JPWO2019054412A1 - 硬化性組成物 - Google Patents
硬化性組成物 Download PDFInfo
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- JPWO2019054412A1 JPWO2019054412A1 JP2019542265A JP2019542265A JPWO2019054412A1 JP WO2019054412 A1 JPWO2019054412 A1 JP WO2019054412A1 JP 2019542265 A JP2019542265 A JP 2019542265A JP 2019542265 A JP2019542265 A JP 2019542265A JP WO2019054412 A1 JPWO2019054412 A1 JP WO2019054412A1
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- 239000000203 mixture Substances 0.000 title claims abstract description 118
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- 239000000178 monomer Substances 0.000 claims abstract description 144
- 125000002091 cationic group Chemical group 0.000 claims abstract description 4
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 44
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- 229910052760 oxygen Inorganic materials 0.000 claims description 44
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- 230000035699 permeability Effects 0.000 claims description 13
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- NVKGJHAQGWCWDI-UHFFFAOYSA-N 4-[4-amino-2-(trifluoromethyl)phenyl]-3-(trifluoromethyl)aniline Chemical compound FC(F)(F)C1=CC(N)=CC=C1C1=CC=C(N)C=C1C(F)(F)F NVKGJHAQGWCWDI-UHFFFAOYSA-N 0.000 description 13
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 9
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- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 7
- 125000001309 chloro group Chemical group Cl* 0.000 description 7
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- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
- 239000006096 absorbing agent Substances 0.000 description 6
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- 125000003277 amino group Chemical group 0.000 description 6
- 150000004984 aromatic diamines Chemical class 0.000 description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 6
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 5
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 5
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- 239000000853 adhesive Substances 0.000 description 5
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- 125000003545 alkoxy group Chemical group 0.000 description 5
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 5
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- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 5
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- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 4
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- MXPYJVUYLVNEBB-UHFFFAOYSA-N 2-[2-(2-carboxybenzoyl)oxycarbonylbenzoyl]oxycarbonylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OC(=O)C1=CC=CC=C1C(=O)OC(=O)C1=CC=CC=C1C(O)=O MXPYJVUYLVNEBB-UHFFFAOYSA-N 0.000 description 4
- GWHLJVMSZRKEAQ-UHFFFAOYSA-N 3-(2,3-dicarboxyphenyl)phthalic acid Chemical compound OC(=O)C1=CC=CC(C=2C(=C(C(O)=O)C=CC=2)C(O)=O)=C1C(O)=O GWHLJVMSZRKEAQ-UHFFFAOYSA-N 0.000 description 4
- QYIMZXITLDTULQ-UHFFFAOYSA-N 4-(4-amino-2-methylphenyl)-3-methylaniline Chemical compound CC1=CC(N)=CC=C1C1=CC=C(N)C=C1C QYIMZXITLDTULQ-UHFFFAOYSA-N 0.000 description 4
- WVDRSXGPQWNUBN-UHFFFAOYSA-N 4-(4-carboxyphenoxy)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OC1=CC=C(C(O)=O)C=C1 WVDRSXGPQWNUBN-UHFFFAOYSA-N 0.000 description 4
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 4
- HYDATEKARGDBKU-UHFFFAOYSA-N 4-[4-[4-(4-aminophenoxy)phenyl]phenoxy]aniline Chemical group C1=CC(N)=CC=C1OC1=CC=C(C=2C=CC(OC=3C=CC(N)=CC=3)=CC=2)C=C1 HYDATEKARGDBKU-UHFFFAOYSA-N 0.000 description 4
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- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- SOLUNJPVPZJLOM-UHFFFAOYSA-N trizinc;distiborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-][Sb]([O-])([O-])=O.[O-][Sb]([O-])([O-])=O SOLUNJPVPZJLOM-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
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Abstract
Description
従って、本発明の目的は、表面硬度及び屈曲性に優れた積層体を形成可能な硬化性組成物、該硬化性組成物を硬化させてなる硬化膜、及び該硬化膜を含む積層体を提供することにある。
[2]カチオン重合性モノマー(B)は、1以上のエポキシ基及び/又は1以上のオキセタニル基を有する環状エーテル化合物(B−1)を含む、[1]に記載の硬化性組成物。
[3]環状エーテル化合物(B−1)は、2以上のエポキシ基及び/又は2以上のオキセタニル基を有するビス環状エーテル化合物(B−1−1)を含む、[2]に記載の硬化性組成物。
[4]カチオン重合性モノマー(B)はビニルオキシ化合物(B−2)をさらに含む、[1]〜[3]のいずれかに記載の硬化性組成物。
[5]硬化性組成物100質量部に対して、多官能(メタ)アクリレートモノマー(A)の含有量は5〜80質量部であり、環状エーテル化合物(B−1)の含有量は5〜80質量部であり、ビニルオキシ化合物(B−2)の含有量は3〜60質量部である、[4]に記載の硬化性組成物。
[6]ビニルオキシ化合物(B−2)の含有量は、多官能(メタ)アクリレートモノマー(A)及びカチオン重合性モノマー(B)の総量100質量部に対して、3〜50質量部である、[4]又は[5]に記載の硬化性組成物。
[7]環状エーテル化合物(B−1)は、1以上のラジカル重合性官能基を有するラジカル重合性環状エーテル化合物(B−1−2)を含む、[2]〜[6]のいずれかに記載の硬化性組成物。
[8]硬化性組成物100質量部に対して、多官能(メタ)アクリレートモノマー(A)の含有量は5〜50質量部であり、ビス環状エーテル化合物(B−1−1)の含有量は3〜30質量部であり、ラジカル重合性環状エーテル化合物(B−1−2)の含有量は5〜40質量部である、[7]に記載の硬化性組成物。
[9]ラジカル重合性環状エーテル化合物(B−1−2)の含有量は、ビス環状エーテル化合物(B−1−1)1質量部に対して、0.1〜10質量部である、[7]又は[8]に記載の硬化性組成物。
[10]ラジカル重合開始剤(C)及びカチオン重合開始剤(D)をさらに含む、[1]〜[9]のいずれかに記載の硬化性組成物。
[11]ラジカル重合開始剤(C)の含有量は、多官能(メタ)アクリレートモノマー(A)100質量部に対して、1〜15質量部であり、カチオン重合開始剤(D)の含有量は、カチオン重合性モノマー(B)100質量部に対して、1〜15質量部である、[10]に記載の硬化性組成物。
[12]無機粒子をさらに含む、[1]〜[11]のいずれかに記載の硬化性組成物。
[13]無機粒子が反応性シリカ粒子である場合、反応性シリカ粒子の含有量は、硬化性組成物の質量に対して、1〜70質量%である、[12]に記載の硬化性組成物。
[14][1]〜[13]のいずれかに記載の硬化性組成物を硬化させてなる硬化膜。
[15][14]に記載の硬化膜が、基材フィルムの少なくとも一方の面に積層された、積層体。
[16]基材フィルムはポリイミド系高分子を含んでなる、[15]に記載の積層体。
[17]酸素透過度は、800cc/(m2・24h・atm)以下である、[15]又は[16]に記載の積層体。
[18][15]〜[17]のいずれかに記載の積層体を含む、フレキシブルディスプレイ。
本発明の硬化性組成物は、多官能(メタ)アクリレートモノマー(A)と、カチオン重合性モノマー(B)とを含有する。
多官能(メタ)アクリレートモノマー(A)とは、分子内に2個以上の(メタ)アクリロイルオキシ基を有する化合物を意味し、本発明における多官能(メタ)アクリレートモノマー(A)は、3官能(メタ)アクリレートモノマー、4官能(メタ)アクリレートモノマー及び8官能(メタ)アクリレートモノマーからなる群から選択される少なくとも2種を含む。なお、本明細書において、用語「(メタ)アクリレート」とは、「アクリレート」又は「メタクリレート」を意味し、用語「(メタ)アクリロイル」も同様に、「アクリロイル」又は「メタクリロイル」を意味する。
本明細書において、表面硬度とは本発明の積層体における硬化膜側の表面の硬さを示す。屈曲性とは本発明の積層体を屈曲させた時に、クラック等の発生を抑制できる特性を意味する。酸素バリア性とは、酸素を透過させにくい特性を意味し、酸素バリア性が高いほど、酸素透過性又は酸素透過度が低いことを示す。耐反り性とは反りが起こりにくい特性を意味し、耐反り性が高いほど、反りが起こりにくいことを示す。
本発明の硬化性組成物はカチオン重合性モノマー(B)を含有する。カチオン重合性モノマー(B)とは、分子内にカチオン重合性基を有する化合物を意味する。カチオン重合性モノマー(B)は、積層体の表面硬度、屈曲性、酸素バリア性、及び耐反り性の観点から、1以上のエポキシ基及び/又は1以上のオキセタニル基を有する環状エーテル化合物(B−1)並びにビニルオキシ化合物(B−2)から選択される少なくとも1種を含むことが好ましい。
環状エーテル化合物(B−1)としては、例えば分子内に1以上のエポキシ基を有するエポキシ化合物[エポキシ化合物(b)と称する]、分子内に1以上のオキセタニル基を有するオキセタン化合物[オキセタン化合物(b)と称する]、1以上のラジカル重合性官能基を有するラジカル重合性環状エーテル化合物(B−1−2)などが挙げられる。エポキシ化合物(b)、オキセタン化合物(b)、及びラジカル重合性環状エーテル化合物(B−1−2)は単独又は二種以上組合せて使用できる。
ビニルオキシ化合物(B−2)とは、分子内に1以上のビニルオキシ基を有する化合物を意味する。特にビニルオキシ化合物(B−2)は2以上のビニルオキシ基を有する化合物が好ましい。これらのビニルオキシ化合物(B−2)は単独又は2種以上組合せて使用できる。ビニルオキシ化合物(B−2)はモノマー又はオリゴマーであってもよいが、好ましくはモノマーである。
本発明の硬化性組成物は、ラジカル重合開始剤(C)及びカチオン重合開始剤(D)を含んでよい。迅速に硬化させやすいという観点から、光ラジカル重合開始剤(C)及び光カチオン重合開始剤(D)を含むことが好ましい。硬化性組成物中に光ラジカル重合開始剤を含有すると、ラジカル重合性化合物である多官能(メタ)アクリレートモノマー(A)を迅速に硬化させることができる。光ラジカル重合開始剤は、可視光線、紫外線、X線、電子線のような活性エネルギー線の照射により、ラジカル重合性化合物の硬化を開始できるものであれば特に限定されず、その具体例としては、アセトフェノン、3−メチルアセトフェノン、ベンジルジメチルケタール、1−(4−イソプロピルフェニル)−2−ヒドロキシ−2−メチルプロパン−1−オン、2−メチル−1−[4−(メチルチオ)フェニル]−2−モルホリノプロパン−1−オン及び2−ヒドロキシ−2−メチル−1−フェニルプロパン−1−オン等のアセトフェノン系開始剤;ベンゾフェノン、4−クロロベンゾフェノン及び4,4′−ジアミノベンゾフェノン等のベンゾフェノン系開始剤;2,2−ジメトキシ−1,2−ジフェニルエタン−1−オン、1−ヒドロキシーシクロヘキシル−フェニル−ケトン等のアルキルフェノン系開始剤;ベンゾインプロピルエーテル及びベンゾインエチルエーテル等のベンゾインエーテル系開始剤;4−イソプロピルチオキサントン等のチオキサントン系開始剤;ビス(2,4,6−トリメチルベンゾイル)−フェニルホスフィンオキサイド等のアシルホスフィンオキサイド系開始剤;その他、キサントン、フルオレノン、カンファーキノン、ベンズアルデヒド、アントラキノン等が挙げられる。これらの光ラジカル重合開始剤は単独又は二種以上組合せて使用できる。これらの光ラジカル重合開始剤の中でも、アルキルフェノン系開始剤、アシルホスフィンオキサイド系開始剤などが好ましい。
(1)硬化膜、積層体
本発明は、前記硬化性組成物を硬化させてなる硬化膜を包含する。該硬化膜は、前記硬化性組成物の硬化物である。本発明の硬化膜は、本発明の硬化性組成物からなるため、表面硬度及び屈曲性に優れている。さらに本発明の硬化膜は、優れた酸素バリア性及び耐反り性も有する。
*は結合手を表し、
Zは、単結合、−O−、−CH2−、−CH2−CH2−、−CH(CH3)−、−C(CH3)2−、−C(CF3)2−、−Ar−、−SO2−、−CO−、−O−Ar−O−、−Ar−CH2−Ar−、−Ar−C(CH3)2−Ar−又は−Ar−SO2−Ar−を表す。Arはフッ素原子で置換されていてもよい炭素数6〜20のアリーレン基を表し、具体例としてはフェニレン基が挙げられる。
Z1、Z2及びZ3は、それぞれ独立して、単結合、−O−、−CH2−、−CH2−CH2−、−CH(CH3)−、−C(CH3)2−、−C(CF3)2−、−SO2−又は−CO−を表す。
1つの例は、Z1及びZ3が−O−であり、かつ、Z2が−CH2−、−C(CH3)2−、−C(CF3)2−又は−SO2−である。Z1とZ2との各環に対する結合位置、及び、Z2とZ3との各環に対する結合位置は、それぞれ、各環に対してメタ位又はパラ位であることが好ましい。
Bは、単結合、−O−、−CH2−、−CH2−CH2−、−CH(CH3)−、−C(CH3)2−、−C(CF3)2−、−SO2−、−S−、−CO−又は−NR9−を表し、R9は水素原子、ハロゲン原子で置換されていてもよい炭素数1〜12の炭化水素基を表し、
nは0〜4の整数であり、
*は結合手を表す]
で表される構成単位であることが好ましい。
で表される構成単位である。式(10)及び(13)中の複数のA及びA3の少なくとも一部が式(4)で表される基であると、積層体は、高い表面硬度を発現できると同時に、高い透明性を有することができる。
で表される構成単位である。式(10)中の複数のGの少なくとも一部が式(5)で表される基であると、積層体は、高い透明性を発現すると同時に、ポリイミド系高分子の溶媒への溶解性を向上し、樹脂ワニスの粘度を低く抑制することができ、また基材フィルムの加工を容易にすることができる。
これらの中でも、好ましくは4,4’−オキシジフタル酸二無水物、3,3’,4,4’−ベンゾフェノンテトラカルボン酸二無水物、2,2’,3,3’−ベンゾフェノンテトラカルボン酸二無水物、3,3’,4,4’−ビフェニルテトラカルボン酸二無水物、2,2’,3,3’−ビフェニルテトラカルボン酸二無水物、3,3’,4,4’−ジフェニルスルホンテトラカルボン酸二無水物、2,2−ビス(3,4−ジカルボキシフェニル)プロパン二無水物、2,2−ビス(2,3−ジカルボキシフェニル)プロパン二無水物、2,2−ビス(3,4−ジカルボキシフェノキシフェニル)プロパン二無水物、4,4’−(ヘキサフルオロイソプロピリデン)ジフタル酸二無水物(6FDA)、1,2−ビス(2,3−ジカルボキシフェニル)エタン二無水物、1,1−ビス(2,3−ジカルボキシフェニル)エタン二無水物、1,2−ビス(3,4−ジカルボキシフェニル)エタン二無水物、1,1−ビス(3,4−ジカルボキシフェニル)エタン二無水物、ビス(3,4−ジカルボキシフェニル)メタン二無水物、ビス(2,3−ジカルボキシフェニル)メタン二無水物、4,4’−(p−フェニレンジオキシ)ジフタル酸二無水物及び4,4’−(m−フェニレンジオキシ)ジフタル酸二無水物が挙げられ、より好ましくは4,4’−オキシジフタル酸二無水物、3,3’,4,4’−ビフェニルテトラカルボン酸二無水物、2,2’,3,3’−ビフェニルテトラカルボン酸二無水物、4,4’−(ヘキサフルオロイソプロピリデン)ジフタル酸二無水物(6FDA)、ビス(3,4−ジカルボキシフェニル)メタン二無水物及び4,4’−(p−フェニレンジオキシ)ジフタル酸二無水物が挙げられる。これらは単独又は2種以上を組合せて使用できる。
(a)前記樹脂を含む液(樹脂ワニスと称する場合がある)を調製する工程(ワニス調製工程)、
(b)樹脂ワニスを支持材に塗布して塗膜を形成する工程(塗布工程)、及び
(c)塗布された液(塗膜)を乾燥させて、基材フィルムを形成する工程(基材フィルム形成工程)
を含む方法によって製造することができる。
本発明の積層体は、例えば、以下の工程:
(d)本発明の硬化性組成物を基材フィルム上に塗布して塗膜を形成する工程(塗膜形成工程)、
(e)塗膜に高エネルギー線を照射し、塗膜を硬化させて硬化膜を形成する工程(硬化工程)
を含む製造方法によって製造することができる。
本発明の積層体は、画像表示装置の前面板、特にフレキシブルディスプレイの前面板(ウィンドウフィルム)として有用である。本発明では、本発明の積層体を含む画像表示装置、特にフレキシブルディスプレイも提供することができる。本実施形態に係るフレキシブルディスプレイは、例えば、フレキシブル機能層と、フレキシブル機能層に積層された本発明の積層体(前面板として機能する)を有する。すなわち、フレキシブルディスプレイの前面板は、フレキシブル機能層の上の視認側に配置される。この前面板は、フレキシブル機能層を保護する機能を有する。
ポリイミドの粉末(「KPI−MX300F(100)」、河村産業(株)製、ポリスチレン換算重量平均分子量(Mw)=280,000)にDMAcを加えて溶解させた後、分散媒がGBLであるシリカゾルを加え、ポリイミドとシリカの質量比が純分ベースで1:1である、ポリイミドワニスを調製した。ポリイミドワニスに占める、ポリイミド樹脂とシリカとの合計質量は17質量%であった。該ポリイミドワニスを流涎成形した後に乾燥させることで、厚み50μmの基材フィルム1を得た。
(シリカゾルAの調整)
ゾル−ゲル法により作製されたBET径(BET法で測定された平均粒子径)が27nmのアモルファスシリカゾルを原料とし、溶媒置換により、GBL置換シリカゾルAを調製した。
窒素ガス雰囲気下、撹拌機を備えた反応容器に、2,2’−ビス(トリフルオロメチル)ベンジジン(TFMB)45質量部及びジメチルアセトアミド(DMAc)768.55質量部を加え、室温で撹拌しながらTFMBをDMAcに溶解させた。次に、反応容器に4,4’−(ヘキサフルオロイソプロピリデン)ジフタル酸二無水物(6FDA)18.92質量部(0.3モル倍[対TFMB])を添加し、室温で3時間撹拌した。その後、4,4’−オキシビス(ベンゾイルクロリド)(OBBC)4.19質量部(0.1モル倍[対TFMB])、次いでテレフタロイルクロリド(TPC)17.29質量部(0.6モル倍[対TFMB])を反応容器に加え、室温で1時間撹拌した。次いで、反応容器に4−メチルピリジン4.63質量部(0.35モル倍[対TFMB])と無水酢酸13.04質量部(0.9モル倍[対TFMB])とを加え、室温で30分間撹拌後、70℃に昇温し、さらに3.5時間撹拌し、反応液を得た。
得られた反応液を室温まで冷却し、大量のメタノール中に糸状に投入し、析出した沈殿物を取り出し、メタノールに6時間浸漬後、メタノールで洗浄した。次に、100℃にて沈殿物の減圧乾燥を行い、ポリアミドイミドAを得た。ポリアミドイミドAの重量平均分子量は、455,000であった。
ポリアミドイミドAをGBLに溶解させたのち、シリカゾルAをポリアミドイミドA:シリカ粒子=60:40(質量比)になるように添加し、ポリアミドイミドワニスAを製造した。ポリアミドイミドワニスA中の固形分濃度は10質量%になるように調製された。
表1及び2に示す成分を秤量後、撹拌することにより硬化性組成物を調製した。製造例1で得られた基材フィルム1に、硬化性組成物をバーコーター塗工し、80℃で3分間乾燥させた後、窒素雰囲気下、UV照射装置[アイグラフィックス社製6KWI灯コンベア]を用いて、以下の硬化条件でUV硬化することにより、基材フィルム1の一方の面に硬化膜が積層された積層体を得た。硬化膜の厚みは9μmであった。なお、表1及び2に示す各配合成分の配合量は、使用した商品が溶剤等を含む場合は、そこに含まれる有効成分の質量部数を示す。
(硬化条件)
光源ランプ:高圧水銀灯
積算光量:500mJ/cm2
ピーク強度:200mW/cm2
なお、積算光量は上記UV照射装置の積層光量計(365nm)を用いて測定した値である。
表3に示す成分を秤量後、撹拌することにより硬化性組成物を調製した。製造例1で得られた基材フィルム1に代えて、製造例2で得られた基材フィルム2を使用し、硬化膜の厚みが16μmとなるように調整したこと以外は、実施例1〜25と同様にして、基材フィルム2の一方の面に硬化膜が積層された積層体を得た。硬化膜の厚みは16μmであった。なお、表3に示す各配合成分の配合量は、使用した商品が溶剤等を含む場合は、そこに含まれる有効成分の質量部数を示す。
表3に示す成分を秤量後、撹拌することにより硬化性組成物を調製した。製造例1で得られた基材フィルム1に代えて、製造例2で得られた基材フィルム2を使用したこと以外は、実施例1〜25と同様にして、基材フィルム2の一方の面に硬化膜が積層された積層体を得た。硬化膜の厚みは9μmであった。なお、表3に示す各配合成分の配合量は、使用した商品が溶剤等を含む場合は、そこに含まれる有効成分の質量部数を示す。
実施例1〜30、及び比較例1で得られた積層体をJIS K 5600−5−4:1999に準拠して硬化膜の表面の鉛筆硬度を測定した。荷重は750gとした。測定結果を表1〜3に示す。
実施例1〜30、及び比較例1で得られた積層体について、JIS K 5600−5−1:1999に準拠して屈曲試験を行い、以下の評価方法により評価した。評価結果を表1〜3に示す。
実施例1〜30、及び比較例1で得られた積層体を1cm×8cmにカットして、測定サンプルを得た。硬化膜が外側になる向きで、6mm(半径R=3mm)又は4mm(半径R=2mm)のロールそれぞれに測定サンプルを巻きつける操作を連続10回行った。
硬化膜におけるヒビ割れ(クラック)の発生の有無に基づいて、屈曲性を次のように判定した。判定結果を表1〜3に示す。
(屈曲性の判定)
◎…クラックがなく、外観は良好であった。
○…1〜4本のクラックが発生した。
△…クラックが5本以上発生した。
実施例1〜30、及び比較例1で得られた積層体をJIS K 7126−1(差圧法)に準拠して、GTRテック(株)製、差圧式ガス透過率測定装置「GTR−30AS型」を用いて酸素透過度を測定した。測定結果を表1〜3に示す。
実施例1〜30、及び比較例1で得られた積層体を3.5cm×4.0cmにカットして、23℃/50%RHの恒温恒湿の条件下、24時間状態調整した後、測定サンプルを得た。測定サンプルを下側が凸側になるように平面上に静置し、平面から測定サンプルの4つの角部までの高さをそれぞれデジタル寸法測定装置LS−7600(KEYENCE社製)を用いて計測し、得られた4点の値の平均値を反り量とした。
<3官能A(アクリレート)モノマー>
トリメチロールプロパントリアクリレート(「A−TMPT」、新中村化学工業(株)製)
<4官能A(アクリレート)モノマー>
ペンタエリスリトールテトラアクリレート(「A−TMMT」、新中村化学工業(株)製)
<6官能A(アクリレート)モノマー>
ジペンタエリスリトールヘキサアクリレート(「A−DPH」、新中村化学工業(株)製)
<8官能A(アクリレート)モノマー>
トリペンタエリスリトールオクタアクリレート(「A−TPE−H−NS」、新中村化学工業(株)製)
3,4−エポキシシクロヘキシルメチル 3,4−エポキシシクロヘキサンカルボキシレート(「セロキサイド(登録商標)2021P」、ダイセル化学(株)製)
3−エチル−3{[(3−エチルオキセタン−3−イル)メトキシ]メチル}オキセタン(「OXT−221」、東亜合成(株)製)
キシリレンビスオキセタンの混合物(キシリレン骨格の繰り返し単位数が1、2又は3の混合物)(「OXT−121」、東亜合成(株)製)
3,4−エポキシシクロヘキシルメチルメタクリレート(「サイクロマー(登録商標)M100」、ダイセル化学(株)製)
シクロヘキサンジメタノールジビニルエーテル(SIGMA−ALDRICH社製)
アクリロイル修飾シリカ粒子(「PGM−AC−2140Y」、日産化学(株)製、粒子径10〜15nm)
ヨードニウム(4−メチルフェニル)[4−(2−メチルプロピル)フェニル]−ヘキサフルオロホスフェートとプロピレンカーボネートとの3:1(質量比)の混合物(「IRGACURE(登録商標) 250」、BASFジャパン(株)製)
<ラジカル重合開始剤>
1−ヒドロキシ−シクロヘキシル−フェニル−ケトン(「IRGACURE 184」、BASFジャパン(株)製)
シリコーン系レベリング剤(「BYK(登録商標)−307」、ビックケミー・ジャパン(株)製)
Claims (18)
- 3官能(メタ)アクリレートモノマー、4官能(メタ)アクリレートモノマー及び8官能(メタ)アクリレートモノマーからなる群から選択される少なくとも2種を含む多官能(メタ)アクリレートモノマー(A)と、カチオン重合性モノマー(B)とを含有する硬化性組成物であって、3官能(メタ)アクリレートモノマー、4官能(メタ)アクリレートモノマー及び8官能(メタ)アクリレートモノマーの総質量は、多官能(メタ)アクリレートモノマー(A)100質量部に対して、50質量部以上である、硬化性組成物。
- カチオン重合性モノマー(B)は、1以上のエポキシ基及び/又は1以上のオキセタニル基を有する環状エーテル化合物(B−1)を含む、請求項1に記載の硬化性組成物。
- 環状エーテル化合物(B−1)は、2以上のエポキシ基及び/又は2以上のオキセタニル基を有するビス環状エーテル化合物(B−1−1)を含む、請求項2に記載の硬化性組成物。
- カチオン重合性モノマー(B)はビニルオキシ化合物(B−2)をさらに含む、請求項1〜3のいずれかに記載の硬化性組成物。
- 硬化性組成物100質量部に対して、多官能(メタ)アクリレートモノマー(A)の含有量は5〜80質量部であり、環状エーテル化合物(B−1)の含有量は5〜80質量部であり、ビニルオキシ化合物(B−2)の含有量は3〜60質量部である、請求項4に記載の硬化性組成物。
- ビニルオキシ化合物(B−2)の含有量は、多官能(メタ)アクリレートモノマー(A)及びカチオン重合性モノマー(B)の総量100質量部に対して、3〜50質量部である、請求項4又は5に記載の硬化性組成物。
- 環状エーテル化合物(B−1)は、1以上のラジカル重合性官能基を有するラジカル重合性環状エーテル化合物(B−1−2)を含む、請求項2〜6のいずれかに記載の硬化性組成物。
- 硬化性組成物100質量部に対して、多官能(メタ)アクリレートモノマー(A)の含有量は5〜50質量部であり、ビス環状エーテル化合物(B−1−1)の含有量は3〜30質量部であり、ラジカル重合性環状エーテル化合物(B−1−2)の含有量は5〜40質量部である、請求項7に記載の硬化性組成物。
- ラジカル重合性環状エーテル化合物(B−1−2)の含有量は、ビス環状エーテル化合物(B−1−1)1質量部に対して、0.1〜10質量部である、請求項7又は8に記載の硬化性組成物。
- ラジカル重合開始剤(C)及びカチオン重合開始剤(D)をさらに含む、請求項1〜9のいずれかに記載の硬化性組成物。
- ラジカル重合開始剤(C)の含有量は、多官能(メタ)アクリレートモノマー(A)100質量部に対して、1〜15質量部であり、カチオン重合開始剤(D)の含有量は、カチオン重合性モノマー(B)100質量部に対して、1〜15質量部である、請求項10に記載の硬化性組成物。
- 無機粒子をさらに含む、請求項1〜11のいずれかに記載の硬化性組成物。
- 無機粒子が反応性シリカ粒子である場合、反応性シリカ粒子の含有量は、硬化性組成物の質量に対して、1〜70質量%である、請求項12に記載の硬化性組成物。
- 請求項1〜13のいずれかに記載の硬化性組成物を硬化させてなる硬化膜。
- 請求項14に記載の硬化膜が、基材フィルムの少なくとも一方の面に積層された、積層体。
- 基材フィルムはポリイミド系高分子を含んでなる、請求項15に記載の積層体。
- 酸素透過度は、800cc/(m2・24h・atm)以下である、請求項15又は16に記載の積層体。
- 請求項15〜17のいずれかに記載の積層体を含む、フレキシブルディスプレイ。
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Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002287356A (ja) * | 2001-03-28 | 2002-10-03 | Nippon Paint Co Ltd | フォトソルダーレジスト組成物 |
JP2003147017A (ja) * | 2001-02-23 | 2003-05-21 | Fuji Photo Film Co Ltd | 硬化性組成物、それを用いたハードコート処理物品及び画像表示装置 |
JP2012047787A (ja) * | 2010-08-24 | 2012-03-08 | Daicel Corp | 体積ホログラム記録用感光性組成物および媒体製造法 |
JP2014043506A (ja) * | 2012-08-27 | 2014-03-13 | Toyo Ink Sc Holdings Co Ltd | 樹脂組成物、ならびにそれを用いた塗膜 |
JP2014051601A (ja) * | 2012-09-07 | 2014-03-20 | Nippon Shokubai Co Ltd | 光学用成形体 |
JP2015166474A (ja) * | 2010-10-29 | 2015-09-24 | 株式会社クラレ | メタクリル樹脂組成物及び樹脂改質剤並びに成形体 |
JP2016068497A (ja) * | 2014-09-30 | 2016-05-09 | 富士フイルム株式会社 | ハードコートフィルム、ハードコートフィルムの製造方法、偏光板、及び液晶表示装置 |
JP2021080460A (ja) * | 2021-01-28 | 2021-05-27 | 日東電工株式会社 | 活性エネルギー線硬化型接着剤組成物、積層偏光フィルムおよびその製造方法、積層光学フィルムおよび画像表示装置 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009202456A (ja) | 2008-02-28 | 2009-09-10 | Toray Ind Inc | 積層シート |
WO2016171024A1 (ja) * | 2015-04-21 | 2016-10-27 | 株式会社ダイセル | ハードコート層形成用樹脂組成物及びその硬化物 |
-
2018
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Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003147017A (ja) * | 2001-02-23 | 2003-05-21 | Fuji Photo Film Co Ltd | 硬化性組成物、それを用いたハードコート処理物品及び画像表示装置 |
JP2002287356A (ja) * | 2001-03-28 | 2002-10-03 | Nippon Paint Co Ltd | フォトソルダーレジスト組成物 |
JP2012047787A (ja) * | 2010-08-24 | 2012-03-08 | Daicel Corp | 体積ホログラム記録用感光性組成物および媒体製造法 |
JP2015166474A (ja) * | 2010-10-29 | 2015-09-24 | 株式会社クラレ | メタクリル樹脂組成物及び樹脂改質剤並びに成形体 |
JP2014043506A (ja) * | 2012-08-27 | 2014-03-13 | Toyo Ink Sc Holdings Co Ltd | 樹脂組成物、ならびにそれを用いた塗膜 |
JP2014051601A (ja) * | 2012-09-07 | 2014-03-20 | Nippon Shokubai Co Ltd | 光学用成形体 |
JP2016068497A (ja) * | 2014-09-30 | 2016-05-09 | 富士フイルム株式会社 | ハードコートフィルム、ハードコートフィルムの製造方法、偏光板、及び液晶表示装置 |
JP2021080460A (ja) * | 2021-01-28 | 2021-05-27 | 日東電工株式会社 | 活性エネルギー線硬化型接着剤組成物、積層偏光フィルムおよびその製造方法、積層光学フィルムおよび画像表示装置 |
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CN111065669A (zh) | 2020-04-24 |
TWI786185B (zh) | 2022-12-11 |
KR20200052948A (ko) | 2020-05-15 |
WO2019054412A1 (ja) | 2019-03-21 |
CN111065669B (zh) | 2022-07-15 |
TW201925367A (zh) | 2019-07-01 |
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