DE69908152T2 - Abriebfeste und schmutzresistente härtbare fluorierte beschichtung - Google Patents
Abriebfeste und schmutzresistente härtbare fluorierte beschichtung Download PDFInfo
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- DE69908152T2 DE69908152T2 DE69908152T DE69908152T DE69908152T2 DE 69908152 T2 DE69908152 T2 DE 69908152T2 DE 69908152 T DE69908152 T DE 69908152T DE 69908152 T DE69908152 T DE 69908152T DE 69908152 T2 DE69908152 T2 DE 69908152T2
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- coating
- amino resin
- coating composition
- radical
- acid
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- 239000011248 coating agent Substances 0.000 title claims description 51
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- 238000004132 cross linking Methods 0.000 claims description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
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- 229920002554 vinyl polymer Chemical class 0.000 claims description 19
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 17
- 239000003999 initiator Substances 0.000 claims description 13
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- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 238000006897 homolysis reaction Methods 0.000 description 1
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- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
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- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- LUCXVPAZUDVVBT-UHFFFAOYSA-N methyl-[3-(2-methylphenoxy)-3-phenylpropyl]azanium;chloride Chemical compound Cl.C=1C=CC=CC=1C(CCNC)OC1=CC=CC=C1C LUCXVPAZUDVVBT-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical class C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- FTJXXXSSRCHQKC-UHFFFAOYSA-N n-(2-cyanoethyl)prop-2-enamide Chemical compound C=CC(=O)NCCC#N FTJXXXSSRCHQKC-UHFFFAOYSA-N 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
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- 125000004043 oxo group Chemical group O=* 0.000 description 1
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- 229910052760 oxygen Inorganic materials 0.000 description 1
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- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
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- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
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- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
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- ROEHNQZQCCPZCH-UHFFFAOYSA-N tert-butyl 2-tert-butylperoxycarbonylbenzoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1C(=O)OC(C)(C)C ROEHNQZQCCPZCH-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
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- ZFDIRQKJPRINOQ-UHFFFAOYSA-N transbutenic acid ethyl ester Natural products CCOC(=O)C=CC ZFDIRQKJPRINOQ-UHFFFAOYSA-N 0.000 description 1
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- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- 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
- C09D161/00—Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
- C09D161/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
-
- 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
- C09D133/00—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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
- C09D133/16—Homopolymers or copolymers of esters containing halogen 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
- C09D179/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09D161/00 - C09D177/00
-
- 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
- C09D5/16—Antifouling paints; Underwater paints
-
- 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
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US136185 | 1998-08-19 | ||
| US09/136,185 US6168866B1 (en) | 1998-08-19 | 1998-08-19 | Abrasion and stain resistant curable fluorinated coating |
| PCT/US1999/002979 WO2000011095A1 (en) | 1998-08-19 | 1999-02-11 | Abrasion and stain resistant curable fluorinated coating |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69908152D1 DE69908152D1 (de) | 2003-06-26 |
| DE69908152T2 true DE69908152T2 (de) | 2004-04-01 |
Family
ID=22471723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69908152T Expired - Fee Related DE69908152T2 (de) | 1998-08-19 | 1999-02-11 | Abriebfeste und schmutzresistente härtbare fluorierte beschichtung |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6168866B1 (https=) |
| EP (1) | EP1114107B1 (https=) |
| JP (1) | JP2002523548A (https=) |
| KR (1) | KR100553925B1 (https=) |
| AR (1) | AR021760A1 (https=) |
| AU (1) | AU741534B2 (https=) |
| BR (1) | BR9914285A (https=) |
| CA (1) | CA2338789C (https=) |
| DE (1) | DE69908152T2 (https=) |
| ES (1) | ES2194443T3 (https=) |
| WO (1) | WO2000011095A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009029153A1 (de) * | 2009-09-03 | 2011-03-17 | Evonik Degussa Gmbh | Waschpermanente Wandbeläge |
Families Citing this family (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7320829B2 (en) | 1998-03-05 | 2008-01-22 | Omnova Solutions Inc. | Fluorinated polymer and amine resin compositions and products formed therefrom |
| US6686051B1 (en) | 1998-03-05 | 2004-02-03 | Omnova Solutions Inc. | Cured polyesters containing fluorinated side chains |
| JP2002505218A (ja) * | 1998-03-05 | 2002-02-19 | オムノヴア ソリユーシヨンズ インコーポレーテツド | 清掃容易なポリマーラミネート |
| US6383651B1 (en) | 1998-03-05 | 2002-05-07 | Omnova Solutions Inc. | Polyester with partially fluorinated side chains |
| US6673889B1 (en) * | 1999-06-28 | 2004-01-06 | Omnova Solutions Inc. | Radiation curable coating containing polyfuorooxetane |
| US6403760B1 (en) | 1999-12-28 | 2002-06-11 | Omnova Solutions Inc. | Monohydric polyfluorooxetane polymer and radiation curable coatings containing a monofunctional polyfluorooxetane polymer |
| US6962966B2 (en) | 1999-12-28 | 2005-11-08 | Omnova Solutions Inc. | Monohydric polyfluorooxetane oligomers, polymers, and copolymers and coatings containing the same |
| US6465566B2 (en) | 2000-07-06 | 2002-10-15 | Omnova Solutions Inc. | Anionic waterborne polyurethane dispersions containing polyfluorooxetanes |
| US6465565B1 (en) | 2000-07-06 | 2002-10-15 | Omnova Solutions, Inc. | Anionic waterborne polyurethane dispersions containing polyfluorooxetanes |
| JP4631137B2 (ja) * | 2000-08-01 | 2011-02-16 | 日東紡績株式会社 | 末端にメルカプト基を有するアリルアミン類重合体およびその製造方法 |
| US6689346B1 (en) * | 2000-10-25 | 2004-02-10 | L'oreal | Reshapable hair styling composition comprising acrylic copolymers |
| WO2002039148A1 (en) | 2000-11-09 | 2002-05-16 | Reflexite Corporation | Elastical optical structure |
| US6660828B2 (en) | 2001-05-14 | 2003-12-09 | Omnova Solutions Inc. | Fluorinated short carbon atom side chain and polar group containing polymer, and flow, or leveling, or wetting agents thereof |
| CA2447132C (en) * | 2001-05-14 | 2008-10-07 | Omnova Solutions Inc. | Polymeric surfactants derived from cyclic monomers having pendant fluorinated carbon groups |
| US20040146706A1 (en) * | 2001-06-19 | 2004-07-29 | Toshihiro Kasai | Protective film,adhesive sheet and floor surface protective structure |
| US6645478B2 (en) * | 2001-06-22 | 2003-11-11 | L'oreal S.A. | Reshapable hair styling composition comprising (meth)acrylic copolymers of four or more monomers |
| US6667378B2 (en) * | 2001-06-22 | 2003-12-23 | L'oreal, S.A. | Reshapable hair styling composition comprising heterogeneous (meth)acrylic copolymer particles |
| US20030147833A1 (en) * | 2001-12-20 | 2003-08-07 | L'oreal | Reshapable hair styling non-rinse composition comprising (meth)acrylic copolymers |
| CA2367898A1 (en) * | 2002-01-16 | 2003-07-16 | 3M Innovative Properties Company | Process for preparing improved abrasive article |
| US20030203980A1 (en) * | 2002-04-30 | 2003-10-30 | Valdes Reynaldo A. | Sol-gel composition, methods for manufacturing sol-gels, and applications for sol-gels |
| DE10252865A1 (de) * | 2002-11-12 | 2004-05-27 | Kronotec Ag | Verfahren zum Erzeugen eines strukturierten Dekors in einer Holzwerkstoffplatte |
| DE10252866B3 (de) | 2002-11-12 | 2004-04-29 | Kronotec Ag | Paneel und Verfahren zur Herstellung eines Paneels |
| US7617651B2 (en) * | 2002-11-12 | 2009-11-17 | Kronotec Ag | Floor panel |
| DE10252863B4 (de) * | 2002-11-12 | 2007-04-19 | Kronotec Ag | Holzfaserplatte, insbesondere Fussbodenpaneel |
| DE50309830D1 (de) * | 2002-11-15 | 2008-06-26 | Flooring Technologies Ltd | Einrichtung bestehend aus zwei miteinander verbindbaren Bauplatten und einem Einsatz zum Verriegeln dieser Bauplatten |
| US20040109947A1 (en) * | 2002-12-09 | 2004-06-10 | Weinert Raymond J. | Stain resistant coatings for flexible substrates, substrates coated therewith and related methods |
| DE10306118A1 (de) | 2003-02-14 | 2004-09-09 | Kronotec Ag | Bauplatte |
| US7678425B2 (en) | 2003-03-06 | 2010-03-16 | Flooring Technologies Ltd. | Process for finishing a wooden board and wooden board produced by the process |
| DE20304761U1 (de) * | 2003-03-24 | 2004-04-08 | Kronotec Ag | Einrichtung zum Verbinden von Bauplatten, insbesondere Bodenpaneele |
| DE10362218B4 (de) * | 2003-09-06 | 2010-09-16 | Kronotec Ag | Verfahren zum Versiegeln einer Bauplatte |
| DE20315676U1 (de) * | 2003-10-11 | 2003-12-11 | Kronotec Ag | Paneel, insbesondere Bodenpaneel |
| US7506481B2 (en) * | 2003-12-17 | 2009-03-24 | Kronotec Ag | Building board for use in subfloors |
| US6995222B2 (en) * | 2003-12-17 | 2006-02-07 | 3M Innovative Properties Company | Coating compositions with reactive fluorinated copolymers having pendant perfluoropolyether groups |
| DE102004005047B3 (de) * | 2004-01-30 | 2005-10-20 | Kronotec Ag | Verfahren und Einrichtung zum Einbringen eines die Feder einer Platte bildenden Streifens |
| DE102004011531C5 (de) * | 2004-03-08 | 2014-03-06 | Kronotec Ag | Holzwerkstoffplatte, insbesondere Fußbodenpaneel |
| DE102004011931B4 (de) * | 2004-03-11 | 2006-09-14 | Kronotec Ag | Dämmstoffplatte aus einem Holzwerkstoff-Bindemittelfaser-Gemisch |
| DE102005042658B3 (de) * | 2005-09-08 | 2007-03-01 | Kronotec Ag | Bauplatte, insbesondere Fußbodenpaneel |
| DE102005042657B4 (de) * | 2005-09-08 | 2010-12-30 | Kronotec Ag | Bauplatte und Verfahren zur Herstellung |
| US7854986B2 (en) * | 2005-09-08 | 2010-12-21 | Flooring Technologies Ltd. | Building board and method for production |
| DE102005063034B4 (de) | 2005-12-29 | 2007-10-31 | Flooring Technologies Ltd. | Paneel, insbesondere Bodenpaneel |
| US20070178239A1 (en) * | 2006-02-01 | 2007-08-02 | Ecolab Inc. | Protective coating for painted or glossy surfaces |
| DE102006006124A1 (de) * | 2006-02-10 | 2007-08-23 | Flooring Technologies Ltd. | Einrichtung zum Verriegeln zweier Bauplatten |
| DE102006007976B4 (de) * | 2006-02-21 | 2007-11-08 | Flooring Technologies Ltd. | Verfahren zur Veredelung einer Bauplatte |
| US8322754B2 (en) | 2006-12-01 | 2012-12-04 | Tenaris Connections Limited | Nanocomposite coatings for threaded connections |
| JP4541388B2 (ja) * | 2007-08-17 | 2010-09-08 | 株式会社沖データ | 画像形成装置 |
| CN100593557C (zh) * | 2008-01-31 | 2010-03-10 | 中国科学院化学研究所 | 防冰霜涂料及其使用方法 |
| US20090220795A1 (en) * | 2008-02-29 | 2009-09-03 | Ppg Industries Ohio, Inc. | Composites comprising a multi-layer coating system |
| US20100015456A1 (en) * | 2008-07-16 | 2010-01-21 | Eastman Chemical Company | Thermoplastic formulations for enhanced paintability toughness and melt process ability |
| US8865261B2 (en) | 2012-12-06 | 2014-10-21 | Eastman Chemical Company | Extrusion coating of elongated substrates |
| EP2945994B1 (en) | 2013-01-18 | 2018-07-11 | Basf Se | Acrylic dispersion-based coating compositions |
| JP6123354B2 (ja) * | 2013-03-01 | 2017-05-10 | Jnc株式会社 | 熱硬化性組成物 |
| US9920526B2 (en) | 2013-10-18 | 2018-03-20 | Eastman Chemical Company | Coated structural members having improved resistance to cracking |
| US9744707B2 (en) | 2013-10-18 | 2017-08-29 | Eastman Chemical Company | Extrusion-coated structural members having extruded profile members |
| AR100953A1 (es) | 2014-02-19 | 2016-11-16 | Tenaris Connections Bv | Empalme roscado para una tubería de pozo de petróleo |
| KR101657568B1 (ko) | 2015-04-22 | 2016-09-19 | (주) 숲으로벽지 | 내오염성과 내마모성이 향상된 천연소재를 이용한 수성발포 벽지 |
| US10597550B2 (en) | 2015-11-24 | 2020-03-24 | Dow Global Technologies Llc | Aqueous polymer dispersion and process of making the same |
| RU2666851C1 (ru) * | 2017-06-07 | 2018-09-12 | Общество с ограниченной ответственностью "Химфист" (ООО "Химфист") | Способ изготовления гидрофобной, водостойкой облицовочной плитки из древесного материала |
| US20190118221A1 (en) | 2017-10-24 | 2019-04-25 | The Boeing Company | Conformal fluoropolymer coatings |
| JP6999373B2 (ja) * | 2017-11-13 | 2022-01-18 | Toyo Tire株式会社 | タイヤ用ゴム組成物および空気入りタイヤ |
| CN114716913B (zh) * | 2022-03-17 | 2023-03-03 | 中国船舶重工集团公司第七二五研究所 | 一种双亲性防污活性剂及其制备方法 |
| KR102677363B1 (ko) * | 2024-04-09 | 2024-06-21 | 주식회사 수광산업 | 위장용 낚시줄 및 이의 제조방법 |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2841573A (en) | 1955-12-29 | 1958-07-01 | Minnesota Mining & Mfg | Fluorocarbon vinyl-type esters and polymers |
| US2803615A (en) | 1956-01-23 | 1957-08-20 | Minnesota Mining & Mfg | Fluorocarbon acrylate and methacrylate esters and polymers |
| FR2328070A1 (fr) | 1975-10-17 | 1977-05-13 | Ugine Kuhlmann | Produits anti-tache permettant l'elimination facile des salissures au lavage |
| US4513059A (en) | 1982-02-02 | 1985-04-23 | Permacel | Release coating composition |
| US4518649A (en) | 1984-05-11 | 1985-05-21 | Chicopee | Soil releasing textiles containing fluorochemical soil release agents and method for producing same |
| FR2588555B1 (fr) | 1985-10-16 | 1987-12-11 | Atochem | Monomeres acryliques fluores, polymeres en derivant et leur application au traitement hydrofuge et oleofuge de substrats divers |
| JPS62127362A (ja) | 1985-11-28 | 1987-06-09 | Daikin Ind Ltd | 電着塗装用組成物 |
| JPH0623263B2 (ja) | 1986-07-10 | 1994-03-30 | 三菱化成ビニル株式会社 | 塩化ビニル系樹脂成形品 |
| KR880003061A (ko) | 1986-08-07 | 1988-05-13 | 황무영 | 천의 발수(撥水) 가공방법 |
| US4812337A (en) | 1986-11-25 | 1989-03-14 | Kansai Paint Company, Limited | Metallic coating method |
| GB8716198D0 (en) | 1987-07-09 | 1987-08-12 | Ici Plc | Chemical process |
| US4804572A (en) | 1987-12-01 | 1989-02-14 | Imperial Wallcoverings, Inc. | Wall covering with fluorocarbon stain resistant top coating |
| JPH02228351A (ja) | 1989-03-02 | 1990-09-11 | Kansai Paint Co Ltd | 樹脂組成物、硬化性組成物及び塗料組成物 |
| JPH03269184A (ja) | 1990-03-15 | 1991-11-29 | Kao Corp | 耐汚染性壁紙 |
| DE4027594A1 (de) | 1990-08-31 | 1992-03-05 | Herberts Gmbh | Wasserverduennbares copolymerisat, dessen herstellung und verwendung, sowie waessrige ueberzugsmittel |
| US5276175A (en) | 1991-04-02 | 1994-01-04 | Minnesota Mining And Manufacturing Company | Isocyanate derivatives comprising flourochemical oligomers |
| US5292796A (en) | 1991-04-02 | 1994-03-08 | Minnesota Mining And Manufacturing Company | Urea-aldehyde condensates and melamine derivatives comprising fluorochemical oligomers |
| DE59203814D1 (de) * | 1991-07-29 | 1995-11-02 | Ciba Geigy Ag | Lichtstabilisierte Copolymer-Zusammensetzungen als Bindemittel für Lacke. |
| JP3287878B2 (ja) | 1992-07-09 | 2002-06-04 | ダイセル化学工業株式会社 | 塗料用樹脂組成物 |
| US5262444A (en) | 1992-11-30 | 1993-11-16 | Borden, Inc. | Porous plastic film product, useful as a breathable wall covering or filters |
| JP3533751B2 (ja) | 1995-04-26 | 2004-05-31 | 日本油脂Basfコーティングス株式会社 | 熱硬化性塗料組成物 |
| US5597874A (en) | 1995-10-16 | 1997-01-28 | E. I. Du Pont De Nemours And Company | Coating compositions of an acrylic fluorocarbon polymer and a fluorinated polyisocyanate |
-
1998
- 1998-08-19 US US09/136,185 patent/US6168866B1/en not_active Expired - Lifetime
-
1999
- 1999-02-11 ES ES99908123T patent/ES2194443T3/es not_active Expired - Lifetime
- 1999-02-11 DE DE69908152T patent/DE69908152T2/de not_active Expired - Fee Related
- 1999-02-11 BR BR9914285-6A patent/BR9914285A/pt not_active IP Right Cessation
- 1999-02-11 AU AU27629/99A patent/AU741534B2/en not_active Ceased
- 1999-02-11 KR KR1020017002070A patent/KR100553925B1/ko not_active Expired - Fee Related
- 1999-02-11 JP JP2000566356A patent/JP2002523548A/ja active Pending
- 1999-02-11 CA CA002338789A patent/CA2338789C/en not_active Expired - Fee Related
- 1999-02-11 EP EP99908123A patent/EP1114107B1/en not_active Expired - Lifetime
- 1999-02-11 WO PCT/US1999/002979 patent/WO2000011095A1/en not_active Ceased
- 1999-08-10 AR ARP990103982A patent/AR021760A1/es unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009029153A1 (de) * | 2009-09-03 | 2011-03-17 | Evonik Degussa Gmbh | Waschpermanente Wandbeläge |
Also Published As
| Publication number | Publication date |
|---|---|
| KR100553925B1 (ko) | 2006-02-24 |
| US6168866B1 (en) | 2001-01-02 |
| AU2762999A (en) | 2000-03-14 |
| CA2338789C (en) | 2009-01-27 |
| AU741534B2 (en) | 2001-12-06 |
| EP1114107B1 (en) | 2003-05-21 |
| WO2000011095A1 (en) | 2000-03-02 |
| DE69908152D1 (de) | 2003-06-26 |
| ES2194443T3 (es) | 2003-11-16 |
| CA2338789A1 (en) | 2000-03-02 |
| BR9914285A (pt) | 2001-06-19 |
| AR021760A1 (es) | 2002-08-07 |
| KR20010072747A (ko) | 2001-07-31 |
| JP2002523548A (ja) | 2002-07-30 |
| EP1114107A1 (en) | 2001-07-11 |
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