TW201410814A - 高折射層塗敷用組合物及包含該高折射層塗敷用組合物的透明導電膜 - Google Patents
高折射層塗敷用組合物及包含該高折射層塗敷用組合物的透明導電膜 Download PDFInfo
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- TW201410814A TW201410814A TW102125711A TW102125711A TW201410814A TW 201410814 A TW201410814 A TW 201410814A TW 102125711 A TW102125711 A TW 102125711A TW 102125711 A TW102125711 A TW 102125711A TW 201410814 A TW201410814 A TW 201410814A
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- high refractive
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- transparent conductive
- conductive film
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- C08K2003/2241—Titanium dioxide
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Abstract
本發明提供一種包含丙烯酸酯樹脂、芴衍生物樹脂及金屬氧化物粒子的高折射層塗敷用組合物。並且,提供一種包括利用上述高折射層塗敷用組合物形成的高折射層的透明導電膜。
Description
本發明涉及一種高折射層塗敷用組合物及包含該高折射層塗敷用組合物的透明導電膜。
根據檢測位置的方法,觸控面板有光學方式、超聲波方式、靜電容量方式、電阻膜方式等。電阻膜方式的觸控面板的結構為,透明導電膜和附著有透明導電體層的玻璃夾著隔片,相對配置,並向透明導電膜輸電,來計測附著有透明導電體層的玻璃的電壓。另一方面,靜電容量方式的觸控面板以在基材上具有透明導電層為基本結構,以沒有運轉部分為特徵,由於具有高耐久性、高透射率,因此適用於車載用途等。
適用於上述觸控面板的透明導電膜,一般是在透明的膜基材的一面,依次形成從上述膜基材一側到底漆層及導電層,日本專利公開公報第2003-197035號公開了基材膜和導電層之間形成有底漆層的透明導電膜。
但是,上述底漆層是由折射率不同的2個層形成,並且只公開了在基材膜一側配置厚度為600Å的高折射率的氧化鋅-氧化錫類膜且在導電層一側配置厚度為450Å的低折射率的氧化矽膜的結構,未對高折射層
的具體塗敷用組合物進行記載,因此,對用於同時確保高折射率的調節及耐久性的高折射塗敷用組合物的研究還在繼續。
本發明的一實施例提供一種,包含芴(fluorene)衍生物樹脂,從而可以確保高折射率的同時,還可以維持透明導電膜的物理性質的高折射塗敷用組合物。
本發明的再一實施例提供一種,由於容易調節光學特性,從而減少圖案能見度,確保硬度等物理性質的透射率優秀的透明導電膜。
本發明的一實施例提供一種高折射層塗敷用組合物,其包含丙烯酸酯(acrylate)樹脂、芴(fluorene)衍生物樹脂及金屬氧化物粒子。
相對於100重量份的總固體量,可包含約1重量份至約50重量份的上述丙烯酸酯樹脂、約1重量份至約50重量份的上述芴衍生物樹脂以及約5重量份至約80重量份的上述金屬氧化物粒子。
在本發明的一實施例中,該芴衍生物樹脂可以是選自包含芴(fluorene)、芴酮(fluorenone)、2-乙醯胺基芴(2-acetamide fluorene)、2-芴基甲基酮(2-acetyl fluorene)、2-乙醯氨基芴(2-acetamino fluorene)、9-溴-9-苯基芴(9-bromo-9-penylfluorene)、2,7-二氨基芴(2,7-diaminofluorene)、2,7-二(乙醯胺基)芴(2,7-di(acetamide)fluorene),2,7-二乙醯基芴(2,7-diacetylfluorene)、9,9-雙[4-(2-羥乙氧基)苯基]芴(9,9-bis[4-(2-hydroxyethoxy)penyl]fluorene)、9,9-雙(3,4-二羧苯基)芴酐(9,9bis(3,4dicarboxypenyl)fluorene anhydride)、9,9-雙(3-甲基-4-羥苯基)芴(9,9-bis(3-metyl-4-hydroxypenyl)
fluorene)、9,9-雙(4-羥苯基)芴(9,9-bis(4-hydroxypenyl)fluorene)、9,9-雙(4-氨基苯基)芴(9,9-bis(4-aminopenyl)fluorene)、9,9-雙(4-羥基-3-甲基苯基)芴(9,9-bis(4-hydroxy-3-metylpenyl)fluorene)、9,9-雙[4-(2-丙烯醯基乙氧基)苯基]芴(9,9-bis[4-(2-acryloyloxyethoxy)]penyl]fluorene)、9,9-雙[4-(2-羥基-3-丙烯醯基丙氧基)苯基]芴(9,9-bis[4-(2-hydroxy-3-acryloyloxypropoxy)penyl]fluorene)、9,9-雙(4-羥基苯基)芴(9,9-bis(4-hydroxypenyl)fluorene)、2-丙烯酸1,1'[9H-芴-9-亞基雙[4,1-奔氧(2-羥基-3,1-丙烷基)]]酯(2-propenoic acid 1,1’[9H-fluorene-9-ylidenebis[4,1-penylenoxy(2-hydroxy-3,1-propantyl)]]ester)以及它們的組合的群組中的其中一種。
在本發明的一實施例中,該金屬化合物粒子可以是選自包含二氧化鈦(TiO2)、氧化鋯(ZrO2)、氧化鋁(Al2O3)、二氧化錫(SnO2)、氧化銦錫(ITO,indium-tin oxide),氧化銻錫(ATO,antimon-tin oxide)、五氧化二銻(Sb2O5)、三氧化二鈮(Nb2O3)、三氧化二釔(Y2O3)、二氧化矽(SiO2)以及它們的組合的群組中的其中一種。
在本發明的一實施例中,該金屬化合物粒子的平均粒徑可以是約1奈米(nm)至約100奈米(nm)。
在本發明的一實施例中,該高折射層塗敷用組合物還可包含光引發劑。
在本發明的一實施例中,相對於100重量份的總固體量,可包含約1重量份至約15重量份的該光引發劑。
本發明的再一實例提供一種透明導電膜,其包括利用上述高折射層塗敷用組合物形成的高折射層。
在本發明的一實施例中,該透明導電膜可以是透明基材、上述高折射層、低折射層及導電層的層壓結構。
在本發明的一實施例中,該高折射層的折射率可以是約1.6至約1.8。
在本發明的一實施例中,該高折射層的厚度可以是約20奈米(nm)至約150奈米(nm)。
在本發明的一實施例中,該低折射層的厚度可以是約5奈米(nm)至約100奈米(nm)。
在本發明的一實施例中,該透明基材可以是包含選自包含聚對苯二甲酸乙二醇酯(PET)、聚萘二甲酸乙二酯(PEN)、聚醚碸(PES)、聚碳酸酯(PC)、聚丙烯(PP)、聚氯乙烯(PVC)、聚乙烯(PE)、聚甲基丙烯酸甲酯(PMMA)、乙烯-乙烯醇(EVA)、聚乙烯醇(PVA)以及它們的組合的組中的某一種的單層膜或層壓膜。
在本發明的一實施例中,該導電層可包含氧化銦錫(ITO,Indium Tin Oxide)或氟摻雜二氧化錫(FTO,Fluorine-doped Tin Oxide)。
在本發明的一實施例中,該透明基材的單面或雙面還包括硬塗層。
在本發明的一實施例中,擴大包含上述高折射塗敷層組合物的高折射層的折射率範圍,可容易調節蒸鍍導電層的透明導電膜的光學特性。
並且,可以確保上述透明導電膜的鉛筆硬度、耐溶解性等物理性質和氣體阻隔性能等,還可具有優秀的透射率。
1‧‧‧透明基材
2‧‧‧硬塗層
3‧‧‧高折射層
4‧‧‧低折射層
5‧‧‧導電層
10‧‧‧透明導電膜
圖1是簡要表示本發明一實施例的透明導電膜的剖面圖。
圖2是簡要表示本發明再一實施例的透明導電膜的剖面圖。
以下,對本發明的實例進行詳細說明。但這只是作為例示而提出的,本發明並不局限於此,本發明根據所附的申請專利範圍的範疇來定義。
為了明確說明本發明,省略了與說明無關的部分,在說明書全文中,將對相同或類似的結構部件使用相同的附圖標記。
為了在附圖中更明確地表現多個層及區域,放大厚度來表示。而且,在附圖中為了便於說明,誇張顯示了一部分的層和區域的厚度。
以下,在基材的“上部(或下部)”或者基材的“上(或下),,形成任意的結構,不僅意味著任意的結構接觸形成在上述基材的上表面(或下表面),還意味著並不限定上述基材和基材上(或下)形成的任意的結構之間不包括其他結構。
本發明的一實例提供一種高折射層塗敷用組合物,其包含丙烯酸酯樹脂、芴衍生物樹脂及金屬氧化物粒子。
一般情況下,在製備高折射層塗敷用組合物時,為了調節折射率,通常使用氧化鋯(ZrO2)、二氧化鈦(TiO2)、氧化銻錫(ATO)等金
屬氧化物奈米粒子和折射率為約1.49至約1.53的丙烯酸單體以及紫外線固化型反應性低聚物。但是,僅僅以上述金屬氧化物奈米粒子的含量來調節高折射層塗敷用組合物的折射率時,會減少高折射層塗敷用組合物的固化率,從而降低高折射層的物理性質,在確保高折射層的物理性質方面存在困難。
對此,上述高折射層塗敷用組合物同時包含金屬氧化物粒子和芴衍生物樹脂,從而即使減少金屬氧化物粒子的含量的情況下,也能確保高折射層塗敷用組合物的高折射率的同時,還能確保增強的物理特性。
上述高折射層塗敷用組合物可包含丙烯酸酯樹脂,上述丙烯酸酯樹脂可以是光固化型。根據紫外線或電子射線等活性能量線進行固化,賦予耐久性及對於高溫、高濕的外部環境的耐性,進而可作為調節折射率的目的而使用。
此時,上述丙烯酸酯可包含含有烷基(甲基)丙烯酸酯、聚亞烷基二醇(甲基)丙烯酸酯、羧基及包含不飽和雙鍵結合的(甲基)丙烯酸化合物、含有羥基的(甲基)丙烯酸化合物、含有氮的(甲基)丙烯酸化合物等。並且,可以包含環氧(甲基)丙烯酸酯,氨基甲酸酯(甲基)丙烯酸酯,聚酯(甲基)丙烯酸酯,聚醚(甲基)丙烯酸酯等丙烯酸類低聚物。
具體地,上述丙烯酸酯樹脂可以是選自包含雙季戊四醇六丙烯酸酯(Dipentaerythritol hexa-acrylate)、雙季戊四醇五丙烯酸酯(Dipentaerythritol penta-acrylate)、季戊四醇三丙烯酸酯(Pentaerythritol triacrylate)、四甲基醇甲烷四丙烯酸酯(Tetramethylol methane tetra acrylate)、四甲基甲烷三醇丙烯酸酯(Tetramethylol methane triacrylate)、三甲醇基丙烷
三丙烯酸酯(Trimethanol propane triacrylate)、1,6-己二醇二丙烯酸酯(1,6-Hexanediol diacrylate)、聚乙二醇二丙烯酸酯(Polyethylene glycol diacrylate)、二乙二醇丙烯酸酯(Diethylene glycol acrylate)、三乙二醇丙烯酸酯(Triethylene glycol acrylate)、四乙二醇丙烯酸酯(Tetraethylene glycol acrylate)、六乙二醇丙烯酸酯(Hexa-ethylene glycol acrylate)、丙烯酸丙酯(Propyl acrylate)、丙烯酸丁酯(Butylacrylate)、丙烯酸戊酯(Pentylacrylate)、2-乙基己基丙烯酸酯(2-Ethylhexyl acrylate)、丙烯酸辛酯(Octyl acrylate)、丙烯酸壬酯(Nonyl acrylate)、雙酚A二縮水甘油二丙烯酸酯(Bisphenol A diglycidyl diacrylate)、雙酚A環氧丙烯酸酯(Bisphenol A epoxy acrylate)、環氧乙烷-雙酚A二丙烯酸酯(Ethylene oxide-added bisphenol A diacrylate)、2-苯氧基乙基丙烯酸酯(2-phenoxy ethyl acrylate)以及它們的組合的群組中的其中一種。
更具體地,相對於100重量份的高折射層塗敷用組合物的總固體量,可包含約1重量份至約50重量份的上述丙烯酸酯樹脂。包含的上述丙烯酸酯樹脂小於約1重量份時,無法確保組合物的鉛筆硬度和緊貼性;而大於約50重量份時,很難提高折射率,即使調節金屬氧化物粒子含量來提高折射率,也可能很難確保塗敷用組合物的物理性質。因此,將所包含的丙烯酸酯樹脂維持在上述範圍內,從而可容易實現調節折射率的同時,能夠確保物理性質的優點。
上述高折射層塗敷用組合物可包含芴衍生物樹脂,上述芴衍生物樹脂有可能是光固化型樹脂。上述芴衍生物樹脂包含以作為芳烴的芴為中心引導的化合物,用於提高有機物所具有的低折射率,提高耐熱性、
基材粘合性、與無機物的相容性。並且,為了在分子結構上解決高密度所具有的低溶解性,可以與金屬氧化物粒子的表面進行化學結合,還可以包含羥基(hydroxy grou)。
具體地,上述芴衍生物樹脂可以是選自包含芴、芴酮、2-乙醯胺基芴、2-芴基甲基酮、2-乙醯氨基芴、9-溴芴、9-溴-9-苯基芴、2,7-二氨基芴、2,7-二(乙醯胺基)芴,2,7-二乙醯基芴、9,9-雙[4-(2-羥乙氧基)苯基]芴、9,9-雙(3,4-二羧苯基)芴酐、9,9-雙(3-甲基-4-羥苯基)芴、9,9-雙(4-羥苯基)芴、9,9-雙(4-氨基苯基)芴、9,9-雙(4-羥基-3-甲基苯基)芴、9,9-雙[4-(2-丙烯醯基乙氧基)苯基]芴、9,9-雙[4-(2-羥基-3-丙烯醯基丙氧基)苯基]芴、9,9-雙(4-羥基苯基)芴、2-丙烯酸1,1'[9H-芴-9-亞基雙[4,1-奔氧(2-羥基-3,1-丙烷基)]]酯以及它們的組合的群組中的其中一種。
更具體地,相對於100重量份的高折射層塗敷用組合物的總固體量,可包含約1重量份至大約50重量份的上述芴衍生物樹脂。包含的上述芴衍生物樹脂小於約1重量份時,可能無法維持組合物的高折射率,由此會存在包含過量的金屬氧化物粒子的問題。並且,包含的上述芴衍生物樹脂大於約50重量份時,難以確保高折射層的鉛筆硬度,因此,維持上述範圍,可在調節折射率及確保物理性質方面具有優點。
上述高折射層塗敷用組合物可包含金屬氧化物粒子。此時,上述金屬氧化物粒子可以是選自包含二氧化鈦(TiO2)、氧化鋯(ZrO2)、氧化鋁(Al2O3)、二氧化錫(SnO2)、氧化銦錫(ITO,indium-tin oxide)、
氧化銻錫(ATO,antimon-tin oxide)、五氧化二銻(Sb2O5)、三氧化二鈮(Nb2O3)、三氧化二釔(Y2O3)、二氧化矽(SiO2)以及它們的組合的群組中的其中一種。
具體地,相對於100重量份的高折射層塗敷用組合物的總固體量,可包含約5重量份至約80重量份的上述金屬氧化物粒子。包含的上述金屬氧化物粒子小於約5重量份時,存在折射率降低的問題,而大於約80重量份時,可能難以確保組合物的物理性質。因此,與上述金屬氧化物粒子一同包含上述的芴衍生物樹脂,能顯示優秀的高折射率及物理性特點。
上述金屬氧化物粒子的平均粒徑為約1奈米(nm)至約100奈米(nm),具體地可以為約1奈米(nm)至約30奈米(nm)。平均粒徑是測定幾個粒子粒徑來算出的平均值,上述金屬氧化物粒子的平均粒徑脫離上述範圍時,包含上述金屬氧化物粒子的高折射層的表面光照度可能會高,並且,由於光的散射而可能增加霧度(haze)。因此,維持上述金屬氧化物粒子的平均粒徑範圍,從而可容易實現光學特性優秀的高折射層。
上述高折射層塗敷用組合物除了丙烯酸酯樹脂、芴衍生物樹脂及金屬氧化物粒子外,還可包含光引發劑。光引發劑是為了進行光固化反應來形成高折射層塗敷用組合物而使用。具體地,相對於100重量份的總固體量,包含約1重量份至約15重量份的上述光引發劑,從而可促進光固化反應。
作為上述光引發劑可使用選自包含1-羥基-環己基-苯基-酮(1-hydroxy-cyclohexyl-phenyl-ketone)、2-甲基-1-[4-(甲硫基)苯基]-2-嗎啉基丙烷-1-酮(2-methyl-1-[4-(methylthio)phenyl]-2-morpholino
propane-1-one)、苄基二甲基酮(Benzyl dimethyl ketone)、1-(4-十二烷基苯基)-2-羥基-2-甲基丙烷-1-酮(1-(4-dodecyl phenyl)-2-hydroxy-2-methylpropane-1-one)、2-羥基-2-甲基-1-苯基丙烷-1-酮(2-hydroxy-2-methyl-1-methylpropane-1-one)、1-(4-異丙基苯)-2-羥基-2-甲基丙烷-1-酮(1-(4-isopropylphenyl)-2-hydroxy-2-methyl propane-1-one)、二苯甲酮(Benzophenone)、2,2-二甲氧基-2-苯基苯乙酮(2,2-dimethoxy-2-phenyl acetphenone)、2,2-二乙氧基-2-苯基苯乙酮(2,2-diethoxy-2-phenyl acetphenone)、2-羥基-2-甲基-1-丙烷-1-酮(2-hydroxy-2-methyl-1-propane-1-one)、4,4’-二乙氨基苯甲酮(4,4'-diethyl amino benzophenone)、二氯二苯甲酮(Dichloro benzophenone)、2-甲基蒽醌(2-methyl anthraquinone)、2-乙基蒽醌(2-Ettal anthraquinone)、2-甲基硫雜蒽酮(2-methyl thioxanthone)、2-乙基硫雜蒽酮(2-ethyl oxanthone)、2,4-二甲基硫雜蒽酮(2,4-dimethyl thioxanthone)、2,4-二乙基硫雜蒽酮(2,4-diethyl thioxanthone)以及它們的組合的組中的某一種。
在本發明的另一實例提供了透明導電膜,其包括利用包含丙烯酸酯樹脂、芴衍生物樹脂及金屬氧化物粒子的高折射層塗敷用組合物形成的高折射層。
圖1是簡要表示本發明一實施例的透明導電膜的剖面的圖。參照圖1,上述透明導電膜10為透明基材1、硬塗層2、高折射層3、低折射層4及導電層5的層壓結構。
透明基材1可包含透明性和強度優秀的膜。具體地,上述透明基材1可以是包含選自包含聚對苯二甲酸乙二醇酯(PET)、聚萘二甲酸乙
二酯(PEN)、聚醚碸(PES)、聚碳酸酯(PC)、聚丙烯(PP)、聚氯乙烯(PVC)、聚乙烯(PE)、聚甲基丙烯酸甲酯(PMMA)、乙烯-乙烯醇(EVA)、聚乙烯醇(PVA)以及它們的組合的組中的某一種的單層膜或層壓膜的形態。
上述高折射層3及低折射層4在透明基材1和導電層5之間起到提高絕緣性及透射度的作用,此時,高折射層可利用上述的高折射層塗敷用組合物來形成。
上述高折射層的折射率可以是約1.6至約1.8。在形成上述高折射層的過程中,利用包含丙烯酸酯樹脂、芴衍生物樹脂及金屬氧化物粒子的高折射層塗敷用組合物的結果,可將折射率調節為約1.6至約1.8,並可提高透明導電膜整體的能見度及總光線透射率。
上述高折射層3的厚度可以是約20奈米(nm)至約150奈米(nm),上述低折射層4的厚度可以是約5奈米(nm)至約100奈米(nm)。例如,上述高折射層3及低折射層4的合計厚度可以是約25奈米(nm)至約250奈米(nm),上述高折射層3及低折射層4的合計厚度小於約25奈米(nm)時,由於厚度過薄,從而存在透射率及可視性提高效果不充分的問題;而上述高折射層3及低折射層4的合計厚度大於250奈米(nm)時,例如低折射層4的厚度大於約100奈米(nm)時,由於各層的應力加劇,有可能發生裂紋(Crack)及捲曲(Curl)。
上述導電層3形成於上述低折射層4的上部,可包含氧化銦錫(ITO,Indium Tin Oxide)或氟摻雜二氧化錫(FTO,Fluorine-doped Tin Oxide)。
圖2是簡要表示本發明再一實施例的透明導電膜的剖面的
圖,圖2中,在透明基材1的下部還形成有硬塗層2。硬塗層2起到提高表面硬度的作用,只要是丙烯酸類化合物等能利用于形成硬塗層的,就可以沒有限制地利用。
如圖1所示,上述硬塗層2可以只形成在透明基材1的單面,但如圖2所示,可形成在透明基材1的雙面。
以下,提出本發明的具體實施例。但是,以下記載的實施例僅僅是為了具體地例示或說明本發明的,本發明並不局限於此。
根據以下表1中記載的結構及含量包含紫外線固化型丙烯酸酯樹脂、紫外線固化型芴衍生物樹脂及金屬氧化物奈米粒子來製備高折射層塗敷用組合物質。
相對於100重量份的總固體量,混合20重量份的雙季戊四醇六丙烯酸酯、60重量份的HX-920UV(Kyoeisha,共榮社)、15重量份的矽
石微粒子(商品名稱:XBA-ST,一山化學)、5重量份的光聚合引發劑豔佳固(Irgacure)-184(Ciba,汽巴公司)後,用稀釋溶劑甲基乙基酮(MEK)進行稀釋,來製備固體量為45%的硬塗層組合物(折射率1.52)。
將四乙氧基原矽酸(Tetra-ethoxy ortho silicate)和水、乙醇以1:2:2的比例進行混合,並投入0.1莫耳(mol)的硝酸溶液,進行24小時的反應,來合成折射率為1.43的溶膠。將合成的溶膠利用甲基乙基酮(MEK)進行稀釋,來製備了固體量為5%的低折射層塗敷用組合物。
利用美亞棒(Meyer bar)將由製備例2製備的硬塗層組合物,在125微米(μm)的聚對苯二甲酸乙二醇酯(PET)膜上,塗敷成乾燥膜的厚度為1.5微米(μm),再利用180瓦(W)的高壓水銀燈照射300毫焦耳(mJ)的紫外線並進行固化,來製備膜。在上述所製備的膜的反面,使用與上述方法相同的方法將由製備例2製備的硬塗層組合物塗敷成乾燥膜的厚度為1.5微米(μm),並進行固化後,製備出雙面都包括硬塗層的膜。
之後,在雙面都包括硬塗層的膜的單面,利用由製備例1-1製備的高折射層塗敷用組合物,塗敷成乾燥膜的厚度為50奈米(nm),利用180瓦(W)的高壓水銀燈照射300毫焦耳(mJ)的紫外線並進行固化,從而形成高折射層。其後,在上述高折射層,利用由製備例3製備的低折射層塗敷液組合物,塗敷成乾燥膜的厚度為20奈米(nm),在150℃的烤箱中進行1分鐘的固化,從而形成低折射層。此時,利用銦:錫=95:5的氧化銦錫(ITO)靶,
在低折射層形成膜厚度為20奈米(nm)的氧化銦錫(ITO)層,從而製備透明導電膜。
除了高折射層塗敷用組合物適用製備例1-2,塗敷成高折射層厚度為45奈米(nm)以外,以與上述實施例1相同的方法製備透明導電膜。
除了高折射層塗敷用組合物適用製備例1-3,塗敷成高折射層厚度為40奈米(nm)以外,以與上述實施例1相同的方法製備透明導電膜。
除了高折射層塗敷用組合物適用製備例1-4,塗敷成高折射層厚度為50奈米(nm)以外,以與上述實施例1相同的方法製備透明導電膜。
除了高折射層塗敷用組合物適用製備例1-5,塗敷成高折射層厚度為50奈米(nm)以外,以與上述實施例1相同的方法製備透明導電膜。
除了高折射層塗敷用組合物適用製備例1-6,塗敷成高折射層厚度為45奈米(nm)以外,以與上述實施例1相同的方法製備透明導電膜。
利用上述實施例及比較例的透明導電膜來測定以下多個物理性質,並將其結果記載於下清單2中。
1)折射率:利用棱鏡耦合器(Prism coupler),使用532奈米(nm)、632.8奈米、830奈米的鐳射測定各個波長中的折射率,並通過柯西定理
(caushy plot)獲得550奈米中的折射率。
2)鉛筆硬度:以JIS K 5600-5-4為準進行測定。
3)緊貼性:利用切割器將塗敷層表面,以1毫米(mm)的間距及10毫米×10毫米的寬度×長度,切割成棋盤模樣後,利用透明膠帶(Nichiban,米其邦公司)來進行剝離試驗。利用膠帶對同一部位進行3次剝離試驗,在評價後由/100標記緊貼的數位。
4)透射率、透射b*/反射b*:利用CM-5(Konica minolta,柯尼卡美能達公司),來測定總光線透射率及透射b*/反射b*值。
5)蝕刻(Etching)評價:利用正四邊形圖案化的面罩在氧化銦錫(ITO)層塗敷感光性樹脂,進行乾燥固化後,在25℃、5%的鹽酸水溶液中浸漬1分鐘,從而實施氧化銦錫(ITO)層的蝕刻評價。
6)測定蝕刻(Etching)前/後的反射率之差(△R)及確認圖案隱蔽力:在蝕刻(Etching)前/後利用CM-5測定反射率,求得反射率之差,並通過肉眼確認圖案隱蔽力。
表2
◎:非常優秀,○:優秀,△:一般,×:差
通過測定結果,可以瞭解實施例1至實施例3的透明導電膜具有優秀的硬度、透射率及能見度。具體地,包括由不包含芴衍生物的製備例1-4的塗敷用組合物形成的高折射層的比較例1的透明導電膜的情況,測定到的高折射層的折射率低。並且,測定到的透射率及蝕刻前/後反射率之差比實施例1至實施例3高,圖案隱蔽力也差,因此,能夠瞭解作為透明導電膜的光學性質並不優秀。
包括由不包含芴衍生物的製備例1-5的塗敷用組合物形成的
高折射層的比較例2的透明導電膜的情況,由於高折射層的折射率與實施例1相似,因此,具有優秀的光學特性和圖案隱蔽力,但鉛筆硬度和緊貼性方面無法確保物理特性。
並且,包括由包含芴衍生物,但不包含紫外線固化型丙烯酸酯的製備例1-6的塗敷用組合物形成的高折射層的比較例3的透明導電膜的情況,由於包含芴衍生物,因此在高折射層的折射率方面測定到較高的折射率,但在鉛筆硬度和緊貼性方面獲得一般以下的評價,所以,很難適用於透明導電膜。
綜上所述,可知,由同時包含紫外線固化型丙烯酸酯樹脂、紫外線固化型芴衍生物樹脂及金屬氧化物奈米粒子的高折射層塗敷用組合物形成的高折射層的折射率可以是1.6至1.8,包括該高折射層塗敷用組合物的透明導電膜能同時確保硬度、透射率、能見度等優秀的光學特性及物理特性。
雖然本發明已以較佳實施例揭露,然其並非用以限制本發明,任何熟習此項技藝之人士,在不脫離本發明之精神和範圍內,當可作各種更動與修飾,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。
1‧‧‧透明基材
2‧‧‧硬塗層
3‧‧‧高折射層
4‧‧‧低折射層
5‧‧‧導電層
10‧‧‧透明導電膜
Claims (16)
- 一種高折射層塗敷用組合物,其包含丙烯酸酯樹脂、芴衍生物樹脂及金屬氧化物粒子。
- 根據申請專利範圍第1項所述之高折射層塗敷用組合物,其中該丙烯酸酯樹脂或該芴衍生物樹脂是光固化型樹脂。
- 根據申請專利範圍第1項所述之高折射層塗敷用組合物,其中相對於100重量份的總固體量,包含1重量份至50重量份的該丙烯酸酯樹脂、1重量份至50重量份的該芴衍生物樹脂以及5重量份至80重量份的該金屬氧化物粒子。
- 根據申請專利範圍第1項所述之高折射層塗敷用組合物,其中該芴衍生物樹脂選自包含芴、芴酮、2-乙醯胺基芴、2-芴基甲基酮、2-乙醯氨基芴、9-溴芴、9-溴-9-苯基芴、2,7-二氨基芴、2,7-二(乙醯胺基)芴、2,7-二乙醯基芴、9,9-雙[4-(2-羥乙氧基)苯基]芴、9,9-雙(3,4-二羧苯基)芴酐、9,9-雙(3-甲基-4-羥苯基)芴、9,9-雙(4-羥苯基)芴、9,9-雙(4-氨基苯基)芴、9,9-雙(4-羥基-3-甲基苯基)芴、9,9-雙[4-(2-丙烯醯基乙氧基)苯基]芴、9,9-雙[4-(2-羥基-3-丙烯醯基丙氧基)苯基]芴、9,9-雙(4-羥基苯基)芴、2-丙烯酸1,1'[9H-芴-9-亞基雙[4,1-奔氧(2-羥基-3,1-丙烷基)]]酯以及它們有組合的群組中的其中一種。
- 根據申請專利範圍第1項所述之高折射層塗敷用組合物,其中該金屬化合物粒子是選自包含二氧化鈦、氧化鋯、氧化鋁、二氧化錫、氧化銦錫、氧化銻錫、五氧化二銻、三氧化二鈮、三氧化二釔、二氧化矽以及它們 的組合的群組中的其中一種。
- 根據申請專利範圍第1項所述之高折射層塗敷用組合物,其中該金屬化合物粒子的平均粒徑為1奈米100奈米。
- 根據申請專利範圍第1項所述之高折射層塗敷用組合物,其中另包含一光引發劑。
- 根據申請專利範圍第7項所述之高折射層塗敷用組合物,其中100重量份的總固體量包含1重量份至15重量份的該光引發劑。
- 一種透明導電膜,其包括利用如申請專利範圍第1項所述的高折射層塗敷用組合物形成的高折射層。
- 根據申請專利範圍第9項所述的透明導電膜,其中上述透明導電膜為透明基材、上述高折射層、低折射層及導電層的層壓結構。
- 根據申請專利範圍第9項所述之透明導電膜,其中該高折射層的折射率為1.6至1.8。
- 根據申請專利範圍第9項所述之透明導電膜,其中該高折射層的厚度為20奈米至150奈米。
- 根據申請專利範圍第10項所述之透明導電膜,其中該低折射層的厚度為5奈米至100奈米。
- 根據申請專利範圍第10項所述之透明導電膜,其中該透明基材是選自包含聚對苯二甲酸乙二醇酯、聚萘二甲酸乙二酯、聚醚碸、聚碳酸酯、聚丙烯、聚氯乙烯、聚乙烯、聚甲基丙烯酸甲酯、乙烯-乙烯醇、聚乙烯醇以及它們組合的群組中的某一種的單層膜或層壓膜。
- 根據申請專利範圍第10項所述之透明導電膜,其中該導電層包含氧化銦 錫或氟摻雜二氧化錫。
- 根據申請專利範圍第10項所述之透明導電膜,其中在該透明基材的單面或雙面還包括一硬塗層。
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| KR1020120097120A KR101525286B1 (ko) | 2012-09-03 | 2012-09-03 | 고굴절층 코팅용 조성물 및 이를 포함하는 투명 도전성 필름 |
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| TW201410814A true TW201410814A (zh) | 2014-03-16 |
| TWI491688B TWI491688B (zh) | 2015-07-11 |
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| TW102125711A TWI491688B (zh) | 2012-09-03 | 2013-07-18 | 包含高折射層塗敷用組合物的透明導電膜 |
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| JP (1) | JP6150404B2 (zh) |
| KR (1) | KR101525286B1 (zh) |
| CN (1) | CN104603215A (zh) |
| TW (1) | TWI491688B (zh) |
| WO (1) | WO2014035018A1 (zh) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI659855B (zh) * | 2016-05-09 | 2019-05-21 | Lg化學股份有限公司 | 導電透明膜、其製造方法及包括其的觸控面板 |
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| KR20160100143A (ko) * | 2015-02-13 | 2016-08-23 | 동우 화인켐 주식회사 | 필름 터치 센서 |
| JP6419610B2 (ja) * | 2015-03-12 | 2018-11-07 | リンテック株式会社 | 透明導電膜積層用フィルム、その製造方法および透明導電性フィルム |
| KR20160150499A (ko) * | 2015-06-22 | 2016-12-30 | 주식회사 엘지화학 | 도전성 필름 |
| WO2017196034A1 (ko) * | 2016-05-09 | 2017-11-16 | 주식회사 엘지화학 | 도전성 투광 필름 |
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| JP2003080624A (ja) * | 2001-09-07 | 2003-03-19 | Nof Corp | 透明導電材料およびタッチパネル |
| WO2007105627A1 (ja) * | 2006-03-10 | 2007-09-20 | Toyo Ink Mfg. Co., Ltd. | 光学部材用ハードコート性樹脂組成物 |
| JP2009133880A (ja) * | 2006-03-10 | 2009-06-18 | Toyo Ink Mfg Co Ltd | 樹脂組成物 |
| JP2007277467A (ja) * | 2006-04-10 | 2007-10-25 | Sony Chemical & Information Device Corp | 硬化性樹脂組成物 |
| WO2007138946A1 (ja) * | 2006-05-29 | 2007-12-06 | Toyo Ink Mfg. Co., Ltd. | 金属酸化物組成物、硬化膜及び積層体 |
| CN101134818A (zh) * | 2006-08-30 | 2008-03-05 | 三洋电机株式会社 | 有机无机复合体形成用材料、有机无机复合体和使用该复合体的光学元件 |
| JP2008266578A (ja) * | 2007-03-23 | 2008-11-06 | Sanyo Electric Co Ltd | 光学ポリマー材料及び光学部品 |
| US7981986B2 (en) * | 2008-04-29 | 2011-07-19 | 3M Innovative Properties Company | Optical films comprising fluorenol (meth)acrylate monomer |
| KR101099031B1 (ko) * | 2009-06-05 | 2011-12-26 | 한화엘앤씨 주식회사 | 터치 패널용 투명 도전성 필름 및 그 제조방법 |
| JP5408075B2 (ja) * | 2009-10-06 | 2014-02-05 | 日油株式会社 | 透明導電性フィルム |
| CN102034565B (zh) * | 2009-10-06 | 2014-01-29 | 日油株式会社 | 透明导电性膜 |
| KR101049182B1 (ko) * | 2009-11-05 | 2011-07-14 | 한화엘앤씨 주식회사 | 터치 패널용 투명 도전성 기재 및 그 제조방법 |
| KR20110133209A (ko) * | 2010-06-04 | 2011-12-12 | (주)필름앤라이프 | 롤 인쇄용 고굴절 하드코팅 조성물 및 이를 이용한 인쇄필름 |
| JP5760522B2 (ja) * | 2011-03-07 | 2015-08-12 | 帝人株式会社 | 光硬化性樹脂組成物及びその硬化皮膜を有する物品、その製造方法 |
| JP5815304B2 (ja) * | 2011-06-29 | 2015-11-17 | 日揮触媒化成株式会社 | 光学薄膜形成用塗料および光学薄膜 |
| JP5991063B2 (ja) * | 2012-07-31 | 2016-09-14 | 東洋インキScホールディングス株式会社 | 樹脂組成物、ならびにそれを用いた塗膜 |
| JP5885585B2 (ja) * | 2012-05-21 | 2016-03-15 | 昭和電工株式会社 | 硬化性組成物およびその硬化物 |
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- 2013-01-08 JP JP2015529650A patent/JP6150404B2/ja not_active Expired - Fee Related
- 2013-01-08 CN CN201380045906.9A patent/CN104603215A/zh active Pending
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI659855B (zh) * | 2016-05-09 | 2019-05-21 | Lg化學股份有限公司 | 導電透明膜、其製造方法及包括其的觸控面板 |
| US10629327B2 (en) | 2016-05-09 | 2020-04-21 | Lg Chem, Ltd. | Conductive transparent film |
Also Published As
| Publication number | Publication date |
|---|---|
| JP6150404B2 (ja) | 2017-06-21 |
| TWI491688B (zh) | 2015-07-11 |
| CN104603215A (zh) | 2015-05-06 |
| WO2014035018A1 (ko) | 2014-03-06 |
| JP2015535859A (ja) | 2015-12-17 |
| KR20140030666A (ko) | 2014-03-12 |
| KR101525286B1 (ko) | 2015-06-02 |
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