KR20180030999A - 가수분해가능한 결합제 - Google Patents
가수분해가능한 결합제 Download PDFInfo
- Publication number
- KR20180030999A KR20180030999A KR1020187003883A KR20187003883A KR20180030999A KR 20180030999 A KR20180030999 A KR 20180030999A KR 1020187003883 A KR1020187003883 A KR 1020187003883A KR 20187003883 A KR20187003883 A KR 20187003883A KR 20180030999 A KR20180030999 A KR 20180030999A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- monomer
- binder
- groups
- polysiloxane
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000011230 binding agent Substances 0.000 title claims abstract description 122
- -1 polysiloxane copolymers Polymers 0.000 claims abstract description 138
- 239000008199 coating composition Substances 0.000 claims abstract description 82
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 64
- 238000002360 preparation method Methods 0.000 claims abstract description 7
- 239000000178 monomer Substances 0.000 claims description 113
- 230000003373 anti-fouling effect Effects 0.000 claims description 43
- 125000003118 aryl group Chemical group 0.000 claims description 39
- 125000000217 alkyl group Chemical group 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 28
- 238000006116 polymerization reaction Methods 0.000 claims description 26
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 25
- 229920001577 copolymer Polymers 0.000 claims description 23
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 20
- 239000003054 catalyst Substances 0.000 claims description 20
- 125000006651 (C3-C20) cycloalkyl group Chemical group 0.000 claims description 19
- 125000004185 ester group Chemical group 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 239000002904 solvent Substances 0.000 claims description 13
- 239000000049 pigment Substances 0.000 claims description 12
- 125000001931 aliphatic group Chemical group 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 11
- 239000000654 additive Substances 0.000 claims description 10
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 125000002947 alkylene group Chemical group 0.000 claims description 9
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 9
- 239000000945 filler Substances 0.000 claims description 9
- 230000000996 additive effect Effects 0.000 claims description 8
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 239000007795 chemical reaction product Substances 0.000 claims description 6
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- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 2
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 125000006713 (C5-C10) cycloalkyl group Chemical group 0.000 claims description 2
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
- 230000000181 anti-adherent effect Effects 0.000 claims 1
- 239000003911 antiadherent Substances 0.000 claims 1
- 238000005187 foaming Methods 0.000 abstract description 3
- 230000003449 preventive effect Effects 0.000 abstract description 2
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- 229920000642 polymer Polymers 0.000 description 85
- 239000011248 coating agent Substances 0.000 description 62
- 239000003139 biocide Substances 0.000 description 37
- 150000002148 esters Chemical class 0.000 description 35
- 239000004205 dimethyl polysiloxane Substances 0.000 description 32
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- 239000011572 manganese Substances 0.000 description 19
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- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical group [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 13
- 238000005498 polishing Methods 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
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- 125000000896 monocarboxylic acid group Chemical group 0.000 description 9
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 9
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- 125000000524 functional group Chemical group 0.000 description 8
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- 238000004458 analytical method Methods 0.000 description 6
- 238000011109 contamination Methods 0.000 description 6
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- 238000011069 regeneration method Methods 0.000 description 5
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- 229910052725 zinc Inorganic materials 0.000 description 5
- 239000011701 zinc Substances 0.000 description 5
- 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 description 5
- MMWRGWQTAMNAFC-UHFFFAOYSA-N 1,2-dihydropyridine Chemical compound C1NC=CC=C1 MMWRGWQTAMNAFC-UHFFFAOYSA-N 0.000 description 4
- JJTUDXZGHPGLLC-IMJSIDKUSA-N 4511-42-6 Chemical compound C[C@@H]1OC(=O)[C@H](C)OC1=O JJTUDXZGHPGLLC-IMJSIDKUSA-N 0.000 description 4
- VIZORQUEIQEFRT-UHFFFAOYSA-N Diethyl adipate Chemical compound CCOC(=O)CCCCC(=O)OCC VIZORQUEIQEFRT-UHFFFAOYSA-N 0.000 description 4
- DKMROQRQHGEIOW-UHFFFAOYSA-N Diethyl succinate Chemical compound CCOC(=O)CCC(=O)OCC DKMROQRQHGEIOW-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
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- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
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- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
- 229920006243 acrylic copolymer Polymers 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
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- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 238000013270 controlled release Methods 0.000 description 4
- QHNCWVQDOPICKC-UHFFFAOYSA-N copper;1-hydroxypyridine-2-thione Chemical compound [Cu].ON1C=CC=CC1=S.ON1C=CC=CC1=S QHNCWVQDOPICKC-UHFFFAOYSA-N 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
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- 125000004494 ethyl ester group Chemical group 0.000 description 4
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- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 3
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 3
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
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- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 2
- BSDOQSMQCZQLDV-UHFFFAOYSA-N butan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] BSDOQSMQCZQLDV-UHFFFAOYSA-N 0.000 description 2
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- 238000000354 decomposition reaction Methods 0.000 description 2
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- 238000009792 diffusion process Methods 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- XTDYIOOONNVFMA-UHFFFAOYSA-N dimethyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC XTDYIOOONNVFMA-UHFFFAOYSA-N 0.000 description 2
- ALOUNLDAKADEEB-UHFFFAOYSA-N dimethyl sebacate Chemical compound COC(=O)CCCCCCCCC(=O)OC ALOUNLDAKADEEB-UHFFFAOYSA-N 0.000 description 2
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- SHZIWNPUGXLXDT-UHFFFAOYSA-N ethyl hexanoate Chemical compound CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 2
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- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 2
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- 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
- 229960005235 piperonyl butoxide Drugs 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
- 229920000555 poly(dimethylsilanediyl) polymer Polymers 0.000 description 1
- 229920002187 poly[N-2-(hydroxypropyl) methacrylamide] polymer Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000647 polyepoxide Chemical group 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
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- 150000003077 polyols Chemical group 0.000 description 1
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- 230000002028 premature Effects 0.000 description 1
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- HKJYVRJHDIPMQB-UHFFFAOYSA-N propan-1-olate;titanium(4+) Chemical compound CCCO[Ti](OCCC)(OCCC)OCCC HKJYVRJHDIPMQB-UHFFFAOYSA-N 0.000 description 1
- XPGAWFIWCWKDDL-UHFFFAOYSA-N propan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCC[O-].CCC[O-].CCC[O-].CCC[O-] XPGAWFIWCWKDDL-UHFFFAOYSA-N 0.000 description 1
- ZGSOBQAJAUGRBK-UHFFFAOYSA-N propan-2-olate;zirconium(4+) Chemical compound [Zr+4].CC(C)[O-].CC(C)[O-].CC(C)[O-].CC(C)[O-] ZGSOBQAJAUGRBK-UHFFFAOYSA-N 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 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
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
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- 238000007761 roller coating Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
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- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 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
- SYXYWTXQFUUWLP-UHFFFAOYSA-N sodium;butan-1-olate Chemical compound [Na+].CCCC[O-] SYXYWTXQFUUWLP-UHFFFAOYSA-N 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
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- 229940014800 succinic anhydride Drugs 0.000 description 1
- BZWKPZBXAMTXNQ-UHFFFAOYSA-N sulfurocyanidic acid Chemical compound OS(=O)(=O)C#N BZWKPZBXAMTXNQ-UHFFFAOYSA-N 0.000 description 1
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- 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
- 125000005497 tetraalkylphosphonium group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 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
- AKUNSPZHHSNFFX-UHFFFAOYSA-M tributyl(tetradecyl)phosphanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC AKUNSPZHHSNFFX-UHFFFAOYSA-M 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-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
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 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
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical group CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 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
- 150000003672 ureas Chemical class 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
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 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
- 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
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/10—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by other chemical means
- B05D3/107—Post-treatment of applied coatings
- B05D3/108—Curing
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/695—Polyesters containing atoms other than carbon, hydrogen and oxygen containing silicon
- C08G63/6954—Polyesters containing atoms other than carbon, hydrogen and oxygen containing silicon derived from polxycarboxylic acids and polyhydroxy compounds
- C08G63/6956—Dicarboxylic acids and dihydroxy compounds
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
-
- 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
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/44—Block-or graft-polymers containing polysiloxane sequences containing only polysiloxane sequences
-
- 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
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/445—Block-or graft-polymers containing polysiloxane sequences containing polyester sequences
-
- 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
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/46—Block-or graft-polymers containing polysiloxane sequences containing polyether sequences
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of 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; Compositions of derivatives of such polymers
- C08L83/10—Block- or graft-copolymers containing polysiloxane sequences
-
- 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/02—Polyesters derived from dicarboxylic acids and dihydroxy 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
- C09D183/04—Polysiloxanes
- C09D183/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen
-
- 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
- C09D183/10—Block or graft copolymers containing polysiloxane sequences
-
- 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
- C09D183/10—Block or graft copolymers containing polysiloxane sequences
- C09D183/12—Block or graft copolymers containing polysiloxane sequences containing polyether sequences
-
- 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
-
- 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
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/28—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen sulfur-containing groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Paints Or Removers (AREA)
- Polyesters Or Polycarbonates (AREA)
- Silicon Polymers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15176493.3 | 2015-07-13 | ||
| EP15176493 | 2015-07-13 | ||
| PCT/EP2016/066422 WO2017009283A1 (en) | 2015-07-13 | 2016-07-11 | Hydrolysable binder |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20180030999A true KR20180030999A (ko) | 2018-03-27 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020187003883A Withdrawn KR20180030999A (ko) | 2015-07-13 | 2016-07-11 | 가수분해가능한 결합제 |
| KR1020187004146A Active KR102814344B1 (ko) | 2015-07-13 | 2016-07-11 | 방오 조성물 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020187004146A Active KR102814344B1 (ko) | 2015-07-13 | 2016-07-11 | 방오 조성물 |
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| Country | Link |
|---|---|
| US (3) | US20190292404A1 (enExample) |
| EP (2) | EP3322760A1 (enExample) |
| JP (4) | JP7097810B2 (enExample) |
| KR (2) | KR20180030999A (enExample) |
| CN (3) | CN108137954B (enExample) |
| WO (3) | WO2017009297A1 (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20190292404A1 (en) * | 2015-07-13 | 2019-09-26 | Evonik Degussa Gmbh | Hydrolysable binder |
| EP3305840B1 (en) | 2016-10-05 | 2019-11-06 | Evonik Degussa GmbH | Compatibilizer for universal colorant in solventborne alkyd paints |
| JP6913757B2 (ja) | 2017-01-19 | 2021-08-04 | ヨトゥン アーエス | 防汚組成物 |
| EP3461864B1 (de) | 2017-09-28 | 2025-10-29 | Evonik Operations GmbH | Härtbare zusammensetzung auf basis von polysiloxanen |
| EP3489311A1 (en) | 2017-11-24 | 2019-05-29 | Jotun A/S | Antifouling composition |
| EP3489310A1 (en) | 2017-11-24 | 2019-05-29 | Jotun A/S | Antifouling composition |
| EP3524651B1 (de) | 2018-02-08 | 2025-11-26 | Evonik Operations GmbH | Wässrige polyorganosiloxanhybridharz-dispersion |
| EP3853294A4 (en) * | 2018-09-17 | 2022-06-08 | Elevance Renewable Sciences, Inc. | SEGMENTED SILICONE POLYMERS, AND METHODS OF MAKING AND USE THEREOF |
| US11306184B2 (en) | 2018-09-17 | 2022-04-19 | Wilmar Trading Pte. | Functionalized silicone polymers and methods of making and using the same |
| US11680171B2 (en) | 2018-11-29 | 2023-06-20 | Henry Company, Llc | Self-cleaning, dirt pick-up resistant compositions for roof coatings |
| JP7534111B2 (ja) * | 2019-03-26 | 2024-08-14 | 大日本塗料株式会社 | 塗料組成物 |
| EP3719076A1 (de) | 2019-04-01 | 2020-10-07 | Evonik Operations GmbH | Wässrige polyorganosiloxanhybridharz-dispersion |
| PL3744763T3 (pl) | 2019-05-28 | 2024-12-16 | Evonik Operations Gmbh | Dopasowane siloksany polieterowe na bazie SIOC |
| EP3744764A1 (de) | 2019-05-28 | 2020-12-02 | Evonik Operations GmbH | Herstellung von sioc-verknüpften polyethersiloxanen |
| PL3744752T3 (pl) | 2019-05-28 | 2025-02-10 | Evonik Operations Gmbh | Sposób wytwarzania niecyklicznych polisiloksanów funkcjonalizowanych alkoksylem |
| CN110862751A (zh) * | 2019-11-18 | 2020-03-06 | 中国船舶重工集团公司第七二五研究所 | 一种有机硅酯类海洋防污材料及其制备方法 |
| EP3828240A1 (en) | 2019-11-29 | 2021-06-02 | Jotun A/S | Fouling release coating |
| GB2592921B (en) | 2020-03-09 | 2024-04-17 | Jotun As | Hull cleaning robot |
| JP2023519444A (ja) | 2020-03-27 | 2023-05-10 | ヨツン エーエス | 防汚コーティング組成物 |
| US11530362B2 (en) * | 2020-04-23 | 2022-12-20 | The Boeing Company | Organosiloxane-based surface treatments for enhancing the adhesion and lubricity of metal surfaces |
| KR102560679B1 (ko) * | 2020-12-04 | 2023-07-28 | (주)노루페인트 | 변성 에테르 폴리디알킬실록산 화합물, 이의 제조방법 및 이를 포함하는 해상용 방오도료 |
| GB202107159D0 (en) | 2021-03-23 | 2021-06-30 | Jotun As | Monitoring a vessel |
| KR20230172498A (ko) | 2021-03-23 | 2023-12-22 | 요툰 에이/에스 | 정지 물체의 수중 표면의 청결도 모니터링 |
| JPWO2023132147A1 (enExample) | 2022-01-05 | 2023-07-13 | ||
| 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 |
| JP7626108B2 (ja) * | 2022-07-07 | 2025-02-04 | 信越化学工業株式会社 | オルガノポリシロキサンの回収方法、硬化性液状シリコーンゴム組成物及びその製造方法 |
| KR102526375B1 (ko) * | 2022-08-23 | 2023-04-26 | 이동철 | 우수한 내오염성을 갖는 1액형 유성 발수제 조성물 및 이의 제조 방법 |
| KR102710785B1 (ko) * | 2024-03-13 | 2024-09-26 | 주식회사 링크솔루텍 | 내시경 보호를 위한 코팅용 조성물 |
Family Cites Families (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3376657D1 (en) | 1982-08-04 | 1988-06-23 | Dow Corning | Siloxane polyester compositions and use thereof |
| JPS61174273A (ja) * | 1985-01-28 | 1986-08-05 | Nichirin Rubber Kogyo Kk | 防汚塗料 |
| JP2739488B2 (ja) * | 1988-12-29 | 1998-04-15 | 日本ペイント株式会社 | 加水分解型シリコーン樹脂被膜を有する塗装物 |
| US5180843A (en) * | 1990-06-18 | 1993-01-19 | Lenick Jr Anthony J O | Terminal substituted silicone fatty esters |
| US5210133A (en) * | 1992-06-15 | 1993-05-11 | Siltech Inc. | Silicone polyester polymers as delivery systems |
| JPH06220361A (ja) | 1993-01-27 | 1994-08-09 | Toyobo Co Ltd | 防汚塗料用ポリエステル系樹脂組成物 |
| JP2790021B2 (ja) | 1993-09-30 | 1998-08-27 | 日本油脂株式会社 | 塗料組成物 |
| US5414054A (en) * | 1994-06-01 | 1995-05-09 | Miles Inc. | Copolycarbonate having improved low-temperature impact strength |
| JP3389338B2 (ja) | 1994-07-06 | 2003-03-24 | 信越化学工業株式会社 | 加水分解性官能基含有オルガノポリシロキサンの製造方法及び硬化性樹脂組成物 |
| JP3465199B2 (ja) * | 1994-10-05 | 2003-11-10 | 日本ペイント株式会社 | 防汚塗料組成物 |
| SG60054A1 (en) | 1996-04-17 | 1999-02-22 | Nof Corp | Coating composition |
| GB9727261D0 (en) | 1997-12-23 | 1998-02-25 | Courtaulds Coatings Holdings | Fouling inhibition |
| DE60004248T2 (de) | 1999-06-11 | 2004-04-15 | J.C. Hempel's Skibsfarve-Fabrik A/S | Selbstpolierende anwuchsverhindernde anstrichfarbe für wasserfahrzeuge - mit silizium enthaltenden copolymeren und fasern |
| US6774183B1 (en) * | 2000-04-27 | 2004-08-10 | Bostik, Inc. | Copolyesters having improved retained adhesion |
| JP2002265611A (ja) * | 2001-03-07 | 2002-09-18 | Mitsubishi Rayon Co Ltd | ポリエステル系ブロック共重合体 |
| JP4159033B2 (ja) | 2001-03-21 | 2008-10-01 | アクゾ ノーベル ナムローゼ フェンノートシャップ | 弗素化アルキル−又はアルコキシ−含有ポリマー又はオリゴマーを含む付着防止組成物 |
| 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 |
| NO320324B1 (no) | 2002-03-26 | 2005-11-21 | Jotun As | Polymerer og monomerer og anvendelse derav samt fremgangsmate for fremstilling av polymerer og begroingshindrende maling inneholdende polymerer |
| US7297727B2 (en) | 2002-05-28 | 2007-11-20 | Arkema Inc. | Triarylsilyl(meth)acryloyl-containing polymers for marine coating compositions |
| US7807752B2 (en) * | 2003-01-27 | 2010-10-05 | Daikin Industries, Ltd. | Coating composition |
| MY145980A (en) | 2003-03-26 | 2012-05-31 | Sigmakalon Services B V | Process for the preparation of poly(silyl esters)s, and their uses |
| NO323474B1 (no) | 2003-04-29 | 2007-05-21 | Jotun As | Anvendelse av polyanhydrider for fremstilling av begroingshindrende maling og begroingshindrende maling inneholdende polyanhydrider |
| ES2276314T3 (es) | 2003-07-07 | 2007-06-16 | Akzo Nobel Coatings International B.V. | Composiciones de copolimero de ester de sililo. |
| DE102004057382A1 (de) | 2004-11-26 | 2006-06-01 | Huhtamaki Forchheim Zweigniederlassung Der Huhtamaki Deutschland Gmbh & Co. Kg | Verfahren zur Herstellung dünner Schichten eines Silikons, dünnes Silikon und Verwendung |
| EP1879972A4 (en) * | 2005-05-09 | 2008-10-15 | Ndsu Res Foundation | ANTIFOULIN MATERIALS WITH POLYAMINE NETWORK POLYSILOXANES |
| WO2008121308A1 (en) * | 2007-03-28 | 2008-10-09 | The Sherwin-Williams Company | Self-polishing anti-fouling compositions |
| MX2009011841A (es) | 2007-05-01 | 2009-11-18 | Akzo Nobel Coatings Int Bv | Composicion de recubrimiento contra obstrucciones por algas y fauna marina basada en copolimeros de poliorganosiloxano polioxialquileno que se pueden curar. |
| ES2356867T3 (es) | 2007-05-01 | 2011-04-13 | Akzo Nobel Coatings International B.V. | Composiciones de recubrimiento contra incrustaciones que contienen una organosilicona carboxi-funcional. |
| DE102007035646A1 (de) * | 2007-07-27 | 2009-01-29 | Evonik Goldschmidt Gmbh | Über SIC- und über Carbonsäureestergruppen verknüpfte lineare Polydimethylsiloxan-Polyoxyalkylen-Blockcopolymere, ein Verfahren zur ihrer Herstellung und ihre Verwendung |
| DE102007044148A1 (de) * | 2007-09-15 | 2009-03-26 | Evonik Goldschmidt Gmbh | Neuartige siloxanhaltige Blockcopolymere, Verfahren zu deren Herstellung und deren Verwendung für Schmiermittel |
| JP2010004831A (ja) | 2008-06-30 | 2010-01-14 | Bio Sangyo Kk | インジェクション装置、加工食肉製造装置、及び加工食肉の製造方法 |
| US7786241B2 (en) * | 2008-07-16 | 2010-08-31 | O'lenick Kevin Anthony | Polyester silicone resins |
| WO2010018164A1 (en) | 2008-08-11 | 2010-02-18 | Hempel A/S | Novel tie-coat compositions |
| JP2011105809A (ja) * | 2009-11-13 | 2011-06-02 | Mitsubishi Chemicals Corp | ポリシロキサン骨格を有するポリエステルポリオールの製造方法 |
| PT2516559E (pt) | 2009-12-22 | 2015-02-06 | Hempel As | Novas composições de revestimento para controlo de incrustações |
| WO2012066084A1 (de) * | 2010-11-17 | 2012-05-24 | Byk-Chemie Gmbh | Aus urethan-basierten, polysiloxan enthaltenden makromonomeren erhältliche copolymere, verfahren zu deren herstellung und deren verwendung |
| PL2691487T3 (pl) * | 2011-03-31 | 2015-05-29 | Akzo Nobel Coatings Int Bv | Kompozycja powłokowa zapobiegająca zanieczyszczeniom porostowym |
| 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 |
| US8829140B2 (en) * | 2011-05-17 | 2014-09-09 | Momentive Performance Materials Inc. | Polysiloxane-polyorgano block copolymers |
| PL2726559T3 (pl) | 2011-06-30 | 2017-09-29 | Hempel A/S | Powłoki przeciwporostowe na bazie polisiloksanu zawierające enzymy |
| DE102012210294A1 (de) * | 2012-06-19 | 2013-12-19 | Evonik Industries Ag | Bewuchsmindernde-Additive, Verfahren zu deren Herstellung und deren Verwendung in Beschichtungen |
| EP2883897A4 (en) * | 2012-08-10 | 2016-03-30 | Unitika Ltd | POLYARYLATE RESIN, AND RESIN SOLUTION AND FILM USING THE SAME |
| US9828524B2 (en) | 2012-11-13 | 2017-11-28 | Chugoku Marine Paints, Ltd. | Antifouling coating composition, antifouling coating film, antifouling substrate, and method for improving storage stability of antifouling coating compositions |
| JP6072066B2 (ja) | 2012-11-13 | 2017-02-01 | 中国塗料株式会社 | 硬化性オルガノポリシロキサン系防汚性複合塗膜、および該複合塗膜で被覆された防汚基材 |
| FR2999980A1 (fr) * | 2012-12-20 | 2014-06-27 | Bluestar Silicones France | Article presentant des proprietes antisalissures et destine a etre utilise dans des applications aquatiques en particulier marines |
| PL2961805T3 (pl) | 2013-02-26 | 2017-06-30 | Akzo Nobel Coatings International B.V. | Kompozycje przeciwzanieczyszczeniowe z fluorowanym, zawierającym oksyalkilen polimerem lub oligomerem |
| PL2976394T3 (pl) * | 2013-03-20 | 2018-07-31 | Hempel A/S | Nowe systemy powłokowe do zwalczania porastania na bazie polisiloksanu |
| EP2980123B1 (en) * | 2013-03-29 | 2019-05-29 | Idemitsu Kosan Co., Ltd | Polyorganosiloxane and polycarbonate-polyorganosiloxane copolymer |
| JP6728038B2 (ja) * | 2013-10-08 | 2020-07-22 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハー | 反応性官能性シロキサン組成物 |
| ES2699004T3 (es) * | 2013-12-05 | 2019-02-06 | Ppg Coatings Europe Bv | Una composición de recubrimiento |
| US20190292404A1 (en) * | 2015-07-13 | 2019-09-26 | Evonik Degussa Gmbh | Hydrolysable binder |
-
2016
- 2016-07-11 US US15/743,232 patent/US20190292404A1/en not_active Abandoned
- 2016-07-11 WO PCT/EP2016/066451 patent/WO2017009297A1/en not_active Ceased
- 2016-07-11 CN CN201680045925.5A patent/CN108137954B/zh active Active
- 2016-07-11 CN CN201680052312.4A patent/CN108026396A/zh active Pending
- 2016-07-11 JP JP2018501270A patent/JP7097810B2/ja active Active
- 2016-07-11 KR KR1020187003883A patent/KR20180030999A/ko not_active Withdrawn
- 2016-07-11 EP EP16736888.5A patent/EP3322760A1/en active Pending
- 2016-07-11 WO PCT/EP2016/066457 patent/WO2017009301A1/en not_active Ceased
- 2016-07-11 KR KR1020187004146A patent/KR102814344B1/ko active Active
- 2016-07-11 US US15/744,095 patent/US10954395B2/en active Active
- 2016-07-11 WO PCT/EP2016/066422 patent/WO2017009283A1/en not_active Ceased
- 2016-07-11 JP JP2017568051A patent/JP2018522106A/ja not_active Withdrawn
- 2016-07-11 CN CN201680046054.9A patent/CN108271380B/zh active Active
- 2016-07-11 EP EP16736504.8A patent/EP3322759A1/en not_active Withdrawn
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- 2019-12-12 US US16/712,580 patent/US20200115562A1/en not_active Abandoned
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2021
- 2021-09-17 JP JP2021151975A patent/JP7378448B2/ja active Active
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2023
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| JP7378448B2 (ja) | 2023-11-13 |
| CN108137954A (zh) | 2018-06-08 |
| EP3322760A1 (en) | 2018-05-23 |
| JP2024001054A (ja) | 2024-01-09 |
| JP7097810B2 (ja) | 2022-07-08 |
| CN108026396A (zh) | 2018-05-11 |
| US10954395B2 (en) | 2021-03-23 |
| JP2018522106A (ja) | 2018-08-09 |
| KR20180042238A (ko) | 2018-04-25 |
| US20180201795A1 (en) | 2018-07-19 |
| KR102814344B1 (ko) | 2025-05-28 |
| WO2017009301A1 (en) | 2017-01-19 |
| WO2017009297A1 (en) | 2017-01-19 |
| US20200115562A1 (en) | 2020-04-16 |
| EP3322759A1 (en) | 2018-05-23 |
| CN108271380A (zh) | 2018-07-10 |
| JP7431378B2 (ja) | 2024-02-14 |
| WO2017009283A1 (en) | 2017-01-19 |
| CN108271380B (zh) | 2020-10-23 |
| CN108137954B (zh) | 2021-03-19 |
| KR20180042240A (ko) | 2018-04-25 |
| JP2018526485A (ja) | 2018-09-13 |
| US20190292404A1 (en) | 2019-09-26 |
| JP2022000517A (ja) | 2022-01-04 |
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