JP2008533237A - 塗料中の殺生物剤を結合するための方法およびナノ粒子の使用 - Google Patents
塗料中の殺生物剤を結合するための方法およびナノ粒子の使用 Download PDFInfo
- Publication number
- JP2008533237A JP2008533237A JP2008500676A JP2008500676A JP2008533237A JP 2008533237 A JP2008533237 A JP 2008533237A JP 2008500676 A JP2008500676 A JP 2008500676A JP 2008500676 A JP2008500676 A JP 2008500676A JP 2008533237 A JP2008533237 A JP 2008533237A
- Authority
- JP
- Japan
- Prior art keywords
- medetomidine
- nanoparticles
- metal nanoparticles
- cuo
- zno
- 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.)
- Granted
Links
- 239000003973 paint Substances 0.000 title claims abstract description 58
- 238000000034 method Methods 0.000 title claims abstract description 21
- 239000002105 nanoparticle Substances 0.000 title description 46
- 239000003139 biocide Substances 0.000 title description 23
- 230000027455 binding Effects 0.000 title description 3
- 229960002140 medetomidine Drugs 0.000 claims description 60
- HRLIOXLXPOHXTA-UHFFFAOYSA-N medetomidine Chemical compound C=1C=CC(C)=C(C)C=1C(C)C1=CN=C[N]1 HRLIOXLXPOHXTA-UHFFFAOYSA-N 0.000 claims description 58
- QPLDLSVMHZLSFG-UHFFFAOYSA-N CuO Inorganic materials [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims description 42
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 31
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 23
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 20
- 239000002082 metal nanoparticle Substances 0.000 claims description 16
- 238000000576 coating method Methods 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 10
- 229940078552 o-xylene Drugs 0.000 claims description 10
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims description 8
- 229910010413 TiO 2 Inorganic materials 0.000 claims description 8
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 6
- 230000010071 organism adhesion Effects 0.000 claims 14
- 239000011253 protective coating Substances 0.000 claims 6
- 239000000758 substrate Substances 0.000 claims 3
- 239000000463 material Substances 0.000 abstract description 9
- 230000000694 effects Effects 0.000 abstract description 6
- 230000002829 reductive effect Effects 0.000 abstract description 5
- 230000002411 adverse Effects 0.000 abstract description 2
- 230000003373 anti-fouling effect Effects 0.000 description 26
- 239000002245 particle Substances 0.000 description 21
- 230000003115 biocidal effect Effects 0.000 description 14
- 241000238586 Cirripedia Species 0.000 description 12
- 238000001179 sorption measurement Methods 0.000 description 12
- 239000002519 antifouling agent Substances 0.000 description 11
- 229910044991 metal oxide Inorganic materials 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 150000004706 metal oxides Chemical class 0.000 description 8
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 7
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 7
- 230000003993 interaction Effects 0.000 description 7
- 238000005498 polishing Methods 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 239000005510 Diuron Substances 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 230000007613 environmental effect Effects 0.000 description 6
- HDHLIWCXDDZUFH-UHFFFAOYSA-N irgarol 1051 Chemical compound CC(C)(C)NC1=NC(SC)=NC(NC2CC2)=N1 HDHLIWCXDDZUFH-UHFFFAOYSA-N 0.000 description 6
- 239000005747 Chlorothalonil Substances 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 5
- -1 2,3-dimethylphenyl Chemical group 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000005751 Copper oxide Substances 0.000 description 4
- 241000195493 Cryptophyta Species 0.000 description 4
- 238000013459 approach Methods 0.000 description 4
- 229910000431 copper oxide Inorganic materials 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 3
- 238000013270 controlled release Methods 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- 108060003345 Adrenergic Receptor Proteins 0.000 description 2
- 102000017910 Adrenergic receptor Human genes 0.000 description 2
- 206010020772 Hypertension Diseases 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000032798 delamination Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- 150000002605 large molecules Chemical class 0.000 description 2
- 230000001418 larval effect Effects 0.000 description 2
- 229920002521 macromolecule Polymers 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002858 neurotransmitter agent Substances 0.000 description 2
- 125000002560 nitrile group Chemical group 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 2
- 230000000144 pharmacologic effect Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 108020003175 receptors Proteins 0.000 description 2
- 102000005962 receptors Human genes 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- 150000003335 secondary amines Chemical class 0.000 description 2
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000003440 toxic substance Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 1
- BTGAJCKRXPNBFI-OAHLLOKOSA-N (8R)-7-propyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-13,14-diol Chemical compound C([C@H]1N(CCC)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 BTGAJCKRXPNBFI-OAHLLOKOSA-N 0.000 description 1
- UCTWMZQNUQWSLP-VIFPVBQESA-N (R)-adrenaline Chemical compound CNC[C@H](O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-VIFPVBQESA-N 0.000 description 1
- 229930182837 (R)-adrenaline Natural products 0.000 description 1
- HMFNKYMONNOACE-UHFFFAOYSA-N 1-(4-tert-butyl-6-methylsulfanyl-1,3,5-triazin-2-yl)-1-cyclopropylhydrazine Chemical compound CSC1=NC(=NC(=N1)C(C)(C)C)N(C1CC1)N HMFNKYMONNOACE-UHFFFAOYSA-N 0.000 description 1
- PORQOHRXAJJKGK-UHFFFAOYSA-N 4,5-dichloro-2-n-octyl-3(2H)-isothiazolone Chemical compound CCCCCCCCN1SC(Cl)=C(Cl)C1=O PORQOHRXAJJKGK-UHFFFAOYSA-N 0.000 description 1
- YAXGBZDYGZBRBQ-UHFFFAOYSA-N 4,5-dihydro-1,3-oxazol-2-amine Chemical compound NC1=NCCO1 YAXGBZDYGZBRBQ-UHFFFAOYSA-N 0.000 description 1
- 241001474374 Blennius Species 0.000 description 1
- 239000005749 Copper compound Substances 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- 241001195836 Cypris Species 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- BYBLEWFAAKGYCD-UHFFFAOYSA-N Miconazole Chemical compound ClC1=CC(Cl)=CC=C1COC(C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 BYBLEWFAAKGYCD-UHFFFAOYSA-N 0.000 description 1
- 241000237502 Ostreidae Species 0.000 description 1
- 241000131858 Siboglinidae Species 0.000 description 1
- 241000238585 Thoracica Species 0.000 description 1
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000000384 adrenergic alpha-2 receptor agonist Substances 0.000 description 1
- 230000002353 algacidal effect Effects 0.000 description 1
- 239000003619 algicide Substances 0.000 description 1
- 102000030484 alpha-2 Adrenergic Receptor Human genes 0.000 description 1
- 108020004101 alpha-2 Adrenergic Receptor Proteins 0.000 description 1
- 230000003444 anaesthetic effect Effects 0.000 description 1
- 230000036592 analgesia Effects 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 229940082988 antihypertensives serotonin antagonists Drugs 0.000 description 1
- 239000003420 antiserotonin agent Substances 0.000 description 1
- 238000009360 aquaculture Methods 0.000 description 1
- 244000144974 aquaculture Species 0.000 description 1
- 230000037007 arousal Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000004166 bioassay Methods 0.000 description 1
- 231100000704 bioconcentration Toxicity 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 230000036471 bradycardia Effects 0.000 description 1
- 208000006218 bradycardia Diseases 0.000 description 1
- OZVBMTJYIDMWIL-AYFBDAFISA-N bromocriptine Chemical compound C1=CC(C=2[C@H](N(C)C[C@@H](C=2)C(=O)N[C@]2(C(=O)N3[C@H](C(N4CCC[C@H]4[C@]3(O)O2)=O)CC(C)C)C(C)C)C2)=C3C2=C(Br)NC3=C1 OZVBMTJYIDMWIL-AYFBDAFISA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000003943 catecholamines Chemical class 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- JJCFRYNCJDLXIK-UHFFFAOYSA-N cyproheptadine Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2C=CC2=CC=CC=C21 JJCFRYNCJDLXIK-UHFFFAOYSA-N 0.000 description 1
- 229960001140 cyproheptadine Drugs 0.000 description 1
- 238000013480 data collection Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- HRLIOXLXPOHXTA-NSHDSACASA-N dexmedetomidine Chemical compound C1([C@@H](C)C=2C(=C(C)C=CC=2)C)=CN=C[N]1 HRLIOXLXPOHXTA-NSHDSACASA-N 0.000 description 1
- 229960004253 dexmedetomidine Drugs 0.000 description 1
- 229960003638 dopamine Drugs 0.000 description 1
- 229940052760 dopamine agonists Drugs 0.000 description 1
- 239000003136 dopamine receptor stimulating agent Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 229960005139 epinephrine Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- FPCCSQOGAWCVBH-UHFFFAOYSA-N ketanserin Chemical compound C1=CC(F)=CC=C1C(=O)C1CCN(CCN2C(C3=CC=CC=C3NC2=O)=O)CC1 FPCCSQOGAWCVBH-UHFFFAOYSA-N 0.000 description 1
- 229960005417 ketanserin Drugs 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229960002509 miconazole Drugs 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 230000003957 neurotransmitter release Effects 0.000 description 1
- 229960002748 norepinephrine Drugs 0.000 description 1
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- 230000036407 pain Effects 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 230000029553 photosynthesis Effects 0.000 description 1
- 238000010672 photosynthesis Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000011045 prefiltration Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000000018 receptor agonist Substances 0.000 description 1
- 229940044601 receptor agonist Drugs 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229940076279 serotonin Drugs 0.000 description 1
- 230000009870 specific binding Effects 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000001890 transfection Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000003232 water-soluble binding agent Substances 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical compound [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1625—Non-macromolecular compounds organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82B—NANOSTRUCTURES FORMED BY MANIPULATION OF INDIVIDUAL ATOMS, MOLECULES, OR LIMITED COLLECTIONS OF ATOMS OR MOLECULES AS DISCRETE UNITS; MANUFACTURE OR TREATMENT THEREOF
- B82B3/00—Manufacture or treatment of nanostructures by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3442—Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
- C08K5/3462—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/12—Adsorbed ingredients, e.g. ingredients on carriers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2993—Silicic or refractory material containing [e.g., tungsten oxide, glass, cement, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Nanotechnology (AREA)
- Inorganic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Paints Or Removers (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
本願は、2005年3月11日に出願された米国仮特許出願第60/661,083号の優先権を主張する出願であり、この米国仮出願は、参照により本明細書に援用される。
本発明は、水中構造物上における例えばフジツボの定着を特異的かつ効果的に妨げる、ナノ粒子へ結合されたイミダゾール含有化合物(例えば、メデトミジン)の防汚塗料における使用および方法に関する。メデトミジンは、意外なことに、金属およびシリカのナノ粒子へ強力に吸着すると判明し、これは、有効な防汚表面を開発し、そして、例えばフジツボ定着を妨げることにおける均一な放出および効果のための塗料マトリクス中の殺生物剤の分散固定化に関する防汚塗料の性能を改善しようとする試みにおいて特に興味深い特徴である。他の殺生物剤系が、船舶用防汚塗料以外の塗料において、均一な放出のために、同一のナノ粒子相互作用を用いて、使用され得る。
未公開の最近の研究によって、ナノ粒子、例えば、酸化銅(II)および酸化亜鉛(II)(それぞれ、直径33および53nm)は、例えば防汚剤メデトミジンの制御放出を維持するために使用され得ることが示された。ナノ粒子の使用は、それらの極めて大きな比表面積(表面積と粒子体積との比率)のために興味深い。CuOおよびZnO粒子は、それぞれ、29および21m2・g−1の比表面積を生じる。
種々のナノ粒子と殺生物剤との間の相互作用の研究
材料および方法
50mlの溶媒o−キシレンへ、殺生物剤を50mMの総濃度で添加した。次いで、ナノ粒子(シグマ−アルドリッチ・スウェーデンAB(Sigma−Aldrich Sweden AB)、ストックホルム、スウェーデン)を、テストプロトコルに従って関連濃度で添加し、そして各添加後、吸着されていないメデトミジンの濃度(オリオン・ファーマ(Orion Pharma)、ヘルシンキ、フィンランド)を標準HPLC−UV技術で測定した。メデトミジンのUV吸光度最大値は文献から220nmであると判った。HPLC分析の前に、UV吸光度最大値を、UV分光計(GBC 920UV/可視分光計、サイエンティフィック・エクイップメンツ・リミテッド(Scientific Equipments Ltd.)、ビクトリア、オーストラリア)を使用して文献からの値を確認するために調べた。
o−キシレン中においてCuOおよびZnOナノ粒子とメデトミジンおよび他の防汚剤、例えば、クロロタロニル、ジクロフルアニド、シーナイン(SeaNine)、イルガロール、ジウロン、およびトリルフルアニドとを混合する場合(図1、2A)および2B)を参照のこと)、相互作用にかなりの差異が観察される。メデトミジンの大部分は、特にZnOを使用した場合、既に低粒子濃度で吸着される。これは、塗膜を介しての防汚剤の拡散運動を制限するために、少量のメデトミジンおよびナノ粒子の両方を含有する塗料系を設計する可能性を許容する。メデトミジンの吸着は、上記に列挙される他の防汚剤と比較して、非常に好ましい。上記に列挙される防汚剤は、1つの共通の特徴を示す:窒素が、第2級または第3級アミン、ニトリル基としてあるいは複素環中のいずれかで、全ての化合物中に存在する。しかし、研究は、メデトミジンのイミダゾール部分が、粒子表面への吸着について最適な形状を有することを示す。
種々のサイズの粒子と殺生物剤との間の相互作用の研究
材料および方法
使用した種々のナノ粒子(ZnO、CuO、Al2O3、MgO、TiO2、SiO2)は、シグマ(Sigma)(シグマ−アルドリッチ・スウェーデンAB(Sigma−Aldrich Sweden AB)、ストックホルム、スウェーデン)から購入し、そしてさらに精製することなく使用した。50mlのo−キシレンを、50mMのメデトミジン(オリオン・ファーマ(Orion Pharma)、ヘルシンキ、フィンランド)を添加したビーカーへ添加した。次いでナノ粒子を添加し、各添加後に、遊離しているメデトミジンの量をHPLC−UVで測定した(上記例1における通り)。
広い表面積の重要性を調べるために、メデトミジンと種々の金属酸化物ナノ粒子(ZnO、CuO、Al2O3、MgO、TiO2)およびシリカ(SiO2)ならびにマイクロメートルサイズの粒子、CuO(5μm)との相互作用を研究した(図3および4を参照のこと)。ナノ粒子をマイクロメートルサイズの粒子で置換する場合、メデトミジン吸着は、ごく僅かとなるようである。これらの結果は、粒子表面上へのメデトミジン吸着に関する広い表面積の重要性を示している。
ナノ粒子からの殺生物剤の放出速度の研究
材料および方法
これらの研究のために選択した塗料は、溶媒としてキシレンを含む自己研磨塗料、ロトレックAB(Lotrec AB)(リンディンゴ、スウェーデン)製のSPCレファント(SPC Lefant)船舶用塗料であった。1リットル塗料へ、10gのナノ粒子(CuOおよびZnO)(シグマ−アルドリッチ・スウェーデンAB(Sigma−Aldrich Sweden AB)、ストックホルム、スウェーデン)および表面吸着されたメデトミジン(オリオン・ファーマ(Orion Pharma)、ヘルシンキ、フィンランド)またはシーナイン(SeaNine)(ローム・アンド・ハース(Rhome & Haas)、ペンシルベニア州フィラデルフィア、米国)を含有する50ml溶液を添加し、そして5分間激しく撹拌しながら混合した。3重のサンプルを調製し、そして塗料アプリケータを使用して塗り、均一な厚みの塗膜(この場合、200μmであった)を確実にした。塗ったプレートは10×10cmであり、そして8週間、人工海水中に配置した。
メデトミジン−ナノ粒子相互作用(メデトミジン−CuOおよびメデトミジン−ZnO)をまた、放出速度研究のために使用した(図5を参照のこと)。8週間後、メデトミジン−ナノ粒子修飾化塗料は、単一添加剤としてメデトミジンを含む塗料と比較して、メデトミジンの放出量が20%減少した。シーナイン(SeaNine)−ナノ粒子相互作用についての結果は図6に示され、これは、メデトミジン−ナノ粒子組み合わせと類似の放出減少を実証している。
殺生物剤を結合するためにナノ粒子を使用する防汚用塗料の製造
メデトミジン修飾化塗料の1つの例として、これらの研究について選択した典型的な塗料は、主要な溶媒としてキシレンを含有した(ロトレックAB(Lotrec AB)(リンディンゴ、スウェーデン)製のSPCレファント(SPC Lefant)船舶用塗料)。ナノ粒子および殺生物剤の両方を含有する塗料を調製するために、これら2つの成分を、先ず、殺生物剤の非常に強い吸着を可能にする溶媒(例えば、キシレン)中において混合した。典型的に、10gのナノ粒子を、最大10%過剰の吸着されていないメデトミジンと共に、(シンプルなマグネチックスターラーを使用して)50mlのキシレン中において撹拌した。完全な吸着の後(典型的に数分間の混合)、塗料が均一になるまで(これは、撹拌速度に依存して、典型的に5〜10分かかった)非常に激しく撹拌しながら(撹拌は、約0.5〜2Hzで作動するプロペラ様剪断機で行った)、前記溶液を塗料中へ徐々に添加した。
Claims (20)
- 基体へ保護コーティングを塗布することを含む、海洋生物付着生物による基体の海洋生物付着を防止する方法であって、該コーティングが、金属ナノ粒子へ結合されたイミダゾール含有化合物を含有する、方法。
- 前記イミダゾール含有化合物がメデトミジンである、請求項1に記載の海洋生物付着を防止する方法。
- 前記金属ナノ粒子が、CuO、ZnO、TiO2、Al2O3、SiO2、およびMgOからなる群から選択される、請求項1に記載の海洋生物付着を防止する方法。
- 前記金属ナノ粒子がCuOである、請求項3に記載の海洋生物付着を防止する方法。
- 前記金属ナノ粒子がZnOである、請求項3に記載の海洋生物付着を防止する方法。
- 前記保護コーティングがさらにo−キシレンを含む、請求項1に記載の海洋生物付着を防止する方法。
- 前記保護コーティングがさらに船舶用塗料を含む、請求項1に記載の海洋生物付着を防止する方法。
- 前記イミダゾール含有化合物がメデトミジンであり、そして前記金属ナノ粒子が、CuO、ZnO、TiO2、Al2O3、SiO2、およびMgOからなる群から選択される、請求項1に記載の海洋生物付着を防止する方法。
- 前記金属ナノ粒子がCuOである、請求項8に記載の海洋生物付着を防止する方法。
- 前記金属ナノ粒子がZnOである、請求項1に記載の海洋生物付着を防止する方法。
- 金属ナノ粒子へ結合されたイミダゾール含有化合物を含有する保護コーティングを含む、海洋生物付着生物による基体の海洋生物付着を防止するための製品。
- 前記イミダゾール含有化合物がメデトミジンである、請求項11に記載の海洋生物付着を防止するための製品。
- 前記金属ナノ粒子が、CuO、ZnO、TiO2、Al2O3、SiO2、およびMgOからなる群から選択される、請求項11に記載の海洋生物付着を防止するための製品。
- 前記金属ナノ粒子がCuOである、請求項13に記載の海洋生物付着を防止するための製品。
- 前記金属ナノ粒子がZnOである、請求項13に記載の海洋生物付着を防止するための製品。
- 前記保護コーティングがさらにo−キシレンを含む、請求項11に記載の海洋生物付着を防止するための製品。
- 前記保護コーティングがさらに船舶用塗料を含む、請求項11に記載の海洋生物付着を防止するための製品。
- 前記イミダゾール含有化合物がメデトミジンであり、そして前記金属ナノ粒子が、CuO、ZnO、TiO2、Al2O3、SiO2、およびMgOからなる群から選択される、請求項11に記載の海洋生物付着を防止するための製品。
- 前記金属ナノ粒子がCuOである、請求項18に記載の海洋生物付着を防止するための製品。
- 前記金属ナノ粒子がZnOである、請求項18に記載の海洋生物付着を防止するための製品。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US66108305P | 2005-03-11 | 2005-03-11 | |
US60/661,083 | 2005-03-11 | ||
US11/373,661 | 2006-03-10 | ||
US11/373,661 US7311766B2 (en) | 2005-03-11 | 2006-03-10 | Method and use of nanoparticles to bind biocides in paints |
PCT/SE2006/000318 WO2006096128A1 (en) | 2005-03-11 | 2006-03-13 | Method and use of nanoparticles to bind biocides in paints |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2008533237A true JP2008533237A (ja) | 2008-08-21 |
JP5006869B2 JP5006869B2 (ja) | 2012-08-22 |
Family
ID=36953649
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2008500676A Expired - Fee Related JP5006869B2 (ja) | 2005-03-11 | 2006-03-13 | 塗料中の殺生物剤を結合するための方法およびナノ粒子の使用 |
Country Status (12)
Country | Link |
---|---|
US (3) | US7311766B2 (ja) |
EP (1) | EP1856215B1 (ja) |
JP (1) | JP5006869B2 (ja) |
KR (1) | KR101255384B1 (ja) |
CN (1) | CN101166797B (ja) |
CA (1) | CA2600646C (ja) |
DK (1) | DK1856215T3 (ja) |
ES (1) | ES2584440T3 (ja) |
HK (1) | HK1118305A1 (ja) |
PL (1) | PL1856215T3 (ja) |
PT (1) | PT1856215T (ja) |
WO (1) | WO2006096128A1 (ja) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011118526A1 (ja) | 2010-03-23 | 2011-09-29 | 中国塗料株式会社 | 防汚塗料組成物およびその用途 |
JP2016527244A (ja) * | 2013-07-24 | 2016-09-08 | アイ − テック エービー | 表面の海洋生物付着に対する阻害剤としてのエナンチオマーデクスメデトミジンの使用 |
JP2016527243A (ja) * | 2013-07-24 | 2016-09-08 | アイ − テック エービー | 表面の海洋生物付着に対する阻害剤としてのエナンチオマーレボメデトミジンの使用 |
KR20190013889A (ko) * | 2016-07-01 | 2019-02-11 | 주고꾸 도료 가부시키가이샤 | 방오 도료 조성물, 방오 도막, 방오 도막 부착 기재 및 그의 제조 방법, 및 방오 방법 |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060189686A1 (en) * | 2005-01-27 | 2006-08-24 | Lena Martensson | Use of a combination of substances to prevent biofouling organisms |
US7311766B2 (en) * | 2005-03-11 | 2007-12-25 | I-Tech Ab | Method and use of nanoparticles to bind biocides in paints |
WO2007026692A1 (ja) * | 2005-09-01 | 2007-03-08 | Chugoku Marine Paints, Ltd. | 防汚塗料組成物、防汚塗膜、塗膜付き基材、防汚性基材、基材表面への塗膜の形成方法および基材の防汚方法 |
WO2008086402A1 (en) * | 2007-01-09 | 2008-07-17 | Inframat Corporation | Coating compositions for marine applications and methods of making and using the same |
TW200902654A (en) * | 2007-07-12 | 2009-01-16 | Dept Of Fisheries Administration The Council Of Agriculture | Anti-fouling drag reduction coating material for ships |
US20100015349A1 (en) * | 2007-07-16 | 2010-01-21 | Larry Weidman | Marine antifoulant coating |
US7910648B2 (en) * | 2007-07-16 | 2011-03-22 | Reintjes Marine Surface Technologies, Llc | Marine antifoulant coating |
JP2009108257A (ja) * | 2007-10-31 | 2009-05-21 | Chugoku Marine Paints Ltd | 耐スライム性および貯蔵安定性が改良された銅化合物を含有する防汚塗料組成物 |
JP5631863B2 (ja) * | 2008-03-24 | 2014-11-26 | クレムソン・ユニヴァーシティ | 生物付着阻止のための方法及び組成物 |
US20120171272A1 (en) * | 2009-06-17 | 2012-07-05 | Raman Premachandran | Stabilized biocidal dispersion via sub-micronized carrier particles, process for making the same and composition thereof |
WO2011070069A1 (en) | 2009-12-09 | 2011-06-16 | I-Tech Ab | Process for preparation of medetomidine |
KR101321832B1 (ko) * | 2011-05-03 | 2013-10-23 | 주식회사 지엘머티리얼즈 | 방오제용 첨가제, 그 제조방법 및 이를 포함하는 방오제 |
CN107613977A (zh) * | 2015-05-06 | 2018-01-19 | I-技术有限公司 | 用于控制鱼上寄生甲壳纲动物的美托咪定 |
US10064273B2 (en) | 2015-10-20 | 2018-08-28 | MR Label Company | Antimicrobial copper sheet overlays and related methods for making and using |
WO2018087160A1 (en) | 2016-11-09 | 2018-05-17 | I-Tech Ab | Substituted heterocyclic compounds for use in controlling parasitic crustaceans on fish |
SG11201908605XA (en) | 2017-03-29 | 2019-10-30 | I Tech Ab | Antifouling article |
EP4147799A3 (en) | 2017-04-26 | 2023-05-17 | Fast & Fluid Management B.V. | Dispenser for tinting pastes |
CN111655616A (zh) * | 2017-12-13 | 2020-09-11 | 费德里科圣玛利亚理工大学 | 用于减少微生物腐蚀的纳米结构的涂料 |
DE202018001813U1 (de) | 2018-04-09 | 2018-05-22 | I-Tech Ab | Löslicher Behälter für Beschichtungskomponenten |
US10954131B2 (en) | 2018-10-03 | 2021-03-23 | International Business Machines Corporation | Biocidal janus particles |
US12050293B2 (en) | 2018-12-19 | 2024-07-30 | Pgs Geophysical As | Medetomidine compositions having improved anti-fouling characteristics |
KR20230107821A (ko) | 2020-10-21 | 2023-07-18 | 아이-테크 에이비 | 방오 화합물 |
WO2024094746A1 (en) | 2022-11-04 | 2024-05-10 | I-Tech Ab | A medetomidine containing particle and use thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002535255A (ja) * | 1999-01-25 | 2002-10-22 | エルヴィング,ハンス | 表面の海洋生物汚染の阻止 |
JP2004339102A (ja) * | 2003-05-14 | 2004-12-02 | Catalysts & Chem Ind Co Ltd | 抗菌・防黴・防藻性組成物 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19828256A1 (de) * | 1998-06-25 | 1999-12-30 | Bayer Ag | Antifoulingmittel, ein Verfahren zur Herstellung und deren Verwendung sowie daraus hergestellte Antifoulingbeschichtungen |
DE60112943T2 (de) * | 2000-07-06 | 2006-06-14 | Akzo Nobel Coatings Int Bv | Ablagerungverhindernde anstrichzusammensetzung |
JP2003073627A (ja) | 2001-06-18 | 2003-03-12 | Osaka Gas Co Ltd | 防汚塗料 |
DE10219127A1 (de) * | 2002-04-29 | 2003-11-06 | Inst Neue Mat Gemein Gmbh | Substrate mit Biofilm-hemmender Beschichtung |
CN1238447C (zh) * | 2002-06-28 | 2006-01-25 | 王钧宇 | 仿生无毒舰船防污涂料及其制法 |
WO2004085305A2 (en) * | 2003-03-21 | 2004-10-07 | Wayne State University | Metal oxide-containing nanoparticles |
US7311766B2 (en) * | 2005-03-11 | 2007-12-25 | I-Tech Ab | Method and use of nanoparticles to bind biocides in paints |
-
2006
- 2006-03-10 US US11/373,661 patent/US7311766B2/en active Active
- 2006-03-13 KR KR1020077023220A patent/KR101255384B1/ko active IP Right Grant
- 2006-03-13 CA CA2600646A patent/CA2600646C/en not_active Expired - Fee Related
- 2006-03-13 PL PL06717003T patent/PL1856215T3/pl unknown
- 2006-03-13 CN CN2006800078654A patent/CN101166797B/zh not_active Expired - Fee Related
- 2006-03-13 EP EP06717003.5A patent/EP1856215B1/en active Active
- 2006-03-13 ES ES06717003.5T patent/ES2584440T3/es active Active
- 2006-03-13 DK DK06717003.5T patent/DK1856215T3/en active
- 2006-03-13 WO PCT/SE2006/000318 patent/WO2006096128A1/en active Application Filing
- 2006-03-13 JP JP2008500676A patent/JP5006869B2/ja not_active Expired - Fee Related
- 2006-03-13 PT PT67170035T patent/PT1856215T/pt unknown
-
2007
- 2007-07-12 US US11/827,466 patent/US20080249078A1/en not_active Abandoned
-
2008
- 2008-08-26 HK HK08109473.9A patent/HK1118305A1/xx not_active IP Right Cessation
-
2009
- 2009-06-23 US US12/456,775 patent/US7662222B2/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002535255A (ja) * | 1999-01-25 | 2002-10-22 | エルヴィング,ハンス | 表面の海洋生物汚染の阻止 |
JP2004339102A (ja) * | 2003-05-14 | 2004-12-02 | Catalysts & Chem Ind Co Ltd | 抗菌・防黴・防藻性組成物 |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011118526A1 (ja) | 2010-03-23 | 2011-09-29 | 中国塗料株式会社 | 防汚塗料組成物およびその用途 |
KR20120129991A (ko) | 2010-03-23 | 2012-11-28 | 주고꾸 도료 가부시키가이샤 | 방오도료 조성물 및 그의 용도 |
US8840910B2 (en) | 2010-03-23 | 2014-09-23 | Chugoku Marine Paints, Ltd. | Antifouling coating composition and uses of the same |
JP5705212B2 (ja) * | 2010-03-23 | 2015-04-22 | 中国塗料株式会社 | 防汚塗料組成物およびその用途 |
JP2016527244A (ja) * | 2013-07-24 | 2016-09-08 | アイ − テック エービー | 表面の海洋生物付着に対する阻害剤としてのエナンチオマーデクスメデトミジンの使用 |
JP2016527243A (ja) * | 2013-07-24 | 2016-09-08 | アイ − テック エービー | 表面の海洋生物付着に対する阻害剤としてのエナンチオマーレボメデトミジンの使用 |
KR20190013889A (ko) * | 2016-07-01 | 2019-02-11 | 주고꾸 도료 가부시키가이샤 | 방오 도료 조성물, 방오 도막, 방오 도막 부착 기재 및 그의 제조 방법, 및 방오 방법 |
JPWO2018003135A1 (ja) * | 2016-07-01 | 2019-02-14 | 中国塗料株式会社 | 防汚塗料組成物、防汚塗膜、防汚塗膜付き基材及びその製造方法、並びに防汚方法 |
KR102209168B1 (ko) * | 2016-07-01 | 2021-01-28 | 주고꾸 도료 가부시키가이샤 | 방오 도료 조성물, 방오 도막, 방오 도막 부착 기재 및 그의 제조 방법, 및 방오 방법 |
US11254823B2 (en) | 2016-07-01 | 2022-02-22 | Chugoku Marine Paints, Ltd. | Antifouling coating material composition, antifouling coating film, substrate provided with antifouling coating film and production method therefor, and antifouling method |
Also Published As
Publication number | Publication date |
---|---|
DK1856215T3 (en) | 2016-08-15 |
KR101255384B1 (ko) | 2013-04-17 |
CN101166797A (zh) | 2008-04-23 |
PL1856215T3 (pl) | 2017-08-31 |
EP1856215A1 (en) | 2007-11-21 |
HK1118305A1 (en) | 2009-02-06 |
US7311766B2 (en) | 2007-12-25 |
EP1856215B1 (en) | 2016-05-04 |
WO2006096128A1 (en) | 2006-09-14 |
CA2600646C (en) | 2013-07-30 |
CN101166797B (zh) | 2011-03-16 |
KR20070116090A (ko) | 2007-12-06 |
US7662222B2 (en) | 2010-02-16 |
US20060201379A1 (en) | 2006-09-14 |
US20080249078A1 (en) | 2008-10-09 |
CA2600646A1 (en) | 2006-09-14 |
PT1856215T (pt) | 2016-08-02 |
ES2584440T3 (es) | 2016-09-27 |
JP5006869B2 (ja) | 2012-08-22 |
US20090270357A1 (en) | 2009-10-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5006869B2 (ja) | 塗料中の殺生物剤を結合するための方法およびナノ粒子の使用 | |
JP5181097B2 (ja) | 塗料中の殺生物剤を結合するための方法および酸性化修飾ポリマーの使用 | |
CA2617570C (en) | Use of a combination of substances to prevent biofouling organisms | |
CA2594862A1 (en) | Use of a combination of substances to prevent biofouling organisms | |
CN1229022C (zh) | 控释组合物 | |
CN105531330A (zh) | 作为抑制剂的对映异构体右旋美托咪啶在海洋生物污损表面附着的应用 | |
CN105473669A (zh) | 作为抑制剂的对映异构体左旋美托咪啶在海洋生物污损表面附着的应用 | |
US20060217456A1 (en) | Non-toxic coating composition, methods of use thereof and articles protected from attachment of biofouling organisms | |
KR20130027374A (ko) | 헥사데실 메타크릴레이트를 포함하는 방오제 및 방오도료 조성물 | |
TW200923035A (en) | Method and use of nanoparticles to bind biocides in paints |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20090119 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20110902 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20111111 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20120511 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20120525 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20150601 Year of fee payment: 3 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5006869 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
LAPS | Cancellation because of no payment of annual fees |