TW200300443A - Polysiloxane rubber sheet for hot press bonding - Google Patents

Polysiloxane rubber sheet for hot press bonding Download PDF

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Publication number
TW200300443A
TW200300443A TW091134387A TW91134387A TW200300443A TW 200300443 A TW200300443 A TW 200300443A TW 091134387 A TW091134387 A TW 091134387A TW 91134387 A TW91134387 A TW 91134387A TW 200300443 A TW200300443 A TW 200300443A
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Taiwan
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silicone rubber
rubber sheet
sheet
weight
hot
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TW091134387A
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Chinese (zh)
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TWI273126B (en
Inventor
Toru Takamura
Akio Nakano
Hideo Kanai
Toru Tsuchiya
Masahiro Mogi
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Shinetsu Chemical Co
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C59/00Surface shaping of articles, e.g. embossing; Apparatus therefor
    • B29C59/005Surface shaping of articles, e.g. embossing; Apparatus therefor characterised by the choice of material
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/04Carbon
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04Polysiloxanes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01RELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
    • H01R13/00Details of coupling devices of the kinds covered by groups H01R12/70 or H01R24/00 - H01R33/00
    • H01R13/02Contact members
    • H01R13/22Contacts for co-operating by abutting
    • H01R13/24Contacts for co-operating by abutting resilient; resiliently-mounted
    • H01R13/2407Contacts for co-operating by abutting resilient; resiliently-mounted characterized by the resilient means
    • H01R13/2414Contacts for co-operating by abutting resilient; resiliently-mounted characterized by the resilient means conductive elastomers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2383/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
    • C08J2383/04Polysiloxanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/20Applications use in electrical or conductive gadgets

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Laminated Bodies (AREA)

Abstract

This invention provides a polysiloxane rubber sheet for hot press bonding, in which the sheet does not tightly fit with the press tool or article to be press bonded, press bonding process can be improved and also the sheet has good durability and does not contaminate the surrounding. As its characteristics, at least one side of the polysiloxane rubber sheet for hot press bonding has an arithmetic average surface roughness of 0.8–5 μ m.

Description

200300443 經濟部智慧財產局員工消費合作社印製 A7 B7五、發明説明(1 ) 一、 發明所屬之技術領域 本發明係有關被壓粘物進行加熱壓延時介於被壓粘物 與加熱壓粘裝置間之熱壓粘用聚矽氧橡膠薄片者,特別是 有關脫模性良好,且不易污染周圍裝置部品、被壓粘物之 熱壓粘用聚矽氧橡膠薄片。 二、 先行技術 近來使用液晶配電盤做爲手提電腦、文書處理裝置、 攝影相機、領航裝置及手提電視等之展示者逐日增加。爲 使液晶傳動,使連接於液晶配電盤之電極與電極與傳動用L 、SI所搭載之易變性印刷基板(FPC)之導引電極介於各向 異性導電性粘著劑後,進行熱壓延後,務必連接電氣及機 械者,此時,挾於加壓工具與FPC之間,由加壓工具導熱 至各向異性導電性粘著劑之同時,加入均一之壓力爲目的 下,使用熱壓延用薄片。做爲此熱壓延用薄片者,亦有使 用聚四氟乙烯(PTFE)等氟樹脂薄膜者,而爲使壓力更爲 均勻,通常使用低彈性,具柔軟性熱傳導性良好之聚矽氧 橡膠薄片者。 惟,聚矽氧橡膠薄片比氧樹脂薄膜其薄片表面且粘合 性、薄片密合於加壓工具、FPC粘附後,不僅明顯降低壓 粘工程之作業性,同時剝離時薄片劣化、耐久性變差。因 此,做爲熱壓粘用聚矽氧橡膠薄片者如:配合氮化硼於聚 矽氧橡膠後,提高熱傳導性同時於玻璃cross進行補強(特 開平5- 198344號公報),於聚矽氧橡膠配合氮化硼與導電 (請先閱讀背面之注意事項再填寫本頁) •裝· 訂200300443 Printed by the Consumers ’Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs A7 B7 V. Description of the invention (1) I. Technical field to which the invention belongs The present invention relates to the pressing and delaying of the pressed object between the pressed object and the heating and pressing device Those who use the silicone rubber sheet for hot-press bonding are particularly concerned with the silicone rubber sheet for hot-press bonding which has good mold release properties and does not easily contaminate the surrounding device parts and the adherend. 2. Advance Technology Recently, the number of exhibitors using LCD power distribution boards as laptop computers, word processing devices, photography cameras, pilot devices, and portable TVs has increased day by day. In order to make the liquid crystal drive, the electrodes and electrodes connected to the liquid crystal switchboard and the guide electrodes of the volatile printed circuit board (FPC) mounted on the transmission L and SI are interposed with an anisotropic conductive adhesive, and then heat-rolled. After that, be sure to connect the electrical and mechanical people. At this time, between the pressurizing tool and the FPC, heat is transferred from the pressurizing tool to the anisotropic conductive adhesive, and the uniform pressure is added for the purpose of using hot pressing. Extend the sheet. As the sheet for hot calendering, there are also those using fluororesin films such as polytetrafluoroethylene (PTFE). To make the pressure more uniform, usually low-elasticity, soft silicone rubber with good thermal conductivity is used. Thinner. However, the silicone rubber sheet has better adhesiveness on the sheet surface than the oxyresin film. After the sheet is tightly attached to the pressure tool and adhered to the FPC, not only the workability of the press-bonding process is significantly reduced, but the sheet is deteriorated and durable when peeled Worse. Therefore, as the silicone rubber sheet for hot-press bonding, for example: after adding boron nitride to silicone rubber, improve the thermal conductivity and reinforce the glass cross (Japanese Patent Laid-Open No. 5-198344), and use silicone rubber. Rubber with boron nitride and conductivity (Please read the precautions on the back before filling this page) • Binding

本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -5- 200300443 A7 B7 五、發明説明(2 ) (請先閱讀背面之注意事項再填寫本頁) 性物質後,更以玻璃cross補強後附與靜電防止性(特開平 6- 3 6853號公報),於聚矽氧橡膠配合陶瓷、金屬等良好熱 傳導性物質者(特開平6- 289352號公報)、或於聚矽氧橡 膠配合0.5%以下之水份以外之揮發份的碳黑後,改善耐 熱性(特開平7- 11010號公報)等被揭示之,惟,針對薄 片表面之粘合性仍未被改善之。 經濟部智慧財產局員工消費合作社印製 對於薄片表面之粘合性問題,被提出於聚矽氧橡膠薄 片表面薄由使滑石、雲母等鱗片狀粉進行均勻打扮後,降 低薄片粘合性之方法,打粉後,以水洗淨多餘粉末後去除 之方法。又,使聚矽氧橡膠薄片與耐熱性樹脂薄膜藉由複 合化後,減少薄片表面之粘合性,同時具理想強度之熱壓 粘用聚矽氧橡膠複合薄片被揭示之(特開平8- 1 74765號公 報)。惟,此薄片其聚矽氧橡膠與耐熱性樹脂薄膜粘著因 此,比橡膠單體更不具柔軟性之缺點存在。特別是,設置 耐熱性樹脂薄膜於薄片兩面時該傾向更加強烈。此不具柔 軟性者於加壓時無法取得均勻壓力,故,務必增加加壓力 ,惟,此關係被壓延體強度者因此被受限之。此缺點可利 用低硬度橡膠提昇柔軟性後被改善之,惟,爲使橡膠呈低 硬度化,務必減少碳塡充量,近而產生不良熱傳導性之缺 黑占。 又’裝置FPC後,不易洗淨液晶配電盤之沾污,因此 ’務必考量工程上儘量不受沾污爲重,被期待開發一種不 是全依照先行方法者,以不擔心污染周邊裝置部品、被壓 延物之聚矽氧橡膠薄片者。 -6 - 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 200300443 Α7 Β7 五、發明説明(3 ) 三、 發明內容 因此,本發明者針對理想表面脫模性同時不易污染周 邊裝置部品、被壓延物等熱壓粘用聚矽氧橡膠薄膜進行精 密硏討後結果發現,於聚矽氧橡膠薄片之至少一表面具一 定範圍之凹凸後可取得良好結果者,進而完成本發明。 因此,本發明之目的係提供一種薄片不密合於加壓工 具、被壓延物,可改善壓延工程之作業性之同時,薄片自 體耐久性佳而不易污染周邊之熱壓粘用聚矽氧橡膠薄片者 〇 本發明該目的係其薄片之至少一表面具有算術平均〇.8 //m〜0.5//m凹凸者爲特徵之熱壓粘用聚矽氧橡膠薄片後 而達成者。該聚矽氧橡膠薄片以含有其水份以外揮發份爲 0.5重量%以下之碳黑及/或理想極傳導性塡充劑者爲宜。 四、 實施方式 本發明所使用聚矽氧橡膠薄片係配合有機聚矽氧烷與 塡充劑及硬化劑後,呈薄片狀成型後被硬化者。 該有機聚矽氧烷其平均聚合度爲200以上者、以下式 (I)之平均組成所示者宜。This paper size is in accordance with Chinese National Standard (CNS) A4 (210X297 mm) -5- 200300443 A7 B7 V. Description of the invention (2) (Please read the precautions on the back before filling in this page) After the substance is used, the glass Cross reinforcement is accompanied by antistatic properties (Japanese Patent Application Laid-Open No. 6-3853), those with good thermal conductivity such as ceramics and metals in silicone rubber (Japanese Patent Application Laid-open No. 6-289352), or silicone rubber When carbon black with a volatile content other than moisture of 0.5% or less is added, heat resistance is improved (Japanese Patent Application Laid-Open No. 7-11010) and the like. However, the adhesion to the surface of the sheet has not been improved. The problem of the adhesion of the sheet surface printed by the employee cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs was proposed on the surface of the thin silicone rubber sheet. The method of reducing the adhesiveness of the sheet after uniformly dressing scaly powder such as talc and mica After removing the powder, wash the excess powder with water and remove it. In addition, after the silicone rubber sheet and the heat-resistant resin film are compounded, the surface adhesion of the sheet is reduced, and at the same time, a silicone rubber composite sheet for hot pressing with ideal strength is disclosed (Japanese Patent Application Laid-Open No. 8- 1 74765). However, this sheet has the disadvantage that the silicone rubber adheres to the heat-resistant resin film and is less flexible than the rubber alone. This tendency is particularly strong when a heat-resistant resin film is provided on both sides of the sheet. This person who is not flexible cannot obtain a uniform pressure when pressing, so it is necessary to increase the pressure, but this relationship is limited by the strength of the rolled body. This disadvantage can be improved by using low-hardness rubber to improve its flexibility. However, in order to reduce the hardness of the rubber, it is necessary to reduce the carbon charge, which has recently resulted in a lack of poor thermal conductivity. Also, 'It is not easy to clean the contamination of the LCD switchboard after installing the FPC. Therefore, it is necessary to consider that the project is as free from contamination as possible. It is expected to develop a person who does not follow the first method in order to not worry about contaminating peripheral device parts and being rolled Silicone rubber sheet. -6-This paper size is in accordance with Chinese National Standard (CNS) A4 specification (210X297 mm) 200300443 A7 B7 V. Description of the invention (3) III. Summary of the invention Therefore, the inventor aims at the ideal surface release property and does not easily contaminate peripheral devices As a result of precise examination of the silicone rubber film for hot-press bonding such as parts and rolled objects, it was found that those who can obtain good results after having a certain range of unevenness on at least one surface of the silicone rubber sheet have completed the present invention. Therefore, the object of the present invention is to provide a polysiloxane for hot-press bonding, which does not adhere to a pressing tool or a rolled object, can improve the workability of the rolling process, and has good durability of the flake itself without contaminating the surroundings. Rubber sheet 〇 This object of the present invention is achieved by a silicone rubber sheet for hot pressing which is characterized by having at least one surface with an arithmetic mean 0.8 // m ~ 0.5 // m unevenness. The silicone rubber sheet is preferably one containing carbon black and / or an ideal polar conductive filler with a volatile content of 0.5% by weight or less other than its moisture. 4. Embodiment The silicone rubber sheet used in the present invention is a sheet that is formed into a sheet and then hardened after being mixed with an organopolysiloxane and a filler and a hardener. This organic polysiloxane has an average degree of polymerization of 200 or more, and is preferably an average composition represented by the following formula (I).

RnSiO (4- η) /2 ( 1 ) 上式中之R係代表取代或非取代之一價烴基及/或氫氧 基者,η代表1.95〜2.05之正數。做爲r之具體例者如: 甲基、乙基、丙基等院基、環戊基、環己基等之環院基、 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐) (請先閱讀背面之注意事項再填寫本頁) 装· 、1Τ 經濟部智慧財產局員工消費合作社印製 200300443 A7 _B7__ 五、發明説明(4 ) (請先閱讀背面之注意事項再填寫本頁) 乙烯基、烯丙基等脂烯基、苯基、甲苯基等之芳基、或此 等氫原子之部份氯原子、氟原子等被取代之鹵化烴基等例 。本發明中有機聚矽氧烷之主鏈係由二甲基矽氧烷單位所 成者,或此有機聚矽氧烷之主鏈中以導入乙烯基、苯基、 三氟丙基等者爲宜。且,其分子鏈末端以三有機甲矽烷基 或氫氧基所封鏈者即可,做爲此三有機甲矽烷基例者如: 三甲基矽烷基、二甲基乙烯矽烷基、三乙烯矽烷基等示例 者。另外,此有機聚矽氧烷之聚合度爲200以上者宜,25 °C之粘度爲300cs以上者宜。當聚合度低於200時,則硬化 後之機械性強度將降低、變脆之傾向。 做爲塡充劑者,以耐熱性爲優先時,其水份以外之揮 發份以使用〇.5重量%以下之碳黑者宜’以熱傳導性爲優 先時則選擇良好熱傳導性塡充劑者宜。 經濟部智慧財產局員工消費合作社印製 水份以外揮發份爲0.5重量%以下之碳黑不僅可提昇 聚矽氧橡膠薄片之耐熱性且提昇熱傳導性與機械性強度, 藉由導電化附與靜電防止性。碳黑藉由其製造方法被分類 爲爐黑、槽法碳黑、熱碳黑、乙炔碳黑等,惟,水份以外 揮發份爲0.5%以下之碳黑者例如:乙炔碳黑、特開平1-27 2667號所揭示之導電性碳黑等理想者。測定水份以外之 揮發份方法記載於〗IS K 622 1 ”橡膠用碳黑試驗方法”,其具 體內容係置入規定量之碳黑於壺中,於950 °C下加熱7分 鐘後,測定揮發減量。 該碳黑配合量爲100重量份有機聚矽氧烷之20〜150 重量份,特別以40〜100重量份爲更佳。當低於20重量% -8- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 200300443 A7 B7__ 五、發明説明(5 ) 則熱傳導性將不足,反之,高於150重量份則不易配合, 且成型加工性極差。 (請先閱讀背面之注意事項再填寫本頁) 做爲本發明所使用之理想熱傳導性塡充劑例者如:氧 化銘、氮化硼、氮化絕、氫氧化絕、氧化纟S、氧化鋅、石 英等之無機粉末,或銀、鎳、銅、鐵等金屬粉末爲理想者 。此等良好熱傳導性塡充材料之配合量爲100重量份有機 聚矽氧氧烷之50〜1,200重量份者宜,特別以100〜1,000 重量份之範圍內使用者更佳,當低於50重量份時熱傳導性 則不足,反之,大於1,200重量份則成型加工性變差、硬 化後之機械性強度變低,同時失去橡膠柔軟性。又,亦可 倂用碳黑及理想傳導性塡充劑後使用之。 本發明所使用之硬化劑通常使用聚矽氧橡膠之硬化者 ,可適當選自先行公知者。如:原子團反應時爲二-第三-丁基過氧化物、2,5-二甲基-2,5-二(第三-丁基過氧 化)己烷、二枯烯基過氧化物等有機過氧化物例,其配合 量爲100重量份有機聚矽氧烷之0.1〜5重量份者宜。 經濟部智慧財產局員工消費合作社印製 有機聚矽氧烷具有2個以上脂烯基時如1分子中含有2 個以上結合於矽原子之氫原子有機氫化聚矽氧烷與鉑族金 屬系觸媒所成之附加反應硬化劑例者。有機氫化聚矽氧烷 之配合量針對有機聚矽氧烷之脂烯基其結合於矽原子之氫 原子莫耳比(三Si- H/脂烯基)爲0·5〜5之量者宜,鉑族 金屬系觸媒爲有機聚矽氧烷之1 ppm〜1,000- ppm者宜。 有機聚矽氧烷爲含有2個以上矽醇基時,如:具有2 個以上烷氧基、乙醯氧基、酮肟基、丙烯氧基等水解性基 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) _ 9 _ 200300443 A7 B7 五、發明説明(6 ) 之有機矽化合物等縮合反應硬化劑例者。 (請先閱讀背面之注意事項再填寫本頁) 本發明中由其成型難易度觀之,做爲硬化劑者以有機 過氧化物或附加反應硬化劑爲理想使用者。 本發明於必要時亦可添加親水性二氧化矽、疏水性二 氧化矽等之補強性二氧化矽塡充劑、粘土、碳酸鈣、矽藻 土、二氧化鈦等塡充劑、低分子矽氧烷酯、矽醇基之有機 矽化合物等分散劑、矽烷偶合劑、鈦偶合劑等粘合附與劑 、附與難燃性之鉑族金屬系觸媒、橡膠混合物之提昇green 強度之四氟聚乙烯粒子等。 經濟部智慧財產局員工消費合作社印製 做爲本聚矽氧橡膠混合物之配合方法者可利用雙棒滾 輥、捏合器、密閃式混合器、行星混合器等混合機進行該 成份之混煉,一般於使用前添加硬化劑者宜。做爲聚矽氧 橡膠薄片之成型方法者如:於塑模中使配合至硬化劑爲止 之聚矽氧橡膠混合物進行熱壓之硬化方法,以壓延機、擠 壓機等加工呈所定形狀後之熱硬化方法、溶解於液狀聚矽 氧橡膠混合物或甲苯等溶劑中使液化聚矽氧橡膠混合物塗 佈於聚乙烯對苯二甲酸酯(PET)等之薄膜後,乾燥去除溶 劑後進行熱硬化之方法例者。 此成型之聚矽氧橡膠薄片厚度以0.1〜10mm者宜。當 厚度低於0.1mm時,則無法充份追隨被壓延體,造成壓力 不均。反之,大於10 m m以上之厚度則熱導性變差。 本發明中,聚矽氧橡膠薄片之至少一表面具有凹凸後 ,附與降低粘合性之脫模性,惟,該凹凸於算術平均表面 粗糙度務必爲0.8//m〜5/zm者。當凹凸爲〇.8//m以下時 -10- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 200300443 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(7 ) ,則聚矽氧薄片將易粘合,反之,5 // m以上則電極電氣之 接觸不安定均不理想。另外,凹凸設於兩表面時,兩表面 之粗糙度可相同亦可爲不同者。該算術平均表面粗糙度係 依照JIS B 0601爲基準進行測定者。該凹凸依壓紋加工進行 設定者,既價廉且迅速爲極理想者。 附與壓紋於聚矽氧橡膠薄片兩表面之方法有:1)利用 壓延滾輥製造薄片時於粗化表面之塑膠薄膜粗面上分出聚 矽氧橡膠薄片組成物,於硬化前使塑膠面反面之分出薄片 面壓附於附壓紋之滾輥後複製壓紋之後,再由硬化後塑膠 薄膜剝取聚矽氧橡膠之方法,2)使硫化後聚矽氧橡膠薄片 藉由噴砂淸理等粗方法,3)於兩面壓紋加工之塑膠薄膜單 面上進行塗層後,硬化前小心將此卷取後直接置入烤箱進 行硫化後,由塑膠薄膜剝取聚矽氧橡膠之方法等。 本發明熱壓延用聚矽氧薄片具有良好的耐熱性、熱傳 導性、強度及作業性,同時具有做爲聚矽氧橡膠之彈性, 因此,利用加壓成型機於成型層合板、易彎性印刷基板時 熱傳導之同時可均一加壓爲目的下被使用之薄片、介著各 向異性導電性粘合劑使連接於液晶顯示器之電極與傳動用 LSI所搭載之FPC引導電極進行熱壓粘後連接電氣及機械時 所使用之薄片爲特別有改者。 [發明效果] 本發明薄片之至少一表面施予凹凸之熱壓粘用聚矽氧 橡膠薄片係於至少一表面上具有凹凸因此,加壓工具,由 (請先閱讀背面之注意事項再填寫本頁) -裝· 訂RnSiO (4- η) / 2 (1) In the above formula, R represents a substituted or unsubstituted monovalent hydrocarbon group and / or a hydroxyl group, and η represents a positive number from 1.95 to 2.05. As specific examples of r, such as: methyl, ethyl, propyl and other bases, cyclopentyl, and cyclohexyl, and other bases, this paper size applies the Chinese National Standard (CNS) A4 specification (210 × 297 mm) (Please read the precautions on the back before filling out this page) Installation, printed by 1T Intellectual Property Bureau, Ministry of Economic Affairs, Consumer Consumption Cooperative, 200300443 A7 _B7__ V. Description of Invention (4) (Please read the precautions on the back before filling out this page) Examples of aliphatic alkenyl groups such as vinyl and allyl groups, aryl groups such as phenyl and tolyl groups, or halogenated hydrocarbon groups such as partial chlorine atoms and fluorine atoms substituted by such hydrogen atoms. In the present invention, the main chain of the organic polysiloxane is formed by dimethylsiloxane units, or the main chain of the organic polysiloxane is introduced by vinyl, phenyl, trifluoropropyl, or the like. should. In addition, those whose molecular chain ends are sealed with a triorganosilyl group or a hydroxyl group may be used. Examples of the triorganosilyl group include: trimethylsilyl group, dimethylethylene silyl group, and triethylene group. Examples such as silane. In addition, the degree of polymerization of the organic polysiloxane is preferably 200 or more, and the viscosity of 25 ° C is 300 cs or more. When the degree of polymerization is less than 200, the mechanical strength after hardening tends to decrease and become brittle. As a filler, when heat resistance is a priority, volatiles other than water are preferably used with carbon black less than 0.5% by weight. 'When thermal conductivity is a priority, a good thermal conductivity filler is selected. should. Carbon black with a volatile content of less than 0.5% by weight, printed by employees of the Intellectual Property Bureau of the Ministry of Economic Affairs, can not only improve the heat resistance of silicone rubber sheets, but also improve the thermal conductivity and mechanical strength. Preventive. Carbon black is classified into furnace black, channel black, hot carbon black, acetylene carbon black, etc. by its manufacturing method, but those with a volatile content other than moisture of 0.5% or less such as acetylene carbon black, Tokai Ping 1-27 2667 is an ideal one such as conductive carbon black. The method for measuring volatiles other than moisture is described in IS K 622 1 "Test method for carbon black for rubber". The specific content is that a predetermined amount of carbon black is placed in a pot, and it is heated at 950 ° C for 7 minutes. Volatile weight loss. The compounding amount of the carbon black is 20 to 150 parts by weight of 100 parts by weight of the organopolysiloxane, and more preferably 40 to 100 parts by weight. When it is less than 20% by weight -8- This paper size applies the Chinese National Standard (CNS) A4 specification (210X297 mm) 200300443 A7 B7__ V. Description of the invention (5) The thermal conductivity will be insufficient, otherwise, if it is higher than 150 parts by weight Difficult to fit and extremely poor in formability. (Please read the precautions on the back before filling out this page) Examples of ideal thermally conductive radon fillers used in the present invention are: oxide oxide, boron nitride, nitriding oxide, hydroxide oxide, thorium oxide, oxide Inorganic powders such as zinc and quartz, and metal powders such as silver, nickel, copper, and iron are preferred. The blending amount of these good thermally conductive filling materials is preferably 50 to 1,200 parts by weight of 100 parts by weight of organopolysiloxane, and it is particularly preferred for users in the range of 100 to 1,000 parts by weight. When it is less than 50 parts by weight, thermal conductivity is insufficient. On the other hand, when it is more than 1,200 parts by weight, molding processability is deteriorated, mechanical strength after curing is lowered, and rubber flexibility is lost. In addition, carbon black and an ideal conductive filler can also be used. The hardening agent used in the present invention is usually a hardened silicone rubber, and may be appropriately selected from those known in the art. Such as: di-third-butyl peroxide, 2,5-dimethyl-2,5-di (third-butyl peroxide) hexane, dicumenyl peroxide, etc. during radical reaction In the case of organic peroxides, the blending amount is preferably 0.1 to 5 parts by weight of 100 parts by weight of the organopolysiloxane. Printed by the Consumers' Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs. Organic polysiloxanes have two or more aliphatic alkenyl groups. For example, one molecule contains two or more hydrogen atoms bonded to silicon atoms. Organic hydrogenated polysiloxanes are in contact with platinum group metals. Examples of additional reaction hardeners made by the media. The compounding amount of the organic hydrogenated polysiloxane is directed to the aliphatic alkenyl group of the organic polysiloxane, and the molar ratio of the hydrogen atom to the silicon atom (tri Si-H / aliphatic group) is preferably 0.5 to 5 The platinum group metal catalyst is preferably from 1 ppm to 1,000-ppm of organopolysiloxane. When the organopolysiloxane contains more than two silanol groups, for example, it has two or more alkoxy, ethoxyl, ketoxime, and acryloxy hydrolyzable basic paper sizes. Applicable to Chinese National Standards (CNS) A4 specification (210X297 mm) _ 9 _ 200300443 A7 B7 V. Examples of condensation reaction hardeners such as organosilicon compounds (6). (Please read the precautions on the back before filling out this page) In the present invention, from the perspective of the difficulty of molding, organic peroxides or additional reaction hardeners are ideal users as hardeners. In the present invention, when necessary, reinforcing silica dioxide fillers such as hydrophilic silica, hydrophobic silica and the like, clay, calcium carbonate, diatomaceous earth, titanium dioxide and other fillers, and low-molecular-weight siloxanes can also be added. Dispersants such as esters, silanol-based organosilicon compounds, adhesives such as silane coupling agents, titanium coupling agents, platinum group metal catalysts with flame resistance, and PTFE with enhanced green strength Ethylene particles, etc. The blending method printed by the employee's consumer cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs as the compounding method of the silicone rubber mixture can use a double-roller roller, a kneader, a flash mixer, a planetary mixer and other mixing machines to mix the ingredients. In general, it is advisable to add a hardener before use. As a method for forming a silicone rubber sheet, for example, a method of hot pressing a silicone rubber mixture mixed with a curing agent in a mold, and then using a calender, an extruder, etc. to form a predetermined shape. Heat hardening method, dissolving in a liquid silicone rubber mixture or a solvent such as toluene, and applying the liquefied silicone rubber mixture to a film such as polyethylene terephthalate (PET), drying and removing the solvent, and then heating Examples of hardening methods. The thickness of the formed silicone rubber sheet is preferably 0.1 ~ 10mm. When the thickness is less than 0.1 mm, it cannot sufficiently follow the rolled body, resulting in uneven pressure. Conversely, if the thickness is more than 10 mm, the thermal conductivity is deteriorated. In the present invention, after at least one surface of the silicone rubber sheet has unevenness, it is accompanied with a mold release property that reduces adhesiveness. However, the arithmetic average surface roughness must be 0.8 // m to 5 / zm. When the unevenness is less than 0.8 // m-10- This paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm) 200300443 A7 B7 Printed by the Consumer Cooperative of Intellectual Property Bureau of the Ministry of Economic Affairs ), The polysilicon sheet will be easy to adhere. Conversely, if the contact is more than 5 // m, the electrode's electrical contact will be unstable. In addition, when the unevenness is provided on both surfaces, the roughness of the two surfaces may be the same or different. This arithmetic average surface roughness is measured in accordance with JIS B 0601. The unevenness is set by embossing, and it is highly desirable because it is inexpensive and quick. The methods of attaching embossing on both surfaces of the silicone rubber sheet are: 1) When the sheet is manufactured by using a calender roll, the silicone rubber sheet composition is separated on the rough surface of the plastic film, and the plastic is hardened before curing. The method of separating the side of the sheet from the back and pressing it on the roller with embossing, copying the embossing, and then stripping the silicone rubber from the hardened plastic film. 2) The vulcanized silicone rubber sheet is sandblasted. Coarse method, etc. 3) After coating on one side of the plastic film embossed on both sides, carefully take this coil before curing and directly put it in the oven for vulcanization, and then strip the silicone rubber from the plastic film. Method, etc. The polysiloxane sheet for hot calendering of the present invention has good heat resistance, thermal conductivity, strength and workability, and at the same time has the elasticity as a polysiloxane rubber. Therefore, a pressure forming machine is used to form the laminated board, and the bendability is easy. The sheet used for the purpose of uniformly pressing while conducting heat while printing the substrate. After the anisotropic conductive adhesive is used, the electrodes connected to the liquid crystal display and the FPC guide electrode mounted on the transmission LSI are thermally bonded. The sheet used when connecting electrical and mechanical parts is particularly modified. [Effects of the Invention] The silicone rubber sheet for hot-press bonding with unevenness on at least one surface of the sheet of the present invention has unevenness on at least one surface. Therefore, the pressure tool, by (please read the precautions on the back before filling in this (Page)-Bookbinding

本紙張尺度適用中國國家標準(CNS ) A4規格(21〇><297公釐) 11 - 200300443 A7 B7 五、發明説明(8 ) (請先閲讀背面之注意事項再填寫本頁) 被壓延物之脫模性均良好,無法染周邊之優異性。故,不 僅薄片自體耐久性良好,更提昇熱壓延步驟之作業性。且 ’加壓時,薄片不密合可若干移動,不致於壓延部卷起空 氣,可加入均勻的壓力者。 [實施例] 以下,藉由實施例更進行本發明之詳細內容,惟,本 發明不受限於此。 [實施例1] 經濟部智慧財產局員工消費合作社印製 於99.85莫耳%二曱基矽氧烷單位及0.15莫耳% 甲基 乙烯矽氧烷單位所成之平均聚合度爲8,000之100重量份 甲基乙烯聚矽氧烷中以雙棒滾輥配合平均粒徑爲40nm、水 份以外揮發份爲0.10%之50重量份乙炔碳黑及5重量份補 強性二氧化矽 (Aerosil R- 972:商品名、Degussa公司製) ,混煉後呈均一化。針對100重量份此聚矽氧橡膠混合物 添加0.1重量份之氯化鉑酸之異丙醇溶液(含鉑量2重量 %) ,0.05重量份之反應抑制劑乙炔性醇(3-甲基-1- 丁 炔-3-醇),以及下式(2)所示之1.2重量份甲基氫化聚 矽氧烷後,以雙棒滾輥充份混煉後,調製呈硬化性聚砂氧 橡膠混合物。 CHa CH3 (CH3) 3S i 0 (S ί 0) i2 (S ί 0) 12S i (CH3) 3 ⑵This paper size applies Chinese National Standard (CNS) A4 specification (21〇 > < 297mm) 11-200300443 A7 B7 V. Description of the invention (8) (Please read the precautions on the back before filling this page) Calendered The release properties of the materials are good, and the excellent properties of the surroundings cannot be dyed. Therefore, not only the sheet itself has good durability, but also improves the workability of the hot rolling step. In addition, when the sheet is pressed, it can be moved slightly if the sheet is not tight, so that the rolling part does not wind up, and even pressure can be added. [Examples] Hereinafter, the details of the present invention will be further described by examples, but the present invention is not limited thereto. [Example 1] The average degree of polymerization produced by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs printed on 99.85 mole% difluorenylsiloxane units and 0.15 mole% methylvinylsiloxane units is 8,000. 50 parts by weight of acetylene black and 5 parts by weight of reinforcing silica (Aerosil R -972: trade name, manufactured by Degussa), uniform after kneading. For 100 parts by weight of this silicone rubber mixture, add 0.1 part by weight of a solution of chloroplatinic acid in isopropanol (containing 2% by weight of platinum) and 0.05 parts by weight of a reaction inhibitor acetylene alcohol (3-methyl-1 -Butyne-3-ol) and 1.2 parts by weight of methyl hydrogenated polysiloxane represented by the following formula (2), and then fully kneaded with a two-roller roller to prepare a hardened polysand rubber compound . CHa CH3 (CH3) 3S i 0 (S ί 0) i2 (S ί 0) 12S i (CH3) 3 ⑵

CH3 H 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -12 - 200300443 A7 B7 經濟部智慧財產局員工消費合作社印製 五、發明説明(9 ) 利用壓延成型機使取得聚矽氧橡膠混合物分出呈厚度 〇.3 0mm後,複製於算術平均表面粗糙度0.7/z m之單面壓紋 加工厚度100 // m之聚乙烯對苯二甲酸酯(PET)薄膜上。 再使算術平均表面粗糙度爲3.5// m之壓紋滾輥壓對於與 PET薄膜相反側之分出薄片表面上,於聚矽氧橡膠表面複 製壓紋後,以5分鐘時間通過1 60 °C之加熱爐中進行硬化 之。再使聚矽氧橡膠薄片由PET薄膜剝離後,200 °C下進 行後加熱硬化2小時後,製作熱壓粘用聚矽氧橡膠薄片者 〇 利用表面粗糙度計surf test 501 (mithutoyo (股份)製 商品名)進行測定複製壓紋面之表面粗糙度後,算術平均 表面粗糙度爲2.9// m者。 [實施例2] 利用捏合器均勻混煉99.85莫耳%之二甲基矽氧烷單 位及0· 1 5莫耳%甲基乙烯基矽氧烷單位所成之平均聚合度 爲8,000之100重量份甲基乙烯基聚矽氧烷,做爲良好熱傳 導性塡充劑之400重量份氧化鋁粉末(氧化鋁AL- 45:昭 和電工(股份)製商品名),30重量份之比表面積爲 20 0m2 /g之二氧化矽微粉末(Aerosil 200:日本Aerosil (股 份)製商品名),以及下式(3)所示之5重量份α,ω -二羥甲基聚矽氧烷後,於150 t下進行熱處理2小時。Cli HO (Si-〇)i〇h ⑶CH3 (請先閲讀背面之注意事項再填寫本頁) •裝·CH3 H This paper size is in accordance with Chinese National Standard (CNS) A4 specification (210X297 mm) -12-200300443 A7 B7 Printed by the Intellectual Property Bureau of the Ministry of Economic Affairs and Consumer Cooperatives V. Description of the invention (9) Using a calendering machine to obtain polysilicon After the oxygen rubber mixture was separated to a thickness of 0.30 mm, it was copied on a polyethylene terephthalate (PET) film with a single-sided embossing thickness of 100 // m and an arithmetic average surface roughness of 0.7 / zm. Then, the embossing roller with an arithmetic average surface roughness of 3.5 // m was applied to the surface of the separated sheet opposite to the PET film. After the embossing was replicated on the surface of the silicone rubber, it passed through 60 ° in 5 minutes. C is hardened in a heating furnace. After the silicone rubber sheet was peeled from the PET film, it was post-heat-cured at 200 ° C for 2 hours, and then a silicone rubber sheet for thermocompression bonding was produced. Surf test 501 (mithutoyo (share)) (Product name), after measuring the surface roughness of the copy embossed surface, the arithmetic average surface roughness is 2.9 // m. [Example 2] A kneader was used to uniformly knead 99.85 mol% of dimethylsiloxane units and 0.15 mol% of methyl vinyl siloxane units. The average degree of polymerization was 100 weights of 8,000. 400 parts by weight of alumina powder (alumina AL-45: Showa Denko (trade name) manufactured by Showa Denko Corporation) as a thermally conductive filler, and a specific surface area of 20 parts by weight is 20 parts by weight. 0 m 2 / g of silicon dioxide fine powder (Aerosil 200: Japan Aerosil (stock) product name), and 5 parts by weight of α, ω-dimethylol polysiloxane represented by the following formula (3), then Heat treatment was performed at 150 t for 2 hours. Cli HO (Si-〇) i〇h ⑶CH3 (Please read the precautions on the back before filling this page) • Installation ·

本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) -13- 200300443 A7 ___ B7 五、發明説明(10) (請先閲讀背面之注意事項再填寫本頁) 冷卻後’於1 00重量份此聚矽氧橡膠混合物中添加1.5 重量份之做爲硬化劑的有機過氧化物(C- 23:信越化學工 業(股份)製商品名)以雙滾輥進行混合後,利用壓延成 型機分出厚度0.30mm者。再於算術平均表面粗糙度0.7 /z m 之單面被壓紋加工厚度100// m之PET薄膜上進行複製該分 出之聚矽氧橡膠組成物後,再使算術平均表面粗糙度3.5 A m之壓紋滾輥壓附於與ΡΕΊν薄膜相反側分出之薄片表面 上,於聚矽氧橡膠表面複製壓紋後,以5分鐘時間通過160 °C之加熱爐後,進行硬化之。再由pet薄膜剝離此聚矽氧 橡膠薄片後,於200 °C下進行後加熱硬化4小時之後,製 成熱壓粘用聚矽氧橡膠薄片。 ΐ [實施例3] ν 經濟部智慧財產局員工消費合作社印製 於99_85莫耳%二甲基矽氧烷單位及0.15莫耳%甲基 乙烯基矽氧烷所成之平均聚合度8,000之1〇〇重量份甲基乙 烯基聚矽烷中以雙滾輥配合平均粒徑40nm、水份以外揮發 份爲0.10%之50重量份乙炔碳黑以及5重量份補強性二氧 化矽(Aerosil R- 972·· Degussa公司製商品名)進行混煉呈 均一化。針對此100重量份聚矽氧橡膠混合物添加〇. 1重量 份氯化鉑酸之異丙醇溶液(鉑量2重量% ) 、0.05重量份 反應抑制劑之乙炔性醇(3-甲基-1- 丁炔-3-醇)、以 及1,2重量份該(2)式所示之甲基氫化聚矽氧烷,以雙 滾輥充份混煉後調製硬化性聚矽氧橡膠混合物。 -14- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 200300443 A7 B7 五、發明説明(11 ) (請先閱讀背面之注意事項再填寫本頁) 以壓延成型機將此聚矽氧橡膠混合物分出厚度呈 ◦•30mm後,複製於厚度100// m算術平均粗糙度爲0之PET 薄膜上,5分鐘通過1 60 °C之加熱爐後進行硬化之。再由 PET薄膜剝離聚矽氧橡膠薄片後,200 下進行後加熱硬 化2小時後,此薄片單面進行噴砂後,製成算術平均表面 粗糙度具1.8/zm壓紋表面之壓粘用聚矽氧橡膠薄片。 [實施例4] 利用捏合器均勻混煉99.85莫耳%二甲基矽氧烷單位 及0.15莫耳%甲基乙烯基矽氧烷單位所成之平均聚合度爲 8,000之1〇〇重星份甲基乙傭基聚砂氧院’ 400重量份之做 爲良好熱傳導性塡充劑之氧化鋁粉末(氧化鋁AL- 45 :昭 和電工(股份)製商品名),30重量份之比表面積爲 200m2 /g之二氧化矽微粉末(Aerosil 200:日本Aerosil (股 份)製商品名),以及5重量份該式(3)所示之α,ω-二羥甲基聚矽氧烷後,於1 50 °C下進行熱處理2小時。 經濟部智慧財產局員工消費合作社印製 冷卻後,於100重量份此聚矽氧橡膠混合物中添加1.5 重量份之做爲硬化劑之有機過氧化物(C - 2 4:信越化學工 業(股份)製商品名)以雙滾輥進行混合後,溶於二甲苯 後做成60%二甲苯溶液,利用Comma coater於算術平均表 面粗糙度0.7//m單面壓紋加工厚度i〇〇//m之pet薄膜之 壓紋加工面上塗層0.2mm厚度後,將二甲苯於80 °C下進 行蒸發乾燥。再使算術平均表面粗糙度爲3 · 5 // m之壓紋滾 輥壓附於與PET薄膜相反側之塗層薄片表面,於聚矽氧橡 -15- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 200300443 A7 B7 五、發明説明(12) 膠表面複製壓紋後,5分鐘通過1 60 °C加熱爐中,進行硬 化。再由PET薄膜剝離此聚矽氧橡膠薄片,200 °C下進行 後加熱硬化4小時後,製成熱壓粘用聚矽氧橡膠薄片。 [比較例1 ] 使用實施例1之聚矽氧橡膠混合物,利用壓延成型機 分出厚度0.30mm後,複製於厚度100//m算術平均表面粗 糙度爲0之PET薄膜後,5分鐘進行通過160 °C加熱爐後 ,進行硬化之。再由PET薄膜剝離聚矽氧橡膠薄片後,於 薄片表面上藉由紗布將平均粒徑1 3 // m之滑石粉末擦於薄 片上,進行均勻塗佈之。更於乾燥器中,200 °C下進行熱 處理4小時後,將此薄片流水中以海綿擦拭同時洗淨之, 去除多餘粉末後使水份乾燥之後,製作熱壓粘用聚矽氧橡 膠薄片。 [比較例2 ] 使用實施例2之聚矽氧橡膠混合物後,利用壓延成型 機後,分出厚度0.30mm後,複製於厚度100//m之算術平 均表面粗糙度爲0之PET薄膜上,5分鐘通過160 °C加熱 爐後進行硬化之。再由PET薄膜剝離此聚矽氧橡膠薄片, 藉由紗布將平均粒徑爲20 // m之雲母粉末擦於薄片進行均 勻塗佈之。更於乾燥機中200 t:下進行熱處理4小時後, 此薄片於流水中以海綿擦拭洗淨後,去除多餘粉末後使水 份乾燥之後,製成熱壓延用聚矽氧橡膠薄片。 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) _ _This paper size applies Chinese National Standard (CNS) A4 specification (210X297 mm) -13- 200300443 A7 ___ B7 V. Description of the invention (10) (Please read the precautions on the back before filling this page) After cooling, it will be '100 1.5 parts by weight of organic peroxide (C-23: Shin-Etsu Chemical Industry Co., Ltd.) as a hardener is added to the silicone rubber mixture by two parts and mixed with a calender molding machine. Separate 0.30mm thickness. The divided silicone rubber composition was reproduced on a PET film having an arithmetic average surface roughness of 0.7 / zm on one side and embossed to a thickness of 100 // m, and then the arithmetic average surface roughness was 3.5 A m The embossing roller was pressed on the surface of the sheet separated from the opposite side of the PEE film. After the embossing was replicated on the surface of the silicone rubber, it was passed through a heating furnace at 160 ° C for 5 minutes and then hardened. The silicone rubber sheet was peeled from the pet film, and then post-heat-cured at 200 ° C for 4 hours, and then a silicone rubber sheet for thermocompression bonding was prepared.实施 [Example 3] ν The average degree of polymerization of 8,000 mol% dimethylsiloxane units and 0.15 mol% methylvinylsiloxane printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs was 1 〇〇weight parts of methyl vinyl polysilane with a double-roller with an average particle diameter of 40nm, 50 parts by weight of acetylene carbon black with a volatile content of 0.10% other than water, and 5 parts by weight of reinforcing silica (Aerosil R- 972 ·· Degussa's product name) Knead uniformly. To this 100 parts by weight of a silicone rubber mixture, 0.1 part by weight of an isopropanol solution of platinum chloride acid (2% by weight of platinum) and 0.05 parts by weight of an acetylene alcohol (3-methyl-1) as a reaction inhibitor were added. -Butyne-3-ol) and 1,2 parts by weight of methyl hydrogenated polysiloxane represented by the formula (2), and kneaded with a double roll to prepare a curable polysiloxane rubber mixture. -14- This paper size is in accordance with Chinese National Standard (CNS) A4 specification (210X297 mm) 200300443 A7 B7 V. Description of the invention (11) (Please read the precautions on the back before filling this page) The silicone rubber mixture was separated to a thickness of 30 mm, and then copied on a PET film with a thickness of 100 // m and an arithmetic mean roughness of 0, and passed through a heating furnace at 1 60 ° C for 5 minutes and then hardened. After the silicone rubber sheet was peeled off from the PET film, after 200 hours of post-heat hardening, the sheet was sandblasted on one side to make a silicon adhesive for pressure bonding with an arithmetic average surface roughness of 1.8 / zm embossed surface. Oxygen rubber sheet. [Example 4] The average degree of polymerization of 99.85 mole% dimethylsiloxane units and 0.15 mole% methylvinylsiloxane units was uniformly kneaded by a kneader to a weight of 1,000 to 1,000 Hundreds of 400 parts by weight of a methyl ethoxylated polysand oxygen institute, alumina powder (alumina AL-45: trade name of Showa Denko Co., Ltd.) as a good thermal conductivity filler, 30 parts by weight After fine silica powder with a surface area of 200 m 2 / g (Aerosil 200: trade name of Aerosil Japan), and 5 parts by weight of α, ω-dimethylol polysiloxane represented by the formula (3) , Heat treatment at 1 50 ° C for 2 hours. After printed and cooled by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs, 1.5 parts by weight of organic peroxide as a hardener is added to 100 parts by weight of this silicone rubber mixture (C-2 4: Shin-Etsu Chemical Industry Co., Ltd.) (Product name) after mixing with a double roll, dissolving in xylene to make a 60% xylene solution, and using a Comma coater at an arithmetic average surface roughness of 0.7 // m for single-side embossing thickness i〇〇 // m After coating the pet film on the embossed surface with a thickness of 0.2 mm, xylene was evaporated to dryness at 80 ° C. Then, the embossing roller with an arithmetic average surface roughness of 3 · 5 // m is pressed on the surface of the coated sheet opposite to the PET film, and on the surface of polysilicone rubber -15- This paper applies Chinese national standard (CNS ) A4 size (210X297 mm) 200300443 A7 B7 V. Description of the invention (12) After the rubber surface is copied and embossed, it is hardened in a heating furnace at 1 60 ° C for 5 minutes. The silicone rubber sheet was peeled from the PET film, and then post-heat-cured at 200 ° C for 4 hours to prepare a silicone rubber sheet for hot-pressing. [Comparative Example 1] The silicone rubber mixture of Example 1 was used to divide a thickness of 0.30 mm by a calender molding machine, and then copied to a PET film having a thickness of 100 // m and an arithmetic average surface roughness of 0, and passed through it in 5 minutes. After heating at 160 ° C, it is hardened. After the silicone rubber sheet was peeled off from the PET film, talc powder having an average particle size of 1 3 // m was rubbed on the surface of the sheet with gauze, and uniformly coated. In a desiccator, heat-treat at 200 ° C for 4 hours, then wipe the sheet under running water with a sponge while washing it, remove excess powder, and dry the water. Then, make a silicone rubber sheet for thermocompression bonding. [Comparative Example 2] After using the silicone rubber mixture of Example 2 and using a calender molding machine, the thickness was 0.30 mm, and then it was copied on a PET film having an arithmetic average surface roughness of 0 // m in thickness. After passing through a 160 ° C heating furnace for 5 minutes, it was hardened. Then, the silicone rubber sheet was peeled off from the PET film, and the mica powder having an average particle diameter of 20 // m was rubbed on the sheet with gauze and uniformly coated. After 200 hours in a dryer, heat treatment was performed for 4 hours. After the sheet was wiped and washed with running sponge in running water, the excess powder was removed and the water was dried to form a silicone sheet for hot rolling. This paper size applies to China National Standard (CNS) A4 (210X297 mm) _ _

經濟部智慧財產局員工消費合作社印製 、言 (請先閱讀背面之注意事項再填寫本頁)Printed by the Consumers' Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs (Please read the precautions on the back before filling this page)

200300443 A7 B7 五、發明説明(13 ) [比較例3] (請先閲讀背面之注意事項再填寫本頁) 除未進行壓紋加工之外,完全與實施例3同法進行, 製成熱壓粘用聚矽氧薄片。 [比較例4] 將底層塗料C (信越化學工業(股份)製商品名)塗佈 於耐熱性樹脂薄膜厚度1 2 // m之芳香族聚亞胺薄膜 (kapton:東菱 deupone (股份)製商品名)後,室溫下進行 30分鐘乾燥。 另外,利用壓延成型機將實施例1所製成之硬化性聚 石夕氧橡膠混合物分出厚度〇.30mm後,複製於厚度loo# m 之算術平均表面粗糙度爲0之PET薄膜上。再由此薄片上 面進行壓延塗佈該底層塗料之kapton薄膜後,5分鐘時間 通過160 °C加熱爐使聚矽氧橡膠混合物進行硬化之。再進 行剝離PET薄膜後,於乾燥器中200 °C下進行熱處理4小 時後,製成熱壓粘用聚矽氧橡膠複合薄片。 經濟部智慧財產局員工消費合作社印製 (壓延試驗) 於實施例1〜4及比較例1〜4所製成之熱壓延用聚矽 氧橡膠薄片之內面下放置厚度30//m之deapone、japan、 limidade製特氟隆薄膜(特氟隆係註冊商標),接著設置 25// m瀝青銅電極之2片FPC挾著厚度22// m之各方異性 導電粘著劑者係設置於壓延機後,由340 °C下於加熱加壓 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) _ 17 - 200300443 A7 B7 五、發明説明(14) (請先閱讀背面之注意事項再填寫本頁) 工具之熱壓延用聚矽氧橡膠薄片表面側以40kgf/cm2之擠壓 壓力下進行20秒壓延之。重複此壓延後,於對於加壓工具 之薄片密合狀態及均一壓力下進行測定無法加熱硬化各方 異性導電粘著劑爲止之次數。此次數係藉由上下FPC銅電 極之傳導進行確定。 惟,比較例4之熱壓延用聚矽氧橡膠薄片時,使 kapton薄膜側往加壓工具進行測定之。又,薄膜厚度增加 ,熱傳導變差,而加壓時間延長2 5秒。結果如表1所示。 表1 樣品 薄片耐久性重 對於薄片加壓 加壓工具 算術平均表 複壓延次數 工具之密合 之沾污 面粗糙度 (次) 表 裏 實施例1 100 ^fnT Μ te J MN 2.9 0.3 實施例2 47 Μ J 翻E J\\\ 1.2 0.6 實施例3 95 紐 j \\\ 川、 1.8 0.3 實施例4 45 M 1.3 0.7 比較例1 67 te 稍有 0.2 0.3 比較例2 33 ίκ 稍有 0.7 0.6 比較例3 71 有 Μ J \ ΝΝ 0.3 0.3 比較例4 78 Μ 0.2 0.1 經濟部智慧財產局員工消費合作社印製 比較例1、2時,連續使用後加壓工具漸被沾污務必進 行洗淨。反之,實施例1〜4時,不必洗淨加壓工具仍具耐 -18- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 200300443 A7 B7 五、發明説明(15 ) 久性。比較例3時,務必進行2次/1日之洗淨,此時需進 行壓延機之冷卻極爲不便者。 又,針對實施例1與比較例4,除降低加壓工具之擠壓 壓力爲30kgf/cm2之外,相同條件下進行壓延試驗後,證明 實施例1其上下FPC之銅電極間之傳導爲良好者,而比較 例4則出現部份傳導不良。比較例4之熱壓粘用聚矽氧橡 膠複合薄片對於加壓工具之密合與沾污並無問題點,惟, 相較於本發明其壓延時間較長,務必提高擠壓壓力者。 (請先閱讀背面之注意事項再填寫本頁) 裝·200300443 A7 B7 V. Description of the invention (13) [Comparative Example 3] (Please read the precautions on the reverse side before filling out this page) Except that no embossing is performed, it is completely performed in the same way as in Example 3 and made into hot press Adhesive silicone sheet. [Comparative Example 4] Primer C (a Shin-Etsu Chemical Industry Co., Ltd. trade name) was applied to an aromatic polyimide film (kapton: manufactured by Toyo Deupone (Stock Corporation)) with a heat-resistant resin film thickness of 1 2 // m. (Trade name), and then dried at room temperature for 30 minutes. In addition, a calendering machine was used to separate the hardenable polysilicone rubber mixture prepared in Example 1 to a thickness of 0.30 mm, and then copied to a PET film having an arithmetic average surface roughness of 0 in thickness loo # m. Then, the kapton film of the primer coating was calendered on this sheet, and then the silicone rubber mixture was cured in a 160 ° C heating furnace for 5 minutes. After the PET film was peeled, it was heat-treated at 200 ° C in a desiccator for 4 hours to prepare a silicone rubber composite sheet for thermocompression bonding. Printed by the Consumer Cooperative of the Intellectual Property Bureau of the Ministry of Economic Affairs (calendering test) A thickness of 30 // m is placed under the inner surface of the silicone rubber sheet for hot rolling made in Examples 1 to 4 and Comparative Examples 1 to 4. Teflon film (registered trademark of Teflon series) made by deapone, japan, and limidade, followed by 2 pieces of FPC with 25 // m pitch copper electrodes and an anisotropic conductive adhesive with a thickness of 22 // m. After calendering, heating and pressing at 340 ° C, this paper applies Chinese National Standard (CNS) A4 specification (210X 297 mm) _ 17-200300443 A7 B7 V. Description of the invention (14) (Please read the back first (Please note this page, please fill in this page again) The surface of the silicone sheet for hot rolling of the tool is rolled at a pressure of 40 kgf / cm2 for 20 seconds. After repeating this calendering, the number of times until the anisotropic conductive adhesive cannot be heat-hardened by measuring the sheet adhered state of the pressurized tool and the uniform pressure was measured. This number is determined by the conduction of the upper and lower FPC copper electrodes. However, when the silicone rubber sheet for hot rolling of Comparative Example 4 was used, the kapton film side was measured with a pressure tool. In addition, the thickness of the film is increased, the heat conduction is deteriorated, and the pressing time is extended by 25 seconds. The results are shown in Table 1. Table 1 Sample sheet durability and weight The arithmetic average of the sheet pressurizing and pressing tool Table shows the number of times the adhesion of the tool is contaminated surface roughness (times) Table Example 1 100 ^ fnT Μ te J MN 2.9 0.3 Example 2 47 Μ J turned EJ \\\ 1.2 0.6 Example 3 95 New j \\\ Sichuan, 1.8 0.3 Example 4 45 M 1.3 0.7 Comparative Example 1 67 te Slightly 0.2 0.3 Comparative Example 2 33 ίκ Slightly 0.7 0.6 Comparative Example 3 71 Yes Μ J \ Ν0.3 0.3 Comparative Example 4 78 Μ 0.2 0.1 When the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs printed Comparative Examples 1 and 2, the pressurized tools became contaminated after continuous use and must be washed. On the other hand, in Examples 1 to 4, the pressure-resistant tools are not required to be washed and still resistant to -18. This paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) 200300443 A7 B7 V. Description of the invention (15) Persistence . In Comparative Example 3, it is necessary to wash twice a day, and it is extremely inconvenient to cool the calender at this time. In addition, for Example 1 and Comparative Example 4, except that the pressing pressure of the pressing tool was reduced to 30 kgf / cm2, the rolling test was performed under the same conditions, and it was proved that the conductivity between the copper electrodes of the upper and lower FPCs of Example 1 was good In contrast, Comparative Example 4 showed partial conduction failure. The silicone rubber composite sheet for hot press bonding of Comparative Example 4 has no problem with the adhesion and staining of the pressurizing tool. However, compared with the present invention, the rolling time is longer, and it is necessary to increase the extrusion pressure. (Please read the notes on the back before filling this page)

、1T, 1T

經濟部智慧財產局員工消費合作社印製 -19- 本紙張尺度適用中國國家標準(CNS ) Α4規格(210Χ297公釐)Printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs -19- This paper size applies to China National Standard (CNS) Α4 specification (210 × 297 mm)

Claims (1)

200300443 A8 B8 C8 ___D8____ 六、申請專利範圍 1 1. 一種熱壓粘用聚矽氧橡膠薄片,其特徵係其薄片之 至少一表面具有算術平均粗糙度爲0.8//m〜5//m之凹凸者 〇 2. 如申請專利範圍第1項之熱壓粘用聚矽氧橡膠薄片 ,其中該聚矽氧橡膠薄片含有0.5重量%以下之水份以外 揮發份之碳黑者。 3. 如申請專利範圍第1項或第2項之熱壓粘用聚矽氧 橡膠薄片,其中該聚矽氧橡膠薄片爲含有良好熱傳導性塡 充劑者。 4. 如申請專利範圍第1項至第3項中任一項之熱壓粘 用聚矽氧橡膠薄片,其中該聚矽氧橡膠薄片之厚度爲0.1〜 10mm 者。 5. 如申請專利範圍第1項至第4項中任一項之熱壓粘 用聚矽氧橡膠薄片,其中該表面之凹凸係藉由壓紋所設定 者。 (請先閱讀背面之注意事項再填寫本頁) 經濟部智慧財產局員工消費合作社印製 本紙張尺度逋用中國國家揉準(CNS ) A4規格(210X297公釐) -20 - 200300443 (一) 本案指定代表圖爲:無代表圖 (二) 本案代表圖之元件代表符號簡單說明·’ 無代表元件200300443 A8 B8 C8 ___D8____ 6. Scope of patent application 1 1. A silicone rubber sheet for thermocompression bonding, characterized in that at least one surface of the sheet has unevenness with an arithmetic average roughness of 0.8 // m to 5 // m 〇2. For example, the silicone rubber sheet for hot-press bonding according to item 1 of the scope of patent application, wherein the silicone rubber sheet contains carbon black with a volatile content other than moisture of 0.5% by weight or less. 3. For example, the silicone rubber sheet for hot-pressing application of item 1 or 2 of the patent application scope, wherein the silicone rubber sheet is a filler containing a good thermal conductivity. 4. For example, the silicone rubber sheet for hot pressing according to any one of claims 1 to 3, wherein the thickness of the silicone rubber sheet is 0.1 to 10 mm. 5. The silicone rubber sheet for hot pressing according to any one of claims 1 to 4, wherein the unevenness of the surface is set by embossing. (Please read the precautions on the back before filling out this page) The paper size printed by the Consumer Cooperatives of the Intellectual Property Bureau of the Ministry of Economic Affairs uses the Chinese National Standard (CNS) A4 (210X297 mm) -20-200300443 (I) This case The designated representative map is: no representative map (2) simple description of the component representative symbols of the representative map in this case
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