DK149187B - Begroningshaemmende overtraeksmateriale indeholdende en phenyltinforbindelse - Google Patents
Begroningshaemmende overtraeksmateriale indeholdende en phenyltinforbindelse Download PDFInfo
- Publication number
- DK149187B DK149187B DK195779AA DK195779A DK149187B DK 149187 B DK149187 B DK 149187B DK 195779A A DK195779A A DK 195779AA DK 195779 A DK195779 A DK 195779A DK 149187 B DK149187 B DK 149187B
- Authority
- DK
- Denmark
- Prior art keywords
- oxide
- colophonium
- coating material
- trialkyltin
- hydroxide
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims description 20
- -1 PHENYLTIN COMPOUND Chemical class 0.000 title claims description 18
- 230000002401 inhibitory effect Effects 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 111
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 claims description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 20
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical group CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 19
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 18
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 239000011248 coating agent Substances 0.000 claims description 17
- 238000000576 coating method Methods 0.000 claims description 17
- YYNNRJWNBXEQTP-UHFFFAOYSA-N 2-[(4-bromophenyl)sulfonylamino]-3-phenylpropanoic acid Chemical compound C=1C=C(Br)C=CC=1S(=O)(=O)NC(C(=O)O)CC1=CC=CC=C1 YYNNRJWNBXEQTP-UHFFFAOYSA-N 0.000 claims description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 239000007795 chemical reaction product Substances 0.000 claims description 11
- 239000011787 zinc oxide Substances 0.000 claims description 9
- 230000003373 anti-fouling effect Effects 0.000 claims description 8
- 239000011230 binding agent Substances 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 239000000049 pigment Substances 0.000 claims description 7
- 238000002386 leaching Methods 0.000 claims description 6
- 238000012360 testing method Methods 0.000 claims description 5
- QDDILISMHGFOPK-CKYSYVORSA-N [(1s,4ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-1-yl]-tributylstannylmethanone Chemical compound C1CC(C(C)C)=CC2=CCC3[C@](C(=O)[Sn](CCCC)(CCCC)CCCC)(C)CCC[C@]3(C)C21 QDDILISMHGFOPK-CKYSYVORSA-N 0.000 claims description 4
- 230000009467 reduction Effects 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 3
- 239000002519 antifouling agent Substances 0.000 claims description 2
- 239000011521 glass Substances 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 230000000052 comparative effect Effects 0.000 claims 1
- 230000002708 enhancing effect Effects 0.000 claims 1
- 239000000047 product Substances 0.000 claims 1
- REDSKZBUUUQMSK-UHFFFAOYSA-N tributyltin Chemical group CCCC[Sn](CCCC)CCCC.CCCC[Sn](CCCC)CCCC REDSKZBUUUQMSK-UHFFFAOYSA-N 0.000 claims 1
- 239000003973 paint Substances 0.000 description 26
- 230000015572 biosynthetic process Effects 0.000 description 21
- 230000000694 effects Effects 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 3
- 239000012024 dehydrating agents Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 150000007514 bases Chemical class 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- 150000007942 carboxylates Chemical group 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 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 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 1
- 229940112669 cuprous oxide Drugs 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- ODOPKAJVFRHHGM-UHFFFAOYSA-N phenyltin Chemical class [Sn]C1=CC=CC=C1 ODOPKAJVFRHHGM-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- CRHIAMBJMSSNNM-UHFFFAOYSA-N tetraphenylstannane Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CRHIAMBJMSSNNM-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical class C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 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
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1637—Macromolecular compounds
- C09D5/1643—Macromolecular compounds containing tin
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Priority Applications (16)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK195779AA DK149187B (da) | 1979-05-10 | 1979-05-10 | Begroningshaemmende overtraeksmateriale indeholdende en phenyltinforbindelse |
| IL59947A IL59947A (en) | 1979-05-10 | 1980-04-29 | Anti-fouling paint compositions |
| GR61847A GR68514B (ref) | 1979-05-10 | 1980-05-03 | |
| ZA00802678A ZA802678B (en) | 1979-05-10 | 1980-05-05 | Paint composition |
| MX182242A MX152231A (es) | 1979-05-10 | 1980-05-08 | Mejoras a composicion de pintura |
| BR8002889A BR8002889A (pt) | 1979-05-10 | 1980-05-09 | Composicao de tinta para pintura |
| ES491328A ES8105024A1 (es) | 1979-05-10 | 1980-05-09 | Un procedimiento para preparar una composicion de pintura que contiene grupos carboxilatos |
| DE8080301524T DE3062413D1 (en) | 1979-05-10 | 1980-05-09 | Paint composition |
| PT71218A PT71218A (en) | 1979-05-10 | 1980-05-09 | Process for preparing a paint composition |
| EP80301524A EP0019433B1 (en) | 1979-05-10 | 1980-05-09 | Paint composition |
| NO801369A NO801369L (no) | 1979-05-10 | 1980-05-09 | Karboksylatgruppe-holdig maling. |
| CA351,666A CA1130954A (en) | 1979-05-10 | 1980-05-09 | Anti-fouling paint composition |
| JP55060829A JPS599587B2 (ja) | 1979-05-10 | 1980-05-09 | 防汚塗料組成物におけるベンゼンの生成を阻止する方法 |
| AU58273/80A AU527455B2 (en) | 1979-05-10 | 1980-05-09 | Phenyltin paint composition |
| US06/148,126 US4303444A (en) | 1979-05-10 | 1980-05-09 | Method for inhibiting benzene formation in antifouling paints |
| SG804/83A SG80483G (en) | 1979-05-10 | 1983-12-20 | Paint composition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK195779 | 1979-05-10 | ||
| DK195779AA DK149187B (da) | 1979-05-10 | 1979-05-10 | Begroningshaemmende overtraeksmateriale indeholdende en phenyltinforbindelse |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DK195779A DK195779A (da) | 1980-11-11 |
| DK149187B true DK149187B (da) | 1986-03-10 |
Family
ID=8109142
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK195779AA DK149187B (da) | 1979-05-10 | 1979-05-10 | Begroningshaemmende overtraeksmateriale indeholdende en phenyltinforbindelse |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4303444A (ref) |
| EP (1) | EP0019433B1 (ref) |
| JP (1) | JPS599587B2 (ref) |
| AU (1) | AU527455B2 (ref) |
| BR (1) | BR8002889A (ref) |
| CA (1) | CA1130954A (ref) |
| DE (1) | DE3062413D1 (ref) |
| DK (1) | DK149187B (ref) |
| ES (1) | ES8105024A1 (ref) |
| GR (1) | GR68514B (ref) |
| IL (1) | IL59947A (ref) |
| MX (1) | MX152231A (ref) |
| NO (1) | NO801369L (ref) |
| PT (1) | PT71218A (ref) |
| SG (1) | SG80483G (ref) |
| ZA (1) | ZA802678B (ref) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4410363A (en) * | 1981-07-21 | 1983-10-18 | The United States Of America As Represented By The Secretary Of The Navy | Underwater applicable antifoulant paint composition |
| GB8511144D0 (en) * | 1985-05-02 | 1985-06-12 | Int Paint Plc | Marine anti-fouling paint |
| EP2285776B1 (en) * | 2008-05-13 | 2013-01-30 | Invista Technologies S.à.r.l. | Stabilization of triphenylboron-pyridine |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO128713B (ref) * | 1967-07-03 | 1974-01-02 | Takeda Chemical Industries Ltd | |
| US3639583A (en) * | 1968-06-28 | 1972-02-01 | Goodrich Co B F | Biocidal elastomeric compositions |
| US3717606A (en) * | 1971-04-05 | 1973-02-20 | H Lomasney | Solventless coal tar extended antifouling coating |
| GB1457590A (en) * | 1974-04-03 | 1976-12-08 | Int Paint Co | Marine paint |
| JPS52124029A (en) * | 1976-04-13 | 1977-10-18 | Kansai Paint Co Ltd | Antifouling coating compositions |
| US4191579A (en) * | 1976-10-18 | 1980-03-04 | The International Paint Company Limited | Antifouling paint comprising a copolymer containing organo tin salt and a pigment having a component which reacts with sea water and another component which does not react with sea water |
-
1979
- 1979-05-10 DK DK195779AA patent/DK149187B/da unknown
-
1980
- 1980-04-29 IL IL59947A patent/IL59947A/xx unknown
- 1980-05-03 GR GR61847A patent/GR68514B/el unknown
- 1980-05-05 ZA ZA00802678A patent/ZA802678B/xx unknown
- 1980-05-08 MX MX182242A patent/MX152231A/es unknown
- 1980-05-09 PT PT71218A patent/PT71218A/pt unknown
- 1980-05-09 ES ES491328A patent/ES8105024A1/es not_active Expired
- 1980-05-09 NO NO801369A patent/NO801369L/no unknown
- 1980-05-09 JP JP55060829A patent/JPS599587B2/ja not_active Expired
- 1980-05-09 AU AU58273/80A patent/AU527455B2/en not_active Ceased
- 1980-05-09 EP EP80301524A patent/EP0019433B1/en not_active Expired
- 1980-05-09 DE DE8080301524T patent/DE3062413D1/de not_active Expired
- 1980-05-09 BR BR8002889A patent/BR8002889A/pt unknown
- 1980-05-09 US US06/148,126 patent/US4303444A/en not_active Expired - Lifetime
- 1980-05-09 CA CA351,666A patent/CA1130954A/en not_active Expired
-
1983
- 1983-12-20 SG SG804/83A patent/SG80483G/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MX152231A (es) | 1985-06-12 |
| ES491328A0 (es) | 1981-05-16 |
| DK195779A (da) | 1980-11-11 |
| ES8105024A1 (es) | 1981-05-16 |
| JPS55151066A (en) | 1980-11-25 |
| US4303444A (en) | 1981-12-01 |
| IL59947A (en) | 1983-05-15 |
| GR68514B (ref) | 1982-01-11 |
| ZA802678B (en) | 1981-05-27 |
| EP0019433B1 (en) | 1983-03-23 |
| JPS599587B2 (ja) | 1984-03-03 |
| BR8002889A (pt) | 1980-12-23 |
| PT71218A (en) | 1980-06-01 |
| EP0019433A2 (en) | 1980-11-26 |
| IL59947A0 (en) | 1980-06-30 |
| EP0019433A3 (en) | 1980-12-10 |
| AU5827380A (en) | 1980-11-13 |
| CA1130954A (en) | 1982-09-07 |
| NO801369L (no) | 1980-11-11 |
| AU527455B2 (en) | 1983-03-03 |
| SG80483G (en) | 1985-03-08 |
| DE3062413D1 (en) | 1983-04-28 |
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