SU876647A1 - Бистриалкилстанниловые эфиры хлорэндиковой кислоты как антиобрастающий агент в составе полимерного покрыти - Google Patents
Бистриалкилстанниловые эфиры хлорэндиковой кислоты как антиобрастающий агент в составе полимерного покрыти Download PDFInfo
- Publication number
- SU876647A1 SU876647A1 SU782640255A SU2640255A SU876647A1 SU 876647 A1 SU876647 A1 SU 876647A1 SU 782640255 A SU782640255 A SU 782640255A SU 2640255 A SU2640255 A SU 2640255A SU 876647 A1 SU876647 A1 SU 876647A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acid
- agent
- esters
- bistrialkylstannyl
- antiovergrowing
- Prior art date
Links
- 238000000576 coating method Methods 0.000 title claims description 15
- 239000011248 coating agent Substances 0.000 title claims description 5
- 239000002253 acid Substances 0.000 title description 4
- 150000002148 esters Chemical class 0.000 title description 3
- 239000003795 chemical substances by application Substances 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims description 9
- DJKGDNKYTKCJKD-BPOCMEKLSA-N (1s,4r,5s,6r)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene-5,6-dicarboxylic acid Chemical class ClC1=C(Cl)[C@]2(Cl)[C@H](C(=O)O)[C@H](C(O)=O)[C@@]1(Cl)C2(Cl)Cl DJKGDNKYTKCJKD-BPOCMEKLSA-N 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000002519 antifouling agent Substances 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 230000003373 anti-fouling effect Effects 0.000 abstract description 8
- 150000001875 compounds Chemical class 0.000 abstract description 8
- -1 derivatives of chlorinated polycyclic dicarboxylic acids Chemical class 0.000 abstract description 6
- 125000000217 alkyl group Chemical group 0.000 abstract description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 239000003053 toxin Substances 0.000 description 7
- 231100000765 toxin Toxicity 0.000 description 7
- 108700012359 toxins Proteins 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- FLBJFXNAEMSXGL-UHFFFAOYSA-N het anhydride Chemical compound O=C1OC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl FLBJFXNAEMSXGL-UHFFFAOYSA-N 0.000 description 3
- 238000002329 infrared spectrum Methods 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 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 2
- 239000002028 Biomass Substances 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 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 2
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 150000004045 organic chlorine compounds Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 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 2
- 235000014692 zinc oxide Nutrition 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- BQWNRSWYMOOLBV-SQDRRJMKSA-M C(=C\C(=O)O[SnH3])\C(=O)O Chemical compound C(=C\C(=O)O[SnH3])\C(=O)O BQWNRSWYMOOLBV-SQDRRJMKSA-M 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 241000229872 Tolus Species 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
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- MILUHXCABWMFFL-UHFFFAOYSA-N methyl(stannyloxy)stannane Chemical compound C[SnH2]O[SnH3] MILUHXCABWMFFL-UHFFFAOYSA-N 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000012261 resinous substance Substances 0.000 description 1
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 1
- 229950000975 salicylanilide Drugs 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- VIULBFHXDPUWIL-UHFFFAOYSA-N triethyl(triethylstannyloxy)stannane Chemical compound CC[Sn](CC)(CC)O[Sn](CC)(CC)CC VIULBFHXDPUWIL-UHFFFAOYSA-N 0.000 description 1
- DZWGKMVDRPKMPD-UHFFFAOYSA-N tripropyl(tripropylstannyloxy)stannane Chemical compound CCC[Sn](CCC)(CCC)O[Sn](CCC)(CCC)CCC DZWGKMVDRPKMPD-UHFFFAOYSA-N 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
- C09D5/1612—Non-macromolecular compounds
- C09D5/1625—Non-macromolecular compounds organic
- C09D5/1631—Organotin compounds
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
- A01N55/04—Tin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Paints Or Removers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU782640255A SU876647A1 (ru) | 1978-08-08 | 1978-08-08 | Бистриалкилстанниловые эфиры хлорэндиковой кислоты как антиобрастающий агент в составе полимерного покрыти |
| DE2902646A DE2902646C2 (de) | 1978-08-08 | 1979-01-24 | Bis-trialkylstannylderivate chlorierter polycyclischer Dicarbonsäuren, Verfahren zu ihrer Herstellung und Mittel für Aufwuchsverhütungsüberzüge |
| JP54008827A JPS5940398B2 (ja) | 1978-08-08 | 1979-01-30 | 塩素化多環式ジカルボン酸のビス−トリアルキル錫誘導体、その製法及びこの誘導体を含有する防汚剤 |
| ES477519A ES477519A1 (es) | 1978-08-08 | 1979-02-07 | Un metodo para producir derivados de bis-trialcohilestanni- lo. |
| FR7905258A FR2433025B1 (fr) | 1978-08-08 | 1979-02-28 | Derives bis-trialcoylstanniques d'acides polycycliques chlores dicarboxyliques, leur procede de preparation et compositions pour peintures antisalissure les contenant |
| GB7908410A GB2027711B (en) | 1978-08-08 | 1979-03-09 | Bis - trialkylstannyl derivatives of chloroinated polycyclic dicarboxylic acids and antifouling compositions containing same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU782640255A SU876647A1 (ru) | 1978-08-08 | 1978-08-08 | Бистриалкилстанниловые эфиры хлорэндиковой кислоты как антиобрастающий агент в составе полимерного покрыти |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU876647A1 true SU876647A1 (ru) | 1981-10-30 |
Family
ID=20775150
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU782640255A SU876647A1 (ru) | 1978-08-08 | 1978-08-08 | Бистриалкилстанниловые эфиры хлорэндиковой кислоты как антиобрастающий агент в составе полимерного покрыти |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPS5940398B2 (es) |
| DE (1) | DE2902646C2 (es) |
| ES (1) | ES477519A1 (es) |
| FR (1) | FR2433025B1 (es) |
| GB (1) | GB2027711B (es) |
| SU (1) | SU876647A1 (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56148398A (en) * | 1980-04-21 | 1981-11-17 | Mitsubishi Heavy Ind Ltd | Cleaning device |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3517104A (en) * | 1969-05-28 | 1970-06-23 | Pasquale P Minieri | Fungicidal compositions and methods employing dialkyltin,1,4-endoalkylene - 2,3 - dihydrophthages and -1,2,3,6-tetrahydrophthalates |
-
1978
- 1978-08-08 SU SU782640255A patent/SU876647A1/ru active
-
1979
- 1979-01-24 DE DE2902646A patent/DE2902646C2/de not_active Expired
- 1979-01-30 JP JP54008827A patent/JPS5940398B2/ja not_active Expired
- 1979-02-07 ES ES477519A patent/ES477519A1/es not_active Expired
- 1979-02-28 FR FR7905258A patent/FR2433025B1/fr not_active Expired
- 1979-03-09 GB GB7908410A patent/GB2027711B/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2902646C2 (de) | 1982-04-08 |
| GB2027711A (en) | 1980-02-27 |
| JPS5524159A (en) | 1980-02-21 |
| GB2027711B (en) | 1982-11-17 |
| FR2433025B1 (fr) | 1983-05-13 |
| DE2902646A1 (de) | 1980-02-14 |
| JPS5940398B2 (ja) | 1984-09-29 |
| FR2433025A1 (fr) | 1980-03-07 |
| ES477519A1 (es) | 1980-04-01 |
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