JP6913757B2 - 防汚組成物 - Google Patents
防汚組成物 Download PDFInfo
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- JP6913757B2 JP6913757B2 JP2019538629A JP2019538629A JP6913757B2 JP 6913757 B2 JP6913757 B2 JP 6913757B2 JP 2019538629 A JP2019538629 A JP 2019538629A JP 2019538629 A JP2019538629 A JP 2019538629A JP 6913757 B2 JP6913757 B2 JP 6913757B2
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- 230000003373 anti-fouling effect Effects 0.000 title claims description 46
- 239000000203 mixture Substances 0.000 title description 41
- 239000000178 monomer Substances 0.000 claims description 256
- -1 polysiloxane group Polymers 0.000 claims description 164
- 239000011230 binding agent Substances 0.000 claims description 130
- 239000008199 coating composition Substances 0.000 claims description 108
- 229920000642 polymer Polymers 0.000 claims description 99
- 229920001296 polysiloxane Polymers 0.000 claims description 77
- 238000000576 coating method Methods 0.000 claims description 61
- 229910052757 nitrogen Inorganic materials 0.000 claims description 56
- 125000002947 alkylene group Chemical group 0.000 claims description 43
- 239000011248 coating agent Substances 0.000 claims description 39
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 37
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 36
- 125000000217 alkyl group Chemical group 0.000 claims description 36
- 239000003139 biocide Substances 0.000 claims description 36
- 150000002148 esters Chemical class 0.000 claims description 35
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- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 30
- 239000007795 chemical reaction product Substances 0.000 claims description 30
- 125000005842 heteroatom Chemical group 0.000 claims description 30
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 28
- 229910052717 sulfur Inorganic materials 0.000 claims description 28
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 27
- 125000003118 aryl group Chemical group 0.000 claims description 25
- 229910052760 oxygen Inorganic materials 0.000 claims description 25
- 229910052698 phosphorus Inorganic materials 0.000 claims description 23
- 125000006717 (C3-C10) cycloalkenyl group Chemical group 0.000 claims description 21
- 230000003115 biocidal effect Effects 0.000 claims description 21
- 239000003921 oil Substances 0.000 claims description 20
- 125000006651 (C3-C20) cycloalkyl group Chemical group 0.000 claims description 19
- 229920000570 polyether Polymers 0.000 claims description 18
- 229910052802 copper Inorganic materials 0.000 claims description 17
- 239000010949 copper Substances 0.000 claims description 17
- 125000004185 ester group Chemical group 0.000 claims description 17
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 17
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 16
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- 125000006373 (C2-C10) alkyl group Chemical group 0.000 claims description 13
- 229910017711 NHRa Inorganic materials 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 12
- 125000003277 amino group Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 239000000049 pigment Substances 0.000 claims description 12
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- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 11
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 11
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- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(i) oxide Chemical compound [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 claims description 10
- 125000000623 heterocyclic group Chemical group 0.000 claims description 10
- 125000006553 (C3-C8) cycloalkenyl group Chemical group 0.000 claims description 9
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- 239000000654 additive Substances 0.000 claims description 9
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- 125000004149 thio group Chemical group *S* 0.000 claims description 9
- 229910052725 zinc Inorganic materials 0.000 claims description 9
- 239000011701 zinc Substances 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 125000006267 biphenyl group Chemical group 0.000 claims description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 7
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims description 6
- PORQOHRXAJJKGK-UHFFFAOYSA-N 4,5-dichloro-2-n-octyl-3(2H)-isothiazolone Chemical compound CCCCCCCCN1SC(Cl)=C(Cl)C1=O PORQOHRXAJJKGK-UHFFFAOYSA-N 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000002228 disulfide group Chemical group 0.000 claims description 6
- 239000012990 dithiocarbamate Substances 0.000 claims description 6
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 claims description 6
- UQAAJPGPIVQWFF-UHFFFAOYSA-N copper;1h-pyridine-2-thione Chemical compound [Cu].SC1=CC=CC=N1 UQAAJPGPIVQWFF-UHFFFAOYSA-N 0.000 claims description 4
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 3
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- 229940043810 zinc pyrithione Drugs 0.000 claims description 3
- 125000006528 (C2-C6) alkyl group Chemical group 0.000 claims description 2
- QHNCWVQDOPICKC-UHFFFAOYSA-N copper;1-hydroxypyridine-2-thione Chemical compound [Cu].ON1C=CC=CC1=S.ON1C=CC=CC1=S QHNCWVQDOPICKC-UHFFFAOYSA-N 0.000 claims description 2
- BQVVSSAWECGTRN-UHFFFAOYSA-L copper;dithiocyanate Chemical compound [Cu+2].[S-]C#N.[S-]C#N BQVVSSAWECGTRN-UHFFFAOYSA-L 0.000 claims description 2
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- 101710088658 Voltage-dependent N-type calcium channel subunit alpha-1B Proteins 0.000 claims 1
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- 239000004205 dimethyl polysiloxane Substances 0.000 description 33
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- 125000000041 C6-C10 aryl group Chemical group 0.000 description 19
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- 239000011572 manganese Substances 0.000 description 18
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- 239000013535 sea water Substances 0.000 description 14
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- 150000001875 compounds Chemical class 0.000 description 13
- 230000007062 hydrolysis Effects 0.000 description 12
- 101000801643 Homo sapiens Retinal-specific phospholipid-transporting ATPase ABCA4 Proteins 0.000 description 11
- 102100033617 Retinal-specific phospholipid-transporting ATPase ABCA4 Human genes 0.000 description 11
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- 238000005498 polishing Methods 0.000 description 10
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- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
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- 150000003839 salts Chemical class 0.000 description 8
- 125000003396 thiol group Chemical group [H]S* 0.000 description 8
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- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 6
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 6
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- 125000000524 functional group Chemical group 0.000 description 6
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- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 5
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- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- JFOJYGMDZRCSPA-UHFFFAOYSA-J octadecanoate;tin(4+) Chemical compound [Sn+4].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O JFOJYGMDZRCSPA-UHFFFAOYSA-J 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 125000005375 organosiloxane group Chemical group 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000773 poly(2-methyl-2-oxazoline) polymer Polymers 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- JKANAVGODYYCQF-UHFFFAOYSA-N prop-2-yn-1-amine Chemical compound NCC#C JKANAVGODYYCQF-UHFFFAOYSA-N 0.000 description 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 1
- ZJLMKPKYJBQJNH-UHFFFAOYSA-N propane-1,3-dithiol Chemical compound SCCCS ZJLMKPKYJBQJNH-UHFFFAOYSA-N 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 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
- 229960002026 pyrithione Drugs 0.000 description 1
- 125000002943 quinolinyl group Chemical class N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- XOVSRHHCHKUFKM-UHFFFAOYSA-N s-methylthiohydroxylamine Chemical compound CSN XOVSRHHCHKUFKM-UHFFFAOYSA-N 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 125000004469 siloxy group Chemical class [SiH3]O* 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- LZOZLBFZGFLFBV-UHFFFAOYSA-N sulfene Chemical compound C=S(=O)=O LZOZLBFZGFLFBV-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 230000009182 swimming Effects 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
- 229940095064 tartrate Drugs 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- RJSZFSOFYVMDIC-UHFFFAOYSA-N tert-butyl n,n-dimethylcarbamate Chemical compound CN(C)C(=O)OC(C)(C)C RJSZFSOFYVMDIC-UHFFFAOYSA-N 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- LSZKGNJKKQYFLR-UHFFFAOYSA-J tri(butanoyloxy)stannyl butanoate Chemical compound [Sn+4].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O LSZKGNJKKQYFLR-UHFFFAOYSA-J 0.000 description 1
- 229920000428 triblock copolymer Polymers 0.000 description 1
- AKUNSPZHHSNFFX-UHFFFAOYSA-M tributyl(tetradecyl)phosphanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC AKUNSPZHHSNFFX-UHFFFAOYSA-M 0.000 description 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical group CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
- CPRPKIMXLHBUGA-UHFFFAOYSA-N triethyltin Chemical compound CC[Sn](CC)CC CPRPKIMXLHBUGA-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- LFRDHGNFBLIJIY-UHFFFAOYSA-N trimethoxy(prop-2-enyl)silane Chemical compound CO[Si](OC)(OC)CC=C LFRDHGNFBLIJIY-UHFFFAOYSA-N 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical group CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 description 1
- KLQSUMRMAGJXSQ-UHFFFAOYSA-J tris(3-oxobutanoyloxy)stannyl 3-oxobutanoate Chemical compound [Sn+4].CC(=O)CC([O-])=O.CC(=O)CC([O-])=O.CC(=O)CC([O-])=O.CC(=O)CC([O-])=O KLQSUMRMAGJXSQ-UHFFFAOYSA-J 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- ITRNXVSDJBHYNJ-UHFFFAOYSA-N tungsten disulfide Chemical compound S=[W]=S ITRNXVSDJBHYNJ-UHFFFAOYSA-N 0.000 description 1
- ODMTYGIDMVZUER-UHFFFAOYSA-N undecane-1,11-dithiol Chemical compound SCCCCCCCCCCCS ODMTYGIDMVZUER-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- WWOFRRCIVMFEDS-UHFFFAOYSA-N zinc;pyridine Chemical compound [Zn+2].C1=CC=NC=C1.C1=CC=NC=C1.C1=CC=NC=C1.C1=CC=NC=C1 WWOFRRCIVMFEDS-UHFFFAOYSA-N 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 150000003755 zirconium compounds Chemical class 0.000 description 1
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
- 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
- C09D5/1675—Polyorganosiloxane-containing compositions
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
-
- 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
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/14—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers in which at least two but not all the silicon atoms are connected by linkages other than oxygen 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
- 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
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1637—Macromolecular compounds
-
- 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
- C09D7/65—Additives macromolecular
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/019—Specific properties of additives the composition being defined by the absence of a certain additive
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (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)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Silicon Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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EP17152301.2 | 2017-01-19 | ||
EP17152301 | 2017-01-19 | ||
PCT/EP2018/051178 WO2018134291A1 (fr) | 2017-01-19 | 2018-01-18 | Composition antisalissure |
Publications (2)
Publication Number | Publication Date |
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JP2020514482A JP2020514482A (ja) | 2020-05-21 |
JP6913757B2 true JP6913757B2 (ja) | 2021-08-04 |
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JP2019538629A Active JP6913757B2 (ja) | 2017-01-19 | 2018-01-18 | 防汚組成物 |
Country Status (7)
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JP (1) | JP6913757B2 (fr) |
KR (1) | KR102346041B1 (fr) |
CN (1) | CN110431195B (fr) |
DE (1) | DE112018000434B4 (fr) |
GB (1) | GB2573944B (fr) |
SG (1) | SG11201906534XA (fr) |
WO (1) | WO2018134291A1 (fr) |
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EP3719076A1 (fr) | 2019-04-01 | 2020-10-07 | Evonik Operations GmbH | Dispersion aqueuse de résine polyorganosiloxanhybride |
EP3744752B1 (fr) | 2019-05-28 | 2024-10-16 | Evonik Operations GmbH | Procédé de fabrication de polysiloxanes à fonction alkoxy non cycliques |
EP3744763B1 (fr) | 2019-05-28 | 2024-08-14 | Evonik Operations GmbH | Polyethérsiloxanes à base de sioc conçus sur mesure |
EP3744764A1 (fr) | 2019-05-28 | 2020-12-02 | Evonik Operations GmbH | Fabrication de polyéthersiloxanes par une liaison sioc |
JP2023523670A (ja) * | 2020-01-27 | 2023-06-07 | モメンティブ パフォーマンス マテリアルズ インコーポレイテッド | 疎水性コーティング組成物 |
GB2592921B (en) | 2020-03-09 | 2024-04-17 | Jotun As | Hull cleaning robot |
WO2021191388A1 (fr) | 2020-03-27 | 2021-09-30 | Jotun A/S | Composition de revêtement antisalissure |
EP3974481A1 (fr) * | 2020-09-29 | 2022-03-30 | Jotun A/S | Composition de revêtement anti-salissures |
GB202107159D0 (en) | 2021-03-23 | 2021-06-30 | Jotun As | Monitoring a vessel |
JP2024514449A (ja) | 2021-03-23 | 2024-04-02 | ヨツン アクティーゼルスカブ | 水中の静止物体の表面の清浄度の監視 |
EP4337634A1 (fr) | 2021-05-10 | 2024-03-20 | Elantas Europe GmbH | Monomères non dangereux en tant que diluants réactifs pour des résines |
CN115894882B (zh) * | 2022-11-04 | 2024-02-27 | 常州瑞杰新材料科技有限公司 | 一种性能优良的含硫醚的液晶聚合物及其制备方法 |
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US4908061A (en) * | 1986-11-13 | 1990-03-13 | Kansai Paint Co., Ltd. | Antifouling coating |
JP2790021B2 (ja) | 1993-09-30 | 1998-08-27 | 日本油脂株式会社 | 塗料組成物 |
SG60054A1 (en) | 1996-04-17 | 1999-02-22 | Nof Corp | Coating composition |
US6011114A (en) | 1996-07-09 | 2000-01-04 | Dow Corning Corporation | Aqueous emulsions which crosslink by Michael addition reactions to form silicon modified organic compositions |
JPH1045996A (ja) * | 1996-08-05 | 1998-02-17 | Chugoku Marine Paints Ltd | ポリマー組成物 |
GB9624881D0 (en) | 1996-11-29 | 1997-01-15 | Courtaulds Coatings Holdings | Coating compositions |
GB9727261D0 (en) | 1997-12-23 | 1998-02-25 | Courtaulds Coatings Holdings | Fouling inhibition |
DE19803468A1 (de) | 1998-01-29 | 1999-08-05 | Wacker Chemie Gmbh | Durch Michael-Addition-ähnliche Reaktionen vernetzte Aminosiliconölemulsionen |
EP1208167B1 (fr) | 1999-06-11 | 2003-07-30 | J.C. Hempel's Skibsfarve-Fabrik A/S | Composition de peinture antisalissures marine autopolissante comprenant des copolymeres qui contiennent du silicium et des fibres |
JP4166391B2 (ja) * | 1999-11-29 | 2008-10-15 | 中国塗料株式会社 | 光硬化性シリコーンブロックアクリル共重合体、共重合体組成物、およびその塗膜、塗膜付き基材、並びに該共重合体の製造方法 |
NO20020846L (no) | 2002-02-21 | 2003-08-22 | Jotun As | Selvpolerende begroingshindrende maling |
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 |
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US20030225184A1 (en) * | 2002-05-30 | 2003-12-04 | Aubart Mark Anthony | Triarylsilyl(meth)acryloyl-containing polymers for marine coating compositions |
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NO323474B1 (no) | 2003-04-29 | 2007-05-21 | Jotun As | Anvendelse av polyanhydrider for fremstilling av begroingshindrende maling og begroingshindrende maling inneholdende polyanhydrider |
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DE102005007320A1 (de) | 2005-02-17 | 2006-08-24 | Consortium für elektrochemische Industrie GmbH | Durch Michael Additionsreaktion härtbare Zusammensetzungen |
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PL2516559T3 (pl) | 2009-12-22 | 2015-04-30 | Hempel As | Nowe kompozycje powłokowe do zwalczania porostów |
DE102010021465A1 (de) * | 2010-05-25 | 2011-12-01 | Clariant International Ltd. | Wässrige Polyurethan-Polyharnstoff-Dispersionen |
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CN102964974A (zh) * | 2011-04-25 | 2013-03-13 | 陶氏环球技术有限公司 | 湿气固化防污涂料组合物 |
US20140170426A1 (en) | 2011-06-30 | 2014-06-19 | Hempel A/S | Novel fouling control coating compositions |
SG2014012421A (en) | 2011-08-18 | 2014-06-27 | Akzo Nobel Coatings Int Bv | Fouling-resistant composition comprising sterols and/or derivatives thereof |
CN104619741B (zh) * | 2012-09-17 | 2017-06-20 | 3M创新有限公司 | 液体环氧树脂涂料组合物、方法和制品 |
KR102201787B1 (ko) | 2013-02-26 | 2021-01-12 | 아크조노벨코팅스인터내셔널비.브이. | 불소화된 옥시알킬렌-함유 폴리머 또는 올리고머를 포함하는 방오 조성물 |
EP2803710A1 (fr) * | 2013-05-14 | 2014-11-19 | 3M Innovative Properties Company | Film adhésif pour graphismes contenant un revêtement anti-graffitis |
US20160312041A1 (en) | 2013-12-05 | 2016-10-27 | Ppg Coatings Europe B.V. | A Coating Composition |
WO2017009301A1 (fr) | 2015-07-13 | 2017-01-19 | Jotun A/S | Composition antisalissure |
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2018
- 2018-01-18 DE DE112018000434.1T patent/DE112018000434B4/de active Active
- 2018-01-18 GB GB1911875.1A patent/GB2573944B/en active Active
- 2018-01-18 CN CN201880019558.0A patent/CN110431195B/zh active Active
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GB201911875D0 (en) | 2019-10-02 |
GB2573944A (en) | 2019-11-20 |
GB2573944B (en) | 2022-11-09 |
WO2018134291A1 (fr) | 2018-07-26 |
CN110431195A (zh) | 2019-11-08 |
DE112018000434T5 (de) | 2019-10-10 |
KR20190102287A (ko) | 2019-09-03 |
SG11201906534XA (en) | 2019-08-27 |
KR102346041B1 (ko) | 2021-12-31 |
DE112018000434B4 (de) | 2024-05-29 |
JP2020514482A (ja) | 2020-05-21 |
CN110431195B (zh) | 2022-02-08 |
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