JP2004196677A - Sterilizer for marine adhesive bacterium - Google Patents
Sterilizer for marine adhesive bacterium Download PDFInfo
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- JP2004196677A JP2004196677A JP2002364508A JP2002364508A JP2004196677A JP 2004196677 A JP2004196677 A JP 2004196677A JP 2002364508 A JP2002364508 A JP 2002364508A JP 2002364508 A JP2002364508 A JP 2002364508A JP 2004196677 A JP2004196677 A JP 2004196677A
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Abstract
Description
【0001】
【発明の属する技術分野】
本発明は、海洋性付着細菌用殺菌剤に関し、詳しくは船底塗料等に防汚目的で使用される殺菌剤に関するものである。
【0002】
【従来の技術】
海洋性付着生物は、しばしば船底や海中構造物の表面などに群体や群集をなして付着することが知られている。特にフジツボ類などの大型付着生物に起因する船底の汚損は、海水に対する摩擦抵抗を増加させ、船速の低下や燃料の過剰消費を引き起こす原因となっている。また、それらの汚損が、浮力減少や局部・間隙腐食等を引き起こすことも知られ、汚損防止対策は、船舶運行の観点から必要不可欠な対策となっている。
【0003】
従来、汚損防止対策として、船底に防汚剤を添加した塗料の塗布が行われている。この防汚剤には、フジツボ類に対する成長阻害効果がある有機スズが用いられ、付着防止にすぐれた効果をあげていた。
【0004】
しかしながら、有機スズ化合物は難分解性であり、その成長阻害毒性に対する人体や環境への影響が問題となり、1989年、化学物質審査規制法の1種特定化学物質に指定され、製造、輸入が禁止されることになり、最近ではその使用が制限されている。代替品として、亜硝酸銅が利用されているが、銅についても環境ホルモンとして長期的には規制の対象にあり、また溶出濃度も有機スズに比べて4倍以上の高濃度の溶出を必要とするため環境や生態系への蓄積が懸念されている。
【0005】
このような環境や生態系へ負荷の高い付着抑制剤に替わり、環境に負荷の低い付着抑制の方法が提案されている。この方法は、生物付着初期段階に生成される付着性細菌の群生(バイオフィルム)を溶菌酵素によって除去することにより、バイオフィルムによって促進されるフジツボ類幼生の付着を抑制し、結果的に大型付着生物の付着を防止する方法である。しかしながら、船底塗料に要する溶菌酵素の大量培養は経済的に困難であり、より安価で、かつ環境への負荷が低い付着細菌除去剤が求められていた。
【0006】
【発明が解決しようとする課題】
本発明は、上記従来技術の課題を背景になされたもので、天然性有機化合物を用いることにより、安価で環境への影響が少ない海洋性付着細菌用殺菌剤を提供することを目的とする。
【0007】
【課題を解決するための手段】
本発明者らは、バイオフィルムを形成する海洋性付着細菌の耐薬品性について鋭意研究を重ねた結果、保存料や香辛料、日持ち向上剤として用いられる天然有機化合物が、海洋性付着細菌に対して殺菌効果を示すことを見出し、この知見に基づいて本発明をなすに至った。
【0008】
すなわち、本発明は、植物抽出物、香辛料、多糖類、有機酸及びたんぱく質からなる群から選ばれる少なくとも1種を有効成分とする海洋性付着細菌用殺菌剤に関する。
【0009】
本発明の海洋性付着細菌用殺菌剤は、船底塗料用として好適に使用される。
【0010】
本発明の殺菌剤を船底に塗布し、それらの成分を溶出させることによって海洋性付着細菌に由来する生物皮膜を殺滅し海洋性生物の付着抑制を行う際、安価でかつ環境に対して負荷の小さい天然有機化合物を用いることを特徴とする、付着性細菌除去剤を提供するものである。
【0011】
さらに本発明は、生物抽出物、香辛料、多糖類、有機酸及びたんぱく質からなる群から選ばれる少なくとも1種を有効成分とする船底への海洋性生物の付着防止剤に関する。
【0012】
【発明の実施の形態】
本発明は、海洋性付着細菌に対して殺滅効果のある天然有機化合物であり、用いられる天然有機化合物としては、例えば植物抽出物や香辛料、多糖類、有機酸、たんぱく質が用いられる。
【0013】
生物抽出物としては、植物抽出物及び動物抽出物が挙げられる。植物抽出物としては、例えば、タンニン、ヒバ油、ヒノキ油、桂皮酸、没食子酸、レンギョウ抽出物、クマザサ抽出物、孟宗竹抽出物、カラシ、ワサビ油、エゴノキ抽出物、ホオノキ抽出物等が用いられ、動物抽出物としては、キトサン、プロタミン等が用いられる。また、その主要成分やその人工合成物も用いられ、例えば、ヒバ油やヒノキ油の主要成分であるヒノキチオールとトロポロン系有機化合物、もしくはクマザサ抽出物や孟宗竹抽出物の主要成分である2,6-ジメトキシ-1,4-ベンゾキノンやキノン誘導体、もしくはカラシやワサビ油の主要成分であるイソチアン酸アリル化合物等が用いられる。
【0014】
香辛料としては、例えば、シンナモン、キャラウェイ、オレガノ、タイム、クローブ、レモン、ナツメグ、ローレル、サフラン、コリアンダー、山椒、マジョラム、バニラ等が用いられる。また、その主要成分や人工合成物も用いられ、上記香辛料の成分であるシンナミックアルデヒド、シンナミックアルコール、カルボン、カルバクロール、チモール、オイゲノ−ル、リモ−ネン、β−ピネン、シネオール、サフロール、リナノ−ル、シトロネロール、テルピネオール、バニリン等が用いられる。
【0015】
多糖類としては、例えば、寒天オリゴ糖、ペクチン分解物、キトサンとその分解物が用いられる。またキトサンとその分解物については、pH6以上において殺菌性を示すため、酸性を持つ粘土やゼオライト等の無機化合物と混合して用いることが望ましい。
【0016】
有機酸としては、ギ酸、酢酸、プロピオン酸、酪酸、吉草酸、イソ吉草酸、ピバル酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、オレイン酸などのモノカルボン酸、シュウ酸、マロン酸、コハク酸、グルタル酸、アジピン酸、ピメリン酸、スベリン酸、アゼライン酸、セバシン酸などのジカルボン酸、安息香酸、サリチル酸、フタル酸、リンゴ酸またはその誘導体などの芳香族モノまたはジカルボン酸、クエン酸などのトリカルボン酸等が例示される。
【0017】
タンパク質としては、リゾチーム、プロタミン、ポリリジンが例示される。
【0018】
好ましい殺菌剤としては、ヒノキチオール、香辛料類、孟宗竹抽出物が例示される。
【0019】
海洋性付着細菌としては、Pseudomonas属、Alteromonas属、Pseudoalteromonas属に属する付着性細菌が例示され、例えば、Pseudoalteromonas carrageenovora、Pseudoalteromonas atlantica, Pseudoalteromonas carrageenovora, Pseudoalteromonas nigrifaciens, Pseudoalteromonas espejiana, Pseudoalterromonas undina等が挙げられる。
【0020】
本発明の殺菌剤は、船底に直接塗布や塗料に分散して塗布し、海水中で徐々に溶解させることによって、その付着防止効果を発揮する。また例えば、溶出速度を抑制するために、殺菌剤を塗料樹脂に化学結合させ塗布する方法、殺菌剤を粘土、シリカゲル等の多孔性無機担体に吸着させ、それらを塗料に分散して塗布する方法を用いても同様の付着防止効果を発揮する。これらの方法によって溶出した本発明の殺菌剤は、人体や大型動物に対する毒性が無く、また環境に対する蓄積効果も見られないため、環境への影響が少ない。
【0021】
本発明の殺菌剤は、その適用対象に応じて添加量を適宜決定すればよいが、有効成分を約0.005〜20%、好ましくは0.01〜5%程度の有効成分濃度として作用させることが好ましい。
【0022】
本発明の殺菌剤は、その使用目的に応じて、例えば、液剤(水懸濁剤および油剤を含む。)、ペースト剤、粉剤、粒剤などの公知の剤型に製剤化して使用することができる。好ましくは、例えば、液剤が挙げられる。液剤として製剤化するには、式(1)で表わされる化合物を、適宜溶剤に溶解または分散すればよい。このときに使用される溶媒としては、一般式(1)で表わされる化合物を溶解または分散し得る溶剤であれば特に制限はない。
【0023】
これらの溶剤として具体的には、例えば、水、例えば、メタノール、エタノール、n−プロパノール、iso−プロパノール、n−ブタノール、tert−ブタノールなどのアルコール系溶媒、例えば、エチレングリコール、ジエチレングリコール、ポリエチレングリコール、プロピレングリコール、ジプロピレングリコール、トリプロピレングリコール、ポリプロピレングリコール、1,4−ブタンジオール、1,5−ペンタンジオール、エチレングリコールモノメチルエーテル、エチレングリコールモノエチルエーテル、エチレングリコールモノブチルエーテル、ジエチレングリコールモノメチルエーテル、ジエチレングリコールモノエチルエーテル、トリプロピレングリコールモノメチルエーテルなどのグリコール系溶媒、例えば、アセトン、メチルエチルケトン、メチルイソブチルケトンなどのケトン系溶媒、例えば、ジオキサン、テトラヒドロフラン、エチルエーテルなどのエーテル系溶媒、例えば、酢酸エチル、酢酸ブチル、酢酸イソブチルなどのエステル系溶媒、例えば、ベンゼン、トルエン、キシレン、メチルナフタレン、ソルベントナフサなどの芳香族系溶媒、例えば、四塩化炭素、クロロホルム、塩化メチレンなどのハロゲン化炭化水素系溶媒、例えば、ジメチルホルムアミド、ジメチルスルホキシド、アセトニトリルなどの極性溶媒などが挙げられる。これらの溶媒は単独または2種以上併用してもよい。
【0024】
本発明の殺菌剤は、船の船底に施工される船底塗料その他の塗膜形成剤に例えば固形物として或いは液剤として配合することにより含有させて使用した場合には、有効成分が塗膜から海水によって流されてしまうことがなく、その効果を良好に維持することができる。
【0025】
【発明の効果】
本発明により、生物付着防止効果を発揮しながら、安価で環境に対する負荷の小さい生物付着抑制剤を提供できる。
【0026】
【実施例】
次に実施例により本発明を詳細に説明するが、本発明はこれらの例によって何ら限定されるものではない。
実施例1
海洋性付着細菌(Pseudoalteromonas carrageenovora)を5mlの液体培地(MB液培地)に植菌し、温度28℃にて対数増殖期まで振盪培養した。その後、遠心分離を行い、液体培地を除去した。遠心分離後の培養細菌に5mlの海水を加え、遠心分離と海水液の懸濁による細胞洗浄を2回行った後、10mlの海水を加えた。得られた溶液を初期濃度3から5×106cell/mlとなるように希釈し、よく攪拌した後、28℃にて対数増殖初期まで振盪培養した。
【0027】
ヒノキチオール10mgをプラスチックチューブにとり、海水5mlにて希釈後、攪拌した。ときどき振盪しながら2時間放置した。その後遠心分離して、上澄み液0.5mlを対数増殖初期まで振盪培養した菌体液に混入し、増殖曲線を計測した。
【0028】
なお、増殖曲線測定時の振盪速度は70rpm、測定間隔は5分間でTotal運動時間は15時間であった。
【0029】
図1に、ヒノキオール添加した菌体培養液と添加しない培養液の、光学密度の経時変化を示す。ヒノキチオールを添加しない培養液の光学密度は、時間の経過と共に増加した。これは、菌が培養液中で増殖し光学密度が増加したことを意味する。それに対して、ヒノキチオールを添加した培養液の密度は増加せず、菌の増殖を抑制できたことが分かる。
実施例2
桂皮アルコール、バニリン、桂皮アルデヒド、イソチアン酸エチル、ベンゾキノン、各10mgに海水5mLを加え、溶液を調整した。その後、対数増殖初期まで培養した菌体液に溶液-0.5ml混入し増殖曲線を計測したところ、培養液の密度は増加せず菌の増殖を抑制出来た。例として、桂皮アルコールの結果を図2に示す。
【0030】
実施例1,2で海洋性付着細菌用殺菌剤の効果の確認されたヒノキチオール、桂皮アルコール、バニリン、桂皮アルデヒド、イソチアン酸エチル、ベンゾキノンを船底塗料に配合し、被験物に塗布して実際の海域中で予備実験を行うと、これら化合物を配合しない船底塗料を塗布した場合と比較して、フジツボ類などの大型付着生物に起因する汚損防止に顕著な効果があることが確認される。
【図面の簡単な説明】
【図1】ヒノキオール添加した菌体培養液と添加しない培養液(blank)の、光学密度の経時変化を示す。
【図2】桂皮アルコール添加した菌体培養液と添加しない培養液(blank)の、光学密度の経時変化を示す。[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to a bactericide for marine attached bacteria, and more particularly, to a bactericide used for antifouling purposes in ship bottom paints and the like.
[0002]
[Prior art]
It is known that marine periphyton often adheres to the bottom of ships and the surface of underwater structures in groups or as a community. In particular, fouling of the ship bottom caused by large attached organisms such as barnacles increases frictional resistance against seawater, causing a decrease in ship speed and excessive consumption of fuel. It is also known that such fouling causes a decrease in buoyancy, local and crevice corrosion, etc., and antifouling measures are indispensable measures from the viewpoint of ship operation.
[0003]
2. Description of the Related Art Conventionally, as a measure for preventing fouling, a paint containing an antifouling agent has been applied to the bottom of a ship. As this antifouling agent, an organotin having a growth inhibitory effect on barnacles was used, and the effect of preventing adhesion was excellent.
[0004]
However, organotin compounds are hardly decomposable, and their effects on the human body and the environment with respect to their growth inhibitory toxicity have become a problem. In 1989, they were designated as one of the specified chemical substances under the Chemical Substances Control Law, and their production and import were banned. And its use has recently been limited. Copper nitrite is used as a substitute, but copper is also subject to long-term regulation as an environmental hormone, and the elution concentration must be at least four times higher than that of organotin. Therefore, accumulation in the environment and ecosystem is a concern.
[0005]
Instead of such an adhesion inhibitor having a high load on the environment and ecosystem, a method of suppressing adhesion with a low environmental load has been proposed. This method suppresses the adhesion of barnacle larvae promoted by the biofilm by removing the colonies of the adherent bacteria (biofilm) generated in the initial stage of the biofouling by lytic enzymes, and consequently, the large adherence. This is a method to prevent the attachment of living things. However, it is economically difficult to mass-cultivate the lytic enzyme required for ship bottom paint, and there has been a demand for an inexpensive and adhering bacteria-removing agent with a low environmental load.
[0006]
[Problems to be solved by the invention]
The present invention has been made in view of the above-mentioned problems of the related art, and an object of the present invention is to provide a bactericide for marine attached bacteria that is inexpensive and has little effect on the environment by using a natural organic compound.
[0007]
[Means for Solving the Problems]
The present inventors have conducted intensive studies on the chemical resistance of marine adherent bacteria that form biofilms, and found that natural organic compounds used as preservatives, spices, and shelf life improvers are marine resistant bacteria. The present inventors have found that they show a bactericidal effect, and have accomplished the present invention based on this finding.
[0008]
That is, the present invention relates to a bactericide for marine adherent bacteria, comprising as an active ingredient at least one selected from the group consisting of plant extracts, spices, polysaccharides, organic acids, and proteins.
[0009]
The bactericide for marine attached bacteria of the present invention is suitably used for ship bottom paints.
[0010]
When the fungicide of the present invention is applied to the bottom of a ship and the components are eluted, a biofilm derived from marine attached bacteria is killed and the attachment of marine organisms is suppressed. It is intended to provide an agent for removing adherent bacteria, characterized by using a natural organic compound having a small particle size.
[0011]
Furthermore, the present invention relates to an agent for preventing marine organisms from adhering to the bottom of a ship, which contains at least one selected from the group consisting of biological extracts, spices, polysaccharides, organic acids and proteins as active ingredients.
[0012]
BEST MODE FOR CARRYING OUT THE INVENTION
The present invention is a natural organic compound having a killing effect on marine attached bacteria, and examples of the natural organic compound used include plant extracts, spices, polysaccharides, organic acids, and proteins.
[0013]
Biological extracts include plant extracts and animal extracts. As the plant extract, for example, tannin, hiba oil, hinoki oil, cinnamic acid, gallic acid, forsythia extract, Kumazasa extract, Moso bamboo extract, mustard, wasabi oil, egonoki extract, honoki extract and the like are used. As an animal extract, chitosan, protamine and the like are used. In addition, the main components and artificial synthetic products thereof are also used, for example, hinokitiol and tropolone organic compounds, which are the main components of hiba oil and hinoki oil, or 2,6- which is the main component of Kumazasa extract and Moso bamboo extract. For example, dimethoxy-1,4-benzoquinone or a quinone derivative, or an allyl isothiocyanate compound which is a main component of mustard or wasabi oil may be used.
[0014]
As spices, for example, cinnamon, caraway, oregano, thyme, clove, lemon, nutmeg, laurel, saffron, coriander, sansho, marjoram, vanilla and the like are used. In addition, the main components and artificial synthetic products are also used, and the components of the above-mentioned spices are cinamic aldehyde, cinamic alcohol, carvone, carvacrol, thymol, eugenol, limo-nene, β-pinene, cineole, safrole, Linanol, citronellol, terpineol, vanillin and the like are used.
[0015]
As the polysaccharide, for example, agar oligosaccharides, pectin degradation products, chitosan and its degradation products are used. Since chitosan and its decomposed product exhibit bactericidal properties at pH 6 or more, it is desirable to use the mixture with an inorganic compound such as clay or zeolite having acidity.
[0016]
As organic acids, formic acid, acetic acid, propionic acid, butyric acid, valeric acid, isovaleric acid, pivalic acid, lauric acid, myristic acid, palmitic acid, stearic acid, monocarboxylic acids such as oleic acid, oxalic acid, malonic acid, Dicarboxylic acids such as succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, aromatic mono- or dicarboxylic acids such as benzoic acid, salicylic acid, phthalic acid, malic acid or derivatives thereof, citric acid, etc. And the like.
[0017]
Examples of proteins include lysozyme, protamine, and polylysine.
[0018]
Preferred fungicides include hinokitiol, spices, and Moso bamboo extract.
[0019]
Examples of marine adherent bacteria include adherent bacteria belonging to the genera Pseudomonas, Alteromonas, and Pseudoalteromonas.
[0020]
The disinfectant of the present invention exerts its adhesion-preventing effect by being directly applied to the ship bottom or dispersed in a paint and applied and gradually dissolved in seawater. In addition, for example, in order to suppress the dissolution rate, a method of applying a bactericide to the coating resin by chemical bonding, a method of adsorbing the bactericide on a porous inorganic carrier such as clay and silica gel, and dispersing and dispersing them in the coating material. The same anti-adhesion effect can be obtained by using. The bactericide of the present invention eluted by these methods has no toxicity to the human body or large animals, and has no accumulation effect on the environment.
[0021]
The amount of the fungicide of the present invention may be appropriately determined depending on the application target, and the active ingredient is allowed to act at an active ingredient concentration of about 0.005 to 20%, preferably about 0.01 to 5%. Is preferred.
[0022]
The bactericide of the present invention can be formulated and used in known dosage forms such as liquids (including water suspensions and oils), pastes, powders, and granules, depending on the purpose of use. it can. Preferably, for example, a liquid agent is used. In order to formulate a liquid formulation, the compound represented by the formula (1) may be appropriately dissolved or dispersed in a solvent. The solvent used at this time is not particularly limited as long as it can dissolve or disperse the compound represented by the general formula (1).
[0023]
Specific examples of these solvents include, for example, water, for example, alcoholic solvents such as methanol, ethanol, n-propanol, iso-propanol, n-butanol, and tert-butanol, for example, ethylene glycol, diethylene glycol, polyethylene glycol, Propylene glycol, dipropylene glycol, tripropylene glycol, polypropylene glycol, 1,4-butanediol, 1,5-pentanediol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol mono Glycol solvents such as ethyl ether and tripropylene glycol monomethyl ether, for example, Ketone solvents such as ton, methyl ethyl ketone, and methyl isobutyl ketone; for example, ether solvents such as dioxane, tetrahydrofuran, and ethyl ether; for example, ester solvents such as ethyl acetate, butyl acetate, and isobutyl acetate; for example, benzene, toluene, and xylene And aromatic solvents such as methylnaphthalene and solvent naphtha, for example, halogenated hydrocarbon solvents such as carbon tetrachloride, chloroform and methylene chloride, and polar solvents such as dimethylformamide, dimethylsulfoxide and acetonitrile. These solvents may be used alone or in combination of two or more.
[0024]
When the fungicide of the present invention is used by being incorporated into a ship bottom paint or other film forming agent applied to the bottom of a ship, for example, as a solid or as a liquid, the active ingredient is removed from the coating film by seawater. And the effect can be favorably maintained.
[0025]
【The invention's effect】
Advantageous Effects of Invention According to the present invention, it is possible to provide a bioadhesion inhibitor that is inexpensive and has a small impact on the environment while exhibiting a bioadhesion prevention effect.
[0026]
【Example】
Next, the present invention will be described in detail with reference to examples, but the present invention is not limited to these examples.
Example 1
Marine adherent bacteria (Pseudoalteromonas carrageenovora) were inoculated into 5 ml of a liquid medium (MB liquid medium) and cultured at 28 ° C. with shaking until the logarithmic growth phase. Thereafter, the liquid medium was removed by centrifugation. 5 ml of seawater was added to the cultured bacteria after centrifugation, and the cells were washed twice by centrifugation and suspension of the seawater solution, and then 10 ml of seawater was added. The resulting solution was diluted to an initial concentration of 3 to 5 × 10 6 cells / ml, stirred well, and cultured at 28 ° C. with shaking until the beginning of logarithmic growth.
[0027]
Hinokitiol (10 mg) was placed in a plastic tube, diluted with 5 ml of seawater, and stirred. Left for 2 hours with occasional shaking. Thereafter, the mixture was centrifuged, and 0.5 ml of the supernatant was mixed with the bacterial cell fluid cultured with shaking until the beginning of logarithmic growth, and the growth curve was measured.
[0028]
The shaking speed during the measurement of the growth curve was 70 rpm, the measurement interval was 5 minutes, and the total exercise time was 15 hours.
[0029]
FIG. 1 shows the time-dependent changes in the optical density of the cell culture with hinokiol added and the culture with no hinokiol added. The optical density of the culture without added hinokitiol increased over time. This means that the bacteria grew in the culture and the optical density increased. On the other hand, it was found that the density of the culture solution to which hinokitiol was added did not increase, and that the growth of bacteria could be suppressed.
Example 2
5 mL of seawater was added to each of 10 mg of cinnamon alcohol, vanillin, cinnamaldehyde, ethyl isocyanate, and benzoquinone to prepare a solution. After that, 0.5 ml of the solution was mixed with the cell fluid cultured until the beginning of logarithmic growth, and the growth curve was measured. As an example, the results for cinnamon alcohol are shown in FIG.
[0030]
Hinokitiol, cinnamon alcohol, vanillin, cinnamaldehyde, ethyl isocyanate, and benzoquinone, which were confirmed to have the effects of the bactericide for marine attached bacteria in Examples 1 and 2, were blended into the hull bottom paint, applied to the test object, and applied to the actual sea area. Preliminary experiments conducted in this way confirm that there is a remarkable effect on the prevention of fouling caused by large attached organisms such as barnacles, as compared with the case where a ship bottom paint not containing these compounds is applied.
[Brief description of the drawings]
FIG. 1 shows the time-dependent changes in the optical density of a cell culture medium containing hinokiol and a culture medium (blank) not containing hinokiol.
FIG. 2 shows the time-dependent changes in the optical density of a cell culture medium containing cinnamon alcohol and a culture medium (blank) without addition.
Claims (4)
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JP2002364508A JP2004196677A (en) | 2002-12-17 | 2002-12-17 | Sterilizer for marine adhesive bacterium |
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JP2002364508A JP2004196677A (en) | 2002-12-17 | 2002-12-17 | Sterilizer for marine adhesive bacterium |
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Cited By (5)
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JP2007182431A (en) * | 2005-12-05 | 2007-07-19 | Chisso Corp | Antifouling agent |
JP2011519968A (en) * | 2008-05-12 | 2011-07-14 | バイオペイント・ソシエタ・ア・レスポンサビリタ・リミタータ | New environmentally friendly antimicrobial adhesion preventive agent for antifouling paints and antifouling paints containing the same |
WO2017057632A1 (en) * | 2015-09-30 | 2017-04-06 | 隆廣 門谷 | Aquatic attaching organism repellent, paint, and aquatic structure |
WO2017209125A1 (en) * | 2016-06-03 | 2017-12-07 | 花王株式会社 | Biofilm formation inhibitor and biofilm formation inhibiting composition |
CN109593672A (en) * | 2018-12-13 | 2019-04-09 | 山东大学 | One plant of Pseudoalteromonas polysaccharide degradation bacteria and its cultural method and application |
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2002
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2007182431A (en) * | 2005-12-05 | 2007-07-19 | Chisso Corp | Antifouling agent |
JP2011519968A (en) * | 2008-05-12 | 2011-07-14 | バイオペイント・ソシエタ・ア・レスポンサビリタ・リミタータ | New environmentally friendly antimicrobial adhesion preventive agent for antifouling paints and antifouling paints containing the same |
US8398759B2 (en) * | 2008-05-12 | 2013-03-19 | Biopaint S.R.L. | Environmental friendly anti-microbial adhesion agents for anti-fouling paints and anti-fouling paints containing them |
AU2009247593B2 (en) * | 2008-05-12 | 2015-02-12 | Nanto, Inc. | Novel environmental friendly anti-microbial adhesion agents for anti-fouling paints and anti-fouling paints containing them |
WO2017057632A1 (en) * | 2015-09-30 | 2017-04-06 | 隆廣 門谷 | Aquatic attaching organism repellent, paint, and aquatic structure |
JPWO2017057632A1 (en) * | 2015-09-30 | 2018-10-04 | 隆廣 門谷 | Underwater biorepellents, paints, and underwater structures |
WO2017209125A1 (en) * | 2016-06-03 | 2017-12-07 | 花王株式会社 | Biofilm formation inhibitor and biofilm formation inhibiting composition |
CN109219349A (en) * | 2016-06-03 | 2019-01-15 | 花王株式会社 | Composition is used in biofilm formating inhibitor and biofilm formation inhibition |
CN109593672A (en) * | 2018-12-13 | 2019-04-09 | 山东大学 | One plant of Pseudoalteromonas polysaccharide degradation bacteria and its cultural method and application |
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