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EP2451282A2 - Structure plane insecticide comprenant un mélange de chlorfenapyr et un pyrethrinoïde - Google Patents

Structure plane insecticide comprenant un mélange de chlorfenapyr et un pyrethrinoïde

Info

Publication number
EP2451282A2
EP2451282A2 EP10728239A EP10728239A EP2451282A2 EP 2451282 A2 EP2451282 A2 EP 2451282A2 EP 10728239 A EP10728239 A EP 10728239A EP 10728239 A EP10728239 A EP 10728239A EP 2451282 A2 EP2451282 A2 EP 2451282A2
Authority
EP
European Patent Office
Prior art keywords
pyrethroid
chlorfenapyr
mixture
sheet
pets
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.)
Ceased
Application number
EP10728239A
Other languages
German (de)
English (en)
Inventor
Hartmut Leininger
Susanne Stutz
Ulrich Karl
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.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Priority to EP10728239A priority Critical patent/EP2451282A2/fr
Publication of EP2451282A2 publication Critical patent/EP2451282A2/fr
Ceased 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
    • A01N43/34—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
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • 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
    • A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
    • C08G18/6266—Polymers of amides or imides from alpha-beta ethylenically unsaturated carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78—Nitrogen
    • C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
    • C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00—General methods for the manufacture of artificial filaments or the like
    • D01F1/02—Addition of substances to the spinning solution or to the melt
    • D01F1/10—Other agents for modifying properties
    • 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
    • D06M13/395—Isocyanates
    • 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
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters 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
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/285—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides
    • 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
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/285—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides
    • D06M15/29—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides containing a N-methylol group or an etherified N-methylol group; containing a N-aminomethylene group; containing a N-sulfidomethylene group
    • 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
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/31—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated nitriles
    • 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
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • 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
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/36—Biocidal agents, e.g. fungicidal, bactericidal, insecticidal agents

Definitions

  • the invention relates to a fabric, in particular a net which has been coated with a pyrethroid-containing active compound mixture, for the protection of humans and domestic animals against noxious insects, in particular mosquitoes, as well as a method for protecting humans and pets from insect pests and diseases transmitted by them.
  • Mosquito nets impregnated with insecticides have proven to be particularly effective in controlling vector-borne diseases such as malaria, yellow fever, dengue fever, lymphatic filariasis and leishmaniasis.
  • vector-borne diseases such as malaria, yellow fever, dengue fever, lymphatic filariasis and leishmaniasis.
  • use of such nets for example, is one of the pillars of the Global Roll Back Malaria Partnership project and is recommended by the World Health Organization (WHO).
  • WHO World Health Organization
  • the nets must be so impregnated that the insecticidal effect is not lost even after a large number of washes.
  • Corresponding nets treated with specific insecticide-binder combinations are also referred to as LLINs (Long Lasting Insecticidal Nets).
  • pyrethroids are used almost exclusively as insecticides because this class of insecticides not only has a high lethal effect for the insects with at the same time lower toxicity for mammals, but the insect is also put out of action by a rapid paralysis before it becomes an insect Sting and thus the transmission of the disease can come (so-called knock-down effect).
  • the long-standing and increasing use of pyrethroids also carries the risk of an increased occurrence of resistance, especially since these insecticides are also used in agriculture for controlling crop pests. For example, in West and East Africa pyrethroid resistance has spread to Anopheles gambiae and in South Africa to Anopheles funestus.
  • Chlorfenapyr which has a good action against Anopheles mosquitoes, is only slightly toxic to humans and has a different mechanism of pyrethroids (decoupling of oxidative phosphorylation in mitochondria, mitochondrial electron transport inhibitor, METI) has (see, eg. N'Guessan et al., Acta Tropica 102 (2007) 69-78, FW Mosha et al., Tropical Medicine and International Health 13 (5) 2008 644-652, R. N'Guessan et al., Tropical Medicine and International Health 14 (4) (2009) 1-7).
  • the invention therefore relates to a fabric impregnated with an insecticidal mixture containing a) Chlorfenapyr and
  • alpha-cypermethrin (b1), deltamethrin (b2), permethrin (b3) and lambda-cyhalothrin (b4), in an amount of (in each case based on the sheet)
  • the invention further relates to the use of the fabric according to the invention for the protection of humans and domestic animals against insect pests and vector-borne diseases.
  • a sheet according to the invention is characterized by simple manufacture and, in particular in the form of nets, a simple application.
  • Nets according to the invention have a good insecticidal activity, even after repeated washing, even against insects resistant to pyrethroid pests.
  • the insecticidal fabrics show favorable toxicological values and allow effective control even of pesticides resistant insect pests.
  • Insecticides According to the invention, a mixture containing, preferably essentially consisting of, in particular consisting of chlorfenapyr and at least one of said pyrrethroids, is used.
  • alpha-cypermethrin alpha-cypermethrin, deltamethrin, permethrin and / or lambda-cyhalothrin.
  • alpha-cypermethrin alpha-cypermethrin, deltamethrin and permethrin.
  • alpha-cypermethrin Preference is given to the use of a binary mixture of chlorfenapyr and one of the pyrethroids mentioned, but it is also possible to use chlorfenapyr mixed with several, preferably two, pyrethroids.
  • the amounts of insecticide per square meter of fabric are generally and preferably as follows:
  • Chlorfenapyr (a): 50 to 150 mg / m 2 , preferably 70 to 130 mg / m 2 , more preferably 90 to 110 mg / m 2 ; alpha-cypermethrin: 50 to 150 mg / m 2 , preferably 70 to 130 mg / m 2 , more preferably 90 to 110 mg / m 2 ; Deltamethrin: 15 to 45 mg / m 2 , preferably 20 to 40 mg / m 2 , more preferably 25 to 35 mg / m 2 ;
  • Permethrin 50 to 750 mg / m 2 , preferably 75 to 650 mg / m 2 , more preferably 100 to 550 mg / m 2 ; lambda-cyhalothrin: 5 to 30 mg / m 2 , preferably 7.5 to 25 mg / m 2 , particularly preferably 10 to 20 mg / m 2 .
  • the amount ratio of chlorfenapyr: pyrethroid is thus - depending on the active ingredient - generally 0.06-30: 1, preferably 0.1-10: 1, more preferably 0.1-5: 1.
  • the particle size of the insecticides in the aqueous formulation is generally from 50 nm to 20 .mu.m, preferably from 50 nm to 8 .mu.m, more preferably from 50 nm to 4 .mu.m, in particular from 50 nm to 500 nm.
  • Textile materials, non-textile plastic materials, paper, leather, artificial leather, films and other, preferably flexible materials are suitable as a sheet.
  • the sheet used is preferably a textile material, in particular nets made of textile fibers. These may be nets made of natural fibers or synthetic fibers. Of course, it may also be mixtures of two or more different fibers. Examples of natural fibers include cotton, jute or linen fibers. Preferably, they are synthetic fibers of suitable polymers. Examples include polyamides, polyesters, polyacrylonitrile or polyolefins. Preference is given to polyamides, polyolefins and polyesters, particularly preferably polyolefins, in particular polypropylene or polyethylene, and polyesters. Very particular preference is given to polyester fibers, in particular polyethylene terephthalate (PET). The fibers may be mono-, oligo- or multifilaments, which may be smooth or textured.
  • PTT polyethylene terephthalate
  • Polypropylene and polyethylene may be polypropylene or polyethylene homopolymers, respectively. However, it may also be copolymers which comprise, in addition to the ethylene or propylene, small amounts of other comonomers. Suitable comonomers may in particular be other olefins such as ethylene or propylene and 1-butene, 2-butene, isobutene, 1-pentene, 1-hexene, 1-heptene, 1-octene, styrene or ⁇ -methylstyrene, dienes and / or polyenes act. The proportion of comonomers in the polyethylene or polypropylene is generally not more than 20% by weight, preferably not more than 10% by weight. The type and amount of the comonomers are chosen by the skilled person depending on the desired properties of the fiber.
  • Particularly preferred for fiber production are relatively high molecular weight, viscous products, which are characterized in the usual way by their melt flow index (determined according to ISO 1133). It may preferably be at least a polypropylene or polyethylene having a melt flow index MFR (230 0 C, 2.16 kg) of 0.1 to 60 g / 10 min act. Preference is given to polypropylene having a melt flow index MFR (230 ° C., 2.16 kg) of 1 to 50 g / 10 min, more preferably 10 to 45 g / 10 min and, for example, 30 to 40 g / 10 min. Such types of polypropylene are particularly suitable for the production of fibers. Of course, a mixture of several different types of polypropylene can be used.
  • the textile fibers have a thickness of 0.05 to 0.6 mm, preferably 0.1 mm to 0.4 mm, particularly preferably 0.12 to 0.35 mm and very particularly preferably 0.2 up to 0.3 mm.
  • the textile material is used for example in the form of covers or covers, for example for duvet covers, mattresses, pillows, curtains, wall coverings, carpets, window, cabinet and door curtains, blankets, tarpaulins and tarpaulins.
  • the preferably used nets preferably have a pattern of meshes with an even number of corners.
  • the nets may in this case preferably consist only of a single type of stitches, for example, only quadrangular or only hexagonal stitches, or they may also comprise two or more types of different stitches, for example a combination of octagonal and square stitches.
  • the meshes of the net should in this case preferably be substantially similar, ie the mesh may indeed have smaller deviations with regard to shape and the size of the mesh, but the values do not scatter excessively around the mean values.
  • Suitable mesh sizes are in the range of 5 mm, preferably 2.5 mm, in particular 1.5 mm as an upper limit and 0.1 mm, preferably 0.25 mm, particularly preferably 0.5 mm, in particular 0, 7 mm as lower limit.
  • the meshes of the net are preferably selected from the group of square, hexagonal or octagonal meshes.
  • the square meshes are meshes in the form of a parallelogram with sides a and b.
  • the term "parallelogram” also includes the terms “rectangle” and "square.”
  • the smaller angle between the two sides of the parallelogram is generally between 60 and 90.degree ..
  • the parallelogram is one Rectangle:
  • the height h a is the length of the side a.
  • Square meshes are particularly preferred ,
  • a net comprising octagonal stitches therefore additionally comprises at least a second sort of stitches. These can be quadrilateral meshes.
  • the height h a in both the parallelogram, the hexagon and the octagon is 0.1 to 0.99 mm, preferably 0.1 to 0.9 mm, particularly preferably 0.12 to 0.8 mm and most preferably 0.25 to 0.7 mm.
  • the length-to-height ratio b / h a is 1: 1 to 5: 1, preferably 1: 1 to 4: 1 and particularly preferably 2: 1 to 4: 1.
  • the mesh in the case of a ratio b / h a, can be 1: 1 by a square with a side length of 0.1 to 0.99 mm.
  • a larger ratio of b / h a is an elongated structure in one direction. The distance h a of 0.99 mm maximum smaller insects are effectively prevented from passing through the network, while the length may well be greater than 0.99 mm, so that the air permeability of the network is not unduly hindered.
  • the ratio ((h b + h c ) / 2) / h a is 1: 1 to 5: 1, preferably 1: 1 to 4: 1 and particularly preferably 2: 1 to 4: 1.
  • the situation here is analogous to the parallelogram.
  • a ratio of 1: 1 it is a regular hexagon with three equal sides, each having the same distance of not more than 0.99 mm from each other.
  • an elongated hexagon is formed in one direction.
  • the effect in terms of insect or air permeability is like the parallelogram.
  • the ratio ((h b + h c + h d ) / 3) / h a is 1: 1 to 5: 1, preferably 1: 1 to 4: 1 and more preferably 2: 1 to 4: 1.
  • the situation here is analogous to the parallelogram.
  • a ratio of 1: 1 is a regular octagon with four equal sides, each having the same distance of not more than 0.99 mm to each other.
  • a larger ratio ((h b + h c + h d ) / 3) / h a arises an octagon elongated in one direction.
  • the effect with regard to insect or air permeability is similar to that of the parallelogram.
  • edges of the net may be knitted more densely, or thicker textile fibers, which are also made of a different polymer, may be used at intervals for stabilization.
  • the terms “height” and “length” refer to the open area of each stitch without regard to the fibers or coated fibers.
  • the term “mesh size” in the sense of this invention means the mesh size of the mesh, i.e. the open area of each mesh without regard to the fibers or the coated fibers.
  • the thickness of the fibers used to produce the textile material according to the invention is chosen by the person skilled in the art according to the desired properties of the net.
  • the fiber thickness should be such that the net at least 20%, preferably at least 40% and in particular has at least 50% open area. Networks of the type described are commercially available.
  • the networks used may preferably be single-layer networks. However, they can also be so-called spacer fabrics in which two nets are connected to each other by means of monofilaments in a double layer.
  • Impregnation means any type of treatment of the fabric with the insecticide mixture, by which a homogeneous distribution of the mixture on or in the fabric is achieved.
  • homogenous means that the concentration of a particular insecticide is essentially the same at each point of the surface.
  • the impregnation is carried out by coating the fabric or, preferably, mono- or multifilaments or fibers from which the fabric is made, with the insecticide mixture together with a binder (Variant A).
  • the impregnation is effected by mixing the insecticide mixture into a polymer and coextrusion of the polymer and insecticide mixture into a monofilament which is processed into the sheet according to the invention (variant B).
  • the binder is used for fixing the insecticide mixture on the mono- or multifilaments or fibers from which the fabric is produced, or on the end-of-line coating (described below using the example of a net). This ensures that the active ingredient can not be washed or at least only very slowly.
  • the polymeric binder can be any desired binder, provided that the binders are capable of fixing the insecticide mixture, in particular, on textile materials. Preference is therefore given to binders which are known from the field of textile impregnation and textile coating. Of course, a mixture of several, different binders can be used. Examples include (meth) acrylates comprising homo- or copolymers, polyurethanes, polyisocyanurates or waxes, such as polyethylene waxes.
  • binders which can be obtained by polymerization of ethylenically unsaturated Momonere, preferably at least one monomer selected from the group of (meth) acrylates, in particular d- to Ci2-esters of (meth) acrylic acid, crosslinking group-containing ( Meth) acrylates, (meth) acrylic acid, maleic acid or esters of maleic acid, acrylonitrile, styrene, vinyl acetate, vinyl alcohol, ethylene, propylene, allyl alcohol or vinyl chloride.
  • suitable radicals R 2 include in particular methyl, ethyl, n-butyl or 2-ethylhexyl radicals, preferably ethyl, n-butyl or 2-ethylhexyl radicals.
  • the copolymer further comprises 1 to 20% by weight of (meth) acrylic acid or additional functional group-containing (meth) acrylic acid derivatives (B).
  • This may in particular be a (meth) acrylic ester and / or (meth) acrylamide.
  • the functional groups serve to bind the binders on the nets and can also be used for networking.
  • ethylenically unsaturated, preferably monoethylenically unsaturated, monomers (C) other than A and B for example acrylonitrile or styrene.
  • the amount of further monomers is generally 0 to 30 wt.%.
  • R 2 comprises 4 to 8 C atoms and is preferably n-butyl and / or 2- Ethylhexyl- and furthermore 10 to 20 wt.% Of acrylonitrile, 1 to 10 wt.% Of (meth) acrylic acid or a functional group-containing (meth) acrylic acid derivative, in particular (meth) acrylic acid methylolamide.
  • binders can be prepared by methods known to those skilled in the art, preferably by means of emulsion polymerization.
  • an acrylate binder in particular a copolymer, obtainable by emulsion polymerization of components B1 to B4 and optionally B5.
  • component B1 one or more, preferably 1, 2 or 3, more preferably 1 (meth) acrylate (s) of the formula (I) are used,
  • R 1 is H or CH 3 , preferably H, and
  • n-C 10 -alkyl is C 1 -C 10 -alkyl, preferably methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, t-butyl, n-pentyl, sec-pentyl, neopentyl, 1, 2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl or n-decyl, particularly preferably methyl, ethyl, n-butyl or 2- Ethylhexyl, most preferably ethyl, n-butyl or 2-ethylhexyl.
  • component B1 Preferred as component B1 are methyl acrylate, ethyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate and methyl methacrylate. Also preferred are butyl acrylate alone or in admixture with methyl methacrylate or ethyl acrylate. Especially preferred is n-butyl acrylate.
  • Component B2 is at least one monomer selected from the group consisting of N-methylolacrylamide, N-methylolmethacrylamide, N, N'-bismethylolmaleic acid diamide and N, N'-
  • N-methylolacrylamide and N-methylolmethacrylamide Preference is given to N-methylolacrylamide and N-methylolmethacrylamide, in particular N-methylolmethacrylamide.
  • Component B3 used is one or more monomers, preferably one or two monomers of the group of acrylic acid, methacrylic acid, vinylsulfonic acid, maleic acid and fumaric acid. Preference is given to acrylic acid and methacrylic acid; Acrylic acid is particularly preferred.
  • component B4 one or more monomers, preferably one or two monomers from groups B4A and / or B4B are used.
  • Monomers of group B4A are those of the formula (II) and / or (III),
  • Z is CONH 2 , CONH-CH 2 -OR 5 , COO-Y-OH, COO-glycidyl, CHO, CO-Y-OH, preferably CONH 2 ;
  • Y is C 1 -C 6 -alkylene, preferably C 2 -C 6 -alkylene and
  • R 4 , R 5 are the same or different and are a linear or branched C 1 -C 10 -alkyl group; and (meth) acryl-modified benzophenones, as described, for example, in EP-A 0 346 734.
  • Preferred monomers of group B4A are acryetoacetyl acrylates, acetoacetate esters, acrylamide, methacrylamide, maleic acid diamide, N-methoxymethylacrylamide, Nn-butoxymethylacrylamide, 3-hydroxypropyl acrylate, 3-hydroxypropyl methacrylate, 4-hydroxybutyl acrylate, methacrylic acid 4-hydroxybutyl ester, 6-hydroxyhexyl acrylate, 6-hydroxyhexyl methacrylate, hydroxy-3-hydroxypropyl acrylate, 3-hydroxy-3-chloropropyl methacrylate, glycidyl acrylate and glycidyl methacrylate.
  • acrylamide 3-hydroxypropyl methacrylate, butanediol monoacrylate-acetylacetate, glycidyl methacrylate and 4-acryloxybenzophenone.
  • Preferred monomers of group B4 are those of group B4A, wherein the use of one or two monomers from this group is preferred.
  • Preferred monomers of group B5 are those of group B5A, as well as vinylaromatic monomers from group B5B.
  • component B5A it is preferred to use acrylonitrile or methacrylonitrile, preferably acrylonitrile.
  • styrene and ⁇ -methylstyrene are preferred, particularly preferred is styrene.
  • acrylonitrile is used as the monomer of component B5 for the preparation of the acrylate binder.
  • the acrylate binder (B) is obtainable by emulsion polymerization of (data in% by weight are in each case based on the total amount B): b1) 20 to 93 wt .-%, preferably 50 to 90 wt .-%, particularly preferably 60 to 90 Wt .-%, in particular 75 to 85 wt .-%, of component B1;
  • Wt .-% in particular 1 to 3 wt .-% of component B3;
  • component B5 0 to 40 wt .-%, preferably 5 to 40 wt .-%, particularly preferably 5 to 30 wt .-%, in particular 0 or 5 to 26 wt .-% of component B5
  • the weight-average molecular weight of the resulting non-crosslinked emulsion polymers is generally between 40,000 and 250,000 (determined by GPC (gel permeation chromatography)).
  • the molecular weight is generally controlled by the use of chain terminating reagents, for example organosulfur compounds, in conventional amounts.
  • the particularly preferred acrylate binder is generally obtained in the form of an aqueous dispersion and is usually used in this form in the insecticidal formulation according to the invention.
  • the preferred acrylate binder may further include conventional additives known to those skilled in the art, for example, film formers and / or plasticizers, e.g. Adipates, phthalates, butyldiglycol, mixtures of diesters, obtainable by reaction of dicarboxylic acids with straight-chain or branched alcohols. Suitable dicarboxylic acids and alcohols are known to the person skilled in the art.
  • silicone oils and waxes, polysiloxanes, resins having fluorinated hydrocarbon radicals, melamine-formaldehyde condensates, methylol-urea derivatives and curable polyesters are also suitable, with silicone oils being preferred.
  • the preferred silicone oils and waxes are generally linear or cyclic polyorganosiloxanes, preferably polyalkyl and / or phenylsiloxanes, where alkyl is, for example, methyl, ethyl, propyl or octyl, preferably methyl. Particularly preferred are polydimethylsiloxanes, poly (methylphenylsiloxanes) and corresponding compounds in which a part of the methyl groups is replaced by higher alkyl groups.
  • the molecular weight is preferably between 1000 and 150,000.
  • the silicone oils and especially waxes may contain consistency regulators, for example metal soaps such as lithium stearate, highly dispersed silicic acid, PTFE, boron nitride or urea, in order to achieve a pasty or fat-like consistency.
  • consistency regulators for example metal soaps such as lithium stearate, highly dispersed silicic acid, PTFE, boron nitride or urea, in order to achieve a pasty or fat-like consistency.
  • the binders can be used in the form of a formulation in a solvent, preferably as an aqueous formulation.
  • the invention also includes solvent-free formulations.
  • aqueous formulations which contain 55 to 99% by weight of water, preferably 85 to 98% by weight of water and 1 to 45% by weight, preferably 2 to 15% by weight, of solids the sum of all components in the formulation are related.
  • concentration also depends on the adsorption capacity of the textile substrate.
  • the solids are at least one binder, the insecticidal mixture, optionally at least one crosslinker and optionally further components.
  • At least one water-dispersible crosslinker is preferably used.
  • the preferred acrylate binder it is preferably a crosslinker which has free isocyanate groups.
  • These may preferably be isocyanurates which have free isocyanate groups, preferably isocyanurates, which are derived from aliphatic, cycloaliphatic or aromatic diisocyanates having 4 to 12 carbon atoms. Examples include 1,6-hexamethylene diisocyanate, 1,12-dodecane diisocyanate, 2,2 '. and 2,4'-dicyclohexylmethane diisocyanate or 2,4-toluene diisocyanate.
  • isocyanurates based on 1,6-hexamethylene diisocyanate. Particular preference is given to isocyanurates which have additional hydrophilic groups, in particular polyethylene oxide groups.
  • the preparation of such isocyanurates is known to the person skilled in the art. They are preferably used dissolved in polar aprotic solvents, such as ethylene carbonate or propylene carbonate. Further details of the preferred isocyanate group-containing crosslinkers are disclosed in WO 2008/052913, page 34, line 6 to page 35, line 3.
  • an isocyanurate based on 1,6-hexamethylene diisocyanate which has additional polyethylene oxide groups, the isocyanurate being dissolved in propylene carbonate (70% by weight HMDI in propylene carbonate).
  • the amount of free isocyanate groups is about 11 to 12 wt.%, Based on the solution.
  • the crosslinker is preferably used in an amount of 1 to 10 wt.% With respect to the amount of all solids of the formulation.
  • the crosslinkers based on isocyanurates are particularly suitable for crosslinking the abovementioned copolymers.
  • the formulation may further contain typical additives and adjuvants, UV protectants and dyes.
  • Wetting agents and thickeners can be used to achieve a uniform application of the treatment liquor in poorly and therefore inhomogeneously wettable fabrics, such as polyolefin fibers.
  • water-miscible solvents could be used, but this is not preferred because of the environmental impact.
  • the person skilled in the commonly used adjuvants and their concentrations are known.
  • the formulations may preferably comprise antioxidants, peroxide scavengers, UV absorbers and light stabilizers. This is particularly recommended for nets exposed to increased UV radiation outdoors or in greenhouses.
  • the additives mentioned protect both the substrate fibers and the active ingredients from radiation-induced decomposition.
  • UV absorbers are described, for example, in WO 02/46503 or in WO 2007/077101.
  • UV absorbers can be used on the one hand as a component of the formulation for impregnation. However, they can also be incorporated, for example in the case of polyolefins and polyesters, during the production of the fibers. It is also advantageous to use mixtures of several stabilizers which have different protective effects. Based on the weight of the untreated network, 0.2 to 5% by weight, preferably 0.25 to 4% and very particularly preferably 0.5 to 3.5% stabilizer are generally used. The amount in the formulation is adjusted accordingly by a person skilled in the art.
  • the impregnation is carried out by the mixture according to the invention is incorporated directly into a monofilament, which is for example processed into fibers of which the sheet of the invention consists or which are contained therein.
  • the fabric in this variant is a net.
  • thermoplastic polymers preferably based on olefinically unsaturated monomers, for example polyolefins, polyvinyl chloride, polyvinyl alcohols, poly (meth) acrylates, but also polyesters and polycarbonates , And optionally mixtures of said polymers with each other or with thermoplastic elastomers.
  • polyethylene such as low density polyethylene (LDPE) such as linear low density polyethylene (LLDPE), ultra low density polyethylene (ULDPE), medium density polyethylene (MDPE) and high density polyethylene (HDPE), polyethylene resins such as copolymers of ethylene and alpha-olefins having at least three carbon atoms, polypropylene homopolymers, random and block copolymers of propylene and alpha-olefins having four or more carbon atoms, copolymers of ethylene with unsaturated carboxylic acid compounds, eg poly (ethylene-methyl methacrylate) , Poly (ethylene-vinyl acetate) or poly (ethylene-acrylic acid), as well as mixtures of such polymers and copolymers.
  • LDPE low density polyethylene
  • LLDPE linear low density polyethylene
  • ULDPE ultra low density polyethylene
  • MDPE medium density polyethylene
  • HDPE high density polyethylene
  • polyethylene resins such as copolymers of ethylene and alpha-olef
  • thermoplastic elastomers examples include olefin and styrene based thermoplastic elastomers. Preference is given to copolymers with ethylene or propylene as the main component, to block copolymers containing polystyrene and polyisoprene and / or polybutadiene blocks and hydrogenated derivatives of such copolymers.
  • the insecticide mixture and the plastic may be mixed by melt-kneading. It is also first by melt kneading appropriate amounts of insecticide mixture and plastic masterbatch are prepared, which is then diluted by melt kneading with another amount of plastic to the desired concentration.
  • melt kneading appropriate amounts of insecticide mixture and plastic masterbatch are prepared, which is then diluted by melt kneading with another amount of plastic to the desired concentration.
  • different plastics for the masterbatch and the subsequent dilution for example an LLDPE for the masterbatch and an HDPE for diluting the masterbatch.
  • the synthetic material composition optionally contains a powdered carrier material, preferably from the group of talcs, kaolin, clays, finely powdered SiO 2 , carbon and dextrins.
  • a powdered carrier material preferably from the group of talcs, kaolin, clays, finely powdered SiO 2 , carbon and dextrins.
  • the content of pulverulent carrier material is - if present - preferably 0.01 to 10 wt .-%.
  • the pulverulent carrier material can be mixed with the insecticide mixture and the plastic by melt kneading, preferably the insecticide mixture and the powdery material are first mixed and then mixed with the plastic, for example by melt-kneading. More preferably, a mixture of the powdered material and the insecticide mixture is used to prepare a masterbatch.
  • the plastic composition optionally contains conventional additives to thermoplastic molding compositions, such as pigments, antioxidants, lubricants, etc.
  • thermoplastic molding compositions such as pigments, antioxidants, lubricants, etc.
  • insecticide and optionally further additives by melt kneading, preferably at elevated Temperatures, mixed, extruded and processed into pellets.
  • Such pellets can be cast into filament by melt spinning or the extrusion method, from which, according to the Raschel method, nets according to the invention can be weaved.
  • Inventive fabrics are suitable for the protection of humans and domestic animals against insect pests and against vector-transmitted diseases which are transmitted by the noxious insects.
  • Inventive fabrics are also suitable for controlling noxious insects, wherein the fabric according to the invention, preferably in the form of a net, is applied in a building.
  • a flexible sheet according to the invention, in particular a net is applied around a living being or an inanimate object which attracts pest insects as a possible source of food.
  • noxious insects comprises not only insects in the actual sense but also harmful, in particular as a vector for the transmission of diseases responsible arachnids (Arachnida).
  • the fabrics of the invention are particularly suitable for protection against or to combat health and storage pests from the orders Diptera, Siphonaptera, Blattaria, (Blattodea), Dermaptera, Hemiptera, Hymenoptera, Orthoptera, Isoptera, Thysanura, Phthiaraptera, Araneida and Acarina, and the Classes Chilopoda and Diplopoda. They are particularly suitable against Diptera, Hemiptera, Hymenoptera, Acarina and Siphonaptera.
  • Diptera such as Culicidae, Simuliidae, Ceratopogonidae, Tabanidae, Muscidae, Calliphoridae, Oestridae, Sarcophagidae, Hippoboscidae), Siphon naptera ⁇ Pulicidae, Rhopalopsyllidae, Ceratophyllidae) and Acarina ⁇ Ixodidae, Argasidae, Nuttalliellidae), especially against mosquitoes and flies.
  • Diptera such as Culicidae, Simuliidae, Ceratopogonidae, Tabanidae, Muscidae, Calliphoridae, Oestridae, Sarcophagidae, Hippoboscidae
  • Siphon naptera ⁇ Pulicidae, Rhopalopsyllidae, Ceratophyllidae
  • Acarina
  • the substrates according to the invention are suitable against:
  • Centipedes (Chilopoda), e.g. Scutigera coleoptrata,
  • Double Feet e.g. Narceus spp., Web spiders (Araneae), e.g. Latrodectus mactans, and Loxosceles reclusa, mites (Acaridida): e.g. Sarcoptes sp,
  • Parasitic mites ticks (Ixodida), e.g. Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus, Rhiphicephalus sanguineus, Dermacentor andersoni, Dermacenter variabilis, Amblyomma americanum, Ambryomma maculatum, Ornithodorus hermsi, Ornithodorus turicata and Mesostigmata, e.g. Ornithonyssus bacoti and Dermanyssus gallinae, termites (Isoptera), e.g.
  • Calotermes flavicollis Leucotermes flavipes, Heterotermes auerus, Reticulitermes flavipes, Reticulitermes virginicus, Reticulitermes lucifugus, Termes natalensis and Coptotermes formosanus,
  • Cockroaches e.g. Blattella germanica, Blattella asahinae, Periplaneta americana, Periplaneta japonica, Periplaneta brunnea, Periplaneta fuligginosa, Periplaneta australasiae and Blatta orientalis,
  • Diptera such as flies and gnats, eg Aedes aegypti, Aedes albopictus, Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Anopheles crucians, Anopheles albimanus, Anopheles gambiae, Anopheles freeborni, Anopheles leucosphyrus, Anopheles minimus, Anopheles quadrimaculatus, Calliphora vicina, Chrysomya bezziana, Chrysomya hominivorax, Chrysomia macellaria, Chrysops discalis, Chrysops silacea, Chrysops atlanticus, Cochliomyia hominivorax, Cordylobia anthropophaga, Culicoides furens, Culex piens, Culex nigripalpus, Culex quinquefasciatus, Culex tar
  • Earwigs e.g. Forficula auricularia
  • Hemiptera Beaked hens (Hemiptera), such as lice and bedbugs, e.g. Cimex lectularius, Cimex hemipterus, Reduvius senilis, Triatoma spp., Rhodnius prolixus and Arilus critatus,
  • Hymenoptera such as ants, bees, wasps and sawflies, e.g. Crematogaster spp., Hoplocampa minuta, Hoplocampa testudinea, Monomorium pharonnis, Solenopsis geminata, Solenopsis invicta, Solenopsis, Solenopsis xyloni, Pogonomyrmex barbatus, Pogonomyrmex californicus, Dasymutilla occidentalis, Bombus spp.
  • Vespula squamosa Paravespula vulgaris, Paravespula pennsylvanica, Paravespula germanica, Dolichovespula maculata, Vespa crabro, Polistes rubiginosa, Camponotus floridanus and Linepithema humile,
  • Spring bugs such as crickets, grasshoppers and grasshoppers, e.g. Acheta domestica, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femurrubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, No- madacris septemfasciata, Schistocerca americana, Schistocerca gregaria, Dociostaurus maroccanus, Tachycines asynamorus, Oedaleus senegalensis, Zonozerus variegatus, Histoglyphus daganensis, Kraussaria angulifera, Calliptamus italicus, Chortoicetes terminifera and Locusta na pardalina, fleas (Siphonaptera), eg Ctenocephalides felis, Ctenocephalides canis,
  • Zottenschwänze such as silverfish and Ofenfischchen, e.g. Lepisma sac- charina and Thermobia domestica,
  • Lice eg Pediculus humanus capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus eurystemus, Haematopinus suis, Linognathus vituli, Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus.
  • the substrate according to the invention is particularly preferably suitable for the protection against or control of mosquitoes (Culicidae), in particular the genera Anopheles, such as Anopheles gambiae, Anopheles stephensi, Anopheles funestus, Anopheles maculipennis, Anopheles claviger and Anopheles plumbeus; Aedes, as / Aedes aegypti (Stegomyia aegypti), Aedes albopictus; Culex, like Culex quinquefasciatus; Culiseta; Haemogoggus; Mansonia; Ochlerotatus; Psorophora; Sabethes; Toxorhynchites; Verralina; Wyeomyia andmaschinenomyia.
  • Anopheles such as Anopheles gambiae, Anopheles stephensi, Anopheles funestus, Anoph
  • the fabrics according to the invention are preferably suitable for protection against or for controlling Siphonaptera (fleas), in particular Tunga (sand fleas), such as Tunga penetrans.
  • Siphonaptera fleas
  • Tunga sand fleas
  • Tunga penetrans Particular preference is given to fabrics according to the invention, in particular nets, for controlling noxious insects which have resistance to either pyrethroids or chloroflavyrs, preferably pyrethroids.
  • Diseases whose transmission can be prevented are in addition to diseases caused by plasmodia, e.g. Malaria tropicana, Malaria tertiana and Malaria quartana, also diseases caused by parasitic worms, such as filariasis, dis- philosis, virus-induced diseases such as yellow fever, dengue fever, West Nile fever, Chikungunya fever, Rift Valley fever bacterial diseases such as tularemia and Chagas disease (South American trypanosomiasis) caused by the parasitic unicellular trypanosoma cruzi and transmitted by predatory bugs.
  • diseases caused by plasmodia e.g. Malaria tropicana, Malaria tertiana and Malaria quartana
  • diseases caused by parasitic worms such as filariasis, dis- philosis, virus-induced diseases such as yellow fever, dengue fever, West Nile fever, Chikungunya fever, Rift Valley fever bacterial diseases such as tularemia and Chagas disease (South American trypano
  • the fabrics according to the invention are also suitable for protecting crops to be stored, that is to say harvested plants or plant parts, if appropriate also in processed form.
  • the goods to be protected may be wood stacks, fruits, vegetables, cereals, cocoa beans, coffee beans or spices, for example.
  • the goods may still be bales. Examples include bales selected from the group of tea, tobacco or cotton.
  • Feed 2 contains 30 g of sodium peroxydisulfate dissolved in 39.9 g of H 2 O.
  • Table 1 Composition at feed 1 in% by weight pphm (parts per hundred monomers)
  • the amount of the initiator sodium peroxydisulfate is 0.3 part by weight, that of the emulsifier 0.4 part by weight Dowfax 2A1 (Dow) and 0.6 part by weight Lumiten IRA (BASF SE), based on 100 parts by weight of the monomer composition from Table 1.
  • Lumiten IRA
  • the nets used in each case for the experiments were impregnated with an aqueous formulation of the insecticide alpha-cypermethrin, the insecticide Chlorfenapyr, the acrylate binder A8 and an isocyanate-based crosslinker, dried and crosslinked at about 100 ° C. for 1 min.
  • the amount of insecticide as indicated in Table 2 is adjusted by (if necessary after squeezing off under defined conditions) determines the liquid uptake of the network and the concentration of the formulation that adjusts so as to obtain the desired amount per m 2 on the web ,
  • the amount of binder was adjusted according to the insecticidal content.
  • the treated nets were washed several times as indicated in Table 3.
  • the washing was carried out according to the "Montpellier washing procedure" (as described in the WHO WHO PVC, 3/07/2002 "Evaluation of wash resistance of long-lasting insecticidal nets”). It was based on the provision in WO 2005/064072, p 46 worked.
  • the samples were subjected to a biological test as described in WO 2005/064072, page 47. This biological test is in line with WHO's "Cone Test” (WHOPES 96.1) with minor adjustments.

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Abstract

L'invention concerne une structure plane, notamment un filet, imprégnée d'un mélange insecticide et contenant a) du chlorfenapyr et b) un ou plusieurs pyréthroïdes du groupe comprenant alpha-cyperméthrine (b1), deltaméthrine (b2), perméthrine (b3) et lambda-cyhalothrine (b4), en une quantité (chacune relativement à la structure plane) a) de 50 à 150 mg/m2 de chlorfenapyr; b1 ) de 50 à 150 mg/m2 d'alpha-cyperméthrine; b2) de 15 à 45 mg/m2 de deltaméthrine; b3) de 50 à 750 mg/m2 de perméthrine; b4) de 5 à 30 mg/m2 de lambda-cyhalothrine, cette structure plane étant appropriée à la lutte contre des insectes nuisibles dans les bâtiments et à la protection des êtres humains et des animaux domestiques contre de tels insectes nuisibles et contre des maladies vectorielles transmises par ces insectes nuisibles.
EP10728239A 2009-07-09 2010-07-05 Structure plane insecticide comprenant un mélange de chlorfenapyr et un pyrethrinoïde Ceased EP2451282A2 (fr)

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EP10728239A EP2451282A2 (fr) 2009-07-09 2010-07-05 Structure plane insecticide comprenant un mélange de chlorfenapyr et un pyrethrinoïde

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EP09165019 2009-07-09
EP09167790 2009-08-13
EP10728239A EP2451282A2 (fr) 2009-07-09 2010-07-05 Structure plane insecticide comprenant un mélange de chlorfenapyr et un pyrethrinoïde
PCT/EP2010/059557 WO2011003861A2 (fr) 2009-07-09 2010-07-05 Structure plane insecticide destinée à la protection d'êtres humains et d'animaux

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CN102480970A (zh) 2012-05-30
WO2011003861A2 (fr) 2011-01-13
CN102480970B (zh) 2016-01-20
ZA201200873B (en) 2013-05-29
WO2011003861A3 (fr) 2011-07-07
BR112012000491A2 (pt) 2015-10-06
CO6420394A2 (es) 2012-04-16
TW201105237A (en) 2011-02-16
US20120114727A1 (en) 2012-05-10
AR077470A1 (es) 2011-08-31
MX2012000334A (es) 2012-01-30
JP2012532841A (ja) 2012-12-20
KR20120052290A (ko) 2012-05-23

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