LU87872A1 - METHOD FOR CONTROLLING WEEDS IN CORN FIELDS USING A MIXTURE OF ACLONIFEN AND ANOTHER N-CHLORO ACETAMIDE HERBICIDE - Google Patents
METHOD FOR CONTROLLING WEEDS IN CORN FIELDS USING A MIXTURE OF ACLONIFEN AND ANOTHER N-CHLORO ACETAMIDE HERBICIDE Download PDFInfo
- Publication number
- LU87872A1 LU87872A1 LU87872A LU87872A LU87872A1 LU 87872 A1 LU87872 A1 LU 87872A1 LU 87872 A LU87872 A LU 87872A LU 87872 A LU87872 A LU 87872A LU 87872 A1 LU87872 A1 LU 87872A1
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- LU
- Luxembourg
- Prior art keywords
- aclonifen
- alachlor
- mixture
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- 239000000203 mixture Substances 0.000 title claims description 37
- DDBMQDADIHOWIC-UHFFFAOYSA-N aclonifen Chemical compound C1=C([N+]([O-])=O)C(N)=C(Cl)C(OC=2C=CC=CC=2)=C1 DDBMQDADIHOWIC-UHFFFAOYSA-N 0.000 title claims description 18
- 239000002890 Aclonifen Substances 0.000 title claims description 17
- 238000000034 method Methods 0.000 title claims description 17
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- 239000004009 herbicide Substances 0.000 title claims description 9
- HSPSCWZIJWKZKD-UHFFFAOYSA-N n-chloroacetamide Chemical compound CC(=O)NCl HSPSCWZIJWKZKD-UHFFFAOYSA-N 0.000 title description 3
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- 238000003756 stirring Methods 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 150000003608 titanium Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Description
Procédé pour lutter contre les mauvaises herbes dans les champs de maïs à l'aide d'un mélange d'aclonifen et d'un autre herbicide de type N-chloro acétamide L'invention concerne un nouveau procédé pour lutter contre les mauvaises herbes dans les champs de maïs. Elle concerne également les compositions herbicides destinées notamment à mettre en oeuvre le procédé.The invention relates to a new method for controlling weeds in corn fields using a mixture of aclonifen and another herbicide of the N-chloro acetamide type. cornfield. It also relates to the herbicidal compositions intended in particular for implementing the process.
Toutes sortes d'herbicides sont connus pour désherber toutes sortes de cultures. La pratique montre cependant que, malgré la multiplicité des herbicides disponibles, il est souvent difficile de désherber correctement telle ou telle culture particulière. Parmi les cultures posant des problèmes et nécessitant des solutions spécifiques, on peut citer le désherbage du maïs.All kinds of herbicides are known to weed all kinds of crops. However, practice shows that, despite the multiplicity of herbicides available, it is often difficult to properly weed a particular crop. Among the crops causing problems and requiring specific solutions, we can mention the weeding of corn.
Un but de 1'invention est de fournir un moyen satisfaisant pour désherber le maïs , notamment avec des désherbants autres que l'atrazine, le procédé selon 1'invention ayant alors 1'avantage de conduire à diminuer la pollution des eaux souterraines par rapport aux procédés connus mettant en oeuvre l'atrazine et étant par ailleurs plus efficace pour la destruction de certaines mauvaises herbes connues pour être résistantes aux dites triazines..An object of the invention is to provide a satisfactory means for weeding the corn, in particular with weed killers other than atrazine, the method according to the invention then having the advantage of leading to reducing the pollution of groundwater compared to known processes using atrazine and also being more effective for the destruction of certain weeds known to be resistant to said triazines.
On avait bien déjà décrit des compositions à base d'aclonifen dans la demande de brevet européen n' 342 134, mais ces compositions illustraient un moyen particulier d'obtention d'émulsions stables, ce moyen étant un dérivé du titane, et cet état de la technique ne fournissait aucune suggestion en rapport avec les buts de la présente invention et les moyens de parvenir à ces buts.Compositions based on aclonifen have already been described in European patent application No. 342 134, but these compositions illustrated a particular means for obtaining stable emulsions, this means being a derivative of titanium, and this state of the art did not provide any suggestion relating to the aims of the present invention and the means of achieving these aims.
Le procédé selon l'invention est caractérisé en ce que l'on applique à l'endroit où des graines de maïs ont été semées, avant leur levée, un mélange constitué d'aclonifen et d'au moins un herbicide N-chloro acétamide choisi parmi 1'acetochlore, l'alachlore, le metholachlore, le metazachlore, de préférence l'alachlore.The method according to the invention is characterized in that a mixture consisting of aclonifen and at least one chosen N-chloro acetamide herbicide is applied to the place where corn seeds have been sown, before their emergence. among acetochlor, alachlor, metholachlor, metazachlor, preferably alachlor.
Selon un mode opératoire général qui n'est évidemment donné qu'à titre indicatif et non limitatif on considère que la période d'application varie en fonction des conditions climatiques entre 1 à 3 semaines environ après le semisAccording to a general procedure which is obviously only given as an indication and not limiting, it is considered that the application period varies according to the climatic conditions between 1 to 3 weeks approximately after sowing
Le metholachlore est le 2-chloro-6'ethyl-N- (2-methoxy-l-methylethyl) acet-o-toluidide. L'acetochlore est le 2-chloro-N-ethoxymethyl-6'-ethylacet-o-toluidide. L'aclonifen est la 2-chloro 6-nitro 3-phenoxyaniline. L'alachlore est le 2-chloro 2', 6'-diéthyl N-méthoxyméthylacétanilide.Metholachlor is 2-chloro-6'ethyl-N- (2-methoxy-l-methylethyl) acet-o-toluidide. Acetochlor is 2-chloro-N-ethoxymethyl-6'-ethylacet-o-toluidide. Aclonifen is 2-chloro 6-nitro 3-phenoxyaniline. The alachlor is 2-chloro 2 ', 6'-diethyl N-methoxymethylacetanilide.
Doses préférées pour l'alachlore 1 à 3 kg/ha d'aclonifen 1 à 2,5 kg/ha d'alachlore et encore avantageusement 1000 à 1500 g/ha d'aclonifen 1500 à 2500 g/ha d'alachlore Parmi les mauvaises herbes pouvant être détruites on peut citer Setaria sp Chenopodium sp Atriplex sp Mercurialis sp Digitaria sp Solanum spPreferred rates for alachlor 1 to 3 kg / ha of aclonifen 1 to 2.5 kg / ha of alachlor and more advantageously 1000 to 1500 g / ha of aclonifen 1500 to 2500 g / ha of alachlor Among the bad weeds that can be destroyed include Setaria sp Chenopodium sp Atriplex sp Mercurialis sp Digitaria sp Solanum sp
Les procédés définis ci-avant sont le plus souvent mis en oeuvre avec seulement l'aclonifen et un seul autre herbicide, mais on peut également envisager, sans sortir de la présente invention, d'y associer un ou plusieurs pesticides compatibles et, de préférence, complémentaires.The processes defined above are most often carried out with only aclonifen and a single other herbicide, but it is also possible, without departing from the present invention, to associate therewith one or more compatible pesticides and, preferably , complementary.
Pour la mise en oeuvre des procédés herbicides selon l'invention, il est avantageux d'utiliser des produits prêts à l'emploi, la plupart du temps sous forme de compositions comme cela sera décrit ci-après, contenant les deux matières actives. Il est possible également (quoi que non préféré) d'employer un emballage comportant une cloison interne séparant les deux matières actives sous forme ou non de composition. Il s'agit donc dans ce cas de mélange extemporané des matières actives. L'invention a également pour objet les compositions herbicides destinées notamment à mettre en oeuvre le procédé selon l'invention. Le plus souvent, ces compositions herbicides contiennent les matières actives selon l'invention telle que décrite précédemment en association avec les supports solides ou liquides, acceptables en agriculture et les agents tensio-actifs également acceptables en agriculture. En particulier sont utilisables les supports inertes et usuels et les agents tensio-actifs usuels. Ces compositions font également partie de l'invention.For the implementation of the herbicidal processes according to the invention, it is advantageous to use ready-to-use products, most of the time in the form of compositions as will be described below, containing the two active materials. It is also possible (although not preferred) to use a packaging comprising an internal partition separating the two active materials in the form or not of composition. It is therefore in this case an extemporaneous mixture of active ingredients. A subject of the invention is also the herbicidal compositions intended in particular for implementing the method according to the invention. Most often, these herbicidal compositions contain the active materials according to the invention as described above in association with solid or liquid carriers, acceptable in agriculture and surfactants also acceptable in agriculture. In particular, the usual inert supports and the usual surfactants can be used. These compositions are also part of the invention.
Ces compositions peuvent contenir aussi toute sorte d'autres ingrédients tels que, par exemple, des colloïdes protecteurs, des adhésifs, des épaississants, des agents thixotropes, des agents de pénétration, des stabilisants, des séquestrants, etc... ainsi que d'autres matières actives connues à propriétés pesticides (notamment insecticides, fongicides ou herbicides) ou à propriétés régulatrices de la croissance des plantes. Plus généralement les composés utilisés dans l'invention peuvent être associés à tous les additifs solides ou liquides correspondant aux techniques habituelles de la mise en formulation. D'une façon générale, les compositions selon l'invention contiennent habituellement de 0,05 à 95 % environ des matières actives mises en oeuvre selon l'invention, de 1 % à 95 % environ de un ou plusieurs supports solides ou liquides et éventuellement de 0,1 à 50 % (de préférence 5 à 40 %) environ de un ou plusieurs agents tensioactifs.These compositions can also contain all kinds of other ingredients such as, for example, protective colloids, adhesives, thickeners, thixotropic agents, penetrating agents, stabilizers, sequestering agents, etc. other known active ingredients with pesticidal properties (in particular insecticides, fungicides or herbicides) or with properties regulating plant growth. More generally, the compounds used in the invention can be combined with all the solid or liquid additives corresponding to the usual techniques of formulation. In general, the compositions according to the invention usually contain from 0.05 to 95% approximately of the active materials used according to the invention, from 1% to 95% approximately from one or more solid or liquid carriers and optionally from 0.1 to 50% (preferably 5 to 40%) of approximately one or more surfactants.
De préférence le rapport en poids aclonifen/alachlore est compris entre 1/2,5 et 3 avantageusement 1/2,5 et 1.Preferably the aclonifen / alachlor weight ratio is between 1 / 2.5 and 3, advantageously 1 / 2.5 and 1.
Par le terme "support", dans le présent exposé, on désigne une matière organique ou minérale, naturelle ou synthétique, avec laquelle les matières actives sont associées pour faciliter leur application sur la plante, sur des graines ou sur le sol. Ce support est donc généralement inerte et il doit être acceptable en agriculture, notamment sur la plante traitée.By the term "support", in the present description, is meant an organic or mineral, natural or synthetic material, with which the active materials are associated to facilitate their application to the plant, to seeds or to the soil. This support is therefore generally inert and it must be acceptable in agriculture, in particular on the treated plant.
Comme supports solides (ou charges) on peut citer les charges minérales ou synthétiques telles que le kaolin, 1'attapulgite, la montmorillonite, la bentonite, le talc, la terre à foulon, la terre de diatomée, le kieselguhr, les carbonates de calcium et de magnésium, la silice synthétique précipitée, l'alumine, les silicates et silicoaluminates alcalins, les résines, cires, engrais solides. On peut aussi utiliser des charges hydrosolubles telles que les sulfates de sodium ou d'ammonium et l'urée.As solid supports (or fillers) mention may be made of mineral or synthetic fillers such as kaolin, attapulgite, montmorillonite, bentonite, talc, fuller's earth, diatomaceous earth, kieselguhr, calcium carbonates and magnesium, precipitated synthetic silica, alumina, alkali silicates and silicoaluminates, resins, waxes, solid fertilizers. It is also possible to use water-soluble fillers such as sodium or ammonium sulfates and urea.
Comme supports liquides, on peut citer l'eau, les alcools (notamment le butanol), les esters (notamment l'acétate de méthyl-glycol), les cétones (notamment la cyclohexanone et 1'isophorone), les fractions de pétrole, les hydrocarbures aromatiques (notamment les xylènes ou paraffiniques), les hydrocarbures chlorés aliphatiques (notamment le trichloroéthane) ou aromatiques (notamment les chlorobenzènes), les solvants hydrosolubles tels que le diméthylformamide, le diméthylsulfoxyde, la N-méthyl-pyrrolidone. L'agent tensioactif peut être un agent émulsionnant, dispersant ou mouillant de type ionique ou non ionique ou un mélange de tels agents tensioactifs.As liquid carriers, mention may be made of water, alcohols (in particular butanol), esters (in particular methyl glycol acetate), ketones (in particular cyclohexanone and isophorone), petroleum fractions, aromatic hydrocarbons (in particular xylenes or paraffinics), chlorinated aliphatic hydrocarbons (in particular trichloroethane) or aromatic (in particular chlorobenzenes), water-soluble solvents such as dimethylformamide, dimethylsulfoxide, N-methyl-pyrrolidone. The surfactant can be an emulsifying, dispersing or wetting agent of ionic or nonionic type or a mixture of such surfactants.
Comme agents mouillants non ioniques on peut ainsi citer les alkylphénols polyéthoxylés (notamment les octyl-, nonyl- et tributyl- phénols ayant de 6 à 18 motifs oxyéthylène), les alcools gras polyéthoxylés (notamment les alcools de C^g à C^g ayant de 6 à 18 motifs oxyéthylène), les amines grasses polyéthoxylées (notamment l'amine de suif, ou tall oil, ayant de 2 à 40 motifs oxyéthylène), les esters d'acides gras et de polyols (de type glycérine ou sucres) polyéthoxylés (notamment les laurate et stéarate de sorbitan ayant de 5 à 20 motifs oxyéthylène).As nonionic wetting agents, polyethoxylated alkylphenols (in particular octyl-, nonyl- and tributylphenols having from 6 to 18 oxyethylene units) can be cited, polyethoxylated fatty alcohols (in particular alcohols from C ^ g to C ^ g having from 6 to 18 oxyethylene units), polyethoxylated fatty amines (in particular tallow amine, or tall oil, having from 2 to 40 oxyethylene units), polyethoxylated esters of fatty acids and of polyols (of glycerin or sugar type) (in particular sorbitan laurate and stearate having from 5 to 20 oxyethylene units).
Comme agents mouillants anioniques, on peut citer les sels-esters alkylnaphtalène sulfonates (notamment les isopropyl-, butyl- et dibutylnaphtalène sulfonate de sodium ou de potassium, les sels-esters sulfates d'alcools gras (notamment les laurylsulfates de sodium ou de potassium), les sels-esters sulfosucci'nates d'alcools gras (notamment les dioctyl-sulfosuccinates de sodium ou de potassium), les dérivés de la taurine (notamment les alkyltaurates, les aryl-N-méthyltaurides, 1'oleylméthyltauride de sodium).As anionic wetting agents, mention may be made of the alkylnaphthalene sulfonate ester salts (especially sodium or potassium isopropyl-, butyl- and dibutylnaphthalene sulfonate, fatty alcohol ester sulfate salts (especially sodium or potassium lauryl sulfates) , the sulfosucci'nate salt esters of fatty alcohols (in particular sodium or potassium dioctyl sulfosuccinates), taurine derivatives (in particular alkyltaurates, aryl-N-methyltaurides, sodium oleylmethyltauride).
Comme agents dispersants non ioniques, on peut citer les arylphénols polyéthoxylés (notamment les di-et tri-(phényléthyl) phénols comprenant 18 à 40 motifs oxyéthylène).As nonionic dispersing agents, mention may be made of polyethoxylated arylphenols (in particular di- and tri- (phenylethyl) phenols comprising 18 to 40 oxyethylene units).
Comme agents dispersants anioniques, on peut citer les polymères polycarboxyliques salifiés (tels que les polymères polycarboxylates et polyacrylates de sodium), les polycondensats de formol et diphénolsulfonates ou d'alkylnaphtalène sulfonates (notamment de méthylnaphtalène sulfonate de sodium), les esters-sels ou acides phosphoriques d'alkyl- ou aryl-phénols polyoxyéthylénés (notamment les esters phosphoriques de nonylphénols ayant 6 à 18 motifs oxyéthylène sous forme acide ou sel de potassium ainsi que les esters phosphoriques de di- ou tri-(phényléthyl) phénol ayant 18 à 40 motifs oxyéthylène sous forme acide ou sel), les alcools gras polyoxyéthylénés phosphatés (notamment les alcools gras C·^ à C^g ayant 6 à 18 motifs oxyéthylène), les lignosulfonates alcalins ou alcalinoterreux.As anionic dispersing agents, mention may be made of salified polycarboxylic polymers (such as polycarboxylate polymers and sodium polyacrylates), polycondensates of formaldehyde and diphenolsulfonates or of alkylnaphthalene sulfonates (in particular of sodium methylnaphthalene sulfonate), salt esters or acids phosphorics of polyoxyethylenated alkyl- or aryl-phenols (in particular phosphoric esters of nonylphenols having 6 to 18 oxyethylene units in acid or potassium salt form as well as phosphoric esters of di- or tri- (phenylethyl) phenol having 18 to 40 units oxyethylene in acid or salt form), phosphated polyoxyethylenated fatty alcohols (in particular fatty alcohols C · ^ to C ^ g having 6 to 18 oxyethylene units), alkali or alkaline earth lignosulfonates.
Les compositions selon l'invention, surtout lorsqu'il s'agit de granulés autodispersibles, peuvent aussi contenir de 1 à 50 %' en poids de liant naturel ou synthétique.The compositions according to the invention, especially when it is self-dispersible granules, can also contain from 1 to 50% by weight of natural or synthetic binder.
Comme liant naturel, on peut citer l'amidon et ses dérivés (notamment l'amidon modifié et la dextrine), les dérivés de la celluloses (notamment la carboxyméthylcellulose, 1'hydroxyéthylcellulose, 1'hydroxypropylcellulose), les sucres (comme le lactose, le mannitol, le sorbitol), les gommes (telles que la gomme arabique et les gommes xanthane).As natural binder, mention may be made of starch and its derivatives (in particular modified starch and dextrin), cellulose derivatives (in particular carboxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose), sugars (such as lactose, mannitol, sorbitol), gums (such as gum arabic and xanthan gums).
Comme liant synthétique, on peut citer les polymères (notamment l'alcool polyvinylique, le polyacétate de vinyle, la polyvinylpyrrolidone, les polyacrylates alcalins), les polycondensats (spécialement les polyéthers tels que les polyglycols ; les copolycondensats d'anhydride maléique ; les polycondensats de formol et d'alkylnaphtalène sulfonates, tels que le polycondensat de formol et de méthylnaphtalène sulfonate de sodium), les lignosulfonates alcalins.As synthetic binder, mention may be made of polymers (in particular polyvinyl alcohol, polyvinyl acetate, polyvinylpyrrolidone, alkaline polyacrylates), polycondensates (especially polyethers such as polyglycols; maleic anhydride copolycondensates; polycondensates of formalin and alkylnaphthalene sulfonates, such as polycondensate of formalin and sodium methylnaphthalene sulfonate), alkaline lignosulfonates.
La présence d'au moins un agent tensioactif dans les compositions selon l'invention est généralement indispensable car d'une part, les matières actives et/ou le support inerte ne sont pas solubles dans l'eau et d'autre part, l'agent vecteur de l'application est l'eau.The presence of at least one surfactant in the compositions according to the invention is generally essential because, on the one hand, the active materials and / or the inert support are not soluble in water and, on the other hand, the vector agent of the application is water.
Pour leur application, les compositions selon l'invention sont sous des formes assez diverses, solides ou liquides ; il s'agit de formes relativement diluées, tandis que les compositions convenables pour le transport, le commerce et le stockage sont plutôt des compositions concentrées.For their application, the compositions according to the invention are in fairly diverse forms, solid or liquid; these are relatively dilute forms, while the compositions suitable for transport, trade and storage are rather concentrated compositions.
Comme formes de compositions solides, on peut citer les poudres mouillables et les poudres pour poudrage (à teneur en matières actives pouvant aller jusqu'à 100 %) et les granulés (de préférence autodispersibles), notamment ceux obtenus par extrusion, par compactage, par imprégnation d'un support granulé, par granulation à partir d'une poudre (la teneur en matières actives de formule (I) et de groupe (II) dans ces granulés étant entre 0,5 et 80 % pour ces derniers cas).As forms of solid compositions, mention may be made of wettable powders and powders for dusting (with an active ingredient content of up to 100%) and granules (preferably self-dispersible), in particular those obtained by extrusion, by compacting, by impregnation of a granulated support, by granulation from a powder (the content of active materials of formula (I) and of group (II) in these granules being between 0.5 and 80% for the latter cases).
On préfère néanmoins mettre en oeuvre dans l'invention des compositions sous forme liquide. On peut citer les concentrés émulsionnables, les suspensions concentrées et les émulsions concentrées.It is nevertheless preferred to use in the invention compositions in liquid form. Mention may be made of emulsifiable concentrates, concentrated suspensions and concentrated emulsions.
Les suspensions concentrées, qui sont applicables en pulvérisation, sont prépareés de manière à obtenir un produit fluide stable ne se déposant pas (broyage fin) et elles contiennent habituellement de 10 à 75 % de matières actives, de 0,5 à 15% d'agents tensioactifs, de 0,1 à 10 % d'agents thixotropes, de 0 à 10 % d'additifs appropriés, comme des anti-mousses, des inhibiteurs de corrosion, des stabilisants, des agents de pénétration et des adhésifs et, comme support, de l'eau ou un liquide organique dans lequel les matières actives sont peu solubles ou non solubles : certaines matières solides organiques ou des sels minéraux peuvent être dissous dans le support pour aider à empêcher la sédimentation ou comme antigels pour l'eau. A titre d'exemple, voici une composition de suspension concentrée (Exemple 1) : - matières actives 500 g - phosphate de tristyrylphénol polyéthoxylé 50 g - alkylphénol polyéthoxylé 50 g - polycarboxylate de sodium 20 g - éthylène glycol (antigel) 50 g - huile organopolysiloxanique (antimousse) 1 g - polysaccharide (épaississant) 1,5 g - eau 316,5 gThe concentrated suspensions, which are applicable in spraying, are prepared so as to obtain a stable fluid product which does not deposit (fine grinding) and they usually contain from 10 to 75% of active materials, from 0.5 to 15% of surfactants, 0.1-10% thixotropic agents, 0-10% suitable additives, such as defoamers, corrosion inhibitors, stabilizers, penetrating agents and adhesives and, as a carrier , water or an organic liquid in which the active ingredients are not very soluble or insoluble: certain organic solid matters or mineral salts can be dissolved in the support to help prevent sedimentation or as antifreezes for water. As an example, here is a concentrated suspension composition (Example 1): - active ingredients 500 g - polyethoxylated tristyrylphenol phosphate 50 g - polyethoxylated alkylphenol 50 g - sodium polycarboxylate 20 g - ethylene glycol (antifreeze) 50 g - oil organopolysiloxane (antifoam) 1 g - polysaccharide (thickener) 1.5 g - water 316.5 g
Les concentrés émulsionnables ou solubles comprennent le plus souvent 10 à 80 % de matière active, les émulsions ou solutions prêtes à l'application contenant, quant à elles, 0,001 à 20 % de matière active.The emulsifiable or soluble concentrates most often comprise 10 to 80% of active material, the emulsions or solutions ready for application containing, for their part, 0.001 to 20% of active material.
En plus du solvant, les concentrés émulsionnables peuvent contenir, quand c'est nécessaire, 2 à 20 % d'additifs appropriés comme les stabilisants, les agents tensio-actifs, les agents de pénétration, les inhibiteurs de corrosion, les colorants ou les adhésifs précédemment cités. A partir de ces concentrés, on peut obtenir par dilution avec de l'eau des émulsions de toute concentration désirée, qui conviennent particulièrement à l'application sur les cultures. A titre d'exemple, voici la composition de quelques concentrés émulsionnables :In addition to the solvent, emulsifiable concentrates can contain, when necessary, 2 to 20% of suitable additives such as stabilizers, surfactants, penetrating agents, corrosion inhibitors, dyes or adhesives previously cited. From these concentrates, emulsions with any desired concentration can be obtained by dilution with water, which are particularly suitable for application to crops. As an example, here is the composition of some emulsifiable concentrates:
Exemple (formulation) 2 : - matières actives 400 g/1 - dodécylbenzène sulfonate alcalin 24 g/1 - nonylphénol oxyéthylé à 10 molécules d'oxyde d'éthylène 16 g/1 - cyclohexanone 200 g/1 - solvant aromatique q.s.p. 1 litreExample (formulation) 2: - active ingredients 400 g / 1 - alkali dodecylbenzene sulfonate 24 g / 1 - oxyethylated nonylphenol containing 10 molecules of ethylene oxide 16 g / 1 - cyclohexanone 200 g / 1 - aromatic solvent q.s.p. 1 litre
Selon une autre formule de concentré émulsionnable, on utilise :According to another formula of emulsifiable concentrate, the following are used:
Exemple F 3 : - matières actives 250 g - huile végétale époxydée 25 g - mélange de sulfonate d'alcoylaryle et d'éther de polyglycol et d'alcools gras 100 g - diméthylformamide 50 g - xylène 575 gExample F 3: - active ingredients 250 g - epoxidized vegetable oil 25 g - mixture of alkylaryl sulfonate and polyglycol ether and fatty alcohols 100 g - dimethylformamide 50 g - xylene 575 g
Les émulsions concentrées sont des compositions sous forme d'émulsions liquides stables , la matière active étant sous forme liquide par elle-même ou sous forme dissoute dans un solvant . Ces émulsions sont essentiellement aqueuses et, outre l'eau, contiennent habituellement 20 à 80 % de matière active, 0 à 35 % de solvant (ce solvant étant simplement utile pour dissoudre la matière active si celle-ci est solide, et étant généralement utilisé en la quantité minimale pour parvenir à ce but), 1 à 15 % (préférentiellement 2 à 10 % r d'un agent tensioactif hydrosoluble, éventuellement 1 à 12 % (préférentiellement 2 à 6 %) d'un agent tensioactif hydrophobe ou liposoluble, et éventuellement encore divers autres adjuvants comme par exemple 1 à 10 % d'agent stabilisant de l'émulsion, 0 à 5 % d'agent épaississant minéral ou organique et 0 à 10 % d'agents divers tels que antimousses, biocides, antigels, etc...La préparation de ces émulsions s'effectue par ajoût de la phase huileuse (c'est-à-dire liquide organique) à la phase aqueuse sous agitation, suivi d'une homogénéisation par exemple à l'aide d'un broyeur colloïdal.Concentrated emulsions are compositions in the form of stable liquid emulsions, the active material being in liquid form by itself or in form dissolved in a solvent. These emulsions are essentially aqueous and, in addition to water, usually contain 20 to 80% of active material, 0 to 35% of solvent (this solvent being simply useful for dissolving the active material if it is solid, and being generally used in the minimum quantity to achieve this goal), 1 to 15% (preferably 2 to 10% r of a water-soluble surfactant, optionally 1 to 12% (preferably 2 to 6%) of a hydrophobic or liposoluble surfactant, and possibly also various other adjuvants such as for example 1 to 10% of stabilizing agent for the emulsion, 0 to 5% of mineral or organic thickening agent and 0 to 10% of various agents such as defoamers, biocides, antifreezes, etc ... The preparation of these emulsions is carried out by adding the oily phase (that is to say organic liquid) to the aqueous phase with stirring, followed by homogenization for example using a colloid mill.
En ce qui concerne les compositions adaptées au stockage et au transport, elles contiennent plus avantageusement de 0,5 à 95 % (en poids) de substance active.As regards the compositions suitable for storage and transport, they more advantageously contain from 0.5 to 95% (by weight) of active substance.
Ainsi donc, les compositions à usage agricole selon l'invention peuvent contenir les matières actives selon l'invention dans de très larges limites, allant de 0,05 à 95 % (en poids). Leur teneur en agent tensio-actif est avantageusement comprise entre 5 % et 40 % en poids. L'exemple suivant, donné à titre non limitatif, illustre l'invention et montre comment elle peut être mise en oeuvre.Thus, the compositions for agricultural use according to the invention can contain the active materials according to the invention within very wide limits, ranging from 0.05 to 95% (by weight). Their content of surfactant is advantageously between 5% and 40% by weight. The following example, given without limitation, illustrates the invention and shows how it can be implemented.
Les essais sont effectués sur des parcelles élémentaires de 30 m^ chacune envahies naturellement par une flore mixte graminées + dicotylédones.The tests are carried out on elementary plots of 30 m ^ each invaded naturally by a mixed grass + dicotyledonous flora.
Chaque traitement est répété sur deux parcelles différentes adjacentes chacune à une parcelle témoin non traitée. L'application est effectuée en prélevée après le semis à raison de 300 1/ha de bouillie.Each treatment is repeated on two different plots, each adjacent to an untreated control plot. The application is made pre-emergence after sowing at the rate of 300 l / ha of spray.
On effectue un relevé 8 semaines après la levée, on mesure le pourcentage d'efficacité (100 % = 100 % d'herbes détruites).A survey is carried out 8 weeks after emergence, the percentage of effectiveness is measured (100% = 100% of herbs destroyed).
On prépare la bouillie, diluée à l'eau et destinée à être appliquée sur les plantes, à partir des concentrats commerciaux de chacun des constituants. Dans le tableau de présentation des résultats, on a utilisé les abréviations suivantes :The mixture is prepared, diluted with water and intended to be applied to plants, from the commercial concentrates of each of the constituents. In the results presentation table, the following abbreviations were used:
Mauvaise herbes AbréviationsWeeds Abbreviations
AMARANTHUS SP AMAAMARANTHUS SP AMA
ATRIPLEX PATÜLA ATPATRIPLEX PATÜLA ATP
BRASSICA NAPUS BRABRASSICA NAPUS BRA
CHENOPODIUM SP CHSCHENOPODIUM SP CHS
DIGITARIA SP DIGDIGITARIA SP DIG
FALLOPIA CONVOLVULUS FALFALLOPIA CONVOLVULUS FAL
GALIUM APARINE GAPGALIUM APARINE GAP
MATRICARIA SP MATMATRICARIA SP MAT
MERCURIALIS ANNUA MEAMERCURIALIS ANNUA MEA
POLYGONUM AVICULARE POAPOLYGONUM AVICULARE POA
POLYGONUM PERSICARIA POPPOLYGONUM PERSICARIA POP
SETARIA SP SETSETARIA SP SET
SINAPIS ARVENSIS SIASINAPIS ARVENSIS SIA
SOLANUM NIGRUM SONSOLANUM NIGRUM SOUND
STELLARIA MEDIA STESTELLARIA MEDIA STE
VERONICA PERSICA VERVERONICA PERSICA VER
CulturesCultures
MAIS MAISBUT BUT
Les résultats suivants, exprimés en pourcentage de destruction, ont été obtenus en appliquant le mélange aclonifen + alachlore à la dose telle que l'aclonifen soit appliqué à raison de 1 kg/ha et l'alachlor à raison de 1,8 kg/ha.The following results, expressed as percentage of destruction, were obtained by applying the aclonifen + alachlor mixture at the dose such that the aclonifen is applied at the rate of 1 kg / ha and the alachlor at the rate of 1.8 kg / ha .
Mauvaises herbes Prélevée AMA 90 CHS 72 POP 90 DIG 84 SET 95Weeds Pre-emergent AMA 90 CHS 72 POP 90 DIG 84 SET 95
Cultures MAIS 5 A la dose de 1144 g/ha d'aclonifen et 2056 g/ha d'alachlore on obtient les résultats suivants AMA 88 ATP 100 CHS 72 MEA 100 SON 67 DIG 58Crops BUT 5 At the dose of 1144 g / ha of aclonifen and 2056 g / ha of alachlor, the following results are obtained AMA 88 ATP 100 CHS 72 MEA 100 SON 67 DIG 58
Un essai semblable avec une dose de 864 g/ha d'atrazine et 2016 g/ha d'alachlore a donné les résultats suivants : AMA 88 ATP 90 CHS 18 MEA 100 SON 67 DIG 42A similar trial with a dose of 864 g / ha of atrazine and 2016 g / ha of alachlor gave the following results: AMA 88 ATP 90 CHS 18 MEA 100 SON 67 DIG 42
Ces résultats de désherbage du maïs correspondent à des performances satisfaisantes et équivalentes où supérieures à celles de mélanges de type atrazine-alachlore, mais les mélanges de l'invention n'ont pas les inconvénients dus à l'atrazine vis-à-vis des nappes phréatiques. Les mélanges à base d'aclonifen et de pendiméthalin conduisent à des performances herbicides également équivalentes, et avec une situation vis-à-vis des nappes phréatiques également favorable.These corn weeding results correspond to satisfactory and equivalent performances or superior to those of mixtures of the atrazine-alachlor type, but the mixtures of the invention do not have the drawbacks due to atrazine with respect to the sheets. phreatic. Mixtures based on aclonifen and pendimethalin lead to equally equivalent herbicidal performances, and with a situation with regard to groundwater also favorable.
Claims (7)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9000468A FR2656769B1 (en) | 1990-01-11 | 1990-01-11 | HERBICIDE MIXTURES BASED ON ACLONIFEN. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU87872A1 true LU87872A1 (en) | 1992-10-15 |
Family
ID=9392828
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU87872A LU87872A1 (en) | 1990-01-11 | 1991-01-03 | METHOD FOR CONTROLLING WEEDS IN CORN FIELDS USING A MIXTURE OF ACLONIFEN AND ANOTHER N-CHLORO ACETAMIDE HERBICIDE |
Country Status (23)
| Country | Link |
|---|---|
| JP (1) | JPH04217901A (en) |
| KR (1) | KR910014031A (en) |
| AT (1) | AT397334B (en) |
| AU (1) | AU635599B2 (en) |
| BE (1) | BE1005340A0 (en) |
| BR (1) | BR9100192A (en) |
| CA (1) | CA2033481A1 (en) |
| CH (1) | CH682204A5 (en) |
| CS (1) | CS3291A2 (en) |
| DE (1) | DE4100702C2 (en) |
| DK (1) | DK4491A (en) |
| ES (1) | ES2033570B1 (en) |
| FR (1) | FR2656769B1 (en) |
| GB (1) | GB2241892B (en) |
| GR (1) | GR1000823B (en) |
| IE (1) | IE904733A1 (en) |
| IL (1) | IL96923A0 (en) |
| IT (1) | IT1244366B (en) |
| LU (1) | LU87872A1 (en) |
| NL (1) | NL9100029A (en) |
| PT (1) | PT96454A (en) |
| SE (1) | SE9100017L (en) |
| ZA (1) | ZA91197B (en) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4650022A (en) * | 1985-01-09 | 1987-03-17 | Yamaha Hatsudoki Kabushiki Kaisha | Rear wheel steering device for motorcycles |
| US4733742A (en) * | 1987-04-20 | 1988-03-29 | Frye Norman V | Two-wheeled steerable vehicle |
| ES2026391A6 (en) * | 1990-10-30 | 1992-04-16 | Belil Creixell Jose Luis | Rear wheel assembly system for motorcycles and similar vehicles. |
| US6102420A (en) * | 1998-08-05 | 2000-08-15 | Archimedec Handelsonderneming V.O.F. | Walking cycle with steerable front and rear wheel |
| AU2002362367A1 (en) * | 2001-09-20 | 2003-04-01 | Syngenta Participations Ag | Herbicidal composition |
| CN101971807A (en) * | 2010-07-14 | 2011-02-16 | 湖北奥士特奥农药产品研发有限公司 | Pendimethalin and alachlor binary complex herbicide and preparation method thereof |
| AR093999A1 (en) | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | HERBICIDE AGENTS CONTAINING ACLONIFEN |
| AR093998A1 (en) | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | HERBICIDE AGENTS CONTAINING ACLONIFEN |
| DK2934123T3 (en) * | 2012-12-18 | 2021-08-16 | Bayer Cropscience Ag | HERBICIDE MEASURES CONTAINING ACLONIFE |
| AR094000A1 (en) | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | HERBICIDE AGENTS CONTAINING ACLONIFEN |
| AR093995A1 (en) | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | HERBICIDE AGENTS CONTAINING ACLONIFEN |
| AR093997A1 (en) | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | HERBICIDE AGENTS CONTAINING ACLONIFEN |
| AR094006A1 (en) | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | HERBICIDE AGENTS CONTAINING ACLONIFEN |
| CN106472508B (en) * | 2016-09-08 | 2019-03-26 | 中山大学 | Application of the great Hua rose ketone A in prevention and treatment aspergillus flavus and/or aflatoxin contamination |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TR20258A (en) * | 1978-07-15 | 1980-12-08 | Celamerck Gmbh & Co Kg | 2-chloro-6-nitroaniline |
| FR2611437A1 (en) * | 1987-03-05 | 1988-09-09 | Rhone Poulenc Agrochimie | Herbicidal product resulting from the association of aclonifen with oxadiazon or diflufenican |
| FR2630885B1 (en) * | 1988-05-09 | 1991-03-01 | Rhone Poulenc Agrochimie | OIL-IN-WATER PESTICIDE EMULSION, METHOD OF IMPLEMENTING |
| FR2659833B1 (en) * | 1990-03-20 | 1996-10-18 | Rhone Poulenc Agrochimie | HERBICIDE COMBINATION COMPRISING ACLONIFEN AND AT LEAST ONE SUBSTITUTED UREA. |
-
1990
- 1990-01-11 FR FR9000468A patent/FR2656769B1/en not_active Expired - Lifetime
- 1990-12-27 BE BE9001249A patent/BE1005340A0/en not_active IP Right Cessation
- 1990-12-31 CA CA002033481A patent/CA2033481A1/en not_active Abandoned
- 1990-12-31 IE IE473390A patent/IE904733A1/en unknown
-
1991
- 1991-01-03 SE SE9100017A patent/SE9100017L/en not_active Application Discontinuation
- 1991-01-03 LU LU87872A patent/LU87872A1/en unknown
- 1991-01-07 GR GR910100004A patent/GR1000823B/en not_active IP Right Cessation
- 1991-01-08 CS CS9132A patent/CS3291A2/en unknown
- 1991-01-09 AU AU69249/91A patent/AU635599B2/en not_active Ceased
- 1991-01-10 AT AT0004491A patent/AT397334B/en not_active IP Right Cessation
- 1991-01-10 DK DK004491A patent/DK4491A/en not_active Application Discontinuation
- 1991-01-10 IL IL96923A patent/IL96923A0/en unknown
- 1991-01-10 PT PT96454A patent/PT96454A/en not_active Application Discontinuation
- 1991-01-10 NL NL9100029A patent/NL9100029A/en not_active Application Discontinuation
- 1991-01-10 ZA ZA91197A patent/ZA91197B/en unknown
- 1991-01-10 ES ES9100059A patent/ES2033570B1/en not_active Expired - Fee Related
- 1991-01-11 BR BR919100192A patent/BR9100192A/en not_active Application Discontinuation
- 1991-01-11 CH CH71/91A patent/CH682204A5/fr not_active IP Right Cessation
- 1991-01-11 IT ITMI910050A patent/IT1244366B/en active IP Right Grant
- 1991-01-11 KR KR1019910000335A patent/KR910014031A/en not_active Withdrawn
- 1991-01-11 JP JP3069568A patent/JPH04217901A/en active Pending
- 1991-01-11 GB GB9100640A patent/GB2241892B/en not_active Expired - Fee Related
- 1991-01-11 DE DE4100702A patent/DE4100702C2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE4100702A1 (en) | 1991-07-18 |
| DK4491A (en) | 1991-07-12 |
| ATA4491A (en) | 1993-08-15 |
| AT397334B (en) | 1994-03-25 |
| JPH04217901A (en) | 1992-08-07 |
| FR2656769B1 (en) | 1996-11-15 |
| CS3291A2 (en) | 1991-08-13 |
| GR1000823B (en) | 1993-01-25 |
| ITMI910050A1 (en) | 1992-07-11 |
| GB9100640D0 (en) | 1991-02-27 |
| GR910100004A (en) | 1992-06-25 |
| IT1244366B (en) | 1994-07-08 |
| ZA91197B (en) | 1991-11-27 |
| SE9100017L (en) | 1991-07-12 |
| KR910014031A (en) | 1991-08-31 |
| PT96454A (en) | 1991-10-15 |
| SE9100017D0 (en) | 1991-01-03 |
| FR2656769A1 (en) | 1991-07-12 |
| AU6924991A (en) | 1991-07-18 |
| NL9100029A (en) | 1991-08-01 |
| BE1005340A0 (en) | 1993-06-29 |
| CA2033481A1 (en) | 1991-07-12 |
| BR9100192A (en) | 1991-10-22 |
| DE4100702C2 (en) | 2000-01-13 |
| AU635599B2 (en) | 1993-03-25 |
| ITMI910050A0 (en) | 1991-01-11 |
| IL96923A0 (en) | 1992-03-29 |
| CH682204A5 (en) | 1993-08-13 |
| GB2241892A (en) | 1991-09-18 |
| ES2033570B1 (en) | 1994-01-16 |
| ES2033570A1 (en) | 1993-03-16 |
| GB2241892B (en) | 1994-07-27 |
| IE904733A1 (en) | 1991-07-17 |
| DK4491D0 (en) | 1991-01-10 |
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