TW200302847A - Curable organic resin composition - Google Patents

Curable organic resin composition Download PDF

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Publication number
TW200302847A
TW200302847A TW091132072A TW91132072A TW200302847A TW 200302847 A TW200302847 A TW 200302847A TW 091132072 A TW091132072 A TW 091132072A TW 91132072 A TW91132072 A TW 91132072A TW 200302847 A TW200302847 A TW 200302847A
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TW
Taiwan
Prior art keywords
resin composition
organic resin
composition
component
weight
Prior art date
Application number
TW091132072A
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English (en)
Other versions
TWI312356B (en
Inventor
Makoto Iwai
Keiji Wakita
Akihiko Shirahata
Original Assignee
Dow Corning Toray Silicone
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Publication of TW200302847A publication Critical patent/TW200302847A/zh
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Publication of TWI312356B publication Critical patent/TWI312356B/zh

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    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/54Silicon-containing compounds
    • C08K5/544Silicon-containing compounds containing nitrogen
    • C08K5/5475Silicon-containing compounds containing nitrogen containing at least one C≡N bond
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    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04Polyurethanes
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    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/4009Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4045Mixtures of compounds of group C08G18/58 with other macromolecular compounds
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    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
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  • Compositions Of Macromolecular Compounds (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Epoxy Resins (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Description

0) 0)200302847 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、内容、實施方式及圖式簡單說明) 【發明的技術領域】 本發明係揭示關於硬化性有機組合物。細言之,係關於 成形性優良、當硬化之時對於金屬等之底材黏著性優越之 硬化性有機樹脂組合物。 【先前技藝】 先前,環氧樹脂如與含環氧基之有機矽烷、含氨基之有 機燒氧基石夕烧或、含魏基有機烧氧基石夕烧混合,可增強黏著 性’係被眾所皆知之事。例如特開昭6 3 - 3 0 9 5 6 6號中提議 於環氧樹脂粉狀塗料中混合有機矽烷偶合劑之^環氧丙氧 基丙基曱基二乙氧基石夕烧,N -苯基·γ -氨基丙基三曱氧基石夕 燒’ γ-巯基丙基三曱氧基矽烷等以增強塗料組合物之黏著 性。且、特開平2_ 1 8 5 5 84號公報中提議於環氧樹脂中添加 Υ -織基丙基三甲氧基矽烷之黏著劑組合物。然而含環氧基 之燒氧基矽烷而混合出之組合物,對於金屬等之底材之黏 著性未必充分。根據用途是無法使用的。再者,含氨基之 有機烧氧基矽烷或含巯基有機烷氧基矽烷之混合組合物 存在著顯著失去了環氧樹脂原本硬化性問題。 另一方面,含硫氰基之有機烷氧基矽烷及此含硫氰基之 有機烧氧基石夕烧混合出之有機橡朦組合物係被知曉的。例 如特開平4-277534號公報中提議在乙丙二烯橡膠(EPDM) 裡混合硫氰基丙基三甲氧基矽烷之組合物。該組合物於有 機過氧化物存在下硫化後物理性質的惡化微少;可成為 t %永久變形率微小之橡膠成形品。並且特開平5-214171 200302847 (2) 號公報中提議在天然橡膠(NR)、苯乙烯丁二烯橡膠 (SBR)、EPDM等可能硫化之有機橡膠裡混合硫氰基丙基三 甲氧基矽烷之組合物。該組合物於硫存在下如硫化可成為 物理性質的惡化微少之橡膠成形品。但是由於含硫氰基之 有機烷氧基矽烷中混合有機樹脂之下,改良後之該有機樹 脂之成形性及對金屬等之底材的黏著性之有機樹脂組合 物是不為所知的。 【發明所欲解決之問題】 本發明者們之專注努力下之成果,發現若於環氧樹脂裡 混合含硫氰基之有機烷氧基矽烷下將可解決上述之問 題。此外,發現了若於酚醛樹脂、醯亞胺樹脂等之熱固性 有機樹脂裡混合含硫氰基之有機烷氧基矽烷,即可增強該 黏著性以達到本發明。 換句話說本發明之目的係提供卓越的成形性、當硬化之 時熱固性有機樹脂組合物此物不喪失其硬化性而硬化、對 於金屬等底材之黏著性優越之硬化性有機樹脂組合物。 【解決問題之手段】 本發明係揭示關於一種硬化性有機樹脂組合物,其特徵 在於包含(A)硬化性有機樹脂(100重量部)及(B)—般式: X-R^SiCORqnR^.n (式中 X是 NCS-或 SCN-; R1 是亞烷基或 烷撐氧基亞烷基;R2及R3是一價烴基;η是1、2或3)表示 之含硫氰基之有機烷氧基矽烷或含異硫氰基之有機烷氧 基矽烷(0.01〜100重量部)。 【發明之實施型態】 200302847 (3) 其說明係(A)硬化性有機樹脂於常溫呈現液體或固體, 藉由加熱、紫外線、放射線、電子射線等之高熱能線照射 等若能硬化之有機樹脂即為良好。雖該種類是未被限制 的,但於加熱下硬化之有機樹脂(熱固性有機樹脂)是合乎 理想的。做為該硬化有機樹脂可例舉為環氧樹脂、酚醛樹 脂、甲醛樹脂、二曱苯樹脂、二曱苯-甲醛樹脂、酮·曱醛 樹脂、呋喃樹脂、尿醛樹脂、醯亞胺樹脂、三聚氰胺樹脂、 醇酸樹脂、不飽和聚脂樹脂、苯胺樹脂、磺胺樹脂、矽樹 脂。其中,環氧樹脂、酚醛樹脂及醯亞胺樹脂是合乎理想 的。 (B)成分係本發明組合物之一種特徵成分,其具有增強 本發明組合物之成形性、增強對於金屬等的底材之黏著性 的功能。該(B)成分為一般式:X-R^SiCOR^nR^.n (式中X 是NCS-或SCN- ; R1是亞烷基或烷撐氧基亞烷基;R2及R3 是一價烴基;η是1、2或3)表示之含硫氰基之有機烷氧基 矽烷或含異硫氰基之有機烷氧基矽烷。 上述一般式中,就做為R1之亞烷基而言,可例示為亞甲 基、次乙基、曱基亞曱基、亞丙基、曱基次乙基、丁烯基。 再者,就做為R1之烷撐氧基亞烷基而言,可例示為亞曱羥 基亞甲基、亞曱經基次乙基、乙烯經基次乙基、乙稀經基 亞丙基。就做為R2及R3之一價烴基而言,可例示為甲基、 乙基、丙基、異丙基等之院基;乙烤基、稀丙基、丁稀基 等之鏈烯基;苯基、曱苯基、二曱苯基等之芳基。η是1、 2或3,較佳為2及3。 200302847
就做為該(B)成分之含硫氰基之有機烷氧基矽烷或含異 硫氰基之有機烷氧基矽烷而言,可例示為如下之化合物。 NCS(CH2)3Si(OCH3)3 NCS(CH2)3Si(OCH2CH3)3 NCS(CH2)3Si[OCH(CH3)2]3 NCS(CH2)3Si[0(CH2)2CH3]3 NCS(CH2)3Si[0(CH2)3CH3]3 NCSCH2CH(CH3)CH2Si(OCH3)3 NCSCH2CH(CHT)CH2Si(OCH2CH3)3 SCN(CH2)3Si(OCH3)3 SCN(CH2)3Si(OCH2CH3)3 SCN(CH2)3Si[OCH(CH3)2]3 SCNCH2CH(CH3)CH2Si(OCH3)3 SCNCH2CH(CH3)CH2Si(OCH2CH3)3 SCNCH2CH(CH3)CH2Si[OCH(CH3)2]3 SCNCH2CH(CH3)CH2Si[0(CH2)3CH3]3 NCS(CH2)3SiCH3(OCH3)2 NCS(CH2)3SiCH3(OCH2CH3)2 NCS(CH2)3Si(OC6H5)3 NCSCH2CH(CH3)CH2SiCH3(OCH3)3 相對於100重量部之(A)成分,(B)成分之混合量為 0.01〜100重量部之範圍内,較佳為0.1〜50重量部之範圍 内。因若過少即會令金屬等之底材之黏著性低落;若過多 即會令機械強度低落。 200302847
(5) 本發明組合物係包含上述之(A)成分及(B)成分。但該些 成分包括於(A)成分裡添加混合之各種眾所皆知之添加 劑。例如為促進(A)成分硬化可混合硬化劑或硬化催化 劑、無機填充物、光增感劑、增塑劑、撓性賦予劑。在此 若顯示硬化劑或硬化催化劑一例,可例示為一級或二級之 氨基化合物、三級胺化合物、鋁或鍅等有機金屬化合物、 磷化氫等之有機磷化合物、硼配合物、有機銨鹽、有機硫 鹽、有機過氧化物等。就做為一種無機填充物而言,可例 示為玻璃纖維、石綿、氧化鋁纖維、為氧化鋁及二氧化矽 成分之陶瓷纖維、硼化纖維、氧化鍅纖維、碳化矽纖維、 金屬纖維、聚酯纖維、一芳香族聚醯胺纖維、尼龍纖維、 苯酚纖維、天然之動植物纖維等之纖維狀填充物;熔融二 氧化矽、沉澱二氧化矽、氣相法白炭黑、燃燒二氧化矽、 氧化鋅、燃燒黏土、炭黑、玻璃珠、氧化鋁、滑石、氧化 #弓、黏土、氫氧化铭、硫酸鋇、二氧化鈦、氮化銘、碳化 矽、氧化鎂、氧化鈹、高嶺土、雲母、氧化锆等之粉粒體 狀填充物。就做為一種增塑劑或撓性賦予劑而言,可例示 為高級脂肪酸金屬鹽、酯蠟、矽油、有機功能基含有矽油、 矽橡膠、有機橡膠。 本發明組合物係包含上述之(A)成分及(B)成分。必要之 應對係藉由均等混合上述之添加劑即可容易製造。就做為 一種為製造本發明組合物之裝置而言,可例示為連續混合 撥壓機、1 〇 s s m i X e r、捏合混合機、m i X i n g r ο 11等。且、從 本發明組合物中取得成形品係以做為(A)成分的成形方法
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(6) 其先前眾所皆知之方法。例如可以適用於壓模方法、傳遞 模塑法、注射成形方法、鑄封成形方法、鑄塑成形方法、 塗覆成形方法等。 如同以上本發明之組合物係卓越的成形性、對於金屬等 之底材接著性優越。因此,活用其如此之特質,例如就做 為一有用之封閉劑或黏著劑,被使用於電器、電子零件。 【實施例】 以下係以實施例來詳細說明本發明組合物。此外,其實 施例中之黏度係2 5 °C之數值。且硬化性有機樹脂組合物之 成形性、黏著性、黏度變化率係以下示之方法評價。 〇成形性 硬化性有機樹脂組合物加壓下,其流動性係由螺旋流動 之測定來評價。螺旋流動係以EMMI規格(EMM 1-1-66)做為 基準方法來測定。 〇黏著性(A) 將其硬化性有機樹脂組合物,夾於兩片錄板(長度5 c m、 寬度1 cm、厚度0.5 mm)之間。於既定溫度、壓力之下壓 縮成形,製成鎳板與硬化性有機樹脂組合物之硬化物所整 體化之黏著實驗物體。將該實驗物體之兩片鎳板之端部各 自固定於拉伸試驗機之夾具,於50mm /分之拉伸速度下向 垂直方向拉伸,剝下有機樹脂組合物之硬化物與鎳板。緊 接之以肉眼觀察硬化性有機樹脂組合物之硬化物與鎳板 之斷裂面之斷裂狀態。結果係如下所揭示。 ◎符號:黏著性極為良好(於硬化性有機樹脂之硬化物 200302847 ⑺ 層遭破壞。凝聚破壞率1〇〇%以上) 〇符號:黏著性良好(一部分界面已分裂。凝聚破壞率 9 5 %以上) X符號:黏著性不良(於硬化性有機樹脂之硬化物及鎳 板之界面分裂。凝聚破壞率5 〇 %以下) 黏著性(B) 將其硬化性有機樹脂組合物,夾於兩片鎳板(長度5 c m、 寬度1 cm、厚度0· 5 mm)之間。於既定溫度、壓力之下壓 縮成形,製成_鎳板與硬化性有機樹脂組合物之硬化物所整 體化之黏著實驗物體。再者,同於上述,製成銅板與硬化 性有機樹脂組合物之硬化物其整體化之黏著實驗物體。將 該些實驗物體之兩片金屬板之端部各自固定於拉伸試驗 機之夾具,於50 mm/分之拉伸速度下向垂直方向拉伸,剝 下硬化性有機樹脂組合物之硬化物與金屬板。此時,測定 必要之分裂應力,做為黏著力(Kgf/cm2)。 〇黏度變化率 將製造後之硬化性有機樹脂組合物於23 t:下放置24小 時,測定黏度之增加程度,做為黏度變化率。黏度變化率 =(24小時放置後的硬化性有機樹脂組合物之黏度-製造後 立即之硬化性有機樹脂組合物之黏度)xl00/製造後立即的 硬化性有機樹脂組合物之黏度。 【實施例1】 3 5重量部之盼搭樹脂(三井化學股份有限公幻製造:苯 酚漆用酚醛樹脂、MILEX XLC-3L、軟化點70°C、170當量 200302847
之羥基)、3重量部之3 -硫氰基丙基三甲氧基矽烷 {NCS(CH2)3Si(OCH3)3}、65重量部之熔融石英粉末、4重 量部之環六亞甲基四胺及1重量部之加洛巴壌以9 0 °C加熱 滾壓來混煉,製造出硬化性酚醛樹脂組合物。粉碎該組合 物,將該組合物夾於兩片鎳板(長度5 c m、寬度1 c m、厚 度0.5 mm)之間,於溫度175°C、壓力70 kg/cm2、加熱3分 鐘之條件下壓縮成形。其後,以1 8 0 °C加熱2小時完成硬 化,製造出鎳板及酚醛樹脂組合物之硬化物成整體化之黏 著實驗物體。關·於該實驗物體對硬化性有機樹脂之鎳板的 黏著性係藉前述黏著實驗(A)中所記載之方法來測定,其 結果揭不於表1。 【比較實例1】 於實施例1,以3 -環氧丙氧基丙基三曱氧基矽烷取代3 -硫氰基丙基三曱氧基矽烷來混合之外,皆與實施例1相同 地來製造苯酚漆用酚醛樹脂。對於該組合物之鎳板的黏著 性與實施例1之測定相同,其結果一併記於表1。 【比較實例2】 於實施例1,除3 -硫氰基丙基三曱氧基矽烷無混合之 外,皆與實施例1相同地來製造苯酚漆用酚醛樹脂。對於 該組合物之鎳板的黏著性與實施例1之測定相同,其結果 一併記於表1。 【表1】
測定項目 實施例1 比較實例1 比較實例2 黏著性(A) ◎ X X -13- 200302847
【實施例2】 其包含單位40摩爾%之CH3Si03/2、單位10摩爾%之 C6H5(CH3)Si02/2、單位 40摩 _ %之 C6H5Si03/2及單位 10摩 爾%之(C6H5)2Si02/2,直接連結於矽原子之含有5重量%羥 基之1 3重量部的曱基苯基聚矽氧烷樹脂及1 3重量部之正 甲酚漆用酚醛環氧樹脂(日本化藥股份有限公司製造: EOCN- 1 02 0、軟化點80 °C、220當量之環氧樹脂)、2重量部 之3-硫氰基丙基三曱氧基矽烷{NCS(CH2)3SiCH3(OCH3)2}、74 重量部之熔@ 英粉末、0 · 9 0重量部之鋁乙酸丙銅配位基 及1重量部之加洛巴蠟以9 0 °C加熱滾壓來混煉,製造出熱 固性環氧樹脂組合物。測定該熱固性樹脂組合物之螺旋流 動。緊接之將該熱固性樹脂組合物夾於兩片鎳板(長度5 cm、寬度lcm、厚度0.5 mm)之間,於溫度175 °C、壓力70 kg/cm2、加熱2分鐘之條件下壓縮成形。其後,以180°C加 熱1 2小時完成硬化,製造出鎳板及硬化性樹脂組合物之硬 化物成整體化之黏著實驗物體。關於該實驗物體對硬化性 樹脂組合物之鎳板的黏著性係藉前述黏著實驗(A)中所記 載之方法來測定,其結果揭示於表2。 【實施例3】 於實施例2,以3-異硫氰基丙基三曱氧基矽烷 {SCN(CH2)3Si(OCH3)3}取代3-硫氰基丙基曱基二曱氧基矽 烷3 -硫氰基丙基三曱氧基矽烷來混合之外,皆與實施例2 相同地來製造熱固性環氧樹脂組合物。該組合物之螺旋流 動及對鎳板之黏著性與實施例2之測定相同,其該些結果 -14- 200302847 (ίο) 揭示於表2。 【比較實例3】 於實施例2 ,以3- Μ基丙基三甲氧基石夕烧
{HS(CH2)3Si(OCH3)3}取代3-硫氰基丙基甲基二曱氧基石夕 烷來混合之外,皆與實施例2相同地來製造熱固性環氧樹 脂組合物。以前述黏著實驗(A)裡$己載之方法來測定該組 合物之對鎳板之黏著性與螺旋流動,該些結果一併記於表 2 〇 【比較實例4 1 於實施例2 ’除3 -硫氰基丙基曱基一曱氧基秒烧無混人 之外,皆與實施例2相同地來製造熱固性環氧樹脂組人 物。該組合物之成形性(螺旋流動)及對鎳板之黏著性與實 施例2之測定相同,該些結果一併記於表2。 【表2】
測定項目 實施例2 實施例3 比較實例3 比較實例4 螺旋流動(英对) 42 39 21 13 黏著性(A) ◎ 〇 〇 X 【實施例4】 3 5重量部之丁烯二酸聚醯亞胺-三氮雜苯型之熱固性聚 亞胺樹脂(MITSUBISHI GAS CHEMICAL股份有限公司製 造)、4重量部之3-硫氰基丙基三曱氧基矽烷 {NCS(CH2)3Si(OCH3)3}、65重量部之熔融石英粉末、1重 量部之加洛巴堪及0 · 3 2重量部之苯甲酸鋁以9 0 °C加熱滾 -15- 200302847
(11) 壓來混煉,製造出熱固性醯亞胺樹脂組合物。測定該組合 物之螺旋流動。緊接之將該組合物夾於兩片鎳板(長度5 cm、寬度lcm、厚度0.5mm)之間,於溫度220 °C、壓力70 kg/cm2、加熱4分鐘之條件下壓縮成形。其後,以23 0°C加 熱3小時完成硬化,製造出鎳板及熱固性醯亞胺樹脂組合 物之硬化物成整體化之黏著實驗物體。關於該實驗物體對 熱固性醯亞胺樹脂組合物之鎳板的黏著性係藉前述黏著 實驗(A)中所記載之方法來測定,其結果揭示於表3。 【比較實例5 l· 於實施例4,除3 -硫氰基丙基三曱氧基矽烷無混合之 外,皆與實施例4相同地來製造熱固性醯亞胺樹脂組合 物。該組合物之螺旋流動及對鎳板之黏著性與實施例4之 測定相同,該些結果一併記於表3。 【表3】
測定項目 實施例4 比較實例5 螺旋流動(英忖) 52 43 黏著牲(A) ◎ X 【實施例5】 7 5重量部之正曱酚漆用酚醛環氧樹脂(日本化藥股份有 限公司製造·· EOCN- 1 020、軟化點80°C、220當量之環氧 樹脂)、2 6 0重量部之容融二氧化石夕、1重量部之加洛巴4鼠、 3 5重量部之苯酚漆用酚醛樹脂(三井化學股份有限公司製 造:MILEX XLC-3L、軟化點70°C、170當量之羥基)、0.6 -16- 200302847 (12)
重量部之三苯基構、5重量部之3 -硫氰基丙基三甲氧基石夕 烧{N C S ( C Η 2 ) 3 S i (Ο C Η 3) 3},以9 0 °C加熱滾壓來混煉,製造 出熱固性環氧樹脂組合物。測定該組合物之螺旋流動。緊 接之,將該組合物夾於兩片鎳板(長度5 cm、寬度1 cm、 厚度0.5 mm)之間’於溫度150C、壓力70 kg/cm2、加熱3 分鐘之條件下壓縮成形。其後,以1 8 0 °C加熱4小時完成硬 化,製造出鎳板及熱固性環氧組合物之硬化物成整體化之 黏著實驗物體。關於該實驗物體對熱固性環氧樹脂組合物 之鎳板的黏著性係藉前述黏著實驗(A)中所記載之方法來 測定,其結果揭示於表4。 【比較實例6】 於實施例5,以3 -環氧丙氧基丙基三甲氧基矽烷取代3 -硫氰基丙基三曱氧基矽烷來混合之外,皆與實施例5相同 地來製造熱固性環氧樹脂組合物。以前述黏著實驗(A)裡 記載之方法來測定該組合物對鎳板之黏著性與螺旋流 動,該些結果一併記於表4。 【比較實例7】 於實施例5,除3-硫氰基丙基三曱氧基矽烷{NCS(CH2}3Si(OCH3}3}無混 合之外,皆與實施例5相同地來製造熱固性環氧樹脂組合 物。 該組合物以前述黏著實驗(A)裡記載之方法來測定該組 合物對#板之黏著性與螺旋流動,該些結果一併記於表4。 -17- 200302847
(13) 【表4】 測定項目 實施例5 比較實例6 比較實例7 螺旋流動(英吋) 55 53 52 黏著性(A) ◎ X X 【實施例6】 於室溫中將20重量部之液體環氧樹脂(UNION CARBIDE 公司製造:ERL-4221)、22重量部之液體酸脫水物(3及4-甲基己烧及泥鄰苯二曱酸酐)、0.3重量部之鋅酸錫、2重量 一一 * —夺-. 部之3-硫氰基丙基三甲氧基矽烷{NCS(CH2)3Si(〇CH3)3}充— 分混合後消泡以製造熱固性液體環氧樹脂組合物。測定該 組合物之黏度變化率。緊接之,將該組合物夾於兩片鎳板 或兩片銅板(各長度5 cm、寬度1 cm、厚度0· 5 mm)之間, 於溫度120°C、壓力70 kg/cm2、加熱3分鐘之條件下壓縮成 形。其後’以1 5 0 °c加熱3小時完成硬化,製造出鎳板或銅 板與熱固性環氧組合物之硬化物成整體化之黏著實驗物 y 體。關於該些實驗物體係藉前述黏著實驗(B)中所記載之一 方法來測定,其結果揭示於表5。 _ 【比較實例8】 於實施例6,以3-巯基丙基三甲氧基矽烷取代3·硫氰基丙 基二甲氧基矽烷來混合之外,皆與實施例6相同地來製造 熱固性環氧樹脂組合物。以前述黏著實驗(B)裡記載之方 法來測定該組合物之黏著性與黏度變化率,該些結果一併 記於表5。 【比較實例9】 -18- 200302847 (14) 於貫施例6 ’以3-¾氧丙氧基丙基二甲氧基碎烧取代3-硫氰基丙基三甲氧基矽烷來混合之外,皆與實施例6相同 地來製造熱固性環氧樹脂組合物。以前述黏著實驗(B)裡 記載之方法來測定該組合物之黏著性與黏度變化率,該些 結果一併記於表5。 【比較實例1 0】 於實施例6,除3 -硫氰基丙基三曱氧基矽烷無混合之 外,皆與實施例6相同地來製造熱固性環氧樹脂組合物。 與實施例6同樣使其硬化。以前述黏著實驗(B)裡記載之方 法來測定該組合物之黏著性與黏度變化率,該些結果一併 記於表5。 【表5】 測定項目 實施例6 比較實例8 比較實例9 比較實例10 黏度變化倍率 2 無能測定 13 4 (膠凝作用) 黏著性(B)(kgf/cm2) 鎳板 182 85 62 59 銅板 121 89 52 53 【發明之功效】 本發明之一種硬化性有機樹脂組合物,其包含(A)成分 及(B)成分。特別是因含有(B)成分之一般式: X-Ri-SUOR^nR^-n (式中 X是 NCS-或 SCN- ; R1是亞烷基或 200302847
(15) 烷撐氧基亞烷基;R2及R3是一價烴基;η是1、2或3)表示 之含硫氰基之有機烷氧基矽烷或含異硫氰基之有機烷氧 基矽烷(0.01〜100重量部),使其具有卓越的成形性、當硬 化之時熱固性有機樹脂此物不喪失其硬化性而硬化、對於 金屬等之底材之黏著性優越之特徵。 -20-

Claims (1)

  1. 200302847 拾、申請專利範圍 1 . 一種硬化性有機樹脂組合物,其特徵在於包含:(A)硬 化性有機樹脂(100重量部);及(B) —般式: X-RLSiCOR^nR^-n (式中 X是 NCS -或 SCN-; R1是亞烷 基或烷撐氧基亞烷基;R2及R3是一價烴基;η是1、2或 3)表示之含硫氰基之有機烷氧基矽烷或含異硫氰基之 有機烷氧基矽烷(〇·〇1〜100重量部)。 2. 如申請專利範圍第1項之硬化性有機樹脂組合物,其中 (Α)成分係_戴®性有機樹脂。 3. 如申請專利範圍第1至2項中任一項之硬化性有機樹脂 組合物,其中(A)成分係紛酸樹脂。 4. 如申請專利範圍第1至2項中任一項之硬化性有機樹脂 組合物,其中(A)成分係環氧樹脂。 5. 如申請專利範圍第1至2項中任一項之硬化性有機樹脂 組合物,其中(A)成分係醯亞胺樹脂。 6. 如申請專利範圍第1項之硬化性有機樹脂組合物,其中 (B)成分係3-硫氰基丙基三曱氧基矽烷。 7. 如申請專利範圍第1項之硬化性有機樹脂組合物,其中 (B)成分係3-硫氰基丙基曱基二曱氧基矽烷。 8. 如申請專利範圍第1項之硬化性有機樹脂組合物,其中 (B)成分係3-異硫氰基丙基三曱氧基矽烷。 200302847 陸、(一)、本案指定代表圖為:第 圖 (二)、本代表圖之元件代表符號簡單說明: 柒、本案若有化學式時,請揭示最能顯示發明特徵的化學 式:
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