JP4828775B2 - 組成物硬化方法及びエネルギー重合性組成物 - Google Patents
組成物硬化方法及びエネルギー重合性組成物 Download PDFInfo
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- JP4828775B2 JP4828775B2 JP2002505878A JP2002505878A JP4828775B2 JP 4828775 B2 JP4828775 B2 JP 4828775B2 JP 2002505878 A JP2002505878 A JP 2002505878A JP 2002505878 A JP2002505878 A JP 2002505878A JP 4828775 B2 JP4828775 B2 JP 4828775B2
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- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 229960003424 phenylacetic acid Drugs 0.000 description 1
- 239000003279 phenylacetic acid Substances 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 238000006303 photolysis reaction Methods 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 230000015843 photosynthesis, light reaction Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001921 poly-methyl-phenyl-siloxane Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920000307 polymer substrate Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 229940107700 pyruvic acid Drugs 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003254 radicals Chemical group 0.000 description 1
- 238000010107 reaction injection moulding Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- MBDNRNMVTZADMQ-UHFFFAOYSA-N sulfolene Chemical compound O=S1(=O)CC=CC1 MBDNRNMVTZADMQ-UHFFFAOYSA-N 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical group 0.000 description 1
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- AEOGRWUNSVGMMJ-UHFFFAOYSA-N trimethylgermane Chemical compound C[GeH](C)C AEOGRWUNSVGMMJ-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical class C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 1
- BPLUKJNHPBNVQL-UHFFFAOYSA-N triphenylarsine Chemical compound C1=CC=CC=C1[As](C=1C=CC=CC=1)C1=CC=CC=C1 BPLUKJNHPBNVQL-UHFFFAOYSA-N 0.000 description 1
- HVYVMSPIJIWUNA-UHFFFAOYSA-N triphenylstibine Chemical compound C1=CC=CC=C1[Sb](C=1C=CC=CC=1)C1=CC=CC=C1 HVYVMSPIJIWUNA-UHFFFAOYSA-N 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/08—Saturated oxiranes
- C08G65/10—Saturated oxiranes characterised by the catalysts used
- C08G65/105—Onium compounds
-
- 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)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Paints Or Removers (AREA)
- Polymerization Catalysts (AREA)
- Epoxy Resins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/603,548 | 2000-06-26 | ||
| US09/603,548 US6635689B1 (en) | 2000-06-26 | 2000-06-26 | Accelerators for cationic polymerization catalyzed by iron-based catalysts |
| PCT/US2000/029855 WO2002000757A1 (en) | 2000-06-26 | 2000-10-31 | Accelerators for cationic polymerization catalyzed by iron-based catalysts |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004502002A JP2004502002A (ja) | 2004-01-22 |
| JP2004502002A5 JP2004502002A5 (enExample) | 2007-12-20 |
| JP4828775B2 true JP4828775B2 (ja) | 2011-11-30 |
Family
ID=24415906
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002505878A Expired - Fee Related JP4828775B2 (ja) | 2000-06-26 | 2000-10-31 | 組成物硬化方法及びエネルギー重合性組成物 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US6635689B1 (enExample) |
| EP (1) | EP1297049B1 (enExample) |
| JP (1) | JP4828775B2 (enExample) |
| KR (1) | KR100723897B1 (enExample) |
| AT (1) | ATE285429T1 (enExample) |
| AU (1) | AU2001214438A1 (enExample) |
| DE (1) | DE60016980T2 (enExample) |
| WO (1) | WO2002000757A1 (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6777460B2 (en) * | 2002-12-23 | 2004-08-17 | 3M Innovative Properties Company | Curing agents for cationically curable compositions |
| US20050250929A1 (en) * | 2004-05-10 | 2005-11-10 | 3M Innovative Properties Company | Ferrocenium-derived catalyst for cationically polymerizable monomers |
| GB2432160A (en) * | 2005-11-14 | 2007-05-16 | Sun Chemical Ltd | Energy curable cyclic carbonate compositions |
| US20070256995A1 (en) * | 2006-05-08 | 2007-11-08 | Northrop Grumman Corporation | Expandable modular rack design |
| US7651830B2 (en) * | 2007-06-01 | 2010-01-26 | 3M Innovative Properties Company | Patterned photoacid etching and articles therefrom |
| US20090288770A1 (en) * | 2008-05-23 | 2009-11-26 | Loctite (R&D) Limited | Surface-promoted cure of one-part cationically curable compositions |
| US20090288771A1 (en) * | 2008-05-23 | 2009-11-26 | Loctite (R&D) Limited | Surface-promoted cure of one-part radically curable compositions |
| US8399099B1 (en) * | 2008-05-23 | 2013-03-19 | Henkel Ireland Limited | Coating compositions |
| CN102301277B (zh) | 2008-12-05 | 2013-07-17 | 3M创新有限公司 | 使用非线性热聚合的三维制品 |
| WO2010094634A1 (en) | 2009-02-17 | 2010-08-26 | Loctite (R & D) Limited | Cationically curable compositions and a primer therefor |
| US8389758B2 (en) | 2009-06-05 | 2013-03-05 | 3M Innovative Properties Company | Benzoxazine-thiol adducts |
| US8383706B2 (en) | 2009-06-05 | 2013-02-26 | 3M Innovative Properties Company | Benzoxazine-thiol adducts |
| US8920019B2 (en) * | 2009-07-17 | 2014-12-30 | Vita-Mix Corporation | Method and apparatus for making food products |
| US9371477B2 (en) | 2012-12-27 | 2016-06-21 | 3M Innovative Properties Company | Polymerizable composition including a benzoxazine and an acid-forming peroxide catalyst, article, and method |
| US9896599B2 (en) | 2013-04-30 | 2018-02-20 | 3M Innovative Properties Company | Process for preparing poly(benzoxazines) |
| CN105612198B (zh) | 2013-10-16 | 2017-10-13 | 3M创新有限公司 | 苯并噁嗪聚合 |
| JP6723238B2 (ja) * | 2014-11-20 | 2020-07-15 | ダウ グローバル テクノロジーズ エルエルシー | 促進剤組成物 |
| EP3307807A1 (en) | 2015-06-09 | 2018-04-18 | 3M Innovative Properties Company | Ammonium salt catalyzed benzoxazine polymerization |
| JP2022127332A (ja) * | 2021-02-19 | 2022-08-31 | デクセリアルズ株式会社 | カチオン硬化剤及びその製造方法、並びにカチオン硬化性組成物 |
| US20250020996A1 (en) * | 2023-07-07 | 2025-01-16 | Feng Lu | Organotin photoresists and method of developing photolithography pattern |
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| JPS60184518A (ja) * | 1984-02-10 | 1985-09-20 | チバ‐ガイギー アーゲー | 硬化可能な組成物及びその使用法 |
| JPH0269516A (ja) * | 1988-08-04 | 1990-03-08 | Ciba Geigy Ag | カチオン重合性物質用の硬化剤結合物 |
| JPH08511570A (ja) * | 1993-06-16 | 1996-12-03 | ミネソタ マイニング アンド マニュファクチャリング カンパニー | 導電性接着剤組成物 |
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| US3907706A (en) | 1973-07-06 | 1975-09-23 | Minnesota Mining & Mfg | Latent catalyst systems for cationically polymerizable materials |
| US4297458A (en) | 1980-07-14 | 1981-10-27 | General Electric Company | Curable epoxy resins |
| US4442197A (en) | 1982-01-11 | 1984-04-10 | General Electric Company | Photocurable compositions |
| DE3369398D1 (en) | 1982-05-19 | 1987-02-26 | Ciba Geigy Ag | Curable compositions containing metallocen complexes, activated primers obtained therefrom and their use |
| DE3366408D1 (en) | 1982-05-19 | 1986-10-30 | Ciba Geigy Ag | Photopolymerisation with organometal salts |
| US4518676A (en) | 1982-09-18 | 1985-05-21 | Ciba Geigy Corporation | Photopolymerizable compositions containing diaryliodosyl salts |
| US5191101A (en) | 1982-11-22 | 1993-03-02 | Minnesota Mining And Manufacturing Company | Energy polymerizable compositions containing organometallic initiators |
| US5089536A (en) | 1982-11-22 | 1992-02-18 | Minnesota Mining And Manufacturing Company | Energy polmerizable compositions containing organometallic initiators |
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| EP0152377B1 (de) | 1984-02-10 | 1987-12-09 | Ciba-Geigy Ag | Härtbare Zusammensetzung und deren Verwendung |
| US4503211A (en) | 1984-05-31 | 1985-03-05 | Minnesota Mining And Manufacturing Co. | Epoxy resin curing agent, process and composition |
| JPS6136302A (ja) | 1984-07-30 | 1986-02-21 | Toshiba Corp | 光重合性組成物 |
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| JPH0699652B2 (ja) | 1986-01-28 | 1994-12-07 | 関西ペイント株式会社 | 複層膜形成用カチオン電着塗料組成物 |
| US4788235A (en) | 1987-11-23 | 1988-11-29 | Minnesota Mining And Manufacturing Company | Phosphite modified epoxy resin |
| DE3814876A1 (de) | 1988-05-02 | 1989-11-16 | Henkel Kgaa | Lichtinduziert dunkelhaertende klebstoffe |
| EP0388837B1 (de) * | 1989-03-21 | 1996-04-10 | Ciba-Geigy Ag | Initiatoren für kationisch polymerisierbare Materialien |
| CA2082258A1 (en) | 1990-04-23 | 1991-10-24 | Michael C. Palazzotto | Energy curable cationically and free-radically polymerizable pressure sensitive compositions |
| US5059701A (en) | 1990-09-20 | 1991-10-22 | Minnesota Mining And Manufacturing Company | Methods for preparation of cyclopentadienyliron (II) arenes |
| JPH05202132A (ja) | 1991-11-29 | 1993-08-10 | Tosoh Corp | ポリプロピレンの製造方法 |
| EP0623151B1 (en) | 1992-01-22 | 1995-11-08 | Minnesota Mining And Manufacturing Company | Photoactivatable, thermally curable epoxy compositions |
| US5252694A (en) | 1992-01-22 | 1993-10-12 | Minnesota Mining And Manufacturing Company | Energy-polymerization adhesive, coating, film and process for making the same |
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| US7575653B2 (en) | 1993-04-15 | 2009-08-18 | 3M Innovative Properties Company | Melt-flowable materials and method of sealing surfaces |
| US5494943A (en) | 1993-06-16 | 1996-02-27 | Minnesota Mining And Manufacturing Company | Stabilized cationically-curable compositions |
| US5744557A (en) | 1993-06-16 | 1998-04-28 | Minnesota Mining And Manufacturing Company | Energy-curable cyanate/ethylenically unsaturated compositions |
| DE4340949A1 (de) | 1993-12-01 | 1995-06-08 | Thera Ges Fuer Patente | Lichtinitiiert kationisch härtende Epoxidmasse und ihre Verwendung |
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2000
- 2000-06-26 US US09/603,548 patent/US6635689B1/en not_active Expired - Lifetime
- 2000-10-31 DE DE60016980T patent/DE60016980T2/de not_active Expired - Lifetime
- 2000-10-31 WO PCT/US2000/029855 patent/WO2002000757A1/en not_active Ceased
- 2000-10-31 AU AU2001214438A patent/AU2001214438A1/en not_active Abandoned
- 2000-10-31 JP JP2002505878A patent/JP4828775B2/ja not_active Expired - Fee Related
- 2000-10-31 EP EP00976699A patent/EP1297049B1/en not_active Expired - Lifetime
- 2000-10-31 AT AT00976699T patent/ATE285429T1/de not_active IP Right Cessation
- 2000-10-31 KR KR1020027017622A patent/KR100723897B1/ko not_active Expired - Fee Related
-
2003
- 2003-09-02 US US10/653,669 patent/US6906156B2/en not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60184518A (ja) * | 1984-02-10 | 1985-09-20 | チバ‐ガイギー アーゲー | 硬化可能な組成物及びその使用法 |
| JPH0269516A (ja) * | 1988-08-04 | 1990-03-08 | Ciba Geigy Ag | カチオン重合性物質用の硬化剤結合物 |
| JPH08511570A (ja) * | 1993-06-16 | 1996-12-03 | ミネソタ マイニング アンド マニュファクチャリング カンパニー | 導電性接着剤組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE60016980D1 (de) | 2005-01-27 |
| WO2002000757A1 (en) | 2002-01-03 |
| EP1297049A1 (en) | 2003-04-02 |
| US20040048943A1 (en) | 2004-03-11 |
| DE60016980T2 (de) | 2005-12-15 |
| US6635689B1 (en) | 2003-10-21 |
| US6906156B2 (en) | 2005-06-14 |
| AU2001214438A1 (en) | 2002-01-08 |
| JP2004502002A (ja) | 2004-01-22 |
| KR20030017563A (ko) | 2003-03-03 |
| ATE285429T1 (de) | 2005-01-15 |
| EP1297049B1 (en) | 2004-12-22 |
| KR100723897B1 (ko) | 2007-06-04 |
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