NO333352B1 - Ny (poly)oksyalkylenblokksilylester-kopolymer, antigroende beleggsammensetning, antigroende belegg dannet fra antigroende beleggsammensetning, antigroende fremgangsmate som anvender antigroende beleggsammensetning og skrog eller undervannsstruktur dekket med antigroende belegg - Google Patents
Ny (poly)oksyalkylenblokksilylester-kopolymer, antigroende beleggsammensetning, antigroende belegg dannet fra antigroende beleggsammensetning, antigroende fremgangsmate som anvender antigroende beleggsammensetning og skrog eller undervannsstruktur dekket med antigroende belegg Download PDFInfo
- Publication number
- NO333352B1 NO333352B1 NO20015198A NO20015198A NO333352B1 NO 333352 B1 NO333352 B1 NO 333352B1 NO 20015198 A NO20015198 A NO 20015198A NO 20015198 A NO20015198 A NO 20015198A NO 333352 B1 NO333352 B1 NO 333352B1
- Authority
- NO
- Norway
- Prior art keywords
- group
- antifouling
- carbon atoms
- silyl ester
- coating composition
- Prior art date
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- 239000003208 petroleum Substances 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- FOKZHJCFBNVOAV-UHFFFAOYSA-N propyl 2-hydroxy-3-phenoxyprop-2-enoate Chemical compound CCCOC(=O)C(O)=COC1=CC=CC=C1 FOKZHJCFBNVOAV-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- WJSXSXUHWBSPEP-UHFFFAOYSA-N pyridine;triphenylborane Chemical compound C1=CC=NC=C1.C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 WJSXSXUHWBSPEP-UHFFFAOYSA-N 0.000 description 1
- YBBJKCMMCRQZMA-UHFFFAOYSA-N pyrithione Chemical compound ON1C=CC=CC1=S YBBJKCMMCRQZMA-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 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
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- PQSIXYSSKXAOFE-UHFFFAOYSA-N tri(propan-2-yl)silyl prop-2-enoate Chemical compound CC(C)[Si](C(C)C)(C(C)C)OC(=O)C=C PQSIXYSSKXAOFE-UHFFFAOYSA-N 0.000 description 1
- LPUCKLOWOWADAC-UHFFFAOYSA-M tributylstannyl 2-methylprop-2-enoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C(C)=C LPUCKLOWOWADAC-UHFFFAOYSA-M 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- PGQNYIRJCLTTOJ-UHFFFAOYSA-N trimethylsilyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)O[Si](C)(C)C PGQNYIRJCLTTOJ-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
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- 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
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
- C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
-
- 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
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/336—Polymers modified by chemical after-treatment with organic compounds containing silicon
-
- 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
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
- C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C08G81/024—Block or graft polymers containing sequences of polymers of C08C or C08F and of polymers of C08G
- C08G81/025—Block or graft polymers containing sequences of polymers of C08C or C08F and of polymers of C08G containing polyether sequences
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- 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
- C09D153/00—Coating compositions based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
-
- 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
- C09D5/1656—Antifouling paints; Underwater paints characterised by the film-forming substance
- C09D5/1662—Synthetic film-forming substance
- C09D5/1668—Vinyl-type polymers
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/926—Polyamide containing a plurality of oxyalkylene groups
-
- 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]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Details Of Rigid Or Semi-Rigid Containers (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000325525 | 2000-10-25 | ||
JP2000325526 | 2000-10-25 |
Publications (3)
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NO20015198D0 NO20015198D0 (no) | 2001-10-24 |
NO20015198L NO20015198L (no) | 2002-04-26 |
NO333352B1 true NO333352B1 (no) | 2013-05-13 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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NO20015198A NO333352B1 (no) | 2000-10-25 | 2001-10-24 | Ny (poly)oksyalkylenblokksilylester-kopolymer, antigroende beleggsammensetning, antigroende belegg dannet fra antigroende beleggsammensetning, antigroende fremgangsmate som anvender antigroende beleggsammensetning og skrog eller undervannsstruktur dekket med antigroende belegg |
Country Status (13)
Country | Link |
---|---|
US (1) | US6828030B2 (ko) |
EP (1) | EP1201700B1 (ko) |
KR (1) | KR100467300B1 (ko) |
CN (1) | CN1182214C (ko) |
AT (1) | ATE240362T1 (ko) |
DE (1) | DE60100271T2 (ko) |
DK (1) | DK1201700T3 (ko) |
ES (1) | ES2201017T3 (ko) |
HK (1) | HK1043693A1 (ko) |
NO (1) | NO333352B1 (ko) |
PT (1) | PT1201700E (ko) |
SG (1) | SG97209A1 (ko) |
TW (1) | TWI241314B (ko) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1308484A1 (en) * | 2001-10-30 | 2003-05-07 | Sigma Coatings B.V. | Use of silylesters of rosin in self-polishing antifouling paints |
JP4361239B2 (ja) * | 2002-03-06 | 2009-11-11 | 中国塗料株式会社 | 防汚塗料組成物、該組成物からなる塗膜、該塗膜で被覆された基材、および防汚方法 |
EP1405850B1 (en) * | 2002-10-01 | 2007-03-07 | Nippon Oil Corporation | (Meth)acrylic compound having an oxetanyl group and liquid crystal film produced by using the same |
MY145980A (en) * | 2003-03-26 | 2012-05-31 | Sigmakalon Services B V | Process for the preparation of poly(silyl esters)s, and their uses |
WO2005005516A1 (en) | 2003-07-07 | 2005-01-20 | Akzo Nobel Coatings International B.V. | Silyl ester copolymer compositions |
CN101675085A (zh) * | 2007-03-23 | 2010-03-17 | 株式会社日本触媒 | 含有聚亚烷基二醇链的硫醇聚合物、硫醇改性的单体、其混合物和水泥外加剂 |
US20100183540A1 (en) * | 2007-07-06 | 2010-07-22 | Jotun A/S | Branched polymer and antifouling coating composition comprising the polymer |
US8025918B2 (en) * | 2007-11-16 | 2011-09-27 | Rhodia, Inc. | High definition printing with waterborne inks on non-porous substrates |
US20110237469A1 (en) * | 2008-08-11 | 2011-09-29 | M-I Australia Pty Ltd. | Compositions and methods for inhibiting emulsion formation in hydrocarbon bodies |
CN102051101B (zh) * | 2010-11-18 | 2012-07-04 | 浙江大学 | 一种常温固化防污减阻水凝胶软涂层的制备方法 |
JP5782174B2 (ja) * | 2011-03-31 | 2015-09-24 | アクゾ ノーベル コーティングス インターナショナル ビー ヴィ | 汚損防止塗料組成物 |
WO2013052181A2 (en) * | 2011-06-17 | 2013-04-11 | Ndsu Research Foundation | Functionalized silicones with polyalkylene oxide side chains |
EP2726560B1 (en) * | 2011-06-30 | 2017-03-01 | Hempel A/S | High solids antifouling paint composition |
JP5916490B2 (ja) | 2012-04-09 | 2016-05-11 | 中国塗料株式会社 | 船底塗膜の摩擦抵抗予測方法および、該方法を用いた塗膜性能評価方法、塗膜性能評価装置 |
EP2864379A1 (en) | 2012-06-22 | 2015-04-29 | PPG Coatings Europe B.V. | Antifouling coating composition |
US8822616B1 (en) * | 2013-02-08 | 2014-09-02 | Rohm And Haas Electronic Materials Llc | Block copolymer formulation and methods relating thereto |
CN103396513B (zh) * | 2013-07-24 | 2016-03-02 | 华南理工大学 | 一种主链断裂型聚丙烯酸类硅烷酯树脂的制备方法及应用 |
GB2558739B (en) * | 2016-11-11 | 2020-05-06 | Jotun As | A silyl ester copolymer and use thereof in an antifouling composition |
DE102017101978B4 (de) | 2017-02-01 | 2023-02-02 | Fachhochschule Kiel | Transparente, kratzfeste Schicht mit Antifouling-Eigenschaften und Verfahren zur Herstellung derselben |
JP6579413B1 (ja) * | 2018-04-20 | 2019-09-25 | 日東化成株式会社 | 防汚塗料組成物 |
CN114846040A (zh) * | 2019-12-25 | 2022-08-02 | Dic株式会社 | 聚合物和包含该聚合物的涂布组合物 |
Family Cites Families (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4593055A (en) | 1983-01-17 | 1986-06-03 | M&T Chemicals Inc. | Erodible ship-bottom paints for control of marine fouling |
EP0131626B1 (en) | 1983-01-17 | 1989-05-24 | M & T Chemicals, Inc. | Erodible paints for control of marine fouling |
JPS61238848A (ja) * | 1985-04-17 | 1986-10-24 | Shin Etsu Chem Co Ltd | 室温硬化性組成物 |
US4652610A (en) * | 1986-01-03 | 1987-03-24 | Ppg Industries, Inc. | Compositions based on silicon-containing resins having hydrolyzable groups |
JPS6357675A (ja) | 1986-08-28 | 1988-03-12 | Chugoku Toryo Kk | 防汚性コ−テイング材 |
JPS63215780A (ja) | 1987-03-04 | 1988-09-08 | Dainippon Ink & Chem Inc | 防汚塗料用樹脂 |
GB8824003D0 (en) | 1988-10-13 | 1988-11-23 | Int Paint Plc | Coating compositions |
JP2664974B2 (ja) * | 1989-01-27 | 1997-10-22 | 東芝シリコーン株式会社 | 徐溶性コーティング材用ビヒクル |
AU633152B2 (en) * | 1989-10-18 | 1993-01-21 | Toray Thiokol Company Limited | Polysulfide polyether, method of producing same, polymer composition and curable composition |
GB9006318D0 (en) | 1990-03-21 | 1990-05-16 | Courtaulds Coatings Ltd | Coating compositions |
JP2956263B2 (ja) | 1991-02-18 | 1999-10-04 | 日本油脂株式会社 | 塗料組成物 |
JPH04264168A (ja) | 1991-02-18 | 1992-09-18 | Nippon Oil & Fats Co Ltd | 塗料組成物 |
JP2956262B2 (ja) | 1991-02-18 | 1999-10-04 | 日本油脂株式会社 | 塗料組成物 |
JPH0582865A (ja) | 1991-03-27 | 1993-04-02 | Zexel Corp | エキシマレーザ発振器 |
JP2500117B2 (ja) | 1991-07-30 | 1996-05-29 | セントラル硝子株式会社 | 保護被覆を施した機能性膜付ガラス |
JPH06157941A (ja) | 1992-11-17 | 1994-06-07 | Nippon Oil & Fats Co Ltd | 防汚性塗料組成物及びそれを用いた防汚性塗膜の形成方法 |
JPH06157940A (ja) | 1992-11-17 | 1994-06-07 | Nippon Oil & Fats Co Ltd | 防汚性塗料組成物及びそれを用いた防汚性塗膜の形成方法 |
JP3261220B2 (ja) | 1993-06-30 | 2002-02-25 | 日本油脂ビーエーエスエフコーティングス株式会社 | 水中防汚塗料組成物 |
JP2790021B2 (ja) | 1993-09-30 | 1998-08-27 | 日本油脂株式会社 | 塗料組成物 |
JP3279437B2 (ja) | 1994-06-24 | 2002-04-30 | 大日本塗料株式会社 | 防汚塗料組成物 |
GB9415239D0 (en) | 1994-07-28 | 1994-09-21 | Courtaulds Coatings Holdings | Coating compositions |
JP3396349B2 (ja) | 1994-11-21 | 2003-04-14 | 日本油脂ビーエーエスエフコーティングス株式会社 | 生物付着防止用塗料組成物 |
JP3451786B2 (ja) | 1995-03-29 | 2003-09-29 | 日本油脂Basfコーティングス株式会社 | 塗料組成物 |
JP3474673B2 (ja) | 1995-03-30 | 2003-12-08 | 日本油脂Basfコーティングス株式会社 | 塗料組成物 |
JP3474672B2 (ja) | 1995-03-30 | 2003-12-08 | 日本油脂Basfコーティングス株式会社 | 塗料組成物 |
JPH08277372A (ja) | 1995-04-04 | 1996-10-22 | Nippon Oil & Fats Co Ltd | 塗料組成物 |
JP3565988B2 (ja) | 1995-05-29 | 2004-09-15 | 住友化学工業株式会社 | 表面コート剤、その硬化膜およびその硬化膜被覆の合成樹脂成形品 |
JP3696333B2 (ja) | 1995-06-01 | 2005-09-14 | 中国塗料株式会社 | 防汚塗料組成物、この防汚塗料組成物から形成されている塗膜および該防汚塗料組成物を用いた防汚方法並びに該塗膜で被覆された船体または水中構造物 |
JP3681216B2 (ja) * | 1995-06-01 | 2005-08-10 | 中国塗料株式会社 | 防汚塗料組成物、この防汚塗料組成物から形成されている塗膜および該防汚塗料組成物を用いた防汚方法並びに該塗膜で被覆された船体または水中構造物 |
JP3715713B2 (ja) | 1995-06-01 | 2005-11-16 | 中国塗料株式会社 | 防汚塗料組成物、この防汚塗料組成物から形成されている塗膜および該防汚塗料組成物を用いた防汚方法並びに該塗膜で被覆された船体または水中構造物 |
JP3906936B2 (ja) | 1995-06-01 | 2007-04-18 | 中国塗料株式会社 | 防汚塗料組成物、この防汚塗料組成物から形成されている塗膜および該防汚塗料組成物を用いた防汚方法並びに該塗膜で被覆された船体または水中構造物 |
JPH0948951A (ja) | 1995-08-08 | 1997-02-18 | Tonen Corp | 着色コーティング用組成物及びそれを用いた着色ガラスとその製造方法 |
JP3874486B2 (ja) | 1996-04-17 | 2007-01-31 | Basfコーティングスジャパン株式会社 | 塗料組成物 |
KR100484290B1 (ko) * | 1996-12-30 | 2006-01-12 | 고려화학 주식회사 | 도료조성물 |
PL200670B1 (pl) * | 1998-12-28 | 2009-01-30 | Chugoku Marine Paints | Kopolimer sililo(met)akrylanowy, sposób jego wytwarzania, przeciwporostowa kompozycja do malowania zawierająca kopolimer sililo(met)akrylanowy oraz jej zastosowanie |
-
2001
- 2001-10-22 SG SG200106527A patent/SG97209A1/en unknown
- 2001-10-23 DE DE2001600271 patent/DE60100271T2/de not_active Expired - Lifetime
- 2001-10-23 AT AT01308986T patent/ATE240362T1/de not_active IP Right Cessation
- 2001-10-23 ES ES01308986T patent/ES2201017T3/es not_active Expired - Lifetime
- 2001-10-23 US US09/983,181 patent/US6828030B2/en not_active Expired - Lifetime
- 2001-10-23 DK DK01308986T patent/DK1201700T3/da active
- 2001-10-23 PT PT01308986T patent/PT1201700E/pt unknown
- 2001-10-23 EP EP20010308986 patent/EP1201700B1/en not_active Expired - Lifetime
- 2001-10-24 TW TW90126231A patent/TWI241314B/zh not_active IP Right Cessation
- 2001-10-24 KR KR10-2001-0065672A patent/KR100467300B1/ko not_active IP Right Cessation
- 2001-10-24 NO NO20015198A patent/NO333352B1/no not_active IP Right Cessation
- 2001-10-25 CN CNB01135836XA patent/CN1182214C/zh not_active Expired - Fee Related
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2002
- 2002-05-29 HK HK02103998A patent/HK1043693A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
TWI241314B (en) | 2005-10-11 |
NO20015198L (no) | 2002-04-26 |
ATE240362T1 (de) | 2003-05-15 |
KR100467300B1 (ko) | 2005-01-24 |
HK1043693A1 (en) | 2002-09-20 |
EP1201700B1 (en) | 2003-05-14 |
DE60100271T2 (de) | 2004-05-27 |
KR20020032366A (ko) | 2002-05-03 |
CN1182214C (zh) | 2004-12-29 |
DK1201700T3 (da) | 2003-09-15 |
DE60100271D1 (de) | 2003-06-18 |
SG97209A1 (en) | 2003-07-18 |
EP1201700A1 (en) | 2002-05-02 |
US20020156224A1 (en) | 2002-10-24 |
CN1361219A (zh) | 2002-07-31 |
US6828030B2 (en) | 2004-12-07 |
ES2201017T3 (es) | 2004-03-16 |
NO20015198D0 (no) | 2001-10-24 |
PT1201700E (pt) | 2003-09-30 |
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