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AU2012211399B2 - Herbicidal compositions as dispersions comprising diflufenican and flurtamone - Google Patents
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AU2012211399B2 - Herbicidal compositions as dispersions comprising diflufenican and flurtamone - Google Patents

Herbicidal compositions as dispersions comprising diflufenican and flurtamone Download PDF

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AU2012211399B2
AU2012211399B2 AU2012211399A AU2012211399A AU2012211399B2 AU 2012211399 B2 AU2012211399 B2 AU 2012211399B2 AU 2012211399 A AU2012211399 A AU 2012211399A AU 2012211399 A AU2012211399 A AU 2012211399A AU 2012211399 B2 AU2012211399 B2 AU 2012211399B2
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diflufenican
flurtamone
dispersions
herbicidal
active substances
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AU2012211399A1 (en
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Gerhard Frisch
Janine Rude
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Bayer CropScience AG
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Bayer CropScience AG
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Abstract

The present invention relates to formulations in the form of aqueous dispersions comprising diflufenican and flurtamone and a mixture of anionic surfactants from the group of the naphthalenesulphonates or from the group of the condensates of naphthalenesulphonates with formaldehyde, nonionic surfactants from the group of the di and tri-block copolymers of alkylene oxides, and polybasic organic acids, to which, if appropriate, thickeners, further agrochemical active substances and further customary adjuvants and additives may be added. In addition, the present invention relates to herbicidal compositions comprising, as components, diflufenican, flurtamone and flufenacet. The aqueous dispersions and herbicidal compositions are useful in the crop protection sector.

Description

1 Description Herbicidal compositions as dispersions comprising diflufenican and flurtamone 5 The invention, the subject of this application, is directed to a herbicidal composition comprising diflufenican, flurtamone and flufenacet and to a process for combating undesirable plant growth, which process comprises the application of an effective amount of a composition comprising diflufenican, flurtamone and flufenacet. ) The problem to be solved by the present invention should be seen in the task to provide a mixture on the base of diflufenican and flurtamone which have improved properties in the control of dicot weeds, such as Galium aparine (GALAP), and monocot weeds, such as loose silky bent (APESV ), Alopecurus myosuroides (ALOMY) and in particular the one-year panicle Poa annua (POAAN) in comparison to the mixture of diflufenican and flurtamone at low doses. The invention, the subject of the application, relates to the field of formulations comprising plant protection agents. It relates in particular to a herbicidal composition comprising diflufenican, flurtamone and flufenacet. ) More broadly disclosed in the present application are: * formulations in the form of aqueous dispersions which comprise at least the herbicidal active substances diflufenican and flurtamone and which are stable on storage after exchange of alkylphenol polyethoxylates in the formulations and * herbicidal compositions which, in addition to the herbicidal active substances .5 diflufenican and flurtamone, additionally comprise the active substance flufenacet. Herbicidal active substances are generally not used in their pure form. Depending on the field of application and the type of application, and on physical, chemical and biological parameters, the active substances are used as a mixture with conventional auxiliaries and additives as 30 active substance formulation. The combinations with additional active substances, in order to broaden the spectrum of activities and/or to protect crop plants (e.g., through safeners, antidotes), are also known. Formulations of herbicidal active substances should generally exhibit high chemical and 35 physical stability, good applicability and user friendliness, and a broad biological action with high selectivity.
2 Aqueous dispersions for herbicidal active substances are known, inter alia, from EP-A-0 514 768 (US 5 707 926) or EP-A-0 592 880 (US 5376621). The herbicidal active substances diflufenican and flurtamone are used alone and as a mixture (tank mix, coformulation), inter alia, as aqueous suspension concentrates (SC), for example with the trade name Carat@ 350 SC. A disadvantage of the formulations underlying this or similar products is the fact that they comprise surfactants from the group consisting of the alkyl phenol polyethoxylates (APE) which, because of their delayed biodegradability, are classified as doubtful. On attempting to manufacture APE-free formulations for this active substance mixture, undesirable effects were produced, such as flocculation, agglomeration and/or crystal growth, resulting in satisfactory storage stability no longer being guaranteed. Although mixtures of the herbicidal active substances diflufenican and flurtamone show a good herbicidal action, there always exists a broad scope for improvements. Thus, the users desire, with regard to the amounts which have to be expended, more flexible solutions with the same to increased activity, for example in the combating of harmful grasses, such as wind grass and Poa species. The aim of one embodiment of the invention was: * to make available an aqueous formulation comprising plant protection agents, which comprises at least the active substances diflufenican and flurtamone, which is free from alkylphenol polyethoxylates and which exhibits a satisfactory stability on storage, and * to discover a herbicidal composition which exhibits the abovementioned improvements to the herbicidal active substance mixture of diflufenican and flurtamone. J The invention, the subject of the application, is directed to a herbicidal composition comprising diflufenican, flurtamone and flufenacet. In a further embodiment of the invention: * aqueous dispersions comprising diflufenican and flurtamone and a "surfactant/organic 0 acid mixture" consisting of anionic surfactants from the group consisting of naphthalenesulfonates or from the group consisting of the condensation products of naphthalenesulfonates with formaldehyde, nonionic surfactants from the group consisting of the di- and triblock copolymers of alkylene oxides and polybasic organic acids, to which also thickeners, additional agrochemical active substances, preferably 5 flufenacet, and additional standard auxiliaries and additives can optionally be added, and * herbicidal compositions which, in addition to the herbicidal active substances diflufenican and flurtamone, additionally comprise the active substance flufenacet.
3 The present invention accordingly relates to aqueous dispersions which comprise a) the herbicidal active substances diflufenican and flurtamone, b) one or more anionic surfactants from the group consisting of the naphthaleesulfonates or from the group consisting of the condensation products of naphthalenesulfonates with formaldehyde, c) one or more nonionic surfactants from the group consisting of the di- and triblock copolymers of alkylene oxides, d) one or more polybasic organic acids, e) optionally one or more thickeners, f) optionally one or more agrochemical active substances other than component a), preferably the herbicidal active substance flufenacet, 9) optionally one or more additional standard auxiliaries and additives, and water. The dispersions according to the invention show an outstanding stability on storage. They are stable on storage at ambient temperature for at least 2 years and show, in this connection, no undesirable effects, such as, e.g., crystal growth. o In a preferred embodiment, these dispersions comprise a) 0.1 to 50% of diflufenican and 0.1 to 50% of flurtamone, b) 0.1 to 510% of one or more anionic surfactants from the group consisting of the naphthalenesulfonates or from the group consisting of the condensation products of naphthalenesulfonates with formaldehyde, insisting of the di 25 c) 0.1 to 20% of one or more nonionic surfactants from the group co and triblock copolymers of alkylene oxides, d) 0.05 to 10% of one or more polybasic organic acids, e) 0 to 5% of one or more thickeners,ial active substances other than component a), f) o to 50% of one or more agrochemnicaaciesbt 30 preferably 0.1 to 50% of flufenacet, g) 0 to 20% of one or more additional standard auxiliaries and additives, 4 ind ?0 to 70% of water. A particularly preferred embodiment is composed of dispersions according to the invention in which are present a) 0.5 to 20% of diflufenican and 0.5 to 30% of flurtamone, b) 0.2 to 5% of one or more anionic surfactants from the group consisting of the naphthalenesulfonates or from the group consisting of the condensation products of naphthalenesulfonates with formaldehyde, c) 0.5 to 14% of one or more nonionic surfactants from the group consisting of the di and triblock copolymers of alkylene oxides, d) 0.1 to 5% of one or more polybasic organic acids, e) 0.05 to 2.5% of one or more thickeners, ) 0 to 40% of one or more agrochemical active substances other than component a), preferably 0.5 to 22% of flufenacet, g) 0 to 15% of one or more additional standard auxiliaries and additives, and 20 to 60% of water. A very particularly preferred embodiment is composed of dispersions according to the invention in which are present a) 2 to 16% of diflufenican and 4 to 22% of flurtaione, b) 0.3 to 1.5% of one or more anionic surfactants from the group consisting of the naphthalenesulfonates or from the group consisting of the condensation products of 5 naphthalenesulfonates with formaldehyde, c) 1 to 10% of one or more nonionic surfactants from the group consisting of the di and triblock copolymers of alkylene oxides, d) 0.2 to 2% of one or more polybasic organic acids, e) 0.075 to 1.5% of one or more thickeners, 30 f) 4 to 22% of flufenacet, g) 0 to 15% of one or more additional standard auxiliaries and additives, and 5 30 to 55% of water. All percentage values are, here and throughout the description, percentages by weight (% by weight) and refer, unless otherwise defined, to the relative weight of the 5 respective component, based on the total weight of the formulation. The herbicidal active substances a) diflufenican (251) and flurtamone (392) are, as individual substances or as a mixture, e.g., known from "The Pesticide Manual", 13th edition (2003), The British Crop Protection Council (note: index number in 10 brackets). The proportion of these active substances in the dispersions according to the invention (component a)) can, for diflufenican, be 0.1 - 50% by weight, preferably 0.5 - 20% by weight, particularly preferably 2 - 16% by weight, and, for flurtamone, be 0.1 - 50% by weight, preferably 0.5 - 30% by weight, particularly preferably 4 - 22% 15 by weight. Examples of anionic surfactants b) from the group consisting of the naphthalenesulfonates are Galory@ MT 800 (sodium dibutylnaphthalenesulfonic acid) and Nekal@ BX (alkylnaphthalenesulfonate). Examples of anionic surfactants 20 b) from the group consisting of the condensation products of naphthalenesulfonates with formaldehyde are Galoryl@ DT 201 (naphthalenesulfonic acid hydroxy polymer with formaldehyde and methylphenol sodium salt), Galoryl@ DT 250 (condensation product of phenol- and naphthalenesulfonates) and Reserve@ C (condensation product of phenol- and naphthalenesulfonates). Preference is given to 25 naphthalenesulfonates 1,2-substituted by dibutyl or diisobutyl, such as, e.g., products such as Galoryl@ MT 800 (CFPI-Nufarm) and Nekal@ BX (BASF). The proportion of the anionic surfactants in the dispersions according to the invention (component b)) can be 0.1 - 10% by weight, preferably 0.2 - 5% by weight, particularly preferably 0.3 - 1.5% by weight. 30 Possible nonionic surfactants c) from the group consisting of the di- and triblock copolymers of alkylene oxides are, e.g., compounds synthesized on the basis of 6 ethylene and propylene oxide with average molar masses between 200 and 10 000 g/mol, preferably 1000 to 4000 g/mol, the proportion by weight of the polyethoxylated block varying between 10 and 80%, such as, e.g., Synperonic@ PE series (Uniqema), Pluronic@ PE series (BASF), VOP@ 32 or Genapol@ PF series 5 (Clariant). Products such as Pluronic@ PE 10500 are preferred, for example. The proportion of the nonionic surfactants in the dispersions according to the invention (component c)) can be 0.1 - 20% by weight, preferably 0.5 - 14% by weight, particularly preferably I - 10% by weight. 10 Examples of polybasic organic acids d) are, e.g., citric acid, tartaric acid, succinic acid, maleic acid, fumaric acid, and the like. Citric acid is preferred. The proportion of the polybasic organic acids in the dispersions according to the invention (component d)) can be 0.05 - 10% by weight, preferably 0.1 - 5% by weight, particularly preferably 0.2 - 2% by weight. 15 Suitable thickeners e) optionally added are, for example: 1) modified natural silicates, such as chemically modified bentonites, hectorites, attapulgites, montmorillonites, smectites or other silicate minerals, such as Bentone@ (Elementis), Attagel@ (Engelhard), Agsorb@ (Oil-Dri Corporation) or 20 Hectorite@ (Akzo Nobel), 2) thickeners based on synthetic polymers, such as thickeners of the Thixin@ or Thixatrol@ series (Elementis) and also Rhodopol@ (Rhodia) and Kelzan@ S (Kelco Corp.), 3) synthetic. silicates, such as silicates of the Sipernat@, Aerosil@ or Durosil@ series 25 (Degussa), of the CAB-0-SIL@ series (Cabot) or of the Van Gel series (R.T. Vanderbilt). Organic- and/or inorganic-based thickeners are preferred, such as, e.g., products such as Bentone@ EW (Elementis) and Rhodopol@ 23 (Rhodia). The proportion in the dispersions according to the invention of thickeners optionally 30 added (component e)) can be up to 5% by weight, preferably 0.05 - 2,5% by weight, particularly preferably 0.075 - 1.5% by weight.
7 Herbicides, fungicides, insecticides, plant growth regulators, safeners and the like are suitable as agrochemical active substances f) other than component a) optionally added. These active substances are, for example, known from "The Pesticide Manual", 13th edition (2003), The British Crop Protection Council (note; index 5 number in brackets). Preference is given to herbicides, such as flufenacet (369), loxynil (467), bromoxynil (95), bifenox (75), aclonifen (8), trifluralin (836), clodinafop-propargyl (156), oxadiazon (600), oxadiargyl (599), pyraflufen-ethyl (691), carbetamide (117), terbuthylazine (775), active substances based on phenylurea, such as isoproturon 10 (475), diuron (281), linuron (489), active substances based on phenoxyacetic or phenoxypropionic and phenoxybutyric acids, such as MCPA (499), mecoprop (503), mecoprop-P (504), 2,4-D (211), fluazifop-butyl (361), diclofop-methyl (238), fenoxaprop-P-ethyl (339), and also in each case the derivatives thereof in the form of acids or esters. The herbicidal active substances flufenacet and isoproturon are 15 particularly preferred and flufenacet is very particularly preferred. The proportion in the dispersions according to the invention of agrochemical active substances other than component a) (component f)) optionally added can be up to 50% by weight, preferably up to 40% by weight, particularly preferably up to 30% by weight. In the case of the herbicidal active substance flufenacet, the proportion can 20 be 0.1 - 50% by weight, preferably 0.5 - 22% by weight, particularly preferably 4 22% by weight. The additional standard auxiliaries and additives g) optionally added are, for example, antifoaming agents, antifreeze agents, structuring agents, preservatives, 25 antioxidants, colorants, aromatic principles, wetting agents, anti-drift agents, deposit builders, penetrating agents (adjuvants), fertilizers and additional surfactants other than the components b) and c). Suitable antifoaming agents are surface-active compounds based on silicone or 30 silane, such as the Tegopren@ products (Goldschmidt), the SE@ products (Wacker), and also the Bevaloid@, Rhodorsil@ and Silcolapse@ products (Rhodia, Dow Coming, Reliance, GE, Bayer). SE@ (Wacker), Rhodorsil@ and Silcolapse@ products 8 (Rhodia) are preferred and, e.g., products such as Silcolapse@ 5020 are particularly preferred. Suitable antifreeze agents are those from the group consisting of ureas, diols and polyols, such as ethylene glycol and propylene glycol, preferably propylene glycol. 5 Suitable preservatives are, e.g., products such as Acticide@ MBS (biocide, Thor Chemie). Suitable antioxidants, colorants, aromatic principles, wetting agents, anti-drift agents, deposit builders, penetrating agents (adjuvants) and fertilizers are known to a person skilled in the art. Additional surfactants other than the components b) and c) which 10 are suitable are, for example, emulsifiers and dispersants. Possible emulsifiers and dispersants are, eg., nonionic emulsifiers and dispersants, e.g.: 1) polyalkoxylated, preferably polyethoxylated, saturated and unsaturated aliphatic 15 alcohols, - with 8 to 24 carbon atoms in the alkyl radical, which is derived from the corresponding fatty acids or from petrochemical products, and - with 1 to 100, preferably 2 to 50, ethylene oxide units (EO), the free hydroxyl group optionally being alkoxylated, and 20 - which, e.g., are available commercially as Genapol@ X and Genapol@ 0 series (Clariant), Crovol@ M series (Croda) or Lutensol@ series (BASF); 2) polyalkoxylated, preferably polyethoxylated, hydroxyfatty acids or glycerides comprising hydroxyfatty acids, such as, e.g., ricinine or castor oil, with a degree of ethoxylation of between 10 and 80, preferably 25 to 40, such as, e.g., 25 Emulsogen@ EL series (Clariant) or Agnique@ CSO series (Cognis); 3) polyalkoxylated, preferably polyethoxylated, sorbitan esters, such as, e.g., Atplus@ 309 F (Uniqema) or Alkamuls@ series (Rhodia). Preferred nonionic emulsifiers and dispersants are, e.g., polyethoxylated alcohols and polyethoxylated triglycerides comprising hydroxyfatty acids. 30 Ionic emulsifiers and dispersants are also possible, e.g.: 1) polyalkoxylated, preferably polyethoxylated, emulsifiers/dispersants which are 9 sonically modified, e.g. by conversion of the terminal free hydroxyl functional group of the polyethylene oxide block to give a sulfate or phosphate ester (e.g., as alkali metal and alkaline earth metal salts), such as, e.g., Genapol@ LRO or Dispersogen 3618 (Clariant), Emulphor@ (BASF) or Crafol@ AP (Cognis); 5 2) alkali metal and alkaline earth metal salts of alkylarylsulfonic acids with a linear or branched alkyl chain, such as phenylsulfonate CA or phenylsulfonate CAL (Clariant), Atlox@ 3377BM (ICI), Empiphos@ TM series (Huntsman); 3) polyelectrolytes, such as lignosulfonates, polystyrenesulfonate or sulfonated unsaturated or aromatic polymers (polystyrenes, polybutadienes or polyterpenes), 10 such as Tamol@ series (BASF), Morwet@ D425 (Witco), Kraftsperse@ series (Westvaco), Borresperse@ series (Borregard). Preferred ionic emulsifiers/dispersants are, e.g., salts of alkylarylsulfonic acids and lignosulfonates. 15 The proportion in the dispersions according to the invention of the additional standard auxiliaries and additives (component g)) optionally added can be up to 20% by weight, preferably up to 15% by weight. The proportion of the component water in the dispersions according to the invention 20 can be 20 - 70% by weight, preferably 20 - 60% by weight, particularly preferably 30 - 55% by weight. The abovementioned formulation auxiliaries of the components b), c), d), e) and g) are known to a person skilled in the art and/or are described, for example, in: 25 Watkins, "Handbook of Insecticide Dust Diluents and Carriers", 2nd Ed., Darland Books, Caldwell, N.J.; H.v. Olphen, "Introduction to Clay Colloid Chemistry", 2nd Ed., J. Wiley & Sons, N.Y.; C. Marsden, "Solvents Guide", 2nd Ed., Interscience, N.Y. 1963; McCutcheon's "Detergents and Emulsifiers Annual", MC Publ. Corp., Ridgewood, N.J.; Sisley and Wood, "Encyclopedia of Surface Active Agents", Chem. 30 Publ. Co. Inc., N.Y., 1964; Sch.6nfeldt, "Grenzflachenaktive Athylenoxidaddukte" [Surface-active ethylene oxide adducts], Wiss. Verlagsgesell., Stuttgart, 1976; Winnacker-KUchler, "Chemische Technologie" [Chemical Technology], Volume 7, 10 4th edition, C. Hanser Verlag, Munich, 1986. The combination of the active substances diflufenican, flurtamone and flufenacet is novel per se and accordingly another subject matter of the invention is a herbicidal 5 composition comprising, as components, the active substances diflufenican, flurtamone and flufenacet. These active substances form the herbicidal composition and are used for this either alone and/or as partial or total mixture (tank mix, coformulation), simultaneously or sequentially. 10 This active substance mixture (3-component combination) is very highly suitable as herbicidal composition and solves the problems posed. In addition, it can be advantageous to add additional plant protection agents, alone or mixtures thereof, to this 3-component combination. Mention may in particular be made here of additional herbicides, safeners, plant growth regulators, insecticides, acaricides, nematicides, 15 fungicides and bactericides, and also substances which are effective as adjuvants. Examples of herbicides are, e.g., from the groups consisting of ALS inhibitors (acetolactate synthetase inhibitors, such as sulfonylureas), carbamates, thiocarbamates, haloacetanilides, phenylpyrazolines (such as pinoxaden), 20 substituted phenoxy-, naphthoxy- and phenoxyphenoxycarboxylic acid derivatives and also heteroaryloxyphenoxyalkanecarboxylic acid derivatives, such as quinolyloxy-, quinoxalyloxy-, pyridyloxy-, benzoxazolyloxy- and benzothiazolyloxyphenoxyalkanecarboxylic acid esters, cyclohexanedione derivatives, imidazolinones, phosphorus-comprising herbicides (e.g., of glufosinate 25 type or of glyphosate type), pyrimidinyloxypyridinecarboxylic acid derivatives, pyrimidyloxybenzoic acid derivatives, triazolopyrimidinesulfonamide derivatives and also S-(N-aryl-N-alkylcarbamoylmethyl)dithiophosphoric acid esters, ureas and also hydroxybenzonitriies. 30 Examples of safeners are, e.g., 4-dichloroacetyl-1-oxa-4-azaspiro[4.5]decane (AD-67), 1-dichloroacetyl-hexahydro-3,3,8a-trimethylpyrrolo[1,2-a]pyrimidin-6(2H)- 11 one (dicyclonone, BAS-145138), 4-dichloroacetyl-3,4-dihydro-3-methyl-2H-1,4 benzoxazine (benoxacor), cloquintocet, (5-chloroquinolin-8-yioxy)acetic acid 1 -methylhexyl ester (cloquintocet-mexyl), a-(cyanomethoxyimino)phenylacetonitrile (cyornetrinil), 2,2-dichloro-N-(2-oxo-2-(2-propenylamino)ethyl)-N-(2-propenyl) 5 acetamide (DKA-24), 2,2-dichloro-N,N-di(2-propenyl)acetamide (dichlormid), N-(4-methylphenyl)-N'-(1-methyl-1-phenylethyl)urea (Dymron), 4,6-dichloro-2-phenyl pyrimidine (fenclorim), 1-(2,4-dichlorophenyl)-5-trichloromethyl-1H-1,2,4-triazole-3 carboxylic acid ethyl ester (fenchlorazole-ethyl), 2-chloro-4-(trifluoromethyl)thiazole 5-carboxylic acid phenylmethyl ester (flurazole), 4-chloro-N-((1,3-dioxolan 10 2-yl)methoxy)-a-trifluoroacetophenonoxime (fluxofenim), 3-dichloroacetyl 5-(2-furanyl)-2,2-dimethyloxazolidine (furilazole, MON-13900), ethyl 4,5-dihydro 5,5-diphenyl-3-isoxazolecarboxylate (isoxadifen-ethyl), diethyl 1-(2,4-dichlorophenyl)-4,5-dihydro-5-methyl-1 H-pyrazole-3,5-dicarboxylate (mefenpyr-diethyl), 2-dichloromethyl-2-methyl-1,3-dioxolane (MG-191), 15 1,8-naphthalic acid anhydride, o-((1,3-dioxolan-2-yl)methoxyimino)phenylacetonitrile (oxabetrinil), 2,2-dichloro-N-((1,3-dioxolan-2-yl)methyl)-N-(2-propenyl)acetamide (PPG-1292), 3-dichloroacetyl-2,2-dimethyloxazolidine (R-28725), 3-dichloroacetyl 2,2,5-trimethyloxazolidine (R-29148), 1-(2-chlorophenyl)-5-phenyl-1 H-pyrazole 3-carboxylic acid methyl ester, 4-cyclopropylaminocarbonyl-N-(2-methoxybenzoyl) 20 benzenesulfonamide (cyprosulfamide), 4-isopropylaminocarbonyl-N (2-methoxybenzoyl)benzenesulfonamide and N-(2-methoxybenzoyl) 4-[(methylaminocarbonyl)amino]benzenesulfonamide. Examples of insecticides are, e.g., from the groups consisting of carbamates, 25 organophosphates, pyrethroids and chloronicotinyls (such as acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazine, thiacoprid, thiamethoxam). Examples of fungicides are, e.g., from the groups consisting of ergosterol 30 biosynthesis inhibitors (such as fenhexamid, azaconazole, bitertanol, bromuconazole, cyproconazole, diclobutrazol, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, etaconazole, fenbuconazole, fluquinconazole, 12 flusilazole, flutriafol, furconazole, furconazole-cis, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, paclobutrazol, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, voriconazole, imazalil, imazalil sulfate, 5 oxpoconazole, fenarimol, flurprimidol, nuarimol, pyrifenox, triforine, pefurazoate, prochloraz, triflumizole, viniconazole, aldimorph, dodemorph, dodemorph acetate, fenpropimorph, tridemorph, fenpropidin, spiroxamine, naftifine, pyributicarb, terbinafine) and respiratory chain inhibitors (e.g., complex liI, such as azoxystrobin, cyazofamid, dimoxystrobin, enestrobin, famoxadone, fenamidone. fluoxastrobin, 0 kresoxim-methyl, metominostrobin, orysastrobin, pyraclostrobin, picoxystrobin, trifloxystrobin). For application, the dispersions or herbicidal compositions according to the invention can be diluted in the normal way, e.g. using water, It can be advantageous to add, to 5 spray mixtures obtained, additional agrochemical active substances (e.g., tank mix components in the form of appropriate formulations) and/or auxiliaries and additives standard for application, e.g. self-emulsifying oils, such as vegetable oils or liquid paraffins, and/or fertilizers. The present invention also accordingly relates to those herbicidal compositions based on the dispersions according to the invention. 0 The dispersions or herbicidal compositions according to the invention exhibit an outstanding herbicidal activity against a broad spectrum of economically important harmful monocotyledonous and dicotyledonous plants. Even perennial weeds which sprout from rhizomes, root stocks or other perennial organs and which are difficult to 25 combat are successfully included. In this connection, the compositions can be applied, e.g., in the presowing, preemergence or postemergence method. Specifically, mention may be made, by way of example, of some representatives of the mono- and dicotyledonous weed flora which can be controlled by the dispersions or herbicidal compositions according to the invention, without the designation 30 resulting in a limitation to certain species. In the case of the monocotyledonous weed species, Apera spica-venti, Avena spp., 13 Alopecurus spp., Brachiaria spp., Digitaria spp., Lolium spp., Echinochloa spp., Panicum spp., Phalaris spp., Poa spp., Setaria spp. and also Bromus spp., such as Bromus catharticus, Bromus secalinus, Bromus erectus, Bromus tectorum and Bromus japonicus, and Cyperus species from the group of the annuals and, in the 5 case of the perennial species, Agropyron, Cynodon, Imperata and also Sorghum and even perennial Cyperus species, e.g., are successfully included. With dicotyledonous weed species, the spectrum of activity applies to species such as, e.g., Abutilon spp., Amaranthus spp., Chenopodium spp., Chrysanthemum spp., 10 Galium spp., such as Galium aparine, lpomoea spp., Kochia spp., Lamium spp., Matricaria spp., Pharbitis spp., Polygonum spp., Sida spp., Sinapis spp., Solanum spp., Stellaria spp., Veronica spp. and Viola spp., Xanthium spp., in the case of the annuals, and Convolvulus, Cirsium, Rumex and Artemisia with the perennial weeds. 15 Harmful plants occurring under the specific cultivation conditions in rice, such as, e.g., Echinochloa, Sagittaria, Alisma, Eleocharis, Scirpus and Cyperus, are likewise combated in an outstanding fashion by the dispersions or herbicidal compositions according to the invention. 20 If the dispersions or herbicidal compositions according to the invention are applied to the soil surface before germination, then either the emergence of the weed seedlings is completely prevented or the weeds grow until they have reached the cotyledon stage but then their growth ceases and finally, after 3 to 4 weeks have elapsed, they completely die. 25 On application of the dispersions or herbicidal compositions according to the invention to the green parts of the plants in the postemergence method, a drastic halt in growth likewise occurs very quickly after the treatment and the weed plants stay in the growth stage present at the time of application or completely die after a certain 30 time, so that in this way competition by weeds, which is harmful for the crop plants, is eliminated very early and with lasting effect.
14 The dispersions or herbicidal compositions according to the invention are distinguished by a rapidly commencing and longlasting herbicidal action. The resistance to rain of the active substances in the combinations according to the invention is generally good. A particular advantage is crucially that the dosages of 5 herbicidal compounds which are used in the herbicidal compositions and which are effective can be adjusted to such a low value that their soil action is optimally low. Accordingly, not only is their use finally possible in sensitive crops but groundwater contamination is virtually avoided. A substantial reduction in the amount of the active substances which has to be expended is made possible by the active substance 10 combination according to the invention. The properties and advantages mentioned are of use in the practical combating of weeds in order to keep agricultural crops free from undesirable competing plants and accordingly to safeguard and/or to increase the yields in terms of quality and 15 quantity. The technical standard is, with regard to the properties described, clearly exceeded by these new dispersions or compositions. Although the dispersions or herbicidal compositions according to the invention exhibit an outstanding herbicidal activity with regard to mono- and dicotyledonous 20 weeds, crop plants of economically important crops, e.g. dicotyledonous crops, such as soya, cotton, rape, sugar beet, or gramineous crops, such as wheat, barley, rye, oats, millet, rice or corn, are only insignificantly damaged or completely undamaged. The dispersions or the components of the herbicidal composition according to the invention, for these reasons, are very well suited to the selective combating of 25 undesirable plant growth in agriculturally useful plants or in ornamental plants. In addition, the dispersions according to the invention or the components of the herbicidal composition exhibit outstanding growth-regulatory properties in crop plants. They intervene in a regulatory manner in the plants' metabolism and can 30 accordingly be used for the selective influencing of plant contents and for making it easier to harvest, such as, e.g., by controlling desiccation and stunted growth. Furthermore, they are also suitable for the general control and inhibition of 15 undesirable vegetative growth, without in this connection killing the plants. Inhibition of vegetative growth plays a major role in many mono- and dicotyledonous crops since lodging can be reduced or completely prevented through this. 5 Because of their herbicidal and plant-growth-regulatory properties, the dispersions or the components of the herbicidal composition according to the invention can also be used for combating harmful plants in crops of known genetically modified plants or genetically modified plants still to be developed. The transgenic plants are generally distinguished by particular advantageous properties, for example by resistance to 10 certain pesticides, mainly certain herbicides, resistance to plant diseases or causative agents of plant diseases, such as certain insects or microorganisms, such as fungi, bacteria or viruses. Other particular properties relate, e.g., to the harvested crops with regard to amount, quality, storability, composition and special ingredients. Thus, transgenic plants with increased starch content or modified quality of the 15 starch or those with a different fatty acid composition of the harvested crops are known. Preference is given to the use of the dispersions or herbicidal compositions according to the invention in economically important transgenic crops of useful and 20 ornamental plants, e.g. of gramineous crops, such as wheat, barley, rye, oats, millet, rice and com, or also crops of sugar beet, cotton, soya, rape, potato, tomato, peas and other kinds of vegetable. Preferably, the dispersions or compositions according to the invention can be used as herbicides in crops of useful plants which are resistant to the phytotoxic effects of the herbicides or which have been made 25 resistant by genetic engineering. When the dispersions or herbicidal compositions according to the invention are used in transgenic crops, effects often occur, in addition to the effects with regard to harmful plants to be observed in other crops, which are specific for the application in 30 the respective transgenic crop, for example a modified or specially broadened weed spectrum which can be combated, modified amounts to be expended which can be used for the application, preferably good ability to be combined with the herbicides to 16 which the transgenic crop is resistant, and influencing of growth and yield of the transgenic crop plants. Another subject matter of the present invention is furthermore a process for 5 combating undesirable plant growth, preferably in crop plants, such as cereals (e.g., wheat, barley, rye, oats, rice, corn, millet), sugar beet, sugar cane, rape, cotton and soya, particularly preferably in monocotyledonous crops, such as cereals, e.g. wheat, barley, rye, oats, hybrids thereof, such as triticale, rice, corn and millet, one or more dispersions or the components of the herbicidal composition according to the 0 invention being applied to the harmful plants, plant parts, plant seeds or the area on which the plants are growing, e.g. the area under cultivation. The crop plants can also be modified by genetic engineering or obtained by mutation selection and are preferably tolerant to acetolactate synthase (ALS) inhibitors. 5 The dispersions according to the invention can be prepared according to processes known to a person skilled in the art; for example according to Houben-Weil, by wet milling by means of bead mills (see: Winnacker-KOchler, "Chemische Technologie" [Chemical Technology], Volume 7, 4th edition, C. Hanser Verlag, Munich, 1986; :0 Wade van Valkenburg, "Pesticide Formulations", Marcel Dekker, N.Y., 1973; K. Martens, "Spray Drying Handbook", 3rd Ed., G. Goodwin Ltd., London, 1979). A uniform particle distribution of the relevant active substances is optionally advantageous in this connection, in order additionally to further prevent crystal growth and flocculation. 25 Examples of aqueous dispersions according to the invention are found in the following table.
17 The terms used in the following examples have the following meaning: diflufenican = common name (BSI, draft E-ISO, (m) draft F-ISO); IUPAC name: 2',4'-difluoro-2-(a,a,g-trifluoro-m 5 tolyloxy)nicotinanilide (Bayer CropScience) flurtamone = common name (BSI, ANSI, draft E-ISO); IUPAC name: (RS)-5-methylamino-2-phenyl-4-(a,g,a-trifluoro-m tolyl)furan-3(2H)-one (Bayer CropScience) Nekal@ BX alkylnaphthalenesulfonic acid sodium salt (BASF) 10 Pluronic@ PE 10500 = propylene oxide/ethylene oxide (PO/EO) block polymer (BASF) citric acid = polybasic organic acid Bentone@ EW = modified sheet silicate (Elementis) Rhodopol@ 23 = xanthan derivate (Rhodia) 15 flufenacet = common name (BSI, pa ISO); IUPAC name: 4'-fluoro-N isopropyl-2-(5-trifluoromethyl-1,3,4-thiadiazol-2 yloxy)acetanilide (Bayer CropScience) Silcolapse@ 5020 = silicone antifoaming agent (Rhodia) propylene glycol = antifreeze agent 20 Acticide@ MBS = preservative (biocide, Thor Chemie) Preparation of an aqueous dispersion: For the preparation of the examples mentioned in table 1, water is first placed in a vessel. Diflufenican and flurtamone and also the additional constituents of the 25 formulation are subsequently added with stirring. The sequence of the addition of the additional components is generally unimportant, A wet milling, for example by means of a bead mill, is optionally carried out subsequently.
18 Table 1 (figures follow in percentage by weight) Component Example No. 1 2 3 4 5 6 7 a Diflufenican 10.7 10.5 10.3 15.7 8 4 12 a Flurtamone 10.7 10.5 14.8 11 20 8 12 b Nekal@ BX 0.5 0.7 0.8 0.6 0.4 0.6 1 Pluronic@ PE c 10500 5 6 6.3 7 7 7 6 d Citric acid 0.5 0.6 0.7 0.7 0.4 0.6 1 e Bentone@ EW 0.1 0.1 0.1 0.2 0.1 0.1 0.1 e Rhodopol@ 23 0.1 0.2 0.1 0.1 0.2 0.2 0.1 f Flufenacet 10.7 15.3 10.3 11 8 22 12 g Silcolapse@5020 1 0.8 1.2 1 1.5 1 1 g Propylene glycol 8 7 7.5 6 10 9 8 g Acticide@ MBS 0.2 0.1 0.2 0.2 0.2 0.2 0.2 Water 52.5 48.2 47.7 46.5 44.2 47.3 46.6 Total: 100 100 100 100 100 100 100 Stability of the aqueous dispersion: The dispersions according to the invention of examples I to 7 exhibit an excellent 5 stability on storage. They are stable at ambient temperature for at least 2 years and at 50*C for at least 3 months without visible change. Herbicidal action: 10 1. The herbicidal action of the dispersions according to the invention with regard to all important harmful plants achieves at least the level of the APE-comprising dispersions or herbicidal compositions comprising diflufenican and flurtamone known from the state of the art (as individual substances and in a mixture with one another and/or additional agrochemical active substances). 15 2. The action of the herbicidal compositions according to the invention comprising the active substances diflufenican, flurtamone and flufenacet as 19 components (3-component combination) corresponds to the requirements and accordingly solves the problem posed (inter alia, provision of more flexible solutions, with regard to the amounts which have to be expended, with the same to increased activity). In field trials, it was established, inter alia, that, by the use of the 3-component combination, the amounts of application products necessary in the combating of harmful grasses, such as wind grass and Poa species, could be reduced by up to 40%, in comparison with the 2-component combination (diflufenican and flurtamone active substance mixture). In addition, with the same amount expended, a greater activity of the 3-component combination compared with the 2 component combination was established. Figures 1 to 7 depict a comparison of the herbicidal efficacy of Bacara Forte (actives: diflufenican + Flurtamone + Flufenacet), Bacara (actives: diflufenican + Flurtamone) on Dicot Weed - Galium aparine (GALAP), Monocot Weeds - 'Bentgrass/Windham' (APESV), Alopecurus myosuroides (ALOMY) and Poa annua (POAAN). The comparison tests between "Bacara" and "Bacara Forte" show clearly the existence of a strong synergistic effect with its strongest effect in the control of POAAN both in pre- and post emergence application (see p. 7-8). Comprises/comprising and grammatical variations thereof when used in this specification are to be taken to specify the presence of stated features, integers, steps or components or groups thereof, but do not preclude the presence or addition of one or more other features, integers, steps, components or groups thereof.

Claims (3)

1. A herbicidal composition comprising diflufenican, flurtamone and flufenacet.
2. A process for combating undesirable plant growth, which process comprises the application of an effective amount of a composition as claimed in claim 1 to the plants, plant parts, seed or the area on which plants are growing.
3. The use of a herbicidal composition comprising diflufenican, flurtamone and flufenacet in combating undesirable plant growth. BAYER CROPSCIENCE AG WATERMARK PATENT AND TRADE MARKS ATTORNEYS P30892AU01
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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0531116A1 (en) * 1991-09-04 1993-03-10 Rhone-Poulenc Agriculture Ltd. Herbicidal compositions
WO2003028467A1 (en) * 2001-09-27 2003-04-10 Syngenta Participations Ag Herbicidal composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0531116A1 (en) * 1991-09-04 1993-03-10 Rhone-Poulenc Agriculture Ltd. Herbicidal compositions
WO2003028467A1 (en) * 2001-09-27 2003-04-10 Syngenta Participations Ag Herbicidal composition

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE CROPU [Online]ORTMAYR J: "Herold - for fall bentgrass and weed control in winter cereals. (Herold - zur Windhalm- und Unkrautbekaempfung im Herbst in Wintergetreide)" XP002454010 retrieved from STN Database accession no. 1999-88286 *
PFLANZENARZT (52, NO. 9-10, 20-21, 1999) 1 FIG. 1 TAB. CODEN: PFLZAQ AV - NO REPRINT ADDRESS., 1999. *

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