JP2007523974A - 熱安定性のカチオン光硬化性組成物 - Google Patents
熱安定性のカチオン光硬化性組成物 Download PDFInfo
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- JP2007523974A JP2007523974A JP2006550160A JP2006550160A JP2007523974A JP 2007523974 A JP2007523974 A JP 2007523974A JP 2006550160 A JP2006550160 A JP 2006550160A JP 2006550160 A JP2006550160 A JP 2006550160A JP 2007523974 A JP2007523974 A JP 2007523974A
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- Prior art keywords
- alkyl
- group
- phenyl
- acid
- phenyliodonium
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- 239000000203 mixture Substances 0.000 title claims abstract description 119
- 125000002091 cationic group Chemical group 0.000 title claims abstract description 15
- 150000001875 compounds Chemical class 0.000 claims abstract description 56
- 239000003381 stabilizer Substances 0.000 claims abstract description 56
- 150000003839 salts Chemical class 0.000 claims abstract description 27
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000012952 cationic photoinitiator Substances 0.000 claims abstract description 11
- -1 haloalkyl sulfonate Chemical compound 0.000 claims description 195
- 125000000217 alkyl group Chemical group 0.000 claims description 66
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 35
- 238000000576 coating method Methods 0.000 claims description 30
- 229910052739 hydrogen Inorganic materials 0.000 claims description 30
- 239000002253 acid Substances 0.000 claims description 29
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 27
- 239000001257 hydrogen Substances 0.000 claims description 26
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- 125000003118 aryl group Chemical group 0.000 claims description 21
- 125000001931 aliphatic group Chemical group 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 18
- 150000002431 hydrogen Chemical class 0.000 claims description 17
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- 229910052717 sulfur Inorganic materials 0.000 claims description 12
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- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims description 4
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- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 3
- 241000723346 Cinnamomum camphora Species 0.000 claims description 3
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- 125000002993 cycloalkylene group Chemical group 0.000 claims description 3
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- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 2
- BUZHLYBJNNZTPL-UHFFFAOYSA-N pentane-1,2,4,5-tetracarboxylic acid Chemical compound OC(=O)CC(C(O)=O)CC(C(O)=O)CC(O)=O BUZHLYBJNNZTPL-UHFFFAOYSA-N 0.000 claims description 2
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- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 125000003696 stearoyl group Chemical group O=C([*])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
- 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
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229940073455 tetraethylammonium hydroxide Drugs 0.000 description 1
- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 239000005028 tinplate Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 125000000297 undecanoyl group Chemical group O=C([*])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
- 125000002948 undecyl 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])[H] 0.000 description 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- INRGAWUQFOBNKL-UHFFFAOYSA-N {4-[(Vinyloxy)methyl]cyclohexyl}methanol Chemical compound OCC1CCC(COC=C)CC1 INRGAWUQFOBNKL-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- 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
- G03F7/0037—Production of three-dimensional images
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/24—Di-epoxy compounds carbocyclic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/68—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- 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
- G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Epoxy Resins (AREA)
- Polymerisation Methods In General (AREA)
- Polymerization Catalysts (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Paints Or Removers (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US53975204P | 2004-01-27 | 2004-01-27 | |
| PCT/EP2005/050157 WO2005070989A2 (en) | 2004-01-27 | 2005-01-17 | Thermally stable cationic photocurable compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007523974A true JP2007523974A (ja) | 2007-08-23 |
| JP2007523974A5 JP2007523974A5 (enExample) | 2008-02-28 |
Family
ID=34807263
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006550160A Pending JP2007523974A (ja) | 2004-01-27 | 2005-01-17 | 熱安定性のカチオン光硬化性組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US20050165141A1 (enExample) |
| EP (1) | EP1709099A2 (enExample) |
| JP (1) | JP2007523974A (enExample) |
| KR (1) | KR20070004649A (enExample) |
| TW (1) | TW200538481A (enExample) |
| WO (1) | WO2005070989A2 (enExample) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006316206A (ja) * | 2005-05-16 | 2006-11-24 | Fujifilm Holdings Corp | インク組成物、インクジェット記録方法、印刷物、平版印刷版の製造方法、及び、平版印刷版 |
| JP2007186566A (ja) * | 2006-01-12 | 2007-07-26 | Fujifilm Corp | インク組成物、インクジェット記録方法、印刷物、平版印刷版の製造方法、及び、平版印刷版 |
| JP2007238777A (ja) * | 2006-03-09 | 2007-09-20 | Fujifilm Corp | インク組成物、インクジェット記録方法、印刷物、平版印刷版の製造方法、及び、平版印刷版 |
| JP2008248150A (ja) * | 2007-03-30 | 2008-10-16 | Fujifilm Corp | インク組成物、インクジェット記録方法、印刷物、平版印刷版の作製方法及び平版印刷版 |
| JP2009120628A (ja) * | 2007-11-12 | 2009-06-04 | Fujifilm Corp | インク組成物、インクカートリッジ、インクジェット記録方法及び印刷物 |
| JP2009144057A (ja) * | 2007-12-14 | 2009-07-02 | Fujifilm Corp | インクジェット記録用インク組成物、及び、インクジェット記録方法 |
| JP2011090147A (ja) * | 2009-10-22 | 2011-05-06 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
| WO2017110744A1 (ja) * | 2015-12-25 | 2017-06-29 | コニカミノルタ株式会社 | 水系インクおよびインクジェット捺染方法 |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005029188A1 (ja) * | 2003-09-24 | 2005-03-31 | Hitachi Chemical Co., Ltd. | 感光性エレメント、レジストパターンの形成方法及びプリント配線板の製造方法 |
| US20060172230A1 (en) | 2005-02-02 | 2006-08-03 | Dsm Ip Assets B.V. | Method and composition for reducing waste in photo-imaging applications |
| US9975302B2 (en) * | 2005-12-21 | 2018-05-22 | Carl Zeiss Vision Austalia Holdings Limited | Primer layer coating compositions |
| JP4929722B2 (ja) * | 2006-01-12 | 2012-05-09 | 日立化成工業株式会社 | 光硬化型ナノプリント用レジスト材及びパターン形成法 |
| US7696260B2 (en) | 2006-03-30 | 2010-04-13 | Dsm Ip Assets B.V. | Cationic compositions and methods of making and using the same |
| US8067643B2 (en) * | 2006-04-13 | 2011-11-29 | Basf Se | Sulphonium salt initiators |
| ES2603838T3 (es) * | 2006-10-24 | 2017-03-01 | Basf Se | Composiciones fotocurables catiónicas térmicamente estables |
| US20090115060A1 (en) | 2007-11-01 | 2009-05-07 | Infineon Technologies Ag | Integrated circuit device and method |
| EP2242774B2 (fr) * | 2008-02-15 | 2018-09-26 | Catalyse | Composition auto-reparante. materiaux a auto-reparation procedes d' autoreparation et applications |
| EP2428842A1 (en) * | 2010-09-14 | 2012-03-14 | Rohm and Haas Electronic Materials LLC | Photoresists comprising multi-amide component |
| JP2013065011A (ja) * | 2011-09-09 | 2013-04-11 | Rohm & Haas Electronic Materials Llc | マルチアミド成分を含むフォトレジスト |
| FR2996227A1 (fr) | 2012-10-02 | 2014-04-04 | Bluestar Silicones France | Composition de resine organique reticulable/polymerisable par voie cationique comprenant un borate de iodonium et degageant une odeur acceptable |
| WO2014053714A1 (fr) | 2012-10-02 | 2014-04-10 | Bluestar Silicones France Sas | Composition reticulable/polymerisable par voie cationique comprenant un borate de iodonium et degageant une odeur acceptable |
| GB201508178D0 (en) * | 2015-05-13 | 2015-06-24 | Photocentric Ltd | Method for making an object |
| JP6286396B2 (ja) * | 2015-08-13 | 2018-02-28 | 株式会社ダイセル | 硬化性組成物及びその硬化物 |
| JP2018534392A (ja) * | 2015-10-02 | 2018-11-22 | スリーエム イノベイティブ プロパティズ カンパニー | 化学線開始型エポキシ接着剤及びそれから製造された物品 |
| US20180033609A1 (en) * | 2016-07-28 | 2018-02-01 | QMAT, Inc. | Removal of non-cleaved/non-transferred material from donor substrate |
| CN110408300B (zh) * | 2018-04-26 | 2021-06-25 | 中钞特种防伪科技有限公司 | 100%固含量的保护性紫外光固化涂料组合物及其涂层和应用 |
| US11846886B2 (en) * | 2020-11-23 | 2023-12-19 | International Business Machines Corporation | Photoacid generator |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004051922A (ja) * | 2002-07-24 | 2004-02-19 | Konica Minolta Holdings Inc | 活性光線硬化型インク、画像形成方法、印刷物、記録装置 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3888752A (en) * | 1973-11-28 | 1975-06-10 | Gen Motors Corp | Phosphite ester antioxidants in radiation cured styrene butadiene elastomers |
| US4138255A (en) * | 1977-06-27 | 1979-02-06 | General Electric Company | Photo-curing method for epoxy resin using group VIa onium salt |
| US4299938A (en) * | 1979-06-19 | 1981-11-10 | Ciba-Geigy Corporation | Photopolymerizable and thermally polymerizable compositions |
| US4339567A (en) * | 1980-03-07 | 1982-07-13 | Ciba-Geigy Corporation | Photopolymerization by means of sulphoxonium salts |
| US4404355A (en) * | 1980-10-08 | 1983-09-13 | Ciba-Geigy Corporation | Heat curable epoxy resin compositions |
| JPH02169619A (ja) * | 1988-12-23 | 1990-06-29 | Toshiba Corp | 封止用エポキシ樹脂組成物及びこれを用いてなる光半導体素子 |
| US5352712A (en) * | 1989-05-11 | 1994-10-04 | Borden, Inc. | Ultraviolet radiation-curable coatings for optical fibers |
| KR910012820A (ko) * | 1989-12-20 | 1991-08-08 | 로레인 제이. 프란시스 | 황산화제 배합물을 함유하는 유리 라디칼 중합성 조성물 |
| JP2868672B2 (ja) * | 1992-08-31 | 1999-03-10 | 沖電気工業株式会社 | シリコーン樹脂組成物及びこれを用いたケイ酸ガラス薄膜の製造方法 |
| TW269017B (enExample) * | 1992-12-21 | 1996-01-21 | Ciba Geigy Ag | |
| EP0683200B1 (en) * | 1994-05-19 | 2001-09-26 | General Electric Company | Stabilizer composition |
| US5554644A (en) * | 1994-06-08 | 1996-09-10 | Warner-Lambert Company | Tachykinin (NK2) antagonists |
| US5468895A (en) * | 1994-10-19 | 1995-11-21 | General Electric Company | Amine stabilized amorphous phosphite |
| TW460509B (en) * | 1996-07-12 | 2001-10-21 | Ciba Sc Holding Ag | Curing process for cationically photocurable formulations |
| WO1998014416A1 (en) * | 1996-10-04 | 1998-04-09 | Betzdearborn Inc. | Compositions and methods for inhibiting vinyl aromatic monomer polymerization |
| US6281311B1 (en) * | 1997-03-31 | 2001-08-28 | Pmd Holdings Corp. | Controlled free radical polymerization process |
| JPH11175402A (ja) * | 1997-12-10 | 1999-07-02 | Fujitsu Ltd | カード型記憶媒体及びカード型記憶媒体のアクセス制御方法並びにカード型記憶媒体用アクセス制御プログラムを記録したコンピュータ読み取り可能な記録媒体 |
| US6444733B1 (en) * | 1999-03-01 | 2002-09-03 | Ciba Specialty Chemicals Corporation | Stabilizer combination for the rotomolding process |
| SG98433A1 (en) * | 1999-12-21 | 2003-09-19 | Ciba Sc Holding Ag | Iodonium salts as latent acid donors |
| US6372350B1 (en) * | 2000-06-16 | 2002-04-16 | Loctite Corporation | Curable epoxy-based compositions |
| US6750267B2 (en) * | 2001-12-24 | 2004-06-15 | University Of Massachusetts Lowell | Radiation-curable polymeric composition |
| JP4219820B2 (ja) * | 2002-04-03 | 2009-02-04 | 協和発酵ケミカル株式会社 | ポリアルケニルエーテル系樹脂 |
| US20040087687A1 (en) * | 2002-10-30 | 2004-05-06 | Vantico A&T Us Inc. | Photocurable compositions with phosphite viscosity stabilizers |
| US20040191674A1 (en) * | 2003-03-28 | 2004-09-30 | Yukio Hanamoto | Chemical amplification resist composition |
-
2005
- 2005-01-17 WO PCT/EP2005/050157 patent/WO2005070989A2/en not_active Ceased
- 2005-01-17 KR KR1020067017287A patent/KR20070004649A/ko not_active Ceased
- 2005-01-17 JP JP2006550160A patent/JP2007523974A/ja active Pending
- 2005-01-17 EP EP05701522A patent/EP1709099A2/en not_active Withdrawn
- 2005-01-21 US US11/040,716 patent/US20050165141A1/en not_active Abandoned
- 2005-01-26 TW TW094102282A patent/TW200538481A/zh unknown
-
2007
- 2007-05-14 US US11/803,274 patent/US20070225395A1/en not_active Abandoned
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004051922A (ja) * | 2002-07-24 | 2004-02-19 | Konica Minolta Holdings Inc | 活性光線硬化型インク、画像形成方法、印刷物、記録装置 |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006316206A (ja) * | 2005-05-16 | 2006-11-24 | Fujifilm Holdings Corp | インク組成物、インクジェット記録方法、印刷物、平版印刷版の製造方法、及び、平版印刷版 |
| JP2007186566A (ja) * | 2006-01-12 | 2007-07-26 | Fujifilm Corp | インク組成物、インクジェット記録方法、印刷物、平版印刷版の製造方法、及び、平版印刷版 |
| JP2007238777A (ja) * | 2006-03-09 | 2007-09-20 | Fujifilm Corp | インク組成物、インクジェット記録方法、印刷物、平版印刷版の製造方法、及び、平版印刷版 |
| JP2008248150A (ja) * | 2007-03-30 | 2008-10-16 | Fujifilm Corp | インク組成物、インクジェット記録方法、印刷物、平版印刷版の作製方法及び平版印刷版 |
| JP2009120628A (ja) * | 2007-11-12 | 2009-06-04 | Fujifilm Corp | インク組成物、インクカートリッジ、インクジェット記録方法及び印刷物 |
| JP2009144057A (ja) * | 2007-12-14 | 2009-07-02 | Fujifilm Corp | インクジェット記録用インク組成物、及び、インクジェット記録方法 |
| JP2011090147A (ja) * | 2009-10-22 | 2011-05-06 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
| WO2017110744A1 (ja) * | 2015-12-25 | 2017-06-29 | コニカミノルタ株式会社 | 水系インクおよびインクジェット捺染方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2005070989A3 (en) | 2005-12-01 |
| US20070225395A1 (en) | 2007-09-27 |
| KR20070004649A (ko) | 2007-01-09 |
| US20050165141A1 (en) | 2005-07-28 |
| WO2005070989A2 (en) | 2005-08-04 |
| TW200538481A (en) | 2005-12-01 |
| EP1709099A2 (en) | 2006-10-11 |
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