TW201803909A - 硬化性組成物,硬化物之製造方法及其硬化物 - Google Patents
硬化性組成物,硬化物之製造方法及其硬化物 Download PDFInfo
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- TW201803909A TW201803909A TW106110862A TW106110862A TW201803909A TW 201803909 A TW201803909 A TW 201803909A TW 106110862 A TW106110862 A TW 106110862A TW 106110862 A TW106110862 A TW 106110862A TW 201803909 A TW201803909 A TW 201803909A
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Abstract
本發明係提供硬化物之玻璃轉移溫度高,密著性優異的硬化性組成物、硬化物之製造方法及其硬化物。
本發明之硬化性組成物,其係含有:陽離子聚合性成分(A)15~90質量份、陽離子聚合起始劑(B)1~10質量份、自由基聚合性成分(C)10~50質量份、自由基聚合起始劑(D)1~10質量份及選自由下述式(I)
表示之單體所得之聚合物、由下述式(II)
表示之單體所得之聚合物等所成群組之重量平均分子量1,000~30,000的聚合物(E)1~20質量份,使(A)與(C)與(E)之合計成為100質量份,(A)係以多元醇之環氧丙基化物等(A1)及氧雜環丁烷化合物(A2)為必須成分,(A1)為35~65質量份,自由基聚合性成分(C)係以具有環氧基及乙烯性不飽和基之化合物(C1)等為必須成分。
Description
本發明係有關硬化性組成物、硬化物之製造方法及其硬化物,詳細為有關硬化物之玻璃轉移溫度高,密著性優異的硬化性組成物、硬化物之製造方法及其硬化物。
硬化性組成物係使用於油墨、塗料、各種塗覆劑、接著劑、光學構件等的領域。關於這種硬化性組成物之改良,有各種的報告。
例如下述專利文獻1~3中提案含有陽離子聚合性成分及自由基聚合性成分之能量線硬化性組成物及其硬化物。具體而言,專利文獻1中,提案初期硬化性及接著性優異的偏光板用接著劑組成物。又,專利文獻2中,提案即使以透濕度低之樹脂薄膜作為保護膜時,光照射後,也能快速展現接著力,且對於各種力,經過一定時間後之接著力為良好,耐久試驗後亦不產生問題,耐濕熱試驗結束後之接著力亦良好之低黏度的光硬化性接著劑。此外,專利文獻3中,提案含有不飽和脂環式環氧酯化合物之可兼具高耐熱性或高折射率化與透明性的活性能量線聚合性
樹脂組成物。
專利文獻1:日本特開2014-105218號公報
專利文獻2:日本特開2015-040283號公報
專利文獻3:日本特開2015-168757號公報
但是,即使為專利文獻1~3所提案之硬化性組成物,對於硬化性及密著性,亦有不一定能夠滿足的情況,現狀為期望能夠高度兼具硬化性及密著性之新穎的硬化性組成物。
因此,本發明之目的為提供硬化物之玻璃轉移溫度高,密著性優異的硬化性組成物、硬化物之製造方法、及其硬化物。
本發明人等為了解決上述課題而精心探討的結果,發現若為具有特定組成之硬化性組成物時,即可克服上述課題,而完成本發明。
亦即,本發明之硬化性組成物,其係含有:
陽離子聚合性成分(A)15~90質量份、陽離子聚合起始劑(B)1~10質量份、自由基聚合性成分(C)10~50質量份、自由基聚合起始劑(D)1~10質量份及選自由下述式(I)
(式中,X為碳原子數1~7之烷基、碳原子數1~7之烷氧基、碳原子數6~12之芳基、碳原子數6~12之芳氧基或碳原子數6~10之脂環式烴基、或此等之基中之氫原子經選自由環氧基、氧雜環丁烷基、羥基及羧基所成群之1種以上之基所取代者)表示之單體所得之聚合物、由下述式(II)
(式中,R1表示氫原子、甲基或鹵素原子,X’為碳原子數1~7之烷基、碳原子數6~12之芳基或碳原子數6~10之脂環式烴基、或此等之基中之氫原子經選自由環氧基、氧雜環丁烷基、羥基及羧基所成群之1種以上之基所取代者)表示之單體所得之聚合物、選自前述式(I)表示之單體之二種以上之單體所得之聚合物、選自前述式(II)表示之單體之二種以上之單體所得之聚合物及由前述式(I)表示之單體及前述式(II)表示之單體所得之聚合物所成群組之重量平均分子量1,000~30,000的聚合物(E)1~20質
量份,使前述陽離子聚合性成分(A)與前述自由基聚合性成分(C)與前述聚合物(E)之合計成為100質量份,前述陽離子聚合性成分(A)係以多元醇之環氧丙基化物或多元醇環氧烷加成物之環氧丙基化物(A1)及氧雜環丁烷化合物(A2)為必須成分,相對於前述陽離子聚合性成分(A)與前述自由基聚合性成分(C)與前述聚合物(E)之合計100質量份時,前述多元醇之環氧丙基化物或多元醇環氧烷加成物之環氧丙基化物(A1)為35~65質量份,前述自由基聚合性成分(C)係以具有環氧基及乙烯性不飽和基之化合物(C1)或碳原子數2~20的多元醇之丙烯酸酯或碳原子數2~20的多元醇之甲基丙烯酸酯(C2)為必須成分。在此,重量平均分子量係指在四氫呋喃(THF)溶劑中,藉由GPC測量,以苯乙烯換算求得的重量平均分子量。
本發明之硬化性組成物中,前述陽離子聚合性成分(A)進一步含有芳香族環氧化合物(A3)為佳。又,本發明之硬化性組成物中,前述芳香族環氧化合物(A3)為多官能芳香族環氧化合物為佳。此外,本發明之硬化性組成物中,前述聚合物(E)為由前述式(I)表示之單體及前述式(II)表示之單體所得的聚合物,前述式(I)中之X為碳原子數6~12之芳基,前述式(II)中之X’為碳原子數1~7之烷基,前述烷基經環氧基所取代為佳。
本發明之硬化性組成物之製造方法,其係對本發明之硬化性組成物進行活性能量線照射,或進行加
熱。
本發明之硬化物,其係本發明之硬化性組成物的硬化物。
依據本發明時,可提供硬化物之玻璃轉移溫度高,密著性優異的硬化性組成物、硬化物之製造方法及其硬化物。本發明之硬化性組成物,特別是可用於接著劑。
以下詳細說明本發明之硬化性組成物。
本發明之硬化性組成物,其係含有:陽離子聚合性成分(A)15~90質量份、陽離子聚合起始劑(B)1~10質量份、自由基聚合性成分(C)10~50質量份、自由基聚合起始劑(D)1~10質量份及選自由下述式(I)表示之單體所得之聚合物、由下述式(II)表示之單體所得之聚合物、選自前述式(I)表示之單體之二種以上之單體所得之聚合物、選自前述式(II)表示之單體之二種以上之單體所得之聚合物及由前述式(I)表示之單體及前述式(II)表示之單體所得之聚合物所成群之重量平均分子量1,000~30,000的聚合物(E)1~20質量份。
本發明之硬化性組成物中,前述陽離子聚合性成分(A)係以多元醇之環氧丙基化物或多元醇環氧烷加成物之環氧丙基化物(A1)及氧雜環丁烷化合物
(A2)為必須成分,且相對於陽離子聚合性成分(A)與自由基聚合性成分(C)與聚合物(E)之合計100質量份時,多元醇之環氧丙基化物或多元醇環氧烷加成物之環氧丙基化物(A1)為35~65質量份。又,自由基聚合性成分(C)係以具有環氧基及乙烯性不飽和基之化合物(C1)或碳原子數2~20的多元醇之丙烯酸酯或碳原子數2~20之多元醇的甲基丙烯酸酯(C2)為必須成分。
在此,式(I)中,X為碳原子數1~7之烷基、碳原子數1~7之烷氧基、碳原子數6~12之芳基、碳原子數6~12之芳氧基或碳原子數6~10之脂環式烴基、或此等之基中之氫原子經選自由環氧基、氧雜環丁烷基、羥基及羧基所成群之1種以上之基所取代者。
在此,式(II)中,R1表示氫原子、甲基或鹵素原子,X’為碳原子數1~7之烷基、碳原子數6~12之芳基或碳原子數6~10之脂環式烴基、或此等之基中之氫原子經選自由環氧基、氧雜環丁烷基、羥基及羧基所成群之1種以上
之基所取代者。
本發明之硬化性組成物的陽離子聚合性成分(A)係藉由以能量線照射或加熱活性化的陽離子聚合起始劑,產生高分子化或交聯反應的化合物。可列舉環氧化合物、氧雜環丁烷化合物、乙烯醚化合物等。
本發明之硬化性組成物的陽離子聚合性成分(A)係以多元醇的環氧丙基化物或多元醇環氧烷加成物的環氧丙基化物(A1)及氧雜環丁烷化合物(A2)作為必須成分,但是也可使用其他的環氧化合物,例如芳香族環氧化合物(A3)及脂環式環氧化合物(A4)等。
上述多元醇之環氧丙基化物、或多元醇環氧烷加成物的環氧丙基化物(A1),可列舉將多元醇或多元醇環氧烷加成物進行環氧丙基化者,且環氧丙基化物的分子量為250以上者為佳。
上述多元醇的環氧丙基化物或多元醇環氧烷加成物的環氧丙基化物(A1),可列舉1,4-丁二醇二環氧丙醚、1,6-己二醇二環氧丙醚、新戊二醇二環氧丙醚、丙三醇之三環氧丙醚、三羥甲基丙烷之三環氧丙醚、山梨醣醇之四環氧丙醚、二季戊四醇之六環氧丙醚、聚乙二醇之二環氧丙醚、聚丙二醇之二環氧丙醚、二環戊二烯二甲醇二環氧丙醚等之多元醇之環氧丙醚,及藉由將1種或2種以上之環氧烷與丙二醇、三羥甲基丙烷、丙三醇等之脂肪族多元醇進行加成所得之聚醚多元醇的聚環氧丙醚化物、脂肪族長鏈二元酸之二環氧丙酯。
多元醇之環氧丙基化物或多元醇環氧烷加成物之環氧丙基化物(A1),進一步可列舉脂肪族高級醇之單環氧丙醚或高級脂肪酸之環氧丙基酯、環氧化大豆油、環氧基硬脂酸辛酯、環氧基硬脂酸丁酯、環氧化大豆油、環氧化聚丁二烯等。
多元醇的環氧丙基化物或多元醇環氧烷加成物的環氧丙基化物(A1)係含有飽和縮合環者,可提高硬化物之硬化性及密著性,故較佳。
上述多元醇的環氧丙基化物或多元醇環氧烷加成物的環氧丙基化物(A1)可使用市售品,可列舉例如Denacol EX-121、Denacol EX-171、Denacol EX-192、Denacol EX-211、Denacol EX-212、Denacol EX-313、Denacol EX-314、Denacol EX-321、Denacol EX-411、Denacol EX-421、Dcnacol EX-512、Denacol EX-521、Denacol EX-611、Denacol EX-612、Denacol EX-614、Denacol EX-622、Denacol EX-810、Denacol EX-811、Denacol EX-850、Denacol EX-851、Denacol EX-821、Denacol EX-830、Denacol EX-832、Denacol EX-841、Denacol EX-861、Denacol EX-911、Denacol EX-941、Denacol EX-920、Denacol EX-931(nagase chemtex(股)公司製);EpoliteM-1230、Epolite40E、Epolite100E、Epolite200E、Epolite400E、Epolite70P、Epolite200P、Epolite400P、Epolite1500NP、Epolite1600、Epolite80MF、Epolite100MF(共榮社化學(股)公司
製)、ADEKA GLYCIROLED-503、ADEKA GLYCIROLED-503G、ADEKA GLYCIROLED-506、ADEKA GLYCIROLED-523T、ADEKA Resin-4088S、ADEKA Resin-4080E((股)ADEKA公司製)等。
上述氧雜環丁烷化合物(A2)可列舉3,7-雙(3-氧環丁基)-5-氧雜-壬烷、1,4-雙[(3-乙基-3-氧環丁基甲氧基)甲基]苯、1,2-雙[(3-乙基-3-氧環丁基甲氧基)甲基]乙烷、1,3-雙[(3-乙基-3-氧環丁基甲氧基)甲基]丙烷、乙二醇雙(3-乙基-3-氧環丁基甲基)醚、三乙二醇雙(3-乙基-3-氧環丁基甲基)醚、四乙二醇雙(3-乙基-3-氧環丁基甲基)醚、1,4-雙(3-乙基-3-氧環丁基甲氧基)丁烷、1,6-雙(3-乙基-3-氧環丁基甲氧基)己烷等之二官能脂肪族氧雜環丁烷化合物、3-乙基-3-[(苯氧基)甲基]氧雜環丁烷、3-乙基-3-(己氧基甲基)氧雜環丁烷、3-乙基-3-(2-乙基己氧基甲基)氧雜環丁烷、3-乙基-3-(羥基甲基)氧雜環丁烷、3-乙基-3-(氯甲基)氧雜環丁烷等之一官能氧雜環丁烷化合物等。此等可1種單獨使用或組合2種以上使用。特別是多官能氧雜環丁烷化合物,提高硬化物之硬化性及密著性,故較佳。
上述氧雜環丁烷化合物(A2)可使用市售品,可列舉例如2-羥基乙基乙烯醚、二乙二醇單乙烯醚、4-羥基丁基乙烯醚(丸善石油化學(股)公司製);ARON OXETANEOXT-121、OXT-221、EXOH、POX、OXA、OXT-101、OXT-211、OXT-212(東亞合成(股)
公司製)、ETERNACOLL OXBP、OXTP(宇部興產(股)公司製)等。
上述芳香族環氧化合物(A3)係指含有芳香環的環氧化合物,而芳香族環氧化合物(A3)之具體例,可列舉酚、甲酚、丁酚等具有至少1個芳香族環的多元酚或其環氧烷加成物之單/聚環氧丙醚化物,可列舉例如雙酚A、雙酚F、或此等再加成有環氧烷之化合物之環氧丙醚化物或環氧基酚醛清漆樹脂;間苯二酚或氫醌、兒茶酚等之具有2個以上之酚性羥基的芳香族化合物之單/聚環氧丙醚化物;苯基二甲醇或苯基二乙醇、苯基二丁醇等之具有2個以上之醇性羥基之芳香族化合物之環氧丙醚化物;鄰苯二甲酸、對苯二甲酸、偏苯三甲酸等之具有2個以上之羧酸的多元酸芳香族化合物之環氧丙酯、苯甲酸之環氧丙酯、苯乙烯氧化物或二乙烯基苯之環氧化物等。
上述芳香族環氧化合物(A3)可使用市售品,可列舉例如Denacol EX-146、Denacol EX-147、Denacol EX-201、Denacol EX-203、Denacol EX-711、Denacol EX-721、Oncoat EX-1020、Oncoat EX-1030、Oncoat EX-1040、Oncoat EX-1050、Oncoat EX-1051、Oncoat EX-1010、Oncoat EX-1011、Oncoat1012(nagase chemtex(股)公司製);OGSOLPG-100、OGSOLEG-200、OGSOLEG-210、OGSOLEG-250(大阪氣體化學(股)公司製);HP4032、HP4032D、HP4700(DIC(股)公司製);ESN-475V(新日鐵住金化學(股)公
司製);EpikoteYX8800(三菱化學(股)公司製);Marproof G-0105SA、Marproof G-0130SP(日油(股)公司製);EPICLONN-665、EPICLONHP-7200(DIC(股)公司製);EOCN-1020、EOCN-102S、EOCN-103S、EOCN-104S、XD-1000、NC-3000、EPPN-501H、EPPN-501HY、EPPN-502H、NC-7000L(日本化藥(股)公司製);ADEKA ResinEP-4000、ADEKA ResinEP-4005、ADEKA ResinEP-4100、ADEKA ResinEP-4901((股)ADEKA公司製);TECHMORE VG-3101L((股)Printec公司製)等。上述芳香族環氧化合物(A3)中,多官能者因硬化性優異,故較佳。
上述脂環式環氧化合物(A4)係指環氧乙烷環不經由鍵結基而直接鍵結於飽和環者。脂環式環氧化合物(A4)之具體例,可列舉藉由將具有至少1個脂環式環之多元醇的聚環氧丙醚化物或含有環己烯或環戊烯環之化合物以氧化劑進行環氧化所得的含有環己烯氧化物或環戊烯氧化物的化合物。可列舉例如3,4-環氧基環己基甲基-3,4-環氧基環己烷羧酸酯、3,4-環氧基-1-甲基環己基-3,4-環氧基-1-甲基己烷羧酸酯、6-甲基-3,4-環氧基環己基甲基-6-甲基-3,4-環氧基環己烷羧酸酯、3,4-環氧基-3-甲基環己基甲基-3,4-環氧基-3-甲基環己烷羧酸酯、3,4-環氧基-5-甲基環己基甲基-3,4-環氧基-5-甲基環己烷羧酸酯、雙(3,4-環氧基環己基甲基)己二酸酯、3,4-環氧基-6-甲基環己烷羧酸酯、亞甲基雙(3,4-環氧基環己烷)、丙烷-
2,2-二基-雙(3,4-環氧基環己烷)、2,2-雙(3,4-環氧基環己基)丙烷、二環戊二烯二環氧化物、伸乙基雙(3,4-環氧基環己烷羧酸酯)、環氧基六氫鄰苯二甲酸二辛酯、環氧基六氫鄰苯二甲酸二-2-乙基己酯、1-環氧基乙基-3,4-環氧基環己烷、1,2-環氧基-2-環氧基乙基環己烷、α-蒎烯氧化物、檸檬烯二氧化物等。脂環式環氧化合物(A4)從提高密著性的觀點,較佳為3,4-環氧基環己基甲基-3,4-環氧基環己烷羧酸酯或3,4-環氧基-1-甲基環己基-3,4-環氧基-1-甲基己烷羧酸酯。
上述脂環式環氧化合物(A4)可使用市售品,可列舉例如CELLOXID 2021P、CELLOXID 2081、CELLOXID 2000、CELLOXID 3000((股)DAICEL公司製)等。
上述乙烯醚化合物,可列舉例如二乙二醇單乙烯醚、三乙二醇二乙烯醚、n-十二烷基乙烯醚、環己基乙烯醚、2-乙基己基乙烯醚、2-氯乙基乙烯醚、乙基乙烯醚、異丁基乙烯醚、三乙二醇乙烯醚、2-羥基乙基乙烯醚、4-羥基丁基乙烯醚、1,6-環己烷二甲醇單乙烯醚、乙二醇二乙烯醚、1,4-丁二醇二乙烯醚、1,6-環己烷二甲醇二乙烯醚等。
上述陽離子聚合性成分(A)中,上述多元醇之環氧丙基化物或多元醇環氧烷加成物之環氧丙基化物(A1)、氧雜環丁烷化合物(A2)、芳香族環氧化合物(A3)、脂環式環氧化合物(A4)及乙烯醚化合物之使
用比例係相對於陽離子聚合性成分(A)與自由基聚合性成分(C)與聚合物(E)之合計為100質量份時,多元醇之環氧丙基化物或多元醇環氧烷加成物之環氧丙基化物(A1)50~90質量份、氧雜環丁烷化合物(A2)10~50質量份、芳香族環氧化合物(A3)0~50質量份、脂環式環氧化合物(A4)0~30質量份、乙烯醚化合物0~20質量份時,可提高黏度、塗佈性、反應性及硬化性,故較佳。
本發明之硬化性組成物的陽離子聚合起始劑(B)係指藉由能量線照射或加熱可釋放使陽離子聚合開始之物質的化合物時,皆可使用,較佳為藉由能量線照射釋放出路易斯酸之鎓鹽的複鹽或其衍生物。此化合物之代表性者,可列舉下述通式、[A]r+[B]r-表示之陽離子與陰離子的鹽。
此處,陽離子[A]r+較佳為鎓類,其構造例如可以下述通式[(R2)aQ]r+表示。
再者,此處,R2係碳原子數為1~60,也可含有幾個碳原子以外之原子的有機基。a為1~5之整數。a個之R2可各自獨立為相同或相異。又,至少1個為具有芳香環之如上述的有機基較佳。Q為選自由S、N、Se、Te、P、As、Sb、Bi、O、I、Br、Cl、F、N=N所成群之原子或
原子團。又,陽離子[A]r+中之Q的原子價為q時,r=a-q之關係(惟,N=N視為原子價0)必須成立。
又,陰離子[B]r-較佳為鹵化物錯合物,其構造例如可以下述通式[LYb]r-表示。
此外,在此,L為鹵化物錯合物之中心原子的金屬或半金屬(Metalloid),其係B、P、As、Sb、Fe、Sn、Bi、Al、Ca、In、Ti、Zn、Sc、V、Cr、Mn、Co等。Y為鹵素原子。b為3~7之整數。又,陰離子[B]r-中之L的原子價當作p時,r=b-p之關係必須成立。
上述通式之陰離子[LYb]r-的具體例,可列舉肆(五氟苯基)硼酸根、四(3,5-二氟-4-甲氧基苯基)硼酸根、四氟硼酸根(BF4)-、六氟磷酸根(PF6)-、六氟銻酸根(SbF6)-、六氟砷酸根(AsF6)-、六氯銻酸根(SbCl6)-等。
又,陰離子[B]r-亦可使用下述通式[LYb-1(OH)]r-表示之構造者。L、Y、b係與上述相同。又,其他可使用之陰離子,可列舉過氯酸離子(ClO4)-、三氟甲基亞硫酸離子(CF3SO3)-、氟磺酸離子(FSO3)-、甲苯磺酸陰離子、三硝基苯磺酸陰離子、樟腦磺酸根、九氟丁烷磺酸根、十六氟辛烷磺酸根、四芳基硼酸根、肆(五氟苯基)硼酸根等。
本發明之硬化性組成物中,如此鎓鹽之中,
以使用下述(甲)~(丙)之芳香族鎓鹽特別有效。可由此等之中以1種單獨使用或混合2種以上使用。
(甲)苯基重氮鎓六氟磷酸鹽、4-甲氧基苯基重氮鎓六氟銻酸鹽、4-甲基苯基重氮鎓六氟磷酸鹽等之芳基重氮鎓鹽
(乙)二苯基錪六氟銻酸鹽、二(4-甲基苯基)錪六氟磷酸鹽、二(4-tert-丁基苯基)錪六氟磷酸鹽、甲苯基異丙苯基錪肆(五氟苯基)硼酸鹽等之二芳基錪鹽
(丙)下述群I或群II表示之鋶陽離子與六氟銻離子、六氟磷酸根離子、肆(五氟苯基)硼酸根離子等之鋶鹽
又,其他較佳者可列舉(η5-2,4-環戊二烯-1-基)[(1,2,3,4,5,6-η)-(1-甲基乙基)苯]-鐵-六氟磷酸鹽等之鐵-芳烴錯合物、或參(乙醯丙酮)鋁、參(乙醯乙酸乙酯)鋁、參(水楊醛)鋁等之鋁錯合物與三苯基矽烷醇等之矽烷醇類的混合物;噻吩鎓鹽、四氫噻吩鐵鹽(thiolanium)、苄基銨、吡啶鎓鹽、鉼鹽(hydrazinium)等之鹽;二乙烯三胺、三乙烯三胺、四乙烯五胺等之聚烷基多胺類;1,2-二胺基環己烷、1,4-二胺基-3,6-二乙基環己烷、異佛爾酮二胺等之脂環式多胺類;m-苯二甲胺、二胺基二苯基甲烷、二胺基二苯基碸等之芳香族多胺類;藉由一般方法使上述多胺類與苯基環氧丙醚、丁基環氧丙醚
、雙酚A-二環氧丙醚、雙酚F-二環氧丙醚等之環氧丙醚類或羧酸之環氧丙酯類等的各種環氧樹脂反應所製造的聚環氧基加成改質物;藉由一般方法使上述有機多胺類與鄰苯二甲酸、間苯二甲酸、二聚酸等之羧酸類反應所製造的醯胺化改質物;藉由一般方法使上述多胺類與甲醛等之醛類及酚、甲酚、二甲酚、第三丁基酚、間苯二酚等之於核具有至少一個醛化反應性場所的酚類反應所製造的曼尼希(Mannich)化改質物;多元羧酸(草酸、丙二酸、琥珀酸、戊二酸、己二酸、庚二酸、辛二酸、壬二酸、癸二酸、十二烷二酸、2-甲基琥珀酸、2-甲基己二酸、3-甲基己二酸、3-甲基戊二酸、2-甲基辛二酸、3,8-二甲基癸二酸、3,7-二甲基癸二酸、氫化二聚酸、二聚酸等之脂肪族二羧酸類;鄰苯二甲酸、對苯二甲酸、間苯二甲酸、萘二羧酸等之芳香族二羧酸類;環己烷二羧酸等之脂環式二羧酸類;偏苯三甲酸、均苯三甲酸(Trimesic Acid)、蓖麻油脂肪酸之三聚物等之三羧酸類;均苯四酸等之四羧酸類等)之酸酐;雙氰胺、咪唑類、羧酸酯、磺酸酯、胺醯亞胺等。
此等之中,就實用面與提高光感度的觀點,使用芳香族錪鹽、芳香族鋶鹽、鐵-芳烴錯合物為佳;相對於陽離子聚合起始劑(B)100質量%,又更佳為含有至少0.1質量%以上之具有下述構造之芳香族鋶鹽。
此處,式中,R11、R12、R13、R14、R15、R16、R17、R18、R19及R20各自獨立地表示氫原子、鹵素原子、碳原子數1~10之烷基、碳原子數1~10之烷氧基或碳原子數2~10之酯基,R21、R22、R23及R24各自獨立地表示氫原子、鹵素原子或碳原子數1~10之烷基,R25表示氫原子、鹵素原子、碳原子數1~10之烷基或選自下述化學式(A)~(C)中的任一取代基,Anq-表示q價的陰離子,p表示使電荷為中性的係數。
此處,式中,R11、R12、R13、R14、R15、R16、R17、R18、R19、R20、R21、R22、R23、R24、R26、R27、R28、R29、R35、R36、R37、R38及R39各自獨立地表示氫原子、鹵
素原子、碳原子數1~10之烷基、碳原子數1~10之烷氧基或碳原子數2~10之酯基,R30、R31、R32、R33及R34各自獨立地表示氫原子、鹵素原子或碳原子數1~10之烷基。
上述通式(1)表示之化合物中,R11、R12、R13、R14、R15、R16、R17、R18、R19、R20、R21、R22、R23、R24、R25、R26、R27、R28、R29、R30、R31、R32、R33、R34、R35、R36、R37、R38及R39表示之鹵素原子,可列舉氟、氯、溴、碘等。
R11、R12、R13、R14、R15、R16、R17、R18、R19、R20、R21、R22、R23、R24、R25、R26、R27、R28、R29、R30、R31、R32、R33、R34、R35、R36、R37、R38及R39表示之碳原子數1~10之烷基,可列舉甲基、乙基、丙基、異丙基、丁基、s-丁基、t-丁基、異丁基、戊基、異戊基、t-戊基、己基、環己基、庚基、辛基、壬基、乙基辛基、2-甲氧基乙基、3-甲氧基丙基、4-甲氧基丁基、2-丁氧基乙基、甲氧基乙氧基乙基、甲氧基乙氧基乙氧基乙基、3-甲氧基丁基、2-甲硫基乙基、氟甲基、二氟甲基、三氟甲基、氯甲基、二氯甲基、三氯甲基、溴甲基、二溴甲基、三溴甲基、二氟乙基、三氯乙基、二氯二氟乙基、五氟乙基、七氟丙基、九氟丁基、十氟戊基、十三氟己基、十五氟庚基、十七氟辛基、甲氧基甲基、1,2-環氧基乙基、甲氧基乙基、甲氧基乙氧基甲基、甲硫基甲基、乙氧基乙基、丁氧基甲基、t-丁硫基甲基、4-戊烯氧基甲基、三氯乙氧基甲基、雙(2-氯乙氧基)甲基、甲氧基環
己基、1-(2-氯乙氧基)乙基、1-甲基-1-甲氧基乙基、乙基二硫乙基、三甲基甲矽烷基乙基、t-丁基二甲基甲矽烷氧基甲基、2-(三甲基甲矽烷基)乙氧基甲基、t-丁氧基羰基甲基、乙氧基羰基甲基、乙基羰基甲基、t-丁氧基羰基甲基、丙烯醯氧基乙基、甲基丙烯醯氧基乙基、2-甲基-2-金剛烷氧基羰基甲基、乙醯基乙基、2-甲氧基-1-丙烯基、羥基甲基、2-羥基乙基、1-羥基乙基、2-羥基丙基、3-羥基丙基、3-羥基丁基、4-羥基丁基、1,2-二羥基乙基等。
R11、R12、R13、R14、R15、R16、R17、R18、R19、R20、R21、R22、R23、R24、R26、R27、R28、R29、R35、R36、R37、R38及R39表示之碳原子數1~10之烷氧基,可列舉甲氧基、乙氧基、丙氧基、異丙氧基、丁氧基、s-丁氧基、t-丁氧基、異丁氧基、戊氧基、異戊氧基、t-戊氧基、己氧基、環己氧基、環己基甲氧基、四氫呋喃氧基、四氫吡喃氧基、2-甲氧基乙氧基、3-甲氧基丙氧基、4-甲氧基丁氧基、2-丁氧基乙氧基、甲氧基乙氧基乙氧基、甲氧基乙氧基乙氧基乙氧基、3-甲氧基丁氧基、2-甲硫基乙氧基、三氟甲氧基等。
R11、R12、R13、R14、R15、R16、R17、R18、R19、R20、R21、R22、R23、R24、R26、R27、R28、R29、R35、R36、R37、R38及R39表示之碳原子數2~10之酯基,可列舉甲氧基羰基、乙氧基羰基、異丙氧基羰基、苯氧基羰基、乙醯氧基、丙醯氧基、丁醯氧基、氯乙醯氧基、二氯
乙醯氧基、三氯乙醯氧基、三氟乙醯氧基、t-丁基羰氧基、甲氧基乙醯氧基、苯甲醯氧基等。
本發明之硬化性組成物的自由基聚合性成分(C)係以具有環氧基及乙烯性不飽和基之化合物(C1)或碳原子數2~20之醇的丙烯酸酯或碳原子數2~20之醇的甲基丙烯酸酯(C2)為必須成分。
上述具有環氧基及乙烯性不飽和基的化合物(C1),可列舉例如環氧基丙烯酸酯或環氧基甲基丙烯酸酯,具體而言,使以往公知之芳香族環氧樹脂、脂環式環氧樹脂、脂肪族環氧樹脂等與丙烯酸或甲基丙烯酸反應所得的丙烯酸酯。此等之環氧基丙烯酸酯或環氧基甲基丙烯酸酯之中,特佳為醇類之環氧丙醚的丙烯酸酯或甲基丙烯酸酯。
上述碳原子數2~20之醇的丙烯酸酯或碳原子數2~20之醇的甲基丙烯酸酯(C2),可列舉使分子中具有至少1個羥基的芳香族或脂肪族醇及其環氧烷加成物與丙烯酸或甲基丙烯酸反應所得的丙烯酸酯或甲基丙烯酸酯。具體而言,可列舉2-乙基己基丙烯酸酯、2-羥基乙基丙烯酸酯、2-羥基丙基丙烯酸酯、異戊基丙烯酸酯、月桂基丙烯酸酯、十八烷基丙烯酸酯、異辛基丙烯酸酯、四氫糠基丙烯酸酯、異莰基丙烯酸酯、苄基丙烯酸酯、1,3-丁二醇二丙烯酸酯、1,4-丁二醇二丙烯酸酯、1,6-己二醇二丙烯酸酯、二乙二醇二丙烯酸酯、三乙二醇二丙烯酸酯、新戊二醇二丙烯酸酯、聚乙二醇二丙烯酸酯、聚丙二醇二丙烯
酸酯、三羥甲基丙烷三丙烯酸酯、季戊四醇四丙烯酸酯、二季戊四醇六丙烯酸酯、ε-己內酯改質二季戊四醇六丙烯酸酯、2-乙基己基甲基丙烯酸酯、2-羥基乙基甲基丙烯酸酯、2-羥基丙基甲基丙烯酸酯、異戊基甲基丙烯酸酯、月桂基甲基丙烯酸酯、十八烷基甲基丙烯酸酯、異辛基甲基丙烯酸酯、四氫糠基甲基丙烯酸酯、異莰基甲基丙烯酸酯、苄基甲基丙烯酸酯、1,3-丁二醇二甲基丙烯酸酯、1,4-丁二醇二甲基丙烯酸酯、1,6-己二醇二甲基丙烯酸酯、二乙二醇二甲基丙烯酸酯、三乙二醇二甲基丙烯酸酯、新戊二醇二甲基丙烯酸酯、聚乙二醇二甲基丙烯酸酯、聚丙二醇二甲基丙烯酸酯、三羥甲基丙烷三甲基丙烯酸酯、季戊四醇四甲基丙烯酸酯、二季戊四醇六甲基丙烯酸酯、ε-己內酯改質二季戊四醇六甲基丙烯酸酯等。又,此等之丙烯酸酯或甲基丙烯酸酯之中,特佳為多元醇之聚丙烯酸酯類或多元醇之聚甲基丙烯酸酯類。
上述自由基聚合性成分(C)可使用(C1)或(C2)以外,藉由以能量線照射或加熱活性化之自由基聚合起始劑,進行高分子化或交聯反應的化合物,可列舉例如烯丙基胺基甲酸酯化合物、不飽和聚酯化合物、苯乙烯系化合物等。自由基聚合性成分(C)中之上述(C1)成分及(C2)成分的比例,較佳為50質量%以上。
本發明之硬化性組成物的自由基起始劑(D)無特別限制,可使用習知者。可使用例如苯乙酮系化合物、苄基系化合物、二苯甲酮系化合物、噻噸酮系化合物
等之酮系化合物、肟系化合物等。
本發明之硬化性組成物的聚合物(E)係選自由上述式(I)表示之單體所得之聚合物、由上述式(II)表示之單體所得之聚合物、選自上述式(I)表示之單體之二種以上之單體所得之聚合物、選自上述式(II)表示之單體之二種以上之單體所得之聚合物及由上述式(I)表示之單體及上述式(II)表示之單體所得之聚合物所成群,且重量平均分子量以聚苯乙烯換算為1,000~30,000。
上述式(I)中之X表示之碳原子數1~7之烷基,可列舉甲基、乙基、丙基、iso-丙基、丁基、sec-丁基、tert-丁基、iso-丁基、戊基、iso-戊基、tert-戊基、己基、2-己基、3-己基、環己基、4-甲基環己基、庚基、2-庚基、3-庚基、iso-庚基、tert-庚基等。此等之中,從硬化性的觀點,碳原子數1~4之烷基或以選自由環氧基、氧雜環丁烷基、羥基及羧基所成群之1種以上之基進行部分取代之碳原子數1~4之烷基為佳。
上述式(I)中之X表示之碳原子數1~7之烷氧基,可列舉甲氧基、乙氧基、丙氧基、iso-丙氧基、丁氧基、sec-丁氧基、tert-丁氧基、iso-丁氧基、戊氧基、iso-戊氧基、tert-戊氧基、己氧基、2-己氧基、3-己氧基、環己氧基、4-甲基環己氧基、庚氧基、2-庚氧基、3-庚氧基、iso-庚氧基、tert-庚氧基等。此等之中,從硬化性的觀點,碳原子數1~4之烷氧基或以選自由環氧基、氧雜環丁烷基、羥基及羧基所成群之1種以上之基進行部分取代
之碳原子數1~4之烷氧基為佳。
上述式(I)中之X表示之碳原子數6~12之芳基,可列舉苯基、甲基苯基、萘基等。
上述式(I)中之X表示之碳原子數6~12之芳氧基,可列舉苯氧基、甲基苯氧基、萘氧基等。
上述式(I)中之X表示之碳原子數6~10之脂環式烴基,可列舉環己基、甲基環己基、降莰基、雙環戊基、雙環辛基、三甲基雙環庚基、三環辛基、三環癸基、螺辛基、螺雙環戊基、金剛烷基、異莰基等。
此等之烷基、烷氧基、芳基、芳氧基及脂環式烴基,可為此等之基中的氫原子經選自由環氧基、氧雜環丁烷基、羥基及羧基所成群之1種以上之基所取代。
上述式(I)中,X之一部分為經環氧基或氧雜環丁烷基取代時之式(I)表示的單體,可列舉例如下述式(1)~(3)表示之單體。
在此,式(1)中,R3表示氫原子或碳原子數1~6之烷基,m為1~6之整數。
在此,式(2)中,R4表示氫原子或碳原子數1~6之烷基,n為1~6之整數。
在此,式(3)中,R5表示氫原子或碳原子數1~6之烷基,s為1~6之整數。
上述式(II)中,以R1所表示的鹵原子,可列舉氟、氯、溴、碘等。
上述式(II)中,X’之碳原子數1~7之烷基、碳原子數6~12之芳基或碳原子數6~10之脂環式烴基,可列舉與上述式(I)同樣者。
上述式(II)中,X’之一部分經環氧基或氧雜環丁烷基取代時,作為式(II)所表示之單體,可列舉下述式(4)~(6)所表示者。
在此,式(4)中,R1係與上述式(II)相同,R6表示氫原子或碳原子數1~6之烷基,t為1~6之整數。
在此,式(5)中,R1係與上述式(II)相同,R7表示氫原子或碳原子數1~6之烷基,q為1~6之整數。
在此,式(6)中,R1係與上述式(II)相同,R8表示氫原子或碳原子數1~6之烷基,y為1~6之整數。
上述聚合物(E)中,構成聚合物之單體的使用比例係上述X為經選自由環氧基、環雜環丁烷基、羥基及羧基所成群之1種以上之基取代之碳原子數1~7之烷基、碳原子數6~12之芳基或碳原子數6~10之脂環式烴基時,使上述(I)或(II)表示之單體成為10~100質量%來使用,由於接著性提高,故較佳。
本發明之硬化性組成物中,上述陽離子聚合性成分(A)係15~90質量份,較佳為50~80質量份,上述陽離子聚合起始劑(B)為1~10質量份,較佳為1~6質量份,上述自由基聚合性成分(C)為10~50質量份,較佳為10~20質量份,上述自由基聚合起始劑(D)為1~10質量份,較佳為1~5質量份,上述聚合物(E)為1~20質量份,
較佳為5~15質量份。上述調配比例以外時,硬化物之硬化性及密著性有變差的疑慮。又,陽離子聚合性成分(A)與自由基聚合性成分(C)與聚合物(E)之合計為100質量份。
本發明之硬化性組成物中,可依需要進一步使用增感劑及/或增感助劑。增感劑係於較陽離子聚合起始劑(B)所顯示之極大吸收波長更長的波長顯示極大吸收,促進藉由陽離子聚合起始劑(B)之聚合起始反應的化合物。又,增感助劑係更進一步促進增感劑之作用的化合物。
增感劑及增感助劑可列舉蒽系化合物、萘系化合物等。
蒽系化合物可列舉例如下述式(7)表示者。
此處,式(7)中,R50及R51各自獨立地表示氫原子、碳原子數1~6之烷基或碳原子數2~12之烷氧基烷基,R52表示氫原子或碳原子數1~6之烷基。
列舉上述式(7)表示之蒽系化合物之具體例時,有如以下的化合物。
可列舉例如9,10-二甲氧基蒽、9,10-二乙氧基蒽、9,10-二丙氧基蒽、9,10-二異丙氧基蒽、9,10-二丁氧
基蒽、9,10-二戊氧基蒽、9,10-二己氧基蒽、9,10-雙(2-甲氧基乙氧基)蒽、9,10-雙(2-乙氧基乙氧基)蒽、9,10-雙(2-丁氧基乙氧基)蒽、9,10-雙(3-丁氧基丙氧基)蒽、2-甲基-或2-乙基-9,10-二甲氧基蒽、2-甲基-或2-乙基-9,10-二乙氧基蒽、2-甲基-或2-乙基-9,10-二丙氧基蒽、2-甲基-或2-乙基-9,10-二異丙氧基蒽、2-甲基-或2-乙基-9,10-二丁氧基蒽、2-甲基-或2-乙基-9,10-二戊氧基蒽、2-甲基-或2-乙基-9,10-二己氧基蒽等。
萘系化合物可列舉例如下述式(8)表示者。
此處,式(8)中,R53及R54各自獨立地表示碳原子數1~6之烷基。
列舉上述式(8)表示之萘系化合物之具體例時,有如以下的化合物。
可列舉例如4-甲氧基-1-萘酚、4-乙氧基-1-萘酚、4-丙氧基-1-萘酚、4-丁氧基-1-萘酚、4-己氧基-1-萘酚、1,4-二甲氧基萘、1-乙氧基-4-甲氧基萘、1,4-二乙氧基萘、1,4-二丙氧基萘、1,4-二丁氧基萘等。
相對於上述陽離子聚合性成分(A)而言,增感劑及增感助劑之使用比例無特別限定,只要在不阻礙本發明之目的的範圍內,大致以通常使用比例使用即可,例
如相對於上述陽離子聚合性成分(A)100質量份,由提高硬化性的觀點,增感劑及增感助劑各自為0.1~3質量份為佳。
本發明之硬化性組成物中,可依需要使用矽烷偶合劑。矽烷偶合劑可使用例如二甲基二甲氧基矽烷、二甲基二乙氧基矽烷、甲基乙基二甲氧基矽烷、甲基乙基二乙氧基矽烷、甲基三甲氧基矽烷、甲基三乙氧基矽烷、乙基三甲氧基矽烷、乙基三甲氧基矽烷等之烷基官能性烷氧基矽烷、乙烯基三氯矽烷、乙烯基三甲氧基矽烷、乙烯基三乙氧基矽烷、烯丙基三甲氧基矽烷等之烯基官能性烷氧基矽烷、3-甲基丙烯醯氧基丙基三乙氧基矽烷、3-甲基丙烯醯氧基丙基三甲氧基矽烷、3-甲基丙烯醯氧基丙基甲基二乙氧基矽烷、3-甲基丙烯醯氧基丙基甲基二甲氧基矽烷、2-甲基丙烯醯氧基丙基三甲氧基矽烷、γ-環氧丙氧基丙基三甲氧基矽烷、γ-環氧丙氧基丙基甲基二乙氧基矽烷、β-(3,4-環氧基環己基)乙基三甲氧基矽烷等之環氧基官能性烷氧基矽烷、N-β(胺基乙基)-γ-胺基丙基三甲氧基矽烷、γ-胺基丙基三乙氧基矽烷、N-苯基-γ-胺基丙基三甲氧基矽烷等之胺基官能性烷氧基矽烷、γ-巰基丙基三甲氧基矽烷等之巰基官能性烷氧基矽烷、四異丙烷氧化鈦、四正丁烷氧化鈦等之鈦烷氧化物類、鈦二辛氧基雙(伸辛基甘醇酸鹽)、鈦二異丙氧基雙(乙基乙醯乙酸鹽)等之鈦螯合物類、四乙醯丙酮鋯、三丁氧基單乙醯丙酮鋯等之鋯螯合物類、三丁氧基單硬脂酸鋯等之鋯醯化物
類類、甲基三異氰酸酯矽烷等之異氰酸酯矽烷類等。
上述矽烷偶合劑之使用量並無特別限定,通常,相對於硬化性組成物中之固形物全部量100質量份,為0.01~20質量份的範圍。
於本發明之硬化性組成物,依需要藉由使用熱可塑性有機聚合物,亦可改善硬化物的特性。熱可塑性有機聚合物,可列舉例如聚苯乙烯、聚甲基丙烯酸甲酯、甲基丙烯酸甲酯丙烯酸乙酯共聚物、甲基丙烯酸甲酯甲基丙烯酸環氧丙酯共聚物、聚(甲基)丙烯酸、苯乙烯-(甲基)丙烯酸共聚物、(甲基)丙烯酸-甲基丙烯酸甲酯共聚物、(甲基)丙烯酸環氧丙酯-聚甲基(甲基)丙烯酸酯共聚物、聚乙烯基縮丁醛、纖維素酯、聚丙烯醯胺、飽和聚酯等。
本發明之硬化性組成物中,亦可依需要進一步使用紫外線吸收劑、或於常溫為不活性,且因加熱至特定溫度/光照射/酸等會使保護基脫離而活性化,展現紫外線吸收能力的化合物。
又,只要不損及本發明之效果時,可依需要添加多元醇、無機填料、有機填料、顏料、染料等之著色劑、消泡劑、增黏劑、界面活性劑、平坦劑、難燃劑、觸變劑、稀釋劑、可塑劑、安定劑、聚合抑制劑、紫外線吸收劑、抗氧化劑、抗靜電劑、流動調整劑、接著促進劑等之各種樹脂添加物等。
本發明之硬化性組成物中,無特別限定,可
使用通常所用之可溶解或分散上述(A)、(B)、(C)、(D)及(E)之各成分的溶劑。溶劑可列舉例如甲基乙基酮、甲基戊基酮、二乙基酮、丙酮、甲基異丙基酮、甲基異丁基酮、環己酮、2-庚酮等之酮類;乙醚、二噁烷、四氫呋喃、1,2-二甲氧基乙烷、1,2-二乙氧基乙烷、丙二醇單甲醚、二丙二醇二甲醚等之醚系溶劑;乙酸甲酯、乙酸乙酯、乙酸-n-丙酯、乙酸異丙酯、乙酸n-丁酯、乙酸環己酯、乳酸乙酯、琥珀酸二甲酯、2,2,4-三甲基-1,3-戊二醇異丁酸(Texanol)等之酯系溶劑;乙二醇單甲醚、乙二醇單乙醚等之溶纖劑系溶劑;甲醇、乙醇、異-或n-丙醇、異-或n-丁醇、戊醇等之醇系溶劑;乙二醇單甲基乙酸酯、乙二醇單乙基乙酸酯、丙二醇-1-單甲醚-2-乙酸酯(PGMEA)、二丙二醇單甲醚乙酸酯、3-甲氧基丁基乙酸酯、乙氧基乙基丙酸酯等之醚酯系溶劑;苯、甲苯、二甲苯等之BTX系溶劑;己烷、庚烷、辛烷、環己烷等之脂肪族烴系溶劑;松節油、D-檸檬烯、蒎烯等之萜烯系烴油;礦油精、Swasol#310(Cosmo松山石油(股)公司製)、Solvesso#100(Exxon化學社)等之鏈烷烴系溶劑;四氯化碳、氯仿、三氯乙烯、二氯甲烷、1,2-二氯乙烷等之鹵化脂肪族烴系溶劑;氯苯等之鹵化芳香族烴系溶劑;碳酸丙烯酯、卡必醇系溶劑、苯胺、三乙基胺、吡啶、乙酸、乙腈、二硫化碳、N,N-二甲基甲醯胺、N,N-二甲基乙醯胺、N-甲基吡咯烷酮、二甲基亞碸、水等。此等溶劑可使用1種或以2種以上之混合溶劑使用。
本發明之硬化性組成物會提高硬化性、接著性、液體保存安定性,故水分量為5質量份以下較佳,又更佳為3質量份以下。水分過多時,有產生白濁或成分析出之疑慮,故不佳。
本發明之硬化性組成物以輥塗佈器、淋幕式塗佈器、各種之印刷、浸漬等之公知手段適用於支撐基體上。又,也可一旦施於薄膜等之支撐基體上後,轉印於其他支撐基體上,其適用方法並無限制。
上述支撐基體之材料,無特別限制,可使用通常所使用者,可列舉例如玻璃等之無機材料;二乙醯基纖維素、三乙醯基纖維素(TAC)、丙醯基纖維素、丁醯基纖維素、乙醯基丙醯基纖維素、硝基纖維素等之纖維素酯;聚醯胺;聚醯亞胺;聚胺基甲酸酯;環氧樹脂;聚碳酸酯;聚對苯二甲酸乙二酯、聚萘二甲酸乙二酯、聚對苯二甲酸丁二酯、聚-1,4-環己烷二亞甲基聚對苯二甲酸酯、聚乙烯-1,2-二苯氧基乙烷-4,4’-二羧酸酯、聚對苯二甲酸丁二酯等之聚酯;聚苯乙烯;聚乙烯、聚丙烯、聚甲基戊烯等之聚烯烴;聚乙酸乙烯酯、聚氯乙烯、聚氟乙烯等之乙烯基化合物;聚甲基丙烯酸甲酯、聚丙烯酸酯等之丙烯酸系樹脂;聚碳酸酯;聚碸;聚醚碸;聚醚酮;聚醚醯亞胺;聚氧乙烯、降莰烯樹脂、環烯烴聚合物(COP)等之高分子材料。又,亦可對上述支撐基體進行電暈放電處理、火焰處理、紫外線處理、高頻處理、輝光放電處理、活性電漿處理、雷射處理等之表面活性化處理。
藉由能量線照射本發明之硬化性組成物使硬化的方法中,能量線可列舉紫外線、電子線、X射線、放射線、高頻等,紫外線在經濟上最佳。紫外線之光源,可列舉紫外線雷射、水銀燈、氙雷射、金屬鹵素燈等。
藉由加熱使本發明之硬化性組成物硬化的方法的條件為70~250℃、1~100分鐘。可於預烤(PAB;Pre applied bake)後加壓進行後烘烤(PEB;Post exposure bake);亦可以不同的數階段的溫度烘烤。加熱條件雖依各成分之種類及摻合比例而異,但例如70~180℃下,烘箱為5~15分鐘,加熱板則為1~5分鐘。然後,為了使塗膜硬化,藉由於180~250℃,較佳為200~250℃,烘箱為30~90分鐘,加熱板則為5~30分鐘進行加熱處理,可得到硬化膜。
本發明之硬化性組成物或其硬化物之具體的用途,可列舉接著劑、眼鏡、以攝影用透鏡為代表之光學材料、塗料、塗覆劑、襯墊(lining)劑、油墨、阻劑、液狀阻劑、印刷版、彩色電視、PC監視器、行動資訊終端、數位相機、有機EL、觸控面板等之顯示元件、絕緣清漆、絕緣薄片、層合板、印刷基板、半導體裝置用/LED封裝用/液晶注入口用/有機EL用/光元件用/電絕緣用/電子零件用/分離膜用等之封裝劑、成形材料、油灰、玻璃纖維含浸劑、木粉填料、半導體用/太陽電池用等之鈍化膜、層間絕緣膜、保護膜、液晶顯示裝置之背光所使用之稜鏡透鏡薄片、投影電視等之螢幕所使用之菲涅耳透鏡薄片、
雙凸透鏡薄片等之透鏡薄片之透鏡部、或使用這種薄片之背光等、微透鏡等之光學透鏡、光學元件、光連接器、光波導、光學造形用鑄型劑等。
本發明之顯示裝置可列舉於透明支撐體上依需要設置有底塗層、抗反射層、偏光元件層、相位差層、雙折射率層、光散射層、硬質塗層、潤滑層、保護層等之各層者,於各層可使用由本發明之硬化物所成的薄膜。
以下列舉實施例等更詳細說明本發明,但本發明不限定於此等實施例。
以下述[表1]~[表6]所示之調配,將各成分充分地混合,得到各實施例1~19之硬化性組成物及比較例1~8之硬化性組成物。又,實施例及比較例之單位為質量份。
陽離子聚合性成分(A)係使用下述化合物。
化合物(A1-1):新戊二醇二環氧丙醚
化合物(A1-2):1,4-丁二醇二環氧丙醚
化合物(A2-1):ARON OXETANEOXT-221(東亞合成(股)公司製)
化合物(A3-1):雙酚型二環氧丙醚
化合物(A3-2):TECHMORE VG3101(芳香族3官
能環氧樹脂:(股)Printec公司製)
陽離子聚合起始劑(B)為使用下述化合物(B-1)。
化合物(B-1):下述式(9)表示之化合物及下述式(10)表示之化合物之混合物的碳酸丙烯酯50%溶液
自由基聚合性成分(C)為使用下述化合物。
化合物(C1-1):環氧基酯M-600A(共榮社化學(股)公司製)
化合物(C1-2):環氧基酯70PA(共榮社化學(股)公司製)
化合物(C2-1):1,6-己二醇二丙烯酸酯
自由基聚合起始劑(D)為使用下述化合物(D-1)。
化合物(D-1):IRGACURE184(BASF公司製)
聚合物(E)為使用下述化合物(E-1)及(E-2)。
聚合物(E-1):甲基丙烯酸甲酯75質量份與環氧丙基甲基丙烯酸酯25之共聚物(重量平均分子量7,000)
聚合物(E’)為使用下述化合物(E’-1)及(E’-2)。
化合物(E’-1):甲基丙烯酸甲酯75質量份與環氧丙基甲基丙烯酸酯25之共聚物(重量平均分子量800)
化合物(E’-2):甲基丙烯酸甲酯75質量份與環氧丙基甲基丙烯酸酯25之共聚物(重量平均分子量35,000)
對於所得之實施例1~19及比較例1~8之各硬化性組成物,依據下述步驟評價玻璃轉移溫度(Tg)、彈性模數及密著性之評價。結果併記於[表1]~[表6]。
將所得之實施例1~19及比較例1~8之各硬化性組成物分別以塗佈棒塗佈於聚對苯二甲酸乙二酯(PET)薄膜上形成30μm的厚度,使用金屬鹵素燈照射3000mJ/cm2之能量。24小時後,自薄膜取出接著劑硬化物,使用(股)Hitachi High-Tech Science製之黏彈性測量裝置(DMA7100),測量Tg及80℃下的彈性模數。
對於所得之實施例1~19及比較例1~8之硬化性組成物
分別以E型黏度計測量25℃下的黏度。
將上述所得之實施例1~19及比較例1~8之硬化性組成物,各自塗佈於一片經電暈處理PMMA薄膜(住友化學(股)公司製:Technolloy 125S001)後,使用層合機與另一片經電暈放電處理的COP(環烯烴聚合物、日本Zeon(股)公司製:型號Zeonor Film 14-060)薄膜貼合,使用無電極紫外光燈透過COP薄膜照射相當於1000mJ/cm2之光進行接著,以得到試驗片。對於所得之試驗片進行90度剝離試驗。
由[表1]~[表6]得知本發明之硬化性組成物係硬化物之玻璃轉移溫度高及密著性優異。
Claims (7)
- 一種硬化性組成物,其係含有:陽離子聚合性成分(A)15~90質量份、陽離子聚合起始劑(B)1~10質量份、自由基聚合性成分(C)10~50質量份、自由基聚合起始劑(D)1~10質量份及選自由下述式(I)
- 如請求項1之硬化性組成物,其中前述陽離子聚合性成分(A)進一步含有芳香族環氧化合物(A3)。
- 如請求項2之硬化性組成物,其中前述芳香族環氧化合物(A3)為多官能芳香族環氧化合物。
- 如請求項1之硬化性組成物,其中前述聚合物(E)為由前述式(I)表示之單體及前述式(II)表示之單體所得 的聚合物,前述式(I)中之X為碳原子數6~12之芳基,前述式(II)中之X’為碳原子數1~7之烷基,前述烷基經環氧基所取代。
- 一種硬化性組成物之硬化方法,其係將活性能量線照射於如請求項1~4中任一項之硬化性組成物。
- 一種硬化性組成物之硬化方法,其係將如請求項1~4中任一項之硬化性組成物進行加熱。
- 一種硬化物,其係如請求項1~4中任一項之硬化性組成物的硬化物。
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JP4667145B2 (ja) * | 2004-07-22 | 2011-04-06 | 三井化学株式会社 | 光硬化型樹脂組成物及びそれからなるプラスチック用樹脂組成物 |
JP5296575B2 (ja) * | 2009-03-06 | 2013-09-25 | 住友化学株式会社 | 光硬化性接着剤組成物、偏光板とその製造法、光学部材及び液晶表示装置 |
JP5240380B1 (ja) * | 2011-07-05 | 2013-07-17 | Jsr株式会社 | 樹脂組成物、重合体、硬化膜および電子部品 |
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JP6164609B2 (ja) | 2013-08-23 | 2017-07-19 | 東亞合成株式会社 | 光硬化性接着剤組成物、偏光板とその製造法、光学部材及び液晶表示装置 |
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WO2015068454A1 (ja) * | 2013-11-07 | 2015-05-14 | 積水化学工業株式会社 | 有機エレクトロルミネッセンス表示素子用封止剤 |
KR101719883B1 (ko) * | 2013-12-25 | 2017-03-24 | 도아고세이가부시키가이샤 | 광 경화성 접착제 조성물, 편광판과 그 제조법, 광학 부재 및 액정 표시 장치 |
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JP6222637B2 (ja) * | 2014-03-19 | 2017-11-01 | 富士フイルム株式会社 | 重合性非線形光学材料、非線形光学膜、光学素子、光変調素子、及び非線形光学膜の製造方法 |
JP6292400B2 (ja) * | 2014-06-06 | 2018-03-14 | 東亞合成株式会社 | プラスチック製フィルム又はシート用活性エネルギー線硬化型接着剤組成物 |
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CN118185235A (zh) | 2024-06-14 |
KR20180132724A (ko) | 2018-12-12 |
WO2017170883A1 (ja) | 2017-10-05 |
TWI788285B (zh) | 2023-01-01 |
CN108884299A (zh) | 2018-11-23 |
KR102356381B1 (ko) | 2022-01-26 |
JP6993766B2 (ja) | 2022-01-14 |
JP2017179163A (ja) | 2017-10-05 |
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