JP2651499B2 - Resin composition for antifouling paint - Google Patents
Resin composition for antifouling paintInfo
- Publication number
- JP2651499B2 JP2651499B2 JP28741887A JP28741887A JP2651499B2 JP 2651499 B2 JP2651499 B2 JP 2651499B2 JP 28741887 A JP28741887 A JP 28741887A JP 28741887 A JP28741887 A JP 28741887A JP 2651499 B2 JP2651499 B2 JP 2651499B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- antifouling
- resin
- acid
- resin composition
- 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.)
- Expired - Fee Related
Links
- 239000003973 paint Substances 0.000 title claims description 31
- 230000003373 anti-fouling effect Effects 0.000 title claims description 28
- 239000011342 resin composition Substances 0.000 title claims description 14
- 239000011347 resin Substances 0.000 claims description 37
- 229920005989 resin Polymers 0.000 claims description 37
- 239000000178 monomer Substances 0.000 claims description 22
- 229920001577 copolymer Polymers 0.000 claims description 17
- 239000013535 sea water Substances 0.000 claims description 14
- 238000004090 dissolution Methods 0.000 claims description 11
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 10
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 9
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 9
- OGHKVCJFHNKOEC-UHFFFAOYSA-N 1-methoxyethane-1,2-diol;2-methylprop-2-enoic acid Chemical compound COC(O)CO.CC(=C)C(O)=O OGHKVCJFHNKOEC-UHFFFAOYSA-N 0.000 claims description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 6
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 6
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical group COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 description 21
- 238000000576 coating method Methods 0.000 description 21
- 239000002519 antifouling agent Substances 0.000 description 19
- 238000012360 testing method Methods 0.000 description 13
- -1 sodium carboxylate Chemical class 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- 239000000243 solution Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 238000010828 elution Methods 0.000 description 6
- 230000007062 hydrolysis Effects 0.000 description 6
- 238000006460 hydrolysis reaction Methods 0.000 description 6
- 230000007774 longterm Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 4
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 4
- 229940112669 cuprous oxide Drugs 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 3
- ZTCLCSCHTACERP-AWEZNQCLSA-N N-[(1S)-1-[3-chloro-5-fluoro-2-[[2-methyl-4-(2-methyl-1,2,4-triazol-3-yl)quinolin-8-yl]oxymethyl]phenyl]ethyl]-2-(difluoromethoxy)acetamide Chemical compound C1=C(C=C(C(=C1Cl)COC1=CC=CC2=C(C=3N(N=CN=3)C)C=C(C)N=C12)[C@@H](NC(=O)COC(F)F)C)F ZTCLCSCHTACERP-AWEZNQCLSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 3
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 150000002736 metal compounds Chemical class 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000005498 polishing Methods 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229910052714 tellurium Inorganic materials 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 2
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 238000004088 simulation Methods 0.000 description 2
- 239000003784 tall oil Substances 0.000 description 2
- 239000011269 tar Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- DWKNOLCXIFYNFV-HSZRJFAPSA-N 2-[[(2r)-1-[1-[(4-chloro-3-methylphenyl)methyl]piperidin-4-yl]-5-oxopyrrolidine-2-carbonyl]amino]-n,n,6-trimethylpyridine-4-carboxamide Chemical compound CN(C)C(=O)C1=CC(C)=NC(NC(=O)[C@@H]2N(C(=O)CC2)C2CCN(CC=3C=C(C)C(Cl)=CC=3)CC2)=C1 DWKNOLCXIFYNFV-HSZRJFAPSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-hydroxyoctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
- AAYSXEMBWUMDIZ-UHFFFAOYSA-N 2-methyl-n,n-dipropylprop-2-enamide Chemical compound CCCN(CCC)C(=O)C(C)=C AAYSXEMBWUMDIZ-UHFFFAOYSA-N 0.000 description 1
- YQIGLEFUZMIVHU-UHFFFAOYSA-N 2-methyl-n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C(C)=C YQIGLEFUZMIVHU-UHFFFAOYSA-N 0.000 description 1
- CCIDRBFZPRURMU-UHFFFAOYSA-N 2-methyl-n-propylprop-2-enamide Chemical compound CCCNC(=O)C(C)=C CCIDRBFZPRURMU-UHFFFAOYSA-N 0.000 description 1
- CXKCZFDUOYMOOP-UHFFFAOYSA-N 3,5-dichlorobenzoic acid Chemical compound OC(=O)C1=CC(Cl)=CC(Cl)=C1 CXKCZFDUOYMOOP-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
- NNJMFJSKMRYHSR-UHFFFAOYSA-N 4-phenylbenzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC=CC=C1 NNJMFJSKMRYHSR-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 241000238586 Cirripedia Species 0.000 description 1
- 229910021595 Copper(I) iodide Inorganic materials 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- MWHHJYUHCZWSLS-UHFFFAOYSA-N FC=1C=C(C=CC1C1=C2CNC(C2=C(C=C1)C=1NC(=CN1)C)=O)NC(=O)NC1=C(C=C(C=C1F)F)F Chemical compound FC=1C=C(C=CC1C1=C2CNC(C2=C(C=C1)C=1NC(=CN1)C)=O)NC(=O)NC1=C(C=C(C=C1F)F)F MWHHJYUHCZWSLS-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- RPJAQOVNRDOGAY-UHFFFAOYSA-L copper(1+);sulfite Chemical compound [Cu+].[Cu+].[O-]S([O-])=O RPJAQOVNRDOGAY-UHFFFAOYSA-L 0.000 description 1
- LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 description 1
- GQDHEYWVLBJKBA-UHFFFAOYSA-H copper(ii) phosphate Chemical compound [Cu+2].[Cu+2].[Cu+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GQDHEYWVLBJKBA-UHFFFAOYSA-H 0.000 description 1
- RSJOBNMOMQFPKQ-UHFFFAOYSA-L copper;2,3-dihydroxybutanedioate Chemical compound [Cu+2].[O-]C(=O)C(O)C(O)C([O-])=O RSJOBNMOMQFPKQ-UHFFFAOYSA-L 0.000 description 1
- PWGQHOJABIQOOS-UHFFFAOYSA-N copper;dioxido(dioxo)chromium Chemical compound [Cu+2].[O-][Cr]([O-])(=O)=O PWGQHOJABIQOOS-UHFFFAOYSA-N 0.000 description 1
- SVOAENZIOKPANY-UHFFFAOYSA-L copper;octadec-9-enoate Chemical compound [Cu+2].CCCCCCCCC=CCCCCCCCC([O-])=O.CCCCCCCCC=CCCCCCCCC([O-])=O SVOAENZIOKPANY-UHFFFAOYSA-L 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 235000019855 cupric citrate Nutrition 0.000 description 1
- 239000011641 cupric citrate Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 229960005215 dichloroacetic acid Drugs 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical class CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000012690 ionic polymerization Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- UETZVSHORCDDTH-UHFFFAOYSA-N iron(2+);hexacyanide Chemical compound [Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] UETZVSHORCDDTH-UHFFFAOYSA-N 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- WFKDPJRCBCBQNT-UHFFFAOYSA-N n,2-dimethylprop-2-enamide Chemical compound CNC(=O)C(C)=C WFKDPJRCBCBQNT-UHFFFAOYSA-N 0.000 description 1
- QRWZCJXEAOZAAW-UHFFFAOYSA-N n,n,2-trimethylprop-2-enamide Chemical compound CN(C)C(=O)C(C)=C QRWZCJXEAOZAAW-UHFFFAOYSA-N 0.000 description 1
- YHOSNAAUPKDRMI-UHFFFAOYSA-N n,n-di(propan-2-yl)prop-2-enamide Chemical compound CC(C)N(C(C)C)C(=O)C=C YHOSNAAUPKDRMI-UHFFFAOYSA-N 0.000 description 1
- RKSYJNCKPUDQET-UHFFFAOYSA-N n,n-dipropylprop-2-enamide Chemical compound CCCN(CCC)C(=O)C=C RKSYJNCKPUDQET-UHFFFAOYSA-N 0.000 description 1
- OJBZOTFHZFZOIJ-UHFFFAOYSA-N n-acetyl-2-methylprop-2-enamide Chemical compound CC(=O)NC(=O)C(C)=C OJBZOTFHZFZOIJ-UHFFFAOYSA-N 0.000 description 1
- RUSRUYULUAYXIP-UHFFFAOYSA-N n-acetylprop-2-enamide Chemical compound CC(=O)NC(=O)C=C RUSRUYULUAYXIP-UHFFFAOYSA-N 0.000 description 1
- QISNULGCGWEUKY-UHFFFAOYSA-N n-ethyl-2-methylidenebutanamide Chemical compound CCNC(=O)C(=C)CC QISNULGCGWEUKY-UHFFFAOYSA-N 0.000 description 1
- ZIWDVJPPVMGJGR-UHFFFAOYSA-N n-ethyl-2-methylprop-2-enamide Chemical compound CCNC(=O)C(C)=C ZIWDVJPPVMGJGR-UHFFFAOYSA-N 0.000 description 1
- SWPMNMYLORDLJE-UHFFFAOYSA-N n-ethylprop-2-enamide Chemical compound CCNC(=O)C=C SWPMNMYLORDLJE-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 description 1
- WDFKEEALECCKTJ-UHFFFAOYSA-N n-propylprop-2-enamide Chemical compound CCCNC(=O)C=C WDFKEEALECCKTJ-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000011297 pine tar Substances 0.000 description 1
- 229940068124 pine tar Drugs 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound 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
- 230000005855 radiation Effects 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000003902 seawater pollution Methods 0.000 description 1
- 235000015170 shellfish Nutrition 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 229910021654 trace metal Inorganic materials 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 125000005389 trialkylsiloxy group Chemical group 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical class CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- STDMRMREKPZQFJ-UHFFFAOYSA-H tricopper;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Cu+2].[Cu+2].[Cu+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O STDMRMREKPZQFJ-UHFFFAOYSA-H 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】 〔発明の目的〕 (産業上の利用分野) 本発明は新規な海中構造物の防汚塗料用樹脂組成物に
関する。DETAILED DESCRIPTION OF THE INVENTION [Object of the Invention] (Industrial application field) The present invention relates to a novel resin composition for an antifouling paint for marine structures.
さらに詳細には塗膜が強固でかつ適度な水可溶性を有
し、樹脂自身が加水分解によって防汚剤としての金属化
合物を海中に放出するため、塗料中に配合する防汚剤を
減らすことが可能な、しかも長期防汚性を有する船底な
らびに海中構造物などに用いられる海水防汚塗料用樹脂
組成物に関するものである。In more detail, since the coating film is strong and has a suitable water solubility, and the resin itself releases a metal compound as an antifouling agent into the sea by hydrolysis, it is necessary to reduce the amount of antifouling agent to be incorporated into the paint. The present invention relates to a resin composition for seawater antifouling paints that can be used and has a long-term antifouling property and is used for ship bottoms and underwater structures.
(従来の技術) 水面下にある物体の表面は、通常、多層のペイント被
膜に覆われており、そして海に棲んでいる藻やフジツボ
などの生物の生長を防ぐために、通常はトップコートと
して防汚性ペイントが塗布されている。(Prior Art) The surface of an object under water is usually covered with a multi-layer paint film, and is usually protected as a top coat to prevent the growth of living organisms such as algae and barnacles living in the sea. Dirty paint is applied.
ところで、かかる防汚性ペイントは、それ自体が毒物
である亜酸化銅の如き徐々に海水と反応して水溶性塩を
生長する防汚剤を含んでおり、これらの防汚剤は水溶性
塩の形で順次ペイントフィルムから溶出されていく。By the way, such antifouling paints contain antifouling agents such as cuprous oxide, which itself is a poison, which gradually reacts with seawater to grow water-soluble salts. It is sequentially eluted from the paint film in the form of
しかしながら、これら防汚剤の溶出過程において、そ
の溶出速度が均一になるように制御することが難しく、
しかも防汚性ペイントが塗布されている船を就航させた
り、再就航させ始めた直後に、望ましくないほど速かに
溶出が起こり、その結果、必要以上に高濃度の毒性の防
汚剤が船のまわりに存在することとなり防汚剤の浪費と
水の汚染を怠起させることとなるし、また溶出が或る程
度進行したのちには防汚剤の濃度が低下する結果、海中
に棲息する上記生物の生長が増進されることとなる。However, in the dissolution process of these antifouling agents, it is difficult to control the dissolution rate to be uniform,
In addition, the dissolution occurs undesirably quickly as soon as the ship to which the antifouling paint has been applied enters service or begins to re-enter, resulting in an unnecessarily high concentration of toxic antifouling agent. Around the seawater, which results in waste of the antifouling agent and neglect of water contamination, and after a certain degree of elution, the concentration of the antifouling agent decreases, resulting in inhabiting in the sea. The growth of the organism will be enhanced.
これらの事実の結論として、防汚剤の溶出速度を均一
になるように人為的にコントロールすることのできる樹
脂の開発が期待されている。As a conclusion of these facts, development of a resin that can be artificially controlled so that the dissolution rate of the antifouling agent becomes uniform is expected.
この種の防汚剤の溶出速度を或る程度均一にさせ、比
較的長期に亘って前記海生物の生長ないしはその増進を
抑制させうる物質として、たとえばトリブチルチンオキ
サイドを側鎖にもつ共重合体がある。しかしながらこの
共重合体は加水分解によりトリブチルチンオキサイドを
生成するため、これが海水汚染の原因となり魚介類への
影響が重大である。Copolymers having tributyltin oxide as a side chain as a substance capable of making the dissolution rate of this kind of antifouling agent uniform to some extent and suppressing the growth or promotion of the marine organism for a relatively long period of time, for example. There is. However, since this copolymer produces tributyltin oxide by hydrolysis, this causes seawater pollution and seriously affects fish and shellfish.
そのほかにも、加水分解性に優れるカルボキシル基、
ジメチルアミノ基またはヒドロキシル基などの官能基を
側鎖にもった(共)重合体が用いられてはいるけれど
も、これらの(共)重合体にしても、それらのいずれも
が長期に亘って均一になる溶出速度を保持しうるもので
はないし、また亜酸化銅の如き金属系の防汚剤を用いた
塗料にカルボキシル基、ヒドロキシル基含有共重合体を
用いると塗料の安定性が極端に悪くなるという点を露呈
する。また、この種のトップコートの樹脂成分として古
くからロジン系樹脂が用いられているが、長期防汚性に
欠ける欠点を有している。In addition, carboxyl groups with excellent hydrolyzability,
Although a (co) polymer having a functional group such as a dimethylamino group or a hydroxyl group in a side chain is used, even when these (co) polymers are used, all of them are uniform over a long period of time. If the carboxyl group- and hydroxyl group-containing copolymer is used in a paint using a metal-based antifouling agent such as cuprous oxide, the stability of the paint becomes extremely poor. The point is revealed. In addition, although rosin-based resins have been used for a long time as a resin component of this type of top coat, they have a drawback that they lack long-term antifouling properties.
本発明者は、さきにビニル系共重合体の側鎖にトリア
ルキルシロキシ基でブロックしたカルボキシレートを持
たせた加水分解性に優れ、かつセルフポリシング型塗膜
を与える塗料樹脂組成物を提供した。(特願昭62−4978
35号)。かかる樹脂は海水中等のアルカリ条件下で加水
分解され、カルボン酸ナトリウム塩の形で防汚剤ととも
に可溶化するものであるが、長期の使用性や公衆衛生的
見地からできるだけ防汚剤の使用量を少なくするという
観点から評価すると、まだ改良の余地を残すものであ
る。The present inventor has provided a coating resin composition which has a carboxylate blocked with a trialkylsiloxy group on the side chain of a vinyl copolymer and has excellent hydrolyzability and gives a self-polishing coating film. . (Japanese Patent Application No. 62-4978
No. 35). Such a resin is hydrolyzed under alkaline conditions such as seawater and solubilized together with an antifouling agent in the form of a sodium carboxylate.However, from the viewpoint of long-term use and public health, the amount of the antifouling agent used is as small as possible. When evaluated from the viewpoint of reducing the number, there is still room for improvement.
(発明が解決しようとする問題点) 従って、本発明の主目的は、樹脂の側鎖部に加水分解
により親水基が生成せられるような基を有し、海水中で
適度の加水分解を受けて溶出する型の造膜性に優れた樹
脂をベースとし、高価でかつ海水汚染の見地からその使
用が望ましくないとされているトリブチルスズ塩に依存
せぬ新規な防汚塗料用樹脂組成物を提供することにあ
る。(Problems to be Solved by the Invention) Therefore, a main object of the present invention is to provide a resin having a group capable of generating a hydrophilic group by hydrolysis in a side chain portion thereof, and to undergo moderate hydrolysis in seawater. Provides a novel resin composition for antifouling paints that is based on a resin with excellent film forming properties that elutes and elutes, and does not depend on tributyltin salt, which is expensive and its use is considered undesirable from the viewpoint of seawater contamination Is to do.
(問題点を解決するための手段) 本発明を概略すれば、本発明は、 (i) 主成分がメチルビニルエーテル、N−ビニルピ
ロリドン、メタクリル酸メトキシエチレングリコール、
またアクリルアミドから選ばれる単量体で構成される水
溶性共重合体あるいはロジンのような微溶解性樹脂の0.
1〜30重量%に、 (ii) 微加水分解性樹脂として、 ●一般式 ●一般式 5〜30部 ●酢酸ビニル及び/又はC1−C2の低級アルキル(メタ)
アクリレート ……40〜90部 から構成される共重合体を70〜99.9重量%配合させて得
られる、とりわけ長期防汚性に優れる防汚塗料用樹脂組
成物に関するものである。(Means for Solving the Problems) To summarize the present invention, the present invention provides: (i) main components are methyl vinyl ether, N-vinylpyrrolidone, methoxyethylene glycol methacrylate,
In addition, water-soluble copolymers composed of monomers selected from acrylamide or a slightly soluble resin such as rosin are used.
1 to 30% by weight, (ii) as a slightly hydrolyzable resin ● General formula 5-30 parts ● vinyl acetate and / or C 1 -C 2 lower alkyl (meth)
Acrylate: A resin composition for an antifouling paint which is obtained by mixing 70 to 99.9% by weight of a copolymer composed of 40 to 90 parts, and which has particularly excellent long-term antifouling properties.
以下、本発明の構成について詳しく説明する。 Hereinafter, the configuration of the present invention will be described in detail.
本発明の防汚塗料用樹脂組成物を構成する水溶性樹脂
(共)重合体としては、メチルビチルエーテル、N−ビ
ニルピロリドン、メタクリル酸メトキシエチレングリコ
ールまたはアクリルアミドを主成分とする単量体から構
成される(共)重合体である。The water-soluble resin (co) polymer constituting the resin composition for an antifouling paint of the present invention is composed of a monomer containing methylbityl ether, N-vinylpyrrolidone, methoxyethylene glycol methacrylate or acrylamide as a main component. (Co) polymer.
メチルビニルエーテルと共重合して良好な水溶性を示
すものとしては、エニルビニルエーテル、酢酸ビニル等
を挙げることが出来る。N−ビニルピロリドンと共重合
して良好な水溶性を示すものとしては、酢酸ビニル、メ
チル(メタ)アクリレート等の低級(メタ)アクリレー
トがある。メタクリル酸メトキシエチレングリコール、
アクリルアミドに於ても低級(メタ)アクリレート、酢
酸ビニルなどを30重量%以下で共重合させると良好な水
溶性を示す共重合体が得られる。本発明でいう主成分と
は、水溶性を呈するのに必要な共重合量を意味するもの
である。Examples of those which exhibit good water solubility when copolymerized with methyl vinyl ether include enyl vinyl ether and vinyl acetate. Examples of those exhibiting good water solubility by copolymerizing with N-vinylpyrrolidone include lower (meth) acrylates such as vinyl acetate and methyl (meth) acrylate. Methoxyethylene glycol methacrylate,
Even when acrylamide is copolymerized with a lower (meth) acrylate, vinyl acetate or the like at 30% by weight or less, a copolymer having good water solubility can be obtained. The main component in the present invention means a copolymerization amount necessary for exhibiting water solubility.
本発明に用いられるロジンとは、酸価が120以上で融
点が40℃以上であるロジンであって、松ヤニから生成さ
れるガムロジン、松の根や切り株より抽出されるウッド
ロジン、またはクラフトパルプの副産物トール油より分
離されるトール油ロジンなどを含むので微溶性である。The rosin used in the present invention is a rosin having an acid value of 120 or more and a melting point of 40 ° C. or more, gum rosin produced from pine tar, wood rosin extracted from pine roots and stumps, or kraft pulp. Since it contains tall oil rosin separated from by-product tall oil, it is slightly soluble.
これらの水溶性樹脂あるいは微溶性樹脂の水不溶性樹
脂への配合割合は、ポリメチルビニルエーテル、ポリ−
N−ビニルピロリドン、ポリメタクリル酸メトキシエチ
レングリコール、ポリアクリルアミドなどの水溶性樹脂
の場合は0.1〜30重量部、好ましくは2〜15重量部であ
り、ロジンのように微溶性樹脂の場合は20〜30重量部で
ある。The mixing ratio of the water-soluble resin or the slightly soluble resin to the water-insoluble resin is, for example, polymethyl vinyl ether or poly-methyl vinyl ether.
In the case of a water-soluble resin such as N-vinylpyrrolidone, poly (methoxyethylene glycol methacrylate), or polyacrylamide, the amount is 0.1 to 30 parts by weight, preferably 2 to 15 parts by weight, and in the case of a slightly soluble resin such as rosin, 20 to 30 parts by weight. 30 parts by weight.
これらの使用量が50重量部をこえると、初期の防汚剤
の溶出速度が大きすぎ、長期に亘り均一に塗膜を減少さ
せることができなくなる。また塗膜の耐水性が極端に低
下する。0.1重量部以下では、初期および長期に亘って
溶出速度が小さく、3ケ月後ぐらいから、ほとんど防汚
剤の溶出はなく防汚効果は極端に減少する。If the amount used exceeds 50 parts by weight, the initial dissolution rate of the antifouling agent is too high, and it is impossible to uniformly reduce the coating film over a long period of time. Further, the water resistance of the coating film is extremely reduced. When the amount is less than 0.1 part by weight, the dissolution rate is low over the initial and long term, and after about three months, there is almost no dissolution of the antifouling agent, and the antifouling effect is extremely reduced.
本発明のもう1つの重要な樹脂成分である加水分解性
を有する水不溶性樹脂は、海水中において前記した水溶
性樹脂、微溶性樹脂の溶出と共に、アルカリPH域で徐々
に加水分解され、防汚剤と共に海水に溶出する。この溶
出過程で順序に新しい塗膜面が形成、いわゆるセルフポ
リシング型の塗膜が形成される。The water-insoluble resin having a hydrolyzability, which is another important resin component of the present invention, is gradually hydrolyzed in an alkaline PH region together with the elution of the water-soluble resin and the slightly soluble resin described above in seawater, and is thus stain-resistant. Elutes in seawater with the agent. In this elution process, a new coating film surface is formed in order, that is, a so-called self-polishing coating film is formed.
本発明に使用する海水中への溶出速度を調節する役割
をもつ微加水分解性樹脂の組成において、もっとも重要
な成分は一般式〔I〕,〔II〕,〔III〕で示される単
量体であり、これらの単量体成分を含有する樹脂はアル
カリPH域で加水分解され、銅などの有機酸塩とカルボン
酸を生成する。In the composition of the slightly hydrolyzable resin having a role of controlling the dissolution rate in seawater used in the present invention, the most important component is a monomer represented by the general formula [I], [II] or [III]. The resin containing these monomer components is hydrolyzed in an alkaline pH range to produce an organic acid salt such as copper and a carboxylic acid.
前記〔I〕,〔II〕,〔III〕で示される単量体は、
例えば、(i)(メタ)アクリル酸あるいはビニル系カ
ルボン酸などの不飽和有機酸、(ii)銅、亜鉛、テルル
などのアルカリ金属よりもイオン化傾向の小さい金属の
酸化物または水酸化物、及び(iii)一価の有機酸の三
者のエステル化反応により合成されることができる。
(以下、〔I〕,〔II〕,〔III〕で示される単量体を
金属含有不飽和単量体という。) 前記(i)不飽和有機酸としては、メタクリル酸、ア
クリル酸、クロトン酸、イタコン酸、マレイン酸もしく
はフマル酸;マレイン酸モノアルキル(C1−C4)エステ
ル、フマル酸モノアルキル(C1−C4)エステル、もしく
はイタコン酸モノアルキル(C1−C4)エステル;または
β−ヒドロキシエチル(メタ)アクリレート、β−ヒド
ロキシプロピル(メタ)アクリレート、β−ヒドロキシ
ブチル(メタ)アクリレート、4−ヒドロキシブチル
(メタ)アクリレート、上記β−ヒドロキシエチル(メ
タ)アクリレートにεカプロラクトンを付加させたもの
〔たとえばプラクセルFM、FAシリーズ(ダイセル(株)
製)〕とか、一般名ポリエチレングリコールモノメタク
リレートで表わされる「ブレンマーPE」シリーズ(日本
油脂(株)製)もしくは一般名ポリプロピレングリコー
ルモノメタクリレートで表わされる「ブレンマーPP」
(日本油脂(株)製)シリーズの如き公知慣用の水酸基
含有ビニル系単量体とR5の無水物として無水コハク酸、
無水フタル酸の如き公知慣用の酸無水物との付加物など
が代表例である また(ii)金属の酸化物または水酸化物の金属種とし
ては、Cu、Zn、Teのほかに、周期律表のII b族、III a
族、IV a族(例えばSn、Pb、Si)、VI a族(例えばS
e)、VI b族(例えばCr、Mo)、VII族(例えばMn)、VI
II族(例えばFe、Co、Ni)などを用いても良い。Cu、Z
n、Teは好ましい金属成分であり、要はアルカリ金属よ
りイオン化傾向の小さい金属が用いられる。これら金属
成分は、従来のSn系の毒性防汚剤などを極力少なく利用
して、かつ効果をあげるために使用するものである。The monomers represented by the above [I], [II], and [III] are:
For example, (i) an unsaturated organic acid such as (meth) acrylic acid or a vinyl carboxylic acid, (ii) an oxide or hydroxide of a metal having a lower ionization tendency than an alkali metal such as copper, zinc, and tellurium, and (Iii) It can be synthesized by a three-part esterification reaction of a monovalent organic acid.
(Hereinafter, the monomers represented by [I], [II], and [III] are referred to as metal-containing unsaturated monomers.) As the (i) unsaturated organic acid, methacrylic acid, acrylic acid, crotonic acid , Itaconic acid, maleic acid or fumaric acid; monoalkyl maleate (C 1 -C 4 ) ester, monoalkyl fumarate (C 1 -C 4 ) ester, or monoalkyl itaconate (C 1 -C 4 ) ester; Or β-hydroxyethyl (meth) acrylate, β-hydroxypropyl (meth) acrylate, β-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, and β-hydroxyethyl (meth) acrylate with ε-caprolactone Those added [for example, Praxel FM, FA series (Daicel Corporation)
") Or" Blemmer PE "series represented by polyethylene glycol monomethacrylate (manufactured by NOF Corporation) or" Blemmer PP "represented by polypropylene glycol monomethacrylate
(Nippon Oil & Fats Co., Ltd.) series and a commonly used hydroxyl group-containing vinyl monomer and succinic anhydride as an anhydride of R 5 ;
Typical examples include adducts with known and common acid anhydrides such as phthalic anhydride. (Ii) Examples of metal species of metal oxides or hydroxides include Cu, Zn, Te, and periodic II b group table, III a
Family, IV a group (e.g. Sn, Pb, Si), VI a group (e.g., S
e), VI b group (eg Cr, Mo), VII group (eg Mn), VI
Group II (for example, Fe, Co, Ni) may be used. Cu, Z
n and Te are preferable metal components. In short, a metal having a lower ionization tendency than an alkali metal is used. These metal components are used to minimize the use of conventional Sn-based toxic antifouling agents and the like, and to increase the effect.
前記(iii)一価の有機酸としては、酢酸、プロピオ
ン酸、安息香酸、サリチル酸、乳酸、3,5−ジクロル安
息香酸、ラウリン酸、ステアリン酸ニトロ安息香酸、リ
ノール酸、リシノール酸、1,2−ヒドロキシステアリン
酸、パルビン酸、アビエチン酸、ナフテン酸、クロル酢
酸、ジクロル酢酸、吉草酸、p−フェニル安息香酸など
があげられる。The (iii) monovalent organic acids include acetic acid, propionic acid, benzoic acid, salicylic acid, lactic acid, 3,5-dichlorobenzoic acid, lauric acid, nitrobenzoic acid stearate, linoleic acid, ricinoleic acid, 1,2 -Hydroxystearic acid, parvic acid, abietic acid, naphthenic acid, chloroacetic acid, dichloroacetic acid, valeric acid, p-phenylbenzoic acid and the like.
前記〔I〕,〔II〕,〔III〕で示される金属含有不
飽和単量体の共重合体は、5〜30部、好ましくは5〜20
部である。30部を越えると共重合された側鎖の有機金属
エステルが多くなりすぎて、素早くアルカリ域で加水分
解されるため、長期防汚性は維持できない。しかも単量
体合成時の残存微量金属化合物のために、重合率が上が
りにくくなる。5部以下では、セルフポリシンクリ性に
劣る結果となってしまう。The copolymer of the metal-containing unsaturated monomer represented by the above [I], [II] or [III] is 5 to 30 parts, preferably 5 to 20 parts.
Department. When the amount exceeds 30 parts, the amount of the copolymerized side chain organometallic ester becomes too large and is quickly hydrolyzed in an alkaline region, so that the long-term antifouling property cannot be maintained. In addition, the polymerization rate is hardly increased due to the remaining trace metal compound at the time of monomer synthesis. If it is less than 5 parts, the result will be inferior to the self-polysyncrin property.
本発明において、前記した金属含有不飽和単量体の次
に重要な成分は、前記一般式〔IV〕で表わされる化合物
である。その具体例としては、アクリルアミド、メタク
リルアミド、N−メチルアクリルアミド、N−エチルア
クリルアミド、N−プロピルアクリルアミド、N−イソ
プロピルアクリルアミド、N,N−ジメチルアクリルアミ
ド、N,N′−ジエチルアクリルアミド、N,N−ジプロピル
アクリルアミド、N,N−ジイソプロピルアクリルアミ
ド、N−アセチルアクリルアミド、N−メチルメタクリ
ルアミド、N−エチルメタクリルアミド、N−プロピル
メタクリルアミド、N−イソプロピルメタクリルアミ
ド、N,N−ジメチルメタクリルアミド、N,N−ジプロピル
メタアクリルアミド、N−アセチルメタクリルアミドな
どがある。In the present invention, the next important component after the above-mentioned metal-containing unsaturated monomer is a compound represented by the above general formula [IV]. Specific examples thereof include acrylamide, methacrylamide, N-methylacrylamide, N-ethylacrylamide, N-propylacrylamide, N-isopropylacrylamide, N, N-dimethylacrylamide, N, N'-diethylacrylamide, N, N- Dipropylacrylamide, N, N-diisopropylacrylamide, N-acetylacrylamide, N-methylmethacrylamide, N-ethylmethacrylamide, N-propylmethacrylamide, N-isopropylmethacrylamide, N, N-dimethylmethacrylamide, N, N-dipropyl methacrylamide, N-acetyl methacrylamide and the like.
上記一般式〔IV〕で示される化合物の具体例として説
明した単量体の単独重合物は水溶性であるが、本発明に
おいて該単量体を5〜30部用いると水不溶性のものとな
る。5重量部以下では、長期に亘る塗膜の均一な溶出は
認められず、従って安定的な防汚性を保持することがで
きない。30部以上では、初期の消耗度(溶出速度)が大
きいが、長期に亘って防汚性を保持することはできない
し、また塗膜の耐水性が極端に低下してしまう。The homopolymer of the monomer described as a specific example of the compound represented by the general formula [IV] is water-soluble, but becomes insoluble when 5 to 30 parts of the monomer is used in the present invention. . When the amount is less than 5 parts by weight, uniform elution of the coating film over a long period of time is not recognized, so that stable antifouling property cannot be maintained. When the amount is more than 30 parts, the initial degree of consumption (elution rate) is large, but the antifouling property cannot be maintained for a long time, and the water resistance of the coating film is extremely reduced.
本発明において、前記〔I〕〜〔IV〕で説明した単量
体成分に次いで重要な単量体成分は酢酸ビニル、及び/
又はメチル、エチルのメタクリレート、アクリレートで
ある。すなわち海水中での塗膜の耐水性、強固なフィル
ムをつくるのにこれらの単量体成分は必要なものであ
る。C3以上の(メタ)アクリレートになると塗膜の疎水
性が増し、他成分の加水分解性を疎外することになるの
で好ましくない。In the present invention, an important monomer component next to the monomer components described in the above [I] to [IV] is vinyl acetate, and / or
Or methyl and ethyl methacrylates and acrylates. That is, these monomer components are necessary for forming a water-resistant and strong film of the coating film in seawater. It becomes a C 3 or more (meth) acrylate increases the hydrophobicity of the coating film, it means that alienating hydrolysis of other components is not preferred.
以上に説明した本発明の防汚塗料用樹脂組成物を構成
する各種単量体から、水溶性樹脂、微加水分解性樹脂を
得るための重合方法としては、ラジカル重合触媒の存在
下で溶液重合するのが簡便であるが、懸濁、塊状、イオ
ン重合、光重合、放射線重合も利用可能である。共重合
体の平均分子量は5,000〜80,000のものが使用可能で、
好ましくは7,000〜30,000のものである。From the various monomers constituting the antifouling paint resin composition of the present invention described above, a water-soluble resin, a polymerization method for obtaining a slightly hydrolyzable resin includes solution polymerization in the presence of a radical polymerization catalyst. Although it is convenient to carry out, suspension, bulk, ionic polymerization, photopolymerization, and radiation polymerization can also be used. The average molecular weight of the copolymer can be used from 5,000 to 80,000,
It is preferably from 7,000 to 30,000.
なお、本発明の前記した防汚性塗料樹脂組成物に対し
て、公知慣用の防汚剤や顔料などが配合される。The antifouling paint resin composition of the present invention is blended with known and commonly used antifouling agents and pigments.
そのうちでも代表的なものを挙げれば、防汚剤として
亜酸化亜鉛、クロム酸亜鉛、クロム酸ストロンチウム、
クロム酸第二銅、クエン酸第二銅、フェロシアン酸第二
銅、キノリン第二銅、δ−ハイドロキノリン第二銅、オ
レイン酸第二銅、硝酸第二銅、リン酸第二銅、酒石酸第
二銅、酸化第1銅、沃化第一銅、または亜硫酸第1銅な
どであり、また防汚剤に有機錫化合物、トリアジン化合
物、有機硫黄化合物などを併用することは何ら妨げるも
のではない。Among them, typical examples include anti-fouling agents such as zinc suboxide, zinc chromate, strontium chromate,
Cupric chromate, cupric citrate, cupric ferrocyanate, cupric quinoline, cupric δ-hydroquinoline, cupric oleate, cupric nitrate, cupric phosphate, tartaric acid Copper (II) cuprous oxide, cuprous oxide, cuprous iodide, cuprous sulfite, etc., and use of an organic tin compound, a triazine compound, an organic sulfur compound, or the like in combination with an antifouling agent does not impede. .
本発明の防汚塗料用樹脂組成物においては、その他、
通常使用されている着色顔料、体質顔料、有機溶剤等を
自由に選択し、使用できることは勿論のことである。In the antifouling paint resin composition of the present invention, other,
It is needless to say that commonly used coloring pigments, extenders, organic solvents and the like can be freely selected and used.
かくして得られる本発明の防汚塗料用樹脂組成物は、
船底塗料、または漁網用塗料などとして用いられる。The resin composition for antifouling paint of the present invention thus obtained is
Used as ship bottom paint or fishing net paint.
次に、本発明を参考例、実施例および比較例により、
更に具体的に説明するが、本発明はこれら実施例に限定
されるものではない。なお、以下に於て部および%は特
にことわりのない限り、すべて重量基準である。Next, the present invention by reference examples, examples and comparative examples,
Although described more specifically, the present invention is not limited to these examples. In the following, all parts and percentages are by weight unless otherwise specified.
参考例−1〔メチルビニルエーテル系共重合体の調製
例〕 撹拌機およびモノマー圧入ライン、触媒圧入ラインを
装備したオートクレーブにあらかじめ脱水処理したキシ
レンを800部仕込んだのち、700℃まで昇温したのちメチ
ルビニルエーテル900部、エチルビチルエーテル100部、
三フッ化ホウ素ジエチルエーテラート10部を4時間かけ
て圧入した。圧入終了後5時間70℃で反応を継続し、不
揮発分50.7%、粘度O−P(ガードナー粘度)の樹脂溶
液を得た。以下、このものを(a−1)と称す。Reference Example-1 [Preparation Example of Methyl Vinyl Ether Copolymer] 800 parts of previously dehydrated xylene was charged into an autoclave equipped with a stirrer, a monomer injection line, and a catalyst injection line, and then heated to 700 ° C., followed by methyl addition. 900 parts of vinyl ether, 100 parts of ethyl bityl ether,
10 parts of boron trifluoride diethyl etherate were injected over 4 hours. After completion of the injection, the reaction was continued at 70 ° C. for 5 hours to obtain a resin solution having a nonvolatile content of 50.7% and a viscosity of OP (Gardner viscosity). Hereinafter, this is referred to as (a-1).
参考例−2〔N−ビニルピロリドン共重合体の調製〕 温度計、還流冷却器、撹拌機および窒素ガス導入口を
備えた四つ口にフラスコにキシレン400部、n−ブタノ
ール、400部を仕込んだのち、N2を液中に30分ブローし
たのち、100℃に昇温し、キシレン100部、n−ブタノー
ル100部、ターシヤリーブチルパーオクテート(TBPO)1
0部、N−ビニルピロリドン80部、メチルメタクリレー
ト200部を5時間で滴下したのち、さらに100℃で10時間
反応を継続したのち、不揮発部50.4%、粘度U−Vの樹
脂溶液を得た。以下、このものを(a−2)と称す。Reference Example-2 [Preparation of N-vinylpyrrolidone copolymer] 400 parts of xylene, n-butanol and 400 parts were charged into a four-necked flask equipped with a thermometer, a reflux condenser, a stirrer, and a nitrogen gas inlet. it then, after 30 minutes blowing N 2 in the liquid, the temperature was raised to 100 ° C., 100 parts of xylene, 100 parts of n- butanol, Tashiya butyl peroxide octoate (TBPO) 1
After 0 parts, 80 parts of N-vinylpyrrolidone and 200 parts of methyl methacrylate were added dropwise over 5 hours, the reaction was further continued at 100 ° C. for 10 hours to obtain a resin solution having a nonvolatile portion of 50.4% and a viscosity of UV. Hereinafter, this is referred to as (a-2).
参考例−3〔メタクリル酸メトキシエチレングリコール
系共重合体の調製例〕 参考例−2と同様の装置に、n−ブタノール600部、
キシレン200部を仕込んだのち、100℃に昇温し、キシレ
ン200部、TBPO8部、ジターシャリーブチルパーオキサイ
ド2部、メタクリル酸メトキシエチレングリコール400
部、メチルメタクリレート100部を4時間で滴下したの
ち、さらに100℃で8時間反応を継続したのち、不揮発
分50.2%、粘度X−Yの樹脂溶液を得た。以下、このも
のを(a−3)と称す。Reference Example-3 [Preparation example of methoxyethylene glycol methacrylate-based copolymer] In the same apparatus as Reference Example-2, 600 parts of n-butanol were added.
After charging 200 parts of xylene, the temperature was raised to 100 ° C., 200 parts of xylene, 8 parts of TBPO, 2 parts of ditertiary butyl peroxide, methoxyethylene glycol methacrylate 400
And 100 parts of methyl methacrylate were added dropwise over 4 hours, and the reaction was further continued at 100 ° C. for 8 hours to obtain a resin solution having a nonvolatile content of 50.2% and a viscosity of XY. Hereinafter, this is referred to as (a-3).
参考例−4〔アクリルアミド系共重合体の調製例〕 参考例−2と同様の装置に、n−ブタノール1000部、
アクリルアミド850部、メチルメタクリレート150部、TB
PO20部を仕込んだのち徐々に100℃まで昇温したのち、
8時間反応後、TBPOを2部加え反応を継続した。6時間
後に不揮発分50.1%、粘度Zの透明な樹脂溶液を得た。
以下、このものを(a−4)と称す。Reference Example-4 [Preparation Example of Acrylamide-Based Copolymer] In the same apparatus as Reference Example-2, 1000 parts of n-butanol were added.
Acrylamide 850 parts, methyl methacrylate 150 parts, TB
After charging PO20 part, gradually raise the temperature to 100 ° C,
After the reaction for 8 hours, 2 parts of TBPO was added and the reaction was continued. After 6 hours, a transparent resin solution having a nonvolatile content of 50.1% and a viscosity of Z was obtained.
Hereinafter, this is referred to as (a-4).
参考例−5〔微加水分解性樹脂の調製例−1〕 参考例−2と同様の装置に、n−ブタノール300部、
トルエン300部を仕込んだのち105℃まで昇温を行ない、
第1表に示す単量体組成、即ちステアリル銅メタクリレ
ート100部、N,N−ジメチルアクリルアミド20部、メチル
アクリレート400部、メチルメタクリレート300部、ブチ
ルセロソルブ400部、TBPO15部の混合物を3時間で滴下
した。105℃で反応を継続し、4時間毎にTBPO2部づつ4
回追加しながら20時間で反応を終了し、不揮発分50.4
%、粘度Z2の青色の樹脂溶液を得た。以下、このものを
(b−1)と称す。Reference Example-5 [Preparation Example 1 of slightly hydrolyzable resin] In the same apparatus as Reference Example-2, 300 parts of n-butanol were added.
After charging 300 parts of toluene, the temperature was raised to 105 ° C,
A monomer composition shown in Table 1, that is, a mixture of 100 parts of stearyl copper methacrylate, 20 parts of N, N-dimethylacrylamide, 400 parts of methyl acrylate, 300 parts of methyl methacrylate, 400 parts of butyl cellosolve, and 15 parts of TBPO was dropped in 3 hours. . Continue the reaction at 105 ° C and add 4 parts of TBPO every 4 hours.
The reaction was completed in 20 hours with additional
% To obtain a blue resin solution viscosity of Z 2. Hereinafter, this is referred to as (b-1).
参考例−6〔微加水分解性樹脂の調製例−2〕〜参考例
−11〔微加水分解性樹脂の調製例−7〕 参考例−6と同様の装置、操作にて第1表に示す単量
体組成にて微加水分解性の樹脂溶液を得た。調製した樹
脂溶液を、以下、それぞれ(b−2)〜(b−7)と称
す。Reference Example-6 [Preparation Example-2 of Slightly Hydrolyzable Resin] to Reference Example-11 [Preparation Example-7 of Slightly Hydrolyzable Resin] Table 1 shows the same apparatus and operation as in Reference Example-6. A slightly hydrolyzable resin solution having a monomer composition was obtained. Hereinafter, the prepared resin solutions are referred to as (b-2) to (b-7), respectively.
参考例−12〜13〔微加水分解性樹脂の調製例〕 参考例−6と同様の装置、操作にて、第1表に示す単
量体組成にて微加水分解性の樹脂溶液を得た。以下、こ
れを(b−8)、(b−9)と称す。Reference Examples -12 to 13 [Examples of preparation of slightly hydrolyzable resin] By the same apparatus and operation as in Reference Example-6, a slightly hydrolyzable resin solution was obtained with the monomer composition shown in Table 1. . Hereinafter, these are referred to as (b-8) and (b-9).
〔塗装試験板の作成〕 第2表に示される組成に基づいて実施例1〜7の防汚
塗料と比較対照1〜4の防汚塗料を調製し、後掲する如
き要領に従って性能の比較検討を行なった。 [Preparation of Painted Test Plate] The antifouling paints of Examples 1 to 7 and the antifouling paints of Comparative Controls 1 to 4 were prepared based on the compositions shown in Table 2, and their performance was compared and examined according to the procedures described later. Was performed.
<性能試験要領> 〔I〕ロータリー試験 サンドブラストした10cm×10cm×0.8cmの銅板にエッ
チングプライマーを塗膜厚5μmに1回塗装し、さらに
タールビニル系船底防錆塗料を塗膜厚70μmに1回塗装
した。 <Performance test procedure> [I] Rotary test An etching primer was applied once on a sandblasted 10 cm x 10 cm x 0.8 cm copper plate to a coating thickness of 5 µm, and a tar vinyl-based ship bottom rust preventive paint was applied once to a coating thickness of 70 µm. Painted.
次いで、実施例1−7、比較例1−4の各防汚塗料を
塗膜厚60μmで3回塗装し、得られたそれぞれの試験板
を海面下に垂下された回転ドラムの外側に取り付け、試
験板に対し海水の速度が、10ノットになるようにドラム
を回転させ、3ケ月間のロータリー試験を行い、初期膜
厚と経時変化後の膜厚差を測定して自己研磨性を評価し
た。試験結果を第3表に示す。Next, each of the antifouling paints of Example 1-7 and Comparative Example 1-4 was applied three times with a coating thickness of 60 μm, and each of the obtained test plates was attached to the outside of a rotating drum suspended below the sea surface. The drum was rotated so that the speed of seawater against the test plate became 10 knots, a rotary test was performed for three months, and the difference between the initial film thickness and the film thickness after aging was measured to evaluate the self-polishing property. . Table 3 shows the test results.
〔II〕シミュレーション試験 サンドブラストした10cm×10cm×1mmの銅板に下塗防
錆塗料としてタールエポキシ塗料を塗膜厚125μmで2
回塗装し、さらにタールビニル系の中塗り塗料を塗膜厚
70μmに1回塗装した。次いで実施例1−7、比較例1
−4の各防汚塗料を塗膜100μmで3回塗装し、得られ
たそれぞれの試験板を前述のロータリー試験を1ケ月間
行ない、さらにそのあと1.5mの海中に1ケ月間浸漬せし
めることを以って1サイクルの試験期間とした。船舶の
運航を想定したシミュレーション試験を行ない、1サイ
クル毎の防錆性を試験塗膜上の付着生成の占有面積
(%)で以って表示した。試験結果を第4表にまとめて
示す。なお銅の溶出速度の測定結果を第5表に示す。[II] Simulation test A 10 cm x 10 cm x 1 mm sand-blasted copper plate was coated with a tar epoxy paint as an undercoat rust preventive paint with a coating thickness of 125 µm.
Times, and then apply a tar-vinyl intermediate coating
Coating was performed once at 70 μm. Next, Example 1-7, Comparative Example 1
-4 Each of the antifouling paints is applied three times with a coating film of 100 μm, and the obtained test plate is subjected to the above-mentioned rotary test for one month, and then immersed in a 1.5 m sea for one month. Thus, the test period was one cycle. A simulation test was performed assuming the operation of a ship, and the rust prevention for each cycle was indicated by the occupation area (%) of the formation of adhesion on the test coating film. The test results are summarized in Table 4. Table 5 shows the measurement results of the elution rate of copper.
(表中の単位μg/cm2/day) 〔発明の効果〕 本発明の特定の水溶性(あるいは微溶解性)重合体成
分と、海水中への溶出速度の調節機能と自ら海水中で加
水分解により防汚性の金属化合物を放出する微加水分解
性樹脂成分とからなる防汚塗料用樹脂組成物は、強固で
かつ適度な水溶性を有する塗膜を形成することができ
る。(Unit μg / cm 2 / day in the table) [Effects of the Invention] A specific water-soluble (or slightly soluble) polymer component of the present invention, a function of controlling the dissolution rate into seawater, and a microparticle capable of releasing an antifouling metal compound by hydrolysis in seawater by itself. The resin composition for an antifouling paint comprising a hydrolyzable resin component can form a strong and moderately water-soluble coating film.
従って、本発明の防汚塗料用樹脂組成物は、塗料中に
配合する防汚剤を減らすことが可能であり、かつ長期に
亘り防汚系を有するため船底、海中構造物などの表面塗
装に極めて有用なものである。Therefore, the resin composition for antifouling paints of the present invention can reduce the amount of antifouling agents to be incorporated into the paint, and has an antifouling system for a long period of time, so that it can be used for surface coating of ship bottoms, underwater structures, etc. It is extremely useful.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 龍野 陽一 広島県広島市安佐南区八木2―14―15 (72)発明者 清水 重男 広島県広島市中区吉島東1―10―19 (56)参考文献 特開 昭58−42668(JP,A) 特開 昭62−57464(JP,A) ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Yoichi Tatsuno 2-14-15 Yagi, Asaminami-ku, Hiroshima City, Hiroshima Prefecture (72) Inventor Shigeo Shimizu 1-10-19, Yoshishima Higashi, Naka-ku, Hiroshima City, Hiroshima Prefecture (56) References JP-A-58-42668 (JP, A) JP-A-62-57464 (JP, A)
Claims (1)
ルピロリドン、メタクリル酸メトキシエチレングリコー
ル、アクリルアミドである水溶性(共)重合体、または
ロジンより選ばれる少なくとも1種以上の化合物 ……0.1〜30重量%、 及び、下記(i),(ii),(iii)の単量体を共重合
させて得られる海水中への溶出速度の調節剤としての微
加水分解性樹脂 ……70〜90.99重量%、 からなる防汚塗料用樹脂組成物。 ●(i).一般式 ●(ii).一般式 ●(iii).酢酸ビニル及び/又はC1−C2の低級アルキ
ル(メタ)アクリレート ……40〜90部A water-soluble (co) polymer whose main component is methyl vinyl ether, N-vinylpyrrolidone, methoxyethylene glycol methacrylate, acrylamide, or at least one compound selected from rosin 0.1 to 30% by weight %, And a slightly hydrolyzable resin as a regulator of the dissolution rate into seawater obtained by copolymerizing the following monomers (i), (ii) and (iii): 70 to 90.99% by weight A resin composition for an antifouling paint comprising: ● (i). General formula ● (ii). General formula ● (iii). Vinyl acetate and / or C 1 -C 2 lower alkyl (meth) acrylate ...... 40-90 parts
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28741887A JP2651499B2 (en) | 1987-11-16 | 1987-11-16 | Resin composition for antifouling paint |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28741887A JP2651499B2 (en) | 1987-11-16 | 1987-11-16 | Resin composition for antifouling paint |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01129077A JPH01129077A (en) | 1989-05-22 |
JP2651499B2 true JP2651499B2 (en) | 1997-09-10 |
Family
ID=17717073
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP28741887A Expired - Fee Related JP2651499B2 (en) | 1987-11-16 | 1987-11-16 | Resin composition for antifouling paint |
Country Status (1)
Country | Link |
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JP (1) | JP2651499B2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006183059A (en) * | 1996-04-17 | 2006-07-13 | Basf Coatings Japan Ltd | Paint composition |
JP4118356B2 (en) * | 1996-12-12 | 2008-07-16 | 日本ペイント株式会社 | Antifouling paint composition |
DK1496089T3 (en) | 2000-03-28 | 2012-01-30 | Nippon Paint Co Ltd | Antifouling coating |
US8076390B2 (en) | 2005-12-01 | 2011-12-13 | Uvic Industry Partnerships Inc. | Antifouling polymeric agent for marine applications |
SG11202103381YA (en) * | 2018-10-05 | 2021-05-28 | Chugoku Marine Paints | Antifouling coating composition, antifouling coating film, substrate with antifouling coating film and method for producing same |
-
1987
- 1987-11-16 JP JP28741887A patent/JP2651499B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH01129077A (en) | 1989-05-22 |
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