AU2012203814B2 - Herbicidal suspension - Google Patents

Abstract

C :NRPonbM>CC LB\442683_ .DOC-266/2012 Abstract A herbicidal suspension comprising (1) a sulfonylurea compound or its salt as a herbicidal component, (2) at least 5 one surfactant selected from the group consisting of an alkoxylated sorbitol fatty acid ester and an alkoxylated sorbitan fatty acid ester, and (3) a water-immiscible diluent. A method for controlling undesired plants or inhibiting their growth, which comprises applying a 10 herbicidally effective amount of the herbicidal suspension to the undesired plants or to a place where they grow.

Description

Australian Patents Act 1990 - Regulation 3.2A ORIGINAL COMPLETE SPECIFICATION STANDARD PATENT Invention Title "Herbicidal suspension" The following statement is a full description of this invention, including the best method of performing it known to us:- WO 2006/098156 PCT/JP2006/303918 DESCRIPTION This application is a divisional of Australian Patent Application No. 2006224071, the entire content of which is incorporated herein by reference. HERBICIDAL SUSPENSION 5 TECHNICAL FIELD The present invention relates to a herbicidal suspension containing a sulfonylurea compound or its salt as a herbicidally active ingredient, and having a stable herbicidal effect, safety for crops and practically 10 satisfactory effects. BACKGROUND ART In recent years, various studies have been conducted to obtain agricultural chemicals which stably exhibit a 15 favorable herbicidal effect, which have no harmful effect over crops and which can be used safely. Further,' there is a tendency to employ various additives for agricultural chemicals which can reduce harmful effects of the agricultural chemicals over human and environment 20 as far as possible. Under these circumstances, it has been desired to quickly develop alternatives to conventional agricultural chemicals having the above-described problems, and to supply to the market agricultural chemicals which are 25 human- and environmentally-friendly and which are also practical. EP 0598515 discloses an activity-enhanced herbicidal HI ia I.:'orenKRIXIuI I X nCR (IV,211 I do-4' 11i014 -2 composition comprising a specific sulfonylurea compound, an ethoxylated fatty amine type surfactant and a vegetable oil and/or a mineral oil. However, further studies have been required to accomplish formulations which are sufficiently practical and which also have high added value. DISCLOSURE OF THE INVENTION Namely, the present inventors have conducted studies paying attention to herbicidal effects and toxicity and further paying attention to safety for human and environment. As a result, they have found a herbicidal suspension containing a sulfonylurea compound or its salt as an active ingredient, which is sufficiently practicable such as having favorable physically and chemical characteristics, and which has an advantage such as more excellent herbicidal activity or improved safety for crops. The present invention provides a herbicidal suspension comprising (1) a sulfonylurea compound or its salt as a herbicidal component, (2) at least one surfactant selected from the group consisting of an alkoxylated sorbitol fatty acid ester and an alkoxylated sorbitan fatty acid ester, and (3) a water-immiscible diluent; and a method for controlling undesired plants or inhibiting their growth by means of such a herbicidal suspension. In another aspect the present invention provides a herbicidal suspension comprising (1) from 0.5 to 20 parts by weight of a sulfonylurea compound or its salt as a herbicidal component, selected from the group consisting of flazasulfuron and nicosulfuron, (2) from 0.5 to 35 parts by weight of an alkoxylated sorbitol fatty acid ester as a surfactant, (3) from 0.5 to 55 parts by weight of another surfactant, wherein the other surfactant is i) at least one llrectlin~ernoscmINfpRtIlDCC\REFC.6IK521I Fdoc-4 q3/2FI4 -3 nonionic surfactant selected from the group consisting of a polyoxyethylene castor oil and a polyoxyethylene hydrogenated castor oil, and ii) an alkylaryl sulfonate as an anionic surfactant, (4) a water-immiscible diluent, wherein the water-immiscible diluent is at least one member selected from the group consisting of a vegetable oil, a fatty acid derived from a vegetable oil and an alkyl ester of the fatty acid as the main component of the rest. BEST MODE FOR CARRYING OUT THE INVENTION The sulfonylurea compound is a compound having the following partial structure: -SOzNHCON (wherein X is a hydrogen atom or an alkyl group), and it may, for example, be amidosulfuron, azimsulfuron, bensulfuron-methyl, chlorimuron-ethyl, chlorsulfuron, cinosulfuron, cyclosulfamuron, ethametsulfuron-methyl, ethoxysulfuron, flazasulfuron, flucetosulfuron, flupyrsulfuron, foramsulfuron, halosulfuron-methyl, imazosulfuron, iodosulfuron, isosulfuron-methyl, mesosulfuron-methyl, metsulfuron-methyl, nicosulfuron, oxasulfuron, primisulfuron-methyl, prosulfuron, pyrazosulfuron-ethyl, rimsulfuron, sulfometuron-methyl, sulfosulfuron, thifensulfuron-methyl, triasulfuron, tribenuron-methyl, trifloxysulfuron, triflusulfuron-methyl or tritosulfuron. Among them, azimsulfuron, bensulfuron methyl, flazasulfuron or nicosulfuron is preferred. As the salt of such a sulfonylurea compound, various WO 2006/098156 PCT/JP2006/303918 4 types may be mentioned. It may, for example, be a salt with an alkali metal such as sodium or potassium, a salt with an alkaline earth metal such as magnesium or calcium, or a salt with an amine such as monomethylamine, s dimethylamine or triethylamine. The alkoxylated sorbitol fatty acid ester or the alkoxylated sorbitan fatty acid ester has one or more alkylene oxide moieties at optional positions. Such an alkylene oxide moiety may, for example, be ethylene 10 oxide, propylene oxide, a copolymer thereof or a block copolymer thereof. Among them, ethylene oxide is preferred. The average addition molar amount of the alkylene oxide is from 3 to 150 mols, preferably from 3 to 60 mols. 15 The number of fatty acid ester in the alkoxylated sorbitol fatty acid ester or the alkoxylated sorbitan fatty acid ester may be one or more, and a monoester, a diester, a triester, a tetraester, a pentaester or a hexaester may, for example, be mentioned. Further, in a 20 case where there 'are a plurality of fatty acid esters, they may be the same or different. The fatty acid moiety of the alkoxylated sorbitol fatty acid ester or the alkoxylated sorbitan fatty acid ester may be either saturated or unsaturated and may be 25 linear or branched, and its carbon number may be from about 4 to about 24, preferably from about 10 to about 20. The fatty acid may, for example, be a saturated WO 2006/098156 PCT/JP2006/303918 5 fatty acid such as butyric acid, n-caproic acid, caprylic acid, n-capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, isostearic acid or arachic acid, or an unsaturated fatty acid such as palmitoleic acid, oleic 5 acid, linoleic acid, linolenic acid, monoctic acid, arachidonic acid or docosahexaenoic acid. Lauric acid, stearic acid or oleic acid is, for example, preferred. The water-immiscible diluent may, for example, be a vegetable oil, a fatty acid derived from a vegetable oil, 10 an alkyl ester of the fatty acid (including one having a fatty acid moiety in a vegetable oil alkylated, such as methylated vegetable oil or methylated seed oil) or a mineral oil. The vegetable oil may, for example, be olive oil, is kapok oil, castor oil, papaya oil, camellia oil, coconut oil, sesame oil, corn oil, rice bran oil, peanut oil, cottonseed oil, soybean oil, rapeseed oil, linseed oil, tung oil, sunflower oil or safflower oil. The fatty acid derived from a vegetable oil is a 20 fatty acid derived from the above-described vegetable oil or the like and it may, for example, be a C 12

.

22 saturated or unsaturated fatty acid, such as lauric acid, palmitic acid, stearic acid, oleic acid, linolic acid, linoleic acid, erucic acid or brassidic acid, and the alkyl ester 25 of the fatty acid may, for example, be a C 1

..

8 linear or branched alkyl ester, such as a methyl ester, a butyl ester, an isobutyl ester or an oleyl ester.

WO 2006/098156 PCT/JP2006/303918 6 The mineral oil may, for example, be an aliphatic hydrocarbon such as liquid paraffin or paraffinic petroleum, or an aromatic hydrocarbon such as an alkyl benzene or an alkyl naphthalene. s The above water-immiscible diluents may be a mixture as the case requires. The herbicidal suspension contains (1) a sulfonylurea compound or its salt as a herbicidal component, (2) at least one surfactant (hereinafter 10 referred to as an essential surfactant) selected from the group consisting of an alkoxylated sorbitol fatty acid ester and an alkoxylated sorbitan fatty acid ester and (3) a water-immiscible diluent, and it is prepared as an oil-based herbicidal suspension such as an oil-based 15 suspension concentrate or a gel formulation. For its preparation, various additives may be used as the case requires. Various additives which can be used here may be any additives so long as they are commonly used in this technical field, and for example, another surfactant 20 (a surfactant other than the alkoxylated sorbitol fatty acid ester and the alkoxylated sorbitan fatty acid ester), a solvent, an anti-settling agent, a thickener, an antifoaming agent, an antifreezing agent, an antioxidant, a gelling agent, a dispersion stabilizer, a 25 phytotoxicity reducing agent, an anti-mold agent, a stabilizer, a preservative, and an inorganic ammonium salt, may be mentioned. The following may, for example, WO 2006/098156 PCT/JP2006/303918 7 be mentioned as specific examples of such various additives. Further, such formulations may be prepared in accordance with methods commonly employed in this technical field. 5 The another surfactant includes, for example, anionic surfactants such as a salt of fatty acid, a benzoate, an alkylsulfosuccinate, a dialkylsulfosuccinate, a polycarboxylate, a salt of alkylsulfuric acid ester, an alkyl sulfate, an alkylaryl io sulfate, an alkyl diglycol ether sulfate, a salt of alcohol sulfuric acid ester, an alkyl sulfonate, an alkylaryl sulfonate, an aryl sulfonate, a lignin sulfonate, an alkyldiphenyl ether disulfonate, a polystyrene sulfonate, a salt of alkylphosphoric acid is ester, an alkylaryl phosphate, a styrylaryl phosphate, a salt of polyoxyethylene alkyl ether sulfuric acid ester, a polyoxyethylene alkylaryl ether sulfate, a polyoxyethylene styrylaryl ether sulfate, an ammonium polyoxyethylene styrylaryl ether sulfate, a salt of 20 polyoxyethylene alkylaryl ether sulfuric acid ester, a polyoxyethylene alkyl ether phosphate, a salt of polyoxyethylene alkylaryl phosphoric acid ester, a polyoxyethylene styrylaryl ether phosphoric acid ester or its salt, a salt of a condensate of naphthalene sulfonate 25 with formalin, a salt of a condensate of alkylnaphthalene sulfonate with formalin, a salt of a condensate of phenol sulfonate with formalin and a salt of maleic anhydride WO 2006/098156 PCT/JP2006/303918 8 alkylene copolymer; nonionic surfactants such as a sorbitan fatty acid ester, a glycerin fatty acid ester, a fatty acid polyglyceride, a fatty acid alcohol polyglycol ether, an acetylene glycol, an acetylene alcohol, an 5 oxyalkylene block polymer, a polyoxyethylene alkyl ether, a polyoxyethylene alkylaryl ether, a polyoxyethylene styrylaryl ether, a polyoxyethylene glycol alkyl ether, a polyoxyethylene fatty acid ester, a polyoxyethylene sorbitan fatty acid ester, a polyoxyethylene glycerin 10 fatty acid ester, a polyoxyethylene hydrogenated castor oil, a polyoxyethylene castor oil, a polyoxypropylene fatty acid ester and an alkyl polyglycoside, and cationic surfactants such as an alkoxylated fatty amine. If desired, two or more of them may suitably be used in is combination. In the present invention, the herbicidal suspension preferably contains as another surfactant at least one surfactant selected from the group consisting of the above anionic surfactants, nonionic surfactants and 20 cationic surfactants. Among them, the anionic surfactant is preferably an alkylaryl sulfonate, the nonionic surfactant is preferably a polyoxyethylene castor oil, and the cationic surfactant is preferably an alkoxylated fatty amine. The herbicidal suspension particularly 25 preferably contains a combination thereof. The full effect of the essential surfactant will be achieved when the cationic surfactant such as an WO 2006/098156 PCT/JP2006/303918 9 alkoxylated fatty amine as the another surfactant is incorporated in the herbicidal suspension of the present invention. More particularly, the alkoxylated fatty amine may, for example, be ethoxylated tallow amine, 5 ethoxylated soy amine or ethoxylated coco amine. The average addition molar amount of the alkylene oxide is from 3 to 100, preferably from 5 to 50. Such an embodiment is one of the preferred embodiments of the present invention. 10 The solvent may, for example, be water, solvent naphtha, paraffin, dioxane, acetone, isophorone, methyl isobutyl ketone, chlorobenzene, cyclohexane, dimethyl sulfoxide, dimethylformamide, N-methyl-2-pyrrolidone, an alcohol, acetic acid, butyric acid, isopropyl acetate, is butyl acetate, benzene, an alkylbenzene or an alkylnaphthalene. If desired, two or more of them may suitably be used in combination. The anti-settling agent may, for example, be silica, bentonite-alkylamino complex, bentonite, white carbon or 20 aluminum magnesium silicic acid. If desired, two or more of them may be suitably used in combination. The thickener may, for example, be a heteropolysaccharide such as xanthan gum or guar gum, a water-soluble polymer such as polyvinyl alcohol, a sodium 25 salt of carboxymethyl cellulose or sodium alginate, bentonite or white carbon. If desired, two or more of them may suitably be used in combination.

WO 2006/098156 PCT/JP2006/303918 10 The antifoaming agent may, for example, be polydimethylsiloxane or acetylene alcohol. If desired, two or more of them may suitably be used in combination. The antifreezing agent may, for example, be ethylene s glycol, propylene glycol, glycerin or urea. If desired, two or more of them may suitably be used in combination. The gelling agent may, for example, be silica, organic attapulgite, clay, hydrogenated castor oil, a higher fatty acid ester, a higher alcohol, a salt of 10 dialkyl sulfosuccinic acid ester, a benzoate, an alkyl sulfate, a poly acrylic polymer, or a mixture of a poly acrylic acid copolymer and water, or 12-hydroxystearic acid. If desired, two or more of them may suitably be used in combination. is The stabilizer may, for example, be urea. The preservative may, for example, be formalin, p chloro m-xylenol or 1,2-benzisothiazolin-3-one. If desired, two or more of them may suitably be used in combination. 20 In preparation of the herbicidal suspension of the present invention, the essential surfactant and optional another surfactant may be preliminarily combined, and then the other various components are mixed therewith. Specifically, a surfactant mixture comprising the 25 essential surfactant and the optional another surfactant such as an anionic surfactant or a nonionic surfactant may be preliminarily prepared and used. In such a case, WO 2006/098156 PCT/JP2006/303918 11 the surfactant mixture is prepared so that the amount of the essential surfactant is usually at least 40 parts by weight, preferably from 40 to 90 parts by weight. Such an embodiment is one of the preferred embodiments of the 5 present invention. In the present invention, if desired, another herbicidal compound other than the sulfonylurea compound or its salt may be used in combination, whereby more excellent effects and functionality may be achieved in 10 some cases. For example, the range of plants to be killed may be broadened, the stage at which the herbicidal suspension is applied may be broadened, or the herbicidal activity may be improved in some cases. The sulfonylurea compound or its salt and the another is herbicidal compound may be separately prepared and mixed at the time of application, or they may be prepared into one composition. The present invention includes the above combined herbicidal composition and a method of controlling undesired plants or inhibiting their growth 20 by means of such a composition. As the another herbicidal compound which can be used in combination with the sulfonylurea compound or its salt, the compound groups of the following (1) to (11) (common names, code names) may, for example, be 25 mentioned. Even when not specifically mentioned, in a case where such compounds have salts, alkyl esters or various structural isomers such as optical isomers, they WO 2006/098156 PCT/JP2006/303918 12 are, of course, all included. (1) Those which are believed to exhibit herbicidal effects by disturbing hormone activities of plants, such as a phenoxy type such as 2,4-D, 2,4-DB, 2,4-DP, MCPA, 5 MCPB, MCPP or naproanilide, an aromatic carboxylic acid type such as 2,3,6-TBA, dicamba, dichlobenil, picloram, triclopyr, clopyralid or aminopyralid, and others such as naptalam, benazolin, quinclorac, quinmerac, diflufenzopyr and thiazopyr. 10 (2) Those which are believed to exhibit herbicidal effects by inhibiting photosynthesis of plants, such as a urea type such as chlorotoluron, diuron, fluometuron, linuron, isoproturon, metobenzuron or tebuthiuron, a triazine type such as simazine, atrazine, atratone, 15 simetryn, prometryn, dimethametryn, hexazinone, metribuzin, terbuthylazine, cyanazine, ametryn, cybutryne, triaziflam or propazine, a uracil type such as bromacil, lenacil or terbacil, an anilide type such as propanil or cypromid, a carbamate type such as swep, 20 desmedipham or phenmedipham, a hydroxybenzonitrile type such as bromoxynil, bromoxynil-octanoate or ioxynil, and others such as pyridate, bentazone, amicarbazone and methazole. (3) Quaternary ammonium salt type such as paraquat 25 or diquat, which is believed to be converted to free radicals by itself to form active oxygen in the plant body.

WO 2006/098156 PCT/JP2006/303918 13 (4) Those which are believed to exhibit herbicidal effects by inhibiting chlorophyll biosynthesis of plants and abnormally accumulating a photosensitizing peroxide substance in the plant body, such as a diphenylether type 5 such as nitrofen, chlomethoxyfen, bifenox, acifluorfen sodium, fomesafen, oxyfluorfen, lactofen or ethoxyfen ethyl, a cyclic imide type such as chlorphthalim, flumioxazin, flumiclorac-pentyl or fluthiacet-methyl, and others such as oxadiargyl, oxadiazon, sulfentrazone, 10 carfentrazone-ethyl, thidiazimin, pentoxazone, azafenidin, isopropazole, pyraflufen-ethyl, benzfendizone, butafenacil, metobenzuron, cinidon-ethyl, flupoxam, fluazolate, profluazol, pyrachlonil and flufenpyr-ethyl. is (5) Those which are believed to exhibit herbicidal effects characterized by whitening activities by inhibiting chromogenesis of plants such as carotenoids, such as a pyridazinone type such as norflurazon, chloridazon or metflurazon, a pyrazole type such as 20 pyrazolate, pyrazoxyfen, benzofenap or BAS-670H, and others such as amitrol, fluridone, flurtamone, diflufenican, methoxyphenone, clomazone, sulcotrione, mesotrione, AVH-301, isoxaflutole, difenzoquat, isoxachlortole, benzobicyclon, picolinafen and 25 beflubutamid. (6) Those which exhibit strong herbicidal effects specifically to gramineous plants, such as an WO 2006/098156 PCT/JP2006/303918 14 aryloxyphenoxypropionic acid type such as diclofop methyl, flamprop-M-methyl, pyriphenop-sodium, fluazifop butyl, haloxyfop-methyl, quizalofop-ethyl, cyhalofop butyl, fenoxaprop-ethyl or metamifop-propyl, and a s cyclohexanedione type such as alloxydim-sodium, clethodim, sethoxydim, tralkoxydim, butroxydim, tepraloxydim, caloxydim, clefoxydim or profoxydim. (7) Those which are believed to exhibit herbicidal effects by inhibiting an amino acid biosynthesis of io plants, such as a triazolopyrimidinesulfonamide type such as flumetsulam, metosulam, diclosulam, cloransulam methyl, florasulam, metosulfam or penoxsulam, an imidazolinone type such as imazapyr, imazethapyr, imazaquin, imazamox, imazameth, imazamethabenz or i5 imazapic, a pyrimidinylsalicylic acid type such as pyrithiobac-sodium, bispyribac-sodium, pyriminobac methyl, pyribenzoxim or pyriftalid, a sulfonylaminocarbonyltriazolinone type such as flucarbazone or procarbazone-sodium, and others such as 20 glyphosate-ammonium, glyphosate-isopropylamine, glufosinate-ammonium and bialaphos. (8) Those which are believed to exhibit herbicidal effects by inhibiting cell mitoses of plants, such as a dinitroaniline type such as. trifluralin, oryzalin, 25 nitralin, pendimethalin, ethalfluralin, benfluralin or prodiamine, an amide type such as bensulide, napronamide or pronamide an organic phosphorus type such as WO 2006/098156 PCT/JP2006/303918 15 amiprofos-methyl, butamifos, anilofos or piperophos, a phenylcarbamate type such as propham, chlorpropham or barban, a cumylamine type such as daimuron, cumyluron or bromobutide, and others such as asulam, dithiopyr and 5 thiazopyr. (9) Those which are believed to exhibit herbicidal effects by inhibiting protein biosynthesis or lipid biosynthesis of plants, such as a chloroacetamide type such as alachlor, metazachlor, butachlor, pretilachlor, 10 metolachlor, S-metolachlor, thenylchlor, pethoxamid, acetochlor, propachlor or propisochlor, a carbamate type such as molinate, dimepiperate or pyributicarb, and others such as etobenzanid, mefenacet, flufenacet, tridiphane, cafenstrole, fentrazamide, oxaziclomefone, 15 indanofan, dimethenamid and benfuresate. (10) A thiocarbimate type such as EPTC, butylate, vernolate, pebulate, cycloate, prosulfocarb, esprocarb, thiobencarb, diallate or triallate, and others such as MSMA, DSMA, endothall, ethofumesate, sodium chlorate, 20 pelargonic acid, fosamine, pinoxaden and HOK-201. (11) Those which are believed to exhibit herbicidal effects by being parasitic on plants, such as Xanthomonas campestris, Epicoccosurus nematosurus, Exserohilum monoseras and Drechsrela monoceras. 25 In the present invention, blend proportions of various components cannot generally be defined, since they may suitably be changed depending upon the types of WO 2006/098156 PCT/JP2006/303918 16 the blend components, the formulations or the application sites. A formulation may, for example, be prepared by incorporating the sulfonylurea compound or its salt in a proportion of from 0.5 to 20 parts by weight, preferably 5 from 2 to 10 parts by weight, furthermore preferably from 5 to 10 parts by weight; the essential surfactant in a proportion of from 0.5 to 35 parts by weight, preferably from 1 to 25 parts by weight; another surfactant, if incorporated as the case requires, in a proportion of io from 0.5 to 55 parts by weight, preferably from 1 to 40 parts by weight; a solvent, if incorporated as the case requires, in a proportion of from 0.1 to 30 parts by weight, preferably from 0.5 to 20 parts by weight, an anti-settling agent, if incorporated as the case 15 requires, in a proportion of from 0.1 to 10 parts by weight, preferably from 0.5 to 5 parts by weight; a gelling agent, if incorporated as the case requires, in a proportion of from 0.1 to 50 parts by weight, preferably from 5 to 40 parts by weight; a stabilizer, if 20 incorporated as the case requires, in a proportion of from 0.1 to 20 parts by weight, preferably from 1 to 10 parts by weight; another herbicidal compound, if incorporated as the case requires, in a proportion of from 0.5 to 75 parts by weight, preferably from 0.5 to 50 25 parts by weight, and the water-immiscible diluent as the rest, so that the total would be 100 parts by weight. The herbicidal suspension of the present invention WO 2006/098156 PCT/JP2006/303918 17 thus prepared has favorable and selective herbicidal effect since when it is diluted with water at the time of its use, droplets of oil will be well dispersed, whereby excellent emulsion characteristics will be achieved. 5 The herbicidal suspension of the present invention is capable of controlling a wide range of weeds including, for example, sedges (or Cyperaceae) such as rice flatsedge (Cyperus iria L.) or purple nutsedge (Cyperus rotundus L.), grasses (or gramineae) such as 10 barnyardgrass (Echinochloa crus-galli L.), crabgrass (Digitaria sanguinalis L.), green foxtail (Setaria viridis L.), goosegrass (Eleusine indica L.), wild oat (Avena fatua L.), johnsongrass (Sorghum halepense L.) or quackgrass (Agropyron repens L.), and broadleaves such as 15 velvetleaf (Abutilon theophrasti MEDIC.), tall morning glory (Ipomoea purpurea L.) , common lambsquarters (Chenopodium album L.), prickly sida (Sida spinosa L.), common purslane (Portulaca oleracea L.) , redroot pigweed (Amaranthus retroflexus L.), sicklepod (Cassia 20 obtusifolia L.), black nightshade (Solanum nigrum L.), pale smartweed (Polygonum lapathifolium L.), common chickweed (Stellaria media L.), common cocklebur (Xanthium strumarium L.), flexuous bittercress (Cardamine flexuosa WITH.), henbit (Lamium amplexicaule L.) or 25 threeseeded copperleaf (Acalypha austalis L.), or inhibiting their growth, by applying it to such undesired plants or to a place where they grow, for example, by WO 2006/098156 PCT/JP2006/303918 18 foliar application. Accordingly, its application range extends not only to crop plant fields but also agricultural fields such as orchards, mulberry fields or paddy fields and non-agricultural fields such as forest 5 land, farm roads, play grounds, factory sites or grass plots. The sulfonylurea compound or its salt may be applied in an amount of 1 to 500 g/ha, preferably from 2 to 250 g/ha. Particularly, a herbicidal suspension comprising nicosulfuron or its salt is capable of 10 controlling noxious weeds or inhibiting their growth without presenting phytotoxicity to corn, and it is very useful as a herbicidal composition for corn fields. Nicosulfuron may be applied in an amount of from 2 to 400 g/ha, preferably from 5 to 200 g/ha. 15 EXAMPLES Now, the present invention will be described in further detail with reference to Examples. However, it should be understood that the present invention is by no means restricted to such specific Examples. 20 EXAMPLE 1 (1) Nicosulfuron (purity: 94.5%): 7.23 parts by weight (2) Mixture (surfactant A) containing polyoxyethylene sorbitol tetraoleate as the main 25 component and containing polyoxyethylene castor oil and calcium salt of dodecylbenzenesulfonic acid: 10.35 parts by weight WO 2006/098156 PCT/JP2006/303918 19 (3) Ethoxylated tallow amine (surfactant B): 15.53 parts by weight (4) Bentonite-alkylamino complex: 1.03 parts by weight 5 (5) Urea: 3.11 parts by weight (6) Mixture of methylated seed oil and corn oil: 62.75 parts by weight The above components were mixed, and the mixture was wet-milled by a wet-mill for 15 minutes to prepare an 10 oil-based suspension concentrate. EXAMPLE 2 (1) Nicosulfuron (purity: 94.5%) : 7.23 parts by weight (2) Surfactant A: 10.35 parts by weight 15 (3) Surfactant B: 15.53 parts by weight (4) Bentonite-alkylamino complex: 1.03 parts by weight (5) Urea: 3.11 parts by weight (6) Mixture of methylated seed oil and corn oil: 20 60.68 parts by weight (7) Alcohol: 2.07 parts by weight The above components were mixed, and the mixture was wet-milled by a wet-mill for 15 minutes to prepare an oil-based suspension concentrate. 25 EXAMPLE 3 (1) Nicosulfuron (purity: 94.5%) : 7.23 parts by weight WO 2006/098156 PCT/JP2006/303918 20 (2) Surfactant A: 10.35 parts by weight (3) Surfactant B: 15.53 parts by weight (4) Bentonite-alkylamino complex: 1.03 parts by weight 5 (5) Urea: 3.11 parts by weight (6) Mixture of methylated seed oil and corn oil: 55.25 parts by-weight (7) Alcohol: 7.50 parts by weight The above components were mixed, and the mixture was 10 wet-milled by a wet-mill for 15 minutes to prepare an oil-based suspension concentrate. EXAMPLE 4 (1) Nicosulfuron (purity: 94.5%) : 7.23 parts by weight 15 (2) Mixture (surfactant D) containing polyoxyethylene sorbitan trioleate as the main component and containing polyoxyethylene castor oil and calcium salt of dodecylbenzenesulfonic acid: 10.35 parts by weight 20 (3) Surfactant B: 20.70 parts by weight (4) Hydrophobic fumed silica: 1.03 parts by weight (5) Urea: 1.03 parts by weight (6) Corn oil: 54.48 parts by weight (7) Alcohol: 5.18 parts by weight 25 The above components were mixed, and the mixture was wet-milled by a wet-mill for 15 minutes to prepare an oil-based suspension concentrate.

WO 2006/098156 PCT/JP2006/303918 21 EXAMPLE 5 (1) Flazasulfuron (purity: 95.1%): 7.14 parts by weight (2) Surfactant A: 10.35 parts by weight 5 (3) Surfactant B: 20.70 parts by weight (4) Hydrophobic fumed silica: 1.04 parts by weight (5) Urea: 3.11 parts by weight (6) Corn oil: 52.48 parts by weight (7) Alcohol: 5.18 parts by weight 10 The above components were mixed, and the mixture was wet-milled by a wet-mill for 15 minutes to prepare an oil-based suspension concentrate. EXAMPLE 6 (1) Azimsulfuron (purity: 99.0%): 7.14 parts by is weight (2) Surfactant A: 10.35 parts by weight (3) Surfactant B: 20.70 parts by weight (4) Hydrophobic fumed silica: 1.04 parts by weight (5) Urea: 3.11 parts by weight 20 (6) Corn oil: 52.48 parts by weight (7) Alcohol: 5.18 parts by weight The above components were mixed, and the mixture was wet-milled by a wet-mill for 15 minutes to prepare an oil-based suspension concentrate. 25 EXAMPLE 7 (1) Bensulfuron-methyl (purity: 99.3%): 7.14 parts by weight WO 2006/098156 PCT/JP2006/303918 22 (2) Surfactant A: 10.35 parts by weight (3) Surfactant B: 20.70 parts by weight (4) Hydrophobic fumed silica: 1.04 parts by weight (5) Urea: 3.11 parts by weight s (6) Corn oil: 52.48 parts by weight (7) Alcohol: 5.18 parts by weight The above components were mixed, and the mixture was wet-milled by a wet-mill for 15 minutes to prepare an oil-based suspension concentrate. 10 COMPARATIVE EXAMPLE 1 An oil-based suspension concentrate was prepared in the same manner as in Example 1 except that a mixture (surfactant C) of polyoxyethylene hydrogenated castor oil and dioctylsulfosuccinate was used instead of the 15 surfactant A. COMPARATIVE EXAMPLE 2 An oil-based suspension concentrate was prepared in the same manner as in Example 2 except that the surfactant C was used instead of the surfactant A. 20 COMPARATIVE EXAMPLE 3 An oil-based suspension concentrate was prepared in the same manner as in Example 3 except that the surfactant C was used instead of the surfactant A. COMPARATIVE EXAMPLE 4 25 An oil-based suspension concentrate was prepared in the same manner as in Example 4 except that the surfactant C was used instead of the surfactant D.

WO 2006/098156 PCT/JP2006/303918 23 COMPARATIVE EXAMPLE 5 An oil-based suspension concentrate was prepared in the same manner as in Example 5 except that the surfactant C was used instead of the surfactant A. 5 COMPARATIVE EXAMPLE 6 An oil-based suspension concentrate was prepared in the same manner as in Example 6 except that the surfactant C was used instead of the surfactant A. COMPARATIVE EXAMPLE 7 10 An oil-based suspension concentrate was prepared in the same manner as in Example 7 except that the surfactant C was used instead of the surfactant A. COMPARATIVE EXAMPLE 8 An oil-based suspension concentrate was prepared in 15 the same manner as in Example 1 except that a mixture (surfactant E) of polyoxyethylene nonylphenyl ether, dialkylsulfosuccinate, polyoxyethylene hydrogenated castor oil and polyglycerol esters of fatty acid was used instead of the surfactant A. 20 COMPARATIVE EXAMPLE 9 An oil-based suspension concentrate was prepared in the same manner as in Example 2 except that the surfactant E was used instead of the surfactant A. COMPARATIVE EXAMPLE 10 25 An oil-based suspension concentrate was prepared in the same manner as in Example 3 except that the surfactant E was used instead of the surfactant A.

WO 2006/098156 PCT/JP2006/303918 24 Now, Test Examples of the present invention will be described below. TEST EXAMPLE 1 Each of the oil-based suspension concentrates 5 obtained in Examples and Comparative Examples was diluted with ion-exchange water and charged into a circulation bath of a particle size measuring apparatus (MICROTRAC HRA, model 9320-x100, HONEYELL), followed by circulation for 5 minutes. The droplets size of emulsion diluted 10 1,500 to 2,000 times was measured. The results are shown in Table 1. TABLE 1 Droplets size of Oil-based suspension elsi of concentrate emulsion (wim) (average) Example 1 18.0 Present Eape21. invention Example 2 15.9 Example 3 13.3 Comparative Example 1 21.4 Comparison Comparative Example 2 22.0 Comparative Example 3 15.8 The conditions in this test correspond to a state is where the herbicidal suspension is diluted with water at the time of application. The oil-based suspension concentrates prepared in Comparative Examples 1 to 3 corresponding to formulations similar to formulations as disclosed in Examples of EP 20 0598515, the oil-based suspension concentrates were under a certain emulsified condition, whereas the oil-based suspension concentrates which were herbicidal suspensions WO 2006/098156 PCT/JP2006/303918 25 of the present invention prepared in Examples 1 to 3 were under a more finely emulsified condition, such being excellent. TEST EXAMPLE 2 5 Each of the oil-based suspension concentrates obtained in Examples and Comparative Examples was diluted with CIPAC Standard Water D 600 times, and the diluted concentrate was left at rest for 15 minutes. The diluted concentrate was put in a measurement cell, and 10 measurement was carried out by a colorimeter (CT-310, manufactured by MINOLTA CAMERA Co.) by means of L*a*b* color system (JIS Z 8729: 2004) to determine the color difference (AE) between Example and the corresponding Comparative Example from the following formula. The is results are shown in Table 2. nE= (AL 2 +Aa 2 +Ab 2 ) 1/2 TABLE 2 Oil-based Luminosity Chroma- Chroma- Color suspension (L*) ticity ticity difference concentrate (a*) (b*) (AE) Example 1 57.05 0.54 6.62 13.45 Comparative 70.42 0.42 5.15 Example 1 Example 2 58.48 0.14 4.49 7.25 Comparative 65.63 0.43 5.63 Example 2 Example 3 52.44 0.88 8.08 8.58 Comparative 60.92 1.28 9.32 Example 3 The luminosity (L*) is represented by a numerical 20 value of from 0 to 100, and the larger the value, the WO 2006/098156 PCT/JP2006/303918 26 brighter (the luminosity of the ion-exchanged water is about 100) . As shown in Table 2, the luminosities of the oil-based suspension concentrates which are herbicidal suspensions of the present invention in Examples 1 to 3 5 are smaller than those of the corresponding Comparative Examples 1 to 3. Accordingly, it is understood that the oil-based suspension concentrates of Examples 1 to 3 have deeper color (emulsified condition). Further, the color difference (AE) is evaluated 10 based on evaluation standards (NBS unit, National Bureau of Standard) as shown in the following Table 3 and as a result, there is a significant difference between the herbicidal suspensions of the present invention prepared in Examples 1 to 3 and the concentrates prepared in the 15 corresponding Comparative Examples 1 to 3. TABLE 3 Color difference (AE) Sensual difference 0 to 0.5 Trace 0.5 to 1.5 Slight 1.5 to 3.0 Noticeable 3.0 to 6.0 Appreciable 6.0 to 12.0 Much More than 12.0 Very much TEST EXAMPLE 3 Upland field soil was filled in a 1/1,000,000 ha 20 pot, seeds of crabgrass (Digitaria sanguinalis L.) were sown therein and grown in a green house. When crabgrass reached 3 leaf stage, a prescribed amount (17.5 g a.i./ha) -of each of the oil-based suspension concentrates WO 2006/098156 PCT/JP2006/303918 27 prepared in Examples and Comparative Examples, was diluted with water corresponding to 300 liters/ha, followed by foliar application. On the 21st day after the application of the s herbicide, the growth of crabgrass was visually observed (growth inhibition rate (%)=0:untreated plot to 100:complete kill), whereby the results as shown in Table 4 were obtained. TABLE 4 Oil-based suspeio Growth inhibition suspension rate (% concentrate Example 1 70 Present invention Example 2 70 Example 2 76 Comparative 58 Comparison Example 1 Comparative 3 Example 2 10 TEST EXAMPLE 4 Upland field soil was filled in a 1/1,000,000 ha pot, seeds of corn (Zea mays) were sown therein and grown in a green house in winter. When corn reached 3 leaf 15 stage, a prescribed amount (90 g a.i./ha) of each of the oil-based suspension concentrates prepared in Examples and Comparative Examples was diluted with water corresponding to 300 liters/ha, followed by foliar application. 20 On the 14th day after the application of the herbicide, the growth of corn was visually observed and as a result, the oil-based suspension concentrates which WO 2006/098156 PCT/JP2006/303918 28 were herbicidal suspensions of the present invention prepared in Examples 1 to 3 exhibited a low degree of corn growth inhibition and showed more excellent safety for the crops as compared with the corresponding 5 Comparative Examples 1 to 3. TEST EXAMPLE 5 With respect to the oil-based suspension concentrates prepared in the above Example and Comparative Example, the droplets size of emulsion was 10 measured in accordance with the above Test Example 1. The results are shown in Table 5. TABLE 5 oil-based suspension Droplets size of concentrate emulsion (pm) (average) Present inentn Example 4 17.4 invention Comparison Comparative Example 4 23.1 The oil-based suspensi-on concentrate prepared in 15 Comparative Example 4 corresponding to a formulation similar to the formulation as disclosed in Example of EP 0598515 was under a certain emulsified condition, whereas the oil-based suspension concentrate which was a herbicidal suspension of the present invention prepared 20 in Example 4 was under a more finely emulsified condition, such being excellent. TEST EXAMPLE 6 With respect to the oil-based suspension WO 2006/098156 PCT/JP2006/303918 29 concentrates prepared in the above Examples and Comparative Examples, the droplets size of emulsion was measured in accordance with the above Test Example 1. The results are shown in Table 6. 5 TABLE 6 oil-based suspension Droplets size of concentrate emulsion (pm) (average) Present Example 5 17.2 invention Example 6 14.7 Example 7 13.6 Comparative Example 5 22.6 Comparison Comparative Example 6 22.6 Comparative Example 7 29.8 The oil-based suspension concentrates prepared in Comparative Examples 5 to 7 were under a certain emulsified condition, whereas the oil-based suspension 10 concentrates which were herbicidal suspensions of the present invention prepared in Examples 5 to 7 were under a more finely emulsified condition, such being excellent. TEST EXAMPLE 7 With respect to the oil-based suspension is concentrates prepared in the above Examples and Comparative Examples, the droplets size of emulsion was measured in accordance with the above Test Example 1. The results are shown in Table 7.

WO 2006/098156 PCT/JP2006/303918 30 TABLE 7 oil-based suspension Droplets size of concentrate emulsion (pm) (average) Present Example 1 17.3 invention Example 2 15.9 Example 3 13.5 Comparative Example 8 22.2 Comparison Comparative Example 9 19.7 Comparative Example 10 17.4 The oil-based suspension concentrates prepared in Comparative Examples 8 to 10 corresponding to 5 preparations as disclosed in Examples of EP 0598515 were under a certain emulsified condition, whereas the oil based suspension concentrates which were herbicidal suspensions of the present invention prepared in Examples 1 to 3 were under a more finely emulsified condition, 10 such being excellent. TEST EXAMPLE 8 With respect to the oil-based suspension concentrates prepared in the above Example and Comparative Example, the luminosity and the is chromaticities were measured to determine the color difference in accordance with the above Test Example 2. The results are shown in Table 8. TABLE 8 Oil-based Luminosity Chroma- Chroma- Color suspension L ticity ticity difference concentrate (a*) (b*) (LE) Example 4 49.38 -0.15 6.39 Comparative 53.83 0.07 7.09 4.51 Example_4 53.83 0.07 7.09 WO 2006/098156 PCT/JP2006/303918 31 Since the luminosity (L*) of the oil-based suspension concentrate which is a herbicidal suspension of the present invention prepared in Example 4 is small as compared with the corresponding Comparative Example 4, 5 it is understood that the oil-based suspension concentrate in Example 4 has a deeper color (emulsified condition). Further, it is also understood that there is a significant difference between them with regard to the 10 color difference ([E). TEST EXAMPLE 9 With respect to the oil-based suspension concentrates prepared in the above Examples and Comparative Examples, the luminosity and the 15 chromaticities were measured to determine the color difference in accordance with the above Test Example 2. The results are shown in Table 9. TABLE 9 Oil-based Luminosity Chroma- Chroma- Color suspension L L*) ticity ticity difference concentrate (a*) (b*) ([E) Example 5 34.80 -0.25 3.80 Comparative 52.19 -0.53 3.68 17.4 Example 5 Example 6 33.05 -0.26 3.80 Comparative 17.5 Exapl 6 50.52 -0.54 3.11 Example 6 Example 7 44.29 -0.43 5.03 Comparative 10.5 Example 7 -0.58 4.41 20 Since the luminosities (L*) of the oil-based WO 2006/098156 PCT/JP2006/303918 32 suspension concentrates which are herbicidal suspensions of the present invention prepared in Example 5 to 7 are small as compared with the corresponding Comparative Examples 5 to 7, it is understood that the oil-based 5 suspension concentrates in Example 5 to 7 have a deeper color (emulsified condition). Further, it is also understood that there is a significant difference between Example and the corresponding Comparative Example, with regard to the 10 color difference (AE). TEST EXAMPLE 10 With respect to the oil-based suspension concentrates prepared in the above Examples and Comparative Examples, the luminosity and the 15 chromaticities were measured to determine the color difference in accordance with the above Test Example 2. The results are shown in Table 10. TABLE 10 Oil-based Chroma- Chroma- Color suspension L*) ticity ticity difference concentrate (a*) (b*) (AE) Example 1 48.57 -0.35 4.81 Comparative 58.41 -0.34 6.34 9.96 Example 8 Example 2 44.75 0.15 6.53 Comparative 55.79 -0.07 6.34 11.04 Example 9 Example 3 48.13 -0.05 6.17 Comparative 58.28 0.14 7.68 10.6 Example 10 58.28 0.14 7.68 20 Since the luminosities (L*) of the oil-based WO 2006/098156 PCT/JP2006/303918 33 suspension concentrates which are herbicidal suspensions of the present invention prepared in Example 1 to 3 are small as compared with the corresponding Comparative Examples 8 to 10, it is understood that the oil-based 5 suspension concentrates in Example 1 to 3 have a deeper color (emulsified condition). Further, it is also understood that there is a significant difference between Example and the corresponding Comparative Example, with regard to the 10 color difference (LE). Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.

Claims (6)

1. A herbicidal suspension comprising (1) from 0.5 to 20 parts by weight of a sulfonylurea compound or its salt as a herbicidal component, selected from the group consisting of flazasulfuron and nicosulfuron, (2) from 0.5 to 35 parts by weight of an alkoxylated sorbitol fatty acid ester as a surfactant, (3) from 0.5 to 55 parts by weight of another surfactant, wherein the other surfactant is i) at least one nonionic surfactant selected from the group consisting of a polyoxyethylene castor oil and a polyoxyethylene hydrogenated castor oil, and ii) an alkylaryl sulfonate as an anionic surfactant, (4) a water-immiscible diluent, wherein the water-immiscible diluent is at least one member selected from the group consisting of a vegetable oil, a fatty acid derived from a vegetable oil and an alkyl ester of the fatty acid as the main component of the rest.

2, The herbicidal suspension according to Claim 1, wherein the water-immiscible diluent is a methylated seed oil, a corn oil or a mixture thereof.

3. The herbicidal suspension according to Claim 1 or 2, wherein the sulfonylurea compound or its salt is flazasulfuron.

4. The herbicidal suspension according to Claim 1 or 2, wherein the sulfonylurea compound or its salt is nicosulfuron.

5. A method for controlling undesired plants or inhibiting their growth, which comprises applying a herbicidally I-'rce'-iilowoln''NaPOnhl'-ULL'ktC N[INI I I doc-4.'O I II - 35 effective amount of the herbicidal suspension as defined in any one of Claims 1 to 4 to the undesired plants or to a place where they grow.

6. A herbicidal suspension according to claim 1, substantially as hereinbefore defined with reference to any one of the Examples.