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EP3125688A1 - Agents biocides - Google Patents

Agents biocides

Info

Publication number
EP3125688A1
EP3125688A1 EP15713489.1A EP15713489A EP3125688A1 EP 3125688 A1 EP3125688 A1 EP 3125688A1 EP 15713489 A EP15713489 A EP 15713489A EP 3125688 A1 EP3125688 A1 EP 3125688A1
Authority
EP
European Patent Office
Prior art keywords
iodo
propynyl
agent according
weight
biocidal agent
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.)
Withdrawn
Application number
EP15713489.1A
Other languages
German (de)
English (en)
Inventor
Hermann Uhr
Katrin MÖWS
Monika LAMORATTA
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lanxess Deutschland GmbH
Original Assignee
Lanxess Deutschland GmbH
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Lanxess Deutschland GmbH filed Critical Lanxess Deutschland GmbH
Publication of EP3125688A1 publication Critical patent/EP3125688A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/707—1,2,3- or 1,2,4-triazines; Hydrogenated 1,2,3- or 1,2,4-triazines
    • 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
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/26—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests in coated particulate form
    • A01N25/28—Microcapsules or nanocapsules
    • 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
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • 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
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
    • A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
    • A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom
    • 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
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
    • 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
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
    • 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
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

Definitions

  • the present invention relates to biocidal compositions having excellent fungicidal and algicidal activity, consisting at least of an algicide, propiconazole and an iodopropargyl compound, wherein preferably at least one of the active ingredients is bound, preferably microencapsulated.
  • Biocidal agents containing propiconazole and IPBC are already known from the literature. Such agents are marketed, for example, under the trade name Preventol A 12-TK 20 by Lanxess GmbH in the form of an emulsion concentrate containing about 10% by weight of IPBC and about 10% by weight of propiconazole.
  • JP 2010-126456 A drug combinations of algicides and IPBC are known as wood preservatives.
  • wood preservatives are known from JP 2011-121901 A, which contain triazole compounds and urea compounds, such as, for example, propiconazole and diuron.
  • bound active substances The encapsulated active substances adsorbed to solid carriers or bound in a polymer matrix in distinction to the free active substance in the sense of a slower release are also referred to below as bound active substances.
  • the controlled release is usually diffusion-controlled.
  • the literature discloses a variety of diffusion controlled release systems. These include polymeric nanoparticles, microspheres, porous silica microparticles, inorganic silica structures, sol-gel matrices, and modified nanoclays.
  • capsule material is melamine-formaldehyde resins.
  • melamine-formaldehyde resins For example, it is known from WO 2004/000953 A to introduce biocides in microcapsules with wall materials of special formaldehyde-melanin resins in order to be able to use them in coating materials which have a pH of more than 11.
  • EP 0 758 633 A describes porous granules containing chemical substances, e.g. also contain biocides that release them slowly in the application.
  • microcapsules have become known, which preferably contain zinc pyrithione or irgarol and which are prepared by the fact that aqueous dispersions of polymer solution, active ingredient and low-boiling solvent are freed from the solvent with vigorous stirring and the resulting microcapsules are isolated by filtration (see US 2006/0246144).
  • Another way to prevent the leaching of active ingredients provides the homogeneous distribution of the active ingredient in a polymeric matrix. Such, by extrusion and grinding too obtained biocide-containing thermoplastic polymer particles are described in WO 2009/00650 A.
  • At least one algicide selected from the group of triazine-algicides, urea-algicides and uracil-algicides
  • bound active substances are understood as meaning active substances or mixtures of active substances
  • Encapsulated preferably microencapsulated and / or
  • Bound agents are preferably those which are either encapsulated, preferably microencapsulated, or attached to or on solid support materials or enclosed in a polymer matrix.
  • At least one of the active ingredients is bound, more preferably microencapsulated.
  • At least one algicide is bound, preferably microencapsulated.
  • the at least one iodopropargyl compound is bound, preferably microencapsulated.
  • the algicides are selected from the group of triazine-algicides, urea-algicides and uracil-algicides.
  • Triazine algicides are, for example, terbutryn, cybutryn, propazine or terbutone;
  • urea-algicides are, for example, diuron, benzthiazuron, methabenzthiazuron, tebuthiuron, and isoproturon, a uracil algicide being, for example, terbacil.
  • the algicides are more preferably selected from the group consisting of isoproturon, diuron, cybutryn and terbutryn.
  • Iodopropargyl compounds are preferably selected from the group 3-iodo-2-propynyl-propyl-carbamate, 3-iodo-2-propynyl-butyl-carbamate (IPBC), 3-iodo-2-propynyl-m-chlorophenyl-carbamate, 3 Iodo-2-propynylphenyl carbamate, 3-iodo-2-propynyl-2,4,5-trichlorophenyl ether, 3-iodo-2-propynyl-4-chloro-henylformal (IPCF), di (3-iodo) 2-propynyl) hexyl dicarbamate, 3-iodo-2-propynyl oxyethanol ethyl carbamate, 3-iodo-2-propynyl oxyethanol phenyl carbamate, 3-iodo-2-propynyl thioxothioethyl
  • a particularly preferred iodopropargyl compound is 3-iodo-2-propynyl-butyl-carbamate (IPBC).
  • IPBC 3-iodo-2-propynyl-butyl-carbamate
  • the weight ratio of propiconazole to the sum of iodopropargyl compound (s) can vary widely. In general, the weight ratio of propiconazole to the sum of iodopropargyl compound (s) is 1: 100 to 100: 1, preferably 1:20 to 20: 1, and more preferably 1: 9 to 9: 1.
  • the weight ratio of algicide (s) to the sum of propiconazole and the sum of iodopropargyl compound (s) can vary within a wide range and is generally 1: 100 to 100: 1, preferably 1:20 to 20: 1 and more preferably 1: 9 to 9: 1.
  • biocidal compositions according to the invention generally contain 0.5 to 80% by weight, preferably 1 to 70% by weight, in particular 1 to 60% by weight of active compounds, based on the sum of components A), B) and C).
  • a polymer matrix means particles, preferably monolithic particles, in which the active substance is homogeneously distributed in at least one thermoplastic polymer.
  • the term "homogeneously distributed” is also understood to mean the distribution of an active substance introduced into the at least one thermoplastic polymer after mixing and extrusion.For reasons of clarity, microcapsules having a drug core surrounded by a polymer wall do not belong to the term "polymer matrix" is included.
  • thermoplastic polymers include, for example, polyacrylates, polyalkylene glycols, in particular polyethylene glycols or polyethylene-polypropylene glycol copolymers (Block copolymers or randomly distributed), polyurethanes, polyamides, polyureas, polycarbonates, polyesters or mixtures thereof.
  • thermoplastic polymers not mentioned here or mixtures thereof in which the glass transition temperature T g is 30 to 250 ° C., preferably 50 to 200 ° C.
  • 95% of all particles have a particle size of less than 100 ⁇ , preferably from 1 to 50 ⁇ .
  • the polymer matrix has, for example, an active ingredient content of from 2 to 80% by weight, preferably from 5 to 60% by weight.
  • Bound agents also include those that are bound to or on solid support materials.
  • Support materials are, for example and preferably, calcium carbonate, calcium silicates, aluminum silicates, silica gels, kieselguhr, zeolites, sheet silicates, silica gels, pyrogenic or precipitated silicas or modified silicas.
  • the support materials are pyrogenic or precipitated silicas.
  • the carrier material is either brought directly into contact with the active ingredient or the active ingredients are dissolved in a solvent and evaporated together with the carrier material.
  • the active ingredients can also be brought into a polymer matrix, if the active ingredients are dissolved in monomers and hereby carries out an emulsion polymerization.
  • the emulsion polymerization is a process of radical polymerization of monomers in an aqueous phase.
  • the components necessary for emulsion polymerization are water, a water-soluble initiator and the monomers which must have low water solubility.
  • the result is a polymer dispersion, i. H. a dispersion of the polymer particles formed from the monomer in water.
  • the active ingredient dissolved simultaneously in the monomer is then preferably distributed homogeneously in the polymer.
  • the emulsion polymers are preferably PVC, polystyrene, polyacrylate, polyacrylonitrile and polyvinyl acetate copolymers.
  • Bound agents include and are preferably encapsulated agents, more preferably microencapsulated agents.
  • Encapsulated active substances in particular microencapsulated active substances, are understood as meaning active ingredients which are completely or partially encased by an encapsulating material. They are also called capsules or microcapsules below.
  • Preferred microcapsules are characterized in that they have, for example, a volume-average particle size of 0.3 to 100 ⁇ m.
  • the microcapsules contained have a volume-average particle size of 5 to 40 ⁇ .
  • the microcapsules contained are distinguished by the fact that the D90 value, determined by laser diffraction as a volume-weighted distribution, is preferably less than 40 ⁇ m.
  • Preferred microcapsules contain a melamine-formaldehyde polymer as the encapsulating material.
  • melamine-formaldehyde polymer is understood to mean a polymer in which melamine, typically with molar excess of formaldehyde, has been polycondensed.
  • the encapsulating material of the contained microcapsules may, for example, also contain other synthetic, semisynthetic or natural aminoplast resins.
  • Aminoplast resins are generally understood as meaning polycondensation products of carbonyl compounds with compounds containing NH groups. Of particular interest in this context are urea or phenol-modified melamine-formaldehyde resins (melamine-urea-formaldehyde resins, melamine-phenol-formaldehyde resins).
  • aminoplast resins may be added to the melamine-formaldehyde resin, for example aminoplast resins from a compound containing NH groups and acetaldehyde or glyoxal.
  • urethane resins, cyanamide resins or dicyanamide resins, aniline resins, sulfonamide resins or mixtures of these resins may be added. These resins and their preparation are known in the art.
  • the encapsulating material may also be synthetic materials such as, for example, acrylic polymers and copolymers, polyacrylamide, polyalkylcyanoacrylate, and poly (ethylenevinylacetate), aluminum monostearate, carboxyvinyl polymers, polyamides, poly (methylvinyl ether-maleic anhydride), poly (adipyl-L -lysine), polycarbonates, polyterephthalamide, poly (vinyl acetate phthalate), poly (terephthaloyl-L-lysine), polyarylsulfones, poly (methyl methacrylate), poly (e-caprolactone), polyvinylpyrrolidone, Polydimethylsiloxane, polyoxyethylenes, polyesters, polyglycolic acid, polylactic acid and its copolymers, polyglutamic acid, polylysine, polystyrene, poly (styrene-acrylonitrile), polyimides and polyvinyl alcohol are used.
  • synthetic materials such as, for
  • semisynthetic materials such as cellulose acetate, cellulose acetate butyrate, cellulose acetate nitrate, ethylcellulose, hydroxypropylcellulose, sodium carboxymethylcellulose, hydroxypropylmethylcellulose, methylcellulose, hydroxypropylmethylcellulose phthalate, hydrogenated tallow, myristyl alcohol, glycerol mono- or di-palmitate, hydrogenated castor oil, glyceryl mono- or tristearates and 12-hydroxystearyl alcohol.
  • semisynthetic materials such as cellulose acetate, cellulose acetate butyrate, cellulose acetate nitrate, ethylcellulose, hydroxypropylcellulose, sodium carboxymethylcellulose, hydroxypropylmethylcellulose, methylcellulose, hydroxypropylmethylcellulose phthalate, hydrogenated tallow, myristyl alcohol, glycerol mono- or di-palmitate, hydrogenated castor oil, glyceryl mono- or tristearates and 12-
  • natural materials such as gum arabic, agar, agarose, maltodextrin, sodium alginate, calcium alginate, dextran, fats, fatty acids, cetyl alcohol, milk solids, molasses, gelatin, gluten, albumin, shellac, starches, caseinates, stearines, Sucrose and waxes such as beeswax, carnauba wax and spermaceti wax.
  • biocidal compositions according to the invention can be present in any desired formulation, for example in the form of suspension concentrates, water-dispersible powders, water-dispersible granules or simple powder mixtures, suspension concentrates, powder mixtures and water-dispersible granules being preferred.
  • the formulations may additionally contain other substances, such as stabilizers, container preservatives and other biocides, such as fungicides, algicides, insecticides, acaricides, nematicides, radicides and herbicides or mixtures thereof, preferably fungicides or algicides or mixtures thereof, very preferably algicides.
  • other substances such as stabilizers, container preservatives and other biocides, such as fungicides, algicides, insecticides, acaricides, nematicides, radicides and herbicides or mixtures thereof, preferably fungicides or algicides or mixtures thereof, very preferably algicides.
  • biocidal agents may optionally further contain various adjuvants in addition to the combinations according to the invention.
  • adjuvants there is also the possibility, independently of each other, that they are not included.
  • auxiliaries are, for example:
  • Surfactants such as surfactants.
  • Surfactants may be, for example, nonionic, cationic and amphoteric surfactants, preferably anionic surfactants.
  • Anionic surfactants are, for example, alkyl sulfates, alkyl ether sulfates, alkylaryl sulfonates, alkyl succinates, alkyl sulfosuccinates, N-alkoylsarcosinates, Acyl taurates, acyl isethionates, alkyl phosphates, alkyl ether phosphates,
  • the alkyl ether sulfates, alkyl ether phosphates and alkyl ether carboxylates may each be, for example, from 1 to 10 ethylene oxide or
  • Propylene oxide units preferably 1 to 3 ethylene oxide units.
  • Suitable examples are sodium lauryl sulfate, ammonium lauryl sulfate, sodium lauryl ether sulfate, ammonium lauryl ether sulfate, sodium lauryl sarcosinate, sodium oleyl succinate,
  • biocidal agents according to the invention can be used, for example, by
  • Defoamer As defoamers, surfactants are generally used which are only slightly soluble in the surfactant solution. preferred
  • Defoamers are those derived from natural fats and oils, petroleum derivatives or silicone oils.
  • Wetting agents such as, for example, alkali metal, alkaline earth metal, ammonium salts of aromatic sulfonic acids, for example lignin, phenol, naphthalene and dibutylnaphthalenesulfonic acid, and of fatty acids, alkyl and alkylaryl sulfonates,
  • biocidal agents according to the invention can be used, for example, by
  • Emulsifiers such as, for example, sodium, potassium and ammonium salts of straight-chain aliphatic carboxylic acids of the chain length C 10 -C 2 o, sodium hydroxyoctadecane sulfonate, Sodium, potassium and ammonium salts of hydroxy fatty acids of chain length C 10 -C 2 o and their sulfation or acetylation products, alkyl sulfates, also known as triethanolamine salts, alkyl- (C 10 -C 2 o) -sulfonates, alkyl- (C 10 -) C 2 o) -arylsulfonates,
  • biocidal compositions according to the invention may be, for example, from 0.01 to 15% by weight, preferably from 0.02 to 8% by weight, particularly preferably from 0.05 to 6% by weight and very particularly preferably from 0.1 to 5% by weight .
  • - Containing emulsifiers may be, for example, from 0.01 to 15% by weight, preferably from 0.02 to 8% by weight, particularly preferably from 0.05 to 6% by weight and very particularly preferably from 0.1 to 5% by weight.
  • Dispersants such as alkylphenol polyglycol ethers.
  • the biocidal compositions according to the invention may be, for example, from 0.01 to 15% by weight, preferably from 0.02 to 8% by weight, particularly preferably from 0.05 to 6% by weight and very particularly preferably from 0.1 to 5% by weight .- Containing dispersants.
  • Stabilizers such as cellulose and cellulose derivatives.
  • the biocidal compositions according to the invention may be, for example, from 0.01 to 6% by weight, preferably from 0.01 to 3% by weight, particularly preferably from 0.01 to 2% by weight and very particularly preferably from 0.01 to 1% by weight .- of stabilizers.
  • Stabilizers such as antioxidants, radical scavengers or UV absorbers.
  • Adhesives or protective colloids such as, for example, carboxymethylcellulose, natural and synthetic powdery, granular or latex-form polymers, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and also natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids and paraffin oils.
  • the biocidal compositions according to the invention can be, for example, from 0.01 to 8% by weight, preferably from From 0.05 to 4% by weight, particularly preferably from 0.2 to 3% by weight and very particularly preferably from 0.2 to 2% by weight, of adhesives.
  • the biocidal compositions according to the invention may be, for example, from 0.01 to 20% by weight, preferably from 0.1 to 10% by weight, more preferably from 0.1 to 5% by weight and most preferably from 0.1 to 2% by weight .- included in spreading agents.
  • Fragrances and dyes such as, for example, inorganic pigments, for example iron oxide, titanium oxide, ferrocyan blue and organic dyes, such as alizarin, azo and metal phthalocyanine dyes and trace nutrients, such as salts of iron, manganese, boron,
  • the biocidal compositions according to the invention may contain, for example, in each case from 0.001 to 4% by weight, preferably from 0.01 to 1% by weight, particularly preferably from 0.01 to 0.8% by weight, of fragrances and dyes. ⁇ Buffer substances, buffer systems or pH regulators.
  • the biocidal compositions according to the invention may contain, for example, in each case from 0.01 to 10% by weight, preferably from 0.1 to 5% by weight, of buffer substances, buffer systems or pH regulators.
  • Thickeners such as polysaccharides, xanthan gum, sodium or magnesium silicates, heteropolysaccharides, alginates, carboxymethylcellulose, gum
  • Arabic or polyacrylic acids preferably xanthan gum.
  • De-dusting agents are, for example, polyglycols and polyglycol ethers.
  • the biocidal compositions according to the invention may contain, for example, in each case from 0.01 to 2% by weight, preferably from 0.05 to 1% by weight, particularly preferably from 0.1 to 0.5% by weight, of dedusting agents.
  • biocidal compositions according to the invention may in each case contain from 0.01 to 5% by weight, preferably from 0.05 to 3% by weight, particularly preferably from 0.1 to 2% by weight, of flow agent to improve the flowability of the solids.
  • Container preservatives are, for example, biocides, bactericides and fungicides.
  • the biocidal compositions according to the invention may contain, for example, in each case from 0.01 to 2% by weight, preferably from 0.05 to 1% by weight, of container preservative.
  • the total content of the abovementioned auxiliaries in the biocidal compositions is, for example, from 0.001 to 20% by weight, preferably from 0.1 to 15% by weight and more preferably from 0.1 to 10% by weight.
  • the biocidal agents may further optionally contain water and / or organic solvents such as, for example, oligo- or polyalkylene glycols or triols, or ethers of the abovementioned compounds, in particular having a molecular weight of less than 1000 g / mol.
  • organic solvents such as, for example, oligo- or polyalkylene glycols or triols, or ethers of the abovementioned compounds, in particular having a molecular weight of less than 1000 g / mol.
  • Solid formulations such as, for example, powder mixtures or water-dispersible granules (WG) may also contain solid auxiliaries, for example ground natural minerals, such as kaolins, clays, talc, marble, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, or synthetic inorganic substances, such as finely divided silica, Alumina and silicates or mixtures thereof.
  • solid auxiliaries for example ground natural minerals, such as kaolins, clays, talc, marble, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, or synthetic inorganic substances, such as finely divided silica, Alumina and silicates or mixtures thereof.
  • the solid formulations can be obtained in a manner known per se, for example by intimately mixing the individual components with the solid auxiliaries or by comminuting solid auxiliaries with the individual components. Furthermore, the solid formulations can be obtained by drying, for example spray-drying, a liquid formulation.
  • biocidal compositions according to the invention may also contain further active compounds such as, for example, fungicides, bactericides, algicides and / or insecticides, either in bound or unbound form or free from further active compounds such as, for example, fungicides, bactericides, algicides and / or insecticides.
  • further active compounds such as, for example, fungicides, bactericides, algicides and / or insecticides.
  • fungicides As optionally additionally contained fungicides, bactericides, algicides and / or insecticides can be used, for example:
  • Triazoles such as azaconazole, azocyclotin, bitertanol, bromuconazole, cyproconazole, diclobutrazole, difenoconazole, diniconazole, epoxyconazole, etaconazole, fenbuconazole, fenchlorazole, fenethanil, fluquinconazole, flusilazole, flutriafol, furconazole, hexaconazole, imibenconazole, ipconazole, isozofos, myclobutanil, metconazole, paclobutrazole, Penconazole, prothioconazole, simeoconazole, ( ⁇ ) -cis- 1 - (4-chlorophenyl) -2- (1H-1,2,4-triazol-1-yl) -cycloheptanol, 2- (1-tert-butyl) - 1 - (2-ch
  • Pyridines and pyrimidines such as ancymidol, buthiobate, fenarimol, mepanipyrine, nuarimol, pyroxyfur, triamirole;
  • Succinate dehydrogenase inhibitors such as Benodanil, Carboxim, Carboximsulfoxid, Cyclafluramid, Fenfuram, Flutanil, Furcarbanil, Furmecyclox, Mebenil, Mepronil, Methfuroxam, Metsulfovax, Nicobifene, Pyrocarbolid, Oxycarboxin, Shirlan, Seedvax;
  • Naphthalene derivatives such as terbinafine, naftifine, butenafine, 3-chloro-7- (2-aza-2,7,7-trimethyl-oct-3-en-5-yne);
  • Sulfenamides such as dichlorofluidide, tolylfluanid, folpet, fluorfolpet; Captan, Captofol;
  • Benzimidazoles such as carbendazim, benomyl, fuberidazole, thiabendazole or their salts;
  • Morpholine derivatives such as aldimorph, dimethomorph, dodemorph, falimorph, fenpropidine, fenpropimorph, tridemorph, trimorphamide and their arylsulfonic acid salts, e.g. p-toluenesulfonic acid and p-dodecylphenylsulfonic acid;
  • Benzothiazoles such as: 2-mercaptobenzothiazole;
  • Benzothiophene dioxides such as: benzo [b] thiophene-S, S-dioxide-carboxylic acid cyclohexylamide;
  • Benzamides such as: 2,6-dichloro-N- (4-trifluoromethylbenzyl) benzamide, Tecloftalam;
  • Boron compounds such as: boric acid, boric acid ester, borax;
  • Formaldehyde and formaldehyde-releasing compounds such as benzyl alcohol mono- (poly) hemiformal, 1,3-bis (hydroxymethyl) -5,5-dimethy-limidazolidine-2,4-diones (DMDMH), bisoxazolidines, n-butanol-hemiformal, cis-1 (3-chloroallyl) -3,5,7-triaza-1-azoniaadamantane chloride, 1 - [1,3-bis (hydroxymethyl-2,5-dioxoimidazolidin-4-yl] -1,3-bis (hydroxymethyl) urea .
  • benzyl alcohol mono- (poly) hemiformal 1,3-bis (hydroxymethyl) -5,5-dimethy-limidazolidine-2,4-diones (DMDMH), bisoxazolidines, n-butanol-hemiformal, cis-1 (3-chlor
  • Dazomet dimethylolurea, 4,4-dimethyl-oxazolidines, ethylene glycol hemiformal, 7-ethyl-bicyclooxazolidines, hexa-hydro-S-triazines, hexamethylenetetramine, N-hydroxymethyl-N'-methylthiourea, methylenebis-morpholine, sodium N- (Hydroxy-methyl) glycinate, N-methylol-chloroacetamide, oxazolidines, paraformaldehyde, tauroline, tetrahydro-1,3-oxazine, N- (2-hydroxypropyl) -amine-methanol, tetramethylol-acetylene-diurea (TMAD);
  • Isothiazolinones such as N-methylisothiazolin-3-one, 5-chloro-N-methylisothiazolin-3-one, 4,5-trimethyleneisothiazolinone, 4,5-benzisothiazolinone, N-methylbenzisothiazolinone, N-butylbenzisothiazolinone;
  • Aldehydes such as cinnamaldehyde, formaldehyde, glutardialdehyde, .beta.-bromomethylaldehyde, o-phthalaldehyde;
  • Thiocyanates such as: thiocyanatomethylthiobenzothiazole, methylene bisthiocyanate;
  • Quaternary ammonium compounds and guanidines such as benzalkonium chloride, benzyldimethyltetradecylammonium chloride, benzyldimethyldodecylammonium chloride, dichlorobenzyldimethylalkylammonium chloride, didecyldimethylammonium chloride, dioctyldimethylammonium chloride, N-hexadecyltrimethylammonium chloride, 1 -
  • Iodine derivatives such as diiodomethyl-p-tolylsulfone, 3-iodo-2-propynyl alcohol, 4-chlorophenyl-3-iodopropargylformal, 3-bromo-2,3-diiodo-2-propenylethylcarbamate, 2,3,3-triiodoallylalcohol, 3 Bromo-2,3-diiodo-2-propenylalcohol, 3-iodo-2-propynyl-n-hexylcarbamate, 3-iodo-2-propynylcyclohexylcarbamate, 3-iodo-2-propynylphenylcarbamate;
  • Phenols such as tribromophenol, tetrachlorophenol, 3-methyl-4-chlorophenol, 3,5-dimethyl-4-chlorophenol, dichlorophene, 2-benzyl-4-chlorophenol, triclosan, diclosan, hexachlorophene, p-hydroxybenzoic acid methyl ester, p- Hydroxybenzoic acid ethyl ester, propyl p-hydroxybenzoate, butyl p-hydroxybenzoate, octyl p-hydroxybenzoate, o-phenylphenol, m-phenylphenol, p-phenylphenol, 4- (2-tert-butyl-4-methyl-phenoxy) -phenol, 4- ( 2-isopropyl-4-methyl-phenoxy) -phenol, 4- (2,4-dimethyl-phenoxy) -phenol and their alkali and alkaline earth metal salts;
  • halogenated microbicides such as Bronidox, 2-bromo-2-nitro-1,3-propanediol, 2-bromo-4'-hydroxy-acetophenone, 1-bromo-3-chloro-4,4,5,5-tetramethyl- 2-imidazolediones, ⁇ -bromo- ⁇ -nitrostyrene, chloroacetamide, chloramine T, 1,3-dibromo-4,4,5,5-tetramethyl-2-imidazoledione, dichloroamine T, 3,4-dichloro (3H) -l, 2-dithiol-3-one, 2,2-dibromo-3-nitrile-propionamide, 1, 2-dibromo-2,4-dicyanobutane, halanes, halazone, mucochloric acid, phenyl (2-chloro cyanogen vinyl) sulfone, phenyl (1,2-dichloro-2-cyanovinyl) s,
  • Pyridines such as 1-hydroxy-2-pyridinethione (and its Cu, Na, Fe, Mn, Zn salts), tetrachloro-4-methylsulphonylpyridine, pyrimethanol, mepanipyrim, dipyrrithione, 1-hydroxy-4-methyl-6 - (2,4,4-trimethylpentyl) -2 (1H) -pyridine;
  • Methoxyacrylates or the like such as azoxystrobin, dimoxystrobin, fluoxastrobin, cresoxymethyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, trilloxystrobin, 2,4-dihydro-5-methoxy-2-methyl-4- [2- [[[1 - 3 - (trifluoromethyl) phenyl] ethylidenes] amino] oxy] methyl] phenyl] -3H-l, 2,4-triazol-3-ones (CAS No. 185336-79-2);
  • Metal soaps such as salts of the metals tin, copper and zinc with higher fatty, resinous, naphthenic and phosphoric acids, for example tin, copper, zinc naphthenate, octoate, 2-ethylhexanoate, oleate, phosphate, benzoate;
  • Metal salts such as salts of the metals tin, copper, zinc, as well as chromates and dichromates such as copper hydroxycarbonate, sodium dichromate, potassium dichromate, potassium chromate, copper sulfate, copper chloride, copper borate, zinc fluorosilicate, copper fluorosilicate;
  • Oxides such as: Oxides of the metals tin, copper and zinc, e.g. Tributyltin oxide, CU2O, CuO, ZnO; Oxidizing agents such as hydrogen peroxide, peracetic acid, potassium persulfate;
  • Dithiocarbamates such as Cufraneb, Ferban, potassium N-hydroxymethyl-N'-methyl-dithiobarbamate, Na- or K-dimethyldithiocarbamate, Macozeb, Maneb, Metam, Metiram, Thiram, Zineb, Ziram;
  • Nitriles such as 2,4,5,6-tetrachloroisophthalodinitrile, disodium cyanodithioimidocarbamate;
  • Quinolines such as: 8-hydroxyquinoline and their Cu salts; other fungicides and bactericides such as Bethoxazine, 5-hydroxy-2 (5H) -furanone; 4,5-benzdithiazolinone, 4,5-trimethylenedithiazolinone, N- (2-p-chlorobenzoylethyl) -hexaminium chloride,
  • 2-Oxo-2- (4-hydroxyphenyl) acethydroximic acid chloride tris-N- (cyclohexyldiazeniumdioxy) -aluminum, N- (cyclohexyldiazeniumdioxy) -tributyltin or K-salts, bis-N- (cyclohexyldi- azeniumdioxy ) Copper, Iprovalicarb, Penflufen, Solatenol, Fenhexamid, Spiroxamine, Carpropamid, Diflumetorin, Quinoxyfen, Famoxadone, Polyoxorim, Acibenzolar-S-methyl, Furametpyr, Thiflucamide, Methalaxyl-M, Benthiavalicarb, Metrafenone, Cyflufenamid, Tiadinil, Tea Tree Oil, Phenoxyethanol,
  • the fungicides and bactericides are most preferably: azaconazole, bromuconazole, cyproconazole, dichlobutrazole, diniconazole, hexaconazole, metaconazole, penconazole, propiconazole, tebuconazole, dichlofluanid, tolylfluanid, triadimefon, fluorolepet, methfuroxam, carboxin, benzo [b] thiophene-S, S-dioxide-carboxylic acid cyclohexylamide, fenpiclonil, 4- (2,2-difluoro-1,3-benzodioxol-4-yl) -1H-pyrrole-3-carbonitrile, butenafine, imazalil, N-methylisothiazolinone 3- ⁇ , 5-chloro-N-methylisothia
  • the algicides are preferably: Acetochlor, Acifluorfen, Aclonifen, Acrolein, Alachlor, Alloxydim, Ametryn, Amidosulfuron, Amitrole, Ammonium sulfamate, Anilofos, Asulam, Atrazine, Azafenidine, Aziptrotryn, Azimsulfuron,
  • MCPA MCPA hydrazide, MCPA-thioethyl, MCPB, mecoprop, mecoprop-P, mefenacet, mefluidide, mesosulfuron, metam, metamifop, metamitron, metazachlor, methabenzthiazuron, Methazol, Methoropyrene, Methyldymrone, Methylisothiocyanate, Metobromuron, Metoxuron, Metribuzin, Metsulfuron, Molinate, Monalid, Monolinuron, MSMA, Metolachlor, Metosulam, Metobenzuron,
  • the liquid agents according to the invention contain no further fungicides, bactericides, algicides and / or insecticides.
  • the invention further relates to the use of the biocidal agents according to the invention for the protection of technical materials.
  • Adhesives, glues, paper, cardboard, leather, wood, wood-based materials, wood-plastic composites, paints, coating compositions, plasters, cooling lubricants and heat transfer liquids come into consideration in particular as technical materials. Very particular preference is given to paints, coating materials, plasters, wood and wood-based materials.
  • the invention also relates to a process for the protection of industrial materials against attack and / or destruction by microorganisms, which is characterized by allowing the inventive biocidal agent undiluted or diluted with water to act on the microorganism or its habitat.
  • the invention also relates to engineering materials obtainable by treating engineering materials with the biocidal agents of the invention.
  • biocidal agents of the invention In the case of paints and coating compounds, both the still liquid and the dried system are protected against infestation by microorganisms, especially fungi and algae.
  • microorganisms that can cause degradation or a change in the technical materials
  • bacteria, fungi, yeasts, algae and mucus organisms may be mentioned.
  • the agents according to the invention are preferably used against fungi, in particular molds, wood-discolouring and wood-destroying fungi (Basidiomycetes) and against algae.
  • Algae are preferably prokaryotic algae (Cyanophyta, blue-green algae) such as representatives of the subclass Coccogoneae and the subclass Hormogoneae.
  • the agents also show good activity against eukaryotic representatives from the departments Heterocontophyta, Rhodophyta, Chlorophyta, Euglenophyta, Cryptophyta, Dinophyta and Haptophyta.
  • fungi are microorganisms of the following genera: Alternaria such as Alternaria tenuis, Aspergillus such as Aspergillus niger, Chaetomium such as Chaetomium globosum, Coniophora such as Coniophora puetana, Lentinus such as Lentinus tigrinus, Penicillium such as Penicillium glaucum, Polyporus such as Polyporus versicolor, Aureobasidium , such as Aureobasidium pullulans, sclerophoma, such as Sclerophoma pityophila, Trichoderma, such as Trichoderma viride.
  • Alternaria such as Alternaria tenuis
  • Aspergillus such as Aspergillus niger
  • Chaetomium such as Chaetomium globosum
  • Coniophora such as Coniophora puetana
  • Lentinus such as Lentinus t
  • the application rate of the agents according to the invention depends on the nature and occurrence of the microorganisms to be controlled and on the composition of the material to be protected. The optimum amount of use can be determined by testing easily and in a manner well known to those skilled in the art.
  • the biocidal agent of the invention is used so that the total concentration of the active ingredients according to the components A), B) and C) in the material to be protected from 20 to 10,000 ppm by weight, preferably 50 to 5000 ppm by weight.
  • the advantage of the invention lies in the fact that the biocidal compositions according to the invention show a superior, because reduced Leaching with high efficacy and duration of action.
  • Coadis TM BR3 (50% by weight in H 2 O) (dispersion reagent, aqueous polyacrylate salt solution from Coatex)
  • SILOFOAM®SRE silicon antifoam emulsion defoamer from Wacker
  • Maprenal® water solution (1: 1) (Maprenal® MF 921w / 85WA melamine-formaldehyde binder from INEOS Melamines)
  • Preventol® D7 (can preservative with about 1.5% by weight chloromethylisothiazolinone / methylisothiazolinone 3: 1)
  • Preventol® BIT 20D (container preservative with about 20% by weight of benzisothiazolinone) urea
  • Sipernat® 50 S (precipitated silica, Evonik)
  • Prevento®l A 14-D (suspension containing 20% Diuron, 10% BCM, 3% OIT)
  • Preventol® MP 400 (suspension containing 40% IPBC, manufacturer Lanxess)
  • Soprophor® S25 (emulsifier based on tris-sterylphenyl ether ethoxylates)
  • Preventol® BM 25 (container preservative containing 2.4 wt .-% benzisothiazolinone and
  • Rhodopol G® thickener based on xanthan gum from Solvay Rhodia
  • Pluronic Fl 27 ethylene oxide-propylene oxide block copolymer
  • Oparyl MT 820 sodium didisobutylnaphthalenesulfonate Example 1 (preparation of propiconazole on Sipernat 50 S)
  • the resulting solution was transferred to a 1000 ml slotted pot with impeller stirrer and Ultraturrax. While stirring with an impeller stirrer, 150.09 g of IPBC were added at about 400-420 rpm.
  • Preventol MP 400 At room temperature, 75.57 g of Preventol MP 400, 30 g and 104 g of water were stirred. 25 g of propiconazole were added with stirring to Sipernat 50 S (see Example 1) and stirred for 30 minutes until the suspension was homogeneous. Subsequently, 269.46 g of the capsule suspension from Example 2 were added and homogenized with slow stirring. To this was added with further stirring 0.5 g of Preventol D 7, 0.5 g of Preventol BIT 20 D, 20.0 g of a 3% aqueous solution of Rhodopol G in water (xanthan gum solution) and a further 6 g of water.
  • the homogeneous white suspension contained 9.0 parts by weight diuron, 6.1 parts by weight IPBC and 3.0 parts by weight propiconazole.
  • the viscosity (rotational viscometer RC 20 / Rheotec) was 370.3 mPas at 30 1 / s.
  • Viscosity 237 mPas at 30 1 / s.
  • Example 7 Examination of fungicidal and algicidal activity
  • Pigment distributor A 10% 2.5 polyacrylic acid salt
  • the samples were watered for 24 h in running tap water at a flow rate of 6 L / h (+/- IL) (24 h wash).
  • One set of the non-watered samples was placed under UV irradiation for 4 weeks and visually inspected after 1, 2 and 4 weeks. All samples were subjected to an agar diffusion test (AD test).
  • Ascomycetes and Deuteromycetes (Alternaria altemata, Aspergillus flavus, Aspergillus niger, Aspergillus ustus, Aureobasidium pullulans, Cladosporium herbaru, Paecilomyces variotii, Paecilomyces variotii, Penicillium citrinum and Stachybotrys chartarum) and algae (known facade damaging agents: Phormidium tergestinum, Chlorella vulgaris, Phormidium spec., Desmodesmus communis). Evaluation of the AD test
  • the evaluation of the mold test takes place after 3 weeks of incubation at 29 ° C +/- 1 ° C.
  • Table 1 Results of the AD test against mold and algae in the case of exterior emulsion paint based on PVAc (color no. 1)

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

L'invention concerne des agents biocides ayant une excellente action fongicide et algicide, composés d'au moins un algicide, de propiconazole et d'un composé propargylique iodé, de préférence. De préférence, au moins l'un des ingrédients actifs est lié, de préférence micro-encapsulé.
EP15713489.1A 2014-04-04 2015-03-31 Agents biocides Withdrawn EP3125688A1 (fr)

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EP14163600.1A EP2926659A1 (fr) 2014-04-04 2014-04-04 Moyen biocide
PCT/EP2015/057128 WO2015150430A1 (fr) 2014-04-04 2015-03-31 Agents biocides

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CN109776548B (zh) * 2018-11-14 2020-08-21 浙江农林大学 一种生物质基分子胶囊囊壁材料及利用其制备缓释灭藻微胶囊的方法
WO2020099567A1 (fr) * 2018-11-16 2020-05-22 Lonza Ltd Biocides encapsulés
PL3669654T3 (pl) * 2018-12-18 2022-02-21 Lanxess Deutschland Gmbh Mikrokapsułki zawierające OIT w kombinacji z propikonazolem i/lub IPBC
CN110679591B (zh) * 2019-10-28 2021-09-21 上海悦联生物科技有限公司 一种农药组合物及其制备方法
CN111117327B (zh) * 2020-01-18 2022-02-08 浙江先拓环保科技有限公司 一种粉末防霉剂及其制备方法
JP7454386B2 (ja) * 2020-01-27 2024-03-22 三菱鉛筆株式会社 筆記具用水性インク組成物
JP7324720B2 (ja) * 2020-01-27 2023-08-10 三菱鉛筆株式会社 抗菌粒子水分散体
CN117597489A (zh) * 2021-05-21 2024-02-23 特洛伊技术第二股份有限公司 用于湿态细菌控制的增强的ipbc
EP4436382A1 (fr) * 2021-11-24 2024-10-02 Viance, LLC Compositions de traitement du bois, procédés d'utilisation et bois traité
CN115161201B (zh) * 2022-05-26 2024-03-19 珠海元育生物科技有限公司 一种栅列藻藻株及其培养方法和用途
CN117802623B (zh) * 2023-12-29 2024-09-17 河北金友新材料科技有限公司 一种改性聚乙烯干法纺丝制备双组份抑菌es短纤维的工艺
CN119060591B (zh) * 2024-09-02 2025-09-05 中南林业科技大学 一种功能化水性涂料及其制备方法

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SG11201608171UA (en) 2016-11-29
US20170215421A1 (en) 2017-08-03
MX2016012993A (es) 2017-01-20
CN106163282A (zh) 2016-11-23
EP2926659A1 (fr) 2015-10-07

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