GB2067407A - Pesticidal composition and use - Google Patents
Pesticidal composition and use Download PDFInfo
- Publication number
- GB2067407A GB2067407A GB8041414A GB8041414A GB2067407A GB 2067407 A GB2067407 A GB 2067407A GB 8041414 A GB8041414 A GB 8041414A GB 8041414 A GB8041414 A GB 8041414A GB 2067407 A GB2067407 A GB 2067407A
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- GB
- United Kingdom
- Prior art keywords
- suspension according
- suspension
- oil
- bendiocarb
- surface active
- 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.)
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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
- A01N25/02—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
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
Abstract
A stable liquid formulation of the pesticide bendiocarb, especially for ultra low volume application, comprises the bendiocarb suspended in a chemically inert oil of low volatility and of low solubility for bendiocarb.
Description
SPECIFICATION
Pesticidal composition and use
This invention relates to a new formulation of bendiocarb.
Bendioca rb, 2,2-dimethyl-1 ,3-benzodioxol-4-yl methyl-carbamate, is a known pesticide active for instance against insects. Pesticides are advantageously formulated as liquids so that the formulation can be sprayed on the locus to be treated, or readily measured out and diluted for spraying on the locus to be treated. Thus, pesticides are commonly formulated as emulsifiable concentrates, which are solutions of pesticides and surface active agents in organic solvents, the concentrates in use being diluted with water for spraying. If the pesticide is sufficiently soluble in water, it may be formulated as an aqueous solution. Bendiocarb, however, is not sufficiently soluble in water or in organic solvents commonly used in emulsifiable concentrates to be formulated as an aqueous solution or emulsifiable concentrate.Bendiocarb is also not sufficiently soluble in solvents generally used to make a solution for ultra low volume application; hitherto bendiocarb has not been available as a liquid formulation for ultra low volume application.
A useful liquid formulation of bendiocarb, especially for ultra low volume application, has now been discovered.
Accordingly, the invention provides a stable, pesticidal, liquid suspension of low volatility, comprising bendiocarb suspended in a chemically inert oil of low volatility and of low solubility for bendiocarb.
The invention provides also a process for preparing the suspension, which process comprises admixing the ingredients.
The invention also provides a method of combating pests at a locus infested or liable to be infested with them, which method comprises applying to the locus a pest-combating amount of the suspension.
The suspension, being liquid, avoids any problems of dustiness arising from a powder. The suspension is particularly useful as a ready-to-use formulation and especially useful for ultra low volume application.
A liquid formulation to be useful has to be stable to storage, i.e. the active ingredient must not undergo chemical change to remove the desired properties of the active ingredient and must not separate out and cause problems such as difficulty in measuring out the correct amount and applying a uniform amount of the active ingredient. The present suspension is surprisingly stable. Stability may be assessed in the laboratory by an accelerated storage test. Present suspensions have been found to be stable in such a test for at least 3 months, e.g. at least 6 months, at 40"C.
The suspension preferably exhibits non-Newtonian flow properties. Especially preferred is its being thixotropic. Simple agitation, e.g. a few gentle inversions of a can containing the suspension, makes the thixotropic material readily flowable.
The suspension, being liquid, can be poured out or readily measured out. It can be used straight from its container without further handling or dilution.
The suspension generally contains 5-7009, e.g. 5-500g,of bendiocarb per litre. If too much is contained, a highly viscous non-pourable paste is formed. Conveniently for storage, transport and use, the suspension contains 100-300g e.g. 150-300g of bendiocarb per litre.
The bendiocarb must be sufficiently finely divided. By being finely divided, the sedimentation velocity of the bendiocarb particles is reduced and they present a greater surface area per unit weight; hence they can be held in suspension better. So that also the suspension can pass through the usual equipment for ultra low volume application, the bendiocarb particles in the suspension are preferably substantially all less than 20 microns in largest dimension. Particle sizes in this specification are as measured under a microscope. The majority of the bendiocarb particles by weight are usually 0.05-20, e.g. 3-5, microns in largest dimension.
The oil carries the bendiocarb. Usually there is 300-996 ml, e.g. 500-900 ml, of the oil per litre of suspension. The oil must be chemically inert, i.e. it does not react chemically with the bendiocarb.
The volatility of the suspension depends on that of the oil. Both must be of low volatility, i.e. when 0.3 cubic centimetres of it is placed in a petri dish of diameter 5cm, then after 7 hours storage in still air at 20"C, not more than 20% by weight evaporates; preferably, not more than 10% by weight evaporates, and especially between 0 and 5% by weight evaporates. Because of the low volatility, the bendiocarb particles in use remain associated with the oil, thus facilitating contact with the pest to be combated. The low volatility also makes the present formulation safer by being less liable to ignite and also by preventing the drift in air which would be liable to occur on application of a formulation containing a more volatile oil; the present oil cannot consist for instance of diesel oil.The present oil usually has a flash point greater than 100 C, preferably greater than 120 C. Usually its flash point is between 100 and 300 C, typically 130-200"C.
The oil must be of low solubility for bendiocarb, i.e. its solubility for bendiocarb is below 10g, preferably below 0.05g, per litre of oil at 20"C. If the solubility is too high, crystal growth of the bendiocarb may occur on storage of the formulation.
The kinematic viscosity of the oil is usually between 0 and 100 centistokes, preferably from 5 to 25 centistokes,at 40 C.
The boiling point of the oil usually lies in the range 200-400"C.
The oil can be an animal oil, a vegetable oil (e.g. rape seed oil or cotton seed oil), a mineral oil or a plasticizer oil (e.g. diisooctyl phthalate). The oil can be an ester, for example a glyceride or a phthalate (e.g. a phthalate plasticizer). Preferably, however, the oil is a hydrocarbon, preferably a paraffin oil, especially a highly paraffinic oil (e.g. at least 99% by weight of the oil being paraffinic). The presence of significant amounts of aromatic compounds may cause phytotoxicity problems if the formulation contacts plants. In addition, the solubility of bendiocarb in aromatic oils tends to be too high. Preferably the oil is a highly refined paraffin oil, being of technical or pharmaceutical quality. Suitable oils include Risella EL (from Shell
Oil Company), Fyzol 11 E (from Fisons Limited) or Klearol (from Witco Chemical Corp). A mixture of oils may be employed.
A suspending agent may be present to help hold the bendiocarb in suspension, especially when lower concentrations of bendiocarb are employed. Preferably, the suspension contains 1-1 00g of suspending agent per litre.
The suspending agent usually gives the formulation a gel structure, which causes the formulation to exhibit non-Newtonian, usuallythixotropic, flow properties.
The suspending agent may be a natural, modified natural, or synthetic, material. The suspending agent is generally a swelling or non-swelling mineral clay, often organically modified to confer particular properties.
The clays may be natural or synthetic.
The clays are preferably used in admixture with additives to secure their optimum properties. Suitable additives include (i) mixtures of lower alcohols and water, (ii) propylene carbonate, (iii) acetone, (iv) lower glycol ethers, or (v) gamma-butyrolactone. The additives may be present for instance as 10-50% by weight of the clay.
As natural, swelling clays, there may be used smectite minerals including smectite itself, montmorillonite, bentonite, hectorite, saponite, sauconite, vermiculite, nontronite, kaolinite, halloysite or illite, especially the first four. As non-swelling clays, there may be used attapulgite or sepiolite. As synthetic swelling clays, there may be used hectorite (e.g. Laponite RD or Laponite RDS, both from Laporte).
The suspending agent may be synthetic silica, e.g. pyrogenic silica or fine, precipitated, silica.
The suspending agent may be an organic derivative of castor oil or an inorganically modified derivative of castor oil.
The suspending agent may be a metal stearate, e.g. aluminium stearate.
A mixture of suspending agents may be employed.
A surface active agent is generally present in the formulation, to facilitate wetting of the solid phase into the oil phase, to disperse the particles once wetted, and as an aid to keep the formulation flowable, pourable and pumpable. The formulation usually contains 1-2009, e.g. 1-1 00g, of surface active agent per litre.
The term 'surface active agent' is used in the broad sense to include materials variously called emulsifying agents, dispersing agents and wetting agents. Such agents are well known in the pesticide art.
The surface agents used may comprise anionic surface active agents, for example mono- or di-esters of phosphoric acid with fatty alcohol ethoxylates or with alkyl-phenol ethoxylates, salts of such esters, fatty alcohol sulphates such as sodium dodecyl sulphate, sodium octadecyl sulphate or sodium cetyl sulphate, ethoxylated fatty alcohol sulphates, ethoxylated alkylphenol sulphates, lignin sulphonates, petroleum sulphonates, alkyl-aryl sulphonates such as alkyl-benzene sulphonates or lower alkyl-naphthalene sulphonates, e.g. butyl-naphthalene sulphonate, salts of sulphonated naphthalene-formaldehyde condensates, salts of sulphonated phenol-formaldehyde condensates, or more complex sulphonates such as the amide sulphonates, e.g. the sulphonated condensation product of oleic acid and N-methyl taurine or the dialkyl sulphosuccinates, e.g. the sodium sulphonate of dioctyl succinate.
The surface active agents may also comprise non-ionic agents, for example condensation products of fatty acid esters, fatty alcohols, fatty acid amides or fatty-, alkyl- or alkenyl-substituted phenols with ethylene oxide, fatty esters of polyhydric alcohol ethers e.g. sorbitan fatty acid esters, condensation products of such esters with ethylene oxide e.g. polyoxyethylene sorbitan fatty acid esters, block copolymers of ethylene oxide and propylene oxide, acetylenic glycols such as 2,4,7,9-tetramethyl-5-decyn-4,7-diol, or ethoxylated acetylenic glycols. By 'fatty' is meant herein hydrocarbon of 12-18 carbon atoms.
The surface active agents may also comprise cationic agents, for example alkyl and/or aryl-subsHtuted quaternary ammonium compounds such as cetyl trimethylammonium bromide or ethoxylated tertiary fatty amines.
Non-ionic surface active agents are preferred. Outstanding surface active agents are condensation products with ethylene oxide. Particularly outstanding surface active agents are: (A) Condensation products of alkyl- or alkenyl- substituted phenols with ethylene oxide, e.g. such products whose alkyl or alkenyl groups contain 6-18 carbon atoms and which contain 2-6 moles of ethylene oxide.
Preferred such products are nonyl phenol-ethylene oxide condensates containing 2-6 moles, particularly 4 moles, of ethylene oxide, and especially polyoxyethylene oleylphenol; (B) Condensation products of ethylene oxide with hydrocarbon of 12-18 carbon atom esters of polyhydric alcohol ethers, e.g. containing 2-25 moles of ethylene oxide, such as polyoxyethylene sorbitan oleate and/or laurate; or (C) Condensation products of hydrocarbon of 12-18 carbon atom alcohols with ethylene oxide, e.g. 2-6 moles of ethylene oxide.
A mixture of surface active agents may be employed.
Besides bendiocarb, the suspension may contain other compatible pesticides, e.g. herbicides, plant growth regulants, other insecticides or other acaricides.
The suspension can be prepared by admixing the ingredients. When a suspending agent is employed, it is preferred to apply a high amount of shear to it to disperse it and to invoke its properties. Preferably, the suspending agent is dispersed in at least some of the oil before admixing the bendiocarb therewith.
To use the suspension to combat pests, it can be diluted, for example with water or hydrocarbon e.g.
diesel oil, and then applied, normally by spraying. Alternatively the suspension can be applied undiluted, normally by spraying. The suspension is especially useful for ultra low volume application, and particularly as a space spray, e.g. applied from aircraft or an ultra low volume aerosol generator. For spraying from aircraft, the suspension can be diluted with hydrocarbon to facilitate passage through the spray equipment.
The suspension can be used against public health and agricultural pests, especially public health pests.
The pests are usually arthropods, especially insects. The suspension may be applied indoors, e.g. in buildings (for instance public buildings, houses, flats and warehouses), in aircraft or on ships, e.g. in food preparation or storage areas. It is preferably applied outdoors, however, e.g. in urban areas, rangelands or forests. It is particularly useful against stored product pests and especially flying insect pests such as mosquitoes, flies, grasshoppers, locusts or gypsy moths (Porthetria dispar).
The suspension is also useful against agricultural insect pests. Thus, it can be used on plants, land or the soil. The suspension may be used to dress seed, for example seeds of vegetables, notably brassicas, onions and beans, or cereals, notably wheat, barley, oats and maize. The dressed seed is protected against insects including coleoptera and diptera, for example wireworms (Agriotes Spp), pygmy beetle (Atomaria), collembola and millipedes, symphilids and flea beetles (Chaetocnema Spp). For use as a seed dressing, the suspension may contain an adhesive to facilitate adhesion of the active ingredient to the seed. The amount of adhesive in the suspension may be, for exam ple, 5-50g per litre.
When used indoors on surfaces, the suspension is usually employed at a rate of 10-1000 mg of bendiocarb per square metre. When used outdoors, e.g. at a locus where plants are growing or are to grow, the suspension is usually employed at a rate of 1/8-2, e.g.1/4-2, kg of bendiocarb per hectare. When used as a seed dressing, the suspension is usually employed at a rate of 0.1 -28g, preferably 0.25-lOg, of bendiocarb per kg of seed.
Preferably, the suspension is applied into the atmosphere, as a space spray. For this use, it is preferably applied at a rate of less than 5 litres of liquid per hectare (i.e. as an ultra low volume application), usually 10-5000, e.g. 20-5000, ml per hectare.
Remarkably small amounts of the suspension are required in order to be effective against pests.
The formulation can be applied by conventional equipment, e.g. conventional ultra low volume equipment. It is a feature of preferred formulations, like that of the following Example 1, that when used in commercial spraying equipment, the formulation can be left in the sprayer overnight without the need to flush the system through.
The invention is illustrated by the following Example.
Example 1
The formulation consists, per litre, of:
Bendiocarb technical - to give bendiocarb 2509 Atlox 1045A (Atlas) - polyoxyethylene
sorbitan oleate/laurate, surface active agent 25g
Geopon GO 11 (NL Industries) - organically
modified montmorillonite clay, suspending agent 25g
Risella EL (Shell) - technical grade
mineral oil 750ml
The Atlox 1045A and Geopon GO 11 were dispersed in 450 ml of the Risella oil per litre of ultimate formulation, using the high speed mixer Silverson AXR for 30 minutes. The remaining Risella oil was then added and stirred in, using the same mixer. The bendiocarb was then dispersed in the mixture using the same mixer. Finally, the product was ball milled in a Dyno KDL mixer (from W Bachofen) to give a particle size of 0.5-5 microns in largest dimension by microscopic examination.
The viscosity of the freshly made formulation was 115,000 centipoises, measured at 20"C on a Brookfield viscometer, model RVT, number 3 spindle, at 0.5 revolution per minute.
Example 2
The formulation consists, per litre, of:
Bendiocarb technical, to give bendiocarb 2509 Triton X-207 (polyoxyethylene alkylphenol
containing 20% dinonyl phenol, surface
active agent) 1009
Geopon GO-11 (NL Industries, organically
modified montmorillonite clay, suspending
agent) 10g Propylene carbonate 3.39
Klearol (medicinal grade mineral oil) 690ml
600 Ml of the Klearol per litre of the ultimate formulation were charged to an Attritor 15 ball mill. The Triton and then the bendiocarb were added, and the mixture was milled to a particle size less than 15 microns in largest dimension by microscopic examination.The Geopon was dispersed in the remaining Klearol using a turbine stirrer, and the propylene carbonate was added; the resulting liquor was passed through a Premier 84 laboratory colloid mill to give a stiff gel. The gel was added to the milled material in the Attritor ball mill, and the mixture milled to obtain a homogenous suspension.
The viscosity of the freshly made formulation, as measured as in Example 1 but with a number 2 spindle, was 10,000 centipoises.
Example 3
Following the procedure of Example 2, formulations with the following content per litre were prepared:
Bendiocarb technical, to give bendiocarb 250g
Atlox 1045A (Atlas, polyoxyethylene sorbitan
oleate/laurate, surface active agent) 209 Geopon GO 11 (NL Industries, organically
modified montmorillonite clay, suspending
agent) 20g
Klearol (medicinal grade mineral oil) 755ml
The viscosity of the freshly made formulations, as measured as in Example 1,was 45000-80000 centipoises.
Example 4
The formulation of Example 1 was applied through a Micro-Gen aerosol generator ED2-20A in field trials in the United States of America against mosquitoes. The sprayer was conveyed at 16 kg per hour, and the insecticide was applied at the following rates, assuming an effective dispersal of 100m from the spray route in assessing rates per ha:
ml/min g bendiocarblmin g bendiocarb/ha 53 13.3 5
74 18.5 7
98 24.4 9
Female mosquito adults, either bred from laboratory stock or collected in the field as larvae or pupae, were placed in disposable cylindrical bioassay cages 15 cm diameter x 4.5cm deep with a fine nylon mosquito net with a 1.5 mm mesh at each end. These were suspended from brackets placed in the field so that the cage centres were 160 cm and 40 cm above ground in all tests. Three such brackets were set 15m apart at 50m from the spray route with another three sets at 100m. Therefore 12 cages were exposed in each test. Four control (unsprayed) cages were held upwind from the spray. About 25 mosquitoes were placed in each cage, more or less depending on the numbers available. The cages were left in the field for 15 minutes after spraying in which time the mosquitoes either became moribund or remained healthy. Mortalities were recorded at 12 hours after exposure.
The Culex quinquefasciatus of field origin used in the tests is known to be resistant to malathion and naled.
The results are shown below
Percentage Mortalities at 12 hours Insect.
Control 50m 100m Rate
Females only (Untreated) 160cm 40cm 160cm 40cm ml/min Aedesaegypti L 0 100 100 98 95 74
Aedes F 1 100 100 100 100 98
sollicitans 2 89 79 94 78 74
Aedes L 1 93 98 98 100 74
taeniorhynchus
Aedes L 2 98 77 92 50 74
triseriatus Culexpipiens L 7 100 100 100 100 74
2 100 99 95 83 53
Culex F 0 100 95 91 52 98
quinquefasciatus
Anopheles L 0 100 100 100 100 74
albimanus
L = Laboratory Stock F = Field Stock
Four series of air samples were taken at 5, 10, 25, 50 and 100m from the spray route to measure the level of bendiocarb present in air when sprayed at the rate of 98 ml/min. Air was sampled at the rate of 4 litres/min for 5 minutes to coincide with the passing of the insecticide cloud.The mean concentration of insecticide in the air was 0.016 mg active ingredient per m3 over the 5 minute sampling period, well below the industrial
Threshold Limit Value Time Weighted Average over an 8 hour day or 40 hour working week of 0.2 mg active ingredient per m3.
The formulation worked perfectly through the Micro-Gen sprayer. The formulation could be left in the sprayer overnight without needing to flush the system through.
Example 5
The formulation of Example 3 was sprayed at a developing building site in the United States of America at a rate of 30 ml per minute from a sprayer mounted on a truck travelling at 16 km per hour, giving an effective insecticide swathe of at least 1 00m. This rate is equivalent to 39 bendiocarb per hectare. The control of mosquitoes Culex quinquefasciatus in cages was assessed, as was the control achieved by analogous treatment using malathion at the standard dose rate of 47g malathion per hectare. The bendiocarb treatment gave 100% control while the malathion treatment gave 70% control.
The bendiocarb formulation did not kill larvae, and this is considered of major technical importance in not building up resistance.
Example 6
The formulation of Example 3 was sprayed in the United States of America againstAedes taeniorhynchus (malathion resistant), Culexnigrapalpus and Psorophora columbiae. The sprayer delivered 120 ml per minute and travelled at 16 km per hour. Effective control of all the species was achieved.
Example 7
The formulation of Example 3 was sprayed in the United States of America at 30 ml per minute from a sprayer travelling at 16 km per hour under erratic wind conditions against Psorophora columbiae. Effective control was achieved.
Example 8
The formulation of Example 3 was sprayed from aircraft against grasshoppers late in their season in the
United States of America. A dose of 150g bendiocarb per ha gave 87% control. The standard melathion dose is 6009 melathion per ha, and the standard carbaryl dose is 6809 carbaryl per ha.
Claims (28)
1. A stable, pesticidal, liquid suspension of low volatility, comprising bendiocarb suspended in a chemically inert oil of low volatility and of low solubility for bendiocarb.
2. A suspension according to claim 1 containing 5-700 g of bendiocarb per litre.
3. A suspension according to claim 1 containing 150-3009 of bendiocarb per litre.
4. A suspension according to claim 1 wherein the bendiocarb particles in the suspension are substantially all less than 20 microns in largest dimension.
5. A suspension according to any one of the preceding claims containing 300-996ml of the oil per litre.
6. A suspension according to any one of the preceding claims wherein the oil is of solubility for bendiocarb below 0.05g per litre of oil at 2O0C.
7. A suspension according to any one of the preceding claims wherein the oil is of flash point between 100 and 300 C.
8. A suspension according to any one of the preceding claims wherein the oil is of kinematic viscosity between 0 and 100 centistokes at 400C.
9. A suspension according to claim 8 wherein the kinematic viscosity is from 5 to 25 centistokes at 40"C.
10. A suspension according to any one of the preceding claims wherein the oil is of boiling point 200-400"C.
11. A suspension according to any one of the preceding claims wherein the oil is a paraffin oil.
12. A suspension according to any one of the preceding claims which contains a suspending agent.
13. A suspension according to claim 12 which contains 1 -100g of suspending agent per litre.
14. A suspension according to claim 12 or 13 which is thixotropic.
15. A suspension according to any one of claims 12-14wherein the suspending agent is a montmorillonite clay.
16. A suspension according to any one of the preceding claims which contains a surface active agent.
17. A suspension according to claim 16 which contains 1-2009 of surface active agent per litre.
18. A suspension according to claim 16 or 17 wherein the surface active agent is non-ionic.
19. A suspension according to claim 18 wherein the non-ionic surface active agent is a condensation product with ethylene oxide.
20. A suspension according to claim 19 wherein the non-ionic surface active agent is a condensation product of an alkyl- or alkenyl-substituted phenol with ethylene oxide.
21. A suspension according to claim 19 wherein the non-ionic surface active agent is a condensation product of ethylene oxide with hydrocarbon of 12-18 carbon atom ester of a polyhydric alcohol ether.
22. A suspension according to claim 19 wherein the non-ionic surface active agent is a condensation product of a hydrocarbon of 12-18 carbon atom alcohol with ethylene oxide.
23. A suspension according to any one of the preceding claims which has been diluted with water or hydrocarbon.
24. A process for preparing the suspension claimed in any one of claims 1-22, which process comprises admixing the ingredients.
25. A process for preparing the suspension claimed in any one of claims 12-15, which process comprises dispersing the suspending agent in at least some of the oil before admixing the bendiocarb therewith.
26. A method of combating pests at a locus infested or liable to be infested with them, which method comprises applying to the locus a pest-combating amount of the suspension claimed in any one of claims 1-22 or the diluted suspension claimed in claim 23.
27. A method according to claim 26 wherein the application is outdoors.
28. A method according to claim 26 or 27 wherein 10-5000ml are applied per hectare.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8041414A GB2067407B (en) | 1980-01-18 | 1980-12-29 | Pesticidal composition and use |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8001748 | 1980-01-18 | ||
GB8041414A GB2067407B (en) | 1980-01-18 | 1980-12-29 | Pesticidal composition and use |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2067407A true GB2067407A (en) | 1981-07-30 |
GB2067407B GB2067407B (en) | 1983-07-27 |
Family
ID=26274195
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8041414A Expired GB2067407B (en) | 1980-01-18 | 1980-12-29 | Pesticidal composition and use |
Country Status (1)
Country | Link |
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GB (1) | GB2067407B (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0117363A1 (en) * | 1983-01-22 | 1984-09-05 | Schering Agrochemicals Limited | Insecticidal compositions |
EP0149459A2 (en) * | 1984-01-18 | 1985-07-24 | S.I.P.C.A.M. S.p.A. Società Italiana Prodotti Chimici e per l'Agricoltura Milano | Stabilized fluid suspension of antiparasites in unchlorinated organic solvents and process for the preparation and use thereof |
NL9100706A (en) * | 1990-05-02 | 1991-12-02 | Rhone Poulenc Agriculture | SOLUBLE PACKAGING. |
WO1992001376A1 (en) * | 1990-07-18 | 1992-02-06 | Rhone-Poulenc Agrochimie | Water dispersible gel formulations |
WO1992001378A1 (en) * | 1990-07-18 | 1992-02-06 | Rhone-Poulenc Agrochimie | Gel formulations for use in toxic or hazardous product containerisation systems |
WO1992001374A1 (en) * | 1990-07-18 | 1992-02-06 | Rhone-Poulenc Agrochimie | Containerization system for agrochemicals and the like |
WO1992001375A1 (en) * | 1990-07-18 | 1992-02-06 | Rhone-Poulenc Agrochimie | Gel formulations for hazardous products |
US5248038A (en) * | 1990-07-18 | 1993-09-28 | Rhone-Poulenc Inc. | Containerization system for agrochemicals and the like |
US5280835A (en) * | 1990-05-02 | 1994-01-25 | Rhone-Poulenc Inc. | Laminated bags for containerization of toxic and hazardous materials |
US5395616A (en) * | 1988-06-15 | 1995-03-07 | May & Baker Ltd. | Packaging for liquid products |
US6436439B1 (en) | 1994-08-03 | 2002-08-20 | Syngenta Limited | Gel formulation |
WO2009004281A2 (en) * | 2007-07-03 | 2009-01-08 | Syngenta Limited | Formulations |
WO2012080208A1 (en) | 2010-12-14 | 2012-06-21 | Lamberti Spa | Agrochemical oil dispersion |
WO2017203527A1 (en) | 2016-05-24 | 2017-11-30 | Adama Makhteshim Ltd. | Oil liquid fungicidal formulation |
WO2019175118A1 (en) | 2018-03-13 | 2019-09-19 | Lamberti Spa | Agrochemical oil dispersions |
-
1980
- 1980-12-29 GB GB8041414A patent/GB2067407B/en not_active Expired
Cited By (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0117363A1 (en) * | 1983-01-22 | 1984-09-05 | Schering Agrochemicals Limited | Insecticidal compositions |
EP0149459A2 (en) * | 1984-01-18 | 1985-07-24 | S.I.P.C.A.M. S.p.A. Società Italiana Prodotti Chimici e per l'Agricoltura Milano | Stabilized fluid suspension of antiparasites in unchlorinated organic solvents and process for the preparation and use thereof |
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WO1992001375A1 (en) * | 1990-07-18 | 1992-02-06 | Rhone-Poulenc Agrochimie | Gel formulations for hazardous products |
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Also Published As
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