Pesticidal composition with controlled release

The pesticide composition with cyclopyrimorate, benzobicyclon, triafamone, tripolyphosphate, alkylbenzenesulfonate, and polycarboxylate addresses initial elution control and sustained release, enhancing herbicidal efficacy and reducing phytotoxicity.

JP2025121404APending Publication Date: 2025-08-19MITSUI CHEM AGRO INC
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Patent Information

Application Number
JP2025017803
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Priority Date
2024-02-06
Filing Date
2025-02-05
Publication Date
2025-08-19

AI Technical Summary

Technical Problem

Existing pesticide compositions face challenges in controlling the initial elution of active ingredients, necessitating a formulation that suppresses initial release while ensuring sustained elution over a specified period to maintain efficacy.

Method used

A pesticide composition comprising cyclopyrimorate, benzobicyclon, triafamone, tripolyphosphate, alkylbenzenesulfonate, and polycarboxylate, which collectively control the elution behavior of cyclopyrimorate, enhancing its dissolution characteristics.

Benefits of technology

The composition achieves controlled elution of cyclopyrimorate, ensuring effective herbicidal action over an extended period with reduced phytotoxicity, particularly in rice plants.

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Abstract

To provide a pesticidal composition comprising cyclopyrimorate and an additional pesticidal active component, which shows superior elution characteristics of cyclopyrimorate.SOLUTION: A pesticidal composition contains (1) cyclopyrimorate, (2) benzobicyclon, (3) triafamone, (4) tripolyphosphate, (5) alkylbenzene sulfonate, and (6) polycarboxylate.SELECTED DRAWING: None
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Description

[Technical Field]

[0001] The present invention relates to a pesticide composition in which the release of cyclopyrimorate is controlled. [Background technology]

[0002] Patent Document 1 discloses that cyclopirimorate is an effective pesticide active ingredient that induces bleaching in paddy broadleaf weeds and sedge weeds of the Cyperaceae family, including arrowhead weed, Monochoria kanazawai, and Scirpus bulrush, causing their death. Because cyclopirimorate has a novel HST inhibitory mechanism, it is also effective against resistant weeds. Furthermore, it is compatible with 4-HPPD inhibitors such as pyrazolate, which also have bleaching effects, and combining them produces a dramatic synergistic effect. Furthermore, the combination of cyclopirimorate and pyrazolate is known to have a broader herbicidal spectrum but is highly safe, causing no phytotoxicity to paddy rice.

[0003] Known means for controlling the release of pesticide active ingredients include, for example, means for processing the pesticide active ingredient itself, such as microencapsulation as described in Patent Document 2, and sustained-release bulk powder as described in Patent Document 3, and means for structurally endowing the pesticide with release control properties, such as hydrophobic substance-coated granules as described in Patent Document 4, and hydrophobic substance-containing granules as described in Patent Document 5. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Japanese Patent Application Laid-Open No. 2011-190198 [Patent Document 2] Japanese Patent Application Laid-Open No. 2004-103481 [Patent Document 3] Japanese Patent Application Publication No. 8-92497 [Patent Document 4] Japanese Patent Application Publication No. 10-25202 [Patent Document 5] Japanese Patent Application Laid-Open No. 2000-26206 Summary of the Invention [Problem to be solved by the invention]

[0005] There is a need for a technical means that exhibits elution behavior that suppresses the initial elution of the pesticide composition at the time of treatment, while eluting a certain amount or more of the active ingredient over a specified period that can ensure the efficacy of the pesticide active ingredient. Therefore, an object of the present invention is to provide an agricultural chemical composition containing cyclopirimorate and other agriculturally active ingredients, which exhibits excellent dissolution behavior of cyclopirimorate. [Means for solving the problem]

[0006] As a result of intensive research aimed at solving the above-mentioned problems, the present inventors have surprisingly found that the above-mentioned problems can be solved by using a tripolyphosphate, an alkylbenzene sulfonate, and a polycarboxylate, and have thus completed the present invention.

[0007] That is, the present invention is as follows. [1] A pesticide composition comprising (1) cyclopyrimorate, (2) benzobicyclon, (3) triafamone, (4) tripolyphosphate, (5) alkylbenzenesulfonate, and (6) polycarboxylate. [2] The pesticide composition according to [1], wherein the polycarboxylate is a potassium polycarboxylate. [3] The pesticide composition according to [1] or [2], wherein the tripolyphosphate is sodium tripolyphosphate or potassium tripolyphosphate. [4] The pesticide composition according to [1] or [2], wherein the alkylbenzene sulfonate is a sodium alkylbenzene sulfonate. [5] The pesticide composition according to [3], wherein the alkylbenzene sulfonate is a sodium alkylbenzene sulfonate. [Effects of the Invention]

[0008] According to the present invention, it is possible to provide an agrochemical composition containing cyclopyrimorate, benzobicyclon, and triafamone, which exhibits excellent elution behavior of cyclopyrimorate. DETAILED DESCRIPTION OF THE INVENTION

[0009] Hereinafter, an embodiment of the present invention (hereinafter referred to as "the present embodiment") will be described, but the scope of the present invention should not be interpreted as being limited to the following embodiment.

[0010] The pesticide composition of the present invention comprises: (1) Cyclopirimorate, (2) benzobicyclon, and (3) Contains triafamone, and further: (4) tripolyphosphate, (5) alkylbenzene sulfonates, and (6) Contains polycarboxylate.

[0011] The pesticide composition of the present embodiment contains (1) cyclopyrimorate, (2) benzobicyclon, and (3) triafamone as pesticide active ingredients. The contents of the three pesticidal active ingredients in the pesticide composition in this embodiment are not particularly limited, but as an example, based on the mass of the pesticide composition, are (1) cyclopyrimorate at 4 mass%, (2) benzobicyclone at 3 mass%, and (3) triafamone at 1 mass%. Based on the mass of the pesticide composition, the contents of (1) cyclopyrimorate, (2) benzobicyclon, and (3) triafamone are, for example, the registered contents, respectively: Cyclopyrimorate: 3.6 to 4.4% by mass Benzobicyclon: 2.7 to 3.3% by mass Triafamone: 0.75 to 1.25% by mass may be. In the present embodiment, the term "based on the mass of the pesticide composition" refers to the case where the pesticide composition is taken as 100% by mass, and the same applies hereinafter in this specification.

[0012] The pesticide composition of the present embodiment may contain "other pesticidal active ingredients" other than cyclopyrimorate, benzobicyclon, and triafamone. The pesticide composition may contain one type of "other pesticidal active ingredients," or may contain two or more types of "other pesticidal active ingredients."

[0013] The "other pesticide active ingredient" is not particularly limited, but examples thereof include bleaching-type herbicidal compounds or salts thereof, and acetolactate synthase (ALS)-inhibiting herbicidal compounds or salts thereof.

[0014] Bleaching herbicidal compounds are herbicides that bleach weeds and cause them to wither and die. Examples of bleaching herbicidal compounds include, but are not limited to, pyrazole herbicidal compounds and triketone herbicidal compounds.

[0015] Examples of pyrazole herbicidal compounds include, but are not limited to, pyrazolate, pyrazoxyfen, and benzofenap. Examples of the triketone herbicidal compounds include, but are not limited to, mesotrione, sulcotrione, tefuryltrione, fenquinotrione, and bicyclopyrone.

[0016] Acetolactate synthase (ALS)-inhibiting herbicidal compounds are herbicides that inhibit ALS, thereby inhibiting the synthesis of essential amino acids valine, leucine, and isoleucine, thereby killing weeds. Examples of ALS-inhibiting herbicidal compounds include, but are not limited to, sulfonylurea herbicidal compounds, pyrimidinylsalicylic acid herbicidal compounds, and triazolopyrimidine herbicidal compounds.

[0017] The sulfonylurea herbicidal compound is not particularly limited, but examples thereof include azimsulfuron, bensulfuron methyl, cyclosulfamuron, halosulfuron methyl, ethoxysulfuron, imazosulfuron, pyrazosulfuron ethyl, chlorimuron ethyl, cinosulfuron, metsulfuron methyl, flucetosulfuron, propyrisulfuron, and metazosulfuron. The pyrimidinylsalicylic acid herbicidal compound is not particularly limited, but examples thereof include bispyribac, pyribenzoxim, pyriftalid, pyriminobac-methyl, and pyrimisulfan. The triazolopyrimidine herbicidal compound is not particularly limited, but examples thereof include penoxsulam.

[0018] Examples of "other pesticide active ingredients" include bleaching herbicidal compounds or their salts, and acetolactate synthase (ALS) inhibitor herbicidal compounds or their salts, as well as triazine herbicidal compounds, including, but not limited to, dimethametryn and simetryn.

[0019] The content of the "other pesticidal active ingredient" contained in the pesticide composition of this embodiment may be any amount that allows a suspension formulation to be formulated in the production process of the pesticide composition of this embodiment, and is usually 0.1 to 30 mass% based on the mass of the pesticide composition.

[0020] In order to expand the spectrum of a single pesticide composition, there is a need for a formulation that can reduce the risk of phytotoxicity, particularly in rice plants in the early growth stages, even when the pesticidal active ingredients are further increased. The pesticidal composition of this embodiment not only contains (1) cyclopyrimorate, (2) benzobicyclon, and (3) triafamone as pesticidal active ingredients, but also has the advantage of being able to reduce the risk of phytotoxicity in cases where other pesticidal active ingredients are contained.

[0021] The pesticide composition of the present embodiment contains, in addition to the pesticidal active ingredient, (4) a tripolyphosphate, (5) an alkylbenzene sulfonate, and (6) a polycarboxylate. Tripolyphosphates are generally used for the purposes of improving the disintegration of solid formulations and the elution of pesticide active ingredients in water. In this embodiment, tripolyphosphate is used to exhibit excellent elution behavior of cyclopyrimorate. The tripolyphosphate salt is not particularly limited, and examples thereof include alkali metal salts such as sodium salts and potassium salts. Among them, the tripolyphosphate salt is preferably sodium tripolyphosphate salt or potassium tripolyphosphate salt, and more preferably sodium tripolyphosphate salt. The tripolyphosphates may be used alone or in combination of two or more. The content of tripolyphosphate in the pesticide composition in this embodiment is not particularly limited, but is usually 1 to 6 mass %, and preferably 2 to 5 mass %, based on the mass of the pesticide composition.

[0022] In this embodiment, the pesticide composition contains (4) tripolyphosphate, (5) alkylbenzenesulfonate, and (6) polycarboxylate, and thereby exhibits excellent elution behavior of cyclopyrimorate. Among these, alkylbenzenesulfonate is used for the purpose of favorably controlling the elution behavior of cyclopyrimorate in combination with tripolyphosphate and polycarboxylate. The alkylbenzene sulfonate may be used alone or as a mixture containing an alkylbenzene sulfonate.

[0023] The alkylbenzene sulfonate is not particularly limited, but examples thereof include dodecylbenzene sulfonate, polyoxyalkylene allyl phenyl ether sulfate ammonium salt·alkylbenzene sulfonate, and polyoxyethylene alkyl ether·sorbitan fatty acid ether·alkylbenzene sulfonate. The alkylbenzenesulfonate salt is not particularly limited, but examples thereof include alkali metal salts such as sodium salts and potassium salts, and ammonium salts, etc. Among these, sodium alkylbenzenesulfonate salts are preferred. The alkylbenzene sulfonates may be used alone or in combination of two or more. The content of alkylbenzenesulfonate in the pesticide composition of the present embodiment is not particularly limited, but is usually 1 to 6 mass %, and preferably 1 to 3 mass %, based on the mass of the pesticide composition.

[0024] In this embodiment, the polycarboxylate is used for the purpose of improving the elution of the pesticide active ingredient in water. The polycarboxylate is not particularly limited, and examples thereof include alkali metal salts such as sodium salts and potassium salts, etc. Among these, the polycarboxylate is preferably a potassium polycarboxylate. The polycarboxylates may be used alone or in combination of two or more. The content of the polycarboxylate in the pesticide composition in this embodiment is not particularly limited, but is usually 1 to 6 mass %, and preferably 1 to 3 wt %, based on the mass of the pesticide composition.

[0025] The pesticide composition of the present embodiment may contain "other components" as components other than the above (1) to (6). The "other components" may be components known to be contained in pesticide compositions, and include, but are not limited to, surfactants, binders, disintegrants, stabilizers, pH adjusters, antibacterial and antifungal agents (preservatives), thickeners, antifoaming agents, wetting agents, colorants, solvents, oils, carriers, etc.

[0026] As the surfactant, surfactants that are generally used for the purposes of emulsifying, dispersing, spreading and / or wetting pesticide compositions can be used. The surfactant is not particularly limited, but examples thereof include nonionic surfactants, anionic surfactants, cationic surfactants, and zwitterionic surfactants.

[0027] The anionic surfactant is not particularly limited, and examples thereof include alkali metal salts, alkaline earth metal salts, ammonium salts, and various amine salts of α-olefin sulfonic acid, α-sulfofatty acid, naphthalene sulfonic acid, naphthalene sulfonic acid condensates, phenol sulfonic acid, alkyl naphthalene sulfonic acid, alkenyl sulfonic acid, alkyl sulfonic acid, alkylaryl sulfonic acid, polystyrene sulfonic acid, polyacrylic acid, polycarboxylic acid, condensates of styrene sulfonic acid and carboxylic acid, polyoxyethylene alkyl ether sulfates, polyoxyethylene alkylaryl ether sulfates, alkyl or dialkyl sulfosuccinates, higher fatty acids, polyoxyethylene alkyl ether phosphates, polyoxyethylene alkylaryl ether phosphates, polyoxyethylene arylaryl ether phosphates, and alkali metal salts, alkaline earth metal salts, ammonium salts, and various amine salts of these phosphate esters, polyacrylic acid salts, sodium salts of alkyl naphthalene sulfonic acid formalin condensates, alkyl benzene sulfonates, alkyl sulfate ester salts, and (di)alkyl sulfosuccinates.

[0028] The nonionic surfactant is not particularly limited, but examples thereof include polyoxyethylene polycyclic phenyl ethers, polyoxyethylene alkyl ethers, polyoxyethylene alkylaryl ethers, polyoxyethylene arylaryl ethers, polyoxyethylene alkyl esters, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, copolymers of polyoxyethylene and polyoxypropylene, higher fatty acid alkanolamides, and acetylene diols. The HLB value of the nonionic surfactant is preferably within the range of 9 to 13 in terms of solubility in water and wetting action.

[0029] The cationic surfactant is not particularly limited, but examples thereof include alkylamine salts, quaternary ammonium salts, pyridinium salts, and amine oxides.

[0030] The zwitterionic surfactant is not particularly limited, but examples thereof include amino acid type and betaine type surfactants.

[0031] The surfactant is preferably an anionic surfactant or a nonionic surfactant.

[0032] The binder is not particularly limited, but examples thereof include sodium alginate, polyvinyl alcohol, gum arabic, and sodium carboxymethylcellulose (hereinafter referred to as "sodium CMC").

[0033] The disintegrant is not particularly limited, but examples thereof include CMC sodium and croscarmellose sodium.

[0034] Examples of the stabilizer include hindered phenol-based antioxidants, and benzotriazole-based and hindered amine-based ultraviolet absorbers.

[0035] The pH adjuster is not particularly limited, but examples thereof include phosphoric acid, acetic acid, and sodium hydroxide.

[0036] The antibacterial and antifungal agent (antiseptic) is not particularly limited, but examples thereof include 1,2-benzisothiazolin-3-one.

[0037] The thickener is not particularly limited, but examples thereof include xanthan gum, guar gum, CMC sodium, gum arabic, polyvinyl alcohol, and montmorillonite.

[0038] The antifoaming agent is not particularly limited, but examples thereof include silicone compounds.

[0039] The wetting agent is not particularly limited, but examples thereof include the above-mentioned anionic surfactants and nonionic surfactants.

[0040] The colorant is not particularly limited as long as it is a colorant that is usually used in agricultural chemical compositions, and examples thereof include pigments. The dye is not particularly limited, but examples thereof include brilliant blue FCF, cyanine green G, and eriogreen G.

[0041] The solvents and oils are not particularly limited, but examples thereof include ethanol, isopropanol, 1-butanol, acetic acid, acetic anhydride, acetophenone, methyl oleate, coconut oil, rapeseed oil, soybean oil, castor oil, linseed oil, paraffin oil, kerosene, higher alcohols, cyclohexanol, γ-butyrolactone, fatty acid methyl esters, methylpyrrolidone, dimethyl sulfoxide, chlorobenzene, chlorotoluene, dichloroaniline, normal paraffin, cyclohexanone, acetonitrile, kerosene, machine oil, and aromatic solvents.

[0042] The carrier is not particularly limited, and examples thereof include mineral fine powders commonly used as pesticide carriers, such as bentonite, talc, clay, diatomaceous earth, amorphous silicon dioxide, calcium carbonate, and magnesium carbonate, as well as resin powders such as vinyl chloride, chlorinated polyethylene, and chlorinated polypropylene, sugars such as glucose, sugar, and lactose, organic substances such as carboxymethylcellulose and its salts, starch and its derivatives, microcrystalline cellulose, wood flour, rice bran, bran, rice husk powder, coffee bean powder, cellulose powder, and licorice powder, water-soluble inorganic salts such as sodium sulfate, ammonium sulfate, and potassium chloride, and urea. The content of the carrier in the pesticide composition in this embodiment varies depending on the type of carrier, but is usually 30 to 90 mass %, and preferably 50 to 90 mass %, based on the mass of the pesticide composition.

[0043] The content of the "other components" in the pesticide composition in this embodiment may be set so that the content of each of the components (1) to (6) above and the content of other pesticidal active ingredients totals 100% by mass, based on the mass of the pesticide composition.

[0044] A method for producing the pesticide composition of this embodiment will be described. Note that the following description is merely an example and is not intended to limit the scope of the present invention. The method for producing the pesticide composition in this embodiment includes: (a) wet-milling a mixture containing an agricultural chemical active ingredient (e.g., (1) cyclopyrimorate and (3) triafamone), an activator, and water, and optionally further mixing with a liquid raw material to obtain a slurry containing the agricultural chemical active ingredient; (b) mixing the slurry obtained in step (a) with the remaining pesticide active ingredient (e.g., (2) benzobicyclon) and other auxiliary ingredients, and granulating the mixture to obtain granules. The method for producing the pesticide composition in this embodiment is not particularly limited, and may further include, for example, (c) a step of drying, crushing, and sieving the granules obtained in the step (b). Further, the method for producing the pesticide composition in this embodiment is (a) wet-milling a mixture containing an agricultural chemical active ingredient, an activator, and water, and optionally mixing with a liquid raw material to obtain a slurry containing the agricultural chemical active ingredient; (b) mixing the slurry obtained in the step (a) with other auxiliary ingredients and granulating the mixture to obtain granules.

[0045] The pesticide composition in this embodiment may be a solid pesticide composition or a granular pesticide composition. The particle size of the pesticide composition in this embodiment is usually 0.1 to 5 mmφ, preferably 0.3 to 3 mmφ, and more preferably 0.5 to 2 mmφ, because if the particles are too large, drying of the particles becomes difficult, and if the particles are too small, workability in subdivision deteriorates and powdering occurs during use. The shape of the granules of the pesticide composition is not particularly limited, and may be, for example, cylindrical, spherical, or irregular. The pesticide composition of the present embodiment may contain water. When the pesticide composition contains water, the content of water is usually about 0.1 to 5 mass % based on the mass of the pesticide composition.

[0046] When the pesticide composition of this embodiment is a normal granule, the apparent specific gravity of the pesticide composition is usually 0.50 to 1.50, and preferably 0.80 to 1.20, taking into consideration productivity, mechanical sprayability, and the like.

[0047] The pesticide composition of the present embodiment may be applied to paddy fields by direct manual spraying, or may be applied using a pesticide sprayer.

[0048] The method for using the pesticide composition in this embodiment can be to manually apply it directly into the paddy field from, for example, a box, bottle, or bag with an appropriate opening, or to apply it using a pesticide sprayer. In this embodiment, the "pesticide sprayer" is an apparatus powered by an engine or a motor, such as an unmanned helicopter, a drone, or a power sprayer.

[0049] In order to avoid moisture, the pesticide composition of this embodiment is preferably stored in a moisture-proof container, etc. Such a container is not particularly limited, but examples thereof include bottles, bags, boxes, etc. made of materials in which resin, aluminum, paper, etc. are bonded together as necessary, or materials in which aluminum or silicic acid is vapor-deposited on the surface of resin, paper, etc. [Example]

[0050] The present invention will be described in more detail below with reference to examples and comparative examples, but the present invention is not limited to these. In the description of the examples, "%" means "% by mass" and "parts" means "parts by mass."

[0051] The following ingredients were used: Benzobicyclon slurry (Benzobicyclon, manufactured by SDS Biotech) Air Roll CT-1L (dioctyl sulfosuccinate, manufactured by Toho Chemical Industry Co., Ltd.) Morwet® D-425 Powder (sodium salt of alkylnaphthalenesulfonic acid formalin condensate, manufactured by Nouryon Surface Chemistry AB) Newcol 607-PDE (polyoxyethylene polycyclic phenyl ether, manufactured by Nippon Nyukazai) Asahi Silicone AF128 (silicone emulsion, manufactured by Asahi Dye Manufacturing Co., Ltd.) SURFYNOL104PG50 (acetylene diol, manufactured by Evonik Japan) Cellogen (registered trademark) 5A (sodium carboxymethylcellulose, manufactured by Daiichi Kogyo Seiyaku) GEROPON SC / 213 (potassium polycarboxylate, manufactured by Solvay Nicca) Sodium tripolyphosphate (sodium tripolyphosphate salt, manufactured by Mitsui Chemicals, Shimonoseki) Newcalgen (registered trademark) SX-C (sodium alkylbenzene sulfonate, manufactured by Takemoto Oil & Fat) SURFYNOL104S (acetylene-based dialcohol composition, manufactured by Evonik Japan) Kunigel V2 (bentonite, manufactured by Kunimine Industries) Calcium Carbonate B-90 (calcium carbonate, manufactured by Kahara Lime Chemical Industry Co., Ltd.)

[0052] Example 1 A mixture of 36.2 parts of cyclopyrimorate technical substance (purity 98.5%), 9.1 parts of triafamone technical substance (purity 97.4%), 1.2 parts of Morwet (registered trademark) D-425 Powder, 0.5 parts of Airroll CT-1L, 1.0 part of Newcol 607-PDE, 0.5 parts of Asahi Silicone AF128 (10% aqueous solution), 0.3 parts of SURFYNOL104PG50, and 51.2 parts of water was wet-pulverized in an Attritor (registered trademark) 1S type (manufactured by Nippon Coke and Engineering Co., Ltd.) using steel balls with a particle size (3 / 16 inch≒4.763 mm) to obtain a cyclopyrimorate / triafamone slurry. 11.2 parts of the obtained cyclopyrimorate / triafamone slurry and 6.6 parts of benzobicyclon slurry (purity 45.3%) were mixed to obtain a cyclopyrimorate / triafamone / benzobicyclon slurry.

[0053] The obtained cyclopyrimorate / triafamone / benzobicyclone slurry (17.9 parts), sodium tripolyphosphate (3.0 parts), Cellogen (registered trademark) 5A (1.0 parts), GEROPON SC / 213 (2.0 parts), New Calgen (registered trademark) SX-C (2.0 parts), Kunigel V2 (20.0 parts), calcium carbonate (B-90) (63.51 parts) were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated product was dried in a dryer to obtain a solid pesticide composition (water content: approximately 1% by mass).

[0054] Example 2 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 3.0 parts of sodium tripolyphosphate, 1.0 part of Cellogen (registered trademark) 5A, 1.0 part of GEROPON SC / 213, 3.0 parts of Newcalgen (registered trademark) SX-C, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0055] Example 3 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 3.0 parts of sodium tripolyphosphate, 1.0 part of Cellogen (registered trademark) 5A, 3.0 parts of GEROPON SC / 213, 1.0 part of Newcalgen (registered trademark) SX-C, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0056] Example 4 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 3.0 parts of sodium tripolyphosphate, 1.0 part of Cellogen (registered trademark) 5A, 1.0 part of GEROPON SC / 213, 1.0 part of Newcalgen (registered trademark) SX-C, 20.0 parts of Kunigel V2, and 65.51 parts of calcium carbonate B-90 were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0057] Example 5 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 4.0 parts of sodium tripolyphosphate, 1.0 part of Cellogen (registered trademark) 5A, 1.0 part of GEROPON SC / 213, 2.0 parts of Newcalgen (registered trademark) SX-C, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0058] Example 6 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 5.0 parts of sodium tripolyphosphate, 1.0 part of Cellogen (registered trademark) 5A, 1.0 part of GEROPON SC / 213, 1.0 part of Newcalgen (registered trademark) SX-C, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0059] (Comparative Example 1) 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 7.0 parts of sodium tripolyphosphate, 1.0 part of Cellogen (registered trademark) 5A, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed, and then an appropriate amount of water was added and kneaded. The resulting kneaded mixture was extruded through a 0.8 mm screen and granulated. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0060] (Comparative Example 2) 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 1.0 part of Cellogen® 5A, 7.0 parts of Newcalgen® SX-C, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed, and then an appropriate amount of water was added and kneaded. The resulting kneaded mixture was extruded through a 0.8 mm screen and granulated. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0061] (Comparative Example 3) 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 1.0 part of Cellogen (registered trademark) 5A, 7.0 parts of GEROPON SC / 213, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed, and then an appropriate amount of water was added and kneaded. The resulting kneaded mixture was extruded through a 0.8 mm screen and granulated. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0062] Comparative Example 4 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 1.0 part of Cellogen (registered trademark) 5A, 7.0 parts of SURFYNOL 104S, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed, and then an appropriate amount of water was added and kneaded. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0063] (Comparative Example 5) 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 1.0 part of Cellogen® 5A, 7.0 parts of Morwet® D-425 Powder, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed, and then an appropriate amount of water was added and kneaded. The resulting mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition. Got it.

[0064] (Comparative Example 6) 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 3.0 parts of sodium tripolyphosphate, 1.0 part of Cellogen® 5A, 2.0 parts of SURFYNOL 104S, 2.0 parts of Newcalgen® SX-C, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0065] (Comparative Example 7) 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 3.0 parts of sodium tripolyphosphate, 1.0 part of Cellogen® 5A, 2.0 parts of Morwet® D-425 Powder, 2.0 parts of Newcalgen® SX-C, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed, and then an appropriate amount of water was added and kneaded. The resulting mixture was extruded through a 0.8 mm screen and granulated. The granulated material was dried in a dryer to obtain a solid pesticide composition. Ta.

[0066] (Comparative Example 8) 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 3.0 parts of sodium tripolyphosphate, 1.0 parts of Cellogen (registered trademark) 5A, 2.0 parts of GEROPON SC / 213, 2.0 parts of SURFYNOL104S, 2.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0067] (Comparative Example 9) 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 3.0 parts of sodium tripolyphosphate, 1.0 parts of Cellogen (registered trademark) 5A, 2.0 parts of GEROPON SC / 213, 2.0 parts of Morwet (registered trademark) D-425 Powder, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0068] (Comparative Example 10) 17.9 parts of the cyclopyrimorate / triafamone / benzobicyclone slurry prepared in Example 1, 3.0 parts of sodium tripolyphosphate, 1.0 parts of Cellogen (registered trademark) 5A, 2.0 parts of SURFYNOL 104S, 2.0 parts of Morwet (registered trademark) D-425 Powder, 20.0 parts of Kunigel V2, and 63.51 parts of calcium carbonate B-90 were mixed and then kneaded with an appropriate amount of water. The resulting kneaded mixture was extruded and granulated through a 0.8 mm screen. The granulated material was dried in a dryer to obtain a solid pesticide composition.

[0069] (Test example) 40 mg of the pesticide composition prepared in the Examples and Comparative Examples was weighed out and placed in a container (approximately 25 cm x 30 cm) filled with water (3-degree hard water) to a depth of 3 cm so as to disperse the composition as uniformly as possible, and then allowed to stand. One day and four days after the addition, water samples were collected, and the concentration of cyclopyrimorate in water (ppm) was quantified by HPLC under the following conditions. From the results obtained, the dissolution rate of cyclopyrimorate in water (concentration in water ÷ concentration at 100% dissolution × 100 (%)) was calculated and evaluated according to the following criteria. (Evaluation criteria for cyclopirimorate dissolution rate after 1 day) 〇: 65% or less ×: Exceeding 65% (Evaluation criteria for cyclopirimorate dissolution rate after 4 days) 〇: 85% or more ×: Less than 85%

[0070] (HPLC conditions) Method: Absolute calibration curve method Column: Zorbax SB-phenyl (3.5 μm, 4.6 × 150 mm) Column temperature: 40℃ Mobile phase: Water (0.01% phosphoric acid) / acetonitrile = 55 / 45

[0071] [Table 1]

[0072] In Table 1, A: Tripolyphosphate B: Alkylbenzene sulfonate C: Polycarboxylate D: Acetylenic dialcohol composition E: Sodium salt of alkylnaphthalenesulfonic acid formalin condensate Table 1 also shows the content of each component in the compositions obtained in the examples and comparative examples in terms of mass %.

[0073] As shown in Table 1, the compositions of the examples were able to achieve control of cyclopyrimorate dissolution (1 day later: 65% or less, 4 days later: 85% or more), which was difficult to achieve with the compositions of the comparative examples. [Industrial Applicability]

[0074] According to the present invention, a highly practical pesticide composition can be provided.

Claims

1. A pesticide composition comprising (1) cyclopyrimorate, (2) benzobicyclon, (3) triafamone, (4) tripolyphosphate, (5) alkylbenzenesulfonate, and (6) polycarboxylate.

2. 2. The pesticide composition according to claim 1, wherein the polycarboxylate is a potassium polycarboxylate.

3. 3. The pesticide composition according to claim 1, wherein the tripolyphosphate salt is sodium tripolyphosphate or potassium tripolyphosphate.

4. 3. The pesticide composition according to claim 1, wherein the alkylbenzene sulfonate is a sodium alkylbenzene sulfonate.

5. 4. The pesticide composition according to claim 3, wherein the alkylbenzene sulfonate is a sodium alkylbenzene sulfonate.

Citation Information

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