JP5408836B2 - 組成物及びそれを用いる部材の仮固定剥離方法 - Google Patents
組成物及びそれを用いる部材の仮固定剥離方法 Download PDFInfo
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- JP5408836B2 JP5408836B2 JP2006141023A JP2006141023A JP5408836B2 JP 5408836 B2 JP5408836 B2 JP 5408836B2 JP 2006141023 A JP2006141023 A JP 2006141023A JP 2006141023 A JP2006141023 A JP 2006141023A JP 5408836 B2 JP5408836 B2 JP 5408836B2
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
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- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
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- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 230000001235 sensitizing effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
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- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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Description
IBX:イソボルニルメタクリレート(共栄社化学社製ライトエステルIB−X)15質量部、合計100質量部、(C)極性有機溶媒(D)光重合開始剤としてベンジルジメチルケタール(以下「BDK」と略す)5質量部、重合禁止剤として2,2−メチレン−ビス(4−メチル−6−ターシャリーブチルフェノール)(以下「MDP」と略す)0.1質量部添加して組成物を作成した。得られた組成物を使用して、以下に示す評価方法にて引張せん断接着強さの測定及び剥離試験を行った。それらの結果を表1に示す。
引張せん断接着強さ:JIS K 6850に従い測定した。具体的には被着材として耐熱パイレックスガラス(25mm×25mm×厚さ2.0mm)を用いて、接着部位を直径8mmとして、作成した組成物にて、表面粗さRMax15μm、RMax20μm、RMax30μm、RMax50μm、無処理の2枚の耐熱パイレックス(登録商標)ガラスを貼り合わせ、無電極放電ランプを使用したフュージョン社製硬化装置により、365nmの波長の積算光量2000mJ/cm2の条件にて硬化させ、引張せん断接着強さ試験片を作成した。作成した試験片は、万能試験機を使用して、温度23℃、湿度50%の環境下、引張速度10mm/minで引張せん断接着強さを測定した。
QM:ジシクロペンテニルオキシエチルメタクリレート(ローム&ハース社製QM−657)
TO−1429:2−(1,2−シクロヘキサカルボキシイミド)エチルアクリレート(東亜合成社製TO−1429、以下「TO−1429」と略す)
表3に示す種類の原材料を表3に示す組成で使用したこと以外は実施例1同様にして組成物を作成した。得られた組成物について、実施例1と同様に引張せん断接着強さの測定及び剥離試験を行った。それらの結果を表3に示す。
表面粗さRMax15μm、RMax20μm、RMax30μm、RMax50μm、無処理の条件とした。
Claims (8)
- (A)及び(B)の合計量100質量部中、(A)1,2−ポリブタジエン末端ウレタン(メタ)アクリレート及びジシクロペンタニルジ(メタ)アクリレートからなる群のうちの1種以上である多官能(メタ)アクリレート5〜70質量部、(B)2−(1,2−シクロヘキサカルボキシイミド)エチルアクリレート、フェノール(エチレンオキサイド2モル変性)アクリレート、ジシクロペンテニロキシエチル(メタ)アクリレート、ベンジルメタクリレート及びイソボルニル(メタ)アクリレートからなる群のうちの1種以上である単官能(メタ)アクリレート30〜95質量部、(A)及び(B)成分の合計量100質量部に対して、(C)メタノール、エタノール、イソプロピルアルコール、n−ブタノールからなる群から選ばれる1種以上0.1〜10質量部、(D)光重合開始剤0.1〜20質量部を含有することを特徴とする組成物。
- (A)及び(B)がいずれも疎水性であること特徴とする請求項1記載の組成物。
- 重合禁止剤を含有することを特徴とする請求項1又は請求項2記載の組成物。
- 部材を接着仮固定し、該仮固定された部材を加工後、波長700nm以下の光を透過する材質から成る物品に波長700nm以下の光を再照射後、該加工された部材を温水に浸漬して、前記組成物の硬化体を取り外すことを特徴とする部材の前記仮固定方法に使用してなる請求項1乃至3のいずれか1項に記載の仮固定用組成物。
- 請求項1乃至4のいずれか1項に記載の組成物からなることを特徴とする接着剤組成物。
- 請求項1乃至5のいずれか1項に記載の組成物を用いて、部材を接着仮固定し、該仮固定された部材を加工後、波長700nm以下の光を透過する材質から成る物品に波長700nm以下の光を再照射後、該加工された部材を90℃以下の温水に浸漬して、前記組成物の硬化体を取り外すことを特徴とする部材の前記仮固定方法。
- 部材を接着仮固定する際に基材を用い、前記硬化体が前記基材に残ることを特徴とする請求項6記載の部材の仮固定方法。
- 基材の組成物に対する面の表面粗さ(RMax)が10μm〜50μmであり、しかも、部材の組成物に対する面の表面粗さ(RMax)よりも10μm以上大きいことを特徴とする請求項7記載の部材の仮固定方法。
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