JP2000516983A - フルオロポリマー―エポキシ樹脂半相互貫入網目構造組成物 - Google Patents
フルオロポリマー―エポキシ樹脂半相互貫入網目構造組成物Info
- Publication number
- JP2000516983A JP2000516983A JP10511654A JP51165498A JP2000516983A JP 2000516983 A JP2000516983 A JP 2000516983A JP 10511654 A JP10511654 A JP 10511654A JP 51165498 A JP51165498 A JP 51165498A JP 2000516983 A JP2000516983 A JP 2000516983A
- Authority
- JP
- Japan
- Prior art keywords
- fluoropolymer
- epoxy resin
- composition
- poly
- semi
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
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- 239000012784 inorganic fiber Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- WDAXFOBOLVPGLV-UHFFFAOYSA-N isobutyric acid ethyl ester Natural products CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229920001427 mPEG Polymers 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000012968 metallocene catalyst Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 229940078552 o-xylene Drugs 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
- 235000019645 odor Nutrition 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 125000000913 palmityl 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])[H] 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 229920009441 perflouroethylene propylene Polymers 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 229920006295 polythiol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 238000011417 postcuring Methods 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- UMFCIIBZHQXRCJ-NSCUHMNNSA-N trans-anol Chemical compound C\C=C\C1=CC=C(O)C=C1 UMFCIIBZHQXRCJ-NSCUHMNNSA-N 0.000 description 1
- 150000003624 transition metals Chemical group 0.000 description 1
- 125000005409 triarylsulfonium group Chemical group 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 229920003249 vinylidene fluoride hexafluoropropylene elastomer Polymers 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or 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 a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or 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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on homopolymers or 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 a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or 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 a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/12—Coating compositions based on homopolymers or 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 a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/04—Polymer mixtures characterised by other features containing interpenetrating networks
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2456696P | 1996-08-26 | 1996-08-26 | |
| US78247697A | 1997-01-10 | 1997-01-10 | |
| US08/782,476 | 1997-01-10 | ||
| US60/024,566 | 1997-01-10 | ||
| PCT/US1997/013561 WO1998008906A1 (en) | 1996-08-26 | 1997-08-01 | Fluoropolymer-epoxy resin semi-interpenetrating network composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000516983A true JP2000516983A (ja) | 2000-12-19 |
| JP2000516983A5 JP2000516983A5 (enrdf_load_stackoverflow) | 2005-04-07 |
Family
ID=26698595
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10511654A Pending JP2000516983A (ja) | 1996-08-26 | 1997-08-01 | フルオロポリマー―エポキシ樹脂半相互貫入網目構造組成物 |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0920482A1 (enrdf_load_stackoverflow) |
| JP (1) | JP2000516983A (enrdf_load_stackoverflow) |
| KR (1) | KR100499992B1 (enrdf_load_stackoverflow) |
| AU (1) | AU3904397A (enrdf_load_stackoverflow) |
| WO (1) | WO1998008906A1 (enrdf_load_stackoverflow) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004511641A (ja) * | 2000-10-14 | 2004-04-15 | ローベルト ボツシユ ゲゼルシヤフト ミツト ベシユレンクテル ハフツング | シリコーン変性された１成分系シールコンパウンド |
| JP2007224183A (ja) * | 2006-02-24 | 2007-09-06 | Toyo Ink Mfg Co Ltd | 感エネルギー線酸硬化性組成物 |
| JP2009511297A (ja) * | 2005-10-11 | 2009-03-19 | シーアールシー フォー アドバンスト コンポジット ストラクチャーズ リミテッド | 乾燥強化繊維の結合方法 |
| JP2009522414A (ja) * | 2005-12-30 | 2009-06-11 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 光起電性モジュールに有用なフルオロポリマーコーティングされたフィルム |
| JP2011517724A (ja) * | 2008-04-14 | 2011-06-16 | ダウ グローバル テクノロジーズ エル エルエルシー | エポキシ系組成物の反応発熱を低下させるための吸熱相転移を受ける充填剤の使用 |
| JP2017171714A (ja) * | 2016-03-22 | 2017-09-28 | 富士電機株式会社 | 樹脂組成物 |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6518362B1 (en) | 1998-02-18 | 2003-02-11 | 3M Innovative Properties Company | Melt blending polyphenylene ether, polystyrene and curable epoxy |
| US6235850B1 (en) | 1998-12-11 | 2001-05-22 | 3M Immovative Properties Company | Epoxy/acrylic terpolymer self-fixturing adhesive |
| US6294270B1 (en) | 1998-12-23 | 2001-09-25 | 3M Innovative Properties Company | Electronic circuit device comprising an epoxy-modified aromatic vinyl-conjugated diene block copolymer |
| JP3987243B2 (ja) * | 1999-09-10 | 2007-10-03 | スリーエム イノベイティブ プロパティズ カンパニー | 接着シートおよび被覆用接着シート |
| US6359166B1 (en) | 1999-10-08 | 2002-03-19 | 3M Innovative Properties Company | Oxalate ester blocked phenols |
| US6387508B1 (en) | 2000-09-14 | 2002-05-14 | 3M Innovative Properties Company | Metal bonding film compositions |
| DE10148909A1 (de) * | 2001-09-26 | 2003-04-30 | Inst Polymerforschung Dresden | Bauteile, Halbzeuge und Profile, ganz oder teilweise aus Kunststoff |
| DE102006015499B4 (de) * | 2006-03-31 | 2009-08-27 | Radpro International Gmbh | Thermolumineszenzdosimeter |
| DE102006057142A1 (de) * | 2006-12-01 | 2008-06-05 | Henkel Kgaa | Metallverbindungen als Initiatoren |
| RU2462493C1 (ru) * | 2011-04-05 | 2012-09-27 | Российская Федерация, от имени которой выступает Министерство промышленности и торговли Российской Федерации (Минпромторг России) | Состав для барьерного покрытия |
| KR101857297B1 (ko) | 2011-12-27 | 2018-05-14 | 주식회사 케이씨씨 | 트리플루오라이드기를 함유한 전착 도료용 수지, 그 제조방법 및 그를 포함하는 전착 도료 조성물 |
| EP2861202B1 (en) | 2012-06-18 | 2018-07-18 | 3M Innovative Properties Company | Powder composition for air polishing the surface of hard dental tissue |
| EP2742897A1 (en) | 2012-12-17 | 2014-06-18 | 3M Innovative Properties Company | Nozzle head, hand piece and powder jet device for applying a dental material |
| EP2742898A1 (en) | 2012-12-17 | 2014-06-18 | 3M Innovative Properties Company | Powder jet device for dispensing a dental material |
| US9662180B2 (en) | 2012-12-17 | 2017-05-30 | 3M Innovative Properties Company | Device for dispensing a dental material with locking mechanism |
| US9169393B2 (en) | 2013-07-25 | 2015-10-27 | 3M Innovative Properties Company | Anticorrosion coatings |
| GB201421373D0 (en) | 2014-12-02 | 2015-01-14 | Cytec Ind Inc | Modified amine curing agents, their preparation and use in curable compositions |
| TWI627192B (zh) * | 2015-03-13 | 2018-06-21 | 村田製作所股份有限公司 | Atomic layer deposition inhibiting material |
| CN112384546B (zh) * | 2018-10-17 | 2024-01-16 | 东洋纺株式会社 | 导热性树脂组合物 |
| CN113549169B (zh) * | 2021-06-15 | 2022-12-06 | 南京工业大学 | 一种苯基芴胺类聚合物空穴传输材料及其制备方法和应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1031406A (en) * | 1963-11-05 | 1966-06-02 | Acheson Ind Inc | Low friction materials |
| US4169187A (en) * | 1977-04-01 | 1979-09-25 | E. I. Du Pont De Nemours And Company | Powder coating composition of a mixture of epoxy resins |
| EP0084771A3 (en) * | 1982-01-22 | 1984-02-22 | Allied Corporation | Method of making a powdered primer coating composition |
| DE3602800A1 (de) * | 1985-06-07 | 1986-12-11 | agru Alois Gruber + Sohn oHG, Bad Hall | Verfahren zur oberflaechenmodifizierung von formkoerpern aus polyvinylidenfluorid |
| JPS6241218A (ja) * | 1985-08-19 | 1987-02-23 | Mitsubishi Electric Corp | 半導体封止用エポキシ樹脂組成物 |
| BR8802120A (pt) * | 1987-05-18 | 1988-12-06 | Standard Oil Co Ohio | Processo de encapsular artigo |
| JP2803055B2 (ja) * | 1989-12-04 | 1998-09-24 | 東芝ケミカル株式会社 | 成形用耐熱性樹脂組成物 |
| JPH0462557A (ja) * | 1990-07-02 | 1992-02-27 | Canon Inc | 感光性組成物 |
| JPH05186757A (ja) * | 1992-01-10 | 1993-07-27 | Sumitomo Metal Ind Ltd | ラミネート金属板用接着剤組成物 |
-
1997
- 1997-08-01 EP EP97936354A patent/EP0920482A1/en not_active Withdrawn
- 1997-08-01 KR KR10-1999-7001503A patent/KR100499992B1/ko not_active Expired - Fee Related
- 1997-08-01 AU AU39043/97A patent/AU3904397A/en not_active Abandoned
- 1997-08-01 WO PCT/US1997/013561 patent/WO1998008906A1/en active IP Right Grant
- 1997-08-01 JP JP10511654A patent/JP2000516983A/ja active Pending
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004511641A (ja) * | 2000-10-14 | 2004-04-15 | ローベルト ボツシユ ゲゼルシヤフト ミツト ベシユレンクテル ハフツング | シリコーン変性された１成分系シールコンパウンド |
| JP2009511297A (ja) * | 2005-10-11 | 2009-03-19 | シーアールシー フォー アドバンスト コンポジット ストラクチャーズ リミテッド | 乾燥強化繊維の結合方法 |
| JP2009522414A (ja) * | 2005-12-30 | 2009-06-11 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 光起電性モジュールに有用なフルオロポリマーコーティングされたフィルム |
| JP2007224183A (ja) * | 2006-02-24 | 2007-09-06 | Toyo Ink Mfg Co Ltd | 感エネルギー線酸硬化性組成物 |
| JP2011517724A (ja) * | 2008-04-14 | 2011-06-16 | ダウ グローバル テクノロジーズ エル エルエルシー | エポキシ系組成物の反応発熱を低下させるための吸熱相転移を受ける充填剤の使用 |
| JP2017171714A (ja) * | 2016-03-22 | 2017-09-28 | 富士電機株式会社 | 樹脂組成物 |
| US10597526B2 (en) | 2016-03-22 | 2020-03-24 | Fuji Electric Co., Ltd. | Resin composition |
| JP7221579B2 (ja) | 2016-03-22 | 2023-02-14 | 富士電機株式会社 | 樹脂組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20000035830A (ko) | 2000-06-26 |
| WO1998008906A1 (en) | 1998-03-05 |
| EP0920482A1 (en) | 1999-06-09 |
| AU3904397A (en) | 1998-03-19 |
| KR100499992B1 (ko) | 2005-07-12 |
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