WO1990003112A1 - Lutte antiparasitaire - Google Patents

Lutte antiparasitaire Download PDF

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Publication number
WO1990003112A1
WO1990003112A1 PCT/GB1989/001160 GB8901160W WO9003112A1 WO 1990003112 A1 WO1990003112 A1 WO 1990003112A1 GB 8901160 W GB8901160 W GB 8901160W WO 9003112 A1 WO9003112 A1 WO 9003112A1
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WO
WIPO (PCT)
Prior art keywords
water
oil
pests
surfactant
cosurfactant
Prior art date
Application number
PCT/GB1989/001160
Other languages
English (en)
Inventor
Howard Bernard Dawson
Original Assignee
Nc Development, Inc.
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
Priority claimed from GB878707563A external-priority patent/GB8707563D0/en
Priority claimed from GB888801643A external-priority patent/GB8801643D0/en
Priority claimed from GB888822936A external-priority patent/GB8822936D0/en
Application filed by Nc Development, Inc. filed Critical Nc Development, Inc.
Priority to DE68913754T priority Critical patent/DE68913754T2/de
Priority to AT89911276T priority patent/ATE102432T1/de
Publication of WO1990003112A1 publication Critical patent/WO1990003112A1/fr
Priority to NO911242A priority patent/NO180701C/no
Priority to DK056891A priority patent/DK56891A/da
Priority to FI911555A priority patent/FI103859B1/fi

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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • 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
    • A01N25/02—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 liquids as carriers, diluents or solvents
    • A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels

Definitions

  • Crops that can be protected by means of the invention include tropical and temperate crops and pests which can be controlled by the invention include insect and acarine pests which infest these crops, public health pests and pests which infest or affect wood or timber and other building materials.
  • the invention relates to formulations of water-insoluble oil-soluble substances in water as small particles whose Z average mean size particle size is less than 200 nm.
  • the Z average mean size can be defined as the model free mean of light scattering.
  • Such formulations include microemulsions, micellar solutions and molecular solutions.
  • Microemulsions are one of three identified types of dispersion (as distinct from a molecular solution) of oil, water and surfactant.
  • oil is used in this specification to mean any non-aqueous solvent in which a substance of interest is soluble and which i ⁇ immiscible with water.
  • These three types of dispersion are: microemulsions, micellar solutions and normal emulsions (or macroemulsions) .
  • Macroemulsions appear white or opaque and are characterised by their property to separate into their two original liquid phases on standing; the average particle • diameter will generally be above 200 nm. Microemulsions and micellar solutions are translucent and do not separate. Microemulsions can be considered as having average droplet (or particle) diameters of from 10 to 200 nm, micellar solutions as having average particle diameters of from 2 nm to 10 nm and molecular solutions as having average particle diameters of less than 2 nm. Recent evidence, however, does suggest that microemulsions with droplet diameters below 10 nm are possible. As with macroemulsions, microemulsions can be of the water-in-oil (w/o) or oil-in-water (o/w) type and can be made to invert from one to another.
  • w/o water-in-oil
  • o/w oil-in-water
  • particle or droplet size (usually measured as averages) .
  • Average particle or droplet size may be measured with a laser particle sizer, such as the MALVERN AUTOSIZER 2c (Malvern Instruments, Malvern, Hereford & Worcester) using glass cells as sample containers.
  • nmr measurements are used to resolve theoretical questions regarding the state or location of molecules in microemulsions.
  • the line width for protons in molecules can indicate freedom of the molecules to thermal motion, the broadening of the line indicating greater restriction of motion.
  • the chemical shift of water is different when it is distributed in spheres or in cylindrical or lamellar micelles.
  • FR-A-2187226 corresponds to CA-A-1007985 and discloses insecti cidal compos itions compris ing an anionic surfactant and a hydrotrope.
  • FR-A-1026169 discloses various emulsions , which may be useful in formulating insecticides comprising an alkylsulphonate surfactant and a polar compound such as an alcohol , an amino, a phenol or an acid.
  • US-A-3954967 discloses "microcolloids" containing a resin and a polar solvent.
  • EP-A-0062181 corresponds to US-A-500348 and relates to apparently conventional emulsions containing high HLB surfactants .
  • EP-A-0107009 corresponds t CA-A-1209361 and relates to a development of the subj ect matter disclosed in EP-A- 0062 181 ; . again , emul s ions conta ining high HLB surfactants are disclosed.
  • EP-A-0149051 corresponds to US-A-4737520 also discloses certain emulsion formulations .
  • US-A-4567161 discloses l iquid active ingredient concentrates for the preparation of microemulsions .
  • the microemulsions are stated to be oil-in-water micro ⁇ emulsions .
  • the coemulsifiers are a particular class of glycerin esters having HLB (Hydrophil ic/Lipophilic Balance) values of between 12 and 18.
  • HLB Hydrophil ic/Lipophilic Balance
  • the formulations of US-A-4567161 are said to have special significance for pharmaceutical active substances .
  • the active ingredient can be a number of other substances including herbicides (a number of which are listed) , fungicides, insecticides, acaricides, nematocides or plant growth regulators. No specific fungicides, insecticides, acaricides, nematocides or plant growth regulators are disclosed or even suggested.
  • WO-A-8807326 published on 6th October 1988 and incorporated herein by reference, relates specifically to the use of pesticidal water-miscible formulations whose average particle sizes are at most 200 nm in the protection of cabbages and apples and/or in the control of grey aphid ⁇ on cabbages (Brevicorvne brassicae) , caterpillars on cabbages (Pieris brassicae) , Tortrix larvae in apples and blowfly larvae, and to the protection of stored grain against the lesser grain borer weevil (Rhysopertha dominical .
  • insecticide/acaricides such as pyrethroids (for example, deltamethrin, cypermethrin or permethrin) show good or enhanced biological activity in the protection against other temperate and tropical crops, particularly rice, maize, cotton, soya and fruit other than apples and/or in the control of pests detrimental to such crops, as well as activity against a range of public health pests including houseflies, cockroaches and mosquitoes and pests which infest or affect wood or timber and other building materials.
  • pyrethroids for example, deltamethrin, cypermethrin or permethrin
  • a method of protecting tropical and temperate crops, other than cabbages and apples comprising treating the crops, or a locus for the crops, with an insecticidal and/or acaricidal water- miscible formulation whose average particle size is at most 200 nm; the formulation may comprise water, an insecticidal and/or acaricidal oil, a surfactant and a cosurfactant, the cosurfactant preferably having an HLB of less than 12.
  • the crop to be protected may be, for example, rice, maize, cotton, soya and fruit other than apples.
  • a method of controlling insect pests of the order Lepidoptera other than Tortrix larvae and Pieris brassicae
  • Diptera Coleoptera.
  • Hemiptera other than Brevicorvne brassicae
  • Orthoptera Dictvoptera.
  • Hymenoptera or Isoptera and/or acarine pests comprising treating the pests, or a locus for the pests, with an insecticidal and/or acaricidal water-miscible formulation whose average particle size is at most 200 nm; the formulation may comprise water, an insecticidal and/or acaricidal oil, a surfactant and a cosurfactant, the cosurfactant preferably having an HLB of less than 12.
  • Lepidoptera Members of the order of Lepidoptera which can be controlled include the small cabbage white (Pieris rapae) butterfly, the diamond-back moth (Plutella xylostella) , the codling moth (Cydia pomonella) , cutworms (A ⁇ rotis spp) , the flour moth (Anagasta kuhniella) , Trichoplusia ni, Earias insulana. army worms (Spodoptera littoralis and S. exigua) , corn leaf worm (Heliothis armigera and H. virescens) , Chilo suppresalis and Bo byx mori.
  • Hemiptera which can be controlled include apids including the peach-potato aphid (Myzus persicae) , the black bean aphid (Aphis fabae) , the pea aphid ( Aery tho siphon psium) , the grain aphid (Sitobion avenae) , the rose-grain aphid (Metopholophium dirhodum) , the bird-cherry-oat aphid (Rhopalosiphum padi) , the glasshouse whitefly (Trialeurodes vaporariorum) , the cotton whitefly (Bemisia tabaci) , the rice leaf hopper (Nephatettix virescens) , the rice brown plant hopper (Nilaparvata lugens) and the green shield bug (Nezara viridula) .
  • apids including the peach-potato aphid (
  • Orthoptera which can be controlled include the house cricket (Achaeta domestica) and locusts (Schistocerca gregaria and Locusta migratoria) .
  • locusts Schocusta migratoria
  • Dictyoptera which can be controlled include cockroaches in the genera Blatta and Periplaneta.
  • Hvmenoptera Members of the order of Hvmenoptera which can be controlled include leaf cutting and other ants, including Atta sextans. Acrvomyrmex octospinosus , Megaphonera f oetens , Monomorium pharaoensis . Ecophylla longinoda, Chromatogaster sp . Myrmicaria eumenoides. and Camponotus sp.
  • a method of controlling public health pests particularly the house fly (Musca domestica) , cockroaches (Blatta spp. and Periplaneta spp.) and mosquito (Aedes aegypti) , the method comprising treating the pests, or a locus for the pests, with an insecticidal and/or acaricidal water-miscibl e formulation whose average particle size is at most 200 nm; the formulation may comprise water, an insecticidal and/or acaricidal oil, a surfactant and a cosurfactant, the cosurfactant preferably having an HLB of less than 12.
  • the invention lends itself to the treatment of wood or timber articles, for example to guard against the common furniture beetle, the house longhorn and the death watch beetle as discussed above.
  • Formulations of the invention are thus very suitable for treating roof and other structural timbers of buildings. This overcomes or mitigates the hitherto apparently insoluble problem of how to apply pesticide while avoiding high levels of solvent in confined parts of buildings such as roof spaces; not only are conventional formulations with their typically high solvent levels a considerable fire hazard on storage, mixing and spraying, especially in the presence of electrical wiring, but also they pose a health hazard for the operator.
  • a method of treating wood or timber comprising applying to the wood or timber a pesticidal water-miscible formulation whose average particle size is at most 200 nm; the formulation may comprise water, a pesticidal oil, a surfactant and a co-surfactant, the co-surfactant preferably having an HLB of less than 12.
  • Formulations in accordance with the invention may as indicated above, be used to treat wood or timber articles or other building materials against insect and acarine pests, and additionally they may be used to treat them against fungus, mould, lichen, algae and other plant pests.
  • Fungi which may be controlled by the invention include dry rot (Serpula (merulius) lacrymans) and wet rot (Coniophora souna) .
  • Moulds which may be controlled by the invention include Aspergillus spp. , Penicillium spp. , Paecilomvces spp. , Alternaria spp. and Cladosporium spp.
  • the microemulsion will generally be clear or translucent, except in the viscoelastic gel phase. Micellar solutions and molecular solutions may additionally be clear.
  • the water can be tap water, although distilled water can be used.
  • the amount of water in the microemulsion will depend on many factors but typically for w/o microemulsions will be from 20 to 70% w/v and for o/w microemulsions it shall be from 40 to 95% w/v.
  • the oil need not merely be an "oil” in the sense of a petroleum fraction, although such oils are included; the term “oil” is used to mean any non-aqueous solvent in which a substance of interest is soluble and which is immiscible with water; alternatively, the substance of interest may itself be the oil.
  • the oil may be animal, vegetable, mineral or silicone or some other organic solvent which is water-immiscible, such as an optionally halogenated hydrocarbon.
  • the hydrocarbon may be aliphatic or aromatic or have both aliphatic and aromatic moieties.
  • Typical solvents include xylene, naphthalene, kerosene, isoparaf ins and halogenated hydrocarbons.
  • the surfactant may be any typical emulsifier as found in most macroemulsion systems.
  • the surfactant may be anionic, cationic, zwitterionic or nonionic.
  • Anionic surfactants are more frequently used.
  • Suitable anionic surfactants include hydrocarbon sulphates, sulphonates and sulphamates, especially compounds wherein the hydrocarbon moiety is an alkyl or alkylaryl group. Soaps (hydrocarbyl carboxylates) can also be used, as can sulphocarboxylic acids such as sulphosuccinic acid.
  • anionic detergents examples include alkyl benzene sulphonates and sulphonic acids such as C 8 to C 16 alkyl benzene sulphonates and sulphonic acids including dodecyl benzene sulphonic acid (a predominately straight chain mixture of which compounds is sold under the trade mark NANSA SSA) .
  • alkyl benzene sulphonates and sulphonic acids such as C 8 to C 16 alkyl benzene sulphonates and sulphonic acids including dodecyl benzene sulphonic acid (a predominately straight chain mixture of which compounds is sold under the trade mark NANSA SSA) .
  • anionic surfactants which are acids, as opposed to salts, may be advantageous.
  • an appropriate surfactant can be made by one of skill in the art without undue experimentation.
  • the oil is aromatic, such as xylene or naphthalene
  • a surfactant having an aromatic moiety for example an alkyl benzene sulphonate or an alkyl naphthalene sulphonate.
  • an aliphatic surfactant is preferred such as an alkyl sulphonate or a dialkyl sulphosuccinate (such as dioctyl sulphosuccinate) or a soap.
  • an alkyl sulphonate or a dialkyl sulphosuccinate (such as dioctyl sulphosuccinate) or a soap.
  • a dialkyl sulphosuccinate such as dioctyl sulphosuccinate
  • soap Another factor in determining the choice of surfactant is the type of microemulsion (w/o or o/w) to be produced.
  • HLB surfactants for example having an HLB of from 4 to 9, particularly 4 to 7 tend to stabilise w/o microemulsions and should therefore for preference be used for w/o microemulsions and high HLB surfactants (for example having an HLB of from 9 to 20, particularly 9 to 20) tend to stabilise o/w microemulsions and should thus be used for o/w microemulsions.
  • HLB values may be measured by standard techniques.
  • PIT phase inversion temperature
  • This system is based upon the temperature at which a surfactant causes an o/w emulsion to invert into a w/o emulsion. It provides information concerning the types of oils, phase volume relation ⁇ ships and the concentration of surfactant which could be used. This system is established on the proposition that the HLB of a nonionic surfactant changes with temperature; the inversion of an emulsion type occurs when the hydrophilic and lipophilic tendencies of the surfactant just balance. No emulsion forms at this temperature.
  • Emulsions stabilised with nonionics tend to be o/w types at low temperatures and w/o types at high temperatures. From the microemulsion standpoint, the PIT system has a useful feature in that it can throw light on the chemical type of surfactant preferred to match a given oil.
  • Water-miscible formulations useful in accordance with the invention include a cosurfactant having an HLB of less than 12.
  • cosurfactant having an HLB of less than 12.
  • Two classes of cosurfactants are normally preferred for use, although others may be used.
  • Aliphatic alcohols are a first preferred class. They may have a carbon content of from 5 to 12 or more carbon atoms.
  • Lower homologues for example C 5 to C 7 alcohols
  • C 8 optionally including C 8
  • Nonionic surfactants form a more versatile group of co- surfactants. They can be balanced with the primary surfactant to give systems that are stable as micellar solutions and as both w/o and o/w microemulsions.
  • a whole range of nonionics can be used, including ethylene oxide propylene oxide block copolymers (as typified by the PLURONIC PE or PLURIOL PE range from BASF) and alcohol ethoxylate ⁇ (as typified by the DOBANOL range from Shell) .
  • the HLB of the cosurfactant may be less than 10 or even less than 5.
  • one nonionic cosurfactant is the ethylene oxide propylene oxide block copolymer containing 10% ethylene oxide sold under the trade mark PLURONIC PE 6100 or PLURIOL PE 6100, which has an HLB of 3.0.
  • Other suitable HLB values for cosurfactants are less than 3, for example about 2 or even about 1.
  • a suitable cosurfactant HLB value of from 6 to 8, for example about 7, may be suitable;
  • PLURONIC PE 6100 or PLURIOL PE 6100 is an example of a cosurfactant having such an HLB value.
  • micellar solutions micellar solutions and molecular solutions
  • broad and preferred ranges of the ingredients may be as follows:
  • Oil (including dissolved substance if any) 20 to 50% 30 to 40%
  • the amounts of surfactant and cosurfactant should be kept as low as possible and the amount of water should be kept as high as possible.
  • the above is subject always to the proviso that the total number of percentage parts of the ingredients cannot exceed 100.
  • the broad and preferred concentration ranges of the ingredients can be as follows: Ingredient Broad w/v Preferred w/v
  • Oil (including dissolved substance if any) 1 to 20% 1 to 10%
  • a water- insoluble oil -s oluble insecticide and/or acaricide which it is desired to formulate may be dissolved in an oil , although it is clear that the oil may itself be the active substance.
  • Synthetic pyrethroids are particular candidates for formulation by means of the present invention .
  • One synthetic pyrethroid is deltamethrin , which is the common name for 3 - ( 2 , 2-dibromoethenyl) -2 , 2-dimethyl- cyclopropane carboxylic acid cyano ( 3-phenoxyphenyl) - methyl ester .
  • Deltamethrin is a potent synthetic pyrethroid insecticide/acaricide, the preparation of the racemic mixture of which is described in DE-A- 2439177.
  • Deltamethrin is insoluble in water, but is soluble in organic solvents such as ethanol , acetone, dioxane, xylene and certain petroleum fractions .
  • Other synthetic pyrethroids include cypermethrin (3- ( 2 , 2 -dichloroethenyl ) - 2 , 2 -dimethyl eye l opropane- carboxylic acid cyano ( 3 -phenoxyphenyl) -methyl ester) , permethrin (3- (2 , 2-dichloroethenyl) -2 , 2-dimethylcyclo- propanecarboxylic acid ( 3 -phenoxyphenyl) -methyl ester) and fenvalerate (4-chloro-alpha-(l-methylethyl) benzene- acetic acid cyano ( 3-phenoxyphenyl ) methyl ester.
  • Cypermethrin may be prepared as described in DE-A- 2326077, permethrin may be prepared as described in DE- A-2437882 and DE-A-2544150 , and fenvalerate may be prepared as described in DE-A-2335347.
  • synthetic pyrethroids natural pyrethroids, organophosphorus compounds and carbamates are other examples of insecticide/acaricides useful in the present invention.
  • Organophosphorus compounds include chlorpyritos (0,0- diethy 1-0-3 , 5, 6-trichloro-2-pyridyl phosphorothioate) , chlorpyrif os-methyl (0,0-dimethyl-0-3 ,5,6-trichloro-2- pyridyl phosphorothioate) , fenitrothion (0,0-dimethyl- 0-4-nitro-m-tolyl phosphorothioate) and pirimiphos- methyl (0_-2-diethylamino-6-methylpyrimidin-4-yl-0,0- dimethyl phosphorothioate) .
  • Mixtures of insecticide/acaricides may be particularly suitable for some applications.
  • Cypermethrin is an example of a liquid which can function both as the oil and as a water-insoluble oil-soluble substance.
  • the oil is an insecticide/acaricide the formulation may be free of an oily solvent for the pesticide.
  • pesticides which can be formulated by means of the invention include fungicides and herbicides.
  • Fungicides particularly useful for treating wood or timber or other building materials include pentachlorophenol, zinc salts including zinc octoate and zinc naphthenate, propaconazole and, particularly for dry rot, an alkali metal phenyl phenoxide, such as sodium 2-phenylphenoxide tetrahydrate.
  • micellar solutions With water-in-oil microemulsions, micellar solutions and molecular solutions, it is generally possible to get a higher concentration of the active substance (for example deltamethrin or another synthetic pyrethroid or other pesticide) .
  • the active substance for example deltamethrin or another synthetic pyrethroid or other pesticide.
  • o/w formulations may give a perfectly adequate concentration for end use or even for concentrates for dilution before use.
  • formulations in accordance with the invention can be made very simply. Therefore, formulations useful in the invention may be prepared by mixing the ingredients. Depending on the thermodynamic favourability of the system, the ingredients will tend to form a microemulsion, micellar solution or molecular solution. In practice, however, kinetic considerations may dictate that some agitation is preferably used to assist the mixing. Agitation may be by magnetic or mechanical means or in some cases ultrasonic.
  • the cosurfactant is added and the system is agitated to produce a clear o/w microemulsion. Routine modifications, such as the application of heat or altering the degree of agitation can be made to these basic processes to suit the system in use.
  • Agricultural formulations useful in the invention may have a further advantage in that they use less potentially harmful solvent (such as xylene) per dose than certain conventional formulations, thereby posing less of a threat to the crop being treated, the handler and to the environment in general.
  • solvent such as xylene
  • the concentration of the active substance (for example, deltamethrin) in the formulations useful in the invention may range from as little as 0.1 ppm, 0.01 g/1 or 0.1 g/1 up to 100 or 200 g/1 or more.
  • High concentrations of insecticide/acaricide may range from 10 to 300 g/1, for example 25 to 200 g/1, such as 25 or 100 g/1.
  • deltamethrin or another pyrethroid pesticide 10 to 50 g/1 or 100 g/1 final concentration may be found to be suitable.
  • a formulation containing from 0.1 ppm or 0.05 g/1 ' to 5 g/1, for example 0.1 g/1 to 1 g/1 may be found to be acceptable.
  • a w/o microemulsion was made up from the following ingredients: xylene/deltamethrin concentrate ⁇ 200 ml/1 xylene 200 ml/1
  • the concentrate contained 125 g/1 deltamethrin and gives a final concentration of 25 g/1
  • a litre of the above formulation was prepared by first adding 200 ml xylene to a beaker. 200 ml of the xylene/deltamethrin concentrate was then added to the same beaker. The surfactant and cosurfactant were then added and dissolved in the oil phase. The water was then added, with stirring, to give a clear w/o micro ⁇ emulsion. The formulation was confirmed to be a microemulsion by conductivity measurements. The average particle size of a 1/400 dilution was measured by a MALVERN AUTOSIZER 2c laser particle sizer to be 62.8 + 11.8 n .
  • a formulation was prepared from the following ingredients: Deltamethrin 0.4 g/1
  • a litre of the above formulation was prepared by first adding the xylene to a beaker. Solid deltamethrin was then added and dissolved in the xylene. The NANSA SSA surfactant was then added and dissolved in the oily phase. Subsequently, water was added and the mixture agitated to give a homogeneous macroemulsion. Finally, the (PLURIOL PE 6100) cosurfactant was added and the entire system agitated to produce a clear formulation. The average particle size was measured by a MALVERN AUTOSIZER 2c laser particle sizer to be 0.8 nm, which indicates that the formulation is a molecular solution.
  • a formulation was prepared from the following ingredients:
  • a ready-for-use formulation was made up from the following ingredients:
  • the K'OTHRINE and xylene were mixed and the surfactants dissolved into them; then the water was added from a burette with constant stirring.
  • the average particle size was measured by a MALVERN AUTOSIZER 2c laser particle sizer to be 15.0 + 2.2 nm, showing the formulation to be on the lower size limit for a microemulsion.
  • a ready-for-use formulation was made up from the following ingredients:
  • the K'OTHRINE and xylene were placed in a beaker. To this the PLURIOL and NANSA were added; then this was well mixed. The water was added to this mixture with constant stirring. The average particle size was measured by a MALVERN AUTOSIZER 2c laser particle sizer to be 4.1 + 1.4 nm, showing the formulation to be a micellar solution.
  • a formulation was made up from the following ingredients:
  • the cypermethrin was dissolved in the xylene; to this the PLURIOL PE 8100 and NANSA SSA were added and mixed in well. The water was added slowly with constant stirring until clear. The average particle size of a 1/400 dilution in water was measured by a MALVERN AUTOSIZER 2c laser particle sizer to be 41.2 + 7.0 nm, showing the formulation to be a microemulsion.
  • a formulation was made up from the following ingredients:
  • the cypermethrin was dissolved in the PLURIOL PE 8100 and NANSA SSA. The water was added slowly with constant stirring until clear. The average particle size was measured by a MALVERN AUTOSIZER 2c laser particle sizer to be 7.8 + 1.6 nm, showing the formulation to be a micellar solution. It is expected that a microemulsion would be formed on dilution.
  • a formulation was made up from the following ingredients:
  • the cypermethrin was dissolved in the xylene. To this the PLURIOL PE 8100 and NANSA SSA- were added and mixed in well. The water was added slowly with constant stirring until clear. The average particle size was measured by a MALVERN AUTOSIZER 2c laser particle sizer to be 40.6 + 7.4 nm, showing the formulation to be a microemulsion.
  • a formulation was made up from the following ingredients:
  • the cypermethrin was dissolved in the PLURIOL PE 8100 and NANSA SSA. The water was added slowly with constant stirring until clear. The average particle size was measured by a MALVERN AUTOSIZER 2c laser particle sizer to be 18.1 + 3.9 n , showing the formulation to be a microemulsion.
  • a formulation was made up from the following ingredients:
  • the fenitrothion and the deltamethrin were dissolved in the xylene; to the resulting solution the PLURIOL PE 8100 and the NANSA SSA- were added with stirring. Then the water was added slowly with constant stirring until clear.
  • the average particle size of a 1/400 dilution in water was measured by a MALVERN AUTOSIZER 2c laser particle sizer to be 41.5 + 11.4 nm, showing the diluted formulation to be a microemulsion.
  • a formulation was made up from the following ingredients:
  • the chlorpyrifos-methyl and the deltamethrin were dissolved in the xylene; to the resulting solution the PLURIOL PE 8100 and the NANSA SSA were added with stirring. Then the water was added slowly with constant stirring until clear.
  • the average particle size of a 1/400 dilution in water may be measured by a MALVERN AUTOSIZER 2c laser particle sizer to be about 40 nm, showing the diluted formulation to be a microemulsion.
  • a formulation was made up from the following ingredients:
  • the fenitrothion and the cypermethrin were dissolved in the xylene; to the resulting solution the PLURIOL PE 8100 and the NANSA SSA were added with stirring. Then the water was added slowly with constant stirring until clear.
  • the average particle size of a 1/400 dilution in water may be measured by a MALVERN AUTOSIZER 2c laser particle sizer to be about 40 nm, showing the diluted formulation to be a microemulsion.
  • a formulation was made up from the following ingredients: Chlorpyrifos-methyl 150 g/1
  • the chlorpyrifos-methyl and the cypermethrin were dissolved in the xylene; to the resulting solution the PLURIOL PE 8100 and the NANSA SSA were added with stirring. Then the water was added slowly with constant stirring until clear.
  • the average particle size of a 1/400 dilution in water may be measured by a MALVERN AUTOSIZER 2c laser particle sizer to be about 40 nm, showing the diluted formulation to be a microemulsion.
  • Preparations useful in the invention were tested against the southern corn root worm (Diabrotica undecimpunctata at the 3rd-instar larvae stage.
  • the application method was the standard Potter Tower method, and the application rate was 200 1/ha.
  • Replicates of 10 larvae were placed in 10cm Petri dishes on moist filter paper and sprayed. Maize seedlings were added and the larvae were kept at 20°C with a 16h photoperiod.
  • the following table shows the percentage of dead larvae at 24, 48 and 72h with all data corrected for control mortality.
  • Preparations useful in the invention are compared with the standard AMBURSH cypermethrin emulsifiable concentrate and the standard DECIS deltamethrin emulsifiable concentrate.
  • the percentage mortalities indicate that microemulsion formulations of cypermethrin and deltamethrin have good toxicity against the southern corn root worm.
  • Preparations useful in the invention were tested against Heliothis armigera at the 3rd-instar larvae stage.
  • the application method was a standard Potter Tower method, and the aplication rate was 200 1/ha.
  • Replicates of 10 larvae were placed in 9cm Petri dishes on moist filter paper and sprayed-. Diet was added and the larvae were kept at 20°C with a 16h photoperiod.
  • the following table shows the percentage of dead larvae at 24 , 48 and 72h, with all data corrected for control mortal ity , of preparations useful in the invention compared with the standard AMBUSH cypermethrin emul s i f iabl e concentrate and the standard DECIS deltamethrin emulsifiable concentrate.
  • the deltamethrin microemulsion of Preparation 1 can be seen to be superior to DECIS at rates of 25 and 12 . 5 ppm.
  • Formulations useful in the invention were tested against Thrips tabaci at the late-instar nymph and adult stage.
  • the application method was a standard Potter Tower method and the application rate was 200 1/ha.
  • 5cm diameter discs were cut from marrow leaves and their abaxial surface was sprayed. The discs were then placed in Petri dishes on moist filter paper, treated surface uppermost. 10 Thrips were introduced to each dish, which was kept at 20°C with a 16h photoperiod.
  • the following table shows the percentage of dead Thrips at 24, 48 and 72h, with all data corrected for control mortality, for preparations useful in the invention, compared to a standard DECIS deltamethrin emulsifiable concentrate.
  • compositions useful in the invention were tested against the army worm, Spodoptera litoralis at the 3rd- instar larvae stage.
  • the application method was a standard Potter Tower method and the application rate was 200 1/ha.
  • Replicates of 10 larvae were placed in 9cm Petri dishes on moist filter paper and sprayed. Diet was added and the larvae were kept at 20°C with a 16h photoperiod.
  • the following table shows the percentage of dead larvae at 24, 48 and 72h and at 7 days for preparations useful in the invention compared to the standard AMBUSH cypermethrin emulsifiable concentrate and the standard DECIS deltamethrin emulsifiable concentrate. The percentage of dead larvae at 7 days was included since, for the higher doses, many larvae remained moribund at 72h. All data are corrected for control mortality.
  • Preparations useful in the invention were tested against Heliothis virescens at the 3rd-instar larvae stage.
  • the application method was a standard Potter Tower method, and the application rate was 200 1/ha.
  • Replicates of 10 larvae were placed in 9cm Petri dishes on moist filter paper and sprayed. Diet was added and the larvae were kept at 20°C with a 16h photoperiod.
  • the following table shows the percentage mortality of larvae at 24, 48 and 72h, with all data corrected for control mortality, for formulations useful in the invention, compared to the standard AMBUSH cypermethrin emulsifiable concentrate and the standard DECIS deltamethrin emulsifiable concentrate.
  • Preparation 1 25 30 93 100 100 12.5 30 100 100 100 6.25 30 93 97 100 3.125 30 83 97 100 1.563 30 52 87 92 0.782 30 35 52 46 0.391 30 21 35 28
  • Preparations useful in the invention were tested against the brown rice leaf hopper (Nilaparvata lugens) at the adult stage.
  • the application method was a standard Potter Tower method and the application rate was 200 1/ha.
  • Replicates of 10 nymphs were placed in 5cm Petri dishes, anaesthetised with a small jet of C0 2 and sprayed.
  • the hoppers were then dropped onto a grou of potted rice plants (approximately 2 months old but cut down to a height of 15cm) .
  • the plants were enclosed in a clear plastic collar with a lid of fine nylon mesh. The plants were kept at 20°c with a I6h photoperiod.
  • the following table shows the percentage of live hoppers at 24, 48 and 72h, with all data corrected for control mortality, for preparations useful in the present invention compared to the standard AMBUSH cypermethrin emulsifiable concentrate and the standard DECIS deltamethrin emulsifiable concentrate.
  • AMBUSH 400 30 66 97 100 200 100
  • Preparation 3 400 30 93 100 100 200 100
  • deltamethrin The activity of deltamethrin can be seen to be enhanced when sprayed as a microemulsion in accordance with the invention, compared to the DECIS formulation at applied rates of 12 . 5 ppm and above .
  • Preparations useful in the invention were tested against pyrethroid resistant first instar glasshouse whitefly (Trialeirodes vaporariorum) on french bean leaves.
  • the replicate infested leaves were dipped in appropriate concentrations of the formulation under test and mortality was assessed after one week.
  • a log dose probit response regression line was plotted covering 0 to 90% mortality range , and the LC g o derived by eye from the graphs .
  • the results are shown in the f o l l owing tabl e for preparat i ons use ful in the invention and the standard AMBUSH C cypermethrin emul s i f i ab l e concentrate and the standard DE C IS deltamethrin emulsifiable concentrate .
  • Formulations useful in the present invention were tested against the adult black vine weevil. Ten weevils to be exposed to a spray of the formulation under test were placed under a Potter Tower, and then transferred to clean Petri dishes with untreated food. There were three replicate dishes per product. The application rate was 50 active ingredient per hectare. Mortality- was assessed at from 12 to 24h after exposure, as appropriate, and after seven days.
  • the following table shows the mean percentage mortality of the weevils for preparations useful in the invention, compared to a standard DECIS deltamethrin emulsifiable concentrate preparation and a standard AMBUSH cypermethrin emulsifiable concentrate preparation.
  • Preparation 5 was tested against the house fly (Musca domestica) by measuring the total numbers of M. domestica knocked down during exposure to the formulation (deltamethrin applied at 8mg/m 2 ) sprayed onto three surfaces. The results are shown in the following table, in which the abbreviation KD stands for knock down.

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

Abstract

Les cultures tropicales et tempérées, notamment le riz, le maïs, le coton, le soja et les fruits, peuvent être protégées, en particulier contre les insectes parasitaires des ordres Lepidoptera, Diptera, Coleoptera, Hemiptera, Orthoptera, Dictyoptera, Hymenoptera et Isoptera et les acariens parasitaires, par traitement avec une formulation hydro-miscible pesticide dont la granulométrie est au maximum de 200 nm. Les parasites nuisibles à la santé publique, à savoir la mouche commune (Musca domestica), la blatte (Blatta sp. ou Periplaneta sp.) et le moustique (Aedes aegypti) ainsi que des parasites qui infestent ou attaquent le bois, notamment dans des immeubles, peuvent également être combattus avec de telles formulations. Ces formulations comprennent de l'eau, de l'huile, un tensioactif, et un co-tensioactif, et soit l'huile est un pesticide soit la formulation renferme un pesticide dissous dans de l'huile. Le pesticide peut être un pyréthroïde tel que la cyperméthrine ou la deltaméthrine. Ces formulations peuvent être des solutions moléculaires, des solutions micellaires ou des micro-émulsions (aqueuses ou huileuses) et sont généralement claires.
PCT/GB1989/001160 1987-03-30 1989-09-29 Lutte antiparasitaire WO1990003112A1 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
DE68913754T DE68913754T2 (de) 1988-09-30 1989-09-29 Pestizidale kontrolle.
AT89911276T ATE102432T1 (de) 1988-09-30 1989-09-29 Pestizidale kontrolle.
NO911242A NO180701C (no) 1988-09-30 1991-03-26 Anvendelse av en insekticid og/eller akaricid vannblandbar formulering for skadedyrbekjempelse
DK056891A DK56891A (da) 1988-09-30 1991-03-27 Anvendelse af pesticidpraeparater
FI911555A FI103859B1 (fi) 1988-09-30 1991-03-28 Menetelmä trooppisen ja lauhkean vyöhykkeen viljelykasvien satojen suojaamiseksi ja tuhoeläinten torjumiseksi

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB878707563A GB8707563D0 (en) 1987-03-30 1987-03-30 Chemical formulations
GB888801643A GB8801643D0 (en) 1988-01-26 1988-01-26 Chemical formulations
GB8822936.4 1988-09-30
GB888822936A GB8822936D0 (en) 1988-09-30 1988-09-30 Pesticidal control

Publications (1)

Publication Number Publication Date
WO1990003112A1 true WO1990003112A1 (fr) 1990-04-05

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PCT/GB1989/001160 WO1990003112A1 (fr) 1987-03-30 1989-09-29 Lutte antiparasitaire

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WO (1) WO1990003112A1 (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992003047A1 (fr) * 1988-03-02 1992-03-05 Roussel-Uclaf Formulations pesticides
WO1993014630A1 (fr) * 1992-01-31 1993-08-05 Nc Development, Inc. Pretraitement pesticide pour le bois, par microemulsions ou solution micellaire ou moleculaire
US5827522A (en) * 1996-10-30 1998-10-27 Troy Corporation Microemulsion and method
WO2006002984A1 (fr) * 2004-07-06 2006-01-12 Basf Aktiengesellschaft Compositions de pesticide liquide
WO2008040727A2 (fr) * 2006-10-03 2008-04-10 Basf Se Composition pesticide liquide contenant des composes pesticides n-phenylsemicarbazone
US9295261B2 (en) 2006-03-29 2016-03-29 Agro-Kanesho Co. Ltd. Aqueous microemulsions containing pyrethroid compounds

Citations (8)

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Publication number Priority date Publication date Assignee Title
FR1026169A (fr) * 1950-07-21 1953-04-24 Ets Kuhlmann Procédé nouveau d'utilisation des produits fischer, transformés par la réaction de reed, pour la préparation d'émulsions et de dispersions transparentes et d'extrême finesse
FR2187226A1 (en) * 1972-06-06 1974-01-18 Procter & Gamble Insecticide emulsions - with improved activity stability and clarity
US3954967A (en) * 1971-08-05 1976-05-04 Vanguard Chemical Company, Inc. Method of producing microcolloidal aqueous emulsions of unsaturated organic insecticidal compounds
EP0062181A1 (fr) * 1981-03-26 1982-10-13 Bayer Ag Emulsions du type huile dans l'eau, procédé pour leur préparation et leur utilisation
EP0107009A2 (fr) * 1982-09-25 1984-05-02 Bayer Ag Microémulsions
EP0149051A2 (fr) * 1983-11-29 1985-07-24 Bayer Ag Formulation pesticide soluble dans l'eau
US4567161A (en) * 1982-07-09 1986-01-28 A. Natterman & Cie Gmbh Liquid active ingredient concentrates for preparation of microemulsions
WO1988007326A1 (fr) * 1987-03-30 1988-10-06 Nc Development Inc Formulations chimiques

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1026169A (fr) * 1950-07-21 1953-04-24 Ets Kuhlmann Procédé nouveau d'utilisation des produits fischer, transformés par la réaction de reed, pour la préparation d'émulsions et de dispersions transparentes et d'extrême finesse
US3954967A (en) * 1971-08-05 1976-05-04 Vanguard Chemical Company, Inc. Method of producing microcolloidal aqueous emulsions of unsaturated organic insecticidal compounds
FR2187226A1 (en) * 1972-06-06 1974-01-18 Procter & Gamble Insecticide emulsions - with improved activity stability and clarity
EP0062181A1 (fr) * 1981-03-26 1982-10-13 Bayer Ag Emulsions du type huile dans l'eau, procédé pour leur préparation et leur utilisation
US4567161A (en) * 1982-07-09 1986-01-28 A. Natterman & Cie Gmbh Liquid active ingredient concentrates for preparation of microemulsions
EP0107009A2 (fr) * 1982-09-25 1984-05-02 Bayer Ag Microémulsions
EP0149051A2 (fr) * 1983-11-29 1985-07-24 Bayer Ag Formulation pesticide soluble dans l'eau
WO1988007326A1 (fr) * 1987-03-30 1988-10-06 Nc Development Inc Formulations chimiques

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992003047A1 (fr) * 1988-03-02 1992-03-05 Roussel-Uclaf Formulations pesticides
WO1993014630A1 (fr) * 1992-01-31 1993-08-05 Nc Development, Inc. Pretraitement pesticide pour le bois, par microemulsions ou solution micellaire ou moleculaire
US5827522A (en) * 1996-10-30 1998-10-27 Troy Corporation Microemulsion and method
WO2006002984A1 (fr) * 2004-07-06 2006-01-12 Basf Aktiengesellschaft Compositions de pesticide liquide
US8741324B2 (en) 2004-07-06 2014-06-03 Basf Se Liquid pesticide compositions
US9295261B2 (en) 2006-03-29 2016-03-29 Agro-Kanesho Co. Ltd. Aqueous microemulsions containing pyrethroid compounds
WO2008040727A2 (fr) * 2006-10-03 2008-04-10 Basf Se Composition pesticide liquide contenant des composes pesticides n-phenylsemicarbazone
WO2008040727A3 (fr) * 2006-10-03 2008-09-18 Basf Se Composition pesticide liquide contenant des composes pesticides n-phenylsemicarbazone
EA015485B1 (ru) * 2006-10-03 2011-08-30 Басф Се Жидкая пестицидная композиция, содержащая n-фенилсемикарбазоновые пестицидные соединения
US9504253B2 (en) 2006-10-03 2016-11-29 Basf Se Liquid pesticide composition containing N-phenylsemicarbazone pesticide compounds

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