An electrostatically sprayable insecticidal formulation comprising a solution of from 0.5 to 50% of permethrin or like compound in an organic solvent medium, the medium being formulated so that the formulation has a resistivity at 20°C in the range 1×106 to 1×1010 ohm centimeter and a viscosity at 20°C of 5 to 50 centistokes.
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1. An electrostatically sprayable insecticidal formulation suitable for use in an electrostatic spraying apparatus to spray plants to give an even coating of the insecticide on the leaves of said plants, the formulation having after spraying a spray droplet size in the range of from about 50 to about 200 microns in diameter, and consisting essentially of a solution of from 0.5 to 50% by weight of an insecticide in an inert organic solvent medium, said medium being a mixture of inert organic solvents or a mixture of inert organic solvents and an antistatic agent, formulated so that the formulation has a resistivity at 20°C in the range 1×106 to 1×1010 ohm centimeters, and a viscosity at 20°C in the range 5 to 50 centistokes, and the insecticide being of formula: ##STR6## where r is hydrogen or cyano, and r1 is selected from the group consisting of:
(i) a group of formula: ##STR7## where X is selected from hydrogen, chlorine and methyl, and (ii) a group of formula: ##STR8## where Y and Z are selected from halogen, and methyl, and or Y is hydrogen and Z is methyl or a group of formula r2 r3 C═CH--, where r2 and r3 are selected from chlorine, bromine, methyl, ethyl, halo-substituted methyl and halo-substituted ethyl.
3. An electrostatically sprayable insecticidal formulation as claimed in
4. A method of treating a plant infested by insects, said method consisting essentially of the step of electrostatically spraying the plant with an insecticidally effective amount of a formulation as claimed in
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This is a continuation of application Ser. No. 969,434, filed Dec. 14, 1978, now abandoned.
This invention relates to insecticidal formulations, and more particularly to insecticidal formulations containing permethrin and like insecticides.
Permethrin is a recently discovered (U.K. Pat. No. 1413491 to the National Research Development Corporation) highly active insecticide of formula: ##STR1## It has a broad spectrum of activity at low rates of application, being particularly effective against lepidoptera, and seems likely to be widely used, for example against spruce budworm and pests of cotton. There is a group of related compounds with generally similar properties of permethrin having the general formula: ##STR2## where R is hydrogen or cyano, and R1 is either (i) a group of formula: ##STR3## where X is hydrogen, chlorine or methyl; or (ii) a group of formula: ##STR4## where Y and Z are halogen or methyl or Y is hydrogen and Z is methyl or a group of formula: ##STR5## where R2 and R3 are chlorine or bromine. Additionally, at least one R2 and R3 may be methyl or ethyl, optionally substituted by one or more halogen atoms. This group of insecticides is hereinafter referred to collectively as "permethrin and like compounds".
Permethrin and like compounds, being active at low rates, are well suited to agricultural application by the known ULV (ultra low volume) technique. This method uses relatively concentrated liquid formulations, containing e.g. 5 to 50% by weight of active ingredient, and a correspondingly low rate of application of the formulation per hectare, e.g. 25-100 liters per hectare, in contrast with more usual high volume spray rates of 200-500 liters per hectare, or more. With such relatively concentrated solutions, it is important to ensure that as much as possible of the formulation goes and stays where it is needed, i.e. on the plants being sprayed, and as little as possible is misdirected onto the ground or carried away by the wind. For this purpose, it is useful to apply electrostatically charged sprays. These are attracted to the foliage of plants; electrostatic forces carry them to the underside of leaves as well as to the top surfaces, and even coating is promoted. Hitherto electrostatic spraying of pesticides has not been widely adopted, for lack of convenient, reliable and cheap spraying apparatus. A suitable apparatus is however now available, and is described in U.K. patent application No. 29539/76 (U.S. Ser. No. 812,440). We have also found that ultra-low volume sprays of permethrin and like compounds are biologically more effective in the form of small droplets e.g. below 70 μ in diameter. Such droplets are particularly prone to drift unless electrostatically charged.
The object of the present invention is to provide a class of insecticidal compositions particularly suited to ULV electrostatic spraying, in particular by the apparatus described in U.K. patent application No. 29539/76 (U.S. Ser. No. 812,440).
According to the present invention we provide an electrostatically sprayable insecticidal formulation comprising a solution of from 0.5 to 50% of permethrin and like compounds (as herein defined) in an organic solvent medium, the formulation having a resistivity at 20°C in the range 1×106 to 1×1010 ohm centimeter and a viscosity at 20°C of 1 to 50 centistokes. In general with higher resistivity values (108 to 1010 ohm centimeters), it is preferred to use higher viscosity values, e.g. above 10 centistokes. In this way, lower spray droplet sizes are obtainable.
We find that solutions according to the invention are readily sprayed at satisfactory rates using the apparatus of U.K. patent application No. 29539/76 (U.S. Ser. No. 812,440) and will give a range of mean spray droplet sizes of from about 50 to about 200 microns in diameter, according to the strength of the electrostatic field applied to them (the stronger the field the smaller the droplets), flow rate through the apparatus and other operating conditions.
The resistivity of solutions according to the invention is conveniently measured by measuring the resistance of a cell of standard dimensions containing the solution held at a temperature of 20°C, using, for example, a Keithley electrometer. It is preferred that the resistivity of the solutions be in the range 106 to 5×108 ohm centimeters.
The viscosity of solutions according to the invention is conveniently measured by timing the flow of a measured quantity of the solution through a hole of known size (as is done, for example, in the Redwood viscometer). It is preferred that the viscosity of the solutions is in the range 5 to 25 centistokes.
The resistivity and viscosity of the solutions depend primarily on the properties of the solvents used to make them, though they are also affected by the nature and amount of the dissolved insecticide.
One way of obtaining the desired properties is to mix solvents having various resistivities and viscosities. High-boiling hydrocarbon solvents, e.g. `Solvesso` 150, `Isopar` L and `Exsol` D180/220, are convenient and relatively cheap, but usually have low viscosities (e.g. of the order of 3 centistokes) and high resistivities (e.g. of the order of 1011 ohm centimeters). To bring down the resistivity of these materials, they may be mixed with polar solvents such as alcohols and in particular ketonic solvents. These have lower resistivities but are also usually not viscous enough; for example, the useful solvent cyclohexanone has a resistivity of about 2×106 ohm centimeters, but a viscosity of only about 3 centistokes. However the viscosity of the solution may be increased by addition of more viscous oil-soluble solvents, for example polybutenes e.g. `Hyvis` (Trademark) and long-chain chlorinated hydrocarbon products such as `Cerechlor` (Trademark) C42 or C48. The latter has a high resistivity, greater than 1010 ohm centimeters, and a high viscosity, of the order of 100 centistokes. By suitable adjustment of the proportions of three solvents such as these, a solution of the desired properties can easily be obtained.
The resistivity of solvents and solutions is easily affected by the presence of water or other contaminants. It is not necessary always to use ultra-pure materials, but consistent results will only be obtained from materials of consistent composition; and formulations which have been made up with the desired properties should thereafter be protected from any further contamination, especially by water.
An alternative way of producing a solution with the required properties is to make up a solution of the required viscosity but excessive resistivity (e.g. from a mixture of hydrocarbons and long-chain chlorinated hydrocarbons) and then dose this with an antistatic agent to reduce the resistivity to the desired level. A suitable antistatic agent is sold for use as a static charge dissipator with hydrocarbon fuels under the name `ASA`; it consists of a complex mixture of calcium and chromium cations with various organic acid anions. Other similar materials, e.g. copper oleates, may also be used. This technique is not always suitable by itself for producing solutions having a resistivity below about 108.
Examples of insecticides suitable for use in the solutions of the invention are listed below in Table I. In general, the presence of one or more asymmetric carbon atoms, as well as of a cyclopropane ring and (in some cases) a carbon-carbon double bond in these insecticides leads to the possibility of a number of different stereoisomers and geometrical isomers. The invention visualises using both pure isomers and mixtures of isomers, the former being potentially more active, the latter cheaper.
| TABLE I |
| ______________________________________ |
| COM- |
| POUND COMMON |
| NO NAME R R1 |
| X Y Z |
| ______________________________________ |
| 1 permethrin H (ii) |
| -- H --CH═CCl2 |
| 2 cypermethrin |
| CN (ii) |
| -- H --CH═CCl2 |
| 3 decamethrin |
| CN (ii) |
| -- H --CH═CBr2 |
| 4 H (i) p-Cl -- -- |
| 5 H (ii) |
| -- H --CH═C(CF3)2 |
| 6 CN (ii) |
| -- H --CH═C(CF3)2 |
| 7 H (ii) |
| -- H --CH═C(CF3)Cl |
| 8 CN (ii) |
| -- H --CH═C(CF3)Cl |
| 9 H (ii) |
| -- H --CH═C(CF3)Br |
| 10 CN (ii) |
| -- H --CH═C(CF3)Br |
| 11 phenothrin H (ii) |
| -- H --CH═C(CH3)2 |
| ______________________________________ |
Preferably the concentration of active ingredient is not more than 10% by weight of the solution. If desired, the solutions of the invention may additionally contain quantities of other active ingredients dissolved therein.
The following Examples illustrate the invention.
The following solution was made by mixing together the constituents.
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Technical permethrin |
| 50 |
| "Solvesso" 150 350 |
| Cyclohexanone 100 |
| "Cerechlor" C42 500 |
| ______________________________________ |
Viscosity 21.2 centistokes; resistivity 1.2×108 ohm centimeters (both measured at 20°C).
This solution was tested in the device illustrated in FIGS. 1-3 of U.K. patent application No. 29539/76 (U.S. Ser. No. 812,440), and atomised very satisfactorily.
A formulation ("Formulation A") of permethrin was prepared suitable for ultra-low volume spraying. This had the following composition:
| ______________________________________ |
| Constituent Parts by Weight |
| ______________________________________ |
| Permethrin 50 |
| Cottonseed oil 200 |
| "Isopar" L (trade name for a |
| 750 |
| high-boiling paraffin |
| 1000 |
| fraction) |
| ______________________________________ |
Formulation A had a viscosity of 7.0 centistokes and a resistivity of 1011 ohm cm. Attempts to spray it through the device illustrated in FIGS. 1-3 of U.K. patent application No. 29539/76 were unsuccessful. The formulation was therefore modified to give a composition according to the invention, by mixing the following ingredients.
| ______________________________________ |
| Constituent Parts by Weight |
| ______________________________________ |
| Formulation A 700 |
| "Cerechlor" C48 290 |
| ASA-3 (antistatic additive) |
| 10 |
| 1000 |
| ______________________________________ |
The modified composition had a viscosity of 19.5 centistokes and a resistivity of 2.4×108 ohm cm, and sprayed very satisfactorily through the aforesaid device
The following solution was made by mixing together the constituents.
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Technical cypermethrin |
| 12.5 |
| n-butanol 220 |
| `Solvesso` 100 150 |
| Cottonseed oil to 1000 |
| ______________________________________ |
Viscosity 11.0 centistokes; resistivity 5.4×107 ohm centimeters (both measured at 20°).
This solution atomised satisfactorily when tested as in Example 1.
The following solution is made by mixing together the constituents:
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Compound No. 8 of Table 1 |
| 15 |
| (mixture of isomers) |
| n-butanol 220 |
| `Solvesso` 100 150 |
| Cottonseed oil to 1000 |
| ______________________________________ |
Viscosity 11 centistokes; resistivity 5.4×107 ohm centimeters (both at 20°C)
This solution atomises satisfactorily when tested as in Example 1.
Seven compositions according to the invention were prepared from cypermethrin (compound No. 2 of Table I) by mixing together the constituents. In each case the resulting solution atomised satisfactorily when tested as in Example 1. The cypermethrin used was a technical grade mixture of isomers supplied as a 34% solution in `Aromasol` H hydrocarbon solvent. Viscosity data are given in centistokes and resistivities in ohm centimeters.
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Cypermethrin 12.5 |
| `Aromasol` H 25 |
| n-butanol 220 |
| `Solvesso` 100 150 |
| Cottonseed oil 592.5 |
| 1000 |
| ______________________________________ |
Properties at 20°C: Viscosity 11.0; Resistivity 5.4×107 ; Density 0.886.
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Cypermethrin 12.5 |
| `Aromasol` H 25 |
| n-butanol 220 |
| `Isopar` L 150 |
| Cottonseed oil 592.5 |
| 1000 |
| ______________________________________ |
Properties at 20°C: Viscosity 12.4; Resistivity 6.0×107 ; Density 0.862.
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Cypermethrin 12.5 |
| `Aromasol` H 25 |
| Cyclohexanone 220 |
| `Isopar` L 150 |
| Cottonseed oil 592.5 |
| 1000 |
| ______________________________________ |
Properties at 20°C: Viscosity 15; Resistivity 4.6×107 ; Density 0.896.
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Cypermethrin 12.5 |
| `Aromasol` H 25 |
| `Isopar` L 150 |
| ASA 3 175 |
| Cottonseed oil 637.5 |
| 1000 |
| ______________________________________ |
Properties at 20°C: Viscosity 50: Resistivity 4.7×107 : Density 0.898.
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Cypermethrin 12.5 |
| `Aromasol` H 25 |
| `Exsol` D180/220 |
| 150 |
| ASA 3 175 |
| Cottonseed oil 637.5 |
| 1000 |
| ______________________________________ |
Properties at 20°C: Viscosity 43: Resistivity 4.7×107 : Density 0.898.
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Cypermethrin 12.5 |
| `Aromasol` H 25 |
| Cyclohexanone 220 |
| `Isopar` L 150 |
| Cottonseed oil 592.5 |
| 1000 |
| ______________________________________ |
Properties at 20°C: Viscosity 7; Resistivity 5.0×107 ; Density 0.851.
| ______________________________________ |
| Ingredient Parts by Weight |
| ______________________________________ |
| Cypermethrin 12.5 |
| `Aromasol` H 25 |
| `Hyvis` 30 100 |
| `Isopar` L 200 |
| White Oil 447.5 |
| Cyclohexanone 220 |
| 1000 |
| ______________________________________ |
Properties at 20°C: Viscosity 10; Resistivity 5.1×107 ; Density 0.856.
"Solvesso" 100 and 150 are mixtures of aromatic hydrocarbons with boiling point ranges of 164°-174°C and 190°-208°C, respectively.
"Isopar" L is a mixture of isoparaffinic hydrocarbons with a boiling range of 189°-208°C
"Exsol" D180/220 is a mixture of paraffinic hydrocarbons and cycloparaffinic hydrocarbons having a boiling point range of 182°-220°C
"Aromasol" H is a mixture of aromatic hydrocarbons.
"Cereclor" C42 and C48 are mixtures of chlorinated long chain paraffinic hydrocarbons containing, respectively, 42% and 49% by weight of chlorine.
"Hyvis" 30 is a polybutene thickening agent.
Coffee, Ronald A., Young, Brian W., Middleton, Michael R.
| Patent | Priority | Assignee | Title |
| 4871766, | Jan 17 1986 | Sumitomo Chemical Company, Limited | Oil-in-water pesticidal emulsion |
| 5435992, | Apr 09 1992 | HOECHST SCHERING AGREVO S A | Non-irritating pesticidal compositions |
| 5866514, | Jul 11 1995 | Nippon Petrochemicals Company, Limited | Pesticidal composition to noxious organisms |
| 6482863, | Dec 15 2000 | S C JOHNSON & SON, INC | Insect repellant formulation deliverable by piezoelectric device |
| 6860439, | Mar 01 2002 | Unilever Home & Personal Care USA, division of Conopco, Inc. | Electrostatic spraying of a cosmetic composition |
| 9044002, | Jan 12 2011 | Sumitomo Chemical Company, Limited | Method of controlling harmful arthropod, composition, and electrostatic spray device |
| Patent | Priority | Assignee | Title |
| 3996375, | Dec 28 1973 | Hoechst Aktiengesellschaft | Insecticidal composition for ultra low volume application |
| 4173651, | Jun 23 1975 | Fumakilla Limited | Method for killing insects and/or fungi with electro-mechanical ultrasonic nebulizer and composition for said method |
| GB1209524, | |||
| GB1413491, | |||
| GB1569707, |
| Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
| Nov 29 1982 | Imperial Chemical Industries PLC | (assignment on the face of the patent) | / |
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