KR20100017848A - 플루오르화 계면활성제의 수성 조성물 및 그의 사용 방법 - Google Patents
플루오르화 계면활성제의 수성 조성물 및 그의 사용 방법 Download PDFInfo
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- KR20100017848A KR20100017848A KR1020097026333A KR20097026333A KR20100017848A KR 20100017848 A KR20100017848 A KR 20100017848A KR 1020097026333 A KR1020097026333 A KR 1020097026333A KR 20097026333 A KR20097026333 A KR 20097026333A KR 20100017848 A KR20100017848 A KR 20100017848A
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- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/004—Surface-active compounds containing F
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
- C09D5/024—Emulsion paints including aerosols characterised by the additives
- C09D5/027—Dispersing agents
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/45—Anti-settling agents
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/47—Levelling agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09G—POLISHING COMPOSITIONS; SKI WAXES
- C09G1/00—Polishing compositions
- C09G1/04—Aqueous dispersions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dispersion Chemistry (AREA)
- Paints Or Removers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US93977107P | 2007-05-23 | 2007-05-23 | |
| US60/939,771 | 2007-05-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20100017848A true KR20100017848A (ko) | 2010-02-16 |
Family
ID=39674348
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097026333A Withdrawn KR20100017848A (ko) | 2007-05-23 | 2008-05-21 | 플루오르화 계면활성제의 수성 조성물 및 그의 사용 방법 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8338517B2 (enExample) |
| EP (1) | EP2155830A1 (enExample) |
| JP (1) | JP2010528159A (enExample) |
| KR (1) | KR20100017848A (enExample) |
| CN (1) | CN101679790B (enExample) |
| WO (1) | WO2008147796A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016024653A1 (ko) * | 2014-08-13 | 2016-02-18 | 주식회사 켐프 | 판상 아연분말이 혼합된 안료 분리형 수성도료 조성물 |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101679569A (zh) * | 2007-06-06 | 2010-03-24 | 3M创新有限公司 | 氟化醚组合物以及使用该组合物的方法 |
| MX2011000702A (es) * | 2008-07-18 | 2011-02-24 | 3M Innovative Properties Co | Compuestos de eter fluorados y metodos para usar los mismos. |
| WO2010080473A1 (en) | 2008-12-18 | 2010-07-15 | 3M Innovative Properties Company | Method of contacting hydrocarbon-bearing formations with fluorinated ether compositions |
| US20120053276A1 (en) * | 2010-08-31 | 2012-03-01 | Brilliant Coatings, Inc. | Surface polish and wear coating |
| US8859799B1 (en) | 2013-10-17 | 2014-10-14 | E I Du Pont De Nemours And Company | Partially fluorinated phosphates |
| CN105428508B (zh) * | 2015-12-02 | 2018-08-24 | 开发晶照明(厦门)有限公司 | 封装基板以及led倒装封装结构 |
| TW202035361A (zh) * | 2018-12-12 | 2020-10-01 | 美商3M新設資產公司 | 氟化胺氧化物界面活性劑 |
| WO2021062091A1 (en) | 2019-09-26 | 2021-04-01 | Ecolab Usa Inc. | High alkaline solvent-based degreaser and cleaner with diutan gum as a primary thickening system |
| CN113045272B (zh) * | 2021-03-23 | 2022-04-12 | 广州市长运预拌混凝土有限公司 | 一种绿色环保混凝土及其制备方法 |
Family Cites Families (166)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA761007A (en) | 1967-06-13 | E. Le Bleu Ronald | Polyfluoropolyoxa-alkyl phosphates | |
| US2713593A (en) | 1953-12-21 | 1955-07-19 | Minnesota Mining & Mfg | Fluorocarbon acids and derivatives |
| US3271341A (en) | 1961-08-07 | 1966-09-06 | Du Pont | Aqueous colloidal dispersions of polymer |
| US3492374A (en) | 1963-06-14 | 1970-01-27 | Du Pont | Polyfluoropolyoxa-alkyl phosphates |
| US3274244A (en) | 1963-06-14 | 1966-09-20 | Du Pont | Polyfluoropolyoxa-alkanamidoalkyl compounds |
| US3250808A (en) | 1963-10-31 | 1966-05-10 | Du Pont | Fluorocarbon ethers derived from hexafluoropropylene epoxide |
| US3306855A (en) | 1966-03-24 | 1967-02-28 | Du Pont | Corrosion and rust inhibited poly (hexafluoropropylene oxide) oil compositions |
| US3391099A (en) | 1966-04-25 | 1968-07-02 | Du Pont | Polymerization process |
| DE1668395C3 (de) | 1966-07-11 | 1978-06-15 | Montecatini Edison S.P.A., Mailand (Italien) | Perfluorierte Ketone und Verfahren zu deren Herstellung |
| US3451908A (en) | 1966-07-19 | 1969-06-24 | Montedison Spa | Method for preparing polyoxyperfluoromethylenic compounds |
| US3472894A (en) | 1967-03-07 | 1969-10-14 | Du Pont | Perfluoroalkyl ether bis(hydroxyalkyl) amides |
| US3553179A (en) | 1968-05-06 | 1971-01-05 | Du Pont | Acrylate-type esters of perfluoropoly-oxa-alkaneamidoalkyl alcohols and their polymers |
| US3518195A (en) | 1968-06-05 | 1970-06-30 | Du Pont | Corrosion-inhibited and stabilized perfluorinated polyether oils |
| US3589906A (en) | 1968-10-16 | 1971-06-29 | Du Pont | Photographic layers containing perfluoro compounds and coating thereof |
| US3555100A (en) | 1968-11-19 | 1971-01-12 | Du Pont | Decarbonylation of fluorinated acyl fluorides |
| US3810874A (en) | 1969-03-10 | 1974-05-14 | Minnesota Mining & Mfg | Polymers prepared from poly(perfluoro-alkylene oxide) compounds |
| US3621059A (en) | 1969-07-30 | 1971-11-16 | Du Pont | Amides of hexafluoropropylene oxide polymer acids and polyalklene oxide |
| US3644492A (en) | 1969-07-30 | 1972-02-22 | Du Pont | Esters of hexafluoropropylene oxide polymer acids and polyalkylene glycols |
| US3798265A (en) | 1969-10-22 | 1974-03-19 | Du Pont | Polyfluoroalkoxy alkyl amidocarboxylic acids and salts thereof |
| GB1352560A (en) | 1970-07-17 | 1974-05-08 | Xidex Corp | Fluorocarbon surfactants for vesicular films |
| US3839425A (en) | 1970-09-16 | 1974-10-01 | Du Pont | Perfluoroalkyletheramidoalkyl betaines and sulfobetaines |
| US3646085A (en) | 1970-09-24 | 1972-02-29 | Du Pont | Perfluoroalkyletheramidoalkyltrialkoxysilanes |
| US3721696A (en) | 1970-11-27 | 1973-03-20 | Montedison Spa | Polyoxyperfluoromethylene compounds and process of their preparation |
| US3927072A (en) | 1974-02-04 | 1975-12-16 | Pennwalt Corp | Fluorinated {62 -(alkoxy)-propionates |
| FR2286153A1 (fr) | 1974-09-24 | 1976-04-23 | Ugine Kuhlmann | Procede de polymerisation ou de copolymerisation en emulsion du fluorure de vinylidene |
| US4089804A (en) * | 1976-12-30 | 1978-05-16 | Ciba-Geigy Corporation | Method of improving fluorinated surfactants |
| US4544458A (en) | 1978-11-13 | 1985-10-01 | E. I. Du Pont De Nemours And Company | Fluorinated ion exchange polymer containing carboxylic groups, process for making same, and film and membrane thereof |
| CA1132397A (en) | 1979-02-28 | 1982-09-28 | Hendrik E. Kokelenberg | Fluorine-containing surfactants and their use in hydrophilic colloid coating compositions and light-sensitive silver halide materials |
| US4832879A (en) | 1980-03-04 | 1989-05-23 | Basf Aktiengesellchaft | Substituted 3-fluoroalkoxybenzoyl halides and their preparation |
| US4381384A (en) | 1981-08-17 | 1983-04-26 | E. I. Du Pont De Nemours And Company | Continuous polymerization process |
| US4380618A (en) | 1981-08-21 | 1983-04-19 | E. I. Du Pont De Nemours And Company | Batch polymerization process |
| US4588796A (en) | 1984-04-23 | 1986-05-13 | E. I. Du Pont De Nemours And Company | Fluoroolefin polymerization process using fluoroxy compound solution as initiator |
| US4621116A (en) | 1984-12-07 | 1986-11-04 | E. I. Du Pont De Nemours And Company | Process for copolymerization of tetrafluoroethylene in the presence of a dispersing agent comprising a perfluoroalkoxybenzene sulfonic acid or salt |
| JPS6289713A (ja) | 1985-10-12 | 1987-04-24 | Daikin Ind Ltd | 新規フルオロエラストマー |
| IT1189092B (it) | 1986-04-29 | 1988-01-28 | Ausimont Spa | Processo di polimerizzazione in dispersione acquosa di monomeri fluorurati |
| IT1204903B (it) | 1986-06-26 | 1989-03-10 | Ausimont Spa | Processo di polimerizzazione in dispersione acquosa di monomeri florati |
| IT1223324B (it) | 1987-10-28 | 1990-09-19 | Ausimont Spa | Microemulsioni acquose comprendenti perfluoropolieteri funzionali |
| US5153322A (en) | 1987-10-30 | 1992-10-06 | Minnesota Mining And Manufacturing Company | Perfluoro (cycloaliphatic methyleneoxyalkylene) carbonyl fluorides and derivatives thereof |
| US4861845A (en) | 1988-03-10 | 1989-08-29 | E. I. Du Pont De Nemours And Company | Polymerization of fluoroolefins |
| JPH01268696A (ja) | 1988-04-19 | 1989-10-26 | Daikin Ind Ltd | 含フッ素リン酸エステル及びその製法並びに含フッ素防錆剤 |
| DE3826807A1 (de) | 1988-08-06 | 1990-02-08 | Hoechst Ag | Verfahren zur herstellung von fluorierten carbonsaeurefluoriden |
| DE3828063A1 (de) | 1988-08-18 | 1990-02-22 | Hoechst Ag | Substituierte (2-haloalkoxy-1.1.2-trifluoraethoxy)-styrole, verfahren zu ihrer herstellung und ihre verwendung |
| WO1990006296A1 (en) | 1988-12-02 | 1990-06-14 | Minnesota Mining And Manufacturing Company | Direct fluorination process for making perfluorinated organic substances |
| US5256318A (en) | 1990-04-07 | 1993-10-26 | Daikin Industries Ltd. | Leather treatment and process for treating leather |
| JP2586706B2 (ja) | 1990-08-23 | 1997-03-05 | 信越化学工業株式会社 | オリゴヘキサフルオロプロピレンオキシド誘導体及びその製造方法 |
| JP3240654B2 (ja) | 1991-06-20 | 2001-12-17 | ソニー株式会社 | パーフルオロポリエーテル誘導体及びこれを用いた潤滑剤並びに磁気記録媒体 |
| JP3198542B2 (ja) | 1991-07-24 | 2001-08-13 | ダイキン工業株式会社 | 変性ポリテトラフルオロエチレン被覆用組成物 |
| DE4217366A1 (de) | 1992-05-26 | 1993-12-02 | Bayer Ag | Imide und deren Salze sowie deren Verwendung |
| IT1256721B (it) | 1992-12-16 | 1995-12-15 | Ausimont Spa | Processo per impartire oleo- ed idro-repellenza alla superficie di materiali ceramici porosi |
| DE4300800C2 (de) | 1993-01-14 | 1996-09-19 | Bayer Ag | Hydroxy- und/oder mercaptogruppenhaltige fluorierte Carbonsäureester von Phosphono- und Phosphinocarbonsäuren, ein Verfahren zu ihrer Herstellung sowie deren Verwendung |
| DE4300799C2 (de) | 1993-01-14 | 1996-09-19 | Bayer Ag | Acrylat- und/oder methacrylatgruppenhaltige fluorierte Carbonsäureester von Phosphono- und Phosphinocarbonsäuren, ein Verfahren zu ihrer Herstellung sowie deren Verwendung |
| US5285002A (en) | 1993-03-23 | 1994-02-08 | Minnesota Mining And Manufacturing Company | Fluorine-containing polymers and preparation and use thereof |
| IT1265067B1 (it) | 1993-05-18 | 1996-10-30 | Ausimont Spa | Processo di (co)polimerizzazione in emulsione acquosa di monomeri olefinici fluorurati |
| US5350497A (en) | 1993-05-21 | 1994-09-27 | E. I. Du Pont De Nemours And Company | Production of perfluoro(alkyl vinyl ethers) |
| JP3172983B2 (ja) | 1993-09-20 | 2001-06-04 | ダイキン工業株式会社 | ビニリデンフルオライド系重合体の水性分散液およびその製法 |
| US5488142A (en) | 1993-10-04 | 1996-01-30 | Minnesota Mining And Manufacturing Company | Fluorination in tubular reactor system |
| IT1269517B (it) | 1994-05-19 | 1997-04-01 | Ausimont Spa | Polimeri e copolimeri fluorurati contenenti strutture cicliche |
| IT1270703B (it) | 1994-11-17 | 1997-05-07 | Ausimont Spa | Microemulsioni di fluoropoliossialchileni in miscela con idrocarburi, e loro uso in processi di (co)polimerizzazione di monomeri fluorurati |
| US5550277A (en) | 1995-01-19 | 1996-08-27 | Paciorek; Kazimiera J. L. | Perfluoroalkyl and perfluoroalkylether substituted aromatic phosphates, phosphonates and related compositions |
| US5478905A (en) | 1995-02-06 | 1995-12-26 | E. I. Du Pont De Nemours And Company | Amorphous tetrafluoroethylene/hexafluoropropylene copolymers |
| US5532310A (en) | 1995-04-28 | 1996-07-02 | Minnesota Mining And Manufacturing Company | Surfactants to create fluoropolymer dispersions in fluorinated liquids |
| US5688884A (en) | 1995-08-31 | 1997-11-18 | E. I. Du Pont De Nemours And Company | Polymerization process |
| US5789508A (en) | 1995-08-31 | 1998-08-04 | E. I. Du Pont De Nemours And Company | Polymerization process |
| IT1276072B1 (it) | 1995-10-31 | 1997-10-24 | Ausimont Spa | Processo di (co)polimerizzazione di monomeri fluorurati per ottenere polimeri contenenti idrogeno |
| IT1295535B1 (it) | 1996-07-01 | 1999-05-12 | Ausimont Spa | Processo di polimerizzazione di vinilidenfluoruro (vdf) |
| IT1286028B1 (it) | 1996-07-09 | 1998-07-07 | Ausimont Spa | Processo di polimerizzazione in sospensione di monomeri fluorurati |
| US5763552A (en) | 1996-07-26 | 1998-06-09 | E. I. Du Pont De Nemours And Company | Hydrogen-containing flourosurfacant and its use in polymerization |
| US6013795A (en) | 1996-11-04 | 2000-01-11 | 3M Innovative Properties Company | Alpha-branched fluoroalkylcarbonyl fluorides and their derivatives |
| IT1290428B1 (it) | 1997-03-21 | 1998-12-03 | Ausimont Spa | Grassi fluorurati |
| IT1290462B1 (it) | 1997-04-08 | 1998-12-03 | Ausimont Spa | Polimeri idrogenati modificati |
| KR100524247B1 (ko) | 1997-04-30 | 2005-10-26 | 다이낑 고오교 가부시키가이샤 | 수성 분산 조성물 및 도장물품 |
| EP1015664B1 (en) | 1997-05-02 | 2007-09-26 | Minnesota Mining And Manufacturing Company | Electrochemical fluorination using interrupted current |
| IT1293516B1 (it) | 1997-07-31 | 1999-03-01 | Ausimont Spa | Dispersione di perfluoropolimeri |
| US6184187B1 (en) | 1998-04-07 | 2001-02-06 | E. I. Dupont De Nemours And Company | Phosphorus compounds and their use as corrosion inhibitors for perfluoropolyethers |
| ITMI981519A1 (it) | 1998-07-02 | 2000-01-02 | Ausimont Spa | Processodi polimerizzazione del tfe |
| DE69918723T2 (de) | 1998-10-13 | 2005-07-21 | Daikin Industries, Ltd. | Verfahren zur herstellung von fluorpolymeren |
| DE19857111A1 (de) * | 1998-12-11 | 2000-06-15 | Dyneon Gmbh | Wäßrige Dispersionen von Fluorpolymeren |
| DE60016577T2 (de) | 1999-03-02 | 2005-11-24 | E.I. Du Pont De Nemours And Co., Wilmington | Radikalische polymerisationsmethode für fluorierte copolymere |
| US6395848B1 (en) | 1999-05-20 | 2002-05-28 | E. I. Du Pont De Nemours And Company | Polymerization of fluoromonomers |
| US6429258B1 (en) | 1999-05-20 | 2002-08-06 | E. I. Du Pont De Nemours & Company | Polymerization of fluoromonomers |
| ITMI991269A1 (it) | 1999-06-08 | 2000-12-08 | Ausimont Spa | Miscele di dispersioni di fluoropolimeri |
| JP4855616B2 (ja) | 1999-10-27 | 2012-01-18 | スリーエム イノベイティブ プロパティズ カンパニー | フルオロケミカルスルホンアミド界面活性剤 |
| DE60041121D1 (de) | 1999-10-29 | 2009-01-29 | Asahi Glass Co Ltd | In wasser dispergierte wasser- und ölabweisende zusammensetzung und verfahren zu ihrer herstellung |
| US6255536B1 (en) | 1999-12-22 | 2001-07-03 | Dyneon Llc | Fluorine containing vinyl ethers |
| US6482979B1 (en) | 1999-12-22 | 2002-11-19 | Dyneon Llc | Perfluorinated acid fluorides and preparation thereof |
| US6677414B2 (en) | 1999-12-30 | 2004-01-13 | 3M Innovative Properties Company | Aqueous emulsion polymerization process for the manufacturing of fluoropolymers |
| IT1317847B1 (it) | 2000-02-22 | 2003-07-15 | Ausimont Spa | Processo per la preparazione di dispersioni acquose di fluoropolimeri. |
| US6452038B1 (en) | 2000-06-28 | 2002-09-17 | 3M Innovative Properties Company | Fluoroalkyloxy dispersant |
| JP2002059160A (ja) | 2000-08-11 | 2002-02-26 | Daikin Ind Ltd | 含フッ素陰イオン系界面活性剤の分離方法 |
| US6646088B2 (en) | 2000-08-16 | 2003-11-11 | 3M Innovative Properties Company | Urethane-based stain-release coatings |
| US6846570B2 (en) | 2000-08-17 | 2005-01-25 | Whitford Corporation | Multiple coat non-stick coating system and articles coated with same |
| US6774164B2 (en) | 2000-09-22 | 2004-08-10 | Dupont Dow Elastomers L.L.C. | Process for producing fluoroelastomers with fluorinated anionic surfactants |
| US6512063B2 (en) | 2000-10-04 | 2003-01-28 | Dupont Dow Elastomers L.L.C. | Process for producing fluoroelastomers |
| US6613860B1 (en) | 2000-10-12 | 2003-09-02 | 3M Innovative Properties Company | Compositions comprising fluorinated polyether silanes for rendering substrates oil and water repellent |
| US6632508B1 (en) | 2000-10-27 | 2003-10-14 | 3M Innovative Properties Company | Optical elements comprising a polyfluoropolyether surface treatment |
| US6730760B2 (en) | 2001-01-31 | 2004-05-04 | 3M Innovative Properties Company | Perfluoroelastomers having a low glass transition temperature and method of making them |
| US6656258B2 (en) | 2001-03-20 | 2003-12-02 | 3M Innovative Properties Company | Compositions comprising fluorinated silanes and compressed fluid CO2 |
| US7125941B2 (en) | 2001-03-26 | 2006-10-24 | 3M Innovative Properties Company | Aqueous emulsion polymerization process for producing fluoropolymers |
| US6761964B2 (en) | 2001-04-02 | 2004-07-13 | E. I. Du Pont De Nemours And Company | Fluoropolymer non-stick coatings |
| JP2002308914A (ja) | 2001-04-17 | 2002-10-23 | Daikin Ind Ltd | 含フッ素重合体ラテックスの製造方法 |
| JP2002317003A (ja) | 2001-04-19 | 2002-10-31 | Daikin Ind Ltd | 含フッ素重合体ラテックスの製造方法 |
| EP1253133B1 (en) | 2001-04-24 | 2004-10-06 | 3M Innovative Properties Company | Process of preparing halogenated esters |
| US6750304B2 (en) | 2001-05-02 | 2004-06-15 | 3M Innovative Properties Company | Aqueous emulsion polymerization in the presence of ethers as chain transfer agents to produce fluoropolymers |
| DE60227508D1 (de) | 2001-05-02 | 2008-08-21 | 3M Innovative Properties Co | Emulgatorfreies wässriges emulsionspolymerisationsverfahren zur herstellung von fluorpolymeren |
| US6737489B2 (en) | 2001-05-21 | 2004-05-18 | 3M Innovative Properties Company | Polymers containing perfluorovinyl ethers and applications for such polymers |
| US7045571B2 (en) | 2001-05-21 | 2006-05-16 | 3M Innovative Properties Company | Emulsion polymerization of fluorinated monomers |
| US20040198880A1 (en) * | 2001-06-29 | 2004-10-07 | Shoiji Ouchi | Floor polish composition |
| JP4409122B2 (ja) | 2001-07-18 | 2010-02-03 | Nokクリューバー株式会社 | 軸受用グリース組成物 |
| JP2003043625A (ja) | 2001-08-03 | 2003-02-13 | Konica Corp | 耐傷性を改良した光熱写真画像形成材料 |
| US6689854B2 (en) | 2001-08-23 | 2004-02-10 | 3M Innovative Properties Company | Water and oil repellent masonry treatments |
| US7279522B2 (en) | 2001-09-05 | 2007-10-09 | 3M Innovative Properties Company | Fluoropolymer dispersions containing no or little low molecular weight fluorinated surfactant |
| JP3900883B2 (ja) | 2001-10-05 | 2007-04-04 | ダイキン工業株式会社 | 含フッ素重合体ラテックスの製造方法 |
| US6649272B2 (en) | 2001-11-08 | 2003-11-18 | 3M Innovative Properties Company | Coating composition comprising fluorochemical polyether silane polycondensate and use thereof |
| US6716534B2 (en) | 2001-11-08 | 2004-04-06 | 3M Innovative Properties Company | Coating composition comprising a fluorochemical polyether silane partial condensate and use thereof |
| US6761694B2 (en) * | 2001-12-13 | 2004-07-13 | Allergan, Inc. | Methods for measuring retinal damage |
| JP4191929B2 (ja) | 2002-01-25 | 2008-12-03 | 株式会社ジェムコ | 含フッ素乳化剤の回収方法 |
| ITMI20020260A1 (it) | 2002-02-12 | 2003-08-12 | Ausimont Spa | Dispersioni acquose di fluoropolimeri |
| US6822059B2 (en) | 2002-04-05 | 2004-11-23 | 3M Innovative Properties Company | Dispersions containing bicomponent fluoropolymer particles and use thereof |
| US6833418B2 (en) | 2002-04-05 | 2004-12-21 | 3M Innovative Properties Company | Dispersions containing perfluorovinyl ether homopolymers and use thereof |
| EP1356755B1 (en) * | 2002-04-25 | 2012-05-09 | Panasonic Corporation | Vacuum-cleaner suction tool and vacuum cleaner using the same |
| JP2005527677A (ja) | 2002-05-24 | 2005-09-15 | スリーエム イノベイティブ プロパティズ カンパニー | 弗素化ポリエーテルを含むフルオロケミカル組成物および該組成物による繊維基材の処理 |
| US7425279B2 (en) | 2002-05-24 | 2008-09-16 | 3M Innovative Properties Company | Fluorochemical composition for treatment of a fibrous substrate |
| WO2003100159A1 (en) | 2002-05-24 | 2003-12-04 | 3M Innovative Properties Company | Fluorochemical composition comprising perfluoropolyether and an extender for the treatment of fibrous substrates |
| AU2003234544B2 (en) | 2002-05-24 | 2008-04-03 | 3M Innovative Properties Company | Fluorochemical composition for treatment of a fibrous substrate |
| JP2004018394A (ja) | 2002-06-12 | 2004-01-22 | Daikin Ind Ltd | 含フッ素両親媒性化合物 |
| JP4123272B2 (ja) | 2002-06-17 | 2008-07-23 | ダイキン工業株式会社 | 含フッ素ポリマー分散体及び含フッ素ポリマー分散体製造方法 |
| CN100381366C (zh) | 2002-06-19 | 2008-04-16 | 笹仓机械工程有限公司 | 含氟乳化剂的回收方法 |
| AU2003276878A1 (en) | 2002-09-30 | 2004-04-23 | Daikin Industries, Ltd. | Process for preparing fluorocarboxylic acids |
| US7064170B2 (en) | 2002-10-31 | 2006-06-20 | 3M Innovative Properties Company | Emulsifier free aqueous emulsion polymerization to produce copolymers of a fluorinated olefin and hydrocarbon olefin |
| US20040116742A1 (en) | 2002-12-17 | 2004-06-17 | 3M Innovative Properties Company | Selective reaction of hexafluoropropylene oxide with perfluoroacyl fluorides |
| US6923921B2 (en) | 2002-12-30 | 2005-08-02 | 3M Innovative Properties Company | Fluorinated polyether compositions |
| JP2004358397A (ja) | 2003-06-05 | 2004-12-24 | Daikin Ind Ltd | 界面活性剤、含フッ素重合体の製造方法及び含フッ素重合体水性分散液 |
| JP2004359870A (ja) | 2003-06-05 | 2004-12-24 | Daikin Ind Ltd | 界面活性剤、含フッ素重合体の製造方法及び含フッ素重合体水性分散液 |
| US7589234B2 (en) * | 2003-07-02 | 2009-09-15 | Daikin Industries, Ltd. | Fluoroalkyl carboxylic acid derivative, method for producing fluorine-containing polymer, and aqueous dispersion of fluorine-containing polymer |
| WO2005023822A1 (en) | 2003-08-21 | 2005-03-17 | 3M Innovative Properties Company | Perfluoropolyether amide-linked phosphonates, phosphates, and derivatives thereof |
| ITMI20032050A1 (it) | 2003-10-21 | 2005-04-22 | Solvay Solexis Spa | Processo per la preparazione di dispersori di fluoropolimeri. |
| US20050090613A1 (en) | 2003-10-22 | 2005-04-28 | Daikin Industries, Ltd. | Process for preparing fluorine-containing polymer latex |
| ATE502062T1 (de) | 2003-10-24 | 2011-04-15 | 3M Innovative Properties Co | Wässrige dispersionen von polytetrafluorethylenteilchen |
| US7141537B2 (en) | 2003-10-30 | 2006-11-28 | 3M Innovative Properties Company | Mixture of fluorinated polyethers and use thereof as surfactant |
| US7696268B2 (en) | 2003-10-31 | 2010-04-13 | Daikin Industries, Ltd. | Process for producing aqueous fluoropolymer dispersion and aqueous fluoropolymer dispersion |
| ATE529451T1 (de) | 2003-11-17 | 2011-11-15 | 3M Innovative Properties Co | Wässrige ptfe-dispersionen mit einem niedrigen gehalt an fluorierten emulgatoren |
| ITMI20032377A1 (it) | 2003-12-04 | 2005-06-05 | Solvay Solexis Spa | Copolimeri del tfe. |
| US7803894B2 (en) | 2003-12-05 | 2010-09-28 | 3M Innovatie Properties Company | Coating compositions with perfluoropolyetherisocyanate derived silane and alkoxysilanes |
| JPWO2005056614A1 (ja) | 2003-12-09 | 2007-07-05 | ダイキン工業株式会社 | 含フッ素重合体水性分散体及びその製造方法 |
| US7566762B2 (en) | 2003-12-25 | 2009-07-28 | Daikin Industries, Ltd. | Process for preparing fluoropolymer |
| JP5028801B2 (ja) | 2004-01-13 | 2012-09-19 | 旭硝子株式会社 | 含フッ素ポリエーテル化合物 |
| DE602004016136D1 (de) | 2004-07-05 | 2008-10-09 | 3M Innovative Properties Co | Grundierung aus PTFE für Metallsubstrate |
| JP2006036986A (ja) | 2004-07-28 | 2006-02-09 | Asahi Glass Co Ltd | 含フッ素ポリマーラテックス、その製造方法および含フッ素ポリマー |
| GB0511779D0 (en) | 2005-06-10 | 2005-07-20 | 3M Innovative Properties Co | Aqueous emulsion polymerization of fluorinated monomers in the presence of a partially fluorinated oligomer as an emulsifier |
| GB0514387D0 (en) | 2005-07-15 | 2005-08-17 | 3M Innovative Properties Co | Aqueous emulsion polymerization of fluorinated monomers using a perfluoropolyether surfactant |
| GB0525978D0 (en) * | 2005-12-21 | 2006-02-01 | 3M Innovative Properties Co | Fluorinated Surfactants For Making Fluoropolymers |
| GB0514398D0 (en) | 2005-07-15 | 2005-08-17 | 3M Innovative Properties Co | Aqueous emulsion polymerization of fluorinated monomers using a fluorinated surfactant |
| GB0523853D0 (en) | 2005-11-24 | 2006-01-04 | 3M Innovative Properties Co | Fluorinated surfactants for use in making a fluoropolymer |
| US20070015937A1 (en) | 2005-07-15 | 2007-01-18 | 3M Innovative Properties Company | Process for recovery of fluorinated carboxylic acid surfactants from exhaust gas |
| US20080015304A1 (en) | 2006-07-13 | 2008-01-17 | Klaus Hintzer | Aqueous emulsion polymerization process for producing fluoropolymers |
| JP2007106958A (ja) | 2005-10-17 | 2007-04-26 | Asahi Glass Co Ltd | フッ素系界面活性剤 |
| GB2432836A (en) | 2005-12-01 | 2007-06-06 | 3M Innovative Properties Co | Fluorinated surfactant |
| US20070276103A1 (en) | 2006-05-25 | 2007-11-29 | 3M Innovative Properties Company | Fluorinated Surfactants |
| US7754795B2 (en) * | 2006-05-25 | 2010-07-13 | 3M Innovative Properties Company | Coating composition |
| US8119750B2 (en) | 2006-07-13 | 2012-02-21 | 3M Innovative Properties Company | Explosion taming surfactants for the production of perfluoropolymers |
| CN101541816B (zh) | 2006-12-15 | 2014-03-12 | 3M创新有限公司 | 用于表面处理的具有甲硅烷侧基的含氟氨基甲酸酯化合物 |
| US7745653B2 (en) | 2007-03-08 | 2010-06-29 | 3M Innovative Properties Company | Fluorochemical compounds having pendent silyl groups |
| CN101679569A (zh) | 2007-06-06 | 2010-03-24 | 3M创新有限公司 | 氟化醚组合物以及使用该组合物的方法 |
| CN101821301B (zh) * | 2007-10-12 | 2012-06-27 | 3M创新有限公司 | 制备纯净含氟聚合物的方法 |
| EA201100051A1 (ru) | 2008-07-18 | 2011-08-30 | Зм Инновейтив Пропертиз Компани | Фторсодержащие простые эфиры силанов и способы их использования |
| MX2011000702A (es) | 2008-07-18 | 2011-02-24 | 3M Innovative Properties Co | Compuestos de eter fluorados y metodos para usar los mismos. |
-
2008
- 2008-05-21 KR KR1020097026333A patent/KR20100017848A/ko not_active Withdrawn
- 2008-05-21 CN CN2008800170058A patent/CN101679790B/zh not_active Expired - Fee Related
- 2008-05-21 JP JP2010509509A patent/JP2010528159A/ja not_active Withdrawn
- 2008-05-21 US US12/601,143 patent/US8338517B2/en not_active Expired - Fee Related
- 2008-05-21 EP EP08756012A patent/EP2155830A1/en not_active Withdrawn
- 2008-05-21 WO PCT/US2008/064307 patent/WO2008147796A1/en not_active Ceased
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016024653A1 (ko) * | 2014-08-13 | 2016-02-18 | 주식회사 켐프 | 판상 아연분말이 혼합된 안료 분리형 수성도료 조성물 |
Also Published As
| Publication number | Publication date |
|---|---|
| US8338517B2 (en) | 2012-12-25 |
| CN101679790B (zh) | 2012-09-19 |
| JP2010528159A (ja) | 2010-08-19 |
| US20100168300A1 (en) | 2010-07-01 |
| EP2155830A1 (en) | 2010-02-24 |
| WO2008147796A1 (en) | 2008-12-04 |
| CN101679790A (zh) | 2010-03-24 |
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