WO2017078638A1 - Composition herbicide synergique d'oxadiazon et de clomazone destinée à être utilisée dans du riz - Google Patents

Composition herbicide synergique d'oxadiazon et de clomazone destinée à être utilisée dans du riz Download PDF

Info

Publication number
WO2017078638A1
WO2017078638A1 PCT/TR2016/000156 TR2016000156W WO2017078638A1 WO 2017078638 A1 WO2017078638 A1 WO 2017078638A1 TR 2016000156 W TR2016000156 W TR 2016000156W WO 2017078638 A1 WO2017078638 A1 WO 2017078638A1
Authority
WO
WIPO (PCT)
Prior art keywords
oxadiazon
clomazone
formulation according
formulation
molecules
Prior art date
Application number
PCT/TR2016/000156
Other languages
English (en)
Inventor
Tuncay YILDIZTEKIN
Original Assignee
Entovest Ilaç Kimya Ve Teknoloji̇ Araştirma Merkezi̇ San. Ti̇c.Ltd.Şti̇
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Entovest Ilaç Kimya Ve Teknoloji̇ Araştirma Merkezi̇ San. Ti̇c.Ltd.Şti̇ filed Critical Entovest Ilaç Kimya Ve Teknoloji̇ Araştirma Merkezi̇ San. Ti̇c.Ltd.Şti̇
Publication of WO2017078638A1 publication Critical patent/WO2017078638A1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/82Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms

Definitions

  • the present invention relates to new and synergistic combinations containing oxadiazon and clomazone molecules as active substances developed for ensuring an effective and broad-spectrum weed management through application prior to cultivating rice.
  • Rice is the basic nutritional source for 40% of the world population and a staple food providing 80% of the caloric intake of approximately 2.7 billion people. Cultivated largely in tropical and temperate regions, 90% of rice is grown and consumed by Asian countries.
  • Rice is grown in five different cultivation systems in the world depending on the water regimen. These systems are irrigated rice, rain-fed lowland rice, deep-water rice, upland rice and coastal wetland rice considering the area of cultivation.
  • rice cultivation system is based on continuous irrigation; and rice is cultivated on waterlogged field in this system. The surface of the field is covered in water starting from planting until it is 20 days till the harvest. The height of water is increased gradually depending on the growth of the plant and kept around 15 cm during maximum growth stage.
  • Methods of planting used in irrigated rice cultivation system in the world vary depending on the economic, ecological and social conditions of countries. Such methods are direct seeding in water (by broadcasting, fertilizer distributors and airplanes), drilling in dry land, hill planting and transplanting (by hand or drilling).
  • the underlying problem in weed management is that the herbicides used against the same group of weeds are applied continuously throughout years. Such non-rotation application, in combination with unchanging application method and unchanging application period, results in resistance to herbicides.
  • the present invention is intended to increase the effect derived from the synergy of the single combination of different herbicide molecules in order to eliminate such threat and manage greater number of weeds with a single application.
  • bensulfuron methyl, penoxsulam, bispyribac Na + and other active agents from ALS group were used to manage Cyperus spp, Echinochloa spp, Digitaria sanguinalis (L.)Scop and Diplachne spp. Varying depending on the herbicides, the application period of such active agents is generally post-emergence when the rice has 2-3 to 6-8 leaves.
  • weeds have developed high resistance to FOB, ALS, molecules acting in contact, Auxin hormones and other herbicide active agents acting in contact, and herbicide doses are increased due to such resistance.
  • Such dose increase is possible for three commonly used (3) molecules, which do not cause phytotoxicity in rise. These are cyhalofob butyl, penoxulam and bentazon. Almost all the other molecules result in intolerable phytotoxicity in rice when applied in high doses. Therefore, it is not an alternative or option to increase the dose of molecules that result in phytotoxicity.
  • increasing the dose of the abovementioned cyhalofob butyl, penoxulam and bentazon molecules from among the prior herbicide molecules is not a solution due to the high resistance. Effective weed management is not ensured despite a sevenfold increase in the dose of cyhalofob butyl and fivefold increase in the dose of penoxulam.
  • Oxadiazon is a Protoporphyrinogen oxidase (PPO) inhibitor, which also acts as a chlorophyll inhibitor.
  • PPO Protoporphyrinogen oxidase
  • the chemical name of oxadiazon is 5-tert-butyl-3-(2,4-dichloro-5-isopropoxyphenyl)- l,3,4-oxadiazol-2(3H)-one, and it is a molecule from Oxadiazole family.
  • Oxadiazon is a highly persistent herbicide with a half-life of 3 to 6 months. This herbicide is strongly adsorbed on soil colloids, and it is not easily degradable. Oxadiazon is not considered to be volatile.
  • oxadiazon emulsifiable concentrate (EC), Water-soluble Powder (WP), Granule (G) and others
  • EC emulsifiable concentrate
  • WP Water-soluble Powder
  • G Granule
  • Oxadiazon Emulsifiable Concentrate (EC) formulation caused great damage to the rice in cultivation areas where oxadiazon is used, and intolerable phytotoxicity was observed.
  • EC Oxadiazon Emulsifiable Concentrate
  • the soil was leached at least twice after application of oxadiazon in order to prevent phytotoxicity in rice, in spite of which the death of rice seeds was observed to be at an intolerable level.
  • Oxadiazon was mostly used on lawns and in cultivation of onion, clove and many other agricultural products.
  • Oxadiazon is an herbicide that rather has an effect on seeds.
  • Conventional solid or liquid formulations that contain oxadiazon have been used in rice cultivation, even if not commonly.
  • Oxadiazon doses over 25 g a.i/da prevent germination in rice whereas doses ⁇ 25 g a.i/da result in tolerable phytotoxicity in rise. Even though such dose is tolerable in terms of phytotoxicity, it is extremely unsuccessful in terms of weed management. Therefore, rice farmers cannot use the products that contain oxadiazon unless they are completely out of solutions.
  • oxadiazon is considered independently from phytotoxicity in rice, it is only effective on weeds Echinochloa crus-galli, Cyperus difformis and Alisma plantago- aquatica, for which the effective dose of oxadiazon is > 35 g a.i/da, which results in intolerable phytotoxicity in rice. Due to such phytotoxicity, it is not always possible to apply the effective dose, and oxadiazon is not effective on other weeds that pose a serious problem in paddy fields.
  • Echinochloa oryzoides a species of weed on which oxadiazon has not sufficient effect. Oxadiazon is mostly effective on a couple of broad-leaved weeds whereas it has no effect on narrow-leaved weeds in terms of weed management.
  • the starting dose was increased in order to prevent the amount of oxadiazon, which was lost due to leaching and conditioning, from dropping below the effective dose, and this resulted in economic loss and unnecessary ecological pollutions.
  • high starting doses may prevent germination of rice.
  • high doses of oxadiazon will remain the soil and cause germination of the rice stop completely.
  • the leaching is performed generally after 4 days of applying the herbicide and the planting is performed after conditioning for 6 days.
  • the oxadiazon in soil reduces or completely depletes due to leaching during the conditioning after day 4 or later. This results in germination of new weed seeds in the period of 6 days.
  • only the weed seeds to germinate in the beginning are managed and the weed seeds to emerge later cannot be controlled. In other words, the effect does not last long.
  • Clomazone is a carotenoid biosynthesis inhibition (unknown target), an herbicide that acts by inhibiting chlorophyll, and its chemical name is 2-[2-chlorophenyl)methyl]-4,4-dimethyl-3- isoxazolidinone. It is from the isoxazolidinone family.
  • Clomazone molecule has completely no effect on Cyperus spp, Alisma spp.. Even though it is more effective than oxadiazon on Echinochloa oryzoides, the effectiveness on such weed ends within a short time. Its effect on Echinochloa crus-galli lasts for less than 30 days. Clomazone has never been a solution in rice when used alone. This molecule has a limited use as a part of a program. Clomazone is mostly used in cultivation of soya, canola, tobacco and other agricultural products.
  • Clomazone is not an effective molecule in weed management when used alone and there are only a few weed species controlled by this molecule.
  • clomazone application was tried in two separate techniques.
  • the first technique involves application when rice has 2-3 leaves. In this period, it is desired to use iron-wheeled tractors to apply to herbicide, which significantly damages the rice.
  • the second application technique involves application prior to cultivation.
  • the dose is doubled in this application technique, and such dose increase damages the rice.
  • Clomazone is used alone at 75 g a.i/da dose, which causes severe phytotoxicity and death of rice particularly in sandy soils. Due to such results, use of clomazone molecule is kept to a minimum.
  • Clomazone is effective only on certain narrow-leaved weeds and not effective on some of the narrow-leaved and broad-leaved weeds. Since clomazone has a narrow spectrum, it has always been necessary to use different herbicides, as well.
  • the inventors aim to ensure management of weeds that are resistant to FOB, acetolactate synthase inhibitor (ALS), Auxin hormones and herbicides acting in contact using the invention.
  • ALS acetolactate synthase inhibitor
  • the inventors have also succeeded at managing certain weeds (Echinochloa oryzoides, red rice) that are unmanageable when the two molecules are used separately.
  • the inventors have broadened the narrow spectrums of oxadiazon and clomazone molecules with a dual chlorophyll blockage obtained from the combination in addition to the synergistic effect.
  • the inventors also aim to eliminate all narrow and broad leaved weeds in rice prior to germination of rice.
  • the inventors have intended to eliminate the antagonism problem (elimination of the effect of one molecule by the other) happening in the mixture obtained by putting these two molecules in separate tanks at the disinfestation process, and eliminated such problem though the emulsifiers and solvents used in the formulations.
  • This invention is also included in the scope of the existing application.
  • the inventors have aimed to develop an herbicide that is effective at lower doses without damaging the rice by means of benefiting from the synergy of different molecules for weed management in a safe way in case of rice species that are sensitive to herbicides.
  • the inventors have also aimed to ensure economy by developing an herbicide formulation that may also be effective at lower doses and minimize environmental pollution by minimizing use of chemicals.
  • the inventors have aimed to solve the unsolved weed management problem resulting from resistance by combining certain herbicides from different groups that have the same action mechanism but are effective in different ways.
  • the inventors have aimed to break the resistance by means of applying chlorophyll inhibitor by benefiting from the same action mechanism of the two herbicides and applying the two herbicides separately on the same area.
  • Oxadiazon as Protoporphyrinogen oxidase inhibition (PPO) and clomazone as carotenoid biosynthesis inhibition play a role in prevention of chlorophyll formation.
  • PPO Protoporphyrinogen oxidase inhibition
  • clomazone carotenoid biosynthesis inhibition
  • the inventors have also discovered during the invention that the synergistic action is higher when pendimethalin herbicide molecule is added into the clomazone + oxadiazon combination. Such combination has contributed in management of certain weed species, allowing the inventors to broaden the spectrum and increase the effectiveness. The inventors have also aimed to manage the weeds in the spectrum of both individual molecules at higher levels and permanently through the invention.
  • the inventors have aimed to minimize phytotoxicity in rice by weakening the strong adsorption characteristic of oxadiazon molecule through use of clomazone and decreasing the entrainment rate of clomazone with water by using oxadiazon in order to increase effectiveness in weed management.
  • the inventors have also aimed to develop a formula that eliminates the disadvantages of the herbicides used in weed management in rice cultivation.
  • the inventors aim to develop a product that provides effective weed management and saves on the environment, productivity, costs and workforce by means of developing a formula for use of the combination oxadiazon and clomazone active substances, which has caused no resistance problem yet but are unable to give the desired result when used individually, prior to planting rice and controlling the weeds when they are seeds.
  • the inventors also intend to develop an environmentally safe product by preventing use of generally petroleum-based solvents and emulsifiers that are released from rice parcels into underground and surface waters.
  • the inventors have aimed to manage all weed species that pose a problem in rice cultivation through a single application and increase the yield in rice cultivation areas with an intention of not causing any damage to rice seeds during application.
  • the inventors have aimed to develop a more economical and more ecological new herbicide by decreasing the effective doses of oxadiazon and clomazone molecules when they are used separately through the synergy of the molecules in the combination subject to the invention.
  • the inventors have achieved the targeted objective, and the individual effective doses of each molecule were dropped by more than 30%.
  • the inventors have aimed to ensure effective weed management by lowering the effective doses and solve the problem by applying lower amount of chemicals to the environment. It is another intention of the inventors to solve the weed management problem that individual oxadiazon and clomazone molecules are unable to solve through the synergy derived from the optimum combination of these two molecules.
  • the inventors have intended to decrease the number of disinfestation from 6 to 8 times to once in a season through the invention.
  • the season of application of the invention is pre-cultivation, which is observed to be the easiest and the ideal period to apply the herbicide.
  • the invention has eliminated all the narrow- and broad-leaved weed species located in the field with a single application prior to cultivation. As a result, it was observed that it is a new invention for management of all weed species with a single application prior to cultivation and without entering the cultivated field.
  • the present invention relates to formulation of clomazone and oxadiazon molecules together as a single combination, which are known in the agricultural industry for their weed management effects in rice cultivation areas but unable to manage resistant weeds at the desired level.
  • the invention has eliminated the unsolved weed problem in rice cultivation when these two molecules are used as a combination. Furthermore, these two molecules can be effective on the same weed species while each of the molecules can be effective on different weed species.
  • the weed species on which these two molecules have a joint effect have been managed at a higher level and for a longer duration, and the weed species on which the two molecules have no effect when they are used individually have been managed with a single application thanks to the synergy created.
  • the weed species on which clomazone and oxadiazon have a joint effect can be managed at a higher level and for a longer duration thanks to the synergy of such molecules.
  • the invention is an effective combination that does not damage the rice since it is applied through easy labor and at economical costs in a single dose prior to cultivation and without needing any other herbicide during the time until the harvest.
  • Echinochloa oryzoides 45-65 ⁇ 10 60-90 ; ⁇ 15 j >95 i >52
  • the molecule (A) is found to be effective whereas the molecule (B) has no effect in the weed species number 3.
  • the invention shows great synergy as in the case of the weed species number 3, and the effectiveness was increased and the duration effect was extended with the invention. 4) No synergy is seen in the weed species number 4; however, since other weed species are managed through the applications to be made for this weed species, the invention is especially beneficial since it is easy to use in the industry and provides management of more than one species of weed at a single time.
  • the weed species number 8 is a weed that has great similarities to rice. Therefore, its management in paddy fields is not easy. Whereas the molecules (A) ad (B) have no effect on this weed species when they are used individually, it is observed that the invention that is formulated by the combination of these two molecules effectively manages such unsolvable weed problem.
  • the weed species number 10 is species of weed, which has been the most challenging weed in terms of management in the recent years. Its species is not fully identified yet. Even though the molecules (A) and (B) are not effective on this species when they are used individually, the combination obtained in the invention has surprising level of effect on the species. In the present invention, the strengths of these two molecules have been used to strengthen their weaknesses, and an ideal formula has been developed for effective weed management.
  • the present invention has a broad spectrum, managing all narrow- and broad-leaved weed species such as Echinochloa crus-galli, Cyperus spp., Echinochloa oryzoides, Alisma spp., Digitaria spp., Lindernia spp., Diplachne (leptochloa) spp. red rice, Panicum spp. Echinochloa sp. (Early barnyard grass. A new species yet to be identified in Turkey).
  • narrow- and broad-leaved weed species such as Echinochloa crus-galli, Cyperus spp., Echinochloa oryzoides, Alisma spp., Digitaria spp., Lindernia spp., Diplachne (leptochloa) spp. red rice, Panicum spp. Echinochloa sp. (Early barnyard grass. A
  • the combination of oxadiazon and clomazone molecules subject to the present invention eliminates the need for another herbicide since they are effective on a broad spectrum of weeds thanks to their synergistic action.
  • the synergistic action of the combination of oxadiazon and clomazone molecules subject to the present invention has an effect on a broad spectrum, thus eliminating the need for another herbicide.
  • Another objective of the invention is related to a method of application on the soil prior to cultivation, which aims to develop an easier disinfestation program.
  • the present invention relates to a method of application of a combination of oxadiazon and clomazone molecules in order to eliminate the weeds in paddy fields.
  • the subject method comprises the following steps:
  • the invention should be applied on the soil right after it is harrowed without conditioning.
  • the invention is pulverized onto the surface of the soil using t-jet nozzles to apply the recommended dose.
  • the invention is used with 30-40 liters of water per decare.
  • the device should be calibrated for adjusting the dose.
  • the soil should be irrigated within minimum one (1) day and preferably four (4) days from application of the invention; the seeds should be spread within at least one (1) day, preferably four (4) days and most preferably (6) days from releasing water to the field.
  • Drying periods should not be kept long in order to ensure the invention shows full performance.
  • rice seeds are placed in a container filled with water to break the seed coats.
  • a container filled with water to break the seed coats.
  • Such container may be a sack, wooden box or a plastic container. It is not necessary to break the seed coats.
  • oxadiazon active substance from among the active substances in the invented combination may be applied at a dose between 3.5 g a.i/da and 210 g a.i/da and preferably between 17.5 g a.i/da and 70 g a.i/da on the field.
  • Such doses are 30% less than the individual application doses of oxadiazon in the prior art, proving that the effectiveness of the invention increases depending on the synergy.
  • clomazone active substance in the invented combination is applied at a dose between 3.5 g a.i/da and 280 g a.i/da and preferably between 15 g a.i/da and 95 g a.i/da on the field.
  • the doses range because of the changes resulting from the soil type, weed density and level of resistance, climatologic conditions, species or type of weed and other factors that will affect the effectiveness. Other effective doses to be tested and found depending on the local conditions are also included within the scope.
  • the present invention relates to a combination of oxadiazon + clomazone where the inventors benefit from the synergistic action of the molecules for application of the combination on paddy fields and a method developed for such combination, comprising the following steps:
  • planting used within the scope of the present invention also stands for popped or cracked seeds. In application of the method, it is preferred to soak the seeds; however, any cultivation without performing the germination is included within the scope of the method of application of the invention.
  • the inventors have observed that the seeds of all narrow- and broad- leaved weeds on the field lost their germination strength by or over 95%, for example by 96%, 97%, 98%, 99% or %100, upon application of the combination subject to the invention onto the cultivation field prepared and a surprisingly high effectiveness was obtained in weed management.
  • the individual application doses of each molecule were further decreased by minimum 30%.
  • the paddy field was irrigated within at least 24 hours and preferably 96 hours from the application; and the rice seeds ready to germinate were broadcasted onto the surface of the water within preferably 114 hours from such process.
  • the rice seeds that were soaked in sacks or another suitable container were not affected by the formulation comprising the combination of the two molecules. Therefore, this method, which is very safe for rice, provides high effectiveness in weed management.
  • the composition that contains oxadiazon + clomazone subject to the invention can be used alone.
  • at least one different active agent can be used in addition to the oxadiazon + clomazone active agent within the scope of the present invention.
  • Such other active agent can be mixed in a tank together with the oxadiazon + clomazone composition at the time of application or at another stage of the production of the composition by addition or applied from a different tank at the time of applying the oxadiazon and clomazone combination subject to the invention.
  • Subject additional active agent or agents may be one or more molecules or a combination of molecules selected from the group of HRAC (Herbicide Resistance Action Committee) WSSA (weed science society of America) Group: 5, 6, 7, 9, 10, 11, 12, 13, 14, 15 or benzobicyclon, butachlor, oxadiargyl, pretilachlor, thiobencarb, pentrazamide, quinclorac, paraquat, diquat, quinmerac, Oxyflourfen, amitrole, aclonifen, acifluorfen-Na, bifenox, chlomethoxyfen, fluoroglycofen-ethyl, fomesafen, halosafen, lactofen, azafenidin, carfentrazone- ethyl, sulfentrazone, pyraclonil, profluazol, flufenpyr-ethyl, benzfendizone, butafenacil, pentoxazone, chlor
  • the invention relates to formulation of oxadiazon and clomazone molecules together.
  • the invention may comprise oxadiazon and clomazone in the same formulation types or together with different formulation types.
  • oxadiazon and clomazone may either be formulated together in a single type of formulation or be brought together after they are prepared in different formulation types. If prepared in different formulation types, these formulations may be applied separately or simultaneously or consecutively or at different times.
  • the invention may be a single formulation that contains the same formulation of each molecule comprising the combination or a multiple formulation that contains different formulations of each molecule comprising the combination.
  • the formulation of the invention will be Emulsifiable Concentrate (EC) if both Oxadiazone and Clomazone are in Emulsifiable Concentrate (EC) form.
  • the single formulation type of the invention will be one from Emulsifiable concentrate (EC) oil-in- water or water-in-oil emulsion (EW), suspension concentrate (SC), micro-emulsion concentrate
  • EC Emulsifiable concentrate
  • EW oil-in- water or water-in-oil emulsion
  • SC suspension concentrate
  • SL water dispersible granule
  • WDG water dispersible granule
  • SG soluble granule
  • WP wettable powder
  • D dust
  • G granule
  • E. Gr effervescent granule
  • Tb tablet
  • WSP water soluble package
  • the single formulation type preferred for the invention will be capsule suspension (CS).
  • the formulation of the invention may include without limitation all of the other single formulation types mentioned above / existing in the state of the art.
  • the formulation of the invention will be ZE when Oxadiazon is in Capsule Suspension (CS) form and Clomazone is in Emulsifiable Concentrate (EC) form.
  • the multiple formulation type of the invention may be one from ZC (CS and SC), ZE (CS and EC or CS and SE), ZW (CS and EW), SE (SC and EC or SC and EW) and all the other multiple (multicharacter) formulations.
  • any of the molecules in the combination may be any of the single formulations.
  • the single formulations mentioned above will be individually used as oxadiazon or clomazone formulation type.
  • the formulation type preferred in the invention will be ZE.
  • the formulation of the invention may include without limitation all of the other multiple formulation types mentioned above / existing in the state of the art.
  • the ratio of molecules will be 4.8 units of Clomazone and 0.12 to 6.0 units of oxadiazon.
  • the preferred range or ratio is 4.8 units of clomazone and 2 units of oxadiazon.
  • the unit of oxadiazon to be used can be 0.12, 0.16, 0.18, 0.20, 0.22, 0.24, 0.30, 0.35, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.2, 2.4, 2.6, 2.8, 3.0, 3.2, 3.4, 3.6, 3.8, 4.0, 4.2, 4.4, 4.6, 4.8 or 6.0 or any other unit within the range defined.
  • the invention can be formulated with not only the preferred ratio but also 4.8 units of clomazone and 0.12 to 6.0 units of oxadiazon as indicated above without limitation any limitation.
  • the units of oxadiazon range because of the variables such as the soil type, climatological conditions, weed species, weed density and resistance.
  • Emulsifier mix 0.001-35 0.1-26
  • the amount of oxadiazon used is 0.001-60%, preferably 5-50%, most preferably 10-45%) by weight.
  • the amount of clomazone used is 0.0024- 96%, preferably 0.5-70%), most preferably 1-60% by weight.
  • chlorophyll inhibitor or photosynthesis inhibitor herbicides in addition to WSSA Group: 5, 6, 1, 9, 10, 1 1, 12, 13, 14, 15 are included within the scope of the invention, and one or more selected therefrom can be used as an alternative to either one of oxadiazon or clomazone.
  • the amount of such molecules used can be 0.001-60%) by weight and 0.0024-96%) by weight when they are used as an alternative to oxadiazon and clomazone, respectively.
  • Use of one or more of such alternative molecules as an addition to the clomazone and oxadiazon composition (the invention) is included within the scope of the invention.
  • the total amount of additional molecule or molecules used shall be 0.001-72%) by weight.
  • the emulsifier mix mentioned in the table may be either combination of multiple emulsifiers or an individual emulsifier. Such emulsifiers may be from ionic, anionic and nonionic groups or a combination of such groups.
  • the emulsifier that can be used in the product may be one or a combination by different ratios of more selected from the group of amine ethoxylates, EO/PO block polymers, ether sulfates, saturated alcohol alkoxylates, saturated alcohol ethoxylates, sorbitan ester ethoxylates, tributylphenol ethoxylates, phosphate esters, tristyrylphenol ethoxylates, sulfonation products, polycondensation products, nonylphenol ethoxylates, alkyl benzene sulfonates, castor oil ethoxylates, EO/PO alkoxylation products, saturated alcohol ethoxylates, olein
  • Preferred emulsifiers used in the formulation are tristyrylphenol ethoxylates and nonylphenol ethoxylates.
  • the preferred ratio of the emulsifier mix is 1 : 1 by weight.
  • the amount of emulsifier mix used is 0.001- 35%, preferably 0.01-30% and most preferably 0.1-26% by weight.
  • the solvent mentioned in the Table is the liquid medium in which the Oxadiazon active agent, which is in a solid state under normal conditions, is solved. Since the invention is performed with interfacial surface polymerization, it can only be formulated using non-water-soluble solvents.
  • hydrocarbons such as xylene, benzene, toluene, cyclohexane, solvesso 100, solvesso 150, solvesso 200 and exxsol series in addition to herbal oils derived from oily seeds and ethyl and methyl esters thereof and herbal terpenes are also included within the scope of the patent.
  • a combination of more than one solvent can be used instead of a single solvent.
  • the preferred solvent used in the formulation is xylene in the amount less than that of the conventional technical formulations.
  • the amount of solvent used is 1-60%, preferably 3-50% and most preferably 5-34% by weight.
  • the antimicrobial preservative mentioned in the Table is butylated hydroxytoluene (BHT) and butylated hydroxyanisole (BHA).
  • the amount of antimicrobial preservative used is 0.0001-59%, preferably 0.005-50% and most preferably 0.1-27% by weight.
  • the antifreeze indicated in the table is glycol derivative additives known in water-based pesticide formulations for their antifreeze properties at low temperatures.
  • Such additives are ethylene glycol, monopropylene glycol, dipropylene glycol, diethylene glycol and glycerin.
  • the preferred additive used in the formulation is monopropylene glycol.
  • the amount of antifoam used is 0.001-60%, preferably 0.05-50% and most preferably 0.1-32% by weight.
  • the reactant 1 indicated in Table is organic compounds containing isocyanate functional group.
  • the function of the reactant 1 in the formulation is to create a polyuria capsule wall upon being polymerized in the emulsion droplets-water interface with the help of catalyzer solution after emulsification of the Oxadiazon prepared with the oil phase.
  • the reactant 1 may be methyl isocyanate, methylene diphenyl diisocyanate (MDI), hexamethylene diisocyanate (HDI), toluene diisocyanate (TDI), naphthalene diisocyanate (NDI), methylene bicyclohexyl isocyanate (HMDI) or isoprene diisocyanate (IPDI).
  • the amount of the Reactant 1 used is 0.001- 70%, preferably 0.05-50% and most preferably 0.02-25% by weight.
  • the reactant 2 and reactant 3 indicated in the Table are amines that create a polyuria capsule shell after they enter into polymerization reaction with the reactant 1 that is the isocyanate group.
  • the reactant 2 and reactant 3 are premixed together in water to prepare the catalyzer solution.
  • the catalyzer solution prepared is slowly added onto the Oxadiazon oil base emulsified in water to start the reaction to create the polyuria capsule shell.
  • the amines used in the synthesis of the polyuria capsule shell may be from primary, secondary or tertiary amine groups.
  • the said reactant 2 and reactant 3 includes ethylamine, ethylene diamine, diethylene triamine, triethylene tetramine, dimethylamine, trimethylamine, diethylamine, diisopropylamine, dimethylaminopropylamine, triisopropylamine .
  • the amount of the Reactant 2 used is 0.001- 60%, preferably 0.05-50% and most preferably 0.21-28% by weight.
  • the amount of the Reactant 3 used is 0.001- 70%, preferably 0.05-50% and most preferably 0.15-19% by weight.
  • the stabilizer indicated in the Table is the additives that may be used to adjust the viscosity of the formulation after the polymerization reaction ends. These include xanthan gum, guar gum, gum Arabic, carboxymethyl cellulose, methylcellulose, hydroxypropyl cellulose. The preferred stabilizer used in the formulation is xanthan gum.
  • the amount of the stabilizer used is 0.0001- 30%, preferably 0.05-20% and most preferably 0.02-12% by weight.
  • the carrier is used in the amount that will take up the formulation to 100% by weight.
  • the preferred carrier indicated in the table is water.
  • Antifoam and antimicrobial preservative are the additives that are commonly used in pesticide formulations.
  • the preferred antifoam used in the formulation is silicone-based antifoam.
  • composition of the invention indicated in the Table above is only given for one of the combinations included in the scope of the invention. Production of different ratios (% content) and different formulations using all familiar production techniques is included in the scope of the invention without any limitation.
  • the invention is intended for using the molecules in lower doses than that of their individual uses due to their synergistic action.
  • the invention is the combination of oxadiazon and clomazone, and such two molecules are used within a single combination.
  • a powerful synergistic action was obtained from such discovery, and weed management was accomplished at a lower dose than individual use of the two molecules. This has allowed for using lower doses than the effective doses of the two molecules when they are used individually, and the new doses derived from the synergy have not caused phytotoxicity in rice. While lower dose is sufficient for weed management, corresponding to an amount of herbicide that is within the safe limits for rice.
  • oxadiazon molecule When oxadiazon molecule is used individually at dose 30-100 g a.i/da and clomazone molecule is used individually at dose 45-150 g a.i/da, they are effective allowing for weed management in their spectrum.
  • the doses range due to weed type, soil structure and climatologic conditions. Even though such doses of both molecules are effective on certain weed species, they have a limited use since they cause phytotoxicity higher than the damage threshold in rice.
  • the present invention lowers the doses of these molecules separately thanks to their synergy, resulting in no phytotoxicity in rice. In the combination subject to the invention, the doses are lowered by minimum 30% for both molecules. >92% success has been obtained in weed management at such lower doses thanks to the synergy. Furthermore, the phytotoxicity in rice has been eliminated as a result of the lowered doses.
  • Clomazone molecule that moves fast in sandy soil causes severe phytotoxicity in rice.
  • oxadiazon molecule is strongly adsorbed on all kinds of soil with a persistence of minimum 3-6 months in soil.
  • the present invention has decreased the downward vertical movement rate of clomazone molecule in soil. Clomazone stays on the desired layer of the soil thanks to its binding to oxadiazon, which is strongly adsorbed on soil colloids.
  • the invention decreases the downward vertical movement rate of clomazone and balances the persistency of oxadiazon on the surface of soil by minimizing it.
  • joint use of oxadiazon that is horizontally adsorbed on soil longer than desired and clomazone that has a vertical movement rate faster than desired has brought a balance; thus, the invention both eliminates phytotoxicity and provides effective weed management by maintaining the effective dose in the target area.
  • the balanced maintenance of the invention in the target area is achieved by the combination of the two molecules, which has brought an effective solution to weed management particularly in sandy soils.
  • the ratio of molecules will be 4.8 units of Clomazone and 0.12 to 6.0 units of oxadiazon.
  • the preferred range or ratio is 4.8 units of clomazone and + 2 units of oxadiazon (E.g. 48% clomazone + 20% oxadiazon).
  • ratios are for general applications.
  • the ratios may change depending on the field, geographical conditions, climatological differences, weed species and densities.
  • the invention has ensured obtaining a high synergy for the effectiveness of oxadiazon and clomazone with such ratios at lower doses.
  • the present invention has been designed to eliminate the antagonism in tank mixtures of these two molecules. Coating of both molecules with special adjuvants and polymer coats has prevented molecules from interacting.

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)

Abstract

La présente invention concerne des combinaisons novatrices et synergiques contenant des molécules d'oxadiazon et de clomazone en tant qu'agents actifs mis au point pour assurer la lutte efficace et sur un large spectre des mauvaises herbes, par application, avant de cultiver le riz.
PCT/TR2016/000156 2015-11-06 2016-11-07 Composition herbicide synergique d'oxadiazon et de clomazone destinée à être utilisée dans du riz WO2017078638A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
TR201513945 2015-11-06
TR2015/13945 2015-11-06

Publications (1)

Publication Number Publication Date
WO2017078638A1 true WO2017078638A1 (fr) 2017-05-11

Family

ID=57868314

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/TR2016/000156 WO2017078638A1 (fr) 2015-11-06 2016-11-07 Composition herbicide synergique d'oxadiazon et de clomazone destinée à être utilisée dans du riz

Country Status (1)

Country Link
WO (1) WO2017078638A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020233646A1 (fr) * 2019-05-21 2020-11-26 江苏龙灯化学有限公司 Composition herbicide contenant des microcapsules, procédé de préparation de celle-ci et utilisation de celle-ci
CN117397695A (zh) * 2023-12-14 2024-01-16 济南兄弟作物科学有限公司 一种用于调节水稻催枯的敌草快复合除草剂及其制备方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020004457A1 (en) * 1998-11-10 2002-01-10 Nevill David John Herbicidal composition
CN103858895B (zh) * 2014-03-31 2015-11-04 济南先达化工科技有限公司 一种水稻田增效除草组合物
CN105707086A (zh) * 2016-04-13 2016-06-29 安徽美兰农业发展股份有限公司 一种异噁草松和噁草酮复配乳油及其制备方法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020004457A1 (en) * 1998-11-10 2002-01-10 Nevill David John Herbicidal composition
CN103858895B (zh) * 2014-03-31 2015-11-04 济南先达化工科技有限公司 一种水稻田增效除草组合物
CN105707086A (zh) * 2016-04-13 2016-06-29 安徽美兰农业发展股份有限公司 一种异噁草松和噁草酮复配乳油及其制备方法

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
HÜSREV MENNAN ET AL: "Herbicide Resistant Weed Management Program in Rice", TURKEY 6TH PLANT PROTECTION CONGRESS WITH INTERNATIONAL PARTICIPATION, 8 September 2016 (2016-09-08), http://www.academia.edu/28931794/Herbicide_Resistant_Weed_Management_Program_in_Rice, pages 1, XP055351100 *
J. CAVERO ET AL: "Selectivity and weed control efficacy of some herbicides applied to sprinkler irrigated rice (Oryza sativa L.)", SPANISH JOURNAL OF AGRICULTURAL RESEARCH, vol. 9, no. 2, 16 May 2011 (2011-05-16), ES, pages 597 - 605, XP055350926, ISSN: 1695-971X, DOI: 10.5424/sjar/20110902-159-10 *
MARCO SOBRERO: "Bayer Crop Science Italia - Punto Riso: Con quali prodotti posso utilizzare l'oxadiazon?", WWW.RISOITALIANO.EU, 18 May 2015 (2015-05-18), XP055351082, Retrieved from the Internet <URL:http://www.cropscience.bayer.it/it-IT/News/2015/05/punto-riso-con-quali-prodotti-posso-usare-oxadiazon.aspx> [retrieved on 20170302] *
P MONTEMURRO ET AL: "PRIMI RISULTATI DI PROVE DI DISERBO CHIMICO CON CLOMAZONE NELLA COLTURA DEL FINOCCHIO (FOENICULUM VULGARE)", ATTI GIORNATE FITOPATOLOGICHE, vol. 1, 1 January 2010 (2010-01-01), pages 455 - 460, XP055350945, DOI: http://www.giornatefitopatologiche.it/it/download/23?tok=20170302105207YGZA3P *
RENATO DANIELIS: "Diserbo soia 2010", 10 February 2011 (2011-02-10), pages 1 - 18, XP055350969, Retrieved from the Internet <URL:http://www.ersa.fvg.it/informativa/atti-dei-convegni-ersa/atti-del-convegno-su-mais-e-soia-del-10-febbraio-2011/Presentazione Diserbo soia 2010.pdf> [retrieved on 20170302] *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020233646A1 (fr) * 2019-05-21 2020-11-26 江苏龙灯化学有限公司 Composition herbicide contenant des microcapsules, procédé de préparation de celle-ci et utilisation de celle-ci
CN117397695A (zh) * 2023-12-14 2024-01-16 济南兄弟作物科学有限公司 一种用于调节水稻催枯的敌草快复合除草剂及其制备方法
CN117397695B (zh) * 2023-12-14 2024-03-29 济南兄弟作物科学有限公司 一种用于调节水稻催枯的敌草快复合除草剂及其制备方法

Similar Documents

Publication Publication Date Title
US20050130842A1 (en) Biocidally active combination for agricultural applications
JP2005529943A (ja) 除草用組成物
JP2012017319A (ja) 除草組成物
CN100356849C (zh) 旱地复配除草剂
CN108024538A (zh) 协同杀昆虫组合物
WO2017078638A1 (fr) Composition herbicide synergique d&#39;oxadiazon et de clomazone destinée à être utilisée dans du riz
CN101803598B (zh) 低浓度氟虫双酰胺悬浮剂
CN104351216B (zh) 一种包括氯酯磺草胺与烯草酮的混合除草剂及制备方法
CN108124862A (zh) 一种杀螟药剂的增效助剂及其使用方法
CN106719679A (zh) 一种含氯氟吡啶酯的除草组合物
CN105532657B (zh) 一种用于单子叶作物的除草组合物及其用途
CN103371176A (zh) 一种含草铵膦的农药组合物
WO2017026957A1 (fr) Formulation d&#39;oxadiazone sans phytotoxicité pour le riz
JP2016502548A (ja) 抵抗性有害植物を防除する方法
UA121771C2 (uk) Ад&#39;ювант для агрохімікатів
CN102461527A (zh) 一种含双草醚和禾草丹的混合除草组合物
JP5901544B2 (ja) 殺虫組成物及び昆虫駆除方法
BR102019019008A2 (pt) Composições de ciclohexanodiona oxima estabilizadas
CN104304259B (zh) 一种包括吡氟酰草胺与胺唑草酮的混合除草剂及制备方法
SK93193A3 (en) Herbicidal composition
CN107136092A (zh) 一种除草剂组合物
AU2020205488B2 (en) A liquid anti-pathogenic agricultural composition
Ali Compatibility and Synergism of Certain Insecticides for Control of Thrips (Thripstabacia) on Onion (Allium cepa L.) Plants in the Field
CN102461515B (zh) 一种含双草醚和扑草净的混合除草组合物
BRPI0707740A2 (pt) uso de um fungicida, e, mÉtodo para a produÇço de uma planta de safra tendo nÍveis aumentados de polifenàis

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 16829331

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 16829331

Country of ref document: EP

Kind code of ref document: A1