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    • 专利摘要:
    Suggested are solid agricultural compositions, comprising: (a1) at least one alkoxylated alcohol according to general formula (I) R
    公开号:AU2011378019A1
    申请号:U2011378019
    申请日:2011-09-27
    公开日:2014-04-17
    发明作者:Jianhua Mao；Anbao ZUO
    申请人:Cognis IP Management GmbH；
    IPC主号:A01N25-12
    专利说明:
    WO 2013/044449 PCT/CN2011/080233 5 Solid agricultural compositions Field of invention The present invention belongs to the area of agriculture and refers to new solid biocide compositions comprising special types of surfactants with improved performance. 10 State of the art Biocides, and in particular pesticides such as fungicides, insecticides and herbicides, are im portant auxiliary agents for agriculture in order to protect and to increase crops. Depending on the various and often very specific needs, a magnitude of actives exist, which show very 15 different chemical structures and behaviors. Pesticide products may be formulated as liquids, powders, or granules. Solvents, emulsifiers, dispersing agents and wetting agents are normally incorporated into such compositions in order to ensure that a uniform pesticide formulation has been prepared. Successful em ployment of any pesticide depends upon its proper formulation into a preparation that can 20 be easily diluted with water into ready-to-use mixtures for application onto a targeted pest and/or agricultural substrate. In addition, the market requires additives - so-called "adju vants" - providing additional benefit to the formulation by increasing the performance of the biocides in a synergistic way. Supply industry offers a wide spectrum of products, especially formulations, intending to 25 fulfill all requirements of the end users. Of particular interest are surfactants working at the same time as adjuvants and solvents, wetting agents or emulsifiers. For example, US 6,432,884 (Cognis) also refers to adjuvant compositions comprising fatty acid alkyl esters, like for example oleic acid ethyl ester, and non-ionic surfactants, like for example sorbitan esters. International patent application WO 2004/080177 Al (Cognis) discloses adjuvant 30 compositions comprising fatty acid alkyl esters and a mixture of hydrophilic and hydrophobic emulsifiers. European patent EP 0765602 B1 (Kao) recommends ethoxylated esters of glyc erol or polyglycerol as adjuvants for herbicides. WO 2010 145772 Al (Cognis) recommends ethoxylates of unsaturated fatty alcohols as additives for aqueous solutions of biocides, in particular for tank mixes comprising glyphosate. 35 While biocide compositions typically are offered in liquid forms, the solid, in particular gra nular form has benefits over the liquid form in easy transportation as it contains none or very little solvent or water. The granular form also has advantages of low dust in production, transportation and in application. Granular compositions of biocides, namely of glyphosate, are well known from the state of the art. 1 WO 2013/044449 PCT/CN2011/080233 For example, WO 2009 09711 Al (Excel) discloses a granular formulation comprising 70-72 % b.w. of ammonium glyphosate, 11-22 % b.w. ammonium sulfate, 5-12.5 % b.w. alkyl poly glucosides and 1-3 % b.w. acrylate based copolymers. According to WO 2006 133788 Al (Sipcam) solid glyphosate compositions are obtainable, by 5 adding solid Broenstedt bases like e.g. ammonium sulfate and liquid surfactants to the her bicide in order to obtain a wet cake and subsequently drying and granulation of the mass. Suitable surfactants are chosen from the group consisting of alkanol amides, betaine deriva tives, ethoxylated-propoxylated block copolymers, glycerol esters, glycolic esters, imidazoli nes and its derivatives, lanolin and lecithin derivatives, tertiary and quaternary polyoxyal 10 kylenalkyl amines , polyoxyalkylen alkyl ethers, polyoxyalkylen alkyl aryl ethers, polyoxyal kylen alkyl esters, alkoxylated and non alkoxylated sorbitan esters alkyl glycosides, alkyl po lyglycosides, alkyl sulfates, alkyl phosphates, sulfonated olefins, alkyl aryl sulfonates, poly oxyalkylen alkyl ether sulfates, polyoxyalkylen alkyl ether phosphates, sulfosuccinate deriva tives, and taurates. 15 Very similar is the content of US 2004 102323 Al (Vigil et al.) claiming a solid herbicidal for mulation of N-(phosphonomethyl)glycine, in powder, rule or flake form, soluble or dispersi ble in water, comprising glyphosate (N-(phosphonomethyl)glycine) in the form of hydrosolu ble salt and 5% to 30% in weight of one or more hydrosoluble tension-active agents, which are compatible with glyphosate and solids at ambient temperature, said tension-active 20 agents being selected from the group consisting of alkanol amides, alkyl aryl sul fonates, sulfonated amines and amides, ethoxylated alkyl phenols, carboxylated alcohols, ethoxylated fatty acids, ethoxylated alcohols, sulfated alcohols, sugar and glucose deriva tives, sorbitol derivatives, phosphate esters, imidazoline and its derivatives, lecithin and its derivatives, lignin and its derivatives, ethylene and propylene oxide block poly 25 mers, ethoxylated alcohol sulfates, fatty acid sulfates, naphthalene and alkyl naphthalene sulfonates, dodecyl and tridecyl benzene sulfonates, taurates and their derivatives. Nevertheless, solid formulations have additional challenges compared to liquid forms, which are not satisfied by the products found in the market and known from the state of the art. In particular, granular formulations are required exhibiting a better physical stability, water 30 dispersibility and lower foaming. Therefore, the problem underlying the present invention has been to provide new granular formulations of biocides, in particular granular formulations of glyphosate comprising tai lor-made surfactant additives, in order to overcome the disadvantages explained above. 35 Description of the invention Object of the present invention are solid agricultural compositions, comprising: (at) at least one alkoxylated alcohol according to general formula (I) R 1O(AO)nH (1) In which R 1 stands for an unsaturated, linear hydrocarbon residue having 12 to 22 car 40 bon atoms and 1, 2 or 3 double bonds, AO stands for an ethylene oxide, propylene ox ide and/or butylene oxide unit, and n represents an integer of from 1 to 60; WO 2013/044449 PCT/CN2011/080233 (a2) at least one alkoxylated alcohol according to general formula (II)
    R
    2 0(AO)mH (II) In which R 2 stands for a saturated or an unsaturated, branched hydrocarbon residue having 8 to 36 carbon atoms, AO stands for an ethylene oxide, propylene oxide and/or 5 butylene oxide unit, and m represents an integer of from 1 to 60; (b) at least one biocide, and optionally (c) at least one inert Broenstedt base and/or (d) at least one solvent, emulsifier or polymer, 10 on condition that said compositions represent granules with a water content of less than about 5 and preferably less than about 2.5 % b.w. Surprisingly, it has been observed that the mixture of adducts of alkylene oxide, in particular about 2 to about 60 mol ethylene oxide and/or propylene oxide to (at) unsaturated, linear alcohols and (a2) saturated, but branched alcohols provides a much better stability and dis 15 persibility to the biocide granules compared of standard surfactants, like for example tallow amine ethoxylates. At the same time, foaming is also significantly reduced. Alkoxylated alcohols Alkoxylated unsaturated and/or branched alcohols forming compounds (al) and (a2) repre 20 sent known products which are obtainable according to standard procedures of organic chemistry. Typically, the alcohols are subjected to alkoxylation in the presence of an alkaline catalyst at temperatures of about 100 to 180 *C and pressures of up to 5 bar. It is possible to conduct alkoxylation using an individual alkylene oxide, that means either ethylene oxide, propylene oxide or butylene oxide or to use mixtures (random distribution). Also possible is 25 to add them block-wise. Suitable alcohols for obtaining compounds (a1) encompass unsaturated fatty alcohols having 12 to 22, preferably 18 carbon atoms, like for example palmoleyl alcohol, oleyl alcohol, elaidyl alcohol, linolyl alcohol, linolenyl alcohol, ricinoleyl alcohol, erucyl alcohol and their technical mixtures. Typically, oleyl alcohol is chosen showing a technical grade of purity de 30 fined by its iodine value. Suitable oleyl alcohols typically represent mixtures of unsaturated
    C
    18 and C 2 2 fatty alcohols and saturated C 1 2
    -C
    2 2 fatty alcohols, showing iodine numbers be tween about 50 and about 125, preferably between about 90 and about 100, and are ob tainable from vegetable oils or animal fats. Suitable alcohols for obtaining compounds (a2) typically include guerbet alcohols, obtained 35 by guerbet reaction of linear alcohols, preferably linear C 5 to C 18 alcohols. These alcohols are branched in the beta-position to the hydroxyl group. A very prominent example is 2-ethylhexanol, but also 2-hexyldecanol and 2-octyldodecanol are well-known sources. Nev ertheless, also other branched alcohols can serve as starting material, as for example isos tearyl alcohol or the monomer fraction obtained from the dimerization of unsaturated fatty 40 alcohols.
    WO 2013/044449 PCT/CN2011/080233 The preferred compound (al), however, represents an adduct of on average about 2 to about 15 mol ethylene oxide to oleyl alcohol, the preferred compound (a2) represents an adduct of on average about 2 to about 15 mol ethylene oxide and/or propylene oxide to guerbet alcohol having about 10 to about 24 carbon atoms. These two groups are individu 5 ally preferred, but also in combination. The compounds (al) and (a2) can be added to the biocide composition within wide ranges, for example in weight ratios of unsaturated alcohol alkoxylates and said branched alcohol alkoxylates a1:a2 = about 20:80 to about 80:20. The best results are obtained in ratios by weight of a1:a2 = about 50:50 to about 30:70. The alcohols may be prepared individually and 10 blended later, but it is also possible to subject a mixture of an appropriate unsaturated al cohol and an appropriate branched alcohol to joint alkoxylation. Biocides A biocide (component b) in the context of the present invention is a plant protection agent, 15 more particular a chemical substance capable of killing different forms of living organisms used in fields such as medicine, agriculture, forestry, and mosquito control. Also counted under the group of biocides are so-called plant growth regulators. Usually, biocides are di vided into two sub-groups: o pesticides, which includes fungicides, herbicides, insecticides, algicides, moluscicides, 20 miticides and rodenticides, (here, The Pesticide Manual, 14 edition, BCPC 2006 is included as a reference, it provides information about the individual mode of actions of active ingredients) and o antimicrobials, which includes germicides, antibiotics, antibacterials, antivirals, anti fungals, antiprotozoals and antiparasites. 25 Biocides can also be added to other materials (typically liquids) to protect the material from biological infestation and growth. For example, certain types of quaternary ammonium compounds (quats) can be added to pool water or industrial water systems to act as an algi cide, protecting the water from infestation and growth of algae. 30 a) Pesticides The U.S Environmental Protection Agency (EPA) defines a pesticide as "any substance or mixture of substances intended for preventing, destroying, repelling, or mitigating any pest". A pesticide may be a chemical substance or biological agent (such as a virus or bacteria) used against pests including insects, plant pathogens, weeds, molluscs, birds, mammals, fish, 35 nematodes (roundworms) and microbes that compete with humans for food, destroy prop erty, spread disease or are a nuisance. In the following examples, pesticides suitable for the agrochemical compositions according to the present invention are given: WO 2013/044449 PCT/CN2011/080233 b) Fungicides A fungicide is one of three main methods of pest control - the chemical control of fungi in this case. Fungicides are chemical compounds used to prevent the spread of fungi in gardens and crops. Fungicides are also used to fight fungal infections. Fungicides can either be con 5 tact or systemic. A contact fungicide kills fungi when sprayed on its surface. A systemic fun gicide has to be absorbed by the fungus before the fungus dies. Examples for suitable fungi cides, according to the present invention, encompass the following chemical classes and corresponding examples: o Aminopyrimidines such as bupirimate, 10 o Anilinopyrimidines such as cyprodinil, mepanipyrim, pyrimethanil, o Heteroaromatics such as hymexazol, o Heteroaromatic hydrocarbons such as etridiazole, o Chlorophenyls/Nitroanilines such as chloroneb, dicloran, quintozene, tecnazene, tolclofos-methyl, 15 o Benzamide fungicides such as zoxamide, o Benzenesulfonamides such as flusulfamide, o Benzimidazoles such as acibenzolar, benomyl, benzothiazole, carbendazim, fuberida zole, metrafenone, probenazole, thiabendazole, triazoxide, and benzimidazole pre cursor fungicides, 20 a Carbamates such as propamocarb, diethofencarb, o Carboxamides such as boscalid, diclocymet, ethaboxam, flutolanil, penthiopyrad, thifluzamide o Chloronitriles such chlorothalonil, o Cinnamic acid amides such as dimethomorph, flumorph, 25 o Cyanoacetamide oximes such as cymoxanil, o Cyclopropancarboxamides such as carpropamid, o Dicarboximides such as iprodione, octhilinone, procymidone, vinclozolin o Dimethyldithiocarbamates such ferbam, metam, thiram, ziram, o Dinitroanilines such as fluazinam, 30 a Dithiocarbamates such as mancopper, mancozeb, maneb, metiram, nabam, propineb, zineb, o Dithiolanes such as isoprothiolane, o Glucopyranosyl antibiotics such as streptomycin, validamycin, o Guanidines such as dodine, guazatine, iminoctadine, 35 o Hexopyranosyl antibiotics such as kasugamycin, o Hydroxyanilides such as fenhexamid, o Imidazoles such as imazalil, oxpoconazole, pefurazoate, prochloraz, triflumizole, WO 2013/044449 PCT/CN2011/080233 o Imidazolinones such as fenamidone, o Inorganics such as Bordeaux mixture, copper hydroxide, copper naphthenate, copper oleate, copper oxychloride, copper(II) sulfate, copper sulfate, copper(II) acetate, copper(II) carbonate, cuprous oxide, sulfur, 5 o lsobenzofuranones such as phthalide, o Mandelamides such as mandipropamide, o Morpholines such as dodemorph, fenpropimorph, tridemorph, fenpropidin, piperalin, spiroxamine, aldimorph o Organotins such as fentin, 10 o Oxazolidinones such as oxadixyl, o Phenylamides such as benalaxyl, benalaxyl-M, furalaxyl, metalaxyl, metalaxyl-M, ofurace, o Phenylpyrazoles such as fipronil, o Phenylpyrroles such as fludioxonil, 15 o Phenylureas such as pencycuron, o Phosphonates such fosetyl, o Phthalamic acids such as tecloftalam, o Phthalimides such as captafol, captan, folpet, o Piperazines such as triforine, 20 a Propionamides such as fenoxanil, o Pyridines such as pyrifenox, o Pyrimidines such as fenarimol, nuarimol, o Pyrroloquinolinones such as pyroquilon, o Qils such as cyazofamid, 25 a Quinazolinones such as proquinazid, o Quinolines such as quinoxyfen, o Quinones such as dithianon, o Sulfamides such as tolylfluanid, dichlofluanid, o Strobilurines such as azoxystrobin, dimoxystrobin, famoxadone, fluoxastrobin, 30 kresoxim-methyl, metominostrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, orysastrobin, o Thiocarbamates such as methasulfocarb, o Thiophanates such as thiophanate-methyl, o Thiophencarboxamides such silthiofam, WO 2013/044449 PCT/CN2011/080233 o Triazole fungicides such as azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, epoxiconazole, fenbuconazole, fluquinconazole, flusi lazole, flutriafol, fluotrimazole, hexaconazole, imibenconazole, ipconazole, metcona zole, myclobutanil, penconazole, propiconazole, prothioconazole, simeconazole, te 5 buconazole, tetraconazole, triadimefon, triadimenol, triticonazole, quinconazole o Triazolobenzothidazoles such as tricyclazole, o Valinamide carbamates such as iprovalicarb, benthiavalicarb o Fluopicolide o Pentachlorophenol 10 and their mixtures. c) Herbicides An herbicide is a pesticide used to kill unwanted plants. Selective herbicides kill specific tar gets while leaving the desired crop relatively unharmed. Some of these act by interfering 15 with the growth of the weed and are often based on plant hormones. Herbicides used to clear waste ground are non-selective and kill all plant material with which they come into contact. Herbicides are widely used in agriculture and in landscape turf management. They are applied in total vegetation control (TVC) programs for maintenance of highways and railroads. Smaller quantities are used in forestry, pasture systems, and management of areas 20 set aside as wildlife habitat. In general, active ingredients representing including various chemical classes and corresponding examples can be used o Anilides such as propanil o Aryloxycarboxylic acids e.g. MCPA-thioethyl o Aryloxyphenoxypropionates e.g. clodinafop-propargyl, cyhalofop-butyl, diclofops, 25 fluazifops, haloxyfops, quizalofops, o Chloroacetamides e.g. acetolochlor, alachlor, butachlor, dimethenamid, metolachlor, propachlor o Cyclohexanedione oximes e.g. clethodim, sethoxydim, tralkoxydim, o Benzamides such as isoxaben 30 o Benzimidazoles such as dicamba, ethofumesate o Dinitroanilines e.g. trifluralin, pendimethalin, o Diphenyl ethers e.g. aclonifen, oxyfluorfen, o The glycine derivative glyphosate, a systemic nonselective (it kills any type of plant) herbicide used in no-till burndown and for weed control in crops that are genetically 35 modified to resist its effects, o Hydroxybenzonitriles e.g. bromoxynil, o Imidazolinones e.g. fenamidone, imazapic, imazamox, imazapic, imazapyr, imazaquin, o Isoxazolidinones e.g. clomazone WO 2013/044449 PCT/CN2011/080233 o Paraquat as bypyridylium, o Phenyl carbamates e.g. desmedipham, phenmedipham, o Phenylpyrazoles e.g. pyraflufen-ethyl o Phenylpyrazolines e.g. pinoxaden, 5 o Pyridinecarboxylic acids or synthetic auxins e.g. picloram, clopyralid, and triclopyr, o Pyrimidinyloxybenzoics e.g. bispyrtbac-sodium o Sulfonyureas e.g. amidosulfuron, azimsulfuron, bensulfuron-methyl, chlorsulfuron, flazasulfuron, foramsulfuron, flupyrsulfuron-methyl-sodium, nicosulfuron, rim sulfuron, sulfosulfuron, tribenuron-methyl, trifloxysurlfuron-sodium, triflusulfuron, 10 tritosulfuron, o Triazolopyrimidines e.g. penoxsulam, metosulam, florasulam, o Triketones e.g. mesotriones, sulcotrione, o Ureas e.g. diuron, linuron, o Phenoxycarboxylic acids such as 2,4-D, MCPA, MCPB, mecoprops, 15 o Triazines such as atrazine, simazine, terbuthylazine, and their mixtures. d) Insecticides An insecticide is a pesticide used against insects in all developmental forms. They include 20 ovicides and larvicides used against the eggs and larvae of insects. Insecticides are used in agriculture, medicine, industry and the household. In the following, suitable chemical classes and examples of insecticides are mentioned: o Abamectin, emamectin, o Anthranilic diamides such as rynaxypyr 25 o Synthetic auxins such as avermectin, o Amidines such as amitraz, o Anthranilic diamide such as rynaxypyr, o Carbamates such as aldicarb, carbofuran, carbaryl, methomyl, 2-(1-methylpropyl)phenyl methylcarbamate, 30 a Chlorinated insecticides such as, for example, Camphechlor, DDT, Hexachloro cyclohexane, gamma-Hexachlorocyclohexane, Methoxychlor, Pentachlorophenol, TDE, Aldrin, Chlordane, Chlordecone, Dieldrin, Endosulfan, Endrin, Heptachlor, Mirex, o Juvenile hormone mimics such as pyriproxyfen, o Neonicotinoids such as imidacloprid, clothianidin, thiacloprid, thiamethoxam, 35 o Organophosphorus compounds such as acephate, azinphos-methyl, bensulide, chlo rethoxyfos, chlorpyrifos, chlorpyriphos-methyl, diazinon, dichlorvos (DDVP), dicroto phos, dimethoate, disulfoton, dthoprop, fenamiphos, fenitrothion, fenthion, fosthi- WO 2013/044449 PCT/CN2011/080233 azate, malathion, methamidophos, methidathion, methyl-parathion, mevinphos, naled, omethoate, oxydemeton-methyl, parathion, phorate, phosalone, phosmet, phostebupirim, pirimiphos-methyl, profenofos, terbufos, tetrachlor-vinphos, tribufos, trichlorfon, 5 o Oxadiazines such as indoxacarb, o Plant toxin derived compounds such as derris (rotenone), pyrethrum, neem (azadirachtin), nicotine, caffeine, o Pheromones such cuellure, methyl eugenol, o Pyrethroids such as, for example, allethrin, bifenthrin, deltamethrin, permethrin, 10 resmethrin, sumithrin, tetramethrin, tralomethrin, transfluthrin, o Selective feeding blockers such as flonicamid, pymetrozine, o Spinosyns e.g. spinosad and their mixtures. 15 e) Plant Growth Regulators Plant hormones (also known as phytohormones) are chemicals that regulate plant growth. Plant hormones are signal molecules produced within the plant, and occur in extremely low concentrations. Hormones regulate cellular processes in targeted cells locally and when moved to other locations, in other locations of the plant. Plants, unlike animals, lack glands 20 that produce and secrete hormones. Plant hormones shape the plant, affecting seed growth, time of flowering, the sex of flowers, senescence of leaves and fruits. They affect which tis sues grow upward and which grow downward, leaf formation and stem growth, fruit devel opment and ripening, plant longevity and even plant death. Hormones are vital to plant growth and lacking them, plants would be mostly a mass of undifferentiated cells. In the 25 following, suitable plant growth regulators are mentioned: o Aviglycine, o Cyanamide, o Gibberellins such gibberellic acid, o Quaternary ammoniums such as chlormequat chloride, mepiquat chloride, 30 o Ethylene generators such ethephone, WO 2013/044449 PCT/CN2011/080233 f) Rodenticides Rodenticides are a category of pest control chemicals intended to kill rodents. Rodents are difficult to kill with poisons because their feeding habits reflect their place as scavengers. They would eat a small bit of something and wait, and if they do not get sick, they would 5 continue eating. An effective rodenticide must be tasteless and odorless in lethal concentra tions, and have a delayed effect. In the following, examples for suitable rodenticides are given: Anticoagulants are defined as chronic (death occurs after 1 - 2 weeks post ingestion of the lethal dose, rarely sooner), single-dose (second generation) or multiple dose (first generation) 10 cumulative rodenticides. Fatal internal bleeding is caused by lethal dose of anticoagulants such as brodifacoum, coumatetralyl or warfarin. These substances in effective doses are antivitamins K, blocking the enzymes Kr-2,3-epoxide-reductase (this enzyme is preferentially blocked by 4-hydroxycoumarin/4-hydroxythiacoumarin derivatives) and Kr-quinone-reductase (this enzyme is preferentially blocked by indandione derivatives), de 15 priving the organism of its source of active vitamin K 1 . This leads to a disruption of the vita min K cycle, resulting in an inability of production of essential blood-clotting factors (mainly coagulation factors II (prothrombin), VII (proconvertin), IX (Christmas factor) and X (Stuart factor)). In addition to this specific metabolic disruption, toxic doses of 4-hydroxycoumarin/4-hydroxythiacoumarin and indandione anticoagulants are causing 20 damage to tiny blood vessels (capillaries), increasing their permeability, causing diffuse in ternal bleedings (haemorrhagias). These effects are gradual; they develop in the course of days and are not accompanied by any nociceptive perceptions, such as pain or agony. In the final phase of intoxication the exhausted rodent collapses in hypovolemic circulatory shock or severe anemia and dies calmly. Rodenticidal anticoagulants are either first generation 25 agents (4-hydroxycoumarin type: warfarin, coumatetralyl; indandione type: pindone, dipha cinone, chlorophacinone), generally requiring higher concentrations (usually between 0.005 and 0.1%), consecutive intake over days in order to accumulate the lethal dose, poor active or inactive after single feeding and less toxic than second generation agents, which are de rivatives of 4-hydroxycoumarin (difenacoum, brodifacoum, bromadiolone and flocoumafen) 30 or 4-hydroxy-1-benzothiin-2-one (4-hydroxy-1-thiacoumarin, sometimes incorrectlly referred to as 4-hydroxy-1-thiocoumarin, for reason see heterocyclic compounds), namely difethia lone. Second generation agents are far more toxic than first generation agents, they are generally applied in lower concentrations in baits (usually in the order of 0.001 - 0.005%), and are lethal after single ingestion of bait and are effective also against strains of rodents 35 that have become resistant against first generation anticoagulants; thus the second genera tion anticoagulants are sometimes referred to as "superwarfarins". Sometimes, anticoagu lant rodenticides are potentiated by an antibiotic, most commonly by sulfaquinoxaline. The aim of this association (e.g. warfarin 0.05% + sulfaquinoxaline 0.02%, or difenacoum 0.005% + sulfaquinoxaline 0.02% etc.) is that the antibiotic/bacteriostatic agent suppresses intesti 40 nal/gut symbiotic microflora that represents a source of vitamin K. Thus the symbiotic bacte ria are killed or their metabolism is impaired and the production of vitamin K by them is di minuted, an effect which logically contributes to the action of anticoagulants. Antibiotic agents other than sulfaquinoxaline may be used, for example co-trimoxazole, tetracycline, neomycin or metronidazole. A further synergism used in rodenticidal baits is that of an asso 45 ciation of an anticoagulant with a compound with vitamin D-activity, i.e. cholecalciferol or ergocalciferol (see below). A typical formula used is, e. g., warfarin 0.025 - 0.05% + cholecal- WO 2013/044449 PCT/CN2011/080233 ciferol 0.01%. In some countries there are even fixed three-component rodenticides, i.e. anticoagulant + antibiotic + vitamin D, e. g. difenacoum 0.005% + sulfaquinoxaline 0.02% + cholecalciferol 0.01%. Associations of a second-generation anticoagulant with an antibiotic and/or vitamin D are considered to be effective even against the most resistant strains of 5 rodents, though some second generation anticoagulants (namely brodifacoum and difethia lone), in bait concentrations of 0.0025 - 0.005% are so toxic that no known resistant strain of rodents exists and even rodents resistant against any other derivatives are reliably extermi nated by application of these most toxic anticoagulants. Vitamin K 1 has been suggested and successfully used as an antidote for pets or humans, 10 which/who were either accidentally or intentionally (poison assaults on pets, suicidal at tempts) exposed to anticoagulant poisons. In addition, since some of these poisons act by inhibiting liver functions and in progressed stages of poisoning, several blood-clotting factors as well as the whole volume of circulating blood lacks, a blood transfusion (optionally with the clotting factors present) can save a person's life who inadvertently takes them, which is 15 an advantage over some older poisons. Metal phosphides have been used as a means of killing rodents and are considered sin gle-dose fast acting rodenticides (death occurs commonly within 1-3 days after single bait ingestion). A bait consisting of food and a phosphide (usually zinc phosphide) is left where the rodents can eat it. The acid in the digestive system of the rodent reacts with the 20 phosphide to generate the toxic phosphine gas. This method of vermin control has possible use in places where rodents are resistant to some of the anticoagulants, particularly for con trol of house and field mice; zinc phosphide baits are also cheaper than most sec ond-generation anticoagulants, so that sometimes, in cases of large infestation by rodents, their population is initially reduced by copious amounts of zinc phosphide bait applied, and 25 the rest of the population that survived the initial fast-acting poison is then eradicated by prolonged feeding on anticoagulant bait. Inversely, the individual rodents that survived an ticoagulant bait poisoning (rest population) can be eradicated by pre-baiting them with nontoxic bait for a week or two (this is important to overcome bait shyness, and to get ro dents used to feeding in specific areas by offering specific food, especially when eradicating 30 rats) and subsequently applying poisoned bait of the same sort as used for pre-baiting until all consumption of the bait ceases (usually within 2-4 days). These methods of alternating rodenticides with different modes of action provides a factual or an almost 100% eradication of the rodent population in the area if the acceptance/palatability of bait is good (i.e., ro dents readily feed on it). 35 Phosphides are rather fast acting rat poisons, resulting in that the rats are dying usually in open areas instead of the affected buildings. Typical examples are aluminum phosphide (fumigant only), calcium phosphide (fumigant only), magnesium phosphide (fumigant only) and zinc phosphide (in baits). Zinc phosphide is typically added to rodent baits in amounts of around 0.75-2%. The baits have a strong, pungent garlic-like odor characteristic for 40 phosphine liberated by hydrolysis. The odor attracts (or, at least, does not repulse) rodents, but has a repulsive effect on other mammals; birds, however (notably wild turkeys), are not sensitive to the smell and feed on the bait thus becoming collateral damage. Hypercalcemia. Calciferols (vitamins D), cholecalciferol (vitamin D 3 ) and ergocalciferol (vita min D 2 ) are used as rodenticides, which are toxic to rodents for the same reason that they 45 are beneficial to mammals: they are affecting calcium and phosphate homeostasis in the WO 2013/044449 PCT/CN2011/080233 body. Vitamins D are essential in minute quantities (few IUs per kilogram body weight daily, which is only a fraction of a milligram), and like most fat soluble vitamins they are toxic in larger doses as they readily result in the so-called hypervitaminosis, which is, simply said, poisoning by the vitamin. If the poisoning is severe enough (that is, if the dose of the toxi 5 cant is high enough), it eventually leads to death. In rodents consuming the rodenticidal bait it causes hypercalcemia by raising the calcium level, mainly by increasing calcium absorption from food, mobilising bone-matrix-fixed calcium into ionised form (mainly monohydrogen carbonate calcium cation, partially bound to plasma proteins, [CaHCO 3 ]f), which circulates dissolved in the blood plasma, and after ingestion of a lethal dose the free calcium levels are 10 raised sufficiently so that blood vessels, kidneys, the stomach wall and lungs are mineral ised/calcificated (formation of calcificates, crystals of calcium salts/complexes in the tissues thus damaging them), leading further to heart problems (myocard is sensitive to variations of free calcium levels that are affecting both myocardial contractibility and excitation propagation between atrias and ventriculas) and bleeding (due to capillary damage) and 15 possibly kidney failure. It is considered to be single-dose, or cumulative (depending on con centration used; the common 0.075% bait concentration is lethal to most rodents after a single intake of larger portions of the bait), sub-chronic (death occurring usually within days to one week after ingestion of the bait). Applied concentrations are 0.075% cholecalciferol and 0.1% ergocalciferol when used alone. There is an important feature of calciferols toxi 20 cology which is that they are synergistic with anticoagulant toxicants. This means that mix tures of anticoagulants and calciferols in the same bait are more toxic than the sum of toxici ties of the anticoagulant and the calciferol in the bait so that a massive hypercalcemic effect can be achieved by substantially lower calciferol content in the bait and vice-versa. More pronounced anticoagulant/hemorrhagic effects are observed if calciferol is present. This 25 synergism is mostly used in baits low in calciferol because effective concentrations of calcif erols are more expensive than effective concentrations of most anticoagulants. The histori cally very first application of a calciferol in rodenticidal bait was, in fact, the Sorex product Sorexa* D (with a different formula than today's Sorexa* D) back in the early 1970's, con taining warfarin 0.025% + ergocalciferol 0.1%. Today, Sorexa* CD contains a 0.0025% 30 difenacoum + 0.075% cholecalciferol combination. Numerous other brand products con taining either calciferols 0.075 - 0.1% (e. g. Quintox*, containing 0.075% cholecalciferol) alone, or a combination of calciferol 0.01 - 0.075% with an anticoagulant are marketed. g) Miticides, moluscicides and nematicides 35 Miticides are pesticides that kill mites. Antibiotic miticides, carbamate miticides, forma midine miticides, mite growth regulators, organochlorine, permethrin and organophosphate miticides all belong to this category. Molluscicides are pesticides used to control mollusks, such as moths, slugs and snails. These substances include metaldehyde, methiocarb and aluminium sulfate. A nematicide is a type of chemical pesticide used to kill parasitic nema 40 todes (a phylum of worm). A nematicide is obtained from a neem tree's seed cake; which is the residue of neem seeds after oil extraction. The neem tree is known by several names in the world but was first cultivated in India since ancient times. h) Antimicrobials WO 2013/044449 PCT/CN2011/080233 In the following examples, antimicrobials suitable for agrochemical compositions according to the present invention are given. Bactericidal disinfectants mostly used are those applying o active chlorine (i.e., hypochlorites, chloramines, dichloroisocyanurate and trichloroi socyanurate, wet chlorine, chlorine dioxide, etc.), 5 o active oxygen (peroxides such as peracetic acid, potassium persulfate, sodium per borate, sodium percarbonate and urea perhydrate), o iodine (iodpovidone (povidone-iodine, Betadine), Lugol's solution, iodine tincture, io dinated nonionic surfactants), o concentrated alcohols (mainly ethanol, 1-propanol, called also n-propanol and 10 2-propanol, called isopropanol and mixtures thereof; further, 2-phenoxyethanol and 1- and 2-phenoxypropanols are used), o phenolic substances (such as phenol (also called "carbolic acid"), cresols (called "Ly sole" in combination with liquid potassium soaps), halogenated (chlorinated, bromi nated) phenols, such as hexachlorophene, triclosan, trichlorophenol, tribromophenol, 15 pentachlorophenol, Dibromol and salts thereof), o cationic surfactants such as some quaternary ammonium cations (such as benzalk onium chloride, cetyl trimethylammonium bromide or chloride, didecyldimethylam monium chloride, cetylpyridinium chloride, benzethonium chloride) and others, non-quarternary compounds such as chlorhexidine, glucoprotamine, octenidine di 20 hydrochloride, etc.), o strong oxidizers such as ozone and permanganate solutions; o heavy metals and their salts such as colloidal silver, silver nitrate, mercury chloride, phenylmercury salts, copper sulfate, copper oxide-chloride etc. Heavy metals and their salts are the most toxic and environmentally hazardous bactericides and, there 25 fore, their use is strongly suppressed or forbidden; further, also o properly concentrated strong acids (phosphoric, nitric, sulfuric, amidosulfuric, tolue nesulfonic acids) and o alcalis (sodium, potassium, calcium hydroxides) between pH < 1 or > 13, particularly below elevated temperatures (above 60*C) kill bacteria. 30 As antiseptics (i.e., germicide agents that can be used on human or animal body, skin, mu coses, wounds and the like), few of the above mentioned disinfectants can be used under proper conditions (mainly concentration, pH, temperature and toxicity toward man/animal). Among them, important are o Some properly diluted chlorine preparations (e. g. Daquin's solution, 0.5% sodium or 35 potassium hypochlorite solution, pH-adjusted to pH 7 - 8, or 0.5 - 1% solution of so dium benzenesulfochloramide (chloramine B)), some o iodine preparations such as iodopovidone in various galenics (ointments, solutions, wound plasters), in the past also Lugol's solution, o peroxides as urea perhydrate solutions and pH-buffered 0.1 - 0.25% peracetic acid 40 solutions, o alcohols with or without antiseptic additives, used mainly for skin antisepsis, WO 2013/044449 PCT/CN2011/080233 " weak organic acids such as sorbic acid, benzoic acid, lactic acid and salicylic acid o some phenolic compounds such as hexachlorophene, triclosan and Dibromol, and o cation-active compounds such as 0.05 - 0.5% benzalkonium, 0.5 - 4% chlorhexidine, 0.1 - 2% octenidine solutions. 5 Bactericidal antibiotics kill bacteria; bacteriostatic antibiotics only slow down their growth or reproduction. Penicillin is a bactericide, as are cephalosporins. Aminoglycosidic antibiotics can act in both a bactericidic manner (by disrupting cell wall precursor leading to lysis) or bacteriostatic manner (by connecting to 30s ribosomal subunit and reducing translation fi delity leading to inaccurate protein synthesis). Other bactericidal antibiotics according to the 10 present invention include the fluoroquinolones, nitrofurans, vancomycin, monobactams, co-trimoxazole, and metronidazole Preferred actives are those with systemic or partially systemic mode of action such as for example azoxystrobin. Overall preferred are non-selective herbicides and in particular biocides selected either (i) from the group consisting of paraquat, diquat, glufsinate, glyphosate and its salts, and 15 their mixtures; or (ii) from the group consisting of azoles, strobilurines, diphenyl ethers, anilides, organo phosphates, synthetic pyrethroids, neonicotinoids, oxadiazines, benzoylureas, phenyl carbamates, chloroacetamides, triketones, pyridinecarboxylic acids, cyclohexanedione oximes, phenylpyrazoles, and their mixtures; or 20 (iii) from the group consisting of oxyflurofen, propanil, chlorpyrifos, bifenthrin, deltame thrin, azoxystrobin, krexoxim-methyl, lambda-cyhalothrin, novaluron, lufenuron, imi dacloprid, thiacloprid, indoxacarb, oxyfluorfen, fluroxypyr and its esters, phenmedi pham, desmedipham, acetochlor, tebuconazole, epoxiconazole, propiconazole, fen buconazole, triademenol, fipronil, and their mixtures. 25 The most preferred biocides, however, are glyphosates including their esters and salts, in particular its sodium, potassium, ammonium and isopropylammonium salt and their mix tu res. Inert Broenstedt bases 30 Typically, the inert Broenstedt bases (component c) represent alkaline, ammonium and/or alkaline earth sulfates, preferably ammonium sulfate, potassium sulfate, sodium sulfate, or their mixtures. Optionally small amounts of anti-packing agents as, for example, magnesium carbonate are added. Preferably the inert agent is milled before being added to the other components so as to have particle size lower than 500 micron. 35 Solvents Suitable solvents (component d1) are, for example, Guerbet alcohols based on fatty alcohols having 6 to 18, preferably 8 to 10, carbon atoms, esters of linear C 6
    -C
    2 2 -fatty acids with linear or branched C 6
    -C
    2 2 -fatty alcohols or esters of branched C 6 -C 13 -carboxylic acids with linear or 40 branched C 6
    -C
    2 2 -fatty alcohols, such as, for example, myristyl myristate, myristyl palmitate, myristyl stearate, myristyl isostearate, myristyl oleate, myristyl behenate, myristyl erucate, WO 2013/044449 PCT/CN2011/080233 cetyl myristate, cetyl palmitate, cetyl stearate, cetyl isostearate, cetyl oleate, cetyl behenate, cetyl erucate, stearyl myristate, stearyl palmitate, stearyl stearate, stearyl isostearate, stearyl oleate, stearyl behenate, stearyl erucate, isostearyl myristate, isostearyl palmitate, isostearyl stearate, isostearyl isostearate, isostearyl oleate, isostearyl behenate, isostearyl 5 oleate, oleyl myristate, oleyl palmitate, oleyl stearate, oleyl isostearate, oleyl oleate, oleyl behenate, oleyl erucate, behenyl myristate, behenyl palmitate, behenyl stearate, behenyl isostearate, behenyl oleate, behenyl behenate, behenyl erucate, erucyl myristate, erucyl palmitate, erucyl stearate, erucyl isostearate, erucyl oleate, erucyl behenate and erucyl eru cate. Also suitable are esters of linear C 6
    -C
    2 2 -fatty acids with branched alcohols, in particular 10 2-ethylhexanol, esters of C 1 8
    -C
    3 8 - alkylhydroxy carboxylic acids with linear or branched C 6 -C 2 2 -fatty alcohols, in particular Dioctyl Malate, esters of linear and/or branched fatty acids with polyhydric alcohols (such as, for example, propylene glycol, dimerdiol or trimertriol) and/or Guerbet alcohols, triglycerides based on C 6
    -C
    10 -fatty acids, liquid mono-/di-/triglyceride mixtures based on C 6
    -C
    18 -fatty acids, esters of C 6 - C 22 -fatty alcohols 15 and/or Guerbet alcohols with aromatic carboxylic acids, in particular benzoic acid, esters of
    C
    2 - C 1 2 -dicarboxylic acids with linear or branched alcohols having 1 to 22 carbon atoms (Ce tiol" B)or polyols having 2 to 10 carbon atoms and 2 to 6 hydroxyl groups, vegetable oils, branched primary alcohols, substituted cyclohexanes, linear and branched C 6
    -C
    2 2 -fatty alco hol carbonates, such as, for example, Dicaprylyl Carbonate (Cetiol® CC), Guerbet carbonates, 20 based on fatty alcohols having 6 to 18, preferably 8 to 10, carbon atoms, esters of benzoic acid with linear and/or branched C 6
    -C
    22 -alcohols (e.g. Cetiol® AB), linear or branched, sym metrical or asymmetrical dialkyl ethers having 6 to 22 carbon atoms per alkyl group, such as, for example, dicaprylyl ether (Cetiol® OE), ring-opening products of epoxidized fatty acid es ters with polyols, silicone oils (cyclomethicones, silicone methicone grades, etc.), aliphatic or 25 naphthenic hydrocarbons. The preferred oil components or co-solvents show an ester or an amide structure. Particu larly preferred are adipates (Cetiol" B, Agnique® DiME 6), methyl esters of vegetable oils (Ag nique ME 18RD-F, Agnique® ME 12C-F), alkyl esters (Agnique® AE 3-2EH =2-Ethylhexyl Lactate) and alkyl amides (Agnique* AMD 10) - all products available in the market from Cognis 30 GmbH, Dsseldorf. Emulsifiers Suitable emulsifiers (component d2) include non-ionic and anionic surfactants and their mix tures. Non-ionic surfactants include for example: 35 o products of the addition of 2 to 30 mol ethylene oxide and/or 0 to 5 mol propylene oxide onto linear C 8
    -
    2 2 fatty alcohols, onto C 1 2
    -
    2 2 fatty acids and onto alkyl phenols containing 8 to 15 carbon atoms in the alkyl group; o C 1 2
    /
    1 8 fatty acid monoesters and diesters of addition products of 1 to 30 mol ethylene oxide onto glycerol; 40 o glycerol mono- and diesters and sorbitan mono- and diesters of saturated and un saturated fatty acids containing 6 to 22 carbon atoms and ethylene oxide addition products thereof; o addition products of 15 to 60 mol ethylene oxide onto castor oil and/or hydrogen- WO 2013/044449 PCT/CN2011/080233 ated castor oil; o polyol esters and, in particular, polyglycerol esters such as, for example, polyglycerol polyricinoleate, polyglycerol poly-12-hydroxystearate or polyglycerol dimerate iso stearate. Mixtures of compounds from several of these classes are also suitable; 5 o addition products of 2 to 15 mol ethylene oxide onto castor oil and/or hydrogenated castor oil; o partial esters based on linear, branched, unsaturated or saturated C6/22 fatty acids, ricinoleic acid and 12-hydroxystearic acid and glycerol, polyglycerol, pentaerythritol, dipentaerythritol, sugar alcohols (for example sorbitol), alkyl glucosides (for example 10 methyl glucoside, butyl glucoside, lauryl glucoside) and polyglucosides (for example cellulose); o mono-, di and trialkyl phosphates and mono-, di- and/or tri-PEG-alkyl phosphates and salts thereof; o wool wax alcohols; 15 o polysiloxane/polyalkyl polyether copolymers and corresponding derivatives; o mixed esters of pentaerythritol, fatty acids, citric acid and fatty alcohol and/or mixed esters of C6- 2 2 fatty acids, methyl glucose and polyols, preferably glycerol or polyglyc erol, and o polyalkylene glycols. 20 The addition products of ethylene oxide and/or propylene oxide onto fatty alcohols, fatty acids, alkylphenols, glycerol mono- and diesters and sorbitan mono- and diesters of fatty acids or onto castor oil are known commercially available products. They are homologue mixtures of which the average degree of alkoxylation corresponds to the ratio between the quantities of ethylene oxide and/or propylene oxide and substrate with which the addition 25 reaction is carried out. C 12
    /
    18 fatty acid monoesters and diesters of addition products of eth ylene oxide onto glycerol are known as lipid layer enhancers for cosmetic formulations. The preferred emulsifiers are described in more detail as follows: a) Partial glycerides 30 Typical examples of suitable partial glycerides are hydroxystearic acid monoglyceride, hy droxystearic acid diglyceride, isostearic acid monoglyceride, isostearic acid diglyceride, oleic acid monoglyceride, oleic acid diglyceride, ricinoleic acid monoglyceride, ricinoleic acid di glyceride, linoleic acid monoglyceride, linoleic acid diglyceride, linolenic acid monoglyceride, linolenic acid diglyceride, erucic acid monoglyceride, erucic acid diglyceride, tartaric acid 35 monoglyceride, tartaric acid diglyceride, citric acid monoglyceride, citric acid diglyceride, malic acid monoglyceride, malic acid diglyceride and technical mixtures thereof which may still contain small quantities of triglyceride from the production process. Addition products of 1 to 30, and preferably 5 to 10, mol ethylene oxide onto the partial glycerides mentioned are also suitable. 40 WO 2013/044449 PCT/CN2011/080233 b) Sorbitan esters Suitable sorbitan esters are sorbitan monoisostearate, sorbitan sesquiisostearate, sorbitan diisostearate, sorbitan triisostearate, sorbitan monooleate, sorbitan sesquioleate, sorbitan dioleate, sorbitan trioleate, sorbitan monoerucate, sorbitan sesquierucate, sorbitan dieru 5 cate, sorbitan trierucate, sorbitan monoricinoleate, sorbitan sesquiricinoleate, sorbitan diricinoleate, sorbitan triricinoleate, sorbitan monohydroxystearate, sorbitan sesquihydroxy stearate, sorbitan dihydroxystearate, sorbitan trihydroxystearate, sorbitan monotartrate, sorbitan sesquitartrate, sorbitan ditartrate, sorbitan tritartrate, sorbitan monocitrate, sorbi tan sesquicitrate, sorbitan dicitrate, sorbitan tricitrate, sorbitan monomaleate, sorbitan ses 10 quimaleate, sorbitan dimaleate, sorbitan trimaleate and technical mixtures thereof. Addition products of 1 to 30, and preferably 5 to 10, mol ethylene oxide onto the sorbitan esters mentioned are also suitable. c) Alk(en)yI oligoglycosides 15 The alkyl or alkenyl oligoglycosides representing also preferred emulsifiers may be derived from aldoses or ketoses containing 5 or 6 carbon atoms, preferably glucose. Accordingly, the preferred alkyl and/or alkenyl oligoglycosides are alkyl or alkenyl oligoglucosides. These materials are also known generically as "alkyl polyglycosides" (APG). The alk(en)yl oligogly cosides according to the invention correspond to formula (Ill) 20 R 30[G]p (1ll) wherein R 3 is an alkyl or alkenyl radical having from 6 to 22 carbon atoms, G is a sugar unit having 5 or 6 carbon atoms and p is a number from 1 to 10. The index p in general formula (Ill) indicates the degree of oligomerisation (DP degree), i.e. the distribution of mono- and oligoglycosides, and is a number of 1 to 10. Whereas p in a given compound must always be 25 an integer and, above all, may assume a value of 1 to 6, the value p for a certain alkyl oli goglycoside is an analytically determined calculated quantity which is mostly a broken num ber. Alk(en)yl oligoglycosides having an average degree of oligomerisation p of 1.1 to 3.0 are preferably used. Alk(en)yl oligoglycosides having a degree of oligomerisation below 1.7 and, more particularly, between 1.2 and 1.4 are preferred from the applicational point of view. 30 The alkyl or alkenyl radical R' may be derived from primary alcohols containing 4 to 22 and preferably 8 to 16 carbon atoms. Typical examples are butanol, caproic alcohol, caprylic al cohol, capric alcohol, undecyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, palmitoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, pet roselinyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and tech 35 nical mixtures thereof such as are formed, for example, in the hydrogenation of technical fatty acid methyl esters or in the hydrogenation of aldehydes from Roelen's oxo synthesis. Alkyl oligoglucosides based on hydrogenated C 8
    -C
    1 coconut oil alcohol having a DP of 1 to 3 are preferred. Also suitable are alkoxylation products of alkyl oligoglucosides, for example adducts of 1 to 10 moles ethylene oxide and/or 1 to 5 moles propylene oxide to C 8
    -C
    10 or 40 C 12 -Cis alkyl oligoglucoside having a DP between 1.2 and 1.4.
    WO 2013/044449 PCT/CN2011/080233 d) Alkoxylated vegetable oils and copolymers Suitable emulsifiers are castor oil, rape seed oil, soy bean oil ethoxylated with 3 to 80 moles ethylene oxide (Agnique" CSO 35, Agnique" SBO 10, Agnique" SBO 60). Typical copolymers are ethoxylated and propoxylated block and/or random polymers of C 2
    -C
    2 2 linear or 5 branched alcohols. e) Anionic emulsifiers Typical anionic emulsifiers encompass alkylbenzene sulfonic acids and their salts, as for ex ample calcium dodecylbenzene sulfonate dissolved in isobutanol (Agnique" ABS 65C) or 10 2-ethylhexanol (Agnique® ABS 60C-EH), dialkyl sulfosuccinates, as for example di-2-ethylhexyl sulfosuccinate or dioctyl sulfosuccinate, and polyacrylates having a molar weight of from 1,000 to 50,000. f) Miscellaneous emulsifiers 15 Other suitable emulsifiers are zwitterionic surfactants. Zwitterionic surfactants are sur face-active compounds which contain at least one quaternary ammonium group and at least one carboxylate and one sulfonate group in the molecule. Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N,N-dimethyl ammonium glyci nates, for example cocoalkyl dimethyl ammonium glycinate, 20 N-acylaminopropyl-N,N-dimethyl ammonium glycinates, for example cocoacylaminopropyl dimethyl ammonium glycinate, and 2-alkyl-3-carboxymethyl-3-hydroxyethyl imidazolines containing 8 to 18 carbon atoms in the alkyl or acyl group and cocoacylaminoethyl hy droxyethyl carboxymethyl glycinate. The fatty acid amide derivative known under the CTFA name of Cocamidopropyl Betaine is particularly preferred. Ampholytic surfactants are also 25 suitable emulsifiers. Ampholytic surfactants are surface-active compounds which, in addition to a C 8 /1 8 alkyl or acyl group, contain at least one free amino group and at least one -COOH or -S0 3 H- group in the molecule and which are capable of forming inner salts. Examples of suitable ampholytic surfactants are N-alkyl glycines, N-alkyl propionic acids, N-alkylamino butyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropy glycines, 30 N-alkyl taurines, N-alkyl sarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids containing around 8 to 18 carbon atoms in the alkyl group. Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, cocoacylaminoethyl aminopropionate and
    C
    1 2
    /
    1 8 acyl sarcosine. 35 Polymers Also the polymers (component d3) represent optional ingredients which are added to the formulation to increase stability of the granules. Examples are polyacrylates, polmethacry lates and condensation products of naphthalene sulfonic acid.
    WO 2013/044449 PCT/CN2011/080233 Biocide compositions Depending on the nature of the biocide the products may show the following compositions: (a) about 1 to about 30, and preferably about 8 to about 12 % b.w. mixtures of alkoxy lated alcohols according to formula (I) and (II) 5 (b) about 3 to about 95, and preferably about 50 to 90 and more preferably about 70 to about 85 % b.w. biocides; (c) 0 to about 15, and preferably about 2 to about 8 % b.w. inert Broenstedt bases; (d1) 0 to about 5, and preferably about 2 to about 4 % b.w. solvents; (d2) 0 to about 5, and preferably about 2 to about 4 % b.w. emulsifiers; and 10 (d3) 0 to about 5, and preferably about 2 to about 4 % b.w. polymers; (d4) 0 to about 5, and preferably about 2 to about 4 % b.w. fillers, such as clay. on condition that the numbers add optionally together with not more than about 10 , and preferably about 3 to 5 % b.w. water to 100 % b.w. 15 Industrial application A final embodiment of the present invention is related to the use of mixtures of alkoxylated unsaturated and branched alcohols as defined above as additives and or adjuvants for bio cides and biocide compositions, preferably for compositions representing granules with a water content of less than about 10 % b.w. , and preferably less than about 5 % b.w. 20 WO 2013/044449 PCT/CN2011/080233 Examples Examples 1 to 6, Comparative Example C1 Various surfactant blends were used for making glyphosate granules and the resulting prod ucts were evaluated for its properties. Foam height was determined according to the 5 Ross-Miles Test, appearance, hardness, solubility and stability by observation. The results are compiled in the following Table 1. Examples 1 to 6 are according to the invention, Exam ple C1 serves for comparison. Table 1 10 Properties of glyphosate granules Surfactant blend for water soluble granule (WG) formula Agnique* GPC' 100.0 - - - - - Agnique* FOH 90C-5 2 - - - 50.0 45.0 - Agnique* FOH 90C-10 3 - 50.0 45.0 - - 30.0 30.0 Lutensol* XP 604 - 50.0 45.0 - - 40.0 35.0 Lutensol* XP 1005 - - - 50.0 45.0 30.0 30.0 Hydropalat* 50406 - - 10.0 - 10.0 - 10.0 WG formula Surfactant blend (above) 12.0 12.0 12.0 12.0 12.0 12.0 12.0 Sodium sulfate 2.1 2.1 2.1 2.1 2.1 2.1 2.1 Ammonium sulfate 1.0 1.0 1.0 1.0 1.0 1.0 1.0 Glyphosate ammonium 83.4 83.4 83.4 83.4 83.4 83.4 83.4 salt (96.2 %) Tamol* NN 89067 1.5 1.5 1.5 1.5 1.5 1.5 1.5 WG properties (after adding 2.0 % water to the granules) Appearance Granule Granule Granule Granule Granule Granule Granule Hardness Soft Good Good Good Good Good good Collapsibility 25.0 5.0 5.0 5.0 5.0 5.0 5.0 Foam height [ml] > 10 < 5 < 10 < 5 < 5 <5 < 10 Solubility Poor Good Good Good Good Good Good Stability (54 *C, 2 weeks) Average Good Good Good Good Good Good 1) Tallow amine+15EO; 2) Oleylalcohol+5EO; 3) Oleylalcohol+10 EO; 4) CIO Guerbet alcohol+6EO; 5) CIO Guerbet alcohol+10EO; 6) Polyacrylate; 7) Naphthalene sulfonic acid polycondensate, sodium salt
    权利要求:
    Claims (19)
    [1] 1. Solid agricultural compositions, comprising: (at) at least one alkoxylated alcohol according to general formula (1) 5 R 1 O(AO)nH (1) In which R 1 stands for an unsaturated, linear hydrocarbon residue having 12 to 22 carbon atoms and 1, 2 or 3 double bonds, AO stands for an ethylene oxide, propylene, oxide and/or butylene oxide unit, and n represents an integer of from 1 to 60; 10 (a2) at least one alkoxylated alcohol according to general formula (II) R 2O(AO)mH (II) In which R 2 stands for a saturated, branched hydrocarbon residue having 8 to 36 carbon atoms, AO stands for an ethylene oxide, propylene, oxide and/or buty lene oxide unit, and m represents an integer of from 1 to 60; 15 (b) at least one biocide, and optionally (c) at least one inert Broenstedt base and/or (d) at least one solvent, emulsifier, polymer or filler, on condition that said compositions represent granules with a water content of less 20 than 10 % b.w.
    [2] 2. Compositions according to Claim 1, characterized in that compound (a1) represents an adduct of on average 2 to 15 mol ethylene oxide to oleyl alcohol
    [3] 3. Compositions according to Claim 1, characterized in that compound (a2) represents an adduct of on average 2 to 15 mol ethylene oxide and/or propylene oxide to guerbet 25 alcohol having 10 to 24 carbon atoms.
    [4] 4. Compositions according to any of the preceding Claims 1 to 3, characterized in that said unsaturated alcohol alkoxylates and said branched alcohol alkoxylates are present in a ratio by weight a1:a2 = 20:80 to 80:20.
    [5] 5. Compositions according to any of the preceding Claims 1 to 4, characterized in that 30 said solid compositions contain less than 5 % water.
    [6] 6. Compositions according to any of the preceding Claims 1 to 5, characterised in that they comprise biocides (component b) selected from the group consisting of herbicides, fungicides, insecticides and plant growth regulators.
    [7] 7. Compositions according to any of the preceding Claims 1 to 6, characterised in that 35 they comprise biocides (component b) selected from the group consisting of non-selective herbicides. WO 2013/044449 PCT/CN2011/080233
    [8] 8. Compositions according to any of the preceding Claims 1 to 7, characterised in that they comprise biocides (component b) selected from the group consisting of paraquat, diquat, glufosinate, glyphosate and its salts, and their mixtures.
    [9] 9. Compositions according to any of the preceding Claims 1 to 8, characterised in that 5 they comprise biocides (component b) selected from the group consisting of azoles, strobilurines, diphenyl ethers, anilides, organophosphates, synthetic pyrethroids, neonicotinoids, oxadiazines, benzoylureas, phenyl carbamates, chloroacetamides, triketones, pyridinecarboxylic acids, cyclohexanedione oximes, phenylpyrazoles, and their mixtures.
    [10] 10 10. Compositions according to any of the preceding Claims 1 to 9, characterised in that they comprise biocides (component b) selected from the group consisting of oxyfluro fen, propanil, chlorpyrifos, bifenthrin, deltamethrin, azoxystrobin, krexoxim-methyl, lambda-cyhalothrin, novaluron, lufenuron, imidacloprid, thiacloprid, indoxacarb, oxy fluorfen, fluroxypyr and its esters, phenmedipham, desmedipham, acetochlor, tebu 15 conazole, epoxiconazole, propiconazole, fenbuconazole, triademenol, fipronil, and their mixtures.
    [11] 11. Compositions according to any of the preceding Claims 1 to 10, characterised in that they comprise as biocides glyphosate or one of its esters or salts.
    [12] 12. Compositions according to any of the preceding Claims 1 to 11, characterised in that 20 they comprise as inert Broensted bases (component c) alkaline, ammonium and/or al kaline earth sulfates.
    [13] 13. Compositions according to any of the preceding Claims 1 to 12, characterised in that they comprise solvents (component d1) selected from the group consisting of Guerbet alcohols based on fatty alcohols having 6 to 18 carbon atoms, esters of linear 25 C 6 -C 22 -fatty acids with linear or branched C 6 -C 22 -fatty alcohols or esters of branched C 6 -C 13 -carboxylic acids with linear or branched C 6 -C 22 -fatty alcohols, methyl esters of C 6 -C 2 2 fatty acids, esters of linear C 6 -C 2 2 -fatty acids with branched alcohols, esters of C 18 -C 3 8 - alkyl hydroxy carboxylic acids with linear or branched C 6 -C 22 -fatty alcohols, esters of linear and/or branched fatty acids with polyhydric alcohols and/or Guerbet 30 alcohols, triglycerides based on C 6 -C 10 -fatty acids, liquid mono-/di-/triglyceride mix tures based on C 6 -C 18 -fatty acids, esters of C 6 - C 22 -fatty alcohols and/or Guerbet alco hols with aromatic carboxylic acids, esters of C 2 - C 12 -dicarboxylic acids with linear or branched alcohols having 1 to 22 carbon atoms or polyols having 2 to 10 carbon atoms and 2 to 6 hydroxyl groups, vegetable oils, branched primary alcohols, substituted 35 cyclohexanes, linear and branched C 6 -C 2 2 -fatty alcohol carbonates, Guerbet carbonates, based on fatty alcohols having 6 to 18 carbon atoms, esters of monopropylene glycol with C 2 -C 18 acids and benzoic acid, esters of benzoic acid with linear and/or branched C 6 -C 22 -alcohols, linear or branched, symmetrical or asymmetrical dialkyl ethers having 6 to 22 carbon atoms per alkyl group, ring-opening products of epoxidized fatty acid 40 esters with polyols, silicone oils and/or aliphatic or naphthenic hydrocarbons, mineral oils and their mixtures.
    [14] 14. Compositions according to any of the preceding Claims 1 to 13, characterised in that they comprise emulsifiers (component d2) selected from the group consisting of non-ionic and anionic surfactants or their mixtures. WO 2013/044449 PCT/CN2011/080233
    [15] 15. Compositions according to any of the preceding Claims 1 to 14, characterised in that they comprise polymers (component d3) selected from the group consisting of poly acrylates, polymethacrylates and polycondensation products of naphthalene sulfonic acid. 5
    [16] 16. Compositions according to any of the preceding Claims 1 to 15, characterised in that they comprise: (a) 1 to 30 % b.w. mixtures of alkoxylated alcohols according to formula (I) and (II) (b) 3 to 95 % b.w. biocides; (c) 0 to 15 % b.w. inert Broenstedt bases; 10 (d1) 0 to 5 % b.w. solvents; (d2) 0 to 5 % b.w emulsifiers; and (d3) 0 to 5 % b.w. polymers; (d4) 0 to 5 % b.w. fillers; on condition that the numbers add optionally together with not more than 10 % b.w. 15 water to 100 % b.w.
    [17] 17. Use of mixtures of alkoxylated unsaturated and branched alcohols according to Claim 1 as additives for biocides and biocide compositions.
    [18] 18. Use of mixtures of alkoxylated unsaturated and branched alcohols according to Claim 1 as adjuvants for biocides and biocide compositions. 20
    [19] 19. Use according to Claims 17 and/or 18, characterized in that said biocide compositions represent granules with a water content of less than 5 % b.w.
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    同族专利:
    公开号 | 公开日
    AU2011378019B2|2016-04-28|
    WO2013044449A1|2013-04-04|
    US20140249029A1|2014-09-04|
    AR088173A1|2014-05-14|
    引用文献:
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    BRPI0605346B1|2006-12-15|2016-03-08|Ricardo Amaral Remer|process for obtaining solid glyphosate ammonium salt, water soluble solid active ingredient for pesticide, agricultural pest control process and use of an active ingredient.|US9497971B2|2015-02-24|2016-11-22|Bayer Cropscience Lp|Non-volatile organic compound pesticide formulations|
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    法律状态:
    2016-08-25| FGA| Letters patent sealed or granted (standard patent)|
    2019-05-02| MK14| Patent ceased section 143(a) (annual fees not paid) or expired|
    优先权:
    申请号 | 申请日 | 专利标题
    PCT/CN2011/080233|WO2013044449A1|2011-09-27|2011-09-27|Solid agricultural compositions|
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