(19)
(11)EP 2 863 741 B1

(12)EUROPEAN PATENT SPECIFICATION

(45)Mention of the grant of the patent:
29.07.2020 Bulletin 2020/31

(21)Application number: 13809629.2

(22)Date of filing:  20.06.2013
(51)International Patent Classification (IPC): 
A01N 25/04(2006.01)
A01N 47/16(2006.01)
A01N 25/22(2006.01)
A01P 3/00(2006.01)
(86)International application number:
PCT/JP2013/067585
(87)International publication number:
WO 2014/003082 (03.01.2014 Gazette  2014/01)

(54)

PESTICIDAL COMPOSITION IN THE FORM OF AQUEOUS EMULSION

PESTIZIDZUSAMMENSETZUNG IN FORM EINER WÄSSRIGEN EMULSION

COMPOSITION PESTICIDE SE PRÉSENTANT SOUS LA FORME D'UNE ÉMULSION AQUEUSE


(84)Designated Contracting States:
AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

(30)Priority: 26.06.2012 JP 2012142761

(43)Date of publication of application:
29.04.2015 Bulletin 2015/18

(73)Proprietor: Sumitomo Chemical Company, Limited
Tokyo 104-8260 (JP)

(72)Inventors:
  • YANAGISAWA, Kazuyuki
    Takarazuka-shi, Hyogo, 665-8555 (JP)
  • MIZUTANI, Motofumi
    Tokyo, 104-8260 (JP)

(74)Representative: Thurston, Joanna 
Withers & Rogers LLP 4 More London Riverside
London SE1 2AU
London SE1 2AU (GB)


(56)References cited: : 
EP-A1- 2 245 929
EP-A1- 2 245 931
WO-A1-2006/069580
WO-A2-93/15605
WO-A2-2008/047569
WO-A2-2009/112836
JP-A- 2008 081 430
JP-A- 2009 173 568
JP-A- 2009 173 579
JP-A- 2009 173 596
US-A1- 2003 134 910
EP-A1- 2 245 930
WO-A1-02/00023
WO-A1-2011/028286
WO-A2-2008/032328
WO-A2-2008/047570
JP-A- S5 939 807
JP-A- 2008 081 431
JP-A- 2009 173 578
JP-A- 2009 173 596
JP-A- 2011 522 005
US-A1- 2006 129 021
  
      
    Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention).


    Description

    Technical Field



    [0001] The present invention relates to a pesticidal composition in the form of an aqueous emulsion in which photodegradation of an agriculturally active ingredient has been inhibited.

    BACKGROUND ART



    [0002] Various studies have hitherto been made for the purpose of inhibiting photodegradation of agriculturally active ingredients which are unstable against light. There have been known technologies in which stabilizers such as an ultraviolet absorber are added (see, for example, Patent Document 1). There is also known a pesticidal composition in the form of an aqueous emulsion, which contains a specific water-soluble polymer as a stabilizer in an aqueous continuous phase (see, for example, Patent Document 2). Patent documents 3 to 15 describe emulsion compositions including agrochemical actives.

    [Prior Art Document]


    [Patent Document]



    [0003] 

    [Patent Document 1] : JP 59-39807 A

    [Patent Document 2]: US 2003/0134910 A

    [Patent Document 3]: WO 2008/047569 A2

    [Patent Document 4]: WO 2008/047570 A2

    [Patent Document 5]: EP 2245930 A1

    [Patent Document 6]: EP 2245931 A1

    [Patent Document 7]: EP 2245929 A1

    [Patent Document 8]: JP 2009-173596 A

    [Patent Document 9]: WO 2006/069580

    [Patent Document 10]: WO 02/00023 A1

    [Patent Document 11]: WO 2009/112836 A2

    [Patent Document 12]: WO 2008/032328 A2

    [Patent Document 13]: WO 2011/028286 A1

    [Patent Document 14]: WO 93/15605 A2

    [Patent Document 15]: US 2006/0129021 A1


    DISCLOSURE OF INVENTION


    [Problems to be Solved by the Invention]



    [0004] An object of the present invention is to provide a new pesticidal composition in the form of an aqueous emulsion in which photodegradation of an agriculturally active ingredient has been inhibited.

    [Means for Solving the Problems]



    [0005] The present inventors have intensively studied so as to find a pesticidal composition in the form of an aqueous emulsion in which photodegradation of an agriculturally active ingredient has been inhibited, and found that, in a pesticidal composition in the form of an aqueous emulsion, comprising :
    1. (a) fenpyrazamine
    2. (b) a hydrophobic organic solvent (hereinafter sometimes referred to as a component b) selected from vegetable oils, esters, ketones and paraffins;
    3. (c) a water-soluble polymer dispersing agent (hereinafter sometimes referred to as a component c) selected from one or more water-soluble polymer dispersing agent(s) selected from the group consisting of a vinyl-based polymer of polyvinyl alcohol, polyvinylpyrrolidone, vinyl acetate copolymer, and sodium polyacrylate, and polysaccharides of gum arabic, xanthan gum, rhamsan gum, locust bean gum, guar gum, carrageenan, welan gum, alginic acid, alginate, gum tragacanth, methyl cellulose, ethyl cellulose, sodium carboxymethyl cellulose, hydroxyethyl cellulose, and hydroxypropyl cellulose; and
    4. (d) water (hereinafter sometimes referred to as a component d) ;
    wherein liquid droplets in which fenpyrazamine is suspended or dissolved in the hydrophobic organic solvent are emulsified in an aqueous continuous phase, and also a weight ratio of the fenpyrazamine to the hydrophobic organic solvent is from 5:95 to 70:30; wherein the liquid droplets have average particle diameter of 5 to 60 µm.

    [0006] The present invention includes the followings:
    1. [1] A pesticidal composition in the form of an aqueous emulsion, comprising:
      1. (a) fenpyrazamine;
      2. (b) a hydrophobic organic solvent selected from vegetable oils, esters, ketones, and paraffins;
      3. (c) a water-soluble polymer dispersing agent selected from one or more water-soluble polymer dispersing agent(s) selected from the group consisting of a vinyl-based polymer of polyvinyl alcohol, polyvinylpyrrolidone, vinyl acetate copolymer, and sodium polyacrylate, and polysaccharides of gum arabic, xanthan gum, rhamsan gum, locust bean gum, guar gum, carrageenan, welan gum, alginic acid, alginate, gum tragacanth, methyl cellulose, ethyl cellulose, sodium carboxymethyl cellulose, hydroxyethyl cellulose, and hydroxypropyl cellulose; and
      4. (d) water;
      wherein liquid droplets in which the fenpyrazamine is suspended or dissolved in the hydrophobic organic solvent are emulsified in an aqueous continuous phase, and also a weight ratio of the fenpyrazamine to the hydrophobic organic solvent is from 5:95 to 70:30; wherein the liquid droplets have an average particle diameter of 5 to 60 µm;
    2. [2] The pesticidal composition in the form of an aqueous emulsion according to [1]wherein the hydrophobic organic solvent(s) is/are one or more hydrophobic organic solvent(s) selected from the group consisting of esters, ketones, and paraffins..

    [Effects of the Invention]



    [0007] According to the present invention, it is possible to inhibit photodegradation of an agriculturally active ingredient.

    MODE FOR CARRYING OUT THE INVENTION



    [0008] The pesticidal composition in the form of an aqueous emulsion of the present invention (hereinafter sometimes referred to as a composition of the present invention) is a
    pesticidal composition in the form of an aqueous emulsion (emulsion pesticidal composition) containing fenpyrazamine which is significantly unstable against light, and is a pesticidal composition which can effectively inhibit photodegradation of fenpyrazamine.

    [0009] As used herein, xenon light means a light source in which a gas filled in a tube is xenon. Usually, xenon light means uniquely the same spectrum. Xenon light (290 nm cutoff) means xenon light having a wavelength within a range of 290 nm or more, and xenon light passed through a borosilicate filter corresponds to this.

    [0010] A method for the calculation of a retention rate of fenpyrazamine defined above is more specifically as follows. First, 250 mg of fenpyrazamine is dissolved in 50 ml of a solvent such as acetone, which can sufficiently dissolve fenpyrazamine and also has high volatility, and 1 mL of the solution is added to a glass petri dish having a diameter of 6 cm using a one-mark pipette, spread entirely over the petri dish, and then air-dried at room temperature. The petri dish is covered with a lid made of quartz glass and then set in a weathering tester (manufactured by Q-Lab Corporation under the trade name of Q-SUN Xenon Accelerated Weathering Tester, Model Xe-3) equipped with a borosilicate filter (manufactured by Q-Lab Corporation under the trade name of Daylight-BB Optical Filter) attached thereto. After irradiation with xenon light under the conditions of an intensity at 340 nm of 0.68 W/m2 and a temperature of 35°C (35°C as measured by an insulated black panel thermometer) for 8 hours, the amount of fenpyrazamine remaining on the petri dish is determined by a known determination method such as high-performance liquid chromatography. It is possible to determine a retention rate by calculating as the weight percentage relative to 5 mg of the fenpyrazamine used above.

    [0011] Fenpyrazamine is the agriculturally active ingredient used in the composition of the present invention and is a fungicidally active component. It is solid at normal temperature (25°C). The retention rate after irradiation with xenon light (290 nm cutoff) at an intensity of 0.68 W/m2 at 340 nm for 8 hours according to the method for calculation above-mentioned is 28.1%.

    [0012]  The composition of the present invention usually contains fenpyrazamine in the total amount of 0.5 to 25% by weight, and preferably 2.5 to 15% by weight.

    [0013] In the composition of the present invention, a component b means an organic solvent which is liquid at normal temperature (25°C) and is immiscible in water. Specifically, an organic solvent having water solubility of 20% by weight or less at 25°C is used. Examples of the hydrophobic organic solvent include hydrophobic organic solvents such as vegetable oils, esters, ketones, and paraffins, for example, the following hydrophobic organic solvents:

    Vegetable oils: rapeseed oil, soybean oil, linseed oil, corn oil, and olive oil;

    Esters: diisobutyl adipate, diisodecyl adipate, dialkyl phthalate (didecyl phthalate, etc.), octyl oleate, lauryl oleate, octyldodecyl oleate, and isopropyl myristate;

    Ketones: methyl isobutyl ketone, heptanone, octanone, nonanone, cyclohexanone, and acetophenone; and

    Paraffins: normal paraffin, isoparaffin, cycloparaffin, and liquid paraffin.



    [0014] In the present invention, commercially available paraffin solvents can be used as paraffins. Examples of the commercially available paraffin solvents include NORPAR 13 (normal paraffin, producttrade name of ExxonMobil Chemical Ltd.), NORPAR 15 (normal paraffin, producttrade name of ExxonMobil Chemical Ltd.), ISOPAR E (isoparaffin, trade name of ExxonMobil Chemical Ltd.), ISOPAR G (isoparaffin, trade name of ExxonMobil Chemical Ltd.), ISOPAR L (isoparaffin, trade name of ExxonMobil Chemical Ltd.), ISOPAR H (isoparaffin, trade name of ExxonMobil Chemical Ltd.), ISOPAR M (isoparaffin, trade name of ExxonMobil Chemical Ltd.), MORESCO-WHITE P-40 (liquid paraffin, trade name of MORESCO Corporation), MORESCO-WHITE P-70 (liquid paraffin, trade name of MORESCO Corporation), MORESCO-WHITE P-200 (liquid paraffin, trade name of MORESCO Corporation), EXXSOL DUO (mixed solvent of paraffin and cycloparaffin, trade name of ExxonMobil Chemical Ltd.), EXXSOL D130 (mixed solvent of paraffin and cycloparaffin, trade name of ExxonMobil Chemical Ltd.), and EXXSOL D160 (mixed solvent of paraffin and cycloparaffin, trade name of ExxonMobil Chemical Ltd.) .

    [0015] There is no particular limitation on the component b used in the composition of the present invention, and one or more hydrophobic organic solvent (s) selected from the group consisting of esters, ketones, and paraffins is/are preferably used, and aromatic ketones such as acetophenone are more preferably used.

    [0016] In the composition of the present invention, a weight ratio of fenpyrazamine to the component b is from 5:95 to 70:30, preferably from 15:85 to 70:30, and more preferably from 30:70 to 70:30. The composition of the present invention usually contains the component b in the total amount of 5 to 40% by weight, and preferably 10 to 25% by weight.

    [0017]  In the present invention, the vinyl-based polymer means a polymer obtained by addition polymerization of a monomer having a vinyl group (-CH=CH2), and polysaccharides mean saccharides which are hydrolyzed to form two or more molecules of monosaccharides.

    [0018] The composition of the present invention usually contains the component c in the total amount of 1 to 10% by weight, and preferably 1 to 5% by weight.

    [0019] There is no particular limitation on a component d used in the composition of the present invention, and it is possible to use water which is used in a conventional pesticidal composition in the form of an aqueous emulsion (emulsion pesticidal composition), such as tap water, well water, and deionized water, and deionized water is preferably used.

    [0020] The composition of the present invention usually contains the component d in the amount of 40 to 93% by weight, and preferably 45 to 90% by weight. Substantially, the component c is dissolved in the component d.

    [0021] It is preferred that the composition of the present invention further contains one or more UV protectants. Examples of the UV protectants include benzophenone-based ultraviolet absorbers such as 2,4-dihydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, and 2-hydroxy-4-n-octyl-benzophenone; benzotriazole-based ultraviolet absorbers such as 2-(2-hydroxy-5-methylphenyl) benzotriazole, 2-[2-hydroxy-3-(3,4,5,6-tetrahydrophthalimide-methyl)-5-methylphenyl] benzotriazole, 2-(3-tert-butyl-2-hydroxy-5-methylphenyl)-5-chlorobenzotriazole, 2-(2-hydroxy-5-tert-octylphenyl)benztriazole, and 2- (2-hydroxy-3,5-di-tert-pentylphenyl)benzotriazole; benzoate-based ultraviolet absorbers such as 2,4-di-tert-butylphenyl 3,5-di-tert-butyl-4-hydroxybenzoate; hydroxyphenyltriazine-based ultraviolet absorber such as 2-(2-hydroxy-4-[1-octyloxycarbonylethoxy]phenyl)-4, 6-bis (4-phenylphenyl)-1,3,5-triazine; photostabilizers such as non-sulfonated lignin (for example, manufactured by MeadWestvaco Corporation under the trade name of INDULIN AT) and a hindered amine- based photostabilizer (HALS); and inorganic UV shielding agents such as titanium oxide.

    [0022] Substantially, the UV protectant (hereinafter sometimes referred to as a component e) is suspended or dissolved in the component b. There is no particular limitation on the component e used in the composition of the present invention, and it is preferred to use a component e, which is miscible in the component b, from the viewpoint of emulsion stability of liquid droplets as the component b which contains the component e in the composition in the form of an aqueous emulsion.

    [0023] When the composition of the present invention contains the component e, the total content is usually from 0.1 to 15% by weight, and preferably from 0.5 to 10% by weight.

    [0024] The composition of the present invention may further contain pesticide auxiliary agents used in a conventional pesticidal composition in the form of an aqueous emulsion. Examples of the pesticide auxiliary agents include surfactants, thickeners, defoamers, preservatives, antifreezing agents, pH adjustors and the like.

    [0025] Examples of the surfactants include nonionic surfactants, cationic surfactants, anionic surfactants, and amphoteric surfactants. Examples of nonionic surfactants include polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, polyoxyethylene lanolin alcohol, polyoxyethylene alkyl phenol formalin condensate, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene glyceryl monofatty acid ester, polyoxypropylene glycol monofatty acid ester, polyoxyethylene sorbitol fatty acid ester, polyoxyethylene castor oil derivative, polyoxyethylene fatty acid ester, higher fatty acid glycerol ester, sorbitan fatty acid ester, sucrose fatty acid ester, polyoxyethylene polyoxypropylene block polymer, polyoxyethylene fatty acid amide, alkylol amide, polyoxyethylenealkylamine, and polyoxyethylene alkanediol. Examples of cationic surfactants include alkylamine hydrochlorides such as dodecylamine hydrochloride; alkyl quaternary ammonium salts such as dodecyltrimethyl ammonium salt, alkyldimethylbenzyl ammonium salt, alkylpyridinium salt, alkylisoquinolinium salt, and dialkylmorpholinium salt; benzethonium chloride, and polyalkyl vinyl pyridinium salt. Examples of anionic surfactants include fatty acid sodium such as sodium palmitate; sodium ether carboxylate such as sodium polyoxyethylene lauryl ether carboxylate; amino acid condensates of higher fatty acid, such as sodium lauroyl sarcosine and sodium N-lauroyl glutamate; higher fatty acid ester sulfonates such as higher alkyl sulfonate and lauric acid ester sulfonic acid salt; dialkyl sulfosuccinates such as dioctyl sulfosuccinate; higher fatty acid amide sulfonates such as oleic acid amide sulfonic acid; alkyl aryl sulfonates such as sodium dodecylbenzene sulfonate and diisopropyl naphthalene sulfonate; higher alcohol sulfuric acid ester salts such as formalin condensate of alkyl aryl sulfonate and pentadecane-2-sulfate; polyoxyethylene alkyl phosphates such as dipolyoxyethylene dodecyl ether phosphate; styrene-maleic acid copolymer; and lignin sulfonate.

    [0026] Examples of amphoteric surfactants include N-laurylalanine, N,N,N-trimethylaminopropionic acid, N,N,N-trihydroxyethylaminopropionic acid, N-hexyl-N, N-dimethylaminoacetic acid, 1-(2-carboxyethyl) pyridinium betaine, and lecithin.

    [0027] When the composition of the present invention contains the surfactant, the total content is usually from 0.1 to 20% by weight, and preferably from 0.5 to 10% by weight.

    [0028] Examples of the thickener include natural polysaccharides such as xanthan gum, rhamsan gum, locust bean gum, guar gum, carrageenan, welan gum, alginic acid, alginate, and gum tragacanth; mineral matter powders such as aluminum silicate, magnesium aluminum silicate, smectite, bentonite, hectorite, synthetic hydrated silicic acid, and dry silica; and alumina sol. It is possible to use, as these thickeners, commercially available products as they are. Examples of commercially available products include KELZAN S (trade name of CP Kelco, Inc.) as xanthan gum, VEEGUM Granules (trade name of Vanderbilt Company, Inc.) as aluminum silicate, an Aerosil 200 (trade name of Evonik Degussa Corporation) as dry silica.

    [0029] When the composition of the present invention contains the thickener, the total content is usually from 0.01 to 10% by weight, and preferably from 0.1 to 5% by weight.

    [0030] Examples of the defoamer include silicone-based defoamers such as ANTIFOAM C EMULSION (trade name of Dow Corning Toray Co., Ltd.), ANTIFOAM CE (trade name of Dow Corning Toray Co., Ltd.), TSA730 (trade name of MOMENTIVE PERFORMANCE MATERIALS JAPAN LLC), TSA731 (trade name of MOMENTIVE PERFORMANCE MATERIALS JAPAN LLC), TSA732 (trade name of MOMENTIVE PERFORMANCE MATERIALS JAPAN LLC), and YMA6509 (trade name of MOMENTIVE PERFORMANCE MATERIALS JAPAN LLC); and fluorine-based defoamers such as Fluowet PL80 (trade name of Clariant GmbH).

    [0031] When the composition of the present invention contains the defoamer, the total content is usually from 0.01 to 3% by weight, and preferably from 0.05 to 1% by weight.

    [0032] Examples of the preservative include p-hydroxybenzoic acid ester, salicylic acid derivative, proxel (1,2-benzisothiazolin-3-one), and isothiazolin-3-one derivative (for example, BIOHOPE L (trade name of KI Chemical Industry Co. Ltd.)).

    [0033] When the composition of the present invention contains the preservative, the total content is usually from 0.01 to 5% by weight, and preferably from 0.05 to 3% by weight.

    [0034] Examples of the antifreezing agent include water- soluble glycols such as ethylene glycol and propylene glycol.

    [0035] When the composition of the present invention contains the antifreezing agent, the total content is usually from 0.5 to 30% by weight, and preferably from 1 to 20% by weight.

    [0036] Examples of the pH adjustor include citric acid monohydrate, sorbic acid, potassium sorbate, disodium hydrogen phosphate, dipotassium hydrogen phosphate, and sodium hydroxide.

    [0037] When the composition of the present invention contains the pH adjustor, the total content is usually from 0.01 to 5% by weight, and preferably from 0.5 to 3% by weight.

    [0038] A method for producing a composition of the present invention (hereinafter sometimes referred to as a present production method) will be described, but the present production method is not limited only to the following methods.

    [0039] The present production method includes the following first and second steps.

    [0040] The first step of the present production method is the step of suspending or dissolving fenpyrazamine in a component b to prepare a suspension or a solution of fenpyrazamine. Fenpyrazamine is suspended or dissolved in the component b.

    [0041] As fenpyrazamine is solid at normal temperature (25°C), it is possible to take the form of a suspension depending on solubility of fenpyrazamine in the component b and a weight ratio of fenpyrazamineto the component b. The present suspension of fenpyrazamine can be prepared by finely grinding the solid fenpyrazamine in the component b using a wet grinding mill such as a beads mill. It is also possible to prepare by finely grinding the solid fenpyrazamine with or without adding other components using a dry grinding mill such as a jet mill, and adding the thus obtained finely ground powder to the component b.

    [0042] The solution in which fenpyrazamine is dissolved in a component b can be prepared by dissolving the fenpyrazamine in the component b.

    [0043] When the solid fenpyrazamine is dispersed (that is, suspended) in the component b in the form of fine particles, an average particle diameter of the fine particles is usually 15 µm or less, preferably 1 to 10 µm, and more preferably 1 to 5 µm.

    [0044] When the composition of the present invention contains the component e, the first step includes the step of respectively suspending or dissolving the fenpyrazamine and the component e in the component b to prepare a suspension or a solution of the fenpyrazamine and the component e.

    [0045] In the suspension or solution of fenpyrazamine and the component e, the fenpyrazamine and the component e take any one of the following forms (1) to (4).
    1. (1) Both the fenpyrazamine and the component e are suspended in the component b.
    2. (2) The component e is dissolved in the component b, and fenpyrazamine is suspended in the component b in which the component e has been dissolved.
    3. (3) Fenpyrazamine is dissolved in the component b, and the component e is suspended in the component b in which fenpyrazamine has been dissolved.
    4. (4) Both fenpyrazamine and the component e are dissolved in the component b.


    [0046] The solid fenpyrazamine can take the form (1) or (2) depending on solubility of the solid fenpyrazamine in the component b and a weight ratio of the solid fenpyrazamine to the component b. When the component e is a component e which is solid at normal temperature (25°C) (hereinafter sometimes referred to as a solid component e), the component e can take the form (1) or (3) depending on solubility of the solid component e to the component b and a weight ratio of the solid component e to the component b.

    [0047] Suspensions of (1) to (3) can be prepared by the same operation as in a method for preparing the present suspension a. In the case of preparing the suspension (1), the solid fenpyrazamine and the solid component e may be finely milled at the same time by a wet grinding mill or a dry grinding mill, or the present suspension of fenpyrazamine and a suspension in which the solid component e has been suspended in the component b may be separately prepared, followed by mixing, in the method for preparing the present suspension of fenpyrazamine. In the case of preparing the suspension (2), usually, the component e is dissolved in the component b and then the solid fenpyrazamine is added to the solution. In the case of preparing the suspension (3), usually, the fenpyrazamine is dissolved in the component b and then the solid component e is added to the solution.

    [0048] The solution (4) can be prepared by dissolving fenpyrazamine and the component e in the component b.

    [0049] The second step of the present production method is the step of mixing the suspension or solution obtained in the first step with the aqueous solution of the component c to prepare liquid droplets.

    [0050] In the aqueous solution of the component c used in the second step, the amount of the component c is usually from 0.5 to 30% by weight, and preferably from 1 to 20% by weight, based on the entire amount of the aqueous solution of the component c. To the aqueous solution of the component c, defoamers may be optionally added. The weight of the aqueous solution of the component c used in the second step is usually within a range of 0.8 to 2 times more than that of the suspension or solution obtained in the first step.

    [0051] In the second step, the method for preparing liquid droplets in water includes, for example, a method in which the suspension or solution obtained in the first step is added to the aqueous solution of the component c, followed by stirring using a stirrer. The stirrer used in this case includes, for example, a propeller stirrer, a turbine stirrer, and a highspeed shear stirrer. Specific examples of the stirrer include T.K. Homo Mixer, T.K. Homomic Line Flow, T.K. Pipeline Homo Mixer, and T.K. Filmix manufactured by PRIMIX Corporation; CLEARMIX manufactured by M Technique Co., Ltd.; POLYTRON homogenizer and MEGATRON homogenizer manufactured by KINEMATICA AG; and SUPRATON manufactured by Tsukishima Kikai Co., Ltd.

    [0052] An average particle diameter of liquid droplets existing in water obtained in the second step, that is, liquid droplets in the composition of the present invention , in which the fenpyrazamine is suspended or dissolved in the component b is from 5 to 60 µm, preferably from 10 to 60 µm, and more preferably from 10 to 40 µm.

    [0053] In the present invention, the average particle diameter means a volume median diameter. The volume median diameter refers to a particle diameter at which a cumulative frequency in a volume equivalent frequency distribution is to be 50%, and the volume median diameter can be determined, for example, by wet measurement using a laser diffraction particle size distribution measuring apparatus. More specifically, liquid droplets are dispersed in water and then the volume median diameter is measured using the apparatus. The laser diffraction particle size distribution measuring apparatus includes, for example, Mastersizer 2000 (manufactured by Malvern Instruments Ltd.).

    [0054] It is possible to obtain a pesticidal composition in the form of an aqueous emulsion in which liquid droplets in which the fenpyrazamine is suspended or dissolved in the component b are emulsified in an aqueous continuous phase, by the above production method. To the pesticidal composition in the form of an aqueous emulsion, the pesticide auxiliary agents and water may be further added.

    [0055] The composition of the present invention can be applied to places such as paddy fields, cultivated lands, orchards, grass plot, and non-agricultural lands in the same manner as in the case of a conventional pesticidal composition in the form of an aqueous emulsion. The composition of the present invention is optionally diluted with water and then the obtained water dilution can be applied by a method in which the composition is applied to plants growing in the above places or the soil in the above places. Examples of the method for applying the water dilution include a soil surface application or foliage application method of the water dilution using a known sprinkler.

    [0056] It is also possible to use the water dilution in a seed treatment, a seedling raising box treatment and the like.

    [0057] The composition of the present invention can be applied as it is without being diluted with water and, for example, the composition of the present invention is applied along from levee to levee of paddy fields under flooding. Before application, the composition of the present invention is usually mixed by slightly shaking a vessel containing the composition of the present invention.

    [Example]



    [0058] The present invention will be described in further detail below by way of Examples, but the present invention is not limited only to these Examples.

    [0059] First, Preparation Examples and Comparative Preparation Examples are shown.

    Preparation Example 1



    [0060] Fenpyrazamine was dry-milled by a vertical type jet mill (JOM-0101-type jet mill, manufactured by Seishin Enterprise Co., Ltd.) to prepare fenpyrazamine fine powders having an average particle diameter 5 µπ

    or less. Twenty (20) parts by weight of the obtained fenpyrazamine fine powders were mixed with 10 parts by weight of acetophenone (manufactured by Wako Pure Chemical Industries, Ltd.) to obtain a fenpyrazamine suspension. Then, 30 parts by weight of the suspension was added to 33 parts by weight of an aqueous 5% by weight polyvinyl alcohol (manufactured by The Nippon Synthetic Chemical Industry Co., Ltd. under the trade name of GOHSENOL GH-17) solution. This mixture was stirred by a rotor-stator homogenizer (manufactured by KINEMATICA AG under the trade name of POLYTRON homogenizer) thereby emulsifying the fenpyrazamine suspension in the aqueous polyvinyl alcohol solution to obtain a fenpyrazamine emulsion.

    [0061] To 14.2 parts by weight of deionized water, 0.4 part by weight of magnesium aluminum silicate (manufactured by Vanderbilt Company, Inc. under the trade name of VEEGUM Granules) was added, followed by stirring at room temperature for 15 minutes. To this solution, 0.2 part by weight of xanthan gum (manufactured by CP Kelco, Inc. under the trade name of KELZAN S) and 5 parts by weight of propylene glycol were added. This mixture was stirred at 60°C for 60 minutes. The obtained dispersion was cooled to room temperature, and then 0.2 part by weight of an preservative (manufactured by Arch Chemicals, Inc. under the trade name of proxel GXL) was added to the dispersion to give a viscosity modifying liquid. Twenty (20) parts by weight of the viscosity modifying liquid, 17 parts by weight of water, and 63 parts by weight of the above fenpyrazamine emulsion were mixed together to obtain the composition (1) of the present invention, containing 20% by weight of fenpyrazamine. Liquid droplets of the fenpyrazamine suspension had an average particle diameter of 28.5 µm.

    Preparation Example 2



    [0062] By performing the same operation as in Preparation Example 1, except that the amount of fenpyrazamine fine powders prepared in Preparation Example 1 was changed from 20 parts to 15 parts by weight, and the amount of acetophenone (the same as mentioned above) was changed from 10 parts to 15 parts by weight, the composition (2) of the present invention, containing 15% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine suspension had an average particle diameter of 31.8 µm.

    Preparation Example 3



    [0063] By performing the same operation as in Preparation Example 1, except that 30 parts by weight of a fenpyrazamine solution obtained by uniformly mixing 10 parts by weight of fenpyrazamine with 20 parts by weight of acetophenone (the same as mentioned above) was used in place of 30 parts by weight of the fenpyrazamine suspension, the composition (3) of the present invention, containing 10% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine solution had an average particle diameter of 25.3 µm.

    Preparation Example 4



    [0064] By performing the same operation as in Preparation Example 3, except that the amount of fenpyrazamine was changed from 10 parts by weight to 5 parts by weight, the amount of acetophenone (the same as mentioned above) was changed from 20 parts by weight to 25 parts by weight, and the aqueous 2.5% by weight polyvinyl alcohol (the same as mentioned above) solution was used in place of the aqueous 5 by weight polyvinyl alcohol (the same as mentioned above) solution, the composition (4) of the present invention, containing 5% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine solution had an average particle diameter of 29.3 µm.

    Preparation Example 5



    [0065] By performing the same operation as in Preparation Example 3 performed, except that the amount of fenpyrazamine was changed from 10 parts by weight to 2.5 parts by weight, the amount of acetophenone (the same as mentioned above) was changed from 20 parts by weight to 27.5 parts by weigh, and the aqueous 1.0% by weight polyvinyl alcohol (the same as mentioned above) solution was used in place of the aqueous 5% by weight polyvinyl alcohol (the same as mentioned above) solution, the composition (5) of the present invention, containing 2.5% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine solution had an average particle diameter of 31.9 µm.

    Preparation Example 6



    [0066] By performing the same operation as in Preparation Example 3, except that the average particle diameter of liquid droplets of the fenpyrazamine solution was changed from 25.3 µm to 44.0 µm in the case of stirring using the rotor-stator homogenizer (the same as mentioned above), the composition (6) of the present invention, containing 10% by weight of fenpyrazamine was obtained.

    Preparation Example 7



    [0067] By performing the same operation as in Preparation Example 3, except that the average particle diameter of liquid droplets of the fenpyrazamine solution was changed from 25.3 µm to 14.9 µm in the case of stirring using the rotor-stator homogenizer (the same as mentioned above), the composition (7) of the present invention, containing 10% by weight of fenpyrazamine was obtained.

    Preparation Example 8



    [0068] By performing the same operation as in Preparation Example 3, except that the average particle diameter of liquid droplets of the fenpyrazamine solution was changed from 25.3 µm to 7.8 µm in the case of stirring using the rotor-stator homogenizer (the same as mentioned above), the composition (8) of the present invention, containing 10% by weight of fenpyrazamine was obtained.

    Preparation Example 9



    [0069] By performing the same operation as in Preparation Example 3, except that the aqueous 2.5% by weight polyvinyl alcohol (the same as mentioned above) solution was used in place of the aqueous 5% by weight polyvinyl alcohol (the same as mentioned above) solution, and the average particle diameter of liquid droplets of the fenpyrazamine solution was changed from 25.3 µm to 50.1 µm in the case of stirring using the rotor-stator homogenizer (the same as mentioned above), the composition (9) of the present invention, containing 10% by weight of fenpyrazamine was obtained.

    Preparation Example 10



    [0070] By performing the same operation as in Preparation Example 1, except that the amount of fenpyrazamine fine powders prepared in Preparation Example 1 was changed from 20 parts by weight to 10 parts by weight, and 10 parts by weight of acetophenone (the same as mentioned above) was replaced by 20 parts by weight of liquid paraffin (manufactured by MORESCO Corporation under the trade name of MORESCO- WHITE P-40), the composition (10) of the present invention, containing 10% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine suspension had an average particle diameter of 34.9 µm.

    Preparation Example 11



    [0071] By performing the same operation as in Preparation Example 10, except that the average particle diameter of liquid droplets of the fenpyrazamine suspension was changed from 34.9 µm to 53.1 µm in the case of stirring using the rotor-stator homogenizer (the same as mentioned above), the composition (11) of the present invention, containing 10% by weight of fenpyrazamine was obtained.

    Preparation Example 12 (Comparative)



    [0072] By performing the same operation as in Preparation Example 1, except that the amount of fenpyrazamine fine powders prepared in Preparation Example 1 was changed from 20 parts by weight to 10 parts by weight, and 10 parts by weight of acetophenone (the same as mentioned above) was replaced by 20 parts by weight of an aromatic hydrocarbon (manufactured by ExxonMobil Chemical Ltd. under the trade name of Solvesso 150ND), the composition (12) of the present invention, containing 10% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine suspension had an average particle diameter of 27.3 µm.

    Preparation Example 13 (Comparative)



    [0073] By performing the same operation as in Preparation Example 12, except that the average particle diameter of liquid droplets of the fenpyrazamine suspension was changed from 27.3 µm to 42.6 µm in the case of stirring using the rotor-stator homogenizer (the same as mentioned above), the composition (13) of the present invention, containing 10% by weight of fenpyrazamine was obtained.

    Preparation Example 1



    [0074] By performing the same operation as in Preparation Example 1, except that the amount of fenpyrazamine fine powders prepared in Preparation Example 1 was changed from 20 parts by weight to 10 parts by weight, and 10 parts by weight of acetophenone (the same as mentioned above) was replaced by 20 parts by weight of diisobutyl adipate (manufactured by Kao Corporation under the trade name of Vinisizer 40), the composition (14) of the present invention, containing 10% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine suspension had an average particle diameter of 30.1 µm.

    Preparation Example 15



    [0075] By performing the same operation as in Preparation Example 3, except that the aqueous 5% by weight polyvinyl alcohol (the same as mentioned above) solution was replaced by an aqueous 20% by weight gum arabic (under the trade name of Arabiccol SS, manufactured by SAN-EI YAKUHIN BOEKI K.K.) solution, the composition (15) of the present invention, containing 10% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine solution had an average particle diameter of 21.3 m.

    Preparation Example 16



    [0076] By performing the same operation as in Preparation Example 1, except that the amount of fenpyrazamine fine powders prepared in Preparation Example 1 was changed from 20 parts by weight to 10 parts by weight, and 10 parts by weight of acetophenone (the same as mentioned above) was replaced by 20 parts by weight of isoparaffin (manufactured by ExxonMobil Chemical Ltd. under the trade name of ISOPAR E), the composition (16) of the present invention, containing 10% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine suspension had an average particle diameter of 31.0 µm.

    Preparation Example 17



    [0077] Ten (10) parts by weight of fenpyrazamine, 19 parts by weight of acetophenone (the same as mentioned above), and 1 part by weight of a benzophenone-based ultraviolet absorber (manufactured by BASF Corporation under the trade name of Uvinul 3000) were mixed together to prepare a fenpyrazamine solution. Then, 30 parts by weight of the solution was added to 33 parts by weight of the aqueous 5% by weight polyvinyl alcohol (the same as mentioned above) solution. This mixture was stirred by the rotor-stator homogenizer (the same as mentioned above) thereby emulsifying the fenpyrazamine solution in the aqueous polyvinyl alcohol solution to obtain a fenpyrazamine emulsion.

    [0078] To 14.2 parts by weight of deionized water, 0.4 part by weight of magnesium aluminum silicate (the same as mentioned above) was added, followed by stirring at room temperature for 15 minutes. To this solution, 0.2 part by weight of xanthan gum (the same as mentioned above) and 5 parts by weight of propylene glycol were added. This mixture was stirred at 60°C for 60 minutes. The obtained dispersion was cooled to room temperature, and then 0.2 part by weight of an preservative (the same as mentioned above) was added to the dispersion to give a viscosity modifying liquid. Twenty (20) parts by weight of the viscosity modifying liquid, 17 parts by weight of water, and 63 parts by weight of the above fenpyrazamine emulsion were mixed together to obtain the composition (17) of the present invention, containing 10% by weight of fenpyrazamine . Liquid droplets of the fenpyrazamine solution had an average particle diameter of 17.8 µm.

    Preparation Example 18



    [0079] By performing the same operation as in Preparation Example 17, except that 30 parts by weight of the fenpyrazamine suspension obtained by mixing 10 parts by weight of the fenpyrazamine fine powders prepared in Preparation Example 1, 15 parts by weight of acetophenone (the same as mentioned above), and 5 parts by weight of a benzotriazole-based ultraviolet absorber (manufactured by BASF Corporation under the trade name of TINUVIN571) was used in place of 30 parts by weight of the fenpyrazamine solution, the composition (18) of the present invention, containing 10% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine suspension had an average particle diameter of 28.4 µm.

    Comparative Preparation Example 1



    [0080] By performing the same operation as in Preparation Example 3, except that the amount of fenpyrazamine was changed from 10 parts by weight to 0.8 part by weight, and the amount of acetophenone (the same as mentioned above) was changed from 20 parts by weight to 29.2 parts by weight, the comparative composition (1), containing 0.8% by weight of fenpyrazamine was obtained. Liquid droplets of the fenpyrazamine solution had an average particle diameter of 33.9 µm.

    Comparative Preparation Example 2



    [0081] By performing the same operation as in Preparation Example 1, except that the amount of fenpyrazamine fine powders prepared in Preparation Example 1 was changed from 20 parts by weight to 25 parts by weight, and the amount of acetophenone (the same as mentioned above) was changed from 10 parts by weight to 5 parts by weight. As a result, viscosity of the fenpyrazamine suspension significantly increased, and thus a fenpyrazamine emulsion could not be produced.

    [0082] Next, Test Example will be shown.

    Test Example 1



    [0083] The compositions (1) to (18) of the present invention, and the comparative composition (1) were respectively diluted with water so as to make each active ingredient concentration to 1,120 ppm. Each of the dilutions (100 µL) was added to a glass petri dish having a diameter of 6 cm, uniformly spread and then air-dried at room temperature. The petri dish was covered with a lid made of quartz glass and placed in a weathering tester (manufactured by Q-Lab Corporation under the trade name of Q-SUN Xenon Accelerated Weathering Tester, Model Xe-3) equipped with a borosilicate filter (manufactured by Q-Lab Corporation under the trade name of Daylight-BB Optical Filter) attached thereto, followed by irradiation with xenon light under the conditions of an intensity at 340 nm of 0.68 W/m2 and a temperature of 34°C (34°C as measured by an insulated black panel thermometer) for 6 hours. After irradiation, fenpyrazamine remaining on the petri dish was extracted with acetonitrile, followed by quantitative analysis through high-performance liquid chromatography. A retention rate was determined by calculating as the weight percentage relative to the amount of fenpyrazamine before irradiation.

    [0084] The results are shown in Table 1.
    [Table 1]
    Compositions usedComponent bComponent eComponent a:Component b (weight ratio)Average particle diameter (µm)Retention rate (%)
    Composition (1) of the present invention Acetophenone - 67:33 28.5 46.1
    Composition (2) of the present invention Acetophenone - 50:50 31.8  
    Composition (3) of the present invention Acetophenone - 33:67 25.3 49.9
    composition (4) of the present invention Acetophenone - 17:83 29.3 37.2
    Composition (5) of the present invention Acetophenone - 8:92 31.9 3.3
    Composition (6) of the present invention Acetophenone - 33:67 44.0 46.1
    Composition (7) of the present invention Acetophenone - 33:67 14.9 38.1
    Composition (8) of the present invention Acetophenone - 33:67 7.8 8.6
    Composition (9) of the present invention Acetophenone - 33: 67 50.1 63.1
    Composition (10) of the present invention Liquid paraffin - 33:67 34.9 13.1
    Composition (11) of the present invention Liquid paraffin - 33:67 53.1 22.8
    Composition (12) of the present invention Aromatic hydrocarbon - 33:67 27.3 24.2
    Composition (13) of the present invention Aromatic hydrocarbon - 33:67 42.6 58.2
    Composition (14) of the present invention Diisobutyl adipate - 33:67 30.1 11.2
    Composition (15) of the present invention Acetophenone - 33:67 21.3 24.7
    Composition (16) of the present invention Isoparaffin - 33:67 31.0 24.3
    Composition (17) of the present invention Acetophenone Benzophenone-based ultraviolet absorber 34:66 17.8 78.6
    Composition (18) of the present invention Acetophenone Benzotriazole-based ultraviolet absorber 40:60 28.4 75.7
    Comparative composition (1) Acetophenone - 3:97 33.9 0.6



    Claims

    1. A pesticidal composition in the form of an aqueous emulsion, comprising:

    (a) fenpyrazamine;

    (b) a hydrophobic organic solvent selected from vegetable oils, esters, ketones and paraffins;

    (c) a water-soluble polymer dispersing agent selected from one or more water-soluble polymer dispersing agent(s) selected from the group consisting of a vinyl-based polymer of polyvinylalcohol, polyvinylpyrrolidone, vinyl acetate copolymer, and sodium polyacrylate, and polysaccharides of gum arabic, xanthan gum, rhamsan gum, locust bean gum, guar gum, carrageenan, welan gum, alginic acid, alginate, gum tragacanth, methyl cellulose, ethyl cellulose, sodium carboxymethyl cellulose, hydroxyethyl cellulose, and hydroxypropyl cellulose; and

    (d) water;

    wherein liquid droplets in which the fenpyrazamine is suspended or dissolved in the hydrophobic organic solvent are emulsified in an aqueous continuous phase, and also a weight ratio of the fenpyrazamine to the hydrophobic organic solvent is from 5:95 to 70:30; wherein the liquid droplets have an average particle diameter of 5 to 60 µm.
     


    Ansprüche

    1. Pestizidzusammensetzung in Form einer wässrigen Emulsion, umfassend:

    (a) Fenpyrazamin,

    (b) ein hydrophobes organisches Lösungsmittel, ausgewählt aus pflanzlichen Ölen, Estern, Ketonen und Paraffinen,

    (c) ein wasserlösliches polymeres Dispergiermittel, ausgewählt aus einem oder mehreren wasserlöslichen polymeren Dispergiermitteln, welche(s) aus der Gruppe, die aus einem Polymer auf Vinylbasis aus Polyvinylalkohol, Polyvinylpyrrolidon, Vinylacetat-Copolymer und Natriumpolyacrylat, und Polysacchariden aus Gummiarabikum, Xanthan, Rhamsan, Johannisbrotkernmehl, Guarkernmehl, Carrageen, Welangummi, Alginsäure, Alginat, Traganth, Methylcellulose, Ethylcellulose, Natriumcarboxymethylcellulose, Hydroxyethylcellulose und Hydroxypropylcellulose besteht, ausgewählt ist/sind und

    d) Wasser,

    wobei flüssige Tröpfchen, in denen das Fenpyrazamin in dem hydrophoben organischen Lösungsmittel suspendiert oder gelöst ist, in einer wässrigen kontinuierlichen Phase emulgiert sind, und ferner das Gewichtsverhältnis des Fenpyrazamins zu dem hydrophoben organischen Lösungsmittel 5:95 bis 70:30 beträgt, wobei die flüssigen Tröpfchen einen mittleren Teilchendurchmesser von 5 bis 60 µm aufweisen.
     


    Revendications

    1. Composition pesticide sous la forme d'une émulsion aqueuse, comprenant :

    (a) de la fenpyrazamine ;

    (b) un solvant organique hydrophobe choisi parmi les huiles végétales, les esters, les cétones et les paraffines ;

    (c) un agent dispersant polymère soluble dans l'eau choisi parmi un ou plusieurs agents dispersants polymères solubles dans l'eau choisis dans le groupe constitué par un polymère à base de vinyle de poly(alcool vinylique), polyvinylpyrrolidone, copolymère d'acétate de vinyle, et poly(acrylate de sodium), et les polysaccharides de gomme arabique, gomme xanthane, gomme rhamsane, gomme de caroube, gomme de guar, carraghénane, gomme welane, acide alginique, alginate, gomme adragante, méthylcellulose, éthylcellulose, carboxyméthylcellulose sodique, hydroxyéthylcellulose, et hydroxypropylcellulose ; et

    (d) de l'eau ;

    dans laquelle des gouttelettes liquides dans lesquelles la fenpyrazamine est en suspension ou en solution dans le solvant organique hydrophobe sont émulsionnées dans une phase aqueuse continue, et également le rapport en poids de la fenpyrazamine au solvant organique hydrophobe est de 5/95 à 70/30 ; dans laquelle les gouttelettes liquides ont un diamètre de particule moyen de 5 à 60 µm.
     






    Cited references

    REFERENCES CITED IN THE DESCRIPTION



    This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.

    Patent documents cited in the description