JP6887783B2 - Antifouling paint compositions, antifouling coatings and their uses - Google Patents
Antifouling paint compositions, antifouling coatings and their uses Download PDFInfo
- Publication number
- JP6887783B2 JP6887783B2 JP2016224045A JP2016224045A JP6887783B2 JP 6887783 B2 JP6887783 B2 JP 6887783B2 JP 2016224045 A JP2016224045 A JP 2016224045A JP 2016224045 A JP2016224045 A JP 2016224045A JP 6887783 B2 JP6887783 B2 JP 6887783B2
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- JP
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- Prior art keywords
- antifouling
- group
- antifouling coating
- coating composition
- mass
- 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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- 230000003373 anti-fouling effect Effects 0.000 title claims description 176
- 238000000576 coating method Methods 0.000 title claims description 77
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- 239000008199 coating composition Substances 0.000 claims description 82
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- 239000002184 metal Substances 0.000 claims description 47
- 229910052751 metal Inorganic materials 0.000 claims description 47
- 239000000463 material Substances 0.000 claims description 39
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 36
- 239000002519 antifouling agent Substances 0.000 claims description 33
- 125000004432 carbon atom Chemical group C* 0.000 claims description 32
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- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 229960002140 medetomidine Drugs 0.000 claims description 18
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- BIYQABXZPGYWIZ-UHFFFAOYSA-N 1-(chloromethyldisulfanyl)octane Chemical compound CCCCCCCCSSCCl BIYQABXZPGYWIZ-UHFFFAOYSA-N 0.000 claims description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims description 2
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- 241001474374 Blennius Species 0.000 description 1
- 241000700675 Bugula neritina Species 0.000 description 1
- LLYUJBFGHPSABS-UHFFFAOYSA-N CC(CCCCCCC)SSCl Chemical compound CC(CCCCCCC)SSCl LLYUJBFGHPSABS-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
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- 239000005977 Ethylene Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 241000243320 Hydrozoa Species 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000555745 Sciuridae Species 0.000 description 1
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- 239000002253 acid Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
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- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 238000009360 aquaculture Methods 0.000 description 1
- 244000144974 aquaculture Species 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
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- 238000006243 chemical reaction Methods 0.000 description 1
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- 238000007334 copolymerization reaction Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid ester group Chemical group C(CCCCCCCCCCC)(=O)O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000009503 electrostatic coating Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 description 1
- RBVLUTAXWVILBT-UHFFFAOYSA-N ethyl prop-2-eneperoxoate Chemical compound CCOOC(=O)C=C RBVLUTAXWVILBT-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- SCDFWNDQCMAYQI-UHFFFAOYSA-N octadecan-1-amine;triphenylborane Chemical compound CCCCCCCCCCCCCCCCCCN.C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 SCDFWNDQCMAYQI-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical group CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- FSAJWMJJORKPKS-UHFFFAOYSA-N octadecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C=C FSAJWMJJORKPKS-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- WJSXSXUHWBSPEP-UHFFFAOYSA-N pyridine;triphenylborane Chemical compound C1=CC=NC=C1.C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 WJSXSXUHWBSPEP-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical group O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 238000005464 sample preparation method Methods 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000003351 stiffener Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical group CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical group CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000003871 white petrolatum Substances 0.000 description 1
- PIMBTRGLTHJJRV-UHFFFAOYSA-L zinc;2-methylprop-2-enoate Chemical compound [Zn+2].CC(=C)C([O-])=O.CC(=C)C([O-])=O PIMBTRGLTHJJRV-UHFFFAOYSA-L 0.000 description 1
- XKMZOFXGLBYJLS-UHFFFAOYSA-L zinc;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)C=C XKMZOFXGLBYJLS-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
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
Description
本発明は、防汚塗料組成物に関し、より詳細には漁具(例:ロープ、漁網、浮き子、ブイ)、船舶、水中構造物等の表面への水棲生物の付着による汚染の防止に使用される防汚塗料組成物等に関する。 The present invention relates to an antifouling paint composition, and more specifically, is used for preventing contamination due to adhesion of aquatic organisms to the surface of fishing gear (eg, rope, fishing net, float, buoy), ship, underwater structure, etc. Antifouling paint composition, etc.
従来、火力、原子力発電所の給排水口等の水中構造物、各種海洋土木工事の汚泥拡散防止膜、船舶、漁具(例:ロープ、漁網、浮き子、ブイ)などの接水部分に、水棲生物が付着し生長すると、例えば、基材の表面粗度が増加して船舶の速度の低下および燃費の拡大を招き、また、基材表面に塗布された防食用塗膜が損傷して、水中構造物の強度や機能の低下や、寿命の著しい短縮化といった被害が生ずるおそれがある。さらに、火力、原子力発電所等の海水の給排水管に水棲生物が付着、繁殖すると冷却水の給排水循環に支障をきたすことがある。 Conventionally, aquatic organisms have been used in underwater structures such as water supply and drainage ports of nuclear power plants, sludge diffusion prevention membranes for various marine civil engineering works, ships, fishing gear (eg ropes, fishing nets, floats, buoys), etc. When the material adheres and grows, for example, the surface roughness of the base material increases, which leads to a decrease in the speed of the ship and an increase in fuel consumption, and the anticorrosion coating film applied to the surface of the base material is damaged, resulting in an underwater structure. There is a risk of damage such as deterioration of the strength and function of the object and significant shortening of the life. Furthermore, if aquatic organisms adhere to and propagate in the water supply and drainage pipes of seawater such as thermal power plants and nuclear power plants, the circulation of cooling water supply and drainage may be hindered.
また、養殖網、定置網等の漁網は、海中に長期間設置されるため、この漁網に各種水棲生物例えば、ヒドロゾア等の腔腸動物、アオノリ、ミドロ類等の海藻類、二枚貝類、フジツボ、シロウスボヤ、セルプラ、コケムシ、軟体動物などが多量に付着する。漁網は、水棲生物の付着により、重くなり漁網の取扱い性が低下したり、破損しやすくなったりするため、頻繁に取替える必要がある。さらに、水棲生物の付着により漁網が目詰まりを起こし、海水の流通が阻害され、養殖魚類を死に至らしめるなどの被害が生じる恐れがある。 In addition, since fishing nets such as aquaculture nets and fixed nets are installed in the sea for a long period of time, various aquatic organisms such as coelenterates such as hydrozoa, seaweeds such as green laver and green laver, bivalves, fujitsubo, and white squirrel , Serpra, coelenterates, mollusks, etc. adhere in large quantities. Fishing nets need to be replaced frequently because they become heavier due to the attachment of aquatic organisms, making them less manageable and more vulnerable to damage. Furthermore, the attachment of aquatic organisms may cause clogging of fishing nets, obstructing the flow of seawater, and causing damage such as death of farmed fish.
さらに、火力、原子力発電所等の海水の給排水管に水棲生物が付着、繁殖すると冷却水の給排水循環に支障をきたすことがある。
このような不具合に対して、防汚剤を含有する防汚塗料(防汚塗料組成物)を基材に塗布して水棲生物の付着を防止することが一般的に行われている。
Furthermore, if aquatic organisms adhere to and propagate in the water supply and drainage pipes of seawater such as thermal power plants and nuclear power plants, the circulation of cooling water supply and drainage may be hindered.
In response to such problems, it is common practice to apply an antifouling paint (antifouling paint composition) containing an antifouling agent to a base material to prevent the adhesion of aquatic organisms.
たとえば特許文献1には、加水分解性共重合体と防汚剤としてのメデトミジンとを含有する防汚塗料組成物が開示されており、さらに、この防汚塗料組成物から形成される防汚塗膜が長期防汚性に優れていることが記載されている。 For example, Patent Document 1 discloses an antifouling coating composition containing a hydrolyzable copolymer and medetomidine as an antifouling agent, and further, an antifouling coating formed from the antifouling coating composition. It is described that the membrane has excellent long-term antifouling properties.
また、特許文献2には、ポリシロキサンブロック含有金属塩共重合体とシリコーンオイルと防汚剤を含有する防汚塗料組成物が開示されており、さらに、この防汚塗料組成物から形成される防汚塗膜が長期防汚性に優れていること、具体的には、板の上に防汚塗料組成物を塗布し、乾燥させて得られた試験板を海中に浸漬する試験において優れた長期防汚性が発現したことが記載されている。 Further, Patent Document 2 discloses an antifouling coating composition containing a polysiloxane block-containing metal salt copolymer, silicone oil, and an antifouling agent, and is further formed from this antifouling coating composition. The antifouling coating material has excellent long-term antifouling properties, specifically, it is excellent in a test in which an antifouling coating composition is applied onto a plate and the test plate obtained by drying is immersed in the sea. It is described that long-term antifouling property was exhibited.
しかしながら、特許文献1または2に開示された防汚塗料組成物は、上述のように優れた長期防汚性を発揮するものの、漁網に含浸・塗布した場合には長期防汚性にさらなる改善の余地があることがわかった。さらに、貯蔵安定性の点で改善の余地があることがわかった。 However, although the antifouling coating composition disclosed in Patent Document 1 or 2 exhibits excellent long-term antifouling property as described above, when impregnated and applied to a fishing net, the long-term antifouling property is further improved. It turned out that there was room. Furthermore, it was found that there is room for improvement in terms of storage stability.
このような問題点に鑑み、本発明は、水棲生物による基材の汚損を防止するために使用される防汚塗料組成物であって、貯蔵安定性に優れ、かつ船舶、水中構造物の基材のみならず漁網に含浸・塗布した場合であっても長期間に亘って優れた防汚性を発現することのできる防汚塗料組成物、および該防汚塗料組成物から形成される防汚塗膜等を提供することを目的とする。 In view of these problems, the present invention is an antifouling coating composition used for preventing contamination of a base material by aquatic organisms, which is excellent in storage stability and is a basis for ships and underwater structures. An antifouling paint composition capable of exhibiting excellent antifouling properties for a long period of time even when impregnated and applied not only to a material but also to a fishing net, and an antifouling coating composition formed from the antifouling coating composition. An object of the present invention is to provide a coating film or the like.
本発明者らは研究を重ねたところ、ポリエーテル変性シリコーンオイルとメデトミジンと塗膜形成樹脂を含む防汚塗料が、貯蔵安定性に優れ、かつ漁具(例:ロープ、浮子、ブイ)、船舶、水中構造物等の基材のみならず漁網に含浸・塗布した場合であっても長期防汚性に優れる塗膜等を形成できることを見い出し、本発明を完成するに至った。本発明の要旨は以下のとおりである。 As a result of repeated studies, the present inventors have found that antifouling paints containing polyether-modified silicone oil, medetomidin, and coating resin have excellent storage stability, and fishing gear (eg, ropes, floats, buoys), ships, etc. The present invention has been completed by finding that a coating film having excellent long-term antifouling property can be formed not only on a base material such as an underwater structure but also on a fishing net by impregnation and coating. The gist of the present invention is as follows.
[1]
ポリエーテル変性シリコーンオイル(A)と防汚剤(B)と塗膜形成樹脂(C)とを含有する防汚塗料組成物であって、
前記ポリエーテル変性シリコーンオイル(A)が一般式[I]:
[1]
An antifouling coating composition containing a polyether-modified silicone oil (A), an antifouling agent (B), and a coating film-forming resin (C).
The polyether-modified silicone oil (A) has a general formula [I]:
X1、X2およびX3はそれぞれ独立に炭素数1〜5のアルキル基、フェニル基またはポリエーテル基を示し、
X4は炭素数1〜18のアルキル基またはフェニル基を示し、
mは1以上の整数を示し、
nは0以上の整数を示し、
pは0以上の整数を示し、
前記ポリエーテル基は下式[Ia]:
−R2−A−(R3O)q(R4O)r−R5 ・・・[Ia]
(式[Ia]中、Aは単結合または酸素原子を示し、
R2、R3およびR4はそれぞれ独立に炭素数1〜5の2価の炭化水素基を示し、
R5は炭素数1〜5のアルキル基または水素原子を示し、
qは1〜30の整数を示し、
rは0〜30の整数を示し、
左端の線はケイ素原子への結合を示す。)
で表される。〕で表され、1分子中に少なくとも1つの前記ポリエーテル基を有し、
前記防汚剤(B)としてメデトミジン(B1)を含有する
防汚塗料組成物。
X 1 , X 2 and X 3 independently represent an alkyl group, a phenyl group or a polyether group having 1 to 5 carbon atoms, respectively.
X 4 represents an alkyl or phenyl group having 1 to 18 carbon atoms.
m indicates an integer of 1 or more,
n indicates an integer greater than or equal to 0,
p indicates an integer greater than or equal to 0,
The polyether group has the following formula [Ia]:
−R 2 −A− (R 3 O) q (R 4 O) r −R 5・ ・ ・ [Ia]
(In formula [Ia], A represents a single bond or an oxygen atom,
R 2 , R 3 and R 4 each independently represent a divalent hydrocarbon group having 1 to 5 carbon atoms.
R 5 represents an alkyl group or a hydrogen atom having 1 to 5 carbon atoms.
q indicates an integer from 1 to 30
r represents an integer from 0 to 30
The leftmost line shows the bond to the silicon atom. )
It is represented by. ], Which has at least one of the above-mentioned polyether groups in one molecule.
An antifouling coating composition containing medetomidine (B1) as the antifouling agent (B).
[2]
前記メデトミジン(B1)の含有量が、前記ポリエーテル変性シリコーンオイル(A)100質量部に対して0.01〜1,000質量部である前記[1]に記載の防汚塗料組成物。
[2]
The antifouling coating composition according to the above [1], wherein the content of the medetomidine (B1) is 0.01 to 1,000 parts by mass with respect to 100 parts by mass of the polyether-modified silicone oil (A).
[3]
前記塗膜形成樹脂(C)が、(メタ)アクリル酸金属塩共重合体、ポリエステル金属塩共重合体、シリルエステル含有共重合体、ポリシロキサンブロック含有金属塩共重合体、硫黄含有オルガノポリシロキサンブロックビニル共重合体、塩化ビニル系樹脂、塩化ビニル−酢酸ビニル共重合体、塩化ビニル−ビニルイソブチルエーテル共重合体、塩化ゴム系樹脂、アクリル樹脂、スチレン−ブタジエン系樹脂、ポリエステル系樹脂、エポキシ系樹脂、フェノール系樹脂、合成ゴム、石油系樹脂、ロジンエステル系樹脂、ロジン系石鹸、およびロジンからなる群から選ばれる一種以上である前記[1]または[2]に記載の防汚塗料組成物。
[3]
The coating film-forming resin (C) is a (meth) acrylic acid metal salt copolymer, a polyester metal salt copolymer, a silyl ester-containing copolymer, a polysiloxane block-containing metal salt copolymer, and a sulfur-containing organopolysiloxane. Block vinyl copolymer, vinyl chloride resin, vinyl chloride-vinyl acetate copolymer, vinyl chloride-vinyl isobutyl ether copolymer, rubber chloride resin, acrylic resin, styrene-butadiene resin, polyester resin, epoxy The antifouling coating composition according to the above [1] or [2], which is one or more selected from the group consisting of resins, phenolic resins, synthetic rubbers, petroleum resins, rosin ester resins, rosin soaps, and rosins. ..
[4]
前記防汚剤(B)として、さらにメデトミジン以外の防汚剤(B2)を含有する前記[1]〜[3]のいずれかに記載の防汚塗料組成物。
[4]
The antifouling coating composition according to any one of the above [1] to [3], which further contains an antifouling agent (B2) other than medetomidine as the antifouling agent (B).
[5]
前記メデトミジン以外の防汚剤(B2)が、亜酸化銅、ロダン銅、銅粉、ビスジメチルジチオカルバモイルジンクエチレンビスジチオカーバメート、ジンクジメチルジチオカーバメート、ジンクエチレンビスジチオカーバメート、N,N−ジメチル−N’−(3,4−ジクロロフェニル)尿素、N−(2,4,6−トリクロロフェニル)マレイミド、2−メチルチオ−4−tert−ブチルアミノ−6−シクロプロピルアミノ−1,3,5−トリアジン、テトラエチルチウラムジスルフィド、4,5−ジクロロ−2−n−オクチル−4−イソチアゾリン−3−オン、銅ピリチオン、ジンクピリチオン、2,3−ジクロロ−N−(2',6'−ジエチルフェニル)マレイミド、2,3−ジクロロ−N−(2'−エチル−6'−メチルフェニル)マレイミド、4−ブロモ−2−(4−クロロフェニル)−5−(トリフルオロメチル)−1H−ピロール−3−カルボニトリル、トリフェニルボラン・アミン錯体、ジフェニルメチルボラン・4−イソプロピルビリジン、クロロメチル−n−オクチルジスルフィド、N’,N’−ジメチル−N−フェニル−(N−フルオロジクロロメチルチオ)スルファミド、およびN’,N’−ジメチル−N−トリル−(N−フルオロジクロロメチルチオ)スルファミドからなる群から選ばれる一種以上である前記[4]に記載の防汚塗料組成物。
[5]
Antifouling agents (B2) other than medetomidin include cuprous oxide, rodane copper, copper powder, bisdimethyldithiocarbamoyl disulfide bisdithiocarbamate, disulfide dithiocarbamate, disulfide bisdithiocarbamate, N, N-dimethyl-N. '-(3,4-dichlorophenyl) urea, N- (2,4,6-trichlorophenyl) maleimide, 2-methylthio-4-tert-butylamino-6-cyclopropylamino-1,3,5-triazine, Tetraethylthiuram disulfide, 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one, copper pyrithione, zincpyrythione, 2,3-dichloro-N- (2', 6'-diethylphenyl) maleimide, 2 , 3-Dichloro-N- (2'-ethyl-6'-methylphenyl) maleimide, 4-bromo-2- (4-chlorophenyl) -5- (trifluoromethyl) -1H-pyrrole-3-carbonitrile, Triphenylboran amine complex, diphenylmethylboran 4-isopropylviridine, chloromethyl-n-octyl disulfide, N', N'-dimethyl-N-phenyl- (N-fluorodichloromethylthio) sulfamide, and N', N The antifouling coating composition according to the above [4], which is one or more selected from the group consisting of'-dimethyl-N-tolyl- (N-fluorodichloromethylthio) sulfamide.
[6]
前記防汚剤(B2)を、前記メデトミジン(B1)1質量部に対して600質量部以下の割合で含有する前記[4]または[5]に記載の防汚塗料組成物。
[6]
The antifouling coating composition according to the above [4] or [5], which contains the antifouling agent (B2) in a proportion of 600 parts by mass or less with respect to 1 part by mass of the medetomidine (B1).
[7]
さらに、ポリオレフィン類、ポリスルフィド類、パラフィン類、およびワセリン類からなる群から選ばれた少なくとも1種の可塑性樹脂(D)を含む前記[1]〜[6]のいずれかに記載の防汚塗料組成物。
[7]
The antifouling coating composition according to any one of the above [1] to [6], further containing at least one plastic resin (D) selected from the group consisting of polyolefins, polysulfides, paraffins, and petrolatums. Stuff.
[8]
前記ポリエーテル変性シリコーンオイル(A)のHLBが0.5〜10である前記[1]〜[7]のいずれかに記載の防汚塗料組成物。
[8]
The antifouling coating composition according to any one of the above [1] to [7], wherein the HLB of the polyether-modified silicone oil (A) is 0.5 to 10.
[9]
さらに、CuO、ZnO、TiO2、Al2O3、SiO2、およびMgOからなる群から選択される1種以上の金属酸化物(E)を含む前記[1]〜[8]のいずれかに記載の防汚塗料組成物。
[9]
Further, any one of the above [1] to [8] containing one or more metal oxides (E) selected from the group consisting of CuO, ZnO, TiO 2 , Al 2 O 3 , SiO 2, and MgO. The antifouling paint composition according to the description.
[10]
漁具の塗装に使用される前記[1]〜[9]のいずれかに記載の防汚塗料組成物。
[10]
The antifouling paint composition according to any one of the above [1] to [9], which is used for painting fishing gear.
[11]
前記[1]〜[10]のいずれかに記載の防汚塗料組成物から形成された防汚塗膜。
[11]
An antifouling coating film formed from the antifouling coating composition according to any one of [1] to [10].
[12]
基材と、前記基材の表面に設けられた前記[11]に記載の防汚塗膜とを有する防汚塗膜付き基材。
[12]
A base material with an antifouling coating film having a base material and the antifouling coating film according to the above [11] provided on the surface of the base material.
[13]
前記基材が漁具、船舶または水中構造物である前記[12]に記載の防汚塗膜付き基材。
[13]
The base material with an antifouling coating film according to the above [12], wherein the base material is a fishing gear, a ship, or an underwater structure.
[14]
前記[1]〜[10]のいずれかに記載の防汚塗料組成物で網染めされた漁網。
[14]
A fishing net dyed with the antifouling paint composition according to any one of [1] to [10].
[15]
前記[1]〜[10]のいずれかに記載の防汚塗料組成物を基材に塗布するかまたは含浸させ、次いで硬化させる、基材の防汚方法。
[15]
An antifouling method for a base material, wherein the base material is coated with or impregnated with the antifouling coating composition according to any one of [1] to [10] and then cured.
[16]
基材の表面に、前記[1]〜[10]のいずれかに記載の防汚塗料組成物を塗布するかまたは含浸させる工程と、前記工程により前記基材に塗布されたまたは含浸された前記防汚塗料組成物を硬化させる工程とを備える防汚塗膜付き基材の製造方法。
[16]
The step of applying or impregnating the surface of the base material with the antifouling coating composition according to any one of [1] to [10], and the step of applying or impregnating the base material by the step. A method for producing a base material with an antifouling coating film, which comprises a step of curing the antifouling coating composition.
本発明の防汚塗料組成物は、造膜性に優れている。また本発明の防汚塗料組成物は、貯蔵安定性に優れるため、長期間保存することが可能である。さらに本発明の防汚塗料組成物は、漁具(例:ロープ、浮子、ブイ)、船舶、水中構造物等の基材だけではなく漁網に含浸・塗布した場合であっても長期防汚性を発揮することができる。また、本発明の防汚塗料組成物は、たとえば漁網に用いられた場合、腔腸動物類、藻類、二枚貝類、軟体動物類等の広範な生物種に防汚効果を発揮すると共に、特にフジツボ類および腔腸動物類への長期の防汚効果を発揮する。 The antifouling coating composition of the present invention is excellent in film forming property. Further, since the antifouling coating composition of the present invention is excellent in storage stability, it can be stored for a long period of time. Further, the antifouling coating composition of the present invention provides long-term antifouling property even when impregnated / applied to fishing nets as well as base materials such as fishing gear (eg, ropes, buoys, buoys), ships, and underwater structures. Can be demonstrated. Further, when the antifouling coating composition of the present invention is used for a fishing net, for example, it exerts an antifouling effect on a wide range of organisms such as coelenterates, algae, bivalves and mollusks, and particularly barnacles. Demonstrates a long-term antifouling effect on species and coelenterates.
以下、本発明に係る防汚塗料組成物、防汚塗膜、およびこれらの用途について具体的に説明する。
なお、「(メタ)アクリル((meth)acryl)」は、アクリル(acryl)およびメタクリル(methacryl)を総称する語句である。
Hereinafter, the antifouling coating composition, the antifouling coating film, and their uses according to the present invention will be specifically described.
In addition, "(meth) acrylic ((meth) acryl)" is a general term for acrylic (acryl) and methacryl (methacryl).
[防汚塗料組成物]
本発明の防汚塗料組成物は、ポリエーテル変性シリコーンオイル(A)と防汚剤(B)と塗膜形成樹脂(C)を含有しており、目的に応じて、任意成分をさらに含んでいてもよい。
[Anti-fouling paint composition]
The antifouling coating composition of the present invention contains a polyether-modified silicone oil (A), an antifouling agent (B), and a coating film-forming resin (C), and further contains an arbitrary component depending on the purpose. You may.
(A)ポリエーテル変性シリコーンオイル:
前記ポリエーテル変性シリコーンオイル(A)は下記一般式[I]で表される化合物である。
(A) Polyether-modified silicone oil:
The polyether-modified silicone oil (A) is a compound represented by the following general formula [I].
X1、X2およびX3はそれぞれ独立に炭素数1〜5のアルキル基、フェニル基またはポリエーテル基を示す。X1が複数個存在する場合(すなわち、pが2以上の整数の場合)、これらは互いに同一であっても異なっていてもよい。 X 1 , X 2 and X 3 independently represent an alkyl group, a phenyl group or a polyether group having 1 to 5 carbon atoms, respectively. If X 1 is present a plurality (i.e., if p is an integer of 2 or more), they may being the same or different.
前記炭素数1〜5のアルキル基としては、たとえばメチル基、エチル基、プロピル基、ブチル基およびペンチル基が挙げられる。
X4は炭素数1〜18のアルキル基またはフェニル基を示し、X4が複数個存在する場合(すなわち、nが2以上の整数の場合)、これらは互いに同一であっても異なっていてもよい。炭素数1〜18のアルキル基としては、たとえば炭素数1〜5のアルキル基として例示したもの、ヘキシル基、オクチル基、2−エチルヘキシル基、ラウリル基およびステアリル基が挙げられる。
Examples of the alkyl group having 1 to 5 carbon atoms include a methyl group, an ethyl group, a propyl group, a butyl group and a pentyl group.
X 4 represents an alkyl group or a phenyl group having 1 to 18 carbon atoms, if X 4 is present a plurality (i.e., when n is an integer of 2 or more), be different even they are identical to each other Good. Examples of the alkyl group having 1 to 18 carbon atoms include those exemplified as an alkyl group having 1 to 5 carbon atoms, a hexyl group, an octyl group, a 2-ethylhexyl group, a lauryl group and a stearyl group.
mは1以上の整数を示し、nは0以上の整数を示し、pは0以上の整数を示す。また、式[I]において、 m indicates an integer of 1 or more, n indicates an integer of 0 or more, and p indicates an integer of 0 or more. Further, in the formula [I],
前記ポリエーテル基は式[Ia]:
−R2−A−(R3O)q−(R4O)r−R5 ・・・[Ia]
で表される。
The polyether group is of the formula [Ia] :.
−R 2 −A− (R 3 O) q − (R 4 O) r −R 5・ ・ ・ [Ia]
It is represented by.
式[Ia]において、Aは単結合または酸素原子を示す。また、左端の線は隣接するケイ素原子への結合を示す。
R2、R3およびR4は、それぞれ独立に炭素数1〜5の2価の炭化水素基、好ましくは2価の飽和炭化水素基、より好ましくは炭素数2〜5のアルキレン基を示す。このアルキレン基は、直鎖状または分岐状であってもよく、好ましくは直鎖状である。アルキレン基としては、たとえばメチレン基、エチレン基、トリメチレン基、プロピレン基およびテトラメチレン基が挙げられ、エチレン基およびトリメチレン基が好ましい。
In formula [Ia], A represents a single bond or an oxygen atom. The leftmost line shows the bond to the adjacent silicon atom.
R 2 , R 3 and R 4 independently represent a divalent hydrocarbon group having 1 to 5 carbon atoms, preferably a divalent saturated hydrocarbon group, and more preferably an alkylene group having 2 to 5 carbon atoms. The alkylene group may be linear or branched, preferably linear. Examples of the alkylene group include a methylene group, an ethylene group, a trimethylene group, a propylene group and a tetramethylene group, and an ethylene group and a trimethylene group are preferable.
R2は好ましくはエチレン基またはトリメチレン基であり、R3は好ましくはエチレン基であり、R4は好ましくはトリメチレン基である。
R5は炭素数1〜5のアルキル基または水素原子を示し、好ましくはアルキル基である。このアルキル基としては、たとえばメチル基、エチル基、プロピル基、ブチル基およびペンチル基が挙げられる。
R 2 is preferably an ethylene group or a trimethylene group, R 3 is preferably an ethylene group, and R 4 is preferably a trimethylene group.
R 5 represents an alkyl group or a hydrogen atom having 1 to 5 carbon atoms, and is preferably an alkyl group. Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, a butyl group and a pentyl group.
qは1〜30の整数(繰り返し単位数)を示し、rは0〜30の整数(繰り返し単位数)を示す。
防汚性、またはポリエーテル変性シリコーンオイル(A)と後述する塗膜形成樹脂(C)との相溶性などを考慮すると、前記ポリエーテル基としては、好ましくは、-C3H6-O-(C2H4O)q-C2H5、-C2H4-O-(C3H6O)q-CH3、-C3H6-O-(C2H4O)q-CH3、-C2H4-O-(C3H6O)q-CH3、-C3H6-(C2H4O)q-CH3、-C2H4-(C3H6O)q-CH3、-C3H6-(C2H4O)q-H、-C2H4-(C3H6O)q-H、-C3H6-O-(C3H6O)q-CH3、-CH2-O-(C2H4O)q-CH3、-CH2-O-(C2H4O)q-H、-C2H4-O-(C2H4O)q-CH3、-C2H4-O-(C2H4O)q-H、-CH2-O-(C3H6O)q-CH3、-CH2-O-(C3H6O)q-H、-CH2-O-(C4H8O)q-CH3、-CH2-O-(C4H8O)q-H、-C3H6-O-(C3H6O)q-H、-C4H8-O-(C4H8O)q-H、-C3H6-O-(C2H4O)q-(C3H6O)r-CH3、-C3H6-O-(C2H4O)q-(C3H6O)r-H、-C3H6-O-(C3H6O)q-(C2H4O)r-CH3、および-C3H6-O-(C3H6O)q-(C2H4O)r-Hが挙げられる。これらの化学式において、C2H4は(CH2)2(エチレン基)であり、C3H6は(CH2)3(トリメチレン基)またはCH(CH3)CH2(プロピレン基)であり、好ましくは(CH2)3である。
q indicates an integer of 1 to 30 (number of repeating units), and r indicates an integer of 0 to 30 (number of repeating units).
Antifouling properties, or by considering the compatibility with the polyether-modified silicone oil (A) and later to film-forming resin (C), examples of the polyether group, preferably, -C 3 H 6 -O- (C 2 H 4 O) q -C 2 H 5 , -C 2 H 4 -O- (C 3 H 6 O) q -CH 3 , -C 3 H 6 -O- (C 2 H 4 O) q -CH 3, -C 2 H 4 -O- (C 3 H 6 O) q -CH 3, -C 3 H 6 - (C 2 H 4 O) q -CH 3, -C 2 H 4 - (C 3 H 6 O) q -CH 3 , -C 3 H 6 - (C 2 H 4 O) q -H, -C 2 H 4 - (C 3 H 6 O) q -H, -C 3 H 6 - O- (C 3 H 6 O) q -CH 3 , -CH 2 -O- (C 2 H 4 O) q -CH 3 , -CH 2 -O- (C 2 H 4 O) q -H,- C 2 H 4 -O- (C 2 H 4 O) q -CH 3 , -C 2 H 4 -O- (C 2 H 4 O) q -H, -CH 2 -O- (C 3 H 6 O) ) Q -CH 3 , -CH 2 -O- (C 3 H 6 O) q -H, -CH 2 -O- (C 4 H 8 O) q -CH 3 , -CH 2 -O- (C 4) H 8 O) q -H, -C 3 H 6 -O- (C 3 H 6 O) q -H, -C 4 H 8 -O- (C 4 H 8 O) q -H, -C 3 H 6 -O- (C 2 H 4 O) q- (C 3 H 6 O) r -CH 3 , -C 3 H 6 -O- (C 2 H 4 O) q- (C 3 H 6 O) r -H, -C 3 H 6 -O- (C 3 H 6 O) q- (C 2 H 4 O) r -CH 3 , and -C 3 H 6 -O- (C 3 H 6 O) q- (C 2 H 4 O) r -H can be mentioned. In these chemical formulas, C 2 H 4 is (CH 2 ) 2 (ethylene group) and C 3 H 6 is (CH 2 ) 3 (trimethylene group) or CH (CH 3 ) CH 2 (propylene group). , Preferably (CH 2 ) 3 .
前記ポリエーテル基としては、-(CH2)3-O-(C2H4O)q-CH3、-C2H4-O-((CH2)3O)q-CH3が特に好ましい。
前記ポリエーテル変性シリコーンオイル(A)は、1分子中に少なくとも1つの前記ポリエーテル基を有する。
As the polyether group,-(CH 2 ) 3 -O- (C 2 H 4 O) q -CH 3 and -C 2 H 4 -O-((CH 2 ) 3 O) q -CH 3 are particularly suitable. preferable.
The polyether-modified silicone oil (A) has at least one of the polyether groups in one molecule.
前記ポリエーテル変性シリコーンオイル(A)としては、
(a):前記式[I]において、X1が前記式[Ia]で表されるポリエーテル基であり、X2およびX3がメチル基等のアルキル基またはフェニル基であり、pが1以上の整数である側鎖型ポリエーテル変性シリコーンオイル、
(b):前記式[I]において、X1がメチル基等のアルキル基またはフェニル基であり、X2およびX3が前記式[Ia]で表されるポリエーテル基である両末端型ポリエーテル変性シリコーンオイル、
(c):前記式[I]において、X1ならびにX2およびX3の一方が前記式[Ia]で表されるポリエーテル基であり、X2およびX3の一方がメチル基等のアルキル基またはフェニル基であり、pが1以上の整数であるポリエーテル変性シリコーンオイル、
(d):前記式[I]において、X1、X2およびX3が前記式[Ia]で表されるポリエーテル基であり、pが1以上の整数であるポリエーテル変性シリコーンオイル、
(e):前記式[I]において、X2およびX3の一方が前記式[Ia]で表されるポリエーテル基であり、X1ならびにX2およびX3の一方がメチル基等のアルキル基またはフェニル基であるポリエーテル変性シリコーンオイル
等が挙げられる。これらの中では、防汚性等の観点から、側鎖型ポリエーテル変性シリコーンオイル(a)および両末端型ポリエーテル変性シリコーンオイル(b)が好ましい。
The polyether-modified silicone oil (A) includes
(A): In the formula [I], X 1 is a polyether group represented by the formula [Ia], X 2 and X 3 are an alkyl group such as a methyl group or a phenyl group, and p is 1. Side-chain type polyether-modified silicone oil, which is an integer above
(B): In the formula [I], X 1 is an alkyl group such as a methyl group or a phenyl group, and X 2 and X 3 are a polyether group represented by the formula [Ia]. Ether-modified silicone oil,
(C): In the formula [I], one of X 1, X 2 and X 3 is a polyether group represented by the formula [Ia], and one of X 2 and X 3 is an alkyl such as a methyl group. Polyether-modified silicone oil, which is a group or a phenyl group and p is an integer of 1 or more.
(D): In the formula [I], a polyether-modified silicone oil in which X 1 , X 2 and X 3 are the polyether groups represented by the formula [Ia] and p is an integer of 1 or more.
(E): In the formula [I], one of X 2 and X 3 is a polyether group represented by the formula [Ia], and one of X 1 and X 2 and X 3 is an alkyl such as a methyl group. Examples thereof include polyether-modified silicone oil having a group or a phenyl group. Among these, the side chain type polyether-modified silicone oil (a) and the double-ended type polyether-modified silicone oil (b) are preferable from the viewpoint of antifouling property and the like.
前記ポリエーテル変性シリコーンオイル(A)の数平均分子量は、通常、1,000〜50,000、好ましくは3,000〜10,000程度である。
前記ポリエーテル変性シリコーンオイル(A)は、1種単独でまたは2種以上を組み合わせて用いることができる。
The number average molecular weight of the polyether-modified silicone oil (A) is usually about 1,000 to 50,000, preferably about 3,000 to 10,000.
The polyether-modified silicone oil (A) can be used alone or in combination of two or more.
前記ポリエーテル変性シリコーンオイル(A)の親水性親油性バランス(HLB)は、
前記ポリエーテル基に含まれるエチレンオキシドの量(質量%)を5で割った値(エチレンオキシド量/5)で示され、好ましくは0.5〜10、特に好ましくは1〜7である。このHLBが0.5〜10の範囲にあると防汚剤の溶出量が適度に保たれるため、防汚性が良好な傾向となる。
The hydrophilic lipophilic balance (HLB) of the polyether-modified silicone oil (A) is
It is indicated by the value (amount of ethylene oxide / 5) obtained by dividing the amount (mass%) of ethylene oxide contained in the polyether group by 5, preferably 0.5 to 10 and particularly preferably 1 to 7. When the HLB is in the range of 0.5 to 10, the elution amount of the antifouling agent is appropriately maintained, so that the antifouling property tends to be good.
このようなポリエーテル変性シリコーンオイル(A)は、従来公知の方法で製造することができ、市販品であれば「KF−6016(HLB=4.5)」、「KF−945(HLB=4.0)」、「X−22−6515(HLB=5.7)」、「X−22−6191(HLB=2.0)(いずれも信越化学工業(株)製)、「TSF4446」(東芝シリコーン(株)製、HLB=4.8)、「ST−114PA(HLB=5.6)」、「FZ−2120(HLB=6.0)」(いずれも東レ・ダウコーニング(株)製などが挙げられる。 Such a polyether-modified silicone oil (A) can be produced by a conventionally known method, and if it is a commercially available product, it is "KF-6016 (HLB = 4.5)" or "KF-945 (HLB = 4)". .0) ”,“ X-22-6515 (HLB = 5.7) ”,“ X-22-6191 (HLB = 2.0) (all manufactured by Shin-Etsu Chemical Co., Ltd.), “TSF4446” (Toshiba) Silicone Co., Ltd., HLB = 4.8), "ST-114PA (HLB = 5.6)", "FZ-2120 (HLB = 6.0)" (all manufactured by Toray Dow Corning Co., Ltd., etc. Can be mentioned.
本発明の防汚塗料組成物のポリエーテル変性シリコーンオイル(A)の含有量は、防汚塗料組成物の固形分量を100質量%とすると、好ましくは0.5〜40質量%、さらに好ましくは2〜35質量%である。なお、本発明において「固形分量」とは、防汚塗料組成物または各成分から任意成分である溶剤を除いた場合の量である。たとえば、防汚塗料組成物または各成分を、105℃で3時間放置して溶剤を揮散させた時の残分の量を「固形分量」とすることができる。 The content of the polyether-modified silicone oil (A) in the antifouling coating composition of the present invention is preferably 0.5 to 40% by mass, more preferably 0.5% by mass, assuming that the solid content of the antifouling coating composition is 100% by mass. It is 2 to 35% by mass. In the present invention, the "solid content" is the amount when the solvent, which is an optional component, is removed from the antifouling coating composition or each component. For example, the amount of the residue when the antifouling coating composition or each component is left at 105 ° C. for 3 hours to volatilize the solvent can be defined as the “solid content”.
ポリエーテル変性シリコーンオイル(A)の含有量がこの範囲にあることで、本発明の防汚塗料組成物から得られる防汚塗膜、および本発明の防汚塗料組成物で網染めされた漁網は、防汚性および造膜性に優れる。 When the content of the polyether-modified silicone oil (A) is in this range, the antifouling coating film obtained from the antifouling coating composition of the present invention and the fishing net dyed with the antifouling coating composition of the present invention are used. Is excellent in antifouling property and film forming property.
(B)防汚剤:
本発明の防汚塗料組成物は、防汚剤(B)として、少なくともメデトミジン(B1)を含有する。
(B) Antifouling agent:
The antifouling coating composition of the present invention contains at least medetomidine (B1) as an antifouling agent (B).
<メデトミジン(B1)>
メデトミジンは、(±)−4−[1−(2,3−ジメチルフェニル)エチル]−1H−イミダゾールである。
<Medetomidine (B1)>
Medetomidine is (±) -4- [1- (2,3-dimethylphenyl) ethyl] -1H-imidazole.
本発明の防汚塗料組成物におけるメデトミジン(B1)の含有量は、防汚塗料組成物の固形分量を100質量%とすると、好ましくは0.01〜50質量%、さらに好ましくは0.05〜45質量%である。メデトミジン(B1)の含有量がこの範囲にあることで、本発明の防汚塗料組成物から得られる防汚塗膜、および本発明の防汚塗料組成物で網染めされた漁網は、フジツボ類および腔腸動物(ヒドラ等)類への防汚性が優れる。 The content of medetomidine (B1) in the antifouling coating composition of the present invention is preferably 0.01 to 50% by mass, more preferably 0.05 to, assuming that the solid content of the antifouling coating composition is 100% by mass. It is 45% by mass. When the content of medetomidin (B1) is in this range, the antifouling coating film obtained from the antifouling coating composition of the present invention and the fishing net dyed with the antifouling coating composition of the present invention are barnacles. It also has excellent antifouling properties for coelenterates (hydra, etc.).
また、メデトミジン(B1)の含有量は、ポリエーテル変性シリコーンオイル(A)100質量部に対して、好ましくは0.01〜1,000質量部であり、より好ましくは0.1〜500質量部であり、さらに好ましくは1〜200質量部である。 The content of medetomidine (B1) is preferably 0.01 to 1,000 parts by mass, more preferably 0.1 to 500 parts by mass, based on 100 parts by mass of the polyether-modified silicone oil (A). It is more preferably 1 to 200 parts by mass.
<メデトミジン以外の防汚剤(B2)>
本発明の防汚塗料組成物は、防汚剤(B)としてメデトミジン(B1)を含有することにより優れた防汚性を発現するが、防汚性をより一層向上させるため、必要に応じて、メデトミジン以外の防汚剤(B2)(以下「他の防汚剤(B2)」ともいう。)を含有してもよい。
<Antifouling agent other than medetomidine (B2)>
The antifouling coating composition of the present invention exhibits excellent antifouling property by containing medetomidine (B1) as the antifouling agent (B), but in order to further improve the antifouling property, if necessary. , An antifouling agent (B2) other than medetomidine (hereinafter, also referred to as “another antifouling agent (B2)”) may be contained.
他の防汚剤(B2)としては、たとえば亜酸化銅、ロダン銅、銅粉、ビスジメチルジチオカルバモイルジンクエチレンビスジチオカーバメート、ジンクジメチルジチオカーバメート、ジンクエチレンビスジチオカーバメート、N,N−ジメチル−N’−(3,4−ジクロロフェニル)尿素、N−(2,4,6−トリクロロフェニル)マレイミド、2−メチルチオ−4−tert−ブチルアミノ−6−シクロプロピルアミノ−1,3,5−トリアジン、テトラエチルチウラムジスルフィド、4,5−ジクロロ−2−n−オクチル−4−イソチアゾリン−3−オン、銅ピリチオン、ジンクピリチオン、2,3−ジクロロ−N−(2',6'−ジエチルフェニル)マレイミド、2,3−ジクロロ−N−(2'−エチル−6'−メチルフェニル)マレイミド、4−ブロモ−2−(4−クロロフェニル)−5−(トリフルオロメチル)−1H−ピロール−3−カルボニトリル、トリフェニルボラン・アミン錯体(トリフェニルボラン・ピリジン錯体、トリフェニルボラン・n−オクタデシルアミン、トリフェニルボラン・3−(2−エチルヘキシルオキシ)プロピルアミン等)、ジフェニルメチルボラン・4−イソプロピルビリジン、クロロメチル−n−オクチルジスルフィド、N’,N’−ジメチル−N−フェニル−(N−フルオロジクロロメチルチオ)スルファミド、およびN’,N’−ジメチル−N−トリル−(N−フルオロジクロロメチルチオ)スルファミドが挙げられる。 Other antifouling agents (B2) include, for example, cuprous oxide, rodane copper, copper powder, bisdimethyldithiocarbamoylzincethylenebisdithiocarbamate, zincdimethyldithiocarbamate, zincethylenebisdithiocarbamate, N, N-dimethyl-N. '-(3,4-dichlorophenyl) urea, N- (2,4,6-trichlorophenyl) maleimide, 2-methylthio-4-tert-butylamino-6-cyclopropylamino-1,3,5-triazine, Tetraethylthiuram disulfide, 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one, copper pyrithione, zincpyrythione, 2,3-dichloro-N- (2', 6'-diethylphenyl) maleimide, 2 , 3-Dichloro-N- (2'-ethyl-6'-methylphenyl) maleimide, 4-bromo-2- (4-chlorophenyl) -5- (trifluoromethyl) -1H-pyrrole-3-carbonitrile, Triphenylboran amine complex (triphenylboran pyridine complex, triphenylboran n-octadecylamine, triphenylboran 3- (2-ethylhexyloxy) propylamine, etc.), diphenylmethylboran 4-isopropylviridine, chloro Methyl-n-octyldisulfide, N', N'-dimethyl-N-phenyl- (N-fluorodichloromethylthio) sulfamide, and N', N'-dimethyl-N-tolyl- (N-fluorodichloromethylthio) sulfamide Can be mentioned.
他の防汚剤(B2)は1種単独で用いてもよく、2種以上を併用してもよい。
本発明の防汚塗料組成物における他の防汚剤(B2)の含有量は、耐クラック性などの塗膜物性に悪影響を与えない範囲であれば特に限定されないが、防汚塗料組成物の固形分量を100質量%とすると、好ましくは1〜80質量%、さらに好ましくは5〜60質量%である。また、他の防汚剤(B2)の含有量は、メデトミジン(B1)1質量部に対して、好ましくは600質量部以下であり、より好ましくは1〜400質量部であり、さらに好ましくは2〜200質量部である。
The other antifouling agent (B2) may be used alone or in combination of two or more.
The content of the other antifouling agent (B2) in the antifouling coating composition of the present invention is not particularly limited as long as it does not adversely affect the physical properties of the coating film such as crack resistance, but the antifouling coating composition When the solid content is 100% by mass, it is preferably 1 to 80% by mass, and more preferably 5 to 60% by mass. The content of the other antifouling agent (B2) is preferably 600 parts by mass or less, more preferably 1 to 400 parts by mass, and further preferably 2 with respect to 1 part by mass of medetomidine (B1). ~ 200 parts by mass.
(C)塗膜形成樹脂:
前記塗膜形成性樹脂(C)としては、従来の船底塗料、漁網用防汚剤等に配合されている塗膜形成性樹脂などを使用できる。
(C) Coating film forming resin:
As the coating film-forming resin (C), a coating film-forming resin blended in a conventional ship bottom paint, an antifouling agent for fishing nets, or the like can be used.
海水中で加水分解されることにより(例:(メタ)アクリル酸金属塩系共重合体の場合)または溶解することにより(例:ロジンの場合)、新規な塗膜面が現れるようになる(塗膜の自己更新性)と共に、塗膜中に含まれる防汚剤を放出して防汚効果を発揮することのできる樹脂のほか、非水溶性、非加水分解性の樹脂(例:塩化ビニル系樹脂)を用いることもできる。 By being hydrolyzed in seawater (eg, in the case of (meth) acrylic acid metal salt-based copolymers) or by dissolving (eg, in the case of rosin), a new coating surface appears (eg, in the case of rosin). In addition to resins that can release antifouling agents contained in the coating film to exert an antifouling effect as well as self-renewal properties of the coating film, water-insoluble and non-hydrolyzable resins (eg, vinyl chloride) System resin) can also be used.
前記塗膜形成樹脂(C)としては、(メタ)アクリル酸金属塩共重合体、ポリエステル金属塩共重合体、シリルエステル含有共重合体、ポリシロキサンブロック含有金属塩共重合体、硫黄含有オルガノポリシロキサンブロックビニル共重合体、塩化ビニル系樹脂、塩化ビニル−酢酸ビニル共重合体、塩化ビニル−ビニルイソブチルエーテル共重合体、塩化ゴム系樹脂、アクリル樹脂(前記(メタ)アクリル酸金属塩共重合体、前記シリルエステル含有共重合体、前記ポリシロキサンブロック含有金属塩共重合体、および前記硫黄含有オルガノポリシロキサンブロックビニル共重合体を除く。)、スチレン−ブタジエン系樹脂、ポリエステル系樹脂(前記ポリエステル金属塩共重合体を除く。)、エポキシ系樹脂、フェノール系樹脂、合成ゴム、石油系樹脂、ロジンエステル系樹脂、ロジン系石鹸、およびロジンなどを用いることができる。 Examples of the coating film-forming resin (C) include (meth) acrylic acid metal salt copolymer, polyester metal salt copolymer, silyl ester-containing copolymer, polysiloxane block-containing metal salt copolymer, and sulfur-containing organopoly. Siloxane block vinyl copolymer, vinyl chloride resin, vinyl chloride-vinyl acetate copolymer, vinyl chloride-vinyl isobutyl ether copolymer, rubber chloride resin, acrylic resin (the (meth) acrylic acid metal salt copolymer , The silyl ester-containing copolymer, the polysiloxane block-containing metal salt copolymer, and the sulfur-containing organopolysiloxane block vinyl copolymer are excluded), a styrene-butadiene resin, and a polyester resin (the polyester metal). Salt copolymers are excluded.), Epoxy resins, phenolic resins, synthetic rubbers, petroleum resins, rosin ester resins, rosin soaps, rosins and the like can be used.
前記(メタ)アクリル酸金属塩共重合体、ポリエステル金属塩共重合体またはシリルエステル含有共重合体としては、例えば、特許文献1(国際公開第2011/118526号)に記載されているような加水分解性共重合体が挙げられ、具体的には、
アクリル樹脂(またはポリエステル樹脂)であって、一般式[II]:
COO−M−O−COR6 ・・・[II]
[式[II]において、MはZnまたはCuを示し、R6は1価の有機基を示す。]
で表される側鎖末端基を有する(メタ)アクリル酸金属塩共重合体(またはポリエステル金属塩共重合体)、
一般式[III]:
CH2=C(R7)−COO−M−O−CO−C(R7)=CH2 ・・・[III]
[式[III]において、MはZnまたはCuを示し、R7はそれぞれ独立に水素原子またはメチル基を示す。]
で表される単量体から誘導される構成単位と、前記単量体と共重合し得る他の不飽和単量体から誘導される構成単位とを含む(メタ)アクリル酸金属塩共重合体、および
一般式[IV]:
CH(R8)=C(R9)−COO−SiR10R11R12 ・・・[IV]
[式[IV]において、R9は水素原子またはメチル基を示し、
R10、R11およびR12はそれぞれ独立にヘテロ原子を有してもよい炭素数1〜20の1価の有機基を示し、
R8は水素原子またはR13−O−CO(但し、R13は独立にヘテロ原子を有してもよい炭素数1〜20の1価の有機基またはSiR14R15R16で示されるシリル基を示し、R14、R15およびR16はそれぞれ独立にヘテロ原子を有してもよい炭素数1〜20の1価の有機基を示す。)
を示す。]
で表される単量体から誘導される構成単位と、前記単量体と共重合し得る他の不飽和単量体から誘導される構成単位とを含むシリルエステル含有共重合体が挙げられる。
Examples of the (meth) acrylic acid metal salt copolymer, polyester metal salt copolymer, or silyl ester-containing copolymer include hydrolysis as described in Patent Document 1 (International Publication No. 2011/118526). Degradable copolymers can be mentioned, specifically, degradable copolymers.
Acrylic resin (or polyester resin), general formula [II]:
COO-MO-COR 6 ... [II]
[In formula [II], M represents Zn or Cu, and R 6 represents a monovalent organic group. ]
(Meta) acrylic acid metal salt copolymer (or polyester metal salt copolymer) having a side chain terminal group represented by
General formula [III]:
CH 2 = C (R 7 ) -COO-MO-CO-C (R 7 ) = CH 2 ... [III]
[In formula [III], M represents Zn or Cu, and R 7 independently represents a hydrogen atom or a methyl group. ]
A (meth) acrylic acid metal salt copolymer containing a structural unit derived from a monomer represented by the above and a structural unit derived from another unsaturated monomer copolymerizable with the monomer. , And the general formula [IV]:
CH (R 8 ) = C (R 9 ) -COO-SiR 10 R 11 R 12 ... [IV]
[In formula [IV], R 9 represents a hydrogen atom or a methyl group,
R 10 , R 11 and R 12 each represent a monovalent organic group having 1 to 20 carbon atoms which may independently have a heteroatom.
R 8 is a hydrogen atom or R 13- O-CO (where R 13 is a monovalent organic group having 1 to 20 carbon atoms which may independently have a hetero atom or a silyl represented by Si R 14 R 15 R 16 Indicates a group, and R 14 , R 15 and R 16 each indicate a monovalent organic group having 1 to 20 carbon atoms which may independently have a heteroatom.)
Is shown. ]
Examples thereof include a silyl ester-containing copolymer containing a structural unit derived from the monomer represented by the above and a structural unit derived from another unsaturated monomer copolymerizable with the monomer.
前記一般式[II]における1価の有機基R6としては、炭素数2〜30の飽和もしくは不飽和脂肪族炭化水素基、炭素数3〜20の飽和もしくは不飽和脂環式炭化水素基または炭素数6〜18の芳香族炭化水素基、あるいはこれらの置換体が好ましく、炭素数10〜20の飽和もしくは不飽和脂肪族炭化水素基または炭素数3〜20の飽和もしくは不飽和脂環式炭化水素基、あるいはこれらの置換体がより好ましい。 The monovalent organic group R 6 in the general formula [II] includes a saturated or unsaturated aliphatic hydrocarbon group having 2 to 30 carbon atoms, a saturated or unsaturated alicyclic hydrocarbon group having 3 to 20 carbon atoms, or the like. Aromatic hydrocarbon groups having 6 to 18 carbon atoms, or substituents thereof are preferred, with saturated or unsaturated aliphatic hydrocarbon groups having 10 to 20 carbon atoms or saturated or unsaturated alicyclic hydrocarbons having 3 to 20 carbon atoms. Hydrogen groups, or substituents thereof, are more preferred.
前記一般式[III]または一般式[IV]で表される単量体と共重合し得る他の不飽和単量体としては、たとえば、
(メタ)アクリル酸メチルエステル、(メタ)アクリル酸エチルエステル、(メタ)アクリル酸ブチルエステル、(メタ)アクリル酸2−エチルヘキシルエステル、(メタ)アクリル酸ラウリルエステル、(メタ)アクリル酸トリデシルエステル、(メタ)アクリル酸ステアリルエステル、(メタ)アクリル酸アリルエステル、(メタ)アクリル酸シクロヘキシルエステル、(メタ)アクリル酸ベンジルエステル、(メタ)アクリル酸イソボルニルエステル、(メタ)アクリル酸メトキシエステル、(メタ)アクリル酸エトキシエステル、(メタ)アクリル酸グリシジルエステル、(メタ)アクリル酸テトラヒドロフルフリルエステル、(メタ)アクリル酸ヒドロキシエチルエステル、(メタ)アクリル酸ヒドロキシプロピルエステル、(メタ)アクリル酸ヒドロキシブチルエステルなどの(メタ)アクリル酸エステル類;
(メタ)アクリル酸などのモノカルボン酸類;
イタコン酸、マレイン酸、コハク酸等のジカルボン酸類またはこれらのハーフエステル(モノエステル)もしくはジエステル;
スチレン、α−メチルスチレンなどのスチレン類;および
酢酸ビニル、プロピオン酸ビニルなどのビニルエステル類
が挙げられ、これらは1種単独でまたは2種類以上を組み合わせて用いてもよい。
Other unsaturated monomers that can be copolymerized with the monomer represented by the general formula [III] or the general formula [IV] include, for example,
(Meta) acrylic acid methyl ester, (meth) acrylic acid ethyl ester, (meth) acrylic acid butyl ester, (meth) acrylic acid 2-ethylhexyl ester, (meth) acrylic acid lauryl ester, (meth) acrylic acid tridecyl ester , (Meta) acrylic acid stearyl ester, (meth) acrylic acid allyl ester, (meth) acrylic acid cyclohexyl ester, (meth) acrylic acid benzyl ester, (meth) acrylic acid isobornyl ester, (meth) acrylic acid methoxyester , (Meta) acrylic acid ethoxyester, (meth) acrylic acid glycidyl ester, (meth) acrylic acid tetrahydrofurfuryl ester, (meth) acrylic acid hydroxyethyl ester, (meth) acrylic acid hydroxypropyl ester, (meth) acrylic acid (Meta) acrylic acid esters such as hydroxybutyl ester;
Monocarboxylic acids such as (meth) acrylic acid;
Dicarboxylic acids such as itaconic acid, maleic acid, succinic acid or their half-esters (monoesters) or diesters;
Examples include styrenes such as styrene and α-methylstyrene; and vinyl esters such as vinyl acetate and vinyl propionate, which may be used alone or in combination of two or more.
前記(メタ)アクリル酸金属塩共重合体および前記ポリエステル金属塩共重合体の、GPC法により後述する実施例での条件または同等の条件で測定される重量平均分子量(Mw)は、防汚塗料組成物の粘度、貯蔵安定性、または防汚塗膜等(防汚塗膜および漁網に含浸された防汚塗料組成物)の溶出速度を考慮すると、通常は1,000〜200,000、好ましくは1,000〜100,000である。 The weight average molecular weight (Mw) of the (meth) acrylic acid metal salt copolymer and the polyester metal salt copolymer measured by the GPC method under the conditions of Examples described later or equivalent conditions is the antifouling paint. Considering the viscosity of the composition, storage stability, or the elution rate of the antifouling coating or the like (antifouling coating and antifouling coating composition impregnated in the fishing net), it is usually 1,000 to 200,000, preferably 1,000 to 200,000. Is 1,000 to 100,000.
また前記シリルエステル含有共重合体の、後述する実施例での条件または同等の条件で測定される数平均分子量(Mn)は、防汚塗料組成物の粘度、貯蔵安定性、または防汚塗膜等の溶出速度を考慮すると、通常は1,000〜200,000、好ましくは1,000〜100,000である。 The number average molecular weight (Mn) of the silyl ester-containing copolymer measured under the conditions described in Examples described later or equivalent conditions is the viscosity, storage stability, or antifouling coating film of the antifouling coating composition. In consideration of the dissolution rate of the above, it is usually 1,000 to 200,000, preferably 1,000 to 100,000.
前記ポリシロキサンブロック含有金属塩共重合体としては、特許文献2(特開2006−77095号公報)に記載されているような樹脂が挙げられ、具体的には、下記(A1)〜(A3)からなる群から選ばれる少なくとも1種のポリシロキサンブロック含有金属塩共重合体を用いることができる。
(A1):ポリシロキサンブロック含有重合性不飽和単量体から誘導される構成単位(a11)と、
下式(a12):
CH2=C(R17)−COO−M−O−CO−R18 ・・・(a12)
(式(a12)において、Mは2価の金属原子を示し、R17は水素原子またはメチル基を示し、R18はラジカル反応性を有しない1価の有機基を示す。)
で表される重合性不飽和カルボン酸金属塩から誘導される構成単位(a12)と、
重合性不飽和カルボン酸またはそのエステルから誘導される構成単位(a13)と
を有するポリシロキサンブロック含有金属塩共重合体、
(A2):ポリシロキサンブロック含有重合性不飽和単量体から誘導される構成単位(a21)と、2価金属ジ(メタ)アクリレートから誘導される構成単位(a22)と、重合性不飽和カルボン酸またはそのエステルから誘導される構成単位(a23)とを有するポリシロキサンブロック含有金属塩共重合体、
(A3):ポリシロキサンブロック(a31)と、アクリル樹脂ブロック(a32)とが、下式(a33):
[−M−O−CO−(G−CO−O−)r−(CH2)p−]・・・(a33)
(式中、Mは2価の金属原子を示し、Gは2価の炭化水素基を示し、rは0または1を示し、pは0〜5の整数を示し、左端の線はアクリル樹脂ブロック(a32)の有するCOOで表される基との結合を、右端の線はポリシロキサンブロック(a31)との結合を示す。)
で表される金属含有結合(a33)で結合されたポリシロキサンブロック含有金属塩共重合体。
Examples of the polysiloxane block-containing metal salt copolymer include resins as described in Patent Document 2 (Japanese Unexamined Patent Publication No. 2006-77095), and specifically, the following (A1) to (A3). At least one polysiloxane block-containing metal salt copolymer selected from the group consisting of the above can be used.
(A1): A structural unit (a11) derived from a polysiloxane block-containing polymerizable unsaturated monomer, and
The following formula (a12):
CH 2 = C (R 17 ) -COO-MO-CO-R 18 ... (a12)
(In the formula (a12), M represents a divalent metal atom, R 17 represents a hydrogen atom or a methyl group, and R 18 represents a monovalent organic group having no radical reactivity.)
The structural unit (a12) derived from the polymerizable unsaturated carboxylic acid metal salt represented by
A polysiloxane block-containing metal salt copolymer having a polymerizable unsaturated carboxylic acid or a structural unit (a13) derived from an ester thereof,
(A2): A structural unit (a21) derived from a polysiloxane block-containing polymerizable unsaturated monomer, a structural unit (a22) derived from a divalent metal di (meth) acrylate, and a polymerizable unsaturated carboxylic acid. A polysiloxane block-containing metal salt copolymer having a structural unit (a23) derived from an acid or an ester thereof,
(A3): The polysiloxane block (a31) and the acrylic resin block (a32) are expressed by the following formula (a33):
[-MO-CO- (G-CO-O-) r- (CH 2 ) p- ] ... (a33)
(In the formula, M represents a divalent metal atom, G represents a divalent hydrocarbon group, r represents 0 or 1, p represents an integer of 0 to 5, and the leftmost line is an acrylic resin block. The bond with the group represented by COO of (a32) is shown, and the rightmost line shows the bond with the polysiloxane block (a31).)
A polysiloxane block-containing metal salt copolymer bonded by the metal-containing bond (a33) represented by.
前記ポリシロキサンブロックとしては、たとえば下式(a0)で表される1価基が挙げられる。 Examples of the polysiloxane block include a monovalent group represented by the following formula (a0).
mは5〜7,000の整数を示し、
nは0〜50の整数を示し、
左端の線は、隣接する原子との結合を示す。)
m represents an integer of 5 to 7,000,
n represents an integer from 0 to 50
The leftmost line shows the bond with the adjacent atom. )
前記構成単位(a11)および(a21)を誘導するポリシロキサンブロック含有重合性不飽和単量体としては、たとえば下式:
CH2=CR−COO−(CH2)p−[PS]
(式中、Rは水素原子またはメチル基を示し、pは0〜5の整数を示し、−[PS]は前記式(a0)で表されるポリシロキサンブロックを示す。)
で表されるものが挙げられる。
Examples of the polysiloxane block-containing polymerizable unsaturated monomer for deriving the structural units (a11) and (a21) include the following formula:
CH 2 = CR-COO- (CH 2 ) p- [PS]
(In the formula, R represents a hydrogen atom or a methyl group, p represents an integer of 0 to 5, and − [PS] represents a polysiloxane block represented by the formula (a0).)
The ones represented by are mentioned.
前記式(a12)中の[−O−CO−R18]部分としては、たとえば、
直鎖状でも分岐を有していてもよい飽和脂肪族カルボン酸残基であるプロピオン酸残基(C2H5COO−)、吉草酸残基(CH3(CH2)3COO−)、パルミチン酸残基(CH3(CH2)14COO−)、ミリスチン酸残基(CH3(CH2)12COO−)、ラウリン酸残基(CH3(CH2)10COO−)、ステアリン酸残基(C17H35COO−)、バーサチック酸残基((C3H7)3C−COO−)など;
飽和脂環式カルボン酸残基であるナフテン酸残基(C5H9(CH2)nCOO−)など;
芳香環式カルボン酸残基である安息香酸残基(C6H5COO−)など;
ロジンに含まれる樹脂酸の残基
が挙げられる。
As the [-O-CO-R 18 ] portion in the above formula (a12), for example,
Saturated aliphatic carboxylic acid residues that may be linear or branched, propionic acid residues (C 2 H 5 COO-), valerate residues (CH 3 (CH 2 ) 3 COO-), Palmitic acid residue (CH 3 (CH 2 ) 14 COO-), myristic acid residue (CH 3 (CH 2 ) 12 COO-), lauric acid residue (CH 3 (CH 2 ) 10 COO-), stearic acid Residues (C 17 H 35 COO-), Versatic acid residues ((C 3 H 7 ) 3 C-COO-), etc .;
Naphthenic acid residue (C 5 H 9 (CH 2 ) n COO-), which is a saturated alicyclic carboxylic acid residue;
Benzoic acid residue (C 6 H 5 COO-), which is an aromatic ring-type carboxylic acid residue;
Included are resin acid residues contained in rosin.
これらのうちでは、カルボン酸残基[−O−CO−R18]部分の総炭素数が3〜20個程度のものが好ましく、例えば、バーサチック酸残基、ナフテン酸残基、ロジンに含まれる樹脂酸の残基が、本発明に係る防汚塗膜の造膜性、耐クラック性等の物性、溶出性の点で望ましい。 Among these, those having a total carbon number of about 3 to 20 in the carboxylic acid residue [-O-CO-R 18 ] portion are preferable, and are contained in, for example, versatic acid residue, naphthenic acid residue, and rosin. The residue of the resin acid is desirable in terms of physical properties such as film-forming property and crack resistance of the antifouling coating film according to the present invention, and elution property.
上記ポリシロキサンブロック含有金属塩共重合体(A1)〜(A3)に含まれる2価金属としては、たとえばZn、CuおよびMgが挙げられる。
前記構成単位(a13)および(a23)を誘導する重合性不飽和カルボン酸またはそのエステルから誘導されるとしては、前記一般式[III]または一般式[IV]で表される単量体と共重合し得る他の不飽和単量体と同様な不飽和単量体を用いることができる。
Examples of the divalent metal contained in the polysiloxane block-containing metal salt copolymers (A1) to (A3) include Zn, Cu and Mg.
As derived from the polymerizable unsaturated carboxylic acid or its ester that induces the structural units (a13) and (a23), it is the same as the monomer represented by the general formula [III] or the general formula [IV]. Unsaturated monomers similar to other unsaturated monomers that can be polymerized can be used.
前記ポリシロキサンブロック(a31)としては、前記式(a0)で表されるポリシロキサンブロックが挙げられる。前記アクリル樹脂ブロック(a32)は、アクリル樹脂から、アクリル樹脂のCOOR(Rは水素原子または有機基である。)で表される側鎖の少なくとも1つが有するRを除去した部分である。 Examples of the polysiloxane block (a31) include a polysiloxane block represented by the formula (a0). The acrylic resin block (a32) is a portion from which R of at least one of the side chains represented by COOR (R is a hydrogen atom or an organic group) of the acrylic resin is removed from the acrylic resin.
前記ポリシロキサンブロック含有金属塩共重合体の、液体クロマトグラフィーにより後述する実施例での条件または同等の条件で測定される数平均分子量(Mn)は、共重合体溶液の粘度、共重合体のゲル化防止、または防汚塗膜等の防汚性などの観点から、通常は1,000〜50,000、好ましくは1,000〜10,000、さらに好ましくは2,000〜5,000である。 The number average molecular weight (Mn) of the polysiloxane block-containing metal salt copolymer measured by liquid chromatography under the conditions of Examples described later or equivalent conditions is the viscosity of the copolymer solution and the copolymer. From the viewpoint of preventing gelation or antifouling property of an antifouling coating film or the like, it is usually 1,000 to 50,000, preferably 1,000 to 10,000, and more preferably 2,000 to 5,000. is there.
前記硫黄含有オルガノポリシロキサンブロックビニル共重合体としては、ラジカル重合性を有するビニル系モノマーから誘導される構成単位を有するビニル重合体ブロックと、一般式[V]: The sulfur-containing organopolysiloxane block vinyl copolymer includes a vinyl polymer block having a structural unit derived from a radically polymerizable vinyl-based monomer and a general formula [V] :.
で表され、かつ少なくとも1つの前記硫黄含有有機基を有する硫黄含有オルガノポリシロキサンブロックとを有する共重合体などが挙げられる。この共重合体は、前記ビニル系モノマー(たとえば、ヘテロ原子を含んでいてもよい(メタ)アクリル酸エステル)と、前記硫黄含有オルガノポリシロキサンブロックにおいて前記硫黄含有有機基をメルカプト基(SH基)に置き換えた化合物とを、ラジカル重合開始剤等のラジカル発生源の存在下で反応させることにより、製造することができる。
Examples thereof include a copolymer represented by and having a sulfur-containing organopolysiloxane block having at least one sulfur-containing organic group. In this copolymer, the vinyl-based monomer (for example, a (meth) acrylic acid ester which may contain a hetero atom) and the sulfur-containing organic group in the sulfur-containing organopolysiloxane block are mercapto groups (SH groups). It can be produced by reacting the compound replaced with the above compound in the presence of a radical generation source such as a radical polymerization initiator.
前記アクリル樹脂としては、(メタ)アクリル酸系エステルの単独重合体または共重合体が挙げられ、(メタ)アクリル酸エステルの単独重合体、少なくとも2種以上の(メタ)アクリル酸エステルの共重合体、(メタ)アクリル酸エステル・スチレン系共重合体などが挙げられる。(メタ)アクリル酸系エステルとしては、前記一般式[III]または一般式[IV]で表される単量体と共重合し得る他の不飽和単量体と同様な不飽和単量体を用いることができる。前記アクリル樹脂の、GPC法により後述する実施例での条件または同等の条件で測定されるポリスチレンを標準とした重量平均分子量(Mw)は、好ましくは1,000〜300,000であり、塗工性能、塗膜物性の観点から、より好ましくは20,000〜200,000である。 Examples of the acrylic resin include homopolymers or copolymers of (meth) acrylic acid-based esters, homopolymers of (meth) acrylic acid esters, and copolymerization of at least two or more (meth) acrylic acid esters. Examples thereof include coalescence, (meth) acrylic acid ester / styrene copolymer, and the like. As the (meth) acrylic acid-based ester, an unsaturated monomer similar to other unsaturated monomers that can be copolymerized with the monomer represented by the general formula [III] or the general formula [IV] can be used. Can be used. The weight average molecular weight (Mw) of the acrylic resin based on polystyrene, which is measured by the GPC method in the conditions described later in Examples or equivalent conditions, is preferably 1,000 to 300,000, and is coated. From the viewpoint of performance and physical properties of the coating film, it is more preferably 20,000 to 200,000.
前記塗膜形成樹脂(C)のキシレンの50%溶液の粘度(E型粘度計、トキメック社製「VISCONIC EMD」により測定)は、25℃において好ましくは10〜20,000mPa・sである。また、樹脂のTg(ガラス転移点)が−20〜30℃のものが通常使用できる。 The viscosity of a 50% solution of xylene of the coating film-forming resin (C) (measured by an E-type viscometer, "VISCONIC EMD" manufactured by Tokimec Co., Ltd.) is preferably 10 to 20,000 mPa · s at 25 ° C. Further, a resin having a Tg (glass transition point) of -20 to 30 ° C. can usually be used.
前記塗膜形成樹脂(C)としては、これらの中でも、漁網に塗布した場合の、造膜性および防汚性の点から(メタ)アクリル酸金属塩共重合体、ポリシロキサンブロック含有金属塩共重合体、およびアクリル樹脂が好ましい。 Among these, the coating film-forming resin (C) includes both a (meth) acrylic acid metal salt copolymer and a polysiloxane block-containing metal salt from the viewpoint of film-forming property and antifouling property when applied to a fishing net. Polymers and acrylic resins are preferred.
本発明の防汚塗料組成物における塗膜形成樹脂(C)の含有量は、防汚塗料組成物の固形分量を100質量%とすると、好ましくは10〜99.49質量%、さらに好ましくは20〜97.95質量%である。塗膜形成樹脂(C)の含有量がこの範囲にあることで、本発明の防汚塗料組成物から形成される防汚塗膜は、造膜性および基材への付着性が優れる。 The content of the coating film-forming resin (C) in the antifouling coating composition of the present invention is preferably 10 to 99.49% by mass, more preferably 20%, assuming that the solid content of the antifouling coating composition is 100% by mass. ~ 97.95% by mass. When the content of the coating film-forming resin (C) is in this range, the antifouling coating film formed from the antifouling coating composition of the present invention is excellent in film-forming property and adhesion to a substrate.
(D)可塑性樹脂:
本発明の防汚塗料組成物は可塑性樹脂(D)(ただし、塗膜形成樹脂(C)を除く。)を含んでいてもよい。前記可塑性樹脂(D)としては、たとえばポリオレフィン、ポリスルフィド、流動パラフィン、ワックス、およびワセリンが挙げられる。可塑性樹脂(D)を添加することにより、防汚塗膜等の防汚性を向上させるとともに、さらに防汚塗膜等からの防汚剤(B)の溶出を調整し長期に亘る防汚効果を発揮させることができる。
(D) Plastic resin:
The antifouling coating composition of the present invention may contain a plastic resin (D) (however, the coating film forming resin (C) is excluded). Examples of the plastic resin (D) include polyolefins, polysulfides, liquid paraffins, waxes, and petrolatum. By adding the plastic resin (D), the antifouling property of the antifouling coating film and the like is improved, and the elution of the antifouling agent (B) from the antifouling coating film and the like is adjusted to have a long-term antifouling effect. Can be demonstrated.
前記ポリオレフィンとしては、たとえばポリエチレン、エチレン・α−オレフィン共重合体、ポリプロピレン、およびポリブテンが挙げられ、ポリブテンが好ましく、防汚性の面から数平均分子量が280〜1,500のポリブテンが特に好ましい。このようなポリブテンとしては、市販品であれば、たとえばLV−5、LV−10、LV−25、LV−50、LV−100、HV−35、HV−50、HV−100、およびHV−300(いずれも商品名、JXエネルギー(株))が挙げられる。 Examples of the polyolefin include polyethylene, an ethylene / α-olefin copolymer, polypropylene, and polybutene. Polybutene is preferable, and polybutene having a number average molecular weight of 280 to 1,500 is particularly preferable from the viewpoint of antifouling property. As such polybutene, if it is a commercially available product, for example, LV-5, LV-10, LV-25, LV-50, LV-100, HV-35, HV-50, HV-100, and HV-300. (Both are trade names, JX Energy Co., Ltd.).
前記ポリスルフィドは、下式[VI]:
R−(S)u−R ・・・[VI]
で表わされるジアルキルポリスルフィドである。
The polysulfide has the following formula [VI]:
R- (S) u- R ... [VI]
It is a dialkyl polysulfide represented by.
式[VI]において、2つのRはそれぞれ独立に炭素数が1〜20のアルキル基を表す。
uは2以上の整数であり、防汚塗膜等の防汚性の観点から好ましくは2〜10の整数である。
In the formula [VI], each of the two Rs independently represents an alkyl group having 1 to 20 carbon atoms.
u is an integer of 2 or more, and is preferably an integer of 2 to 10 from the viewpoint of antifouling property of the antifouling coating film and the like.
前記ポリスルフィドとしては、たとえばジエチルペンタスルフィド、ジ-tert-ブチルジスルフィド、ジ-tert-ブチルテトラスルフィド、ジ-tert-ペンチルテトラスルフィド、ジオクチルポリスルフィド、ジ-tert-オクチルペンタスルフィド、ジ-tert-ノニルペンタスルフィド、ジ-tert-ドデシルペンタスルフィド、およびジノナデシルテトラスルフィドが挙げられる。 Examples of the polysulfide include diethylpentasulfide, di-tert-butyldisulfide, di-tert-butyltetrasulfide, di-tert-pentyltetrasulfide, dioctylpolysulfide, di-tert-octylpentasulfide, and di-tert-nonylpenta. Included are sulfides, di-tert-dodecylpentasulfides, and dinonadesyltetrasulfides.
前記流動パラフィンは、原油を蒸留してガソリン分、灯油分軽油分等を除き、スピンドル油からエンジン油までの留分を採り、精製して得られ、主としてアルキルナフテン類からなる液状炭化水素油であり、好ましくは、JISK9003の規定に適合するものである。 The liquid paraffin is a liquid hydrocarbon oil mainly composed of alkylnaphthenes, which is obtained by distilling crude oil to remove gasoline, kerosene, light oil, etc., taking a fraction from spindle oil to engine oil, and refining it. Yes, preferably, it conforms to the provisions of JIS K9003.
前記ワックスとしては、たとえば石油系ワックス、ポリエチレン系ワックス、およびポリプロピレン系ワックスが挙げられる。
前記石油系ワックスとしては、たとえば、パラフィンワックス、マイクロクリスタリンワックス、およびペトロラタムワックスが挙げられ、パラフィンワックスが特に好ましい。
Examples of the wax include petroleum-based wax, polyethylene-based wax, and polypropylene-based wax.
Examples of the petroleum-based wax include paraffin wax, microcrystalline wax, and petrolatum wax, and paraffin wax is particularly preferable.
前記ワセリンとしては、たとえば白色ワセリン、および黄色ワセリンが挙げられる。
このような可塑性樹脂(D)のうちでは、ポリブテンおよびポリスルフィドが防汚効果向上の面から好ましい。
Examples of the petrolatum include white petrolatum and yellow petrolatum.
Among such plastic resins (D), polybutene and polysulfide are preferable from the viewpoint of improving the antifouling effect.
これらは1種単独でまたは2種以上を組み合わせて用いることができる。
本発明の防汚塗料組成物における可塑性樹脂(D)の含有量は、防汚塗料組成物の固形分量を100質量%とすると、好ましくは1〜40質量%、さらに好ましくは5〜30質量%である。可塑性樹脂(D)の含有量がこの範囲にあることで、本発明の組成物から形成される防汚塗膜、および本発明の組成物で網染めされた漁網は柔軟性に優れる。
These can be used alone or in combination of two or more.
The content of the plastic resin (D) in the antifouling coating composition of the present invention is preferably 1 to 40% by mass, more preferably 5 to 30% by mass, assuming that the solid content of the antifouling coating composition is 100% by mass. Is. When the content of the plastic resin (D) is in this range, the antifouling coating film formed from the composition of the present invention and the fishing net dyed with the composition of the present invention are excellent in flexibility.
(E)金属酸化物:
本発明の防汚塗料組成物は、塗膜強度を向上させるために、金属酸化物(E)(前記他の防汚剤(B2)としての亜酸化銅を除く。)を含有してもよい。金属酸化物としては、CuO(酸化銅(II))、ZnO、TiO2、Al2O3、SiO2、およびMgOからなる群から選択される1種以上の金属酸化物が挙げられる。
(E) Metal oxide:
The antifouling coating composition of the present invention may contain a metal oxide (E) (excluding cuprous oxide as the other antifouling agent (B2)) in order to improve the strength of the coating film. .. Examples of the metal oxide include one or more metal oxides selected from the group consisting of CuO (copper oxide (II) oxide), ZnO, TiO 2 , Al 2 O 3 , SiO 2, and MgO.
本発明の防汚塗料組成物における金属酸化物(E)の含有量は、防汚塗料組成物の固形分量を100質量%とすると、好ましくは5〜60質量%、さらに好ましくは10〜50質量%である。 The content of the metal oxide (E) in the antifouling coating composition of the present invention is preferably 5 to 60% by mass, more preferably 10 to 50% by mass, assuming that the solid content of the antifouling coating composition is 100% by mass. %.
その他の成分:
本発明の防汚塗料組成物は、前述した成分の他に、着色顔料、体質顔料、脱水剤、搖変剤、有機酸、溶剤等、一般的な塗料組成物に用いられている各種成分を含んでいてもよい。これらは1種単独で用いてもよく、2種以上併用してもよい。
揺変剤(沈降防止剤・たれ止剤)としてはたとえば、酸化ポリエチレンワックス、脂肪酸アマイドワックス、およびベントンが挙げられる。
Other ingredients:
In addition to the above-mentioned components, the antifouling coating composition of the present invention contains various components used in general coating compositions such as coloring pigments, extender pigments, dehydrating agents, stiffeners, organic acids, and solvents. It may be included. These may be used alone or in combination of two or more.
Examples of the rocking agent (anti-sedimentation agent / anti-sagging agent) include polyethylene oxide wax, fatty acid amide wax, and Benton.
溶剤:
前記溶剤としては、従来の防汚塗料組成物、特に漁網用防汚塗料組成物に配合されている、防汚剤などの各種成分を容易に分散することのできる脂肪族炭化水素系溶剤、芳香族炭化水素系溶剤、ケトン系溶剤、エステル系溶剤、アルコール系溶剤、またはエーテル系溶剤を用いることができる。
solvent:
As the solvent, an aliphatic hydrocarbon solvent and fragrance that can easily disperse various components such as an antifouling agent, which are blended in a conventional antifouling coating composition, particularly an antifouling coating composition for fishing nets, can be easily dispersed. Group hydrocarbon solvents, ketone solvents, ester solvents, alcohol solvents, or ether solvents can be used.
前記脂肪族系炭化水素溶剤としては、たとえばターペンが挙げられる。
前記芳香族炭化水素系溶剤としては、たとえばキシレン、トルエン、エチルベンゼン、トリメチルベンゼン、メチルエチルベンゼン、およびプロピルベンゼンが挙げられる。
Examples of the aliphatic hydrocarbon solvent include tarpen.
Examples of the aromatic hydrocarbon solvent include xylene, toluene, ethylbenzene, trimethylbenzene, methylethylbenzene, and propylbenzene.
前記ケトン系溶剤としては、たとえばメチルエチルケトン、メチルイソブチルケトン、およびメチルエチルイソブチルケトンが挙げられる。
前記エステル系溶剤としては、たとえば酢酸エチル、および酢酸ブチルが挙げられる。
Examples of the ketone solvent include methyl ethyl ketone, methyl isobutyl ketone, and methyl ethyl isobutyl ketone.
Examples of the ester solvent include ethyl acetate and butyl acetate.
前記アルコール系溶剤としては、たとえばエタノール、イソプロピルアルコール、n−ブタノール、およびイソブタノールが挙げられる。
前記エーテル系溶剤としては、たとえばプロピレングリコールモノメチルエーテル、およびプロピレングリコールモノメチルエーテルアセテート(PMAC)が挙げられる。
Examples of the alcohol solvent include ethanol, isopropyl alcohol, n-butanol, and isobutanol.
Examples of the ether solvent include propylene glycol monomethyl ether and propylene glycol monomethyl ether acetate (PMAC).
これらは1種単独でまたは2種以上を組み合わせて用いることができる。
これらの溶剤の中では、溶解力、引火点、蒸発速度の点から、キシレン、エチルベンゼン、酢酸ブチル、およびプロピレングリコールモノメチルエーテルが好ましい。
本発明の防汚塗料組成物における溶剤の配合量は、防汚塗料組成物の量を100質量%とすると、通常10〜90質量%、好ましくは20〜80質量%である。
These can be used alone or in combination of two or more.
Among these solvents, xylene, ethylbenzene, butyl acetate, and propylene glycol monomethyl ether are preferable from the viewpoint of dissolving power, flash point, and evaporation rate.
The blending amount of the solvent in the antifouling coating composition of the present invention is usually 10 to 90% by mass, preferably 20 to 80% by mass, assuming that the amount of the antifouling coating composition is 100% by mass.
[防汚塗料組成物の製造方法]
本発明の防汚塗料組成物は、たとえば所定の量の前記各成分を、塗料組成物の製造における一般的な装置および手法を用いて混合・撹拌することにより製造できる。
[Manufacturing method of antifouling paint composition]
The antifouling coating composition of the present invention can be produced, for example, by mixing and stirring a predetermined amount of each of the above components using a general device and method for producing a coating composition.
[防汚塗料組成物の用途]
本発明の防汚塗料組成物は、たとえば、火力、原子力発電所の給排水口等の水中構造物、湾岸道路、海底トンネル、港湾設備、運河、水路等のような各種海洋土木工事の汚泥拡散防止膜、船舶(例:船底部)、漁具(例:ロープ、漁網、浮き子、ブイ)などの海水または真水と接触する各種基材の表面の防汚にも使用できる。具体的には、本発明の防汚塗料組成物を基材の表面に常法に従って1回〜複数回塗布し、または含浸させ、次いで乾燥させるなどして硬化させることにより、防汚性に優れ、防汚剤成分が長期間に亘って徐放可能であり、厚塗りしても適度の可撓性を有し耐クラック性に優れた防汚塗膜が形成される。このように形成できる本発明の防汚塗膜は、本発明の防汚塗料組成物の固形分からなる。なお、表面に防汚塗膜が設けられた基材を「防汚塗膜付き基材」ともいう。
[Use of antifouling paint composition]
The antifouling coating composition of the present invention prevents the spread of sludge in various marine civil engineering works such as thermal power, underwater structures such as water supply and drainage ports of nuclear power plants, bay roads, submarine tunnels, harbor facilities, canals, and waterways. It can also be used to prevent stains on the surface of various base materials that come into contact with seawater or fresh water such as membranes, ships (eg, bottom of ships), fishing gear (eg, ropes, fishing nets, floats, buoys). Specifically, the antifouling coating composition of the present invention is applied to the surface of a base material once or multiple times according to a conventional method, impregnated, and then dried to cure, thereby excellent in antifouling property. The antifouling agent component can be released slowly over a long period of time, and even if it is applied thickly, an antifouling coating film having appropriate flexibility and excellent crack resistance is formed. The antifouling coating film of the present invention that can be formed in this way comprises the solid content of the antifouling coating composition of the present invention. A base material having an antifouling coating film on the surface is also referred to as a "base material with an antifouling coating film".
また、本発明の防汚塗料組成物は、漁具の塗装、特に漁網の網染めに好ましく使用される。漁網の材質としては、ポリエチレン、ナイロン、麻、金属、ポリエステルなどが挙げられ、このような材質の場合は、防汚塗料組成物が良好に含浸付着する。漁網の網染めは、一般的な手法を用いて行うことができ、例えば、防汚塗料組成物の中に漁網を浸漬して漁網の繊維内あるいは繊維間に防汚塗料組成物を浸透含浸させた後、漁網を引き上げ乾燥させるなどして防汚塗料組成物を硬化させることにより行うことができる。また、敷延あるいは広げて吊るした漁網の表裏面に防汚塗料組成物を静電塗装の方法で、あるいはエアガン、エアレス塗装等の方法で散布してもよい。このように網染めによる漁網の重量増加は、漁網1kg当たり、通常80〜300g程度である。本発明の組成物で網染めされた漁網は、その繊維内または繊維間に本発明の防汚塗料組成物の固形分を有しており、さらにその表面に本発明の防汚塗膜を有していてもよい。 Further, the antifouling coating composition of the present invention is preferably used for painting fishing gear, particularly for net dyeing of fishing nets. Examples of the material of the fishing net include polyethylene, nylon, hemp, metal, polyester and the like, and in the case of such a material, the antifouling paint composition is satisfactorily impregnated and adhered. Net dyeing of fishing nets can be performed using a general method. For example, the fishing net is immersed in the antifouling paint composition and impregnated with the antifouling paint composition in or between the fibers of the fishing net. After that, the fishing net can be pulled up and dried to cure the antifouling paint composition. Further, the antifouling paint composition may be sprayed on the front and back surfaces of the fishing net spread or spread and hung by a method of electrostatic coating, or by a method of air gun, airless coating or the like. As described above, the weight increase of the fishing net by net dyeing is usually about 80 to 300 g per 1 kg of the fishing net. A fishing net dyed with the composition of the present invention has the solid content of the antifouling coating composition of the present invention in or between the fibers, and further has the antifouling coating film of the present invention on the surface thereof. You may be doing it.
本発明の組成物から形成された防汚塗膜ないし防汚塗膜付き基材、本発明のおよび本発明の組成物で網染めされた漁網は、アオサ、フジツボ、アオノリ、セルプラ、カキ、フサコケムシ、ヒドラ等の水棲生物(特にフジツボ、ヒドラ)の付着を長期間継続的に防止できるなど防汚性に優れている。 The antifouling coating film or the base material with the antifouling coating film formed from the composition of the present invention, and the fishing nets dyed with the compositions of the present invention and the present invention include sea lettuce, hydra, green laver, celpra, oyster, and fusakokemushi. , Hydra and other aquatic organisms (especially Fujitsubo and Hydra) can be prevented from adhering continuously for a long period of time and have excellent antifouling properties.
さらに、本発明の基材の防汚方法は、本発明の防汚塗料組成物を基材に塗布するかまたは含浸させ、次いで硬化させるというものであり、この防汚方法により、基材へのアオサ、フジツボ、アオノリ、セルプラ、カキ、フサコケムシ、ヒドラ等の水棲生物(特にフジツボ、ヒドラ)の付着を長期間継続的に防止できる。 Further, the antifouling method for the base material of the present invention is to apply or impregnate the base material with the antifouling coating composition of the present invention and then cure the base material. Adhesion of aquatic organisms (particularly Fujitsubo and Hydra) such as sea lettuce, Fujitsubo, green laver, Serpra, oyster, Bugula neritina, and hydra can be continuously prevented for a long period of time.
以下、本発明を実施例に基づいてさらに具体的に説明するが、本発明の実施態様はこれらの実施例によりなんら限定されるものではない。
[測定方法]
<塗膜形成樹脂の重量平均分子量(Mw)>
塗膜形成樹脂の重量平均分子量(Mw)は、下記条件でGPC(ゲルパーミエーションクロマトグラフィー)法により測定した。
装置 :「HLC−8120GPC」(東ソー(株)製)
カラム:「TSKgel SuperH2000」及び「TSKgel SuperH4000」を連結(いずれも、東ソー(株)製、6mm(内径)×15cm(長さ))
溶離液:テトラヒドロフラン(THF)
流速 :0.500ml/min
検出器:RI
カラム恒温槽温度:40℃
標準物質:ポリスチレン
サンプル調製法:各製造例で調製された重合体溶液に少量の塩化カルシウムを加えて脱水した後、メンブレムフィルターで濾過して得られた濾物をGPC測定サンプルとした。
Hereinafter, the present invention will be described in more detail based on Examples, but the embodiments of the present invention are not limited to these Examples.
[Measuring method]
<Weight average molecular weight (Mw) of coating film forming resin>
The weight average molecular weight (Mw) of the coating film-forming resin was measured by the GPC (gel permeation chromatography) method under the following conditions.
Equipment: "HLC-8120GPC" (manufactured by Tosoh Corporation)
Column: "TSKgel SuperH2000" and "TSKgel SuperH4000" are connected (both manufactured by Tosoh Corporation, 6 mm (inner diameter) x 15 cm (length))
Eluent: tetrahydrofuran (THF)
Flow velocity: 0.500 ml / min
Detector: RI
Column constant temperature bath temperature: 40 ° C
Standard substance: Polystyrene Sample preparation method: The polymer solution prepared in each production example was dehydrated by adding a small amount of calcium chloride, and then filtered through a membrane filter to obtain a filter product as a GPC measurement sample.
<塗膜形成樹脂の数平均分子量(Mn)>
塗膜形成樹脂の数平均分子量(Mn)は、下記条件で液体クロマトグラフィーを用いて測定した。
装置 :「Waters 2695」
カラム:「TSKgel SuperH2000」及び「TSKgel SuperH4000」を連結(いずれも、東ソー(株)製、6mm(内径)×15cm(長さ))
溶離液:テトラヒドロフラン(THF)
流速 :0.6ml/min
検出器:「Shodex RI−104」
カラム恒温槽温度:40℃
<Number average molecular weight (Mn) of coating film forming resin>
The number average molecular weight (Mn) of the coating film-forming resin was measured by liquid chromatography under the following conditions.
Equipment: "Waters 2695"
Column: "TSKgel SuperH2000" and "TSKgel SuperH4000" are connected (both manufactured by Tosoh Corporation, 6 mm (inner diameter) x 15 cm (length))
Eluent: tetrahydrofuran (THF)
Flow velocity: 0.6 ml / min
Detector: "Shodex RI-104"
Column constant temperature bath temperature: 40 ° C
<塗膜形成樹脂溶液の粘度>
塗膜形成樹脂溶液の粘度は、25℃でE型粘度計(トキメック社製「VISCONIC EMD」)により測定した。
<Viscosity of coating film forming resin solution>
The viscosity of the coating film-forming resin solution was measured at 25 ° C. with an E-type viscometer (“VISCONIC EMD” manufactured by Tokimec Co., Ltd.).
[製造例1](アクリル樹脂の製造)
攪拌機、還流冷却機、滴下ロートを備えた4つ口フラスコに、キシレン67質量部を仕込み、撹拌しながら90℃に保持した。ここにイソブチルメタクリレート(IBMA)42質量部、ブチルアクリレート(BA)27質量部、メチルメタクリレート(MMA)18質量部およびt−ブチルパーオキシ−2−エチルヘキサノエート0.09質量部の混合液を2時間かけて滴下した。ここに、滴下終了2時間後に撹拌を続けながらt−ブチルパーオキシ−2−エチルヘキサノエートを0.045質量部ずつ1時間おきに2回加え、更に撹拌を続けながらt−ブチルパーオキシ−2−エチルヘキサノエート0.045質量部を30分おきに2回加えた。その後105℃まで昇温し、30分間撹拌を行った後、キシレンを20重量部加えてアクリル樹脂溶液(ワニスA1)を得た。得られたワニスA1の外観は透明、NV(105℃熱風乾燥機中3時間乾燥後の加熱残分)は50.3%、25℃での粘度は9,200mPa・sであり、ワニスA1に含まれる樹脂の重量平均分子量(Mw)は151,200であった。
[Manufacturing Example 1] (Manufacturing of acrylic resin)
67 parts by mass of xylene was placed in a four-necked flask equipped with a stirrer, a reflux condenser, and a dropping funnel, and the temperature was maintained at 90 ° C. with stirring. Here, a mixed solution of 42 parts by mass of isobutyl methacrylate (IBMA), 27 parts by mass of butyl acrylate (BA), 18 parts by mass of methyl methacrylate (MMA) and 0.09 parts by mass of t-butylperoxy-2-ethylhexanoate is added. It was added dropwise over 2 hours. To this, t-butylperoxy-2-ethylhexanoate was added twice every hour by 0.045 parts by mass while continuing stirring 2 hours after the completion of the dropping, and t-butylperoxy- was further continued while stirring. 0.045 parts by mass of 2-ethylhexanoate was added twice every 30 minutes. Then, the temperature was raised to 105 ° C., and after stirring for 30 minutes, 20 parts by weight of xylene was added to obtain an acrylic resin solution (varnish A1). The appearance of the obtained varnish A1 is transparent, the NV (heat residue after drying in a hot air dryer at 105 ° C. for 3 hours) is 50.3%, and the viscosity at 25 ° C. is 9,200 mPa · s. The weight average molecular weight (Mw) of the contained resin was 151,200.
[製造例2]((メタ)アクリル酸金属塩共重合体の製造)
(金属含有単量体を含む溶液(A2−1)の調製)
冷却器、温度計、滴下ロートおよび攪拌機を備えた四つ口フラスコに、プロピレングリコールモノメチルエーテル(PGM)85.4質量部および酸化亜鉛40.7質量部を仕込み、撹拌しながら75℃に昇温した。続いて、メタクリル酸(MAA)43.1質量部、アクリル酸(AA)36.1質量部、および水5質量部からなる混合物を滴下ロートから3時間かけて等速で滴下した。乳白色状態であった反応溶液は、滴下終了後に透明となった。さらに2時間撹拌した後、プロピレングリコールモノメチルエーテル36質量部を添加して、金属含有単量体を含む溶液(A2−1)を得た。金属含有単量体溶液(A2−1)のNVは44.8%であった。
[Production Example 2] (Production of (meth) acrylic acid metal salt copolymer)
(Preparation of solution (A2-1) containing metal-containing monomer)
85.4 parts by mass of propylene glycol monomethyl ether (PGM) and 40.7 parts by mass of zinc oxide were placed in a four-necked flask equipped with a cooler, a thermometer, a dropping funnel and a stirrer, and the temperature was raised to 75 ° C. with stirring. did. Subsequently, a mixture consisting of 43.1 parts by mass of methacrylic acid (MAA), 36.1 parts by mass of acrylic acid (AA), and 5 parts by mass of water was added dropwise from the dropping funnel at a constant velocity over 3 hours. The reaction solution, which was in a milky white state, became transparent after the completion of dropping. After further stirring for 2 hours, 36 parts by mass of propylene glycol monomethyl ether was added to obtain a solution (A2-1) containing a metal-containing monomer. The NV of the metal-containing monomer solution (A2-1) was 44.8%.
((メタ)アクリル酸金属塩共重合体の製造)
冷却器、温度計、滴下ロートおよび攪拌機を備えた四つ口フラスコに、プロピレングリコールモノメチルエーテル(PGM)15質量部およびキシレン57質量部を仕込み、撹拌しながら100℃に昇温した。続いて、前記金属含有単量体溶液(A2−1)52質量部、メチルメタクリレート(MMA)1質量部、エチルアクリレート(EA)66.2質量部、2−メトキシエチルアクリレート(2−MEA)5.4質量部、アゾビスイソブチロニトリル(AIBN)(日本ヒドラジン工業(株)製)2.5質量部、アゾビスメチルブチロニトリル(AMBN)(日本ヒドラジン工業(株)製)7質量部、連鎖移動剤「ノフマーMSD」(日本油脂(株)製)1質量部、およびキシレン10質量部からなる透明な混合物を滴下ロートから6時間かけて等速で滴下した。滴下終了後にt−ブチルパーオクトエート(TBPO)0.5質量部とキシレン7質量部とを30分かけて滴下し、さらに1時間30分撹拌した後、キシレンを4.4質量部添加して、不溶物がなく、淡黄色透明な、(メタ)アクリル酸金属塩共重合体を含む反応混合物(ワニスA2)を得た。反応混合物(ワニスA2)のNV(105℃熱風乾燥機中3時間乾燥後の加熱残分)は45.6%、25℃での粘度は1,650mPa・sであり、ワニスA2に含まれる樹脂の重量平均分子量(Mw)は5,200であった。
(Production of (meth) acrylic acid metal salt copolymer)
A four-necked flask equipped with a cooler, a thermometer, a dropping funnel and a stirrer was charged with 15 parts by mass of propylene glycol monomethyl ether (PGM) and 57 parts by mass of xylene, and the temperature was raised to 100 ° C. with stirring. Subsequently, 52 parts by mass of the metal-containing monomer solution (A2-1), 1 part by mass of methyl methacrylate (MMA), 66.2 parts by mass of ethyl acrylate (EA), and 2-methoxyethyl acrylate (2-MEA) 5 .4 parts by mass, azobisisobutyronitrile (AIBN) (manufactured by Nippon Hydrazin Industry Co., Ltd.) 2.5 parts by mass, azobismethylbutyronitrile (AMBN) (manufactured by Nippon Hydrazin Industry Co., Ltd.) 7 parts by mass A transparent mixture consisting of 1 part by mass of the chain transfer agent "Nofmer MSD" (manufactured by Nippon Oil & Fats Co., Ltd.) and 10 parts by mass of xylene was added dropwise from the dropping funnel at a constant velocity over 6 hours. After completion of the dropping, 0.5 parts by mass of t-butyl peroctate (TBPO) and 7 parts by mass of xylene were added dropwise over 30 minutes, and after further stirring for 1 hour and 30 minutes, 4.4 parts by mass of xylene was added. A reaction mixture (varnish A2) containing a (meth) acrylic acid metal salt copolymer having no insoluble matter and being pale yellow and transparent was obtained. The NV (heat residue after drying in a hot air dryer at 105 ° C. for 3 hours) of the reaction mixture (varnish A2) was 45.6%, the viscosity at 25 ° C. was 1,650 mPa · s, and the resin contained in the varnish A2. The weight average molecular weight (Mw) of was 5,200.
[製造例3](ポリシロキサンブロック含有金属塩共重合体の製造)
攪拌機、還流冷却器および滴下ロートを備えた4つ口フラスコに、プロピレングリコールモノメチルエーテル20質量部、キシレン82質量部を仕込み90℃に昇温し、その温度で保持した。次いで、このフラスコ内に亜鉛ジメタクリレート7質量部、亜鉛ジアクリレート7質量部、メチルメタクリレート6質量部、エチルアクリレート45質量部、純水0.5質量部、プロピレングリコールモノメチルエーテル16質量部、メタクリロキシプロピルポリジメチルシロキサン(商品名「サイラプレーンFM−0711」、JNC(株)製、数均分子量約1,000)を35質量部、重合用触媒としてアゾビスイソブチロニトリル3質量部の混合液を2時間かけて滴下し、滴下後、約4時間この温度(90℃)を保持して、仕込み量に基づいて算出されるメタクリロキシプロピルポリジメチルシロキサン成分が35質量%であり、亜鉛ジ(メタ)アクリレート中の金属Znの含有量が4.2質量%であり、メチルメタクリレートおよびエチルアクリレートから誘導される成分の含有量が51質量%のポリシロキサンブロック含有金属塩共重合体を含む反応混合物(但し、共重合体の質量を100質量%とする。)を得た。ワニスA3のNV(105℃熱風乾燥機中3時間乾燥後の加熱残分)は45.2%、25℃での粘度は12,000mPa・s、ワニスA3に含まれる樹脂の数平均分子量(Mn)は2,380、固形分酸価は71mgKOH/gであった。
[Production Example 3] (Production of Polysiloxane Block-Containing Metal Salt Copolymer)
In a four-necked flask equipped with a stirrer, a reflux condenser and a dropping funnel, 20 parts by mass of propylene glycol monomethyl ether and 82 parts by mass of xylene were charged, the temperature was raised to 90 ° C., and the temperature was maintained. Next, in this flask, 7 parts by mass of zinc dimethacrylate, 7 parts by mass of zinc diacrylate, 6 parts by mass of methyl methacrylate, 45 parts by mass of ethyl acrylate, 0.5 parts by mass of pure water, 16 parts by mass of propylene glycol monomethyl ether, and methacryloxy. A mixed solution of 35 parts by mass of propylpolydimethylsiloxane (trade name "Silaplane FM-0711", manufactured by JNC Co., Ltd., having a number average molecular weight of about 1,000) and 3 parts by mass of azobisisobutyronitrile as a polymerization catalyst. Was added dropwise over 2 hours, and after the addition, the temperature (90 ° C.) was maintained for about 4 hours, and the methacryloxypropyl polydimethylsiloxane component calculated based on the charged amount was 35% by mass, and zinc di ( A reaction mixture containing a polysiloxane block-containing metal salt copolymer having a metal Zn content of 4.2% by mass and a component derived from methyl methacrylate and ethyl acrylate of 51% by mass in the meta) acrylate. (However, the mass of the copolymer is 100% by mass.) Was obtained. The NV of varnish A3 (heat residue after drying in a hot air dryer at 105 ° C for 3 hours) is 45.2%, the viscosity at 25 ° C is 12,000 mPa · s, and the number average molecular weight of the resin contained in varnish A3 (Mn). ) Was 2,380, and the solid acid value was 71 mgKOH / g.
[防汚塗料組成物の製造]
[実施例1〜40、比較例1〜15]
製造例1〜3により得られたワニスA1、ワニスA2またはワニスA3と他の成分とを、表2〜5に記載の割合でペイントシェーカーを用いて均一に混合することにより、防汚塗料組成物を製造した。各防汚塗料組成物を後述する方法で評価した。結果を表2〜5に示す。
実施例および比較例で使用された原材料の詳細は以下の通りである。
[Manufacturing of antifouling paint composition]
[Examples 1 to 40, Comparative Examples 1 to 15]
An antifouling coating composition is obtained by uniformly mixing the varnish A1, varnish A2 or varnish A3 obtained in Production Examples 1 to 3 with other components at the ratios shown in Tables 2 to 5 using a paint shaker. Manufactured. Each antifouling coating composition was evaluated by the method described later. The results are shown in Tables 2-5.
Details of the raw materials used in the examples and comparative examples are as follows.
[性能評価]
(1)静置防汚性(漁網)
実施例および比較例で調製した防汚塗料組成物のそれぞれに、漁網(ポリエチレン製無結節網(7節、400デニール/50本、縦15cm×横15cm))を1〜3分間程度浸漬し、取り出した後、室内で7日間風乾し、塗膜付き漁網を得た。
この塗膜付き漁網を80cm×40cmのステンレス枠に固定し、広島県広島湾内の海面下約2mに、浸漬した。浸漬開始から2ヶ月毎に、漁網の水棲生物が付着している部分の面積(付着面積)(%)(漁網の全面積を100%とする。)を測定し、下記評価基準に基づいて静置防汚性(漁網)を評価した。
<評価基準>
A:付着面積が0%
B:付着面積が0%より大きく10%未満
C:付着面積が10%以上30%未満
D:付着面積が30%以上50%未満
E:付着面積が50%以上90%未満
F:付着面積が90%以上
[Performance evaluation]
(1) Static antifouling property (fishing net)
A fishing net (polyethylene knotless net (7 nodes, 400 denier / 50 lines, length 15 cm x width 15 cm)) was immersed in each of the antifouling paint compositions prepared in Examples and Comparative Examples for about 1 to 3 minutes. After taking it out, it was air-dried indoors for 7 days to obtain a fishing net with a coating film.
This coated fishing net was fixed to a stainless steel frame of 80 cm × 40 cm and immersed in about 2 m below the sea surface in Hiroshima Bay, Hiroshima Prefecture. Every two months from the start of immersion, the area (attachment area) (%) of the part of the fishing net to which aquatic organisms are attached is measured (the total area of the fishing net is 100%), and it is static based on the following evaluation criteria. The antifouling property (fishing net) was evaluated.
<Evaluation criteria>
A: Adhesion area is 0%
B: Adhesion area is greater than 0% and less than 10% C: Adhesion area is 10% or more and less than 30% D: Adhesion area is 30% or more and less than 50% E: Adhesion area is 50% or more and less than 90% F: Adhesion area is 90% or more
(2)静置防汚性(パネル)
サンドブラスト処理鋼板(縦300mm×横100mm×厚み3.2mm)に、エポキシ系防錆塗料(エポキシAC塗料、商品名「バンノー500」、中国塗料(株)製)をその乾燥膜厚が150μm厚となるように塗布した後、エポキシ系バインダー塗料(商品名「バンノー500N」、中国塗料(株)製)をその乾燥膜厚が100μm厚となるように塗布した。続いて、実施例および比較例で製造した防汚塗料組成物を、その乾燥膜厚が100μmとなるように1回塗布し、室温で7日間乾燥させて、防汚塗膜付き試験板を作製した。なお、前記の3回の塗装間隔はいずれも1day/1coatとした。
(2) Static antifouling property (panel)
Epoxy-based rust preventive paint (epoxy AC paint, trade name "Banno 500", manufactured by China Paint Co., Ltd.) is applied to a sandblasted steel plate (length 300 mm x width 100 mm x thickness 3.2 mm) with a dry film thickness of 150 μm. After that, an epoxy-based binder paint (trade name "Banno 500N", manufactured by China Paint Co., Ltd.) was applied so that the dry film thickness was 100 μm. Subsequently, the antifouling coating composition produced in Examples and Comparative Examples was applied once so that the dry film thickness was 100 μm, and dried at room temperature for 7 days to prepare a test plate with an antifouling coating film. did. The three coating intervals were set to 1 day / 1 coat.
作製された試験板を広島県広島湾内に10ヶ月間静置浸漬し、その間2ヶ月毎に塗膜表面のスライムを除く海中生物が付着している部分の面積(付着面積)(%)(防汚塗膜の全面積を100%とする。)を測定した。そして、下記評価基準に従って、静置防汚性(パネル)を評価した。
<評価基準>
A:付着面積が0%
B:付着面積が0%より大きく10%未満
C:付着面積が10%以上30%未満
D:付着面積が30%以上50%未満
E:付着面積が50%以上90%未満
F:付着面積が90%以上
The prepared test plate was soaked in Hiroshima Bay, Hiroshima Prefecture for 10 months, and every 2 months during that period, the area (adhesion area) (%) (prevention) of the part where marine organisms other than slime on the coating film surface adhered. The total area of the dirty coating film is 100%.) Was measured. Then, the static antifouling property (panel) was evaluated according to the following evaluation criteria.
<Evaluation criteria>
A: Adhesion area is 0%
B: Adhesion area is greater than 0% and less than 10% C: Adhesion area is 10% or more and less than 30% D: Adhesion area is 30% or more and less than 50% E: Adhesion area is 50% or more and less than 90% F: Adhesion area is 90% or more
(3)耐フジツボ性
耐フジツボ性評価は、前記静置防汚性(1)または前記静置防汚性(2)での漁網または試験板の海への浸漬開始から10ヶ月目の付着面積に占めるフジツボが付着している部分の面積(フジツボ付着面積)の割合を測定し、下記評価基準に基づいて耐フジツボ性を評価した。
<評価基準>
A:フジツボ付着面積が0%
B:フジツボ付着面積が0%より大きく10%未満
C:フジツボ付着面積が10%以上30%未満
D:フジツボ付着面積が30%以上50%未満
E:フジツボ付着面積が50%以上90%未満
F:フジツボ付着面積が90%以上
(3) Barnacle resistance The barnacle resistance evaluation is based on the adhesion area of the fishing net or test plate 10 months after the start of immersion in the sea with the static antifouling property (1) or the static antifouling property (2). The ratio of the area of the barnacles attached to the barnacles (barnacles attached area) was measured, and the barnacle resistance was evaluated based on the following evaluation criteria.
<Evaluation criteria>
A: Barnacle adhesion area is 0%
B: Barnacle adhesion area is greater than 0% and less than 10% C: Barnacle adhesion area is 10% or more and less than 30% D: Barnacle adhesion area is 30% or more and less than 50% E: Barnacle adhesion area is 50% or more and less than 90% F : Barnacle adhesion area is 90% or more
(4)耐腔腸動物(ヒドラ)性
耐腔腸動物(ヒドラ)性評価では、前記静置防汚性(1)と同様な方法で作製した塗膜付き漁網を80cm×40cmのステンレス枠に固定し、神奈川県相模湾内の海面下約2mに、浸漬した。浸漬開始から4ヶ月後の付着面積に占めるヒドラが付着している部分の面積(ヒドラ付着面積)の割合を測定し、下記評価基準に基づいて耐ヒドラ性を評価した。
<評価基準>
A:ヒドラ付着面積が0%
B:ヒドラ付着面積が0%より大きく10%未満
C:ヒドラ付着面積が10%以上30%未満
D:ヒドラ付着面積が30%以上50%未満
E:ヒドラ付着面積が50%以上90%未満
F:ヒドラ付着面積が90%以上
(4) Coelenterate (Hydra) In the evaluation of coelenterate (Hydra), a fishing net with a coating film prepared by the same method as the static antifouling property (1) was placed in a 80 cm x 40 cm stainless steel frame. It was fixed and immersed in about 2 m below the sea level in Sagami Bay, Kanagawa Prefecture. The ratio of the area where the hydra was attached (hydra adhesion area) to the adhesion area 4 months after the start of immersion was measured, and the hydra resistance was evaluated based on the following evaluation criteria.
<Evaluation criteria>
A: Hydra adhesion area is 0%
B: Hydra adhesion area is greater than 0% and less than 10% C: Hydra adhesion area is 10% or more and less than 30% D: Hydra adhesion area is 30% or more and less than 50% E: Hydra adhesion area is 50% or more and less than 90% F : Hydra adhesion area is 90% or more
(5)造膜性
実施例および比較例で調製した防汚塗料組成物のそれぞれを、アプリケーターを用いてガラス板上に乾燥膜厚が100μmとなるよう塗布し、室内で2週間乾燥して塗膜を形成した。この塗膜に指先で触れて、以下の基準に基づいて評価を行った。
<評価基準>
◎・・・塗膜に殆ど傷が付かない
○・・・塗膜表面にわずかに傷が付く
□・・・塗膜表面に明らかに傷が付く
△・・・塗膜に容易に塗膜に割れが生じる
×・・・塗膜が容易に塗膜が破壊される
(5) Film-forming property Each of the antifouling coating compositions prepared in Examples and Comparative Examples was applied onto a glass plate using an applicator so that the dry film thickness was 100 μm, and dried and applied indoors for 2 weeks. A film was formed. The coating film was touched with a fingertip and evaluated based on the following criteria.
<Evaluation criteria>
◎ ・ ・ ・ Slightly scratched on the coating film ○ ・ ・ ・ Slightly scratched on the coating film surface □ ・ ・ ・ Clearly scratched on the coating film surface △ ・ ・ ・ Easily applied to the coating film Cracks occur × ・ ・ ・ The coating film is easily destroyed
(6)貯蔵安定性
実施例および比較例で調製した防汚塗料組成物のそれぞれについて、密封した容器に入れて、40℃の恒温器で2ヶ月貯蔵したものを用意し、貯蔵後の塗料状態および粘性を確認し、貯蔵前の状態と比較し、下記評価基準に基づいて評価した。
<評価基準>
5・・・変化なし
4・・・わずかな粘度上昇が認められる
3・・・わずかな粘度上昇および微小な粒が認められる
2・・・大幅な粘度上昇および微小な粒が認められる
1・・・大幅な粘度上昇および粒が認められる
(6) Storage stability Each of the antifouling paint compositions prepared in Examples and Comparative Examples was placed in a sealed container and stored in an incubator at 40 ° C. for 2 months, and the state of the paint after storage was prepared. And the viscosity was confirmed, compared with the state before storage, and evaluated based on the following evaluation criteria.
<Evaluation criteria>
5 ... No change 4 ... Slight increase in viscosity is observed 3 ... Slight increase in viscosity and fine grains are observed 2 ... Significant increase in viscosity and minute grains are observed 1 ...・ Significant increase in viscosity and grains are observed.
Claims (15)
前記ポリエーテル変性シリコーンオイル(A)が一般式[I]:
X1、X2およびX3はそれぞれ独立に炭素数1〜5のアルキル基、フェニル基またはポリエーテル基を示し、
X4は炭素数1〜18のアルキル基またはフェニル基を示し、
mは1以上の整数を示し、
nは0以上の整数を示し、
pは0以上の整数を示し、
前記ポリエーテル基は下式[Ia]:
−R2−A−(R3O)q(R4O)r−R5 ・・・[Ia]
(式[Ia]中、Aは単結合または酸素原子を示し、
R2、R3およびR4はそれぞれ独立に炭素数1〜5の2価の炭化水素基を示し、
R5は炭素数1〜5のアルキル基または水素原子を示し、
qは1〜30の整数を示し、
rは0〜30の整数を示し、
左端の線はケイ素原子への結合を示す。)で表される。〕で表され、1分子中に少なくとも1つの前記ポリエーテル基を有し、
前記防汚剤(B)としてメデトミジン(B1)を含有し、
前記メデトミジン(B1)の含有量が、前記ポリエーテル変性シリコーンオイル(A)100質量部に対して1〜200質量部である
防汚塗料組成物。 An antifouling coating composition containing a polyether-modified silicone oil (A), an antifouling agent (B), and a coating film-forming resin (C).
The polyether-modified silicone oil (A) has a general formula [I]:
X 1 , X 2 and X 3 independently represent an alkyl group, a phenyl group or a polyether group having 1 to 5 carbon atoms, respectively.
X 4 represents an alkyl or phenyl group having 1 to 18 carbon atoms.
m indicates an integer of 1 or more,
n indicates an integer greater than or equal to 0,
p indicates an integer greater than or equal to 0,
The polyether group has the following formula [Ia]:
−R 2 −A− (R 3 O) q (R 4 O) r −R 5・ ・ ・ [Ia]
(In formula [Ia], A represents a single bond or an oxygen atom,
R 2 , R 3 and R 4 each independently represent a divalent hydrocarbon group having 1 to 5 carbon atoms.
R 5 represents an alkyl group or a hydrogen atom having 1 to 5 carbon atoms.
q indicates an integer from 1 to 30
r represents an integer from 0 to 30
The leftmost line shows the bond to the silicon atom. ). ], Which has at least one of the above-mentioned polyether groups in one molecule.
Medetomidine (B1) is contained as the antifouling agent (B) ,
The antifouling coating composition contains 1 to 200 parts by mass of the medetomidine (B1) with respect to 100 parts by mass of the polyether-modified silicone oil (A).
A step of applying or impregnating the surface of the base material with the antifouling coating composition according to any one of claims 1 to 9 , and the step of preventing the base material from being coated or impregnated by the step. A method for producing a base material with an antifouling coating film, which comprises a step of curing the stain coating composition.
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