JP6910347B2 - 硬化性組成物、硬化物の製造方法、およびその硬化物 - Google Patents
硬化性組成物、硬化物の製造方法、およびその硬化物 Download PDFInfo
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- JP6910347B2 JP6910347B2 JP2018509444A JP2018509444A JP6910347B2 JP 6910347 B2 JP6910347 B2 JP 6910347B2 JP 2018509444 A JP2018509444 A JP 2018509444A JP 2018509444 A JP2018509444 A JP 2018509444A JP 6910347 B2 JP6910347 B2 JP 6910347B2
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- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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Description
(式中、Xは、炭素原子数1〜7のアルキル基、炭素原子数1〜7のアルコキシ基、炭素原子数6〜12のアリール基、炭素原子数6〜12のアリールオキシ基もしくは炭素原子数6〜10の脂環式炭化水素基、またはこれらの基中の水素原子が、エポキシ基、オキセタン基、水酸基およびカルボキシル基からなる群より選択される1種以上の基で置換されたものである)で表される単量体から得られるポリマー、下記式(II)、
(式中、R1は、水素原子、メチル基またはハロゲン原子を表し、X’は、炭素原子数1〜7のアルキル基、炭素原子数6〜12のアリール基もしくは炭素原子数6〜10の脂環式炭化水素基、またはこれらの基中の水素原子が、エポキシ基、オキセタン基、水酸基およびカルボキシル基からなる群より選択される1種以上の基で置換されたものである)で表される単量体から得られるポリマー、前記式(I)で表される単量体から選択される二種以上の単量体から得られるポリマー、前記式(II)で表される単量体から選択される二種以上の単量体からな得られるポリマー、並びに前記式(I)で表される単量体および前記式(II)で表される単量体から得られるポリマーからなる群より選択される重量平均分子量1,000〜30,000であって、エポキシ基、オキセタン基、水酸基およびカルボキシル基からなる群より選択される1種以上の基を有するポリマー(E)と、を含有し、
前記カチオン重合性成分(A)が、分子量200以上の多価アルコールのグリシジル化物、または多価アルコールアルキレンオキサイド付加物のグリシジル化物(A1)と、オキセタン化合物(A2)と、を必須成分とし、
前記ラジカル重合性成分(C)が、エポキシ基およびエチレン性不飽和基を有する化合物(C1)、または炭素原子数2〜20であるアルコールのアクリル酸エステルあるいは炭素原子数2〜20であるアルコールのメタクリル酸エステル(C2)を必須成分とし、かつ、
前記分子量200以上の多価アルコールのグリシジル化物、または多価アルコールアルキレンオキサイド付加物のグリシジル化物(A1)における多価アルコールが、縮合環を有する多価アルコールであることを特徴とするものである。ここで、重量平均分子量とは、テトラヒドロフラン(THF)溶媒中、GPCにより測定し、スチレン換算で求めた重量平均分子量をいう。
本発明の硬化性組成物は、カチオン重合性成分(A)と、カチオン重合開始剤(B)と、ラジカル重合性成分(C)と、ラジカル重合開始剤(D)と、下記式(I)で表される単量体から得られるポリマー、下記式(II)で表される単量体から得られるポリマー、下記式(I)で表される単量体から選択される二種以上の単量体から得られるポリマー、下記式(II)で表される単量体から選択される二種以上の単量体からな得られるポリマー、並びに下記式(I)で表される単量体および下記式(II)で表される単量体から得られるポリマーからなる群より選択される重量平均分子量1,000〜30,000であるポリマー(E)と、を含有する。本発明の硬化性組成物においては、カチオン重合性成分(A)は、分子量200以上の多価アルコールのグリシジル化物、または多価アルコールアルキレンオキサイド付加物のグリシジル化物(A1)と、オキセタン化合物(A2)と、を必須成分とし、ラジカル重合性成分(C)は、エポキシ基およびエチレン性不飽和基を有する化合物(C1)、または炭素原子数2〜20であるアルコールのアクリル酸エステルあるいは炭素原子数2〜20であるアルコールのメタクリル酸エステル(C2)を必須成分とする。
[A]r+[B]r−
で表される陽イオンと陰イオンの塩を挙げることができる。
[(R2)aQ]r+
で表すことができる。
[LYb]r−で
表すことができる。
[LYb−1(OH)]r−
で表される構造のものも好ましく用いることができる。L,Y,bは上記と同様である。また、その他用いることのできる陰イオンとしては、過塩素酸イオン(ClO4)−、トリフルオロメチル亜硫酸イオン(CF3SO3)−、フルオロスルホン酸イオン(FSO3)−、トルエンスルホン酸陰イオン、トリニトロベンゼンスルホン酸陰イオン、カンファースルフォネート、ノナフロロブタンスルフォネート、ヘキサデカフロロオクタンスルフォネート、テトラアリールボレート、テトラキス(ペンタフルオロフェニル)ボレート等を挙げることができる。
下記の[表1]〜[表3]に示す配合で各成分を十分に混合して、各々実施例1〜14、参考例1および比較例1〜3の硬化性組成物を得た。なお、実施例および比較例の単位は質量部である。
化合物(A1−1):アデカレジンEP−4088L((株)ADEKA社製)
化合物(A1−2):1,6−ヘキサンジオールジグリシジルエーテル
化合物(A1−3):ネオペンチルグリコールジグリシジルエーテル
化合物(A2−1):アロンオキセタンOXT−221(東亞合成(株)社製)
化合物(A3−1):セロキサイド2021P(脂環式エポキシ:(株)ダイセル社製)
化合物B−1:下記式(9)で表される化合物および下記式(10)で表される化合物の混合物のプロピレンカーボネート50%溶液
化合物(C2−1):1,6−ヘキサンジオールジアクリレート
化合物(C2−2):トリシクロデカンジメタノールジアクリレート
化合物(C2−3):エトキシ化イソシアヌル酸トリアクリレート
化合物(C2−4):テトラヒドロフルフリルアクリレート
化合物(D−1):イルガキュア184(BASF社製)
化合物(E−1):メチルメタクリレート75質量部とグリシジルメタクリレート25質量部の共重合体(重量平均分子量7,000)
化合物(E−2):メチルメタクリレート35質量部、スチレン35質量部及びグリシジルメタクリレート30質量部の共重合体(重量平均分子量8,000)
得られた実施例1〜14、参考例1および比較例1〜3の各硬化性組成物を、それぞれをポリエチレンテレフタレート(PET)フィルム上に、バーコーターで30μmの厚さに塗布し、メタルハライドランプを用いて3000mJ/cm2のエネルギーを照射した。24時間後にフィルムから接着剤硬化物を取り出し、(株)日立ハイテクサイエンス製の粘弾性測定装置(DMA7100)を用いTgおよび80℃における弾性率を測定した。
上記で得られた実施例1〜14、参考例1および比較例1〜3の硬化性組成物を、一枚のコロナ処理PMMAフィルム(住友化学(株)社製:テクノロイ125S001)にそれぞれ塗布した後、もう一枚のコロナ放電処理を施したCOP(シクロオレフィンポリマー、日本ゼオン(株)社製:品番ゼオノアフィルム14−060)フィルムとラミネーターを用いて貼り合わせ、無電極紫外光ランプを用いて1000mJ/cm2に相当する光をCOPフィルム越しに照射して接着して試験片を得た。得られた試験片につき、90度ピール試験を行った。
Claims (7)
- カチオン重合性成分(A)と、カチオン重合開始剤(B)と、ラジカル重合性成分(C)と、ラジカル重合開始剤(D)と、下記式(I)、
(式中、Xは、炭素原子数1〜7のアルキル基、炭素原子数1〜7のアルコキシ基、炭素原子数6〜12のアリール基、炭素原子数6〜12のアリールオキシ基もしくは炭素原子数6〜10の脂環式炭化水素基、またはこれらの基中の水素原子が、エポキシ基、オキセタン基、水酸基およびカルボキシル基からなる群より選択される1種以上の基で置換されたものである)で表される単量体から得られるポリマー、下記式(II)、
(式中、R1は、水素原子、メチル基またはハロゲン原子を表し、X’は、炭素原子数1〜7のアルキル基、炭素原子数6〜12のアリール基もしくは炭素原子数6〜10の脂環式炭化水素基、またはこれらの基中の水素原子が、エポキシ基、オキセタン基、水酸基およびカルボキシル基からなる群より選択される1種以上の基で置換されたものである)で表される単量体から得られるポリマー、前記式(I)で表される単量体から選択される二種以上の単量体から得られるポリマー、前記式(II)で表される単量体から選択される二種以上の単量体からな得られるポリマー、並びに前記式(I)で表される単量体および前記式(II)で表される単量体から得られるポリマーからなる群より選択される重量平均分子量1,000〜30,000であって、エポキシ基、オキセタン基、水酸基およびカルボキシル基からなる群より選択される1種以上の基を有するポリマー(E)と、を含有し、
前記カチオン重合性成分(A)が、分子量200以上の多価アルコールのグリシジル化物、または多価アルコールアルキレンオキサイド付加物のグリシジル化物(A1)と、オキセタン化合物(A2)と、を必須成分とし、
前記ラジカル重合性成分(C)が、エポキシ基およびエチレン性不飽和基を有する化合物(C1)、または炭素原子数2〜20であるアルコールのアクリル酸エステルあるいは炭素原子数2〜20であるアルコールのメタクリル酸エステル(C2)を必須成分とし、かつ、
前記分子量200以上の多価アルコールのグリシジル化物、または多価アルコールアルキレンオキサイド付加物のグリシジル化物(A1)における多価アルコールが、縮合環を有する多価アルコールであることを特徴とする硬化性組成物。 - 前記カチオン重合性成分(A)として、さらに脂環式エポキシ化合物(A3)を含有する請求項1記載の硬化性組成物。
- 前記ポリマー(E)が、前記式(I)で表される単量体および前記式(II)で表される単量体から得られるポリマーであって、前記式(I)中のXが、炭素原子数6〜12のアリール基であり、前記式(II)中のX’が、炭素原子数1〜7のアルキル基であって、前記アルキル基がエポキシ基で置換されている請求項1記載の硬化性組成物。
- 前記カチオン重合性成分(A)が30〜70質量部、前記カチオン重合開始剤(B)が0.001〜10質量部、前記ラジカル重合性成分(C)が30〜60質量部、前記ラジカル重合開始剤(D)が1〜10質量部、前記ポリマー(E)が1〜20質量部であり、前記カチオン重合性成分(A)と、前記ラジカル重合性成分(C)と、前記ポリマー(E)と、の合計が100質量部である請求項1記載の硬化性組成物。
- 請求項1〜4のうちいずれか一項記載の硬化性組成物に、活性エネルギー線を照射することを特徴とする硬化性組成物の硬化方法。
- 請求項1〜4のうちいずれか一項記載の硬化性組成物を、加熱することを特徴とする硬化性組成物の硬化方法。
- 請求項1〜4のうちいずれか一項記載の硬化性組成物の硬化物であることを特徴とする硬化物。
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TW201809020A (zh) | 2018-03-16 |
WO2017170881A9 (ja) | 2021-04-01 |
WO2017170881A1 (ja) | 2017-10-05 |
KR20180132071A (ko) | 2018-12-11 |
CN108779321A (zh) | 2018-11-09 |
KR102356563B1 (ko) | 2022-01-26 |
TWI727026B (zh) | 2021-05-11 |
CN108779321B (zh) | 2021-04-02 |
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