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US20080171661A1 - Water-dispersible agrochemical compositions - Google Patents

Water-dispersible agrochemical compositions Download PDF

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Publication number
US20080171661A1
US20080171661A1 US11/930,706 US93070607A US2008171661A1 US 20080171661 A1 US20080171661 A1 US 20080171661A1 US 93070607 A US93070607 A US 93070607A US 2008171661 A1 US2008171661 A1 US 2008171661A1
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active ingredient
composition
methyl
agrochemical active
primary
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US11/930,706
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John Misselbrook
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Agform Ltd
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Agform Ltd
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Priority to US11/930,706 priority Critical patent/US20080171661A1/en
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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
    • 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
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

Definitions

  • the invention relates to novel chemical compositions in particular, compositions of biologically active agents and their use.
  • the invention is more particularly concerned with granular compositions of low dose-rate agrochemicals, for example pesticides, suitably prepared by an extrusion process, which deliver the active ingredient of the composition efficiently to the substrate, for example a crop, which is to be treated.
  • Dispersible granules may be prepared by extrusion.
  • U.S. Pat. No. 3,954,439 discloses granular compositions of a herbicidal agent and one or more surfactants and processes for the production of such compositions. The process described in U.S. Pat. No. 3,954,439 is applicable to those herbicides which are substantially insoluble in water.
  • This patent states that it is obviously desirable that the granules should have the highest possible content of active herbicidal material.
  • This patent further states that the process is preferably carried out so as to give granules containing at least 50% of active herbicide material and that it is more preferable that the granules should contain more than this, that is at least 80% and even up to 95%.
  • the patent also teaches that it is obviously important to keep the surfactant content down to a minimum, the total amount of surfactant preferably being from 5 to 15%.
  • U.S. Pat. No. 5,872,078 relates to dry, water soluble and/or water dispersible, agriculturally acceptable herbicidal compositions containing N-phosphonomethylglycerine or acceptable water-soluble salt thereof.
  • the composition may comprise further optional ingredients, one of which may be a co-herbicide.
  • co-herbicides A large number of co-herbicides are listed including sulfonylureas such as those available under the trade names Ally, Classic, Oust, Glean and mixtures thereof.
  • a liquid surfactant is added to this mixture and extrusion granulation may be used to process the compositions described to form granules.
  • compositions containing a lower level of a primary active ingredient than conventionally employed in compositions containing the same ingredient, together with a suitable dispersing agent may conferenhanced delivery of the primary active ingredient to the crop to be treated.
  • the invention is particularly applicable to a low use rate agrochemical for instance a pesticide, and especially a water-insoluble agrochemical.
  • the composition may include additional materials in the remaining “formulation space” to provide additional effects.
  • a first aspect of the invention provides an agrochemical composition
  • a primary agrochemical active ingredient preferably a low use rate active ingredient, at a level of less than 50% by weight of the composition and a dispersing agent, preferably a nonionic and/or anionic surfactant(s).
  • compositions according to the first aspect of the invention provide surprisingly beneficial bioavailability of the active for instance by making a larger proportion of the active biologically available in a liquid carrier, for example water, with which the composition is mixed in use than a known composition having a high level of active.
  • the compositions disperse rapidly in the liquid carrier to form stable suspensions of the active material(s) and subsequently dissolve at a rate and to an extent higher than that achieved by conventional compositions containing the same ingredients.
  • This property provides enhanced efficacy of the agrochemicals with attendant reduced crop damage.
  • This enhanced bioavailability means that a given agrochemical effect may be obtained using a lower total amount of agrochemical active thus providing environmental benefits through lower use of agrochemicals.
  • the concentration of the active is lower than conventionally employed, there is a reduced risk that some of the active will not be dispersed or dissolve in the liquid carrier. Hence the risk of poor dispersion or dissolution of the active in a liquid carrier leading to high localized concentrations of the active penetrating to the crop especially the roots of plants and possibly damaging the crop is reduced.
  • a further advantage is that the lower level of primary active ingredient provides enhanced flexibility in formulating a composition as compared to conventional compositions employing high levels of active.
  • the formulator may include a secondary active ingredient or other materials as desired in the composition to provide an optimum effect or balance of properties.
  • the primary active ingredient when low use-rate pesticides, such as water-insoluble compounds including sulfonyl ureas, for example as described in U.S. Pat. No. 5,872,078, are employed as the primary active ingredient with a secondary high rate use pesticide and a suitable dispersing agent at the required level, the rate and extent of solubility and thus the bioavailability, of the primary active or both the actives may be increased as compared to granules containing the equivalent amount of each material alone.
  • the primary and secondary actives are intimately mixed in suitable proportions.
  • optional conventional other ingredients such as one or more additional surfactants are included in the formulation and the ingredients are processed into a suitable form, for example water-dispersible granules.
  • the invention also provides in a preferred embodiment an agrochemical composition
  • agrochemical composition comprising as a primary active ingredient, a low use rate agrochemical active ingredient, at a level of less than 50% by weight of the composition and a secondary active ingredient, preferably a high use rate active ingredient, and a dispersing agent, preferably an anionic and/or nonionic surfactant.
  • compositions provide at least an enhanced effect as regards the primary active and suitably an effect greater than the combined additive affect of both the primary and secondary active is observed where the composition contains a primary and secondary active.
  • low use rate active denotes those agrochemical actives which typically are applied at a rate of less than 100 g/hectare and the term “high use rate” active denotes those agrochemical actives which typically are applied at a rate of more than 1000 g/hectare.
  • compositions of the present invention result in the individual components being used at lower rates and with less phytotoxicity than conventional compositions of the said active materials, against a wide range of pests and diseases.
  • the level of primary active ingredient is suitably selected according to the particular compound to be used but is preferably less than 30% by weight of the composition, especially in the case of a low use rate active.
  • chlorsulfuron may suitably be employed at a level of less than 30%, for example 25% by weight of the composition.
  • the primary active ingredient for example bensulfuron, is present at a level of less than 10% and more preferably less than 2% by weight of the composition.
  • the primary active is present at a level of less than 1%.
  • the composition will contain the primary active at a level at which, on mixing with a liquid carrier, it provides a concentration of active which will provide a beneficial effect in treating crops. This level may suitably be at 0.05% but is preferably at least 0.1% and desirably at least 0.2% by weight of the composition although the precise level may be adjusted according to the particular application and the particular primary active present in the composition.
  • a second active is employed, it is suitably present at a level greater than the level of the primary active ingredient.
  • the secondary active is present at a level of at least 30%, more preferably at least 50%, optimally at least 65%, for example 75% by weight of the composition.
  • the invention comprises a dry, free-flowing, dustless and rapidly dispersing granular formulation containing a low use rate pesticide or mixture of pesticides together with an additional high use rate pesticide.
  • composition and formulation are used herein to have the same meaning.
  • a suitable dispersing agent(s) is/are incorporated into the formulation at a specific ratio so as to enable the rapid dispersion and subsequent dissolution of the low use rate and high use rate active material upon dilution and subsequent application.
  • the weight ratio of dispersing agent to the low use rate primary active ingredient in the composition is 0.1 to 10:1, preferably 0.4 to 6:1, for example about 4:1 and about 5:1.
  • the invention is particularly suitable for, but not limited to, such low use-rate pesticides as: Abamectin, imidazolinone, azoxystrobin, bensulfuron-methyl, carfentrazone-ethyl, chlorsulfuron, cinosulfuron, clodinafop, clopyralid, lambda-cyhalothrin, deltamethrin, diflufenican, emamectin benzoate, fibronil, flurtamone, imazamethabenz-methyl, imazapyr, imazethapyr, imadacloprid, metsulfuron-methyl, milbectin, nicosulfuron, pirimisulfuron-methyl, rimsulfuron, sulfometuron, -methyl, thifensulfuron-methyl, tribenuron-methyl, and tirflusulfuron-methyl.
  • the low use rate pesticide is a
  • Suitable high use rate pesticides include: Abamectin, atrazine, benomylbentazone, bifenox, bromoxynil, captan, carbendazim, chloridazon, chlorothalonil, chlortoluron, lambda-cyhalothrin, cyhexatin, cymoxynil, alpha-cypermethrin, deltamethrin, dimethomorph, diuron, ethofumesate, fibronil, flurtamone, glyphosate, imazamethabenz-methyl, imazapyr, imazethapyr, imadacloprid, isoproturon, linuron, mancozeb, maneb, metamitron, methiocarb, metribuzin, milbectin, oxadixyl, oxyfluorfen, phenmedipham, propanil, propyzamide, simazine,
  • the low use rate pesticide comprises bensulfuron-methyl and the high use rate pesticide comprises propanil.
  • the dispersing agent comprises a surfactant with nonionic surfactants and especially anionic surfactants being preferred.
  • suitable dispersing agents include alkali metal, preferably sodium salts of lignosulphonates, naphthalene sulphonate formaldehyde condensates, tristyrylphenol ethoxylate phosphate esters, aliphatic alcohol ethoxylates, alkylphenol ethoxylates, ethylene oxide/propylene oxide (EO-PO) block copolymers, “comb” graft copolymers and polyvinyl alcohol-vinyl acetate copolymers.
  • Other dispersing agents known in the art may be employed as desired.
  • Suitable wetting agents include: alkali metal salts of alkylaryl sulphonates, alkyl aryl sulphosuccinates and alkyl sulphates, preferably as the sodium salt.
  • Other wetting agents, and other excipients known to those skilled in the art may be employed as desired including disintegrants for example: bentonite, modified starch and polyvinyl pyrrolidone; stabilisers, for example citric acid, polyethylene glycol and butylated hydroxy toluene; and fillers, for example, starch, lactose, china clay, sucrose and kaolin; and flow-aids.
  • the granular compositions are preferably prepared by the method described in PCT application PCT/GB00/00163 the contents of which are hereby incorporated by reference.
  • the process comprises, preparing a mix in the form of a free-flowing powder, preferably a homogeneous powder, comprising the primary active ingredient and a dispersing agent and optionally other components, preferably without forming a paste, and extruding the pre-mix in an extruder, for example a low pressure extruder to form the granules.
  • a pre-mix optionally containing the secondary active ingredient may be mixed with the dispersing agent and the primary active ingredient to form the mix for extrusion.
  • the dispersing agent may be liquid in which case an additional liquid component is not required although a further liquid component may be included as desired.
  • Suitable apparatus for the blending step(s) include a low-shear, high intensity blender such as a Lodige Ploughshare mixer, ribbon, Y-cone, double cone or trough blender, so that a free-flowing powder is formed.
  • the mix is fed directly or indirectly into a suitable low-pressure extruder, such as that described in WO 96/26828, so that the premix is compacted against the apertures in the screen and forced through.
  • the composition of the mix and the extruder settings are such that the formation of a paste before extrusion is avoided and the material being processed remains a free flowing particulate material during the formation of the pre-mix.
  • the material optimally does not form a paste prior to extrusion.
  • the composition may contain one or more liquid components, it may be wet or dry provided that it remains free-flowing and particulate during the process.
  • a paste may be considered as a mass of material, for example an agglomerate, which contains sufficient liquid or is at such a temperature that the particulate material being processed forms into an agglomerate which is mouldable or deformable and which is not free-flowing.
  • a paste does not disintegrate into finer particles on application of shear, for example by rubbing between fingers, but rather remains as an agglomerated mass and the shear acts to mould or deform the agglomerate.
  • the components of the composition are first mixed, for example in a blender so that a uniform blend is obtained which is then passed through a suitable milling system such as an air mill, pin mill or air-swept impact mill so that a fine powder (the pre-mix) comprising an average particle size of 0.5 to 20 microns, or more preferably between 0.5 to 5 microns is obtained.
  • a suitable milling system such as an air mill, pin mill or air-swept impact mill so that a fine powder (the pre-mix) comprising an average particle size of 0.5 to 20 microns, or more preferably between 0.5 to 5 microns is obtained.
  • the powder thus obtained is suitably agglomerated, so that uniform, dust-free granules are obtained, preferably by the process described in PCT/GB00/00163.
  • This preferred method involves the extrusion of the wetted powder which is then in the form of a freely flowing homogeneous powder, in a low temperature, low pressure extruder, for example as described in EP-A-8
  • the low use rate and high use rate agrochemicals may be combined in the formation of the dry pre-mix with the other formulation ingredients for example dispersing agents or alternatively the pre-mix may be prepared with one of the agrochemicals and the other added to the milled pre-mix.
  • This alternative approach is preferred when the high use rate pesticide is propanil which is suitably incorporated in the dry pre-mix, and the low use rate pesticide is then added to the pre-mix and blended with it prior to granulation.
  • the invention provides a method of treating a plant by applying a herbicidally effective amount of a composition according to the present invention to the plant or to the locus of the plant.
  • the present invention enables the composition of the invention to be used at a lower rate of use (mass of composition/unit area, typically grammes per hectare) to achieve a given effect than known compositions.
  • the agrochemical active is applied to the plant or locus of the plant at a rate of use of less than 75%, more preferably less than 50% of the conventional rate of use for the active in commercially available compositions.
  • a composition comprising a sulphonyl urea low use rate active for example bensulfuron is applied in use at a rate of use of less than 50 g/hectare, especially less than 30 g/hectare and optimally less than 20 g/hectare.
  • a commercially available composition containing in excess of 50% by weight of the composition of bensulfuron-methyl may be employed at a rate of use of 60 g/hectare or more.
  • the composition comprises a high use rate secondary active comprising propanil in addition to a sulphonyl urea active, for example bensulfuron, and suitably the secondary active is applied in use at a rate of less than 7000 g/hectare, preferably less than 5000 g/hectare and especially at a rate of less than 3200 g/hectare.
  • a high use rate secondary active comprising propanil in addition to a sulphonyl urea active, for example bensulfuron, and suitably the secondary active is applied in use at a rate of less than 7000 g/hectare, preferably less than 5000 g/hectare and especially at a rate of less than 3200 g/hectare.
  • the treatment is such as to control or kill the weed.
  • the composition is applied to the plant or its locus by means of a liquid carrier, typically water, with which the composition is mixed prior to application.
  • a liquid carrier typically water
  • the composition may be mixed with a liquid carrier to form a concentrate suitable for subsequent mixing with a liquid carrier.
  • the application of the composition to the plant or its locus in solid or concentrate form especially where water is present in the vicinity of the plant through natural precipitation is also within the ambit of the invention.
  • the composition is diluted for use to a level of 10 to 500 mg/l and preferably 20 to 300 mg/l.
  • the dilution is suitably selected according to the composition used, the type of application, the state of growth of the plants to be treated and other factors known to those skilled in the art.
  • the invention provides for use of a composition according to the invention as an agrochemical, for example a low use rate herbicide.
  • This invention relates to novel compositions and to methods of treating plants, for example killing or controlling weeds by applying a reduced amount of the active ingredient(s), suitably diluted in water, than that normally recommended for such active(s) against such weeds.
  • the invention allows for the avoidance of subsequent applications of the said actives, thus further reducing the amount of pesticide used.
  • the chlorsulfuron technical was airmilled using a Gem-T airmill before combining with other components.
  • the technical, Ultrazine and Arylan components were blended until uniform in a high speed blender.
  • the lactose was then added and the formulation blended for a further 15 seconds.
  • 12% distilled water was added whilst blending.
  • the wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen.
  • a compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes.
  • the dried granules were then sieved through 2 mm and 500 micron sieves.
  • the chlorsulfuron technical was airmilled using a Gem-T airmill before combining with other components.
  • the milled chlorsulfuron technical, Ultrazine and Galoryl components were blended until uniform in a high speed blender.
  • the lactose was then added and the formulation blended for a further 15 seconds. 17% distilled water was added whilst blending.
  • the wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen.
  • a compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes.
  • the dried granules were then sieved through 2 mm and 500 micron sieves.
  • the technical and Galoryl DT505 were blended together until uniform.
  • the blend was then airmilled using a Gem-T airmill.
  • the milled premix, Galoryl MT704 and lactose were blended until uniform in a high speed blender.
  • the lactose was then added and the formulation blended for a further 15 seconds.
  • 12% distilled water was added whilst blending.
  • the wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen. A compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes. The dried granules were then sieved through 2 mm and 500 micron sieves.
  • Comparative Example B was prepared using the method set out in Example 2.
  • Londax 60 WG 300 Tap 12 Comparative 60 WG 291 Tap 25
  • Example B Londax 60 WG 75 Tap 19 Comparative 60 WG 73 Tap 46
  • Example B Example 2 1 WG 240 Tap 71
  • a premix of Propanil was prepared as follows:
  • the ingredients were blended in a medium shear, high speed blender for 5 minutes until uniform. The resulting mixture was passed through an air mill to obtain a fine powder. The powder was wetted with 19.5% water (based on the dry weight of powder) and blended until a damp free flowing powder was formed.
  • the premix was used in the following blends with bensulfuron:
  • the technical and Galoryl DT505 were blended together until uniform.
  • the blend was then airmilled using a Gem-T airmill.
  • the milled bensulfuron-methyl and milled propanil premixes, Galoryl MT704 and china clay were blended until uniform in a high speed blender. 17% distilled water was added whilst blending.
  • the wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen.
  • a compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes.
  • the dried granules were then sieved through 2 mm and 500 micron sieves.
  • the technical and Galoryl DT505 were blended together until uniform.
  • the blend was then airmilled using a Gem-T airmill.
  • the milled bensulfuron-methyl and milled propanil premixes, Galoryl MT704 and china clay were blended until uniform in a high speed blender. 17% distilled water was added whilst blending.
  • the wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen.
  • a compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes.
  • the dried granules were then sieved through 2 mm and 500 micron sieves.
  • Example 2 Further solubility testing up to 2 hours was carried out using the same method as for Example 1 except the granules were diluted in 1000 mls water and samples were taken after 5, 30, 60, 90 and 120 minutes. The following results were obtained using 37.5 mgs a.i./litre (all in tap water). Data for Comparative Example B (bensulfuron-methyl 60 WG) and Londax (commercial bensulfuron-methyl 60 WG) at the same dilution rate is shown for comparison.
  • Example B Londax 5 67 42 15 30 67 52 32 60 67 57 39 90 66 57 49 120 69 62 53
  • solubility rate of bensulfuron-methyl in a granule which also contains an active that is used a high rate per hectare is significantly higher compared with diluting the bensulfuron-methyl as a 60 WG.
  • Example 4 The processing method set out in Example 4 was employed, with the bensulfuron-methyl being milled as a premix with the Galoryl DT505. The solubility of the bensulfuron-methyl in the above formulation was then tested using the method set out in Example 4. The following results were obtained using 25 mgs and 31.3 mgs bensulfuron-methyl a.i./litre (in tap water).
  • Example 5 Time (mins) (25 mgs/L) (31.3 mgs/L) 5 89 91 30 90 92 60 94 92 90 93 96 120 97 95
  • Example 4 A composition according to Example 4 was evaluated in the field in comparison with commercial formulations containing the same active ingredients.
  • Stam 80 EDF is a commercial formulation containing 80% propanil in the form of an extruded granule.
  • Londax 60 is a commercial formulation containing 60% bensulfuron-methyl in the form of a fluid bed granule.
  • Treatment 1 Treatment 2
  • Treatment 3 Control % % % % % % % % Weeds % cov. cov. eff. Sympt. cov. eff. Sympt. cov. eff. Sympt. Heteranthera 38.0 37.0 0.0 n.a. 35.0 0.0 n.a. 35.0 0.0 n.a. limosa Heteranthera 0.0 1.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a. reniformis Echinochloa 1.0 1.0 0.0. n.a. 1.0 0.0 n.a. 1.0 0.0 n.a. crus-galli Panicum 1.0 1.0 0.0 n.a.
  • Treatment 1 Treatment 2
  • Treatment 3 Control % % % % % % % % Weeds % cov. cov. eff. Sympt. cov. eff. Sympt. cov. eff. Sympt. Heteranthera 55.0 55.0 70.0 WC 34.0 80.0 W 40.0 50.0 W limosa Heteranthera 0.5 0.0 0.0 n.a. 0.6 0.0 n.a. 0.0 n.a. reniformis Echinochloa 7.0 0.0 0.0 n.a. 1.0 0.0 n.a. 1.0 0.0 n.a. crus-galli Panicum 5.5 0.0 0.0 n.a. 1.0 0.0 n.a.a.
  • Treatment 1 Treatment 2
  • Treatment 3 Control % % % % % % % % Weeds % cov. cov. eff. Sympt. cov. eff. Sympt. cov. eff. Sympt. Heteranthera 55.0 1.0 99.0 W.C. 18.0 80.0 W.C. 2.0 98.0 W limosa Heteranthera 0.0 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a. reniformis Echinochloa 10.0 0.0 0.0 n.a. 1.0 0.0 n.a. 0.0 0.0 n.a. crus-galli Panicum 15.0 0.0 0.0 n.a. 1.0 0.0 n.a. 1.0 0.0 n.a. 1.0 0.0 n.a.a.
  • Treatment 1 Treatment 2
  • Treatment 3 Control % % % % % % % % % Weeds % cov. cov. eff. Sympt. cov. eff. Sympt. cov. eff. Sympt. Heteranthera 37.0 0.0 0.0 n.a. 1.0 0.0 n.a. 0.0 0.0 n.a. limosa Heteranthera 1.0 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 n.a. reniformis Echinochloa 10.0 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a. crus-galli Panicum 15.0 0.0 0.0 n.a.
  • Example 4 (15 g/ha bensulfuron-methyl combined with 3,000 g/ha propanil) provides equivalent control to the commercial products tested when applied at less than 1 ⁇ 3rd of the propanil in the Stam 80 EDF treatment (two applications, one 3200 a.i. g/ha and one 6400 a.i. g/ha propanil) and 1 ⁇ 4 of the Londax rate (one application of 60 g/ha bensulfuron-methyl tank mixed with one application of 3,200 g/ha propanil).

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
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Abstract

The invention relates to novel compositions of biologically active agents containing less than 50% by weight of a low use rate agrochemical active and a dispersing agent, which exhibit enhanced bio-availability on dilution and application in water.

Description

  • This application is a continuation of U.S. patent application Ser. No. 10/069,911 filed on Feb. 26, 2002, claiming priority from PCT Application No. PCT/GB00/03307 filed on Aug. 25, 2000 and United Kingdom Application Serial No. 9920281.4, filed Aug. 26, 1999.
    • BACKGROUND AND SUMMARY OF THE INVENTION
  • The invention relates to novel chemical compositions in particular, compositions of biologically active agents and their use. The invention is more particularly concerned with granular compositions of low dose-rate agrochemicals, for example pesticides, suitably prepared by an extrusion process, which deliver the active ingredient of the composition efficiently to the substrate, for example a crop, which is to be treated.
  • The advantages of dispersible granule formulations of pesticides are known and include their ease of handling and reduced worker exposure compared to powder or liquid formulations. G. A. BELL, “Chemistry and Technology of Agrochemical Formulations”, edited by D. A. Knowles (Kluver, 1998), pages 80-114, describes a range of dispersible granule types and processes for their manufacture.
  • Dispersible granules may be prepared by extrusion. U.S. Pat. No. 3,954,439 discloses granular compositions of a herbicidal agent and one or more surfactants and processes for the production of such compositions. The process described in U.S. Pat. No. 3,954,439 is applicable to those herbicides which are substantially insoluble in water. This patent states that it is obviously desirable that the granules should have the highest possible content of active herbicidal material. This patent further states that the process is preferably carried out so as to give granules containing at least 50% of active herbicide material and that it is more preferable that the granules should contain more than this, that is at least 80% and even up to 95%. The patent also teaches that it is obviously important to keep the surfactant content down to a minimum, the total amount of surfactant preferably being from 5 to 15%.
  • U.S. Pat. No. 5,872,078 relates to dry, water soluble and/or water dispersible, agriculturally acceptable herbicidal compositions containing N-phosphonomethylglycerine or acceptable water-soluble salt thereof. The composition may comprise further optional ingredients, one of which may be a co-herbicide. A large number of co-herbicides are listed including sulfonylureas such as those available under the trade names Ally, Classic, Oust, Glean and mixtures thereof. A liquid surfactant is added to this mixture and extrusion granulation may be used to process the compositions described to form granules.
  • Improved delivery and bioavailability of the active ingredient in agrochemical compositions, especially of water insoluble actives for example sulphonyl ureas, to achieve a desired agrochemical effect is desirable. It is also desirable to achieve this effect in as cost effective manner as possible and conventionally this has been achieved by including as high a level of active ingredient as possible in a formulated composition.
  • We have now surprisingly found that a composition containing a lower level of a primary active ingredient than conventionally employed in compositions containing the same ingredient, together with a suitable dispersing agent may conferenhanced delivery of the primary active ingredient to the crop to be treated. The invention is particularly applicable to a low use rate agrochemical for instance a pesticide, and especially a water-insoluble agrochemical. Furthermore, as this enhanced effect may be achieved at a lower level of active ingredient in the composition, the composition may include additional materials in the remaining “formulation space” to provide additional effects.
  • Accordingly, a first aspect of the invention provides an agrochemical composition comprising a primary agrochemical active ingredient, preferably a low use rate active ingredient, at a level of less than 50% by weight of the composition and a dispersing agent, preferably a nonionic and/or anionic surfactant(s).
  • The compositions according to the first aspect of the invention provide surprisingly beneficial bioavailability of the active for instance by making a larger proportion of the active biologically available in a liquid carrier, for example water, with which the composition is mixed in use than a known composition having a high level of active. The compositions disperse rapidly in the liquid carrier to form stable suspensions of the active material(s) and subsequently dissolve at a rate and to an extent higher than that achieved by conventional compositions containing the same ingredients.
  • This property provides enhanced efficacy of the agrochemicals with attendant reduced crop damage.
  • This enhanced bioavailability means that a given agrochemical effect may be obtained using a lower total amount of agrochemical active thus providing environmental benefits through lower use of agrochemicals.
  • Further, as the concentration of the active is lower than conventionally employed, there is a reduced risk that some of the active will not be dispersed or dissolve in the liquid carrier. Hence the risk of poor dispersion or dissolution of the active in a liquid carrier leading to high localized concentrations of the active penetrating to the crop especially the roots of plants and possibly damaging the crop is reduced.
  • A further advantage is that the lower level of primary active ingredient provides enhanced flexibility in formulating a composition as compared to conventional compositions employing high levels of active. Thus, the formulator may include a secondary active ingredient or other materials as desired in the composition to provide an optimum effect or balance of properties.
  • It has also been surprisingly found that when low use-rate pesticides, such as water-insoluble compounds including sulfonyl ureas, for example as described in U.S. Pat. No. 5,872,078, are employed as the primary active ingredient with a secondary high rate use pesticide and a suitable dispersing agent at the required level, the rate and extent of solubility and thus the bioavailability, of the primary active or both the actives may be increased as compared to granules containing the equivalent amount of each material alone. Optimally, the primary and secondary actives are intimately mixed in suitable proportions. Suitably, optional conventional other ingredients such as one or more additional surfactants are included in the formulation and the ingredients are processed into a suitable form, for example water-dispersible granules.
  • Accordingly the invention also provides in a preferred embodiment an agrochemical composition comprising as a primary active ingredient, a low use rate agrochemical active ingredient, at a level of less than 50% by weight of the composition and a secondary active ingredient, preferably a high use rate active ingredient, and a dispersing agent, preferably an anionic and/or nonionic surfactant.
  • In addition to the advantages referred to above for composition according to the invention, the compositions provide at least an enhanced effect as regards the primary active and suitably an effect greater than the combined additive affect of both the primary and secondary active is observed where the composition contains a primary and secondary active.
  • The term “low use rate” active denotes those agrochemical actives which typically are applied at a rate of less than 100 g/hectare and the term “high use rate” active denotes those agrochemical actives which typically are applied at a rate of more than 1000 g/hectare.
  • The compositions of the present invention result in the individual components being used at lower rates and with less phytotoxicity than conventional compositions of the said active materials, against a wide range of pests and diseases.
  • The level of primary active ingredient is suitably selected according to the particular compound to be used but is preferably less than 30% by weight of the composition, especially in the case of a low use rate active. For example, chlorsulfuron may suitably be employed at a level of less than 30%, for example 25% by weight of the composition. In a preferred embodiment, the primary active ingredient, for example bensulfuron, is present at a level of less than 10% and more preferably less than 2% by weight of the composition. In an especially preferred embodiment the primary active is present at a level of less than 1%. Suitably, the composition will contain the primary active at a level at which, on mixing with a liquid carrier, it provides a concentration of active which will provide a beneficial effect in treating crops. This level may suitably be at 0.05% but is preferably at least 0.1% and desirably at least 0.2% by weight of the composition although the precise level may be adjusted according to the particular application and the particular primary active present in the composition.
  • Where a second active is employed, it is suitably present at a level greater than the level of the primary active ingredient. In a preferred embodiment the secondary active is present at a level of at least 30%, more preferably at least 50%, optimally at least 65%, for example 75% by weight of the composition.
  • The invention comprises a dry, free-flowing, dustless and rapidly dispersing granular formulation containing a low use rate pesticide or mixture of pesticides together with an additional high use rate pesticide. The terms composition and formulation are used herein to have the same meaning.
  • A suitable dispersing agent(s) is/are incorporated into the formulation at a specific ratio so as to enable the rapid dispersion and subsequent dissolution of the low use rate and high use rate active material upon dilution and subsequent application. Suitably, the weight ratio of dispersing agent to the low use rate primary active ingredient in the composition is 0.1 to 10:1, preferably 0.4 to 6:1, for example about 4:1 and about 5:1.
  • The invention is particularly suitable for, but not limited to, such low use-rate pesticides as: Abamectin, imidazolinone, azoxystrobin, bensulfuron-methyl, carfentrazone-ethyl, chlorsulfuron, cinosulfuron, clodinafop, clopyralid, lambda-cyhalothrin, deltamethrin, diflufenican, emamectin benzoate, fibronil, flurtamone, imazamethabenz-methyl, imazapyr, imazethapyr, imadacloprid, metsulfuron-methyl, milbectin, nicosulfuron, pirimisulfuron-methyl, rimsulfuron, sulfometuron, -methyl, thifensulfuron-methyl, tribenuron-methyl, and tirflusulfuron-methyl. Preferably the low use rate pesticide is a sulfonyl urea.
  • Suitable high use rate pesticides include: Abamectin, atrazine, benomylbentazone, bifenox, bromoxynil, captan, carbendazim, chloridazon, chlorothalonil, chlortoluron, lambda-cyhalothrin, cyhexatin, cymoxynil, alpha-cypermethrin, deltamethrin, dimethomorph, diuron, ethofumesate, fibronil, flurtamone, glyphosate, imazamethabenz-methyl, imazapyr, imazethapyr, imadacloprid, isoproturon, linuron, mancozeb, maneb, metamitron, methiocarb, metribuzin, milbectin, oxadixyl, oxyfluorfen, phenmedipham, propanil, propyzamide, simazine, thifensulfuron-methyl and thiram.
  • In an especially preferred embodiment, the low use rate pesticide comprises bensulfuron-methyl and the high use rate pesticide comprises propanil.
  • In a preferred embodiment, the dispersing agent comprises a surfactant with nonionic surfactants and especially anionic surfactants being preferred. Examples of suitable dispersing agents include alkali metal, preferably sodium salts of lignosulphonates, naphthalene sulphonate formaldehyde condensates, tristyrylphenol ethoxylate phosphate esters, aliphatic alcohol ethoxylates, alkylphenol ethoxylates, ethylene oxide/propylene oxide (EO-PO) block copolymers, “comb” graft copolymers and polyvinyl alcohol-vinyl acetate copolymers. Other dispersing agents known in the art may be employed as desired.
  • In addition to the dispersing agent, other components may be present in the composition for example a wetting agent. Suitable wetting agents include: alkali metal salts of alkylaryl sulphonates, alkyl aryl sulphosuccinates and alkyl sulphates, preferably as the sodium salt. Other wetting agents, and other excipients known to those skilled in the art may be employed as desired including disintegrants for example: bentonite, modified starch and polyvinyl pyrrolidone; stabilisers, for example citric acid, polyethylene glycol and butylated hydroxy toluene; and fillers, for example, starch, lactose, china clay, sucrose and kaolin; and flow-aids.
  • The granular compositions are preferably prepared by the method described in PCT application PCT/GB00/00163 the contents of which are hereby incorporated by reference. Suitably the process comprises, preparing a mix in the form of a free-flowing powder, preferably a homogeneous powder, comprising the primary active ingredient and a dispersing agent and optionally other components, preferably without forming a paste, and extruding the pre-mix in an extruder, for example a low pressure extruder to form the granules. A pre-mix optionally containing the secondary active ingredient may be mixed with the dispersing agent and the primary active ingredient to form the mix for extrusion. The dispersing agent may be liquid in which case an additional liquid component is not required although a further liquid component may be included as desired.
  • Suitable apparatus for the blending step(s) include a low-shear, high intensity blender such as a Lodige Ploughshare mixer, ribbon, Y-cone, double cone or trough blender, so that a free-flowing powder is formed. The mix is fed directly or indirectly into a suitable low-pressure extruder, such as that described in WO 96/26828, so that the premix is compacted against the apertures in the screen and forced through.
  • In a preferred embodiment, the composition of the mix and the extruder settings are such that the formation of a paste before extrusion is avoided and the material being processed remains a free flowing particulate material during the formation of the pre-mix. In particular, the material optimally does not form a paste prior to extrusion. However, as the composition may contain one or more liquid components, it may be wet or dry provided that it remains free-flowing and particulate during the process. In this context, a paste may be considered as a mass of material, for example an agglomerate, which contains sufficient liquid or is at such a temperature that the particulate material being processed forms into an agglomerate which is mouldable or deformable and which is not free-flowing. Thus, a paste does not disintegrate into finer particles on application of shear, for example by rubbing between fingers, but rather remains as an agglomerated mass and the shear acts to mould or deform the agglomerate.
  • If desired, the components of the composition, either in sequence, all together or some in sequence and others together are first mixed, for example in a blender so that a uniform blend is obtained which is then passed through a suitable milling system such as an air mill, pin mill or air-swept impact mill so that a fine powder (the pre-mix) comprising an average particle size of 0.5 to 20 microns, or more preferably between 0.5 to 5 microns is obtained. The powder thus obtained is suitably agglomerated, so that uniform, dust-free granules are obtained, preferably by the process described in PCT/GB00/00163. This preferred method involves the extrusion of the wetted powder which is then in the form of a freely flowing homogeneous powder, in a low temperature, low pressure extruder, for example as described in EP-A-812256.
  • Where present, the low use rate and high use rate agrochemicals may be combined in the formation of the dry pre-mix with the other formulation ingredients for example dispersing agents or alternatively the pre-mix may be prepared with one of the agrochemicals and the other added to the milled pre-mix. This alternative approach is preferred when the high use rate pesticide is propanil which is suitably incorporated in the dry pre-mix, and the low use rate pesticide is then added to the pre-mix and blended with it prior to granulation.
  • In a second aspect, the invention provides a method of treating a plant by applying a herbicidally effective amount of a composition according to the present invention to the plant or to the locus of the plant.
  • The present invention enables the composition of the invention to be used at a lower rate of use (mass of composition/unit area, typically grammes per hectare) to achieve a given effect than known compositions. Suitably the agrochemical active is applied to the plant or locus of the plant at a rate of use of less than 75%, more preferably less than 50% of the conventional rate of use for the active in commercially available compositions.
  • In a preferred embodiment, a composition comprising a sulphonyl urea low use rate active for example bensulfuron, is applied in use at a rate of use of less than 50 g/hectare, especially less than 30 g/hectare and optimally less than 20 g/hectare. Typically, a commercially available composition containing in excess of 50% by weight of the composition of bensulfuron-methyl may be employed at a rate of use of 60 g/hectare or more. In another preferred embodiment, the composition comprises a high use rate secondary active comprising propanil in addition to a sulphonyl urea active, for example bensulfuron, and suitably the secondary active is applied in use at a rate of less than 7000 g/hectare, preferably less than 5000 g/hectare and especially at a rate of less than 3200 g/hectare.
  • Where the plant is a weed, suitably, the treatment is such as to control or kill the weed. Generally, the composition is applied to the plant or its locus by means of a liquid carrier, typically water, with which the composition is mixed prior to application. If desired, the composition may be mixed with a liquid carrier to form a concentrate suitable for subsequent mixing with a liquid carrier. The application of the composition to the plant or its locus in solid or concentrate form especially where water is present in the vicinity of the plant through natural precipitation is also within the ambit of the invention.
  • In water, suitably the composition is diluted for use to a level of 10 to 500 mg/l and preferably 20 to 300 mg/l. The dilution is suitably selected according to the composition used, the type of application, the state of growth of the plants to be treated and other factors known to those skilled in the art.
  • In a third aspect, the invention provides for use of a composition according to the invention as an agrochemical, for example a low use rate herbicide.
  • This invention relates to novel compositions and to methods of treating plants, for example killing or controlling weeds by applying a reduced amount of the active ingredient(s), suitably diluted in water, than that normally recommended for such active(s) against such weeds. In addition the invention allows for the avoidance of subsequent applications of the said actives, thus further reducing the amount of pesticide used.
  • The following examples illustrate the invention in an non-limiting manner.
    • EXAMPLE 1 Chlorsulfuron 25 WG
  • Ingredient Trade name % w/w
    Chlorsulfuron technical (95%) (technical a.i.) 26.32
    Sodium lignosulfonate Ultrazine NA 12.50
    Dodedyl benzene sulphonate, Sodium Arylan SX85 5.00
    salt
    Lactose Lactose 56.18
    • Method
  • The chlorsulfuron technical was airmilled using a Gem-T airmill before combining with other components. The technical, Ultrazine and Arylan components were blended until uniform in a high speed blender. The lactose was then added and the formulation blended for a further 15 seconds. 12% distilled water was added whilst blending. The wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen. A compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes. The dried granules were then sieved through 2 mm and 500 micron sieves.
    • COMPARATIVE EXAMPLE A Chlorsulfuron 75 WG
  • Ingredient Trade name % w/w
    Chlorsulfuron technical (95%) 78.95
    technical a.i.)
    Sodium lignosulfonate Ultrazine NA 12.50
    Di isopropyl naphthalene sulfonate, Galoryl MT704 1.00
    sodium salt
    Lactose Lactose 7.55
    • Method
  • The chlorsulfuron technical was airmilled using a Gem-T airmill before combining with other components. The milled chlorsulfuron technical, Ultrazine and Galoryl components were blended until uniform in a high speed blender. The lactose was then added and the formulation blended for a further 15 seconds. 17% distilled water was added whilst blending. The wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen. A compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes. The dried granules were then sieved through 2 mm and 500 micron sieves.
  • The solubility of the compositions produced according to Example 1 and Comparative Example A and Glean (commercially available 75 WG product) and airmilled technical was tested using the method below:
    • Solubility Test Method
  • 200 mls water was poured into a jacketed glass vessel and allowed to reach 25 C. A Grant recirculator was used to maintain the temperature at 25 C+/−1 C. A magnetic stirrer at a set speed was used to stir the water. The specified weight of granules was then added to the water and allowed to disperse for 30 seconds before a timer was started. A 2 mls sample was removed using a syringe after 5 minutes and filtered using a 0.45 micron syringe filter. The solution was then analysed to determine the active concentration using a HPLC method. The theoretical concentration assuming 100% solubility was calculated using an assay obtained using the HPLC.
  • The following data was obtained:
  • Type of % active added
    Dilution water used to water that
    rate (mgs to dilute dissolved after
    Formulation Product a.i./L) granules 5 minutes
    Example 1 25 WG 69 Distilled 98
    Comparative 75 WG 72 Distilled 95
    Example A
    Glean (Du 75 WG 72 Distilled 67
    Pont)
    Airmilled — 91 Distilled <2
    technical
    • Conclusions
  • Both the 75 and 25 extruded WG formulations have a significantly higher solubility in distilled water compared to the commercial product. The technical is not readily soluble in distilled water at this temperature.
    • EXAMPLE 2 Bensulfuron-methyl 1 WG
  • Ingredient Trade name % w/w
    Bensulfuron methyl technical (95%) (technical 1.05
    a.i.)
    Naphthalene sulfonic acid Galoryl DT505 12.70
    Formaldehyde condensate, sodium salt
    Di isopripyl naphthalene sulfonate, Galoryl MT704 1.00
    sodium salt
    Lactose Lactose 85.25
    • Method
  • The technical and Galoryl DT505 were blended together until uniform. The blend was then airmilled using a Gem-T airmill. The milled premix, Galoryl MT704 and lactose were blended until uniform in a high speed blender. The lactose was then added and the formulation blended for a further 15 seconds. 12% distilled water was added whilst blending. The wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen. A compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes. The dried granules were then sieved through 2 mm and 500 micron sieves.
    • COMPARATIVE EXAMPLE B Bensulfuron-methyl 60 WG
  • Ingredient Trade name % w/w
    Bensulfuron methyl technical (95%) (technical 64.21
    a.i.)
    Naphthalene sulfonic acid Galoryl DT505 12.70
    Formaldehyde condensate, sodium salt
    Di isopripyl naphthalene sulfonate, Galoryl MT704 1.00
    sodium salt
    Lactose Lactose 22.08
  • The composition of Comparative Example B was prepared using the method set out in Example 2.
  • The solubility of the compositions of Example 2 and Comparative Example B were then tested using the method detailed in Example 1. The following data was obtained:
  • Type of % active added
    Dilution water used to water that
    rate (mgs to dilute dissolved after
    Formulation Product a.i./L) granules 5 minutes
    Londax 60 WG 300 Tap 12
    Comparative 60 WG 291 Tap 25
    Example B
    Londax 60 WG 75 Tap 19
    Comparative 60 WG 73 Tap 46
    Example B
    Example 2  1 WG 240 Tap 71
    • EXAMPLE 3 Propanil and bensulfuron-methyl combined WG (75% propanil and 0.75% bensulfuron) Propanil Premix
  • A premix of Propanil was prepared as follows:
  • Ingredient Trade name % w/w
    Propanil technical (97.0% a.i.) Technical 82.47
    Starch Paselli 1.00
    Nonionic surfactant and sodium Stepsperse DF 5.00
    Lignosulphonate blend 500
    Modified sodium lignosulphonate Ufoxane 3A 5.00
    Hydrated aluminium silicate China Clay to 1.00
  • The ingredients were blended in a medium shear, high speed blender for 5 minutes until uniform. The resulting mixture was passed through an air mill to obtain a fine powder. The powder was wetted with 19.5% water (based on the dry weight of powder) and blended until a damp free flowing powder was formed. The premix was used in the following blends with bensulfuron:
  • Ingredient Trade name % w/w
    Bensulfuron methyl technical (95%) (technical a.i.) 0.79
    Propanil 80% milled premix 93.75
    Naphthalene sulfonic acid Galoryl DT505 0.31
    Formaldehyde condensate, sodium
    salt
    China clay China clay GTY 5.15
  • The technical and Galoryl DT505 were blended together until uniform. The blend was then airmilled using a Gem-T airmill. The milled bensulfuron-methyl and milled propanil premixes, Galoryl MT704 and china clay were blended until uniform in a high speed blender. 17% distilled water was added whilst blending. The wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen. A compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes. The dried granules were then sieved through 2 mm and 500 micron sieves.
    • EXAMPLE 4 Propanil and bensulfuron-methyl combined WG (75% propanil and 0.375% bensulfuron)
  • Ingredient Trade name % w/w
    Bensulfuron-methyl technical (95%) (technical a.i.) 0.39
    Propanil 80% milled premix — 93.75
    Naphthalene sulfonic acid Galoryl DT505 0.16
    Formaldehyde condensate, sodium salt
    China clay China clay GTY 5.70
  • The technical and Galoryl DT505 were blended together until uniform. The blend was then airmilled using a Gem-T airmill. The milled bensulfuron-methyl and milled propanil premixes, Galoryl MT704 and china clay were blended until uniform in a high speed blender. 17% distilled water was added whilst blending. The wetted premix (free flowing powder) was fed to a basket extruder as described in EP-A-812256 through a 1 mm screen. A compacted extrudate was obtained and the resulting granules dried at 60 C for 8 minutes. The dried granules were then sieved through 2 mm and 500 micron sieves.
  • The above combination formulations were tested using the solubility method detailed in Example 1. The following data was obtained:
  • Type of % active added
    % Dilution water used to water that
    bensulfuron- rate (mgs to dilute dissolved after
    Formulation methyl a.i. a.i./L) granules 5 minutes
    Example 3 0.75 75 Tap 66
    0.75 112.5 Tap 64
    Example 4 0.375 37.5 Tap 83
    0.375 56 Tap 84
  • Further solubility testing up to 2 hours was carried out using the same method as for Example 1 except the granules were diluted in 1000 mls water and samples were taken after 5, 30, 60, 90 and 120 minutes. The following results were obtained using 37.5 mgs a.i./litre (all in tap water). Data for Comparative Example B (bensulfuron-methyl 60 WG) and Londax (commercial bensulfuron-methyl 60 WG) at the same dilution rate is shown for comparison.
  • % active added to water that dissolved
    Time Comparative
    (mins) Example 5 Example B Londax
    5 67 42 15
    30 67 52 32
    60 67 57 39
    90 66 57 49
    120 69 62 53
    • Conclusions
  • The solubility rate of bensulfuron-methyl in a granule which also contains an active that is used a high rate per hectare, is significantly higher compared with diluting the bensulfuron-methyl as a 60 WG.
    • EXAMPLE 5 Propanil and bensulfuron-methyl combined WG (75% propanil and 0.24% bensulfuron)
  • Ingredient Trade name % w/w
    Bensulfuron methyl technical (95%) (technical a.i.) 0.25
    Propanil 80% milled premix — 93.72
    Naphthalene sulfonic acid Galoryl DT505 0.10
    Formaldehyde condensate, sodium salt
    China clay China clay GTY 5.90
  • The processing method set out in Example 4 was employed, with the bensulfuron-methyl being milled as a premix with the Galoryl DT505. The solubility of the bensulfuron-methyl in the above formulation was then tested using the method set out in Example 4. The following results were obtained using 25 mgs and 31.3 mgs bensulfuron-methyl a.i./litre (in tap water).
  • % bensulfuron-methyl active
    added to water that dissolved
    Example 5 Example 5
    Time (mins) (25 mgs/L) (31.3 mgs/L)
    5 89 91
    30 90 92
    60 94 92
    90 93 96
    120 97 95
    • Field Evaluation
  • A composition according to Example 4 was evaluated in the field in comparison with commercial formulations containing the same active ingredients.
    • Treatment Details
  • Treatment
    Number Composition Rate of use (g/Hectare) Product
    Control Untreated Control —
    1 Stam 80 EDF 4,000 g at Growth Stage BBCH 12-13
    8,000 g at Growth Stage BBCH 21-21
    2 Stam 80 EDF + 4,000 g at Growth Stage BBCH 12-13
    Londax 60 100 g at Growth Stage BBCH 12-13
    3 Example 4 4,000 g at Growth Stage BBCH 12-13
  • The above treatments were applied in 400 l water/ha on Rice v. loto against Gramineae family weeds. The weeds were assessed at −1, +4, +16 and +32 days after application by the efficacy assessment guidelines provided by EPPO Guidelines PP1/181(2), PP1/152(2) and 1/62(2).
  • Stam 80 EDF is a commercial formulation containing 80% propanil in the form of an extruded granule. Londax 60 is a commercial formulation containing 60% bensulfuron-methyl in the form of a fluid bed granule.
    • Results
  • Assessment: 1 day before 1st Application
  • Treatment 1 Treatment 2 Treatment 3
    Control % % % % % %
    Weeds % cov. cov. eff. Sympt. cov. eff. Sympt. cov. eff. Sympt.
    Heteranthera 38.0 37.0 0.0 n.a. 35.0 0.0 n.a. 35.0 0.0 n.a.
    limosa
    Heteranthera 0.0 1.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a.
    reniformis
    Echinochloa 1.0 1.0 0.0. n.a. 1.0 0.0 n.a. 1.0 0.0 n.a.
    crus-galli
    Panicum 1.0 1.0 0.0 n.a. 1.0 0.0 n.a. 1.0 0.0 n.a.
    dichotomiflorum
    Scirpus 1.0 1.0 0.0 n.a. 1.0 0.0 n.a. 2.0 0.0 n.a.
    maritimus
    Scirpus 1.0 1.0 0.0 n.a. 2.0 0.0 n.a. 1.0 0.0 n.a.
    mucranatus
  • Assessment: 4 days after 1st Application
  • Treatment 1 Treatment 2 Treatment 3
    Control % % % % % %
    Weeds % cov. cov. eff. Sympt. cov. eff. Sympt. cov. eff. Sympt.
    Heteranthera 55.0 55.0 70.0 WC 34.0 80.0 W 40.0 50.0 W
    limosa
    Heteranthera 0.5 0.0 0.0 n.a. 0.6 0.0 n.a. 0.0 0.0 n.a.
    reniformis
    Echinochloa 7.0 0.0 0.0 n.a. 1.0 0.0 n.a. 1.0 0.0 n.a.
    crus-galli
    Panicum 5.5 0.0 0.0 n.a. 1.0 0.0 n.a. 1.0 0.0 n.a.
    dichotomiflorum
    Scirpus 1.0 4.0 90.0 W 0.0 0.0 n.a. 3.0 70.0 W
    maritimus
    Scirpus 2.0 1.0 60.0 W 2.0 60.0 W 5.0 70.0 W
    mucranatus
  • Assessment: 16 days after 1st Application
  • Treatment 1 Treatment 2 Treatment 3
    Control % % % % % %
    Weeds % cov. cov. eff. Sympt. cov. eff. Sympt. cov. eff. Sympt.
    Heteranthera 55.0 1.0 99.0 W.C. 18.0 80.0 W.C. 2.0 98.0 W
    limosa
    Heteranthera 0.0 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a.
    reniformis
    Echinochloa 10.0 0.0 0.0 n.a. 1.0 0.0 n.a. 0.0 0.0 n.a.
    crus-galli
    Panicum 15.0 0.0 0.0 n.a. 1.0 0.0 n.a. 0.0 0.0 n.a.
    dichotomiflorum
    Scirpus 5.0 0.0 0.0 n.a. 0.0 0.0 n.a. 1.0 98.0 W
    maritimus
    Scirpus 15.0 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a.
    mucranatus
  • Assessment: 32 days after 1st Application
  • Treatment 1 Treatment 2 Treatment 3
    Control % % % % % %
    Weeds % cov. cov. eff. Sympt. cov. eff. Sympt. cov. eff. Sympt.
    Heteranthera 37.0 0.0 0.0 n.a. 1.0 0.0 n.a. 0.0 0.0 n.a.
    limosa
    Heteranthera 1.0 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a.
    reniformis
    Echinochloa 10.0 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a.
    crus-galli
    Panicum 15.0 0.0 0.0 n.a. 2.0 0.0 n.a. 0.0 0,0 n.a.
    dichotomiflorum
    Scirpus 5.0 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a.
    maritimus
    Scirpus 32.0 0.0 0.0 n.a. 0.0 0.0 n.a. 0.0 0.0 n.a.
    mucranatus
    Abbreviations:
    % cov.: % area covered by weeds
    % eff.: % herbicide efficacy (% of weeds showing necrotic symptoms):
    Sympt.: symptoms (W: withered; C: chlorotic; n.a. not applicable)
    • Conclusions
  • The above results demonstrate the composition of Example 4 (15 g/ha bensulfuron-methyl combined with 3,000 g/ha propanil) provides equivalent control to the commercial products tested when applied at less than ⅓rd of the propanil in the Stam 80 EDF treatment (two applications, one 3200 a.i. g/ha and one 6400 a.i. g/ha propanil) and ¼ of the Londax rate (one application of 60 g/ha bensulfuron-methyl tank mixed with one application of 3,200 g/ha propanil).

Claims (10)

1.-49. (canceled)
50. A method for making a composition to treat a plant or a locus of the plant, the method comprising the steps of:
selecting a primary agrochemical active ingredient from metsulfuron-methyl, nicosulfaron, rimsulfuron, tribenuron methyl, thifedsulfuron-methyl, chlorsulfuron, bensulfuron-methyl;
selecting a secondary agrochemical active ingredient from diuron, lunuron, metribuzin, oxyfluorfen and propanil;
providing a dispersing agent; and
extruding a mixture to form a composition wherein the mixture has the primary agrochemical active ingredient, the secondary agrochemical active ingredient and the dispersing agent wherein the primary agrochemical active ingredient is present at a levE of less than 10% of weight of the composition wherein the secondary agrochemical active ingredient is present at a level of more than 50% by weight of the composition.
51. The method according to claim 50 wherein a solubility rate of the primary agrochemical active ingredient is higher than a solubility rate of the primary agrochemical active ingredient in a composition having same levels of the primary agrochemical active ingredient and the secondary agrochemical active ingredient in separate granules.
52. The method according to claim 50 furthing comprising the step of:
selecting the primary agrochemical active ingredient from metsulfuron-methyl, nicosulfuron, rimsulfuron, tribenuron methyl and thifensulfuron-methyl and the secondary active is selected from propanil and diuron.
53. The method according to claim 50 further comprising the step of:
preparing a wetted mixture in the form of a free-flowing powder having the primary agrochemical active ingredient, the secondary agrochemical active ingredient, the dispersing agent and optionally other components wherein at least one of the dispersing agent and optional other component is liquid wherein granules form from the composition.
54. The method according to claim 53 wherein the liquid of the wetted mixture is water.
55. The method according to claim 50 further comprising the step of:
drying the composition to form granules.
56. (canceled)
57. The method according to claim 50 further comprising the step of:
mixing a liquid carrier with the composition for applying to the plant or the locus of the plant to be treated.
58-60. (canceled)
US11/930,706 1999-08-26 2007-10-31 Water-dispersible agrochemical compositions Abandoned US20080171661A1 (en)

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US10/069,911 US6872689B1 (en) 1999-08-26 2000-08-25 Water-dispersible agrochemical compositions
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US10/973,518 US20050059553A1 (en) 1999-08-26 2004-10-25 Water-dispersible agrochemical compositions
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US20050059553A1 (en) 2005-03-17
AU6715500A (en) 2001-03-19
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ATE262277T1 (en) 2004-04-15
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CN100374018C (en) 2008-03-12
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