bis phenol A-type epoxy resin (manufactured by Petrochemical Shell Epoxy Co., Ltd., trade name [r EP828] 50 weight part is added with thermoplastic resin phenoxy resin ( 50 parts by weight of Toto Kasei Co., Ltd. under the trade name "YP50", silane coupling agent (Silane Coupling) (manufactured by Unika Co., Ltd. under the trade name "A-187") 1 part by weight, 2.5 conductive particles 10 parts by weight, 10 parts by weight of each latent hardener, and organic solvent, and then dispersed into 糨 14200200409
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SUNDIAL CONFIDENTIAL 糊狀的接著劑,以這些接著劑在上第⑽,⑻圖的工程 中’製成了實施例1、2的接著膜2〇。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」、「4〇。〇 保存試驗」。 〔室溫保存試驗〕 利用這些貝施例1、2與比較例1、2的接著膜2〇, 在上述第3(a)〜3(d)圖、第4(e)、4(f)圖的工程,在TCP15 與LCDU連接後,測定LCDn上Tcpi5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i、2的接著 膜20 ’在室溫(25t:)下分別保存1日、3日、7日, 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LCDU之後,測定LCDU上Tcpi5剝離時 的剝離強度(保存後剝離強度)。 〔4〇°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 4 C之外,以鈾述的「室溫保存试驗」中相同條件保存接 著膜20,待TCpi5與LCD11連接後,測定保存後剝離強 22 200409785 錢SUNDIAL CONFIDENTIAL Paste adhesive, these adhesives were used in the process of the second and third drawings to prepare the adhesive film 20 of Examples 1 and 2. The following "room temperature storage test" and "40.0 storage test" were performed using the adhesive films 20 of these Examples 1 and 2, respectively. [Room Temperature Storage Test] Using these adhesive films 20 of Examples 1 and 2 and Comparative Examples 1 and 2, the above-mentioned Figures 3 (a) to 3 (d), 4 (e), and 4 (f) In the process shown in the figure, after TCP15 is connected to the LCDU, the peel strength (initial peel strength) of Tcpi5 on the LCDn is measured. In addition, the adhesive films 20 ′ of Examples 1 and 2 and Comparative Examples i and 2 were stored at room temperature (25t :) for 1 day, 3 days, and 7 days, respectively, and each of the adhesive films 20 after storage was the same as described above. After the connection of TCP15 and LCDU, the peeling strength (peeling strength after storage) of Tcpi5 on LCDU was measured. [Storage Test at 40 ° C] This test saves the bonding film 20 under the same conditions in the "room temperature storage test" described in uranium, except that the storage temperature of the bonding film 20 is adjusted from room temperature to 4 C. The TCpi5 and After LCD11 is connected, measure peel strength after storage 22 200409785 money
File:TW 1009F-IPO.doc SUNDIAL CONFIDENTIAL 度。 在上述的「室溫保存試驗」與「40°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%以下畫「〇」,70%以上8〇%以下畫 「△」,70%以下畫「X」以資評估,其評價結果如下表2 所記載。 【表1】File: TW 1009F-IPO.doc SUNDIAL CONFIDENTIAL degree. In the above-mentioned "room temperature storage test" and "40 ° C storage test", if the peel strength after storage reaches 90% or more of the initial peel strength, "◎" is drawn, and 80% or more and 90% or less "0", 70 Above "%" and "80%" draw "△" and below 70% draw "X" for evaluation. The evaluation results are shown in Table 2 below. 【Table 1】
表1 :評價試驗的結果Table 1: Results of evaluation tests
室溫保存 4〇°C保存 3曰 7曰 3曰 7日 實施例1 ◎ ◎ ◎ 〇 實施例2 ◎ ◎ ◎ 〇 比較例1 X X X X 比較例2 X X 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 // m的金屬配線以25 # m的間 隔配置,LCD11是表面積每lcm2的電阻是由1〇〇的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 23 200409785Stored at 40 ° C at room temperature. Stored on the 3rd, 7th, and 3rd days. Example 1 ◎ ◎ ◎ 〇 Example 2 ◎ ◎ ◎ 〇 Comparative Example 1 XXXX Comparative Example 2 XXXX Comparative Examples 1 and 2 in Table 1 above will be implemented The two types of hardener particles used in Examples 1 and 2 were directly added to the adhesive without forming a capsule. In addition, TCP15 is configured with 25 // m metal wiring at 25 # m intervals. LCD11 has a surface area of 1 cm2. The resistance is formed by 100 IT0 electrode 13. The overlap between TCP15 and LCD11 is added. After applying a load of 3Mpa, do heating for 10 seconds to increase the temperature of the coating layer 25 23 200409785
File:TW 1009F-IPO.doc 到13(TC後相連接。 SUNDIAL CONFIDENTIAL· * 從上述表1、2中可看出,在使用將硬化劑粒子31 封入膠囊33中的實施例i、2當中,「室溫保存試驗」與 40 C保存试驗」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1、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。File: TW 1009F-IPO.doc is connected to 13 (TC. SUNDIAL CONFIDENTIAL · * As can be seen from Tables 1 and 2 above, in Examples i and 2 in which hardener particles 31 are enclosed in capsules 33, The evaluation results of the "room temperature storage test" and the 40 C storage test were both good. On the other hand, in Comparative Examples 1 and 2 in which the capsule was not formed and the curing agent was directly added to the adhesive, the results of each storage test were also obtained. All of them were inferior. From these results, it was confirmed that the adhesive using the latent hardener of the present invention has excellent storage stability.
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TCP1^S連接時,首先要在lcdii 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)。The case where the adhesive film is produced using the adhesive agent has been described above, but the application of the present invention is not limited to this. For example, the adhesive agent may be directly used in the form of a paste. The symbol 11 shown in FIG. 6 (a) is the same as that shown in FIG. 3 (a). It is an LCD. When the LCD11 is connected to TCP1 ^ S, it must first be on the surface of the ITO electrode 13 of LCDII and on the surface of TCP15. Adhesive is applied to the connected portions to form a coating layer 45 of the adhesive (FIG. 6 (b)).
然後在上第3(d)圖的工程中進行TCP15的對準位子 後’在上述第4(e)、4(f)圖的工程中,將TCP15與LCD11 相連接,就可得到電氣設備40 (第6(c)圖)。 以上說明了使用接著劑連接TCP15與LCD11的情 形,但是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。Then, after performing the alignment of TCP15 in the process shown in Figure 3 (d) above, in the process shown in Figures 4 (e) and 4 (f) above, connect TCP15 to LCD11 to obtain electrical equipment 40 (Figure 6 (c)). The case where TCP15 and LCD11 are connected using an adhesive has been described above, but the application of the present invention is not limited to this. It can be used for the connection of substrates and semiconductor wafers and in the manufacture of various electrical equipment.
24 20040978524 200409785
File:TW 1009F-IPO.doc ' . 1File: TW 1009F-IPO.doc '. 1
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。 金屬蜇合物可以使用錯蜇合物、鈦蜇合物、鋁蜇合 物等各種金屬蜇合物,其中,最好採用反應性最高的銘蜇 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327t: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3〇χ:以上 350 C以下,熱分解溫度在5〇°C以上500°C以下,軟化溫 度在〇°C以上300。(:以下,玻璃移轉溫度在_4〇t以上3〇〇 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r 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 200409785 pile:TWl 009F-IPO.docSUNDIAL CONFIDENTIAL The above description refers to the case where conductive particles are dispersed in an adhesive, but the application of the present invention is not limited to this. For example, adhesives containing no conductive particles are also included in the scope of the present invention. As the metal compound, various metal compounds such as a complex compound, a titanium compound, and an aluminum compound can be used. Among them, the most reactive compound is preferred. In addition, the method for producing the hardener particles by the spray drying method has been described above, but the present invention is not limited to this. The case of using a fluorinated resin having a melting point of 327t: has been described above, but the scope of use of the present invention is not limited to this, as long as the melting point is within 30 ×: above 350 C, and the thermal decomposition temperature is above 50 ° C and 500 ° C , The softening temperature is above 300 ° C. (: Below, one of conditions such as glass transition temperature of -40 ° C to 300 ° C, etc., thermoplastic resins, bridging resins, gel resins can also be used. For the above resins, for example, look at acrylic Resin (manufactured by Nippon Paint Co., Ltd., trade name "Micro Gel"), Poly-methyl methacrylate resin (r mp series manufactured by Soken Chemical Co., Ltd.), Benzodiguanamine resin ( "Product name" Eposter "made by Japan Catalyst Co., Ltd., Silicon Resin (made by GE Toshiba Silicon Co., Ltd., trade name" Tospar "), etc. The capsules formed by dissolving the resin particles having the above characteristics are Capsule 25 200409785 pile: TWl 009F-IPO.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。 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、酚醛樹脂、乙烯醚 (vinyle ether)樹脂、〇xetane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。 另外’本發明所採用的硅烷偶合劑(SilaneSUNDIAL CONFIDENTIAL In the project, 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 capsules exceed the previous resin temperature range. The above thermosetting resin is described using an epoxy resin as an example, but the application of the present invention is not limited to this. If it is a cationic resin, such as urea resin, melamine resin, phenol resin, vinyl ether resin, oxetane resin, etc., but if the strength of the adhesive after hardening is considered, It is best to use epoxy. In addition, the silane coupling agent (Silane used in the present invention
Coupling),最好能採用下列式子⑹所示的物質。 【化2】Coupling) is preferably a substance represented by the following formula (1). [Chemical 2]
A T X —Si—χ3……一般式(5) X4 (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(Eth〇xy )。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 稀基’尤其最好是具有環氧置換基之Glycidil基。擁有乙 26 200409785 • 1 · 4 1ATX —Si—χ3 …… General formula (5) X4 (In the general formula (5) above, at least one of the substituents X1 to X4 is an alkoxy group. The alkoxy group is best It is methoxy (Methoxy) or ethoxy (Ethoxy). In addition, among the substituents X1 to X4 other than alkoxy, it is preferred that at least one of the substituents is epoxy or ethylene. It is a Glycidil group with an epoxy-substituted group. It has a B 26 200409785 • 1 · 4 1
File:TW1009F-IPO.doc SUNDIAL CONFiL)ENTIAL 浠基的有例如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,例如聚乙晞樹脂、 尿烧樹脂、聚醋酸乙稀酯(Polyvinyl acetate)、醋酸乙烤酯 (Ethylene Vinyle Acetate)、聚 丁二烯(Polybutadiene)橡膠 等橡膠類也可以使用。 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,由於金屬蜇合物所構成之硬化 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 200409785 « 1 4File: TW1009F-IPO.doc SUNDIAL CONFiL) ENTIAL The base is, for example, the Metacryloxipropil base. In addition, all of the substitution groups XI to X4 may be Alchoxy groups, that is, so-called silicates. ) In addition to Phenoxy resins, thermoplastic resins, such as polyethylene resin, urinary resin, Polyvinyl acetate, Ethylene Vinyle Acetate, polybutadiene rubber, etc. Can also be used. In addition to the present invention, additives such as an anti-aging agent, a filler, and a colorant may be added. ® In the adhesive of the present invention, since the hardener particles composed of the metal admixture are coated with capsules, the epoxy resin does not overlap at normal temperature, and the adhesive has high storage stability. In addition, the adhesive of the present invention is hardened due to the cationic superposition reaction of the epoxy resin. The superposition reaction of the cations is lower than the temperature at which the superposition reaction of the conventional hardener occurs in the past. Therefore, the adhesive of the present invention can be cured at a lower temperature and in a shorter time than the conventional adhesive. In summary, although the present invention has been disclosed as # above in a preferred embodiment, it is not intended to limit the present invention. Any person skilled in the art can make various changes without departing from the spirit and scope of the present invention. Changes and retouching, therefore, the scope of protection of the present invention shall be determined by the scope of the appended patent application. 27 200409785 «1 4
File:TW 1009F-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 200409785 SUNDIAL CONFIDENTIAL:File: TW 1009F-IPO.doc SUNDIAL CONFIDENTIAL [Brief description of the drawings] Figures 1 (a) to 1 (c) are explanatory drawings for an example of a latent hardener manufacturing process of the present invention. Figures 2 (a) and 2 (b) are drawings for explaining an example of the process of manufacturing an adhesive film using the adhesive of the present invention. Figures 3 (a) to 3 (d) are drawings for the first half of the engineering description for bonding the LCD and TCP using the adhesive of the present invention. Figures 4 (e) and 4 (f) are diagrams for explaining the semi-process after TCP and LCD are bonded. Fig. 5 is a plan view illustrating the state where the TCP and the LCD are aligned. Figures 6 (a) to 6 (c) are explanatory diagrams of other examples of the bonding process 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 using traditional technology. Description of figure numbers 20, 45: Adhesive (coating layer) 3 0: Potential hardener 31: Hardener particles 32: Capsule material 28 200409785 SUNDIAL CONFIDENTIAL:
File:TW 1009F-IPO.doc 33 :膠囊File: TW 1009F-IPO.doc 33: Capsule
2929
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001170712A JP3802373B2 (en) | 2001-06-06 | 2001-06-06 | Latent curing agent, method for producing latent curing agent, and adhesive |
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| Publication Number | Publication Date |
|---|---|
| TW200409785A true TW200409785A (en) | 2004-06-16 |
| TWI270558B TWI270558B (en) | 2007-01-11 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW91134974A TWI270558B (en) | 2001-06-06 | 2002-12-02 | Latent hardener, manufacturing method for latent hardener, and adhesive |
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| JP (1) | JP3802373B2 (en) |
| TW (1) | TWI270558B (en) |
Families Citing this family (18)
| 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 |
| JP5417982B2 (en) * | 2003-09-08 | 2014-02-19 | デクセリアルズ株式会社 | Latent curing agent |
| 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 |
| 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 |
| US8147720B2 (en) | 2007-01-24 | 2012-04-03 | Sony 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 |
| CN119348260B (en) * | 2024-09-11 | 2025-10-14 | 杭州诗蓝过滤科技有限公司 | Ultra-soft breathable waterproof membrane and preparation method thereof |
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2001
- 2001-06-06 JP JP2001170712A patent/JP3802373B2/en not_active Expired - Lifetime
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| JP3802373B2 (en) | 2006-07-26 |
| TWI270558B (en) | 2007-01-11 |
| JP2002363255A (en) | 2002-12-18 |
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