JP5016224B2 - 組成物及びそれを用いた部材の仮固定方法 - Google Patents
組成物及びそれを用いた部材の仮固定方法 Download PDFInfo
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- JP5016224B2 JP5016224B2 JP2006006962A JP2006006962A JP5016224B2 JP 5016224 B2 JP5016224 B2 JP 5016224B2 JP 2006006962 A JP2006006962 A JP 2006006962A JP 2006006962 A JP2006006962 A JP 2006006962A JP 5016224 B2 JP5016224 B2 JP 5016224B2
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- Prior art keywords
- meth
- acrylate
- composition
- adhesive
- mass
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- 239000000203 mixture Substances 0.000 title claims description 52
- 238000000034 method Methods 0.000 title claims description 18
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- 239000000853 adhesive Substances 0.000 claims description 53
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- 238000006116 polymerization reaction Methods 0.000 claims description 12
- 239000003495 polar organic solvent Substances 0.000 claims description 9
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- 239000003112 inhibitor Substances 0.000 claims description 6
- 239000003999 initiator Substances 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 2
- 238000007598 dipping method Methods 0.000 claims 1
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- 238000012360 testing method Methods 0.000 description 23
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- 238000009835 boiling Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
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- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
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- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
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- IAXXETNIOYFMLW-GYSYKLTISA-N [(1r,3r,4r)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@@]2(C)[C@H](OC(=O)C(=C)C)C[C@@H]1C2(C)C IAXXETNIOYFMLW-GYSYKLTISA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
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- 238000003491 array Methods 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
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- NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
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- QWQFVUQPHUKAMY-UHFFFAOYSA-N 1,2-diphenyl-2-propoxyethanone Chemical compound C=1C=CC=CC=1C(OCCC)C(=O)C1=CC=CC=C1 QWQFVUQPHUKAMY-UHFFFAOYSA-N 0.000 description 1
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- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
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- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 1
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- TZAMQIAPGYOUKF-UHFFFAOYSA-N diethoxyphosphoryl(phenyl)methanone Chemical compound CCOP(=O)(OCC)C(=O)C1=CC=CC=C1 TZAMQIAPGYOUKF-UHFFFAOYSA-N 0.000 description 1
- XVKKIGYVKWTOKG-UHFFFAOYSA-N diphenylphosphoryl(phenyl)methanone Chemical compound C=1C=CC=CC=1P(=O)(C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 XVKKIGYVKWTOKG-UHFFFAOYSA-N 0.000 description 1
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 1
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- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
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- MHCLJIVVJQQNKQ-UHFFFAOYSA-N ethyl carbamate;2-methylprop-2-enoic acid Chemical compound CCOC(N)=O.CC(=C)C(O)=O MHCLJIVVJQQNKQ-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
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- 229940119545 isobornyl methacrylate Drugs 0.000 description 1
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- 150000002576 ketones Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- REEZZSHJLXOIHL-UHFFFAOYSA-N octanoyl chloride Chemical compound CCCCCCCC(Cl)=O REEZZSHJLXOIHL-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 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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- 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
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- 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
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Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
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(登録商標)ガラス(25mm×25mm×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、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。
BDK:ベンジルジメチルケタール(チバ スペシャルティ ケミカルズ社製IRGACURE651)
M101A:フェノールエチレンオキサイド2モル変成アクリレート(東亜合成社製アロニックスM−101A)
BZ:ベンジルメタクリレート(共栄社化学社製ライトエステルBZ)
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)
デンカPVA B−17(電気化学工業社製、鹸化度88mol%、重合度1700)
デンカPVA B−20(電気化学工業社製、鹸化度88mol%、重合度2000)
デンカPVA K−05(電気化学工業社製、鹸化度98mol%、重合度500)
2−HEMA:2-ヒドロキシエチルメタクリレート
MTEGMA:メトシキテトラエチレングリコールモノメタクリレート(新中村化学社製NKエステルM−90G)
Claims (6)
- (A)疎水性である多官能(メタ)アクリレート、(B)疎水性である単官能(メタ)アクリレート、(C)ポリビニルアルコール、(D)光重合開始剤を含有し、(A)を1〜50質量部、(B)を5〜95質量部、(C)を0.1〜20質量部、(D)を0.1〜20質量部含有することを特徴とする光硬化性組成物。
- 更に、重合禁止剤を含有すること特徴とする請求項1記載の光硬化性組成物。
- 更に、極性有機溶媒を含有すること特徴とする請求項1乃至2のいずれか一項に記載の光硬化性組成物。
- 更に、(A)〜(D)に溶解しない粒状物質を含有すること特徴とする請求項1乃至3のいずれか一項に記載の光硬化性組成物。
- 請求項1乃至4のいずれか一項に記載の光硬化性組成物からなることを特徴とする光硬化性接着剤。
- 請求項1乃至5のいずれか一項に記載の光硬化性組成物を用いて、部材を接着仮固定し、該仮固定された部材を加工後、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仮固定方法。
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Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
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KR101660056B1 (ko) * | 2008-07-22 | 2016-09-30 | 덴카 주식회사 | 부재의 가고정·박리 방법 및 그에 적합한 가고정용 접착제 |
JP5570207B2 (ja) * | 2009-12-25 | 2014-08-13 | 日本合成化学工業株式会社 | 偏光板用接着剤、それを用いた偏光板 |
JP5674332B2 (ja) * | 2010-04-14 | 2015-02-25 | 電気化学工業株式会社 | 接着剤組成物及びそれを用いた部材の仮固定方法 |
JP5596205B2 (ja) * | 2013-04-17 | 2014-09-24 | 電気化学工業株式会社 | 部材の搬送方法 |
CN111690373B (zh) * | 2013-10-11 | 2022-09-02 | 株式会社大赛璐 | 粘接剂 |
WO2017061416A1 (ja) * | 2015-10-09 | 2017-04-13 | 株式会社ダイセル | 接着剤 |
CN107501477B (zh) * | 2016-06-14 | 2019-11-05 | 珠海赛纳打印科技股份有限公司 | 一种用于3d喷墨打印的光固化材料及制备和打印方法 |
WO2019004431A1 (ja) * | 2017-06-29 | 2019-01-03 | 株式会社Adeka | 接着剤組成物 |
AU2020270003A1 (en) | 2019-05-03 | 2020-12-03 | Johnson & Johnson Surgical Vision, Inc. | High reactive index, high abbe compositions |
US11708440B2 (en) | 2019-05-03 | 2023-07-25 | Johnson & Johnson Surgical Vision, Inc. | High refractive index, high Abbe compositions |
WO2022090857A1 (en) | 2020-10-29 | 2022-05-05 | Johnson & Johnson Surgical Vision, Inc. | Compositions with high refractive index and abbe number |
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JP2808290B2 (ja) * | 1988-11-22 | 1998-10-08 | 株式会社スリーボンド | 仮固定用接着剤組成物 |
JPH03160077A (ja) * | 1989-11-17 | 1991-07-10 | Denki Kagaku Kogyo Kk | チップ部品仮固形用接着剤組成物 |
JP2903333B2 (ja) * | 1990-05-19 | 1999-06-07 | 株式会社スリーボンド | 仮固定用接着剤組成物 |
JPH10130309A (ja) * | 1996-10-25 | 1998-05-19 | Toagosei Co Ltd | 仮固定用光硬化性組成物及び物品の製造方法 |
JP4601757B2 (ja) * | 2000-02-17 | 2010-12-22 | 株式会社 アーデル | 仮固定用接着剤組成物及びその使用方法 |
JP4326747B2 (ja) * | 2002-04-23 | 2009-09-09 | 株式会社 アーデル | 仮固定用接着剤を用いる加工方法、及び仮固定用接着剤の剥離方法 |
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