EP2618661A2 - Procédé pour protéger des plantes vivantes d'insectes nuisibles avec une structure plane - Google Patents

Procédé pour protéger des plantes vivantes d'insectes nuisibles avec une structure plane

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Publication number
EP2618661A2
EP2618661A2 EP11757892.2A EP11757892A EP2618661A2 EP 2618661 A2 EP2618661 A2 EP 2618661A2 EP 11757892 A EP11757892 A EP 11757892A EP 2618661 A2 EP2618661 A2 EP 2618661A2
Authority
EP
European Patent Office
Prior art keywords
insecticide
sheet
plants
impregnated
plant
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Withdrawn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
EP11757892.2A
Other languages
German (de)
English (en)
Inventor
Thomas ZÜHLKE
Lars Weichel
Michael Habermann
Christian Tomiczek
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 EP11757892.2A priority Critical patent/EP2618661A2/fr
Publication of EP2618661A2 publication Critical patent/EP2618661A2/fr
Withdrawn legal-status Critical Current

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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
    • 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
    • A01N25/34—Shaped forms, e.g. sheets, not provided for in any other sub-group of this main group
    • 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
    • A01N25/08—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 containing solids as carriers or diluents
    • A01N25/10—Macromolecular compounds
    • 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
    • A01N47/02—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 no bond to a nitrogen 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
    • A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur

Definitions

  • the subject of the present invention is a method of protecting live plants from harmful insects by covering with a sheet impregnated with an insecticide the surface of the stem, pseudo-trunk, branch, root ball and / or root area of the plant.
  • a further subject matter is living plants in which the surface of the stem, pseudophor, branch, root ball, and / or root area of the plant is covered with a fabric which is impregnated with an insecticide.
  • the invention also relates to a rectangular sheet which is impregnated with an insecticide and which contains a fastening means which, after tubular covering of the surface of the trunk, pseudobunk or branch of a plant, allows it to be permanently held thereon.
  • insects require living parts of plants for their reproduction or development. For example, Bark beetle and rape beetle in living parts of plants to lay eggs there. Certain insect species, such as e.g. Plants harmful butterflies, longhorn beetles and European beetles lay their eggs on plant parts and the hatching larvae go into woody, living plant parts for their further development. Other insects eat on leaves, needles but also on bark.
  • cork oaks For cork oaks, the valuable cork should be protected from the ingress of cork oak beetle.
  • Various insects hibernate in the bark of living trees and migrate in spring to feed in the treetops. Even in the root area itself and around plants live active pests (such as citrus longhorn beetle, cockchafer, leaf wasp and weevil), which are to prevent the hatching or excursion as well as bark and trunk feeding.
  • Object of the present invention was to find a method for the protection of living plants, such as trees and shrubs, from harmful insects.
  • the object has been achieved by a method for protecting live plants from insect pests by covering them with a fabric impregnated with an insecticide, the surface of the trunk, pseudo-trunk, branch, root ball and / or root area of the plant.
  • Living plants are plants that are biologically active and intact. They are different from dead plants that can not grow anymore. Usually, the roots of living plants have contact with substrate, for example, the soil or substrate in pots. Trees in a growth break, e.g. in winter are also considered living plants. Root-bare plants, such as bare-root trees, can also be living plants as long as they are biologically active and intact.
  • All plants are suitable, which have at least one trunk, pseudo trunk, or branch. Further suitable plants are those with a root ball of at least 3 cm (preferably at least 10 cm, and particularly preferably at least 30 cm) in diameter, for example trees and shrubs. Furthermore, plants having a root area of at least 20 cm in diameter (preferably at least 50 cm) are suitable as plants, for example trees and shrubs.
  • Preferred plants are trees such as conifers (such as pine, spruce, Douglas fir, larch, pine, fir, cedar, stone pine) and deciduous trees (such as maple, acacia, birch, pear, beech, oak (such as cork oak), alder, aspen, ash , Icy berry, hazel, hornbeam, cherry, chestnut, linden, American walnut, poplar, sycamore, peach, olive, robinia, elm, walnut, gum, zebrano, willow, Turkey oak).
  • Particularly preferred plants are deciduous trees.
  • Preferred deciduous trees are fruit trees, such as pome fruit (eg apple, pear, quince, spout [Sorbus domestica]), stone fruits (eg cherry, sour cherry, plum, plum, peach, apricot, nectarine), or as stalks pulled berry fruit (eg currants, gooseberries), with pome fruit and stone fruit being preferred.
  • pome fruit eg apple, pear, quince, spout [Sorbus domestica]
  • stone fruits eg cherry, sour cherry, plum, plum, peach, apricot, nectarine
  • stalks pulled berry fruit eg currants, gooseberries
  • pome fruit and stone fruit being preferred.
  • oaks such as cork oaks are preferred deciduous trees.
  • the plant organs stem, pseudo trunk and branch are known in the art. Also anatomically similar to a stem shaped parts of a plant are understood as a sham trunk.
  • the root ball
  • the diameter of stem, pseudo trunk and branch are usually at least 0.5 cm, preferably at least 2 cm and more preferably at least 5 cm.
  • the root zone of a plant is usually the area in the vicinity of the plant where its roots are wide. This is preferably a circle-like area around the plant on the earth's surface.
  • the surface is covered by the root ball of the plant.
  • the surface is covered by the root region of the plant.
  • the sheet covers the surface of the trunk, pseudo trunk, branch, root ball, and / or root area.
  • cover means that the fabric has at least partially surface contact with the surface.
  • the sheet has at least partially surface contact with the surface.
  • at least 10%, preferably at least 50%, particularly preferably at least 70%, and especially at least 90%, of the fabric have surface contact with the surface.
  • the fabric covers the surface in the process of the invention for a period of at least one week, preferably at least one month, more preferably at least three months, most preferably at least six months, and especially at least twelve months.
  • the sheet can cover the surface for up to 10 years, preferably up to 3 years.
  • Textile materials for example a cotton or polyester fabric
  • non-textile plastic materials paper, leather, artificial leather, plastic film (for example made of polypropylene, polyethylene, polystyrene or cellulose) and others, preferably flexible ones, are suitable as the textile fabric Materials.
  • the fabric usually has an area of at least 0.001 m 2 , preferably of at least 0.005 m 2 and particularly preferably of at least 0.05 m 2 .
  • the area can be up to 100.0 m 2 , preferably up to 30.0 m 2 , particularly preferably up to 3.0 m 2 .
  • the sheet used is preferably a textile material, in particular nets 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.
  • Natural fibers include cotton, jute or linen fibers.
  • 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).
  • PET polyethylene terephthalate
  • the fibers may be mono-, oligo- or multifilaments, which may be smooth or textured.
  • 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, for example, ethylene or propylene and also 1-butene, 2-butene, isobutene, 1-pentene, 1-hexene, 1-heptene, 1-octene, styrene or ⁇ -methylstyrene. Serve 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 one polypropylene or polyethylene having a melt flow index MFR (230 ° C, 2.16 kg) of 0.1 to 60 g / 10 min. It is preferably polypropylene with a melt flow index M FR (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 to 0.3 mm.
  • 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 that the mesh may indeed have smaller deviations with regard to shape and the size of the mesh, but that the values do not scatter excessively around the mean values.
  • the mesh size of the mesh can be varied widely, for example from 0.5 mm to 25 mm, preferably from 1 mm to 20 mm.
  • Preferred mesh sizes are in the range of 5 mm, preferably 2.5 mm, in particular 1.5 mm as the 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 0.1 to 0.99 mm, preferably 0.1 to 0.9 mm, more 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 is a regular hexagon with three equal sides, each having the same distance of not more than 0.99 mm to each other.
  • I h a 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 + hc + 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.
  • an octagon elongated in one direction is formed.
  • the effect of insect or air permeability is similar to the parallelogram.
  • combinations of quadrangular and octagonal meshes can also be used or the shape and size of the meshes can be varied in parts of the mesh.
  • the edges of the mesh may be knitted more densely, or thicker textile fibers, also made of a different polymer, may be intermittently acted upon 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, respectively Textile mesh materials according to this embodiment of the invention are described in WO 2010/012671.
  • the thickness of the fibers used for producing the textile material according to the invention are selected by the person skilled in the art according to the desired properties of the net.
  • the fiber thickness should be such that the net has at least 20%, preferably at least 40% and in particular 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.
  • impregnating means any type of treatment of the fabric with at least one insecticide 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 sheet or, preferably, mono- or multifilaments or fibers from which the sheet is produced, with at least one insecticide together with a binder (variant A).
  • the binder is used to fix the insidicide 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 network). 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.
  • they may be binders which can be obtained by polymerization of ethylenically unsaturated monomers, preferably at least one monomer selected from (meth) acrylates, in particular C 1 to C 12 esters of (meth) acrylic acid, crosslinking groups (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.
  • monomers preferably at least one monomer selected from (meth) acrylates, in particular C 1 to C 12 esters of (meth) acrylic acid, crosslinking groups (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 additionally comprises 1 to 20% by weight of (meth) acrylic acid or additional (meth) acrylic acid derivatives (B) containing functional groups.
  • 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.%.
  • a binder which contains 70 to 90% by weight of an acrylic ester in which R 2 comprises 4 to 8 C atoms and is preferably n-butyl and / or 2-ethylhexyl, and furthermore 10 to 20% by weight of acrylonitrile, 1 to 10% by weight 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.
  • R 1 is H or CH 3 , preferably H, and
  • 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 ethyl, n-butyl or 2-ethylhexyl, very particularly preferred are 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 at least one monomer from the group N-methylol acrylamide, N-methylolmethacrylamide, ⁇ , ⁇ '-Bismethylolmalein Acidklarediamid and ⁇ , ⁇ '- Bismethylolfumarklarediamid is used.
  • N-methylolacrylamide and N-methylolmethacrylamide Preference is given to N-methylolacrylamide and N-methylolmethacrylamide, in particular N-methylolmethacrylamide.
  • one or more monomers preferably one or two monomers of the group acrylic acid, methacrylic acid, vinylsulfonic acid, maleic acid and fumaric acid are used. 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 8 -alkylene, preferably C 2 -C 6 -alkylene and
  • R 4 , R 5 are identical 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 acetoacetoacetyl acrylate, acetoacetyl methacrylate, acrylamide, methacrylamide, maleic acid diamide, N-methoxy methylacrylamide, Nn-butoxymethylacrylamide, 3-hydroxypropyl acrylate, 3-hydroxypropyl methacrylate, 4-hydroxybutyl acrylate, 4-hydroxybutyl methacrylate, 6-hydroxyhexyl acrylate, 6-hydroxyhexyl methacrylate, 2-acrylic acid. hydroxy-3-chloropropyl ester, methacrylic acid-3-hydroxy-3-chloro-propyl ester, glycidyl acrylate and glycidyl methacrylate. Particularly preferred are acrylamide, 3-hydroxypropyl methacrylate, butanediol monoacrylate acetylacetate, glycidyl methacrylate and 4-acryloxybenzophenone.
  • Suitable monomers of group B4B allyl acrylate, Acrylklaremethallylester, allyl methacrylate, Methacrylcic acid diallyl ester, ma- be leinticaimethylallylester, Fumarticachureallylester, Fumar Vietnameseklaremethallylester, phthalic klarediallylester, Phthal Acidimethylallylester, diallyl terephthalate, Te- rephthal Acidimethallylester, p-divinylbenzene, butane-1, 4-diol diallyl ether and Butane-1, 4-diol dimethallylether used.
  • 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.
  • component B5B 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;
  • Wt .-% in particular 0 or 5 to 26 wt .-% of component B5
  • Suitable processes are known to the person skilled in the art and are described, for example, in WO 2005/064072 (page 20, line 20 to page 23, line 15).
  • 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 termination 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. Particular preference is given to polydimethylsiloxanes, poly (methylphenylsiloxanes) and corresponding compounds in which part of the methyl groups has been replaced by higher alkyl groups.
  • the molecular weight is preferably between 1000 and 150,000.
  • the silicone oils, and especially waxes, consistency regulators, e.g. Metal soaps such as lithium stearate, fumed silica, PTFE, boron nitride or urea contain 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.
  • 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. The exact 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 other 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.
  • H MDI 1,6-hexamethylene diisocyanate
  • the amount of free isocyanate groups is about 1 1 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.
  • additives are mentioned in WO 2008/052913 page 35, line 17 to page 37, line 5.
  • dyes and pigments can exert a warning effect, for example on birds or mammals, or cause camouflage of the insecticide nets against insects.
  • dark colors can cause desired shading and reduce the harmful effect of UV light on active ingredients and textile fibers in outdoor applications.
  • 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 Um- far harmfulness.
  • 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 networks that are exposed outdoors or in greenhouses increased UV irradiation.
  • 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. But they can also, for example in polyolefins and polyesters, already be incorporated in the course of 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 admixing at least one insecticide to form a polymer and coextrusion of polymer and at least one insecticide into a monofilament which is processed into the sheet according to the invention (variant B).
  • the impregnation is carried out by incorporating at least one insecticide directly into a monofilament, e.g. is processed into fibers of which the sheet according to 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 if appropriate, mixtures of the stated polymers with one another or with thermoplastic elastomers.
  • polyethylene eg, low density polyethylene (LDPE) such as linear low density polyethylene (LLDPE), ultra low density polyethylene Density (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, for example poly (ethylene-methyl methacrylate), poly (ethylene-vinyl acetate) or poly (ethylene-acrylic acid), and mixtures of such polymers and copolymers.
  • LDPE low density polyethylene
  • LLDPE linear low density polyethylene
  • ULDPE ultra low density polyethylene Density
  • MDPE medium density polyethylene
  • HDPE high density polyethylene
  • polyethylene resins such as copolymers of ethylene and alpha o
  • thermoplastic elastomers examples include olefin and styrene based thermoplastic elastomers. Preference is given on the one hand to copolymers with ethylene or propylene as the main component, and on the other hand to block copolymers comprising polystyrene and polyisoprene and / or polybutadiene blocks and hydrogenated derivatives of such copolymers.
  • an insecticide and the plastic may be mixed by melt-kneading. It is also possible first to prepare a masterbatch by means of melt kneading corresponding amounts of insecticide and plastic, which is then diluted to the desired concentration by melt kneading with a further quantity of plastic. If the masterbatch method is used, it is also possible to use different plastics for the masterbatch and the subsequent dilution, for example an LLDPE for the masterbatch and an HDPE for diluting the masterbatch.
  • the plastic composition optionally contains a powdery carrier material, preferably from the group of talcs, kaolin, clays, finely powdered S1O2 carbon and dextrins.
  • a powdery carrier material preferably from the group of talcs, kaolin, clays, finely powdered S1O2 carbon and dextrins.
  • the content of pulverulent carrier material, if present, is preferably from 0.01 to 10% by weight.
  • the powdery carrier material can be mixed with the insecticide mixture and the plastic by melt kneading, preferably first the insecticide mixture and the powdery material are mixed and then, for example by melt kneading, mixed with the plastic. 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.
  • plastic, insecticide and optionally further additives are mixed by melt kneading, preferably at elevated temperatures, extruded and processed into pellets.
  • Such pellets can be cast into filament by melt spinning or by the extrusion method, from which, according to the Raschel method, nets according to the invention can be weaved. Details of net material and its production for this embodiment of the invention are described, for example, in WO 2008/00471 1.
  • insecticide all known insecticides come into consideration. Particularly suitable insecticides are the following already known active substances (see "The Pesticide Manual", Edition 2003, EC Tanlin):
  • Carbamates for example alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb,
  • Organophosphates for example acephates, azamethiphos, azinphos (-methyl, -ethyl), bromophos-ethyl, bromfenvinfos (-methyl), butathiofos, cadusafos, carbophenothione, chloroethoxyfos, chlorfenvinphos, chloroformes, chlorpyrifos (- methyl / -ethyl), Coumaphos, Cyanofenphos, Cyanophos, Chlorfenvinphos, Demeton-S-methyl, Demeton-S-methylsulphone, Dialifos, Diazinon, Dichlofenthione, Dichlorvos / DDVP, Dicrotophos, Dimethoate, Dimethylvinphos, Dioxabenzofos, Disulfone, EPN, Ethion, Ethoprophos, Etrimfos, Famphur, Fenamiphos, Fenitrothion, Fen
  • Pyrethroids for example acrinathrin, allethrin (d-cis-trans, d-trans) s beta
  • Oxadiazines for example Indoxacarb.
  • Chloronicotinyls for example acetamipride, clothianidin, dinotefuran, imidacoloride, nitenpyram, nithiazines, thiacloprid, thiamethoxam, nicotine, bensultap and cartap.
  • Organochlores for example camphechlor, chlordane, endosulfan, gamma-HCH, HCH, heptachlor, lindane and methoxychlor,
  • Fiproles for example, acetoprole, ethiprole, fipronil, pyrafluprole, pyriprole and vaniliprole.
  • Mectins for example avermectin, emamectin, emamectin benzoate, ivermectin and milbemcycin.
  • juvenile hormone mimetics for example, diofenolan, epofenonans, fenoxycarb, hydroprene, kinoprenes, methoprenes, pyriproxifen and triprene.
  • Amidrazone in question In another form suitable as insecticides Amidrazone in question. Amidrazones, their preparation and their insecticidal activity are well known (see, for example, EP 604 798 A1, JA Furch et al., "Amidrazone: A New Class of Coleopteran Insecticides", ACS Symposium Series 686, Am. Chem. Soc, 1998 18, p. 178 et seq., And DG Kuhn et al., "Cycloalkyl-substituted Amidrazones: A Novel Class of Insect Control Agents", ACS Symposium Series 686, Am. Chem. Soc., 1998, Chapter 19, p 185 ff.). Particularly suitable amidrazones are described in claim 7 of EP 0 604 798 B1, which are hereby incorporated by reference.
  • insecticides which are active against wood pests, in particular against bark and wood-breeding beetle species.
  • these include, for example, such as pyrethroids (eg alpha-cypermethrin).
  • fipronil eg alpha-cypermethrin
  • fipronil e.g alpha-cypermethrin
  • chlorfenapyr e.g. pyrethroids
  • particularly preferred insecticides are alpha-cypermethrin, deltamethrin and permethrin, fipronil, amidrazone and chloroflavin.
  • the insecticides are selected from alpha-cypermethrin, deltamethrin, permethrin, fipronil, and chlorfenapyr.
  • Very particularly preferred insecticides are alpha-cypermethrin, deltamethrin and permethrin.
  • Specially preferred insecticide is alpha-cypermethrin.
  • the insecticide is chlorphenapyr.
  • the sheet is impregnated with an insecticide, for example one, two or three insecticides.
  • insecticide for example one, two or three insecticides.
  • it is impregnated with one or two insecticides, especially with an insecticide.
  • the fabric may contain, in addition to at least one insecticide, other pesticides, such as fungicides, herbicides and / or growth regulators.
  • the amount of insecticide per square meter of fabric depends on the desired duration of the activity and the potency of the insecticide and can be adjusted by a person skilled in the art.
  • the amount can be from 0.1 to 1000 mg / m 2 .
  • the amount of chlorfenapyr is usually 50 to 150 mg / m 2 , preferably 70 to 130 mg / m 2 , particularly preferably 90 to 1 10 mg / m 2 .
  • the amount of alpha-cypermethrin is usually 50 to 150 mg / m 2 , preferably 70 to 130 mg / m 2 , particularly preferably 90 to 1 10 mg / m 2 .
  • the amount of deltamethrin is usually 15 to 45 mg / m 2 , preferably 20 to 40 mg / m 2 , particularly preferably 25 to 35 mg / m 2 .
  • the amount of permethrin is usually 50 to 750 mg / m 2 , preferably 75 to 650 mg / m 2 , particularly preferably 100 to 550 mg / m 2 .
  • the amount of lambda-cyhalothrin is usually 5 to 30 mg / m 2 , preferably 7.5 to 25 mg / m 2 , particularly preferably 10 to 20 mg / m 2 . If chlorphenapyr is used in admixture with a pyrethroid, the amount ratio of chlorfenapyr: pyrethroid is 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 ⁇ , preferably 50 nm to 8 ⁇ , more preferably 50 nm to 4 ⁇ , in particular 50 nm to 500 nm.
  • the dormitornmatrial may contain in addition to the insecticide additionally at least one insect repellent component.
  • suitable insect-repellent components are, for example, ⁇ , ⁇ -diethyl-meta-toluamide (DEET), N, N-diethylphenylacetamide (DEPA), 1- (3-cyclohexan-1-yl-carbonyl) -2-methylpiperine, (2- hydroxymethylcyclohexyl) acetic acid lactones, 2-ethyl-1,3-hexanediol, indalon, methyl neodecanamide (MN DA), ⁇ +/-) - 3-allyl-2-methyl-4-oxocyclopent-2 - (+) - enyl - (+) - transchrysantemate (e-biothrin), limonene, eugenol, (+) eucamalol (1), (-) - l -epi-eucamalol, extracts
  • the insect repellent components and the other pesticides can already be applied to the fabric in advance, for example by spraying a textile material (for example with Fendona® from BASF SE, a spray containing alphacypermethrin).
  • a textile material for example with Fendona® from BASF SE, a spray containing alphacypermethrin.
  • Fendona® dip-it-yourself from BASF SE a preparation containing alphacypermethrin for impregnating nets from textile fibers
  • K-0 TAB® 1 -2-3 from Bayer Crop Science
  • Sheets impregnated with an insecticide are commercially available, especially textile fiber nets.
  • Examples are Interceptor® from BASF SE (polyester mesh impregnated with alphacypermethrin), DuraNet® from Clarke Moquito Control Products Inc. (polyethylene mesh impregnated with alphacypermethrin), Dawa Plus ⁇ from Tanna Netting Co. Ltd. (Polyester net impregnated with deltamethrin), NetProtect® from Bestnet Europe Ltd.
  • 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).
  • insects from the orders Diptera, Siphonaptera, Blattaria, Blattodea, Dermaptera, Hemiptera, Hymenoptera, Orthoptera, Isoptera, Thysanura, Phthiaraptera, Araneida, Lepidoptera, Coleoptera and Acarina, as well as the classes Chilopoda and Diplopoda.
  • Preference is given to insect pests of the order Diptera, Hemiptera, Hymenoptera, Acarina, Lepidoptera, Coleoptera and Siphonaptera.
  • insect pests of the order Lepidoptera and Coleoptera are especially preferred.
  • Examples of harmful insects are:
  • Insects of the order Lepidoptera such as Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Cameraria ohridella, Capua reticulana, Cheimatobia brumata, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias indulsana, Elasmopalpus lignosellus, Estigmene acrea, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranea, Galleria mellonella, Grapholitha funebrana,
  • Beetle (Coleoptera), such as Agrilus sinuatus, Agrilus viridis, Agrilus bigutattus, Agrilus planetipennis, Agriotes lineatus, Agriotes obscurus, Amphimallus solstitialis, Anisandrus dispar, Anoplophora glabripennis, Anoplphora chinensis, Anoplpophora sp., Anthonomus grandis, Anthonomus pomorum , Aphthona euphoridae, Athous haemorrhoidalis, Atomaria linearis, Blastophagus piniperda, Blitophaga undata, Bruchus rufimanus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata, Ceuthorrhynchus assimilis, Ceuth
  • Termites such as Calotermes flavicollis, Leucotermes flavipes, Heterotermes aureus, Reticulitermes flavipes, Reticulitermes virginicus, Reticulitermes lucifugus, Termes natalensis, and Coptotermes formosanus,
  • Cockroaches (Blattaria - Blattodea), like.
  • Blattella germanica Blattella asahinae, Periplantenta americana, Periplaneta japonica, Periplaneta brunnea, Periplaneta fuligginosa, Peri- planeta australasiae, and Blatta orientalis; true beetles (Hemiptera including homoptera) such as Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Eushtistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis, Thy- perdatorum, Acyrthosiphon onobry
  • Ants, bees, wasps, hymenoptera such as Athalia rosae, Atta cephalotes, Atta capiguara, Atta cephalotes, Atta laevigata, Atta robusta, Atta sexdens, Atta texana, Crematogaster spp., Hoplocampa minuta, Hoplocampa testudinea, Monor- norium pharaonis , Solenopsis geminata, Solenopsis invicta, Solenopsis, Solenopsis xyloni, Pogonomyrmex barbatus, Pogonomyrmex californicus, Pheidole megacephala, Dasymutilla occidentalis, Bombus spp.
  • Ants, bees, wasps, hymenoptera such as Athalia rosae, Atta cephalotes, Atta capiguara, Atta cephalotes
  • Vespula squamosa Paravespula vulgaris, Paravespula pennsylvanica, Paravespula germanica, Dolichovespula maculata, Vespa crabro, Polistes rubiginosa, Camponotus floridanus, and Linepithema humile,
  • Arachnoid such as arachnids (Acarina), for example the families Argasidae, Ixodidae and Sarcoptidae, such as Amblyomma americanum, Amblyomma variegatum, Ambryomma maculatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Dermacentor silvarum, Dermacentor andersoni, Dermacentor variabilis, Hyalomma truncatum , Ixodes ricinus, Ixodes rubicundus, Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus, Ornithodorus moubata, Ornithodorus hermsi,
  • Ornithodorus turicata Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes ovis, Rhipicephalus sanguineus, Rhipicephalus appendiculatus,
  • Tetranychidae spp. such as Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae, Panonychus ulmi, Panonychus citri, and Oligonychus pratensis; Araneida, e.g.
  • Silverfish, sting fish such as Lepisma saccharina and Thermobia domestica
  • Centipede Centipede (Chilopoda), such as Scutigera coleoptrata, Millipedes (Diplopoda), like Narceus spp.,
  • Ear creepers such as forficula auricularia, lice (Phthiraptera), such as Pediculus humanus capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus eurysternus, Haematopinus suis, Linognathus vituli, Bovica bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus,
  • Nematodes such as Heterodera glycines, H. avenae, H. schachtii, H. trifolii, H. gottingiana, H. cajani, H. zeae, Globodera rostochiensis, G. pallida, G. tabacum., Meloidogyne arenaria, M. incognita, M. javanica, M. hapla, M. chitwoodi, Ditylenchus destructor, D. dipsaci, D. angustus, Anguina tritici, A. agrostis, Afrina / Anguina wevelli, Pratylenchus penetrans, P. brachyurus, P.
  • pest insects of the order Lepidoptera are those of the family Gracillariidae, especially the subfamilies Thaumetopoeinae, Cossinae, Zeuzerinae, Larentinae, Ennominae.
  • Particularly preferred pest insects of the order Lepidoptera are oak processiffy spinner (Thaumetopoea processionea), pine processducy spinner (Thaumetopoea pityocampa), willow borer (Cossus cos- sul), blue screen (Zeuzera pyrina), sponge spinner (Lymantria dispar), horse chestnut miner moth (Cameraria ohridella), oak winder (Tortrix viridana), Small Frostspanner (Operophtera brumata), and Large Frostspanner (Erannis defoliaria).
  • pest insects of the order Coleoptera are those of the family Curculionidae, Bupraestoidae, Cerambycidae, Scarabaeidae, and Hemiptera, especially the subfamilies Scolytinae, Molytinae, Rhynchophorinae, Agrilinae; Buprestinae, Lamiinae, Melonthinae and Tinginae.
  • Particularly preferred pest insects of the order Coleoptera are book printers (Ips typographus), oak chip beetle (Scolytus intricatus), large elm beetle (Scolytus scolytus), engraver (Pityogenes chalcographus), giant beetle (Dentroctonus micans), mountain pine beetle (Dendroctonus ponderosae), large brown weevil (Hylobius abietis ), Greenrod (Phyllobius spec), palm weevil (Rhynchophorus ferrugineus), beech tree beetle (Agrilus viridis), deciduous beetle (Agrilus spec), white oak bumblebee (Coraebus undatus), poplar ibex (Saperda spec), Asian longhorned beetle (Anoplophora glabripennis), citrus beetle ( Anopolophora
  • the method according to the invention for protecting live cork oaks from harmful insects is suitable by covering the surface of the trunk and / or branch of the cork oaks with a fabric impregnated with an insecticide.
  • the present invention further relates to living plants in which the surface of the stem, pseudobunk, branch, root ball, and / or root area of the plant is covered with a sheet impregnated with an insecticide.
  • the present invention further relates to a rectangular sheet (especially a network of textile fibers) which is impregnated with an insecticide and contains a fastening means which, after tubular covering of the surface of the stem, pseudobunk or branch of a plant, allows it to be permanently held thereon.
  • a rectangular sheet especially a network of textile fibers
  • a fastening means which, after tubular covering of the surface of the stem, pseudobunk or branch of a plant, allows it to be permanently held thereon.
  • the fastening means comprises, for example, an adhesive material, a band, a cord or a hook-and-loop fastener, preferably a hook-and-loop fastener.
  • the attachment means usually connects the adjacent corners when the sheet is in tubular form.
  • the shape of the rectangular sheet is largely rectangular, e.g. square, or trapezoidal. Usually at least two opposite edges are largely parallel. The edges may each have a length of 1 cm to 10.0 m, preferably 5 cm to 5.0 m, and especially 10 cm to 2.5 m.
  • the sheet has a height of 30 cm to 5.0 m, preferably 50 cm to 3.0 m, and particularly preferably 80 cm to 2.2 m
  • the length is usually set to cover the circumference of the stem, pseudo trunk, or branch, usually from 10 cm to 5.0 cm m, preferably at 30 cm to 3.0 m and more preferably at 50 cm to 1, 5 m.
  • the fabric has a height of 0.5 cm to 50 cm, preferably 2 cm to 30 cm, and particularly preferably 4 cm to 20 cm dimensioned to cover the circumference of the trunk, pseudo trunk, or branch, and is usually from 10 cm to 5.0 m, preferably from 30 cm to 3.0 m, and more preferably from 50 cm to 1.5 m.
  • the present invention further relates to a sheet (especially a network of textile fibers) which is impregnated with an insecticide, in the form of a perforated disc, the a continuous interruption between the outer and inner edge.
  • the continuous interruption can be designed as a largely radial cut.
  • the shape of the perforated disc may be circular, oval, square, rectangular, or similar to one of these shapes.
  • the shape of the hole in the perforated disc may be circular, o-val, square, rectangular, or similar to one of these shapes. It is also possible to make the hole in the form of at least one cut (eg a cross cut). In a preferred embodiment, the perforated disc and the hole is substantially circular.
  • the diameter of the hole in the perforated disc is usually 0.1 cm to 2 m, preferably 10 cm to 1, 0 m and especially 30 cm to 80 cm.
  • the diameter of the perforated disc is usually 10 cm to 30 m, preferably 1, 0 m to 20 m, and especially 2.0 m to 10.0 m.
  • the diameter of the hole in the perforated disc is of course smaller than the diameter of the perforated disc.
  • the perforated disc is largely rectangular.
  • the edges may each have a length of 50 cm to 30 m, preferably 1, 0 m to 20 m, and especially 2.0 m to 10.0 m.
  • the edge of the hole may be provided with an elastic material optionally comprising a hook and loop fastener.
  • the perforated disc can be fixed in the area of the outer edge with conventional pegs or the like in the ground.
  • the present invention further relates to the use of the fabrics according to the invention for the protection of living plants from harmful insects.
  • the present invention offers a wide variety of advantages: it is possible to protect individual plants or certain parts of plants from the harmful effects of the insects in a very targeted and precise manner. There is no contamination of the environment, as is the case for example in the spray application. This protects the environment and makes it possible to use it even where there are currently restrictions on the use of insecticides to protect water or certain organisms.
  • the plants are efficiently protected from entering the bark or in the wood of living or brooding insects or insectivorous insects.
  • the insect pests are usually killed by contact with the net. The process is less expensive due to the long-lasting effect and less expensive in the long term than the regular spraying with insecticides.
  • the fabric in the form of fibers is permeable to air, so that there is no impairment of the living plants. Examples
  • Example 1 Tree trunk covered with high net
  • Embodiment 1 uses an Interceptor® mesh from BASF SE impregnated with alphacypermethrin (polyester mesh, 75 denier, 155 mesh, 200 mg alphacypermethrin / m 2 ).
  • the rectangular net has a length of 180 cm and a height of 160 cm.
  • the net is wrapped around the trunk (about 30 cm diameter) of a tree so that it covers the surface of the trunk from the ground up to a height of 180 cm above the ground.
  • the net is fixed to the trunk by a commercial adhesive tape which is glued about 10 cm above the ground and 180 cm above the ground around the trunk and the net covering it.
  • a cord, rubber band or a band (elastic or non-elastic) with Velcro can be used instead of the tape.
  • the Interceptor® net it is also possible to use a DuraNet®, Dawa Plus, NetProtect®, Iconet®, Olyset® or Lifenet®.
  • a Complion® mesh from BASF SE can be used instead of the Interceptor® mesh.
  • Example 2 Tree trunk covered with net in cuff form
  • nets are used as in Example 1.
  • the rectangular net has a length of 20 cm and a height of 10 cm.
  • the net is wrapped around the trunk (about 3 cm diameter) of a tree so that it covers the surface of the trunk at a height of 20 cm (alternatively 60 or 160 cm) above the ground in a width of 10 cm.
  • the net is fixed to the trunk by a commercially available adhesive tape.
  • a cord, rubber band or a band (elastic or non-elastic) with Velcro can be used instead of the tape.
  • the net may be knotted in cuff form at the ends.
  • Example 3 - Tree trunk covered with high net incl. Velcro
  • Example 3 the nets of Example 1 at the top and bottom are provided with a 2 cm wide and 100 cm long bands one side of a hook and loop fastener. At the top and bottom right corner there is a 2 cm wide and 10 cm long band on the opposite side of the hook and loop fastener near the end of the 100 cm long band. This net can now be wrapped around the tree trunk. For attachment, the short end of the band at the corners must now be brought into contact with the long band, so that the Velcro closes. This ensures a secure hold on the tree trunk.
  • Example 4 Root area covered with round net
  • an Interceptor® net is used in the form of a perforated disk with an outer diameter of 5.0 m and a diameter of the hole of 10 cm, wherein is a radial section between the inner hole and the outer edge.
  • the perforated disc is placed around a tree trunk (about 15 cm in diameter) on the ground above the root area, so that the trunk comes to rest in the area of the hole.
  • a tree trunk about 15 cm in diameter
  • the Interceptor® net it is also possible to use a DuraNet®, Dawa Plus, NetProtect®, Iconet®, Olyset® or Lifenet®.
  • a Complion® mesh from BASF SE can be used.
  • Examples 1 to 4 instead of the Interceptor® net, a dark green colored LLIN net is used based on a 100 denier polyester yarn with 45-50 holes per cm 2 , and with 100 mg alpha-cypermethrin per m 2 net area.

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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)
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  • Environmental Sciences (AREA)
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Abstract

La présente invention a pour objet un procédé pour protéger des plantes vivantes d'insectes nuisibles en couvrant avec une structure plane qui est imprégnée d'un insecticide la surface du tronc, du pseudo-tronc, des branches, des racines avec la motte et/ou de la zone racinaire de la plante. L'invention a pour autre objet des plantes vivantes dont la surface du tronc, du pseudo-tronc, des branches, des racines avec la motte et/ou de la zone racinaire de la plante est recouverte d'une structure plane qui est imprégnée d'un insecticide. L'invention concerne également une structure plane rectangulaire qui est imprégnée d'un insecticide et comporte un moyen de fixation qui, après recouvrement tubulaire de la surface du tronc, pseudo-tronc ou branche d'une plante, permet un maintien durable sur celle-ci. L'invention concerne également une structure plane, qui est imprégnée d'un insecticide et a la forme d'une plaque perforée qui présente une interruption continue entre le bord extérieur et le bord intérieur. Enfin, elle concerne aussi l'utilisation de la structure plane pour protéger des plantes vivantes d'insectes nuisibles.
EP11757892.2A 2010-09-23 2011-09-21 Procédé pour protéger des plantes vivantes d'insectes nuisibles avec une structure plane Withdrawn EP2618661A2 (fr)

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EP11757892.2A EP2618661A2 (fr) 2010-09-23 2011-09-21 Procédé pour protéger des plantes vivantes d'insectes nuisibles avec une structure plane

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EP10178770 2010-09-23
PCT/EP2011/066388 WO2012038460A2 (fr) 2010-09-23 2011-09-21 Procédé pour protéger des plantes vivantes d'insectes nuisibles avec une structure plane
EP11757892.2A EP2618661A2 (fr) 2010-09-23 2011-09-21 Procédé pour protéger des plantes vivantes d'insectes nuisibles avec une structure plane

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EP2763536B1 (fr) * 2011-08-22 2016-08-10 Romano Natur GmbH Composition antiparasitaire à activité élevée contre rhynchophorus ferrugineus
CN104396637B (zh) * 2014-10-31 2016-08-24 云南省烟草公司昆明市公司 一种群集式烟草害虫的田间防控方法
MY187947A (en) 2015-04-17 2021-10-31 Basf Agrochemical Products Bv Method for controlling non-crop pests
WO2016195048A1 (fr) * 2015-06-05 2016-12-08 住友化学株式会社 Filet cylindrique et procédé de protection de plantes
WO2018102669A1 (fr) * 2016-12-02 2018-06-07 University Of Florida Research Foundation, Inc. Pesticides incorporés dans un revêtement durable à traitement anti-moustiques de contenants de type peler/coller
IT202100014189A1 (it) * 2021-05-31 2022-12-01 Sachim Srl Supporto in polietilene cui è legato un idrogel caricato con un principio attivo naturale antiparassitario
CN114107368B (zh) * 2021-11-29 2023-05-26 重庆大学 表达反式菊酸的联合表达载体及其在调控番茄vi型腺体腺毛合成反式菊酸中的应用

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2602640A1 (fr) * 1986-08-12 1988-02-19 Decaix Roland Dispositif de protection contre les insectes grimpants
US6108968A (en) * 1998-09-30 2000-08-29 Peng; Hai-Sung Device for exterminating garden pests

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3820464A1 (de) 1988-06-16 1990-02-08 Basf Ag Neue benzophenonderivate und deren herstellung
DE69126969T2 (de) * 1990-04-18 1998-03-05 Procter & Gamble Zusammensetzungen zur bekämpfung von läusen
FR2663502A1 (fr) * 1990-06-20 1991-12-27 Decaix Roland Dispositif de protection des vegetaux contre les insectes.
MY131441A (en) 1992-12-29 2007-08-30 American Cyanamid Co Amidrazones and their use as insecticidal and acaricidal agents
WO1998053663A2 (fr) * 1997-05-30 1998-12-03 Neal Daniel J O Systeme d'apport d'agents horticoles
BR0005598B1 (pt) * 1999-09-16 2013-03-19 mÉtodo para proteger uma planta crescendo contra insetos rastejantes.
KR100764071B1 (ko) 2000-12-06 2007-10-08 시바 스폐셜티 케미칼스 홀딩 인코포레이티드 염색성 폴리올레핀 섬유 및 직물
TR200401424T2 (tr) * 2001-12-22 2004-11-22 DCT�ApS BöcekÁöldürücüÁbattaniye
US20050132500A1 (en) 2003-12-22 2005-06-23 Basf Aktiengesellschaft Composition for impregnation of fibers, fabrics and nettings imparting a protective activity against pests
DE102005062793A1 (de) 2005-12-28 2007-07-05 Basf Ag Stabilisierung von in Polypropylen gelösten Farbstoffen gegenüber Abbau durch Licht
JP2008013508A (ja) 2006-07-07 2008-01-24 Sumitomo Chemical Co Ltd 害虫防除材
DE102006034208B3 (de) * 2006-07-25 2007-10-31 Thomas Merschmann Baumschutzmanschette
JP2008100920A (ja) * 2006-10-17 2008-05-01 Arysta Lifescience Corp 害虫駆除材
EP2079298A1 (fr) 2006-11-03 2009-07-22 Basf Se Procédé et dispositif de protection des plants de récolte
JP2008222554A (ja) * 2007-03-08 2008-09-25 Furukawa Electric Co Ltd:The 害虫駆除テープおよび害虫駆除方法
FR2925825A1 (fr) * 2007-12-28 2009-07-03 Ct De Cooperation Internat En Procede de protection des cultures de legumes feuilles contre les acariens
US9288978B2 (en) * 2008-07-30 2016-03-22 Basf Se Insecticide-impregnated nets and use thereof for protecting against pests
JP2010057476A (ja) * 2008-08-06 2010-03-18 Sumitomo Chemical Co Ltd 害虫防除ネット

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2602640A1 (fr) * 1986-08-12 1988-02-19 Decaix Roland Dispositif de protection contre les insectes grimpants
US6108968A (en) * 1998-09-30 2000-08-29 Peng; Hai-Sung Device for exterminating garden pests

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2012038460A2 *

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TW201216858A (en) 2012-05-01
EA201300390A1 (ru) 2013-10-30
MX2013003299A (es) 2013-07-22
AU2011306963A1 (en) 2013-05-02
AR083087A1 (es) 2013-01-30
KR20130106844A (ko) 2013-09-30
BR112013006895A2 (pt) 2016-07-12
WO2012038460A3 (fr) 2012-09-07
CN103220909A (zh) 2013-07-24
JP2013542926A (ja) 2013-11-28
CA2812229A1 (fr) 2012-03-29
WO2012038460A2 (fr) 2012-03-29

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