CN110036343B - 水溶性组合物、图案形成剂、使用了它们的固化物的制造方法和固化物 - Google Patents
水溶性组合物、图案形成剂、使用了它们的固化物的制造方法和固化物 Download PDFInfo
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- CN110036343B CN110036343B CN201780072576.0A CN201780072576A CN110036343B CN 110036343 B CN110036343 B CN 110036343B CN 201780072576 A CN201780072576 A CN 201780072576A CN 110036343 B CN110036343 B CN 110036343B
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Classifications
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- C—CHEMISTRY; METALLURGY
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F216/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an alcohol radical
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- C08F16/12—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F18/02—Esters of monocarboxylic acids
- C08F18/04—Vinyl esters
- C08F18/08—Vinyl acetate
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/28—Condensation with aldehydes or ketones
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- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
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- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
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- G—PHYSICS
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- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
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- G—PHYSICS
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- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
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- Materials For Photolithography (AREA)
- Compositions Of Macromolecular Compounds (AREA)
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WO2018230564A1 (ja) * | 2017-06-16 | 2018-12-20 | 株式会社Adeka | コーティング組成物 |
WO2019004431A1 (ja) * | 2017-06-29 | 2019-01-03 | 株式会社Adeka | 接着剤組成物 |
JP2020084156A (ja) * | 2018-11-30 | 2020-06-04 | 株式会社Adeka | 組成物、これを含有するバリア膜形成用組成物、これらの硬化物、それからなるガスバリア膜および硬化物の製造方法 |
CN112432931B (zh) * | 2020-11-09 | 2023-04-07 | 合肥乐凯科技产业有限公司 | 一种薄膜涂层固化度的测试方法 |
CN114797513B (zh) * | 2022-04-11 | 2024-01-26 | 云南磷化集团有限公司 | 一种实验室试剂瓶标签保护膜的制备方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08269130A (ja) * | 1995-03-31 | 1996-10-15 | Oji Kako Kk | 陰極線管蛍光面作製用感光性樹脂材料 |
US6136507A (en) * | 1998-03-12 | 2000-10-24 | Goo Chemical Co., Ltd. | Photosensitive resin composition and photoresist ink for manufacturing printed wiring boards |
JP2001133976A (ja) * | 1999-11-05 | 2001-05-18 | Murakami:Kk | 感光性樹脂組成物及びそれを用いたスクリーン印刷用版並びにスクリーン印刷用版の製造方法 |
CN104854155A (zh) * | 2012-12-13 | 2015-08-19 | 株式会社Adeka | 光固化性组合物 |
JP2016139130A (ja) * | 2015-01-23 | 2016-08-04 | 東レ株式会社 | 感光性樹脂組成物、感光性樹脂積層体、および感光性樹脂印刷版原版 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4077927B2 (ja) | 1998-04-27 | 2008-04-23 | 住友化学株式会社 | 樹脂組成物および積層体 |
US20070082965A1 (en) * | 2002-11-28 | 2007-04-12 | Jsr Corporation | Photocuring resin composition, medical device using same and method for manufacturing same |
JP4570406B2 (ja) * | 2004-07-09 | 2010-10-27 | 株式会社カネカ | ポリ乳酸系樹脂発泡粒子およびその成形体 |
JP2007025723A (ja) * | 2006-10-19 | 2007-02-01 | Kunihiro Ichimura | 感活性エネルギー線樹脂組成物、感活性エネルギー線樹脂フィルム及び該フィルムを用いるパターン形成方法 |
JP4943968B2 (ja) | 2007-08-06 | 2012-05-30 | 三菱製紙株式会社 | 感熱記録材料 |
ATE538185T1 (de) * | 2007-08-22 | 2012-01-15 | Datalase Ltd | Laserempfindliche beschichtungszusammensetzung |
JP5791415B2 (ja) | 2011-07-28 | 2015-10-07 | 日本合成化学工業株式会社 | 耐変色性ポリビニルアルコール系樹脂架橋物の製造方法 |
JP6123714B2 (ja) * | 2014-03-19 | 2017-05-10 | 富士ゼロックス株式会社 | 電子写真感光体、プロセスカートリッジ、及び画像形成装置 |
WO2016136752A1 (ja) * | 2015-02-26 | 2016-09-01 | 株式会社Adeka | パターン形成方法およびこれを用いて製造した電子デバイス |
JP6545506B2 (ja) * | 2015-03-31 | 2019-07-17 | 株式会社Adeka | 重合体及び光硬化性組成物 |
-
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08269130A (ja) * | 1995-03-31 | 1996-10-15 | Oji Kako Kk | 陰極線管蛍光面作製用感光性樹脂材料 |
US6136507A (en) * | 1998-03-12 | 2000-10-24 | Goo Chemical Co., Ltd. | Photosensitive resin composition and photoresist ink for manufacturing printed wiring boards |
JP2001133976A (ja) * | 1999-11-05 | 2001-05-18 | Murakami:Kk | 感光性樹脂組成物及びそれを用いたスクリーン印刷用版並びにスクリーン印刷用版の製造方法 |
CN104854155A (zh) * | 2012-12-13 | 2015-08-19 | 株式会社Adeka | 光固化性组合物 |
JP2016139130A (ja) * | 2015-01-23 | 2016-08-04 | 東レ株式会社 | 感光性樹脂組成物、感光性樹脂積層体、および感光性樹脂印刷版原版 |
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JP7096772B2 (ja) | 2022-07-06 |
WO2018117138A1 (ja) | 2018-06-28 |
KR20190098746A (ko) | 2019-08-22 |
TWI753072B (zh) | 2022-01-21 |
CN110036343A (zh) | 2019-07-19 |
KR102478397B1 (ko) | 2022-12-15 |
JPWO2018117138A1 (ja) | 2019-10-31 |
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