WO2012001027A2 - Antifouling benzoate combinations - Google Patents
Antifouling benzoate combinations Download PDFInfo
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- WO2012001027A2 WO2012001027A2 PCT/EP2011/060873 EP2011060873W WO2012001027A2 WO 2012001027 A2 WO2012001027 A2 WO 2012001027A2 EP 2011060873 W EP2011060873 W EP 2011060873W WO 2012001027 A2 WO2012001027 A2 WO 2012001027A2
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- WIPO (PCT)
- Prior art keywords
- component
- benzoate
- composition
- antifouling
- fouling organisms
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/16—Heavy metals; Compounds thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/16—Heavy metals; Compounds thereof
- A01N59/20—Copper
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- 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
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/203—Unsaturated carboxylic acids; Anhydrides, halides or salts thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/203—Unsaturated carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/2035—Aromatic acids
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/35—Heterocyclic compounds
- D06M13/352—Heterocyclic compounds having five-membered heterocyclic rings
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/35—Heterocyclic compounds
- D06M13/355—Heterocyclic compounds having six-membered heterocyclic rings
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
Definitions
- the present invention relates to combinations of a biocidal compound selected from ferric benzoate, aluminium benzoate, barium benzoate and calcium benzoate and the biocidal compound tralopyril, which combinations provide an improved protecting effect against fouling organisms, and the use of these
- compositions comprising a combination of a component (I) and a component (II) in respective proportions to provide a synergistic effect against fouling organisms, whereby component (I) is selected from ferric benzoate, aluminium benzoate, barium benzoate and calcium benzoate, and component (II) is tralopyril; with the proviso that said composition is essentially free of cuprous oxide.
- control is defined to include the inhibition of attachment or settlement of fouling organisms to the surface of an object, the removal of fouling organisms that are attached to the surface of an object, and the growth of fouling organisms.
- Ferric benzoate (CAS Registry Number 14534-87-3) is also known as iron benzoate of iron (III) benzoate and is hereinafter referred to as component (l-a).
- Other biocidal components (I) are aluminium benzoate (l-c), barium benzoate (l-d) and calcium benzoate (l-e).
- WO-2007/061546 discloses stabilized paint compositions containing a hydrolyzable acrylate resin such as copper acrylate, zinc acrylate, or silyl acrylate, a metal salt of pyrithione, cuprous oxide, and a primary stabilizing agent selected from the group consisting of benzoic acid, hydroxypyridine, metal salts of benzoic acid, and hydroxypyridine.
- WO-2007/088172 discloses compositions containing tralopyril and a broad range of zinc compounds such as e.g. ZnO, ZnCI 2 , ZnS0 4 , zineb and zinc pyrithione having a synergistic antifouling effect.
- the wording "essentially free of cuprous oxide" as used herein means that the compositions of the present invention do no comprise cuprous oxide that has been intentionally added to the compositions.
- the common method of controlling the attachment of fouling organisms is by treating the structure to be protected with a coating which comprises an antifouling agent.
- combinations of antifouling biocidal compounds as claimed in the present invention are especially suitable to protect surfaces or objects in constant or frequent contact with water from fouling or attachment or settlement of algae, by applying to said surfaces or objects a composition comprising component (I) and one of the components (II) in respective proportions to provide a synergistic effect against fouling organisms.
- combinations of component (I) and one of the components (II) may be incorporated into the substrate to be protected from fouling.
- Examples of said surfaces or objects are for instance, flexible nets or rigid cages used in marine or freshwater aquaculture, fishing nets, ship hulls, harbor installations, piers and pilings, drying docks, sluice-gates, locks, mooring masts, buoys, offshore oil rigging equipment, drilling platforms, bridges, pipelines, cables, ballast water tanks, ship reservoirs that draw water from infested bodies of water, recreational equipment, such as surfboards, jet skis, and water skis, and any other object in constant or frequent contact with water.
- the invention also provides a method to protect materials, in particular surfaces or objects in frequent or constant contact with water, against fouling organisms by applying to said objects a composition comprising an effective antifouling amount of a combination of a component (I) together with a component (II) wherein the amount of component (I) and component (II) are in respective proportions to provide a synergistic effect against fouling organisms.
- the present invention further provides a method of protecting a surface which comprises applying to the surface a composition comprising an effective antifouling amount of a combination of a component (I) together with a component (II) wherein the amount of component (I) and component (II) are in respective proportions to provide a synergistic effect against fouling organisms.
- An especially important use of the method of the invention comprises a method for inhibiting fouling of nets used in aquaculture, which comprises applying to the net an antifouling composition in accordance with the invention. The effects of biofouling to the aquaculturist are largely detrimental.
- the complex fouling communities that can develop may indirectly cause further stress to stock by affording habitat to a range of 'harmful' diseases and parasites; for example, 'netpen liver disease', amoebic gill disease, the nematode Hysterothylacium disposecum and the sea louse Lepeophtheirus salmonis.
- Fouling can also create 'Health and Safety' concerns, i.e. fouling increases the weight and slipperiness of equipment that is handled and, in the tropics, the frequency of contact with stinging and cutting organisms is raised.
- Another important use of the method of the invention comprises a method for inhibiting fouling of a ship's hull, which comprises applying to the hull an antifouling composition in accordance with the invention.
- Fouling on the hulls of ships for example increases frictional drag with a corresponding decrease in speed and maneuverability and an increase in fuel consumption and increased maintenance costs associated with removal of the fouling.
- compositions comprising a combination of a component (I) together with a component (II) wherein the amount of component (I) and component (II) are in respective proportions to provide a synergistic effect against fouling organisms
- constructions such as, e.g. swimming pools, baths, cooling water circulation circuits and industrial baths in various installations, e.g. in manufacturing plants or in air-conditioning installations, the function of which can be impaired by the presence and/or the multiplication of fouling organisms.
- buildings and parts of buildings such as floors, outer and inner walls or ceilings, or places suffering from dampness such as cellars, bathrooms, kitchens, washing houses and the like, and which are hot-beds for fouling.
- ballast water is treated or disinfection of ballast water to reduce or eliminate the presence of aquatic organisms such as phytoplankton (dinoflagellates and diatoms), crustaceans (crabs, shrimp, copepods, amphipods), rotifers, polychaetes, molluscs, fish, echinoderms, ctenophores, and coelenterates.
- aquatic organisms such as phytoplankton (dinoflagellates and diatoms), crustaceans (crabs, shrimp, copepods, amphipods), rotifers, polychaetes, molluscs, fish, echinoderms, ctenophores, and coelenterates.
- synergistic antifouling compositions of the present invention can also be used in a variety of applications :
- aqueous process fluids e.g. cooling waters, pulp and paper mill process waters and suspensions, secondary oil recovery systems, spinning fluids, metal working fluids, and the like
- aqueous functional fluids e.g. polymer emulsions, water based paints and adhesives, glues, starch slurries, thickener solutions, gelatin, wax emulsions, inks, polishes, pigment and mineral slurries, rubber latexes, concrete additives, drilling mud's, toiletries, aqueous cosmetic formulations, pharmaceutical formulations, and the like.
- fouling organisms is meant to comprise organisms that attach, settle, grow on or adhere to various kinds of surfaces, in particular in humid or aqueous environments such as, marine waters, fresh waters, brackish waters, rain water, and also cooling water, drainage water, waste water and sewage.
- Fouling organisms are Algae such as, for example, Microalgae, e.g. Amphora, Achnanthes, Navicula, Amphiprora, Melosira, Cocconeis, Chlamydomonas, Chlorella, Ulothrix, Anabaena, Phaeodactylum, Porphyridium; Macroalgae, e.g. Enteromorpha,
- Cladophora Ectocarpus, Acrochaetium, Ceramium, Polysiphonia and Hormidium sp.; fungi; microbes; tunicates, including members of the class Ascidiacea such as Ciona intestinalis, Diplosoma listerianium, and Botryllus scheri; members of the class Hydrozoa, including Clava squamata, Hydractinia echinata, Obelia geniculata and Tubularia larynx; bivalves, including Mytilus edulis, Crassostrea virginica, Ostrea edulis, Ostrea chilensia, Dreissena polymorpha (zebra mussels) and Lasaea rubra; bryozoans, including Electra pilosa, Bugula neritina, and Bowerbankia gracilis;
- polychaete worms including Hydroides norvegica; sponges; and members of the class Crustacea, including Artemia, and Cirripedia (barnacles), such as Balanus amphitrite, Lepas anatifera, Balanus balanus, Balanus balanoides, Balanus hameri, Balanus crenatus, Balanus improvisus, Balanus galeatus, and Balanus eburneus; and Elminius modestus, and Verruca.
- Cirripedia barnacles
- the relative proportions of component (I) and component (II) in compositions comprising a combination of component (I) and a component (II) are those proportions which result in a synergistic effect against fouling organisms when compared to a composition including, as an active ingredient, either component (I) alone or a component (II) alone.
- the said synergistic effect may be obtained within various proportions of components (I) and (II) in the composition, depending on the kind of fouling organism towards which effect is measured and the substrate to be treated. Based on the teachings of the present application, determination of the synergistic effect of such combinations can be performed according to the procedures of the Poison Plate Assay as described in Experiment 1. As a general rule, however, it may be said that for most fouling organisms the suitable proportions by weight of the amount of component (I) to component (II) in the combinations should lie in the range from 10:1 to 1 :10.
- this range is from 4:1 to 1 :4, more particularly from 3:1 to 1 :3 or 2:1 to 1 :2.
- a particular ratio of component (I) to component (II) in the compositions of the present invention is from 4:1 to 1 :3, more particularly from 3:1 to 1 :3 or 2:1 to 1 :2.
- the present invention also relates to a composition only containing a combination of the two active ingredients : i.e. a component (I) selected from ferric benzoate (l-a), aluminium benzoate (l-c), barium benzoate (l-d) and calcium benzoate (l-e), and tralopyril as a component (II) - without further active ingredients being present - and one or more carriers.
- a component (I) selected from ferric benzoate (l-a), aluminium benzoate (l-c), barium benzoate (l-d) and calcium benzoate (l-e)
- tralopyril as a component (II) - without further active ingredients being present - and one or more carriers.
- compositions are covered containing a combination of a component (I) selected from ferric benzoate (l-a), aluminium benzoate (l-c), barium benzoate (l-d) and calcium benzoate (l-e) and tralopyril as a component (II); whereby component (I) and component (II) are in respective proportions to provide a synergistic biocidal effect; and one or more carriers.
- a component (I) selected from ferric benzoate (l-a), aluminium benzoate (l-c), barium benzoate (l-d) and calcium benzoate (l-e) and tralopyril as a component (II); whereby component (I) and component (II) are in respective proportions to provide a synergistic biocidal effect; and one or more carriers.
- the suitable proportions by weight of the amount of component (I) to component (II) in these biocidal compositions should lie in the range from 10:1 to 1 :10. Particularly,
- the quantity of each of the active ingredients in compositions comprising a combination of a component (I) and a component (II) will be so that a synergistic effect is obtained.
- the ready to use compositions of the present invention comprise component (I) in an amount of at least 1 wt % based on the total weight of the composition. More particular such ready to use compositions comprise component (I) in an amount from 1 wt% to 40 wt% based on the total weight of the composition.
- the amount of component (II) in said ready to use compositions will be so that a synergistic antifouling effect is obtained.
- the amount of component (II) may range from 1 wt% to 20 wt%, more particular from 2 wt% to 10 wt% based on the total weight of the dry mass of the composition.
- antifouling compounds may be brought into contact with a fouling organism by :
- compositions of the invention include a film-forming component such as a polymer resin solution.
- Exemplary polymer resins include unsaturated polyester resins formed from: a) unsaturated acids or anhydrides, such as maleic anhydride, fumaric acid, itaconic acid and the like; b) saturated acids or anhydrides, such as phthalic anhydride, isophthalic anhydride, terephthalic anhydride, tetrahydrophthalic anhydride, tetrahalophthalic anhydride, adipic acid, sebacic acid, and the like; c) glycols, such as ethylene glycol and the like; d) vinyl monomers, such as styrene, vinyl toluene, chlorostyrene, bromostyrene, acrylates like methylmethacrylate, ethylene glycol dimethacrylate and the like.
- unsaturated polyester resins formed from: a) unsaturated acids or anhydrides, such as maleic anhydride, fumaric acid, itaconic acid and the like; b) saturated acids or anhydr
- Suitable resins include vinyl ethers (like vinylisobutyl ether), copper and zinc acrylates, triorganosilyl acrylates, titanium acrylates, vinyl ester-, vinyl acetate-, and vinyl chloride-based resins, elastomeric components, vulcanized rubbers, rosins, metalresinates and urethane-based resins.
- a composition comprising a combination of a component (I) and a component (II) in respective proportions to provide a synergistic effect against fouling organisms is thus suitably used together with carriers and additives, including wetting agents, dispersing agents, stickers, adhesives, emulsifying agents and the like such as those conventionally employed by the artisan in preparing antifouling compositions.
- the antifouling compositions of the present invention may further comprise suitable substances known in the art of formulation, such as, for example natural or regenerated mineral substances, solvents, dispersants, surfactants, wetting agents, adhesives, thickeners, binders, anti-freeze agents, repellents, color additives, corrosion inhibitors, water-repelling agents, siccatives, UV-stabilizers and other active ingredients.
- suitable surfactants are non-ionic, cationic and/or anionic surfactants having good emulsifying, dispersing and wetting properties.
- surfactants will also be understood as comprising mixtures of surfactants.
- Suitable carriers for solid formulations are any dispersant that does not adversely affect the active ingredients, for example, clays (for example, kaolin, bentonite, acid clay, and the like), talcs (for example, talc powder, agalmatolite powder, and the like), silica's (for example, diatomaceous earth, silicic acid anhydride, mica powder, and the like), alumina, sulfur powder, activated charcoal, and the like.
- clays for example, kaolin, bentonite, acid clay, and the like
- talcs for example, talc powder, agalmatolite powder, and the like
- silica's for example, diatomaceous earth, silicic acid anhydride, mica powder, and the like
- alumina for example, sulfur powder, activated charcoal, and the like.
- Appropriate carriers for liquid formulations are any liquid that does not adversely affect the active ingredients, for example, water, alcohols (for example, methyl alcohol, ethyl alcohol, ethylene glycol, propylene glycol, diethylene glycol, glycerin, etc.), ketones (for example, acetone, methyl ethyl ketone, etc.), ethers (for example, dioxane, tetrahydrofuran, cellosolve, diethylene glycol dimethyl ether, etc.), aliphatic hydrocarbons (for example, hexane, kerosene, etc.), aromatic hydrocarbons (for example, benzene, toluene, xylene, solvent naphtha, methyl naphthalene, etc.), halogenated hydrocarbons (for example, chloroform, carbon tetrachloride, etc.), acid amides (for example, dimethyl formadide, etc.), esters (for example,
- Emulsifiable concentrates of the antifouling compositions according to the present invention can also be obtained upon dilution of the combination of components (I) and (II) with at least a suitable organic solvent (i.e. a liquid carrier) followed by the addition of at least a solvent-soluble emulsifying agent.
- a suitable organic solvent i.e. a liquid carrier
- Solvents suitable for this type of formulation are usually water-immiscible and belong to the hydrocarbon, chlorinated hydrocarbon, ketone, ester, alcohol and amide classes of solvents, and they can be properly selected by those skilled in the art based on the solubility's of components (I) and (II) respectively.
- Emulsifiable concentrates usually contain, in addition to the organic solvent(s), from about 10 to 50% by weight of the combination of active ingredients, from about 2 to 20% of emulsifying agent(s) and up to 20% other additives such as stabilisers, corrosion inhibitors and the like.
- the combination of components (I) and (II) may also be formulated as a suspension concentrate, which is a stable suspension of the active ingredients in a (preferably organic) liquid intended to be diluted with water before use.
- a suspending agent selected from known protective colloids and thixotropic agents.
- liquid formulations like aqueous dispersions and emulsions, for example obtained by diluting a wettable powder or a concentrate (such as previously described) with water, and which may be of the water-in-oil or the oil-in-water type, also lie within the scope of the present invention.
- the present invention also provides protective antifouling compositions, for instance in the form of paints, coatings or varnishes, comprising the said combination of components (I) and (II) together with one or more additives suitable for their formulation.
- the total amount of the combination of components (I) and (II) in such protective compositions may range from 2 to 10% (w/v).
- Suitable additives for use in said protective compositions are quite conventional in the art and include, for instance, at least an organic binder (preferably in aqueous form) such as an acrylic or vinyl- based emulsion or rosin compounds; mineral carriers such as calcium carbonate; surface-active agents such as previously described; viscosity regulators; corrosion inhibitors; pigments such as titanium dioxide; stabilisers such as sodium benzoate, sodium hexametaphosphate and sodium nitrite; mineral or organic colorants and the like.
- organic binder preferably in aqueous form
- mineral carriers such as calcium carbonate
- surface-active agents such as previously described
- viscosity regulators such as previously described
- corrosion inhibitors pigments
- pigments such as titanium dioxide
- stabilisers such as sodium benzoate, sodium hexametaphosphate and sodium nitrite
- mineral or organic colorants and the like are quite conventional in the art and include, for instance, at least an organic binder (preferably in aqueous form) such as an acrylic
- the antifouling compositions according to the present invention can be applied by a number of conventional methods, such as hydraulic spray, air-blast spray, aerial spray, atomising, dusting, scattering or pouring.
- the most appropriate method will be chosen by those skilled in the art in accordance with the intended objectives and the prevailing circumstances, namely the kind of fouling organism to be controlled, the type of equipment available and the type of material to be protected.
- the combination of components (I) and (II) is preferably applied in the form of compositions wherein both said ingredients are intimately admixed in order to ensure simultaneous administration to the materials to be protected.
- Administration or application of both components (I) and (II) can also be a "sequential-combined" administration or application, i.e. component (I) and component (II) are administered or applied alternatively or sequentially in the same place in such a way that they will necessarily become admixed together at the site to be treated. This will be achieved namely if sequential administration or application takes place within a short period of time e.g. within less than 24 hours, preferably less than 12 hours.
- This alternative method can be carried out for instance by using a suitable single package comprising at least one container filled with a formulation comprising the active component (I) and at least one container filled with a formulation comprising an active component (II). Therefore the present invention also
- a composition comprising a component (I) selected from ferric benzoate (l-a), aluminium benzoate (l-c), barium benzoate (l-d) and calcium benzoate (l-e), and - (b) a composition comprising tralopyril as a component (II), as a combination for simultaneous or sequential use, wherein said (a) and (b) are in respective proportions to provide a synergistic effect against fouling organisms;
- Name of the primary compound - ferric benzoate as component (l-a)
- Name of the combination partners - tralopyril as component (II);
- liquid freshwater mineral medium containing the test compounds in one of the concentrations of a dose series is added.
- the liquid freshwater mineral medium is inoculated by adding an aliquot of an actively growing, 3 week old liquid
- BG1 1 culture of algae and incubated at 21 °C, 65% relative humidity, 1000 Lux 16hr/day. The growth is evaluated after three weeks.
- Crustaceans the brine shrimp Artemia salina is used as a model organism for crustaceous marine foulers, such as barnacles. Artemia salina cysts (Great Salt Lake strain) are allowed to hatch in aerated artificial seawater according to Probst. Approximately 20 Artemia salina instar II larvae obtained in this way are added to 300 ⁇ of the same artificial seawater medium. The medium contains the test compounds in a dose range as detailed below ("Concentrations"). The animals are incubated in the laboratory at 25°C and survival of the crustaceans is evaluated after one day.
- Culture medium algae: BG 1 1 liquid mineral medium
- Synergism between component (I) and one of the components (II) was determined by using the Synergy Index method described by by Kull et al. (Kull, F.C., P.C. Eismann, H.D. Sylvestrowicz, and R.L. Mayer (1961 ) "Mixtures of quaternary ammonium compounds and long-chain fatty acids as antifungal agents" Applied Microbiology 9: 538-541 ; also see Zwart Voorspuij, A.J., and C.A.G. Nass (1957) "Some aspects of the notions additivity, synergism and antagonism in the simultaneous activity of two antibacterial agents in vitro" Arch, intern.
- ⁇ Q A is the concentration of compound A in ppm, acting alone, which produced an end point (e.g. MIC),
- Q a is the concentration of compound A in ppm, in the mixture, which produced an end point (e.g. MIC),
- Q B is the concentration of compound B in ppm, acting alone, which produced an end point (e.g. MIC)
- Qe is the concentration of compound B in ppm, in the mixture, which produced an end point (e.g. MIC).
- MIC is the minimum inhibitory concentration, i.e. the lowest concentration of each test compound or mixture of test compounds sufficient to inhibit visible growth.
- Synergy Index When the Synergy Index is greater than 1 .0, antagonism is indicated. When the SI is equal to 1.0, additivity is indicated. When the SI is less than 1 .0, synergism is demonstrated.
- Synergy Index When the Synergy Index is greater than 1 .0, antagonism is indicated. When the SI is equal to 1.0, additivity is indicated. When the SI is less than 1 .0, synergism is demonstrated.
- Table 1 MIC-values (minimum inhibitory concentration in ppm) and synergy index of ferric benzoate (l-a) and tralopyril (II) their combination against Artemia salina
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Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11735823.4A EP2587918B1 (en) | 2010-07-01 | 2011-06-29 | Antifouling benzoate combinations comprising ferric benzoate and tralopyril |
| SG2012091666A SG186326A1 (en) | 2010-07-01 | 2011-06-29 | Antifouling benzoate combinations |
| CN201180033021.8A CN102958363B (en) | 2010-07-01 | 2011-06-29 | Antifouling benzoate combinations |
| KR1020127034056A KR101777222B1 (en) | 2010-07-01 | 2011-06-29 | Antifouling benzoate combinations |
| JP2013517260A JP5865364B2 (en) | 2010-07-01 | 2011-06-29 | Anti-fouling benzoate combination |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10168099.9 | 2010-07-01 | ||
| EP10168099 | 2010-07-01 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2012001027A2 true WO2012001027A2 (en) | 2012-01-05 |
| WO2012001027A3 WO2012001027A3 (en) | 2012-09-13 |
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| Application Number | Title | Priority Date | Filing Date |
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| PCT/EP2011/060873 Ceased WO2012001027A2 (en) | 2010-07-01 | 2011-06-29 | Antifouling benzoate combinations |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP2587918B1 (en) |
| JP (1) | JP5865364B2 (en) |
| KR (1) | KR101777222B1 (en) |
| CN (1) | CN102958363B (en) |
| CL (1) | CL2012003701A1 (en) |
| SG (1) | SG186326A1 (en) |
| WO (1) | WO2012001027A2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8399506B2 (en) | 2006-08-07 | 2013-03-19 | Janssen Pharmaceutica, Nv | Combinations of 4 bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile and oxidizing agents |
| US8512763B2 (en) | 2006-02-01 | 2013-08-20 | Janssen Pharmaceutica, Nv | Combinations of 4 bromo 2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile and metal compounds |
| US8841338B2 (en) | 2001-11-08 | 2014-09-23 | Janssen Pharmaceutica N.V. | Synergistic antifouling compositions comprising 4-bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile |
| US20190185117A1 (en) * | 2017-12-18 | 2019-06-20 | The United States of America, as represented by the Secretary of the Department of the Interior | Hydroxide stabilization as a means of controlling surface fouling associated with wetted surfaces of boats barges and ships |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007061546A2 (en) | 2005-11-23 | 2007-05-31 | Arch Chemicals, Inc. | Paint containing metal salt of pyrithione and cuproux oxide |
| WO2007088172A2 (en) | 2006-02-01 | 2007-08-09 | Janssen Pharmaceutica N.V. | Combinations of 4-bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1h-pyrrole-3-carbonitrile and metal compounds |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04321608A (en) * | 1991-04-22 | 1992-11-11 | K B L Eizen Center:Yugen | Alga-or shellfish-proof composition |
| US5932520A (en) * | 1995-05-23 | 1999-08-03 | American Cyanamid Company | Use of pyrrole compounds as antifouling agents |
| JPH10158102A (en) * | 1996-11-28 | 1998-06-16 | Taki Chem Co Ltd | Growth retarding agent for algae and moss |
| ATE420556T1 (en) * | 2001-11-08 | 2009-01-15 | Janssen Pharmaceutica Nv | SYNERGISTIC ANTI-GROWTH AGENTS CONTAINING 4-BROMO-2-(4-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-H-PYRROLE-3-CARBONITRILE |
| EP1772055A1 (en) * | 2005-10-04 | 2007-04-11 | Rohm and Haas France SAS | Synergistic microbicidal compositions comprising a N-alkyl-1,2-benzoisothiazolin-3-one |
| US7893047B2 (en) * | 2006-03-03 | 2011-02-22 | Arch Chemicals, Inc. | Biocide composition comprising pyrithione and pyrrole derivatives |
| MY145557A (en) * | 2006-04-10 | 2012-02-29 | Janssen Pharmaceutica Nv | Combinations of 4-bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1h-pyrrole-3-carbonitrile and bioooooocidal compounds |
| US7934888B2 (en) * | 2008-01-18 | 2011-05-03 | Viv Suppression, Inc. | Marine anti-foulant system and methods for using same |
| JP5433017B2 (en) * | 2008-12-11 | 2014-03-05 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Antifouling combination comprising 4-bromo-2- (4-chlorophenyl) -5- (trifluoromethyl) -1H-pyrrole-3-carbonitrile |
-
2011
- 2011-06-29 CN CN201180033021.8A patent/CN102958363B/en active Active
- 2011-06-29 KR KR1020127034056A patent/KR101777222B1/en active Active
- 2011-06-29 JP JP2013517260A patent/JP5865364B2/en active Active
- 2011-06-29 EP EP11735823.4A patent/EP2587918B1/en active Active
- 2011-06-29 WO PCT/EP2011/060873 patent/WO2012001027A2/en not_active Ceased
- 2011-06-29 SG SG2012091666A patent/SG186326A1/en unknown
-
2012
- 2012-12-27 CL CL2012003701A patent/CL2012003701A1/en unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007061546A2 (en) | 2005-11-23 | 2007-05-31 | Arch Chemicals, Inc. | Paint containing metal salt of pyrithione and cuproux oxide |
| WO2007088172A2 (en) | 2006-02-01 | 2007-08-09 | Janssen Pharmaceutica N.V. | Combinations of 4-bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1h-pyrrole-3-carbonitrile and metal compounds |
Non-Patent Citations (4)
| Title |
|---|
| B. DEL AMO ET AL., COLLOIDS AND SURFACES A : PHYSICOCHEM. ENG. ASPECTS, vol. 324, 2008, pages 58 - 64 |
| KULL, F.C., P.C. EISMANN, H.D. SYLVESTROWICZ, R.L. MAYER: "Mixtures of quaternary ammonium compounds and long-chain fatty acids as antifungal agents", APPLIED MICROBIOLOGY, vol. 9, 1961, pages 538 - 541 |
| STEINBERG, D.C.: "Measuring synergy", COSMETICS & TOILETRIES, vol. 115, no. 11, 2000, pages 59 - 62, XP009188542 |
| ZWART VOORSPUIJ, A.J., C.A.G. NASS: "Some aspects of the notions additivity, synergism and antagonism in the simultaneous activity of two antibacterial agents in vitro", ARCH. INTERN. PHARMACODYNAMIE, vol. 109, 1957, pages 211 - 228 |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8841338B2 (en) | 2001-11-08 | 2014-09-23 | Janssen Pharmaceutica N.V. | Synergistic antifouling compositions comprising 4-bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile |
| US8841339B2 (en) | 2001-11-08 | 2014-09-23 | Janssen Pharmaceutica N.V. | Synergistic antifouling compositions comprising 4-bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile |
| US8512763B2 (en) | 2006-02-01 | 2013-08-20 | Janssen Pharmaceutica, Nv | Combinations of 4 bromo 2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile and metal compounds |
| US8399506B2 (en) | 2006-08-07 | 2013-03-19 | Janssen Pharmaceutica, Nv | Combinations of 4 bromo-2-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile and oxidizing agents |
| US20190185117A1 (en) * | 2017-12-18 | 2019-06-20 | The United States of America, as represented by the Secretary of the Department of the Interior | Hydroxide stabilization as a means of controlling surface fouling associated with wetted surfaces of boats barges and ships |
| US10800497B2 (en) * | 2017-12-18 | 2020-10-13 | U.S. Geological Survey | Hydroxide stabilization as a means of controlling surface fouling associated with wetted surfaces of boats barges and ships |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2012001027A3 (en) | 2012-09-13 |
| CL2012003701A1 (en) | 2013-08-09 |
| EP2587918A2 (en) | 2013-05-08 |
| JP5865364B2 (en) | 2016-02-17 |
| CN102958363B (en) | 2014-10-29 |
| JP2013529666A (en) | 2013-07-22 |
| KR20130088761A (en) | 2013-08-08 |
| EP2587918B1 (en) | 2015-09-09 |
| SG186326A1 (en) | 2013-01-30 |
| KR101777222B1 (en) | 2017-09-11 |
| CN102958363A (en) | 2013-03-06 |
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