WO2018206253A1 - Pesticide compositions - Google Patents
Pesticide compositions Download PDFInfo
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- WO2018206253A1 WO2018206253A1 PCT/EP2018/060030 EP2018060030W WO2018206253A1 WO 2018206253 A1 WO2018206253 A1 WO 2018206253A1 EP 2018060030 W EP2018060030 W EP 2018060030W WO 2018206253 A1 WO2018206253 A1 WO 2018206253A1
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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
Definitions
- the present technology relates to seed treatments, and in particular seed treatment compositions that have improvements in drying times and plantability.
- Pesticides can be applied directly to plant propagation materials (such as seeds) prior to sowing and/or are used in foliar or furrow applications.
- a seed treatment is any material applied to a seed.
- seed treatments include, inter alia, pesticides, non-pesticide formularies, and mixtures thereof.
- Non-pesticide formularies generally include material such as surfactants, humectants, fillers, and polymers that influence the treated seed characteristics.
- Seed treatments are generally used on a variety of crops to control a variety of pests. Seed treatments are commonly used to ensure uniform stand establishment by protecting against soilborne diseases and insects. Systemic seed treatments may provide an alternative to traditional broadcast sprays of foliar fungicides or insecticides for certain early season airborne diseases and insects.
- Pesticide seed treatments come in a variety of formulations: dry flowables (DF), liquid flowables (LF), true liquids (TL), emulsifiable concentrates (EC), dusts (D), wettable powders (WP), suspoemulsions (SE), water-dispersible granules (WG) and others. Some are registered for use only by commercial applicators using closed application systems, others are readily available for on-farm use as dusts, slurries, water soluble bags, or liquid ready-to-apply formulations.
- DF dry flowables
- LF liquid flowables
- TL true liquids
- EC emulsifiable concentrates
- D dusts
- WP wettable powders
- SE suspoemulsions
- WG water-dispersible granules
- Seed coating additives are seed treatments used to remedy problems such as low seed flowability and excessive dust-off.
- selection of a seed coating additive to reduce dust-off will likely have the adverse effect of decreasing seed flowability.
- selection of a seed coating to increase seed flowability will likely have the adverse effect of increasing dust-off.
- the present technology provides for seed treatment compositions having improved adherence to plant propagation material with low dust-off.
- the compositions of the present technology have particular application in the protection of plant propagation materials, such as seeds, against pests when combined with one or more pesticides.
- the present technology thus provides an improved seed treatment suitable for applying to plant propagation materials.
- the seed treatments of the present technology include propylene glycol and talc. Such additions drastically improve the drying time of the seed treatment compositions, thereby improving the adherence to the seed.
- FIG. 1 is a chart providing the results of Example 2.
- Propylene glycol also called propane- 1,2-diol
- propane- 1,2-diol has the chemical formula C3H8O2.
- the use of propylene glycol in the compositions of the present invention aid in the drying times of the composition after it has been used to treat seeds.
- propylene glycol is sometimes utilized in seed treatment formulations, it is done so for its properties as an antifreeze component and not as a component for reducing drying times.
- the amount of propylene glycol in the composition may be between about 2% and about 8% by weight of the composition.
- the amount of propylene glycol in the composition may be between about 4% and about 6% by weight of the composition.
- the amount of propylene glycol in the composition may be about 5% by weight of the composition.
- talc is utilized to aid in the drying times of the compositions of the present invention.
- certain amounts of talc may be necessary to ensure that the compositions of the present invention do not result in too much dust-off, forcing the composition off of the seed after treating.
- talc is utilized in the composition in an amount less than or equal to about 10% by weight of the composition.
- talc is utilized in the composition in an amount less than or equal to about 9% by weight of the composition, or an amount less than or equal to about
- Talc suitable for the present invention may include SILVERLINE 002 (magnesium silicate) (Fitz Chem of Itasca, IL) and SILVERLINE 202 (magnesium silicate) (Imerys Corporation of Sylacauga, AL).
- the talc may include magnesium silicate.
- the propylene glycol and talc utilized in the compsositions of the present invention may also be expressed in the form of a ratio.
- the ratio of propylene glycol to talc may be from about 2: l to about 1 :2, from about 1.5:1 to about 1 : 1.5, from about 1.2: 1 to about 1 :1.2 all by weight of the composition.
- the propylene glycol to talc may be about 1 :1 ratio by weight of the composition.
- compositions of the present invention may reduce drying times of the compositions once applied to seeds to less than 5 hours.
- compositions of the present invention may reduce drying times of the composition once applied to seeds to less than 2 hours.
- Seed treatment formulations applied to seeds generally comprise a pesticide, surfactants, film- forming polymers, carriers, antifreeze agents, and other formulary additives and when used together provide compositions that are storage stable and are suitable for use in normal seed treatment equipment, such as a slurry seed treater, direct treater, panogen treater or a mist-o-matic treater as well as on-farm hopper-box or planter-box treatments. Propagation materials treated with the compositions dry quickly, have good flowability, suitable coverage and have little or no dust-off.
- the compositions are advantageously combined with a pesticidally effective amount of at least one pesticide.
- Pesticides are intended to cover compounds active against pests which are intended to repel, kill, or control any species designated a pest including weeds, insects, rodents, fungi, bacteria, or other organisms.
- pesticides include those selected from, for example and not for limitation, insecticides, acaricides, bactericides, fungicides, nematicides and molluscicides.
- Suitable additions of insecticidally, acaricidally, nematicidally, or molluscicidally active ingredients are, for example and not for limitation, representatives of the following classes of active ingredients: organophosphorus compounds, nitrophenols and derivatives, formamidines, triazine derivatives, nitroenamine derivatives, nitro- and cyanoguanidine derivatives, ureas, benzoylureas, carbamates, pyrethroids, chlorinated hydrocarbons and Bacillus thuringiensis products.
- the insecticides may include thiamethoxam, abamectin, cyanoimine, acetamiprid, thiodicarb, nitromethylene, nitenpyram, clothianidin, dinotefuran, fipronil, lufenuron, pyripfoxyfen, thiacloprid, fluxofenime; imidacloprid, Chloranthraniliprole, beta cyfiuthrin, lambda cyhalothrin, fenoxycarb, diafenthiuron, pymetrozine, diazinon, disulphoton; profenofos, furathiocarb, cyromazin, cypermethrin, tau-fiuvalinate, spinetoram, spinosad, sulfloxaflor, tefiuthrin or Bacillus thuringiensis products.
- Suitable additions of fungicidally active ingredients are, for example and not for limitation, representatives of the following classes of active ingredients: strobilurins, triazoles, ortho-cyclopropyl-carboxanilide derivatives, phenylpyrroles, and systemic fungicides.
- fungicidally active ingredients include, but are not limited to, the following compounds: azoxystrobin; bitertanol; carboxin; Cu 2 0; cymoxanil;
- cyproconazole cyprodinil; dichlofluamid; difenoconazole; diniconazole; epoxiconazole;
- fenpiclonil fludioxonil; fiuoxastrobin, fluquiconazole; fiusilazole; flutriafol; furalaxyl;
- guazatin hexaconazole; hymexazol; imazalil; imibenconazole; ipconazole; kresoxim-methyl; mancozeb; metalaxyl; mefenoxam; metconazole; myclobutanil, oxadixyl, pefurazoate;
- the pesticides of the present composition may include thiamethoxam, mefenoxam and fludioxonil.
- the pesticidally active compound or compound mixture is present in the composition in an amount of from about 0.05 % to about 50 % by weight, more specifically, from 2 to about 30% by weight of the entire composition.
- the pesticidally active compounds include between about 20 and 30% by weight of the composition.
- Seed treatment application rates with respect to pesticidally active ingredients may be between about 0.5 to 1000 g of pesticidally active compound per 100 kg seed.
- application rate ranges with respect to seed treatments include: 0.5 to 500 g of pesticidally active compound per 100 kg seed; 0.5 to 250 g of pesticidally active compound per 100 kg seed; 0.5 to 100 g of pesticidally active compound per 100 kg seed; 0.5 to 75 g of pesticidally active compound per 100 kg seed; and 0.5 to 55 g of pesticidally active compound per 100 kg seed.
- Seed treatment compositions may also contain at least about 2% up to about 15% by weight of a surface-active agent.
- Compositions may contain from 3% up to 7% by weight of a surface -active agent.
- the surface-active agent may comprise at least one nonionic surfactant and may optionally further comprise one or more anionic surfactants.
- nonionic surfactants include polyarylphenol polyethoxy ethers, polyalkylphenol polyethoxy ethers, polyglycol ether derivatives of saturated fatty acids, polyglycol ether derivatives of unsaturated fatty acids, polyglycol ether derivatives of aliphatic alcohols, polyglycol ether derivatives of cycloaliphatic alcohols, fatty acid esters of polyoxy ethylene sorbitan, alkoxylated vegetable oils, alkoxylated acetylenic diols, polyalkoxylated alkylphenols, fatty acid alkoxylates, sorbitan alkoxylates, sorbitol esters, C 8 - C22 alkyl or alkenyl polyglycosides, polyalkoxy styrylaryl ethers, alkylamine oxides, block copolymer ethers, polyalkoxylated fatty glyceride, polyalkylene glycol ethers
- nonionic sufactants include: Genapol X-060 (Clariant) (ethoxylated fatty alcohol); Sorpohor BSU (Rhodia) (ethoxylated tristyrylphenol); Makon TD- 6 (Stepan) (ethoxylated fatty alcohol); BRIJ 30 (Uniqema) (ethoxylated lauryl alcohol);
- Witconol CO-360 (Witco) (ethoxylated castor oil)
- Toximul 8320 (Stepan) (polyethylene- polypropylene glycol monobutyl ether); and Witconol NP-60 (Witco) (ethoxylated
- nonylphenol nonylphenol
- Suitable nonionic surfactants can be prepared by methods known per se and also are commercially available.
- the anionic surfactant may be any known in the art.
- Anionic surfactants are in general oligomers and polymers, as well as polycondensates, which contain a sufficient number of anionic groups to ensure their water-solubility.
- Anionic surfactants also include alcohol sulfates, alcohol ether sulfates, alkylaryl ether sulfates, alkylaryl sulfonates such as alkylbenzene sulfonates and alkylnaphthalene sulfonates and salts thereof, alkyl sulfonates, mono- or di-phosphate esters of polyalkoxylated alkyl alcohols or alkylphenols , mono- or di- sulfosuccinate esters of C12-C15 alkanols or polyalkoxylated C12-C15 alkanols, alcohol ether carboxylates, phenolic ether carboxylates, polybasic acid esters of ethoxylated polyoxyalkylene glycols consisting of oxybutylene or the residue of tetrahydrofuran, sulfoalkylamides and salts thereof such as N-methyl ⁇ N-oleoyltaurate Na
- anionic surfactants include: Geropon T77 (Rhodia) (N- methyl--N-oleoyltaurate Na salt); Soprophor 4D384 (Rhodia) (tristyrylphenol sulphate); Reax 825 (Westvaco) (ethoxylated lignin sulfonate); Stepfac 8171 (Stepan) (ethoxylated
- nonylphenol phosphate ester nonylphenol phosphate ester
- Stepfac 8181 (tridecyl alcohol ethoxy late phosphate ester), Ninate 401-A (Stepan) (calcium alkylbenzene sulfonate); Emphos CS-131 (Witco) (ethoxylated nonylphenol phosphate ester); Ultrazine NA (sodium lignosulfonate); Ufoxane 3A, NA (sodium lignosulphonate); Morwet D-425 (sodium alkylnapthalenesulfonate), Reax 1425E (lignin sulfonate ethoxylate), and Atphos 3226 (Uniqema) (ethoxylated tridecylalcohol phosphate ester).
- Suitable anionic surfactants can be prepared by methods known per se and also are commercially available.
- certain cationic or zwitterionic surfactants also are suitable for use in the present invention such as alkanol amides of Cs-Cis fatty acids and Cs-Cis fatty amine polyalkoxylates, Cio-Cis alkyldimethylbenzylammonium chlorides, coconut alkyldimethylaminoacetic acids, and phosphate esters of Cs-is fatty amine polyalkoxylates.
- zwitterionic surfactants may be employed as follows: (1) 0.5 - 4% by weight of a wetting agent selected from at least one anionic surfactant.
- Anionic surfactant wetting agents include sulfoalkylamides and salts thereof such as N-methyl ⁇ N-oleoyltaurate Na salt, alkylaryl sulfonates such as alkylbenzene sulfonates and alkylnaphthalene sulfonates and salts thereof and salts of ligninsulfonic acid; (2) 1 - 4% by weight of a dispersing agent selected from at least one anionic surfactant.
- Anionic surfactant dispersing agents include sulfate esters of styrylphenyl alkoxylates, and sulfonate esters of styrylphenyl alkoxylates and their
- compositions may contain between about 1.5 and about 8 % by weight of surface active agents.
- the compositions of the present invention may include about 1 to about 3 % by weight of an anionic surfactant and from about 0.5 to about 3 % by weight of a nonionic surfactant.
- the anionic surfactant may be tridecyl alcohol ethoxylate phosphate ester and the nonionic surfactant may be polyethylene -polypropylene glycol monobutyl ether.
- the compositions of the present invention may include about 1% by weight of the nonionic surfactant and may also include about 2% by weight of an anionic surfactant.
- the composition may include the Morwet D-425 (sodium alkylnapthalenesulfonate) at about 0.2% by weight of the composition, Ultrazine NA (sodium lignosulfonate) at about 2.0% by weight of the composition, Stepfac 8181 (tridecyl alcohol ethoxylate phosphate ester) at about 2.0% by weight of the composition, Toximul 8320 (polyethylene -polypropylene glycol monobutyl ether) at about 1 .0% by weight of the composition, propylene glycol at about 5.0% by weight of the composition, and Silverline 002 (magnesium silicate) at about 5.0% by weight of the composition or at about 10.0% by weight of the composition.
- Morwet D-425 sodium alkylnapthalenesulfonate
- Ultrazine NA sodium lignosulfonate
- Stepfac 8181 tridecyl alcohol ethoxylate phosphate ester
- Toximul 8320 poly
- Seed treatment compositions may also include a humectant.
- a humectant is hygroscopic substance used to retain water.
- the compositions generally contain from 1% to 30 % by weight of the composition.
- commonly used formulation humectants include antifreezes, for example ethylene glycol, propylene glycol and glycerin. In examples where propylene glycol is utilized as a humectant the amount expressed above is in addition to the other amounts provided.
- Film-forming Polymer [0038] Seed treatment composition may also include at least one polymer selected from water-soluble and water-dispersible film-forming polymers.
- Suitable polymers generally have an average molecular weight of at least about 1 ,000 up to about 100,000; more specifically at least about 5,000, up to about 100,000.
- the compositions generally contain from about 0.5% to about 10% by weight of the composition of polymer. In a specific embodiment, the compositions contain from about 1.0% up to about 5% by weight of a film- forming polymer.
- Polymers are generally selected from alkyleneoxide random and block copolymers such as ethylene oxide -propylene oxide block copolymers (EO/PO block copolymers) including both EO-PO-EO and PO-EO-PO block copolymers, ethylene oxide -butylene oxide random and block copolymers, C2-6 alkyl adducts of ethylene oxide -propylene oxide random and block copolymers, C2-6 alkyl adducts of ethylene oxide -butylene oxide random and block copolymers.
- alkyleneoxide random and block copolymers such as ethylene oxide -propylene oxide block copolymers (EO/PO block copolymers) including both EO-PO-EO and PO-EO-PO block copolymers, ethylene oxide -butylene oxide random and block copolymers, C2-6 alkyl adducts of ethylene oxide -propylene oxide random and block copolymers.
- Prospective polymers further include polyoxyethylene-polyoxypropylene monoalkylethers such as methyl ether, ethyl ether, propyl ether, butyl ether or mixtures thereof; vinylacetate/vinylpyrrolidone copolymers; alkylated vinylpyrrolidone copolymers;
- polyvinylpyrrolidone and polyalkyleneglycol including the polypropylene glycols and polyethylene glycols.
- polymers include Pluronic PI 03 (BASF) (EO-PO-EO block copolymer), Pluronic P65 (BASF) (EO-PO-EO block copolymer), Pluronic PI 08 (BASF) (EO- PO-EO block copolymer), Vinamul 18160 (National Starch) (polyvinylacetate), Agrimer 30 (ISP) (polyvinylpyrrolidone), Agrimer VA7w (ISP) (vinyl acetate/vinylpyrrolidone
- compositions and methods lack a film- forming polymer that are provided above. As illustrated in the Examples provided below, the absence of such a film-forming polymer may aid in plantability of the composition. [0042] Antifreeze
- composition may also comprise an antifreeze from about 2 and up to about 30% by weight.
- antifreezes include ethylene glycol, 1,2 -propylene glycol, 1,3- propylene glycol, 1,2-butanediol, 1 ,3-butanediol, 1 ,4-butanediol, 1 ,4-pentanediol, 3-methyl- 1,5-pentanediol, 2,3-dimethyl-2,3-butanediol, trimethylol propane, mannitol, sorbitol, glycerol, pentaerythritol, 1,4-cyclohexanedimethanol, xylenol, bisphenols such as bisphenol A or the like.
- ether alcohols such as diethylene glycol, triethylene glycol, tetraethylene glycol, polyoxyethylene or polyoxypropylene glycols of molecular weight up to about 4000, diethylene glycol monomethylether, diethylene glycol monoethylether, triethylene glycol monomethylether, butoxyethanol, butylene glycol monobutylether, dipentaerythritol, tripentaerythritol, tetrapentaerythritol, diglycerol, triglycerol, tetraglycerol, pentaglycerol, hexaglycerol, heptaglycerol, octaglycerol and the like.
- ethylene glycol propylene glycol
- glycerin ethylene glycol
- propylene glycol the amount expressed above is in addition to the other amounts provided.
- the composition may also contain (e) at least one thickener.
- the thickener is present in the aqueous composition in an amount from about 0.01% to about 25% by weight, more specifically from 0.02 to 10% by weight of the entire composition.
- thickeners water-soluble polymers which exhibit pseudoplastic properties in an aqueous medium
- gum arabic gum karaya
- gum tragacanth gum tragacanth
- guar gum locust bean gum
- xanthan gum carrageenan
- alginate salt casein, dextran, pectin, agar
- 2- hydroxyethyl starch 2-aminoethyl starch
- 2 -hydroxy ethyl cellulose methyl cellulose, carboxymethyl cellulose salt, cellulose sulfate salt
- polyacrylamide alkali metal salts of the maleic anhydride copolymers, alkali metal salts of poly(meth)acrylate, and the like.
- Attapulgite-type clay carrageenan, croscarmellose sodium, furcelleran, glycerol, hydroxypropyl methylcellulose, polystyrene, vinylpyrrolidone/styrene block copolymer, hydroxypropyl cellulose,
- composition according to the invention can be employed together with the adjuvants customary in formulation technology, biocides, biostats, emulsifiers (lethicin, sorbitan, and the like), antifoam agents or application-promoting adjuvants customarily employed in the art of formulation.
- adjuvants customary in formulation technology
- biocides biostats
- emulsifiers lethicin, sorbitan, and the like
- antifoam agents customarily employed in the art of formulation.
- inoculants and brighteners there may be mentioned inoculants and brighteners.
- a coloring agent such as a dye or pigment (and the like such as described in the CFR 180.1001) is included in the seed coating so that an observer can immediately determine that the seeds are treated.
- the dye is also useful to indicate to the user the degree of uniformity of the coating applied.
- inventive compositions contain and/or may be applied together or sequentially with further active compounds.
- further compounds can be fertilizers or micronutrient donors or other preparations that influence plant growth. They can also be selective herbicides, insecticides, fungicides, bactericides, insect growth regulators, plant growth regulators, nematicides, molluscicides or mixtures of several of these preparations.
- the pesticidal compositions of the invention can be prepared by processes known in the art.
- the compositions of the invention can be prepared by a process which comprises the steps: (a) forming a premix with at least one pesticidal compound, at least one surfactant, and water (b) forming a premix of a thickener and water, and (c) sequentially adding the premixes (a) and (b), talc, propylene glycol, the remaining ingredients, and water while stirring to form a homogeneous composition.
- compositions of the invention can be prepared by combining commercially available seed treatment formulations with talc and propylene glycol.
- Pesticidal compositions in accordance with the invention may take the form of aqueous solutions, dispersions, suspensions, emulsions or suspoemulsions.
- aqueous solutions dispersions, suspensions, emulsions or suspoemulsions.
- the composition is a ready for use suspension or suspoemulsion.
- plant propagation material and seed encompass both true seeds and other types of plant propagation material from which plants grow. Plant propagation material itself is commonly referred to as a seed and is defined as such herein. Many seed treatments are applied to true seeds, which have a seed coat surrounding an embryo. Seed treatments are also applied to plant propagation materials such as rhizomes, bulbs, corms or tubers.
- the amount of fungicide, insecticide or other ingredients used in the seed treatment are employed in amounts that do not inhibit generation of the seed or cause phytotoxic damage to the seed.
- the total amount of active ingredients is generally in the range of from about 0.05 % to about 50 % by weight, more specifically, from 15 to about 28% by weight of the entire composition.
- Suitable target seeds are especially those of corn, potatoes, cereals, (wheat, barley, rye, oats, rice), maize, sugar beet, cotton, millet varieties such as sorghum, sun flowers, beans, peas, oil plants such as canola, rape, soybeans, cabbages, tomatoes, eggplants (aubergines), pepper and other vegetables and spices as well as ornamental shrubs and flowers.
- Suitable target seeds also include those of transgenic crop plants of the foregoing varieties.
- Suitable application rates of talc and propylene glycol to plant seeds is between 0.05 to 10.0 g/500g seed; 0.1 to 5.0 g/500g seed; 0.1 to 2.5 g/500g seed; 0.1 to 1.0 g/500g seed; and also between 0.25 to 1.0 g/500 g seed.
- compositions of the invention are applied to the seed as slurry or a soak. There also may be mentioned, e.g., film coating or encapsulation.
- the coating processes are well known in the art, and employ, for seeds, the techniques of film coating or encapsulation, or for the other multiplication products, the techniques of immersion.
- the method of application of the inventive compositions to the seed may be varied and the technology is intended to include any technique that is to be used.
- the compositions of the present technology may be formulated or mixed in the seed treater tank or combined on the seed by overcoating with other seed treating agents.
- the agents to be mixed with the compounds of this invention may be for the control of pests, nutrition, and the control of plant diseases.
- a feature of the technology is that it provides for a treated seed with a reduction in drying times over conventional seed treatments while at the same time reducing excess dust. Accordingly, the formulation aids in reducing the associated health hazards to those who work with treated seeds, such as processing plant employees, truck drivers, warehouse workers, and farmers.
- Still another feature of the technology is the uniform coating of-seeds with non- dusting seed treatment which will not interfere with germination and sprouting of the seed but which will protect the seed against seed-borne pathogens.
- each formulation included thiamethoxam (22.62 % by weight), fludioxonil (1.12 % by weight), and mefenoxam (1.70 % by weight).
- Formulation B also included propylene glycol (5.0 % by weight)
- Formulation C included propylene glycol (5.0 % by weight) and talc (Silverline 002 5.0 % by weight).
- Coating Evaluation - On Film Each of the formulations prior to being applied to seeds were placed on a plastic film and allowed to dry. The drying times of each formulation are provided in the Table below.
- Formulation B Dry to the touch within 1 day
- Formulation C Dry to the touch within 2 hours
- Soybean seeds were then treated with each of the three different formulations (A, B, and C) to measure wet flow (g/sec), and dry flow (g/sec).
- Wet flow Measurement Seeds are taken immediately from the treater and are weighed. The seeds are then placed in a Cox funnel having a 1 .25 inch opening at the stem. The funnel door is opened and a stopwatch concurrently started. The funnel may be tapped lightly if seeds begin to clump. The stopwatch is stopped when the last seed flows from the funnel. The seeds are poured back into the funnel two times and the above procedure repeated for a total of three measurements. The flow measurements are then calculated and averaged.
- Dry flow Measurement Seeds are taken from the treater and allowed to dry completely (approximately 24 hours) and are then weighed. The seeds are then placed in a Cox funnel having a 1.25 inch opening at the stem. The funnel door is opened and a stopwatch concurrently started. The funnel may be tapped lightly if seeds begin to clump. The stopwatch is stopped when the last seed flows from the funnel. The seeds are poured back into the funnel two times and the above procedure repeated for a total of three measurements. The flow measurements are then calculated and averaged.
- compositions (A, B, C, D and E shown in Table 3) were prepared and treated onto soybean seeds, and tested under various conditions to determine the plantability of the seed against untreated soybean seeds.
- the four different compositions were treated on soybean seeds of the variety Waseguro. Once the seeds were treated with the appropriate composition, they were immediately placed in a plastic container. The seeds were then stored at various temperatures and different relative humidity (RH) and were allowed to dry at different intervals.
- RH relative humidity
- the drying times and conditions are provided: (1) seeds stored at 25 °C with RH of 60-70% for 30 mins; (2) seeds stored at 25°C with RH of 60-70% for 3 hours; (3) seeds stored at 25°C with RH of 60-70% for 24 hours; (4) seeds stored at 40°C with RH of 98% for 1 hour; and (5) seeds stored at 40°C with RH of 98% for 4 hours.
- the seeds were placed in a roll-type seeder, which was run for two minutes and the discharged seeds were collected. The weight of the discharged seeds were recorded and each test was repeated three times. Each test was repeated three times (any seeds trapped in the holes were removed after each test). The machine was cleaned after evaluation of each sample and verified to be clean by running the test with untreated seeds in between samples.
- Cruiser FS30 was included as a standard, because this is known to have good plantability
- Toximul 8320 1.00 1.00 1.00 1.00 1.00 1.00 1.00
- a falling seed weight less than 100% indicates impaired plantability compared with untreated seeds.
- formulations A to E of the present invention all give better plantability compared with the CruiserMaxx or Cruiser FS30 commercial standards, especially under high humidity conditions.
- Treatments without binder showed better plantability after 30 minutes drying in comparison with treatments containing the binder (formulations D and E); the presence of a film- forming polymer may inhibit flowability of seeds at certain temperatures and relative humidity. Such finding is of immense importance, as many seeds are planted under very hot and humid conditions.
- CruiserMaxx seed treatment does not contain propylene glycol or talc.
- Table 5 Dust-off and drying time of treated seeds CruiserMaxx (standard) 0.1 mg Remained wet/tacky after 2 weeks
- Dust-off levels were similar for all formulations, and all within acceptable levels for seed treatment formulations.
- the addition of propylene glycol was found to dramatically speed up drying time compared with glycerine in the CruiserMaxx standard. Further, the addition of 5% talc dramatically accelerated drying time without causing dust-off issues. The addition of 10% talc did not further improve drying time. The presence or absence of a binder has little effect on drying time but does marginally improve dusting properties.
- an FT4 instrument was used to measure the resistance of seeds to flow while the seeds are in motion.
- a precision 'blade', or impeller is rotated and moved downwards and upwards through the sample to establish a precise flow pattern.
- This causes many particles/seeds to interact, or flow relative to one another, and the resistance experienced by the blade represents the difficulty of this relative particle movement, or the bulk flow properties.
- This resistance is measured as the force required to move the seeds and presented as Down Energy or Up Energy. The less force, the better the flow properties of a treated seed. Resistance to flow can create issues with seed handling and plantability. Good flow properties related to the tackiness of the seeds not only immediately after treatment but after the drying process.
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Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019561835A JP7488048B2 (ja) | 2017-05-12 | 2018-04-19 | 殺生物剤組成物 |
| JP2022120228A JP7504165B2 (ja) | 2017-05-12 | 2022-07-28 | 殺生物剤組成物 |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762505166P | 2017-05-12 | 2017-05-12 | |
| US62/505,166 | 2017-05-12 |
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| WO2018206253A1 true WO2018206253A1 (en) | 2018-11-15 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2018/060030 Ceased WO2018206253A1 (en) | 2017-05-12 | 2018-04-19 | Pesticide compositions |
Country Status (2)
| Country | Link |
|---|---|
| JP (2) | JP7488048B2 (https=) |
| WO (1) | WO2018206253A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116940235A (zh) * | 2021-03-01 | 2023-10-24 | 先正达农作物保护股份公司 | 杀有害生物配制品 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018206253A1 (en) | 2017-05-12 | 2018-11-15 | Syngenta Participations Ag | Pesticide compositions |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006024333A2 (en) * | 2004-08-17 | 2006-03-09 | Syngenta Participations Ag | Aqueous neonicotinoid compositions for seed treatment |
| WO2006035316A2 (en) * | 2005-04-25 | 2006-04-06 | Syngenta Participations Ag | Fungicidal aqueous compositions for seed treatment |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007039340A (ja) * | 2005-07-05 | 2007-02-15 | Kanebo Cosmetics Inc | 防腐殺菌剤及び皮膚外用組成物 |
| WO2018206253A1 (en) * | 2017-05-12 | 2018-11-15 | Syngenta Participations Ag | Pesticide compositions |
-
2018
- 2018-04-19 WO PCT/EP2018/060030 patent/WO2018206253A1/en not_active Ceased
- 2018-04-19 JP JP2019561835A patent/JP7488048B2/ja active Active
-
2022
- 2022-07-28 JP JP2022120228A patent/JP7504165B2/ja active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006024333A2 (en) * | 2004-08-17 | 2006-03-09 | Syngenta Participations Ag | Aqueous neonicotinoid compositions for seed treatment |
| WO2006035316A2 (en) * | 2005-04-25 | 2006-04-06 | Syngenta Participations Ag | Fungicidal aqueous compositions for seed treatment |
Non-Patent Citations (1)
| Title |
|---|
| "Pesticide Manual", 2001, BRITISH CROP PROTECTION COUNCIL |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116940235A (zh) * | 2021-03-01 | 2023-10-24 | 先正达农作物保护股份公司 | 杀有害生物配制品 |
| US20240147999A1 (en) * | 2021-03-01 | 2024-05-09 | Syngenta Crop Protection Ag | Pesticidal formulations |
Also Published As
| Publication number | Publication date |
|---|---|
| JP7488048B2 (ja) | 2024-05-21 |
| JP2020520347A (ja) | 2020-07-09 |
| JP2022166034A (ja) | 2022-11-01 |
| JP7504165B2 (ja) | 2024-06-21 |
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