JP3772994B2 - Pesticide granule for paddy field - Google Patents
Pesticide granule for paddy field Download PDFInfo
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- JP3772994B2 JP3772994B2 JP17793895A JP17793895A JP3772994B2 JP 3772994 B2 JP3772994 B2 JP 3772994B2 JP 17793895 A JP17793895 A JP 17793895A JP 17793895 A JP17793895 A JP 17793895A JP 3772994 B2 JP3772994 B2 JP 3772994B2
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Description
【0001】
【産業上の利用分野】
本発明は水田用農薬粒剤に関する。詳しくは、本発明は、難水溶性農薬活性成分の水中への溶出量を増し、その効果が十分に発揮できるように改良された水田用農薬粒剤に関する。
【0002】
【従来の技術および発明が解決すべき課題】
農業用薬剤の散布にかかわる製剤形態としては、これまで、粒剤、粉剤、水和剤、フロアブル剤、水溶剤、液剤、乳剤等が知られており、また、最近では、錠剤(ジャンボ剤)、パック剤も開発されている。
粒剤は、散布時の飛散が少ない、適量の施用が容易等の理由により広く使用されている。また、近年、粒剤施用量の少量化(3kg/10aから1kg/10a)の開発がなされる等、省力化、減農薬化の傾向にあわせた開発がされている。
しかし、難水溶性の農薬活性成分を粒剤に加工し水田に散布した場合、農薬活性成分が水中に溶出されなかったり、溶出した農薬活性成分が土壌に吸着され、農薬活性成分の田面水中の濃度が十分に上がらずに活性成分本来の効果を発揮できない場合がある。
特公昭47−24731号、特公昭48−1182号及び特公平3−76281号には、乳剤を粒剤に含浸させ水中への溶出速度を改良した特許が出願公告されている。
しかし、これらの方法によっても農薬活性成分の田面水中の濃度が十分に上がらずに農薬本来の効果を発揮できない場合がある。
【0003】
【課題を解決するための手段】
本発明者等は、このような状況に鑑み、研究を重ねた結果、下記の組成(処方)を有する粒剤を水田に施用した場合、該製剤では田面水へ農薬活性成分を速やかに溶出しその効果を十分に発揮することを見出し、本発明を完成するに至った。
即ち、本発明は、非水溶性有機溶媒に難水溶性農薬活性物質を溶解して成る20℃における比重が0.90以上1.00未満の溶液を、担体に担持被覆せしめて成る水田用農薬粒剤に係わるものである。
本発明の水田用農薬粒剤は、水田へ散布された後、田面水へ難水溶性農薬活性物質を速やかに放出し有効な濃度に保つことが可能である。
以下、本発明の水田用農薬粒剤について詳細に説明する。
【0004】
本発明で使用される難水溶性の農薬活性物質は、水溶性が低く水面施用時に、そのままでは効果が発揮されず、界面活性剤等補助剤の添加が必要な農薬活性物質をいう。例えば、20℃における水に対する溶解度が10ppm 以下の農薬活性成分を挙げることができ、その具体例として、
2−ベンゾチアゾール−2−イルオキシ−N−メチルアセトアニリド、
1−(3−クロロ−4−トリフルオロメチルフェニル)−4−(N,N−ジメチルカルバモイル)−5(4H)−テトラゾリノン、
1−(3−クロロ−4−トリフルオロメトキシフェニル)−4−(N,N−ジプロピルカルバモイル)−5(4H)−テトラゾリノン、
1−フェニル−4−(N−エチル−N−シクロヘプチルカルバモイル)−5(4H)−テトラゾリノン、
1−(3−クロロ−4−イソプロピルフェニル)−4−(N,N−ジプロピルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−クロロフェニル)−4−(N,N−ジプロピルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−クロロシクロヘキセン−1−イル)−4−(N−エチル−N−シクロヘキシルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−クロロ−6−メチルフェニル)−4−(N,N−ジエチルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−クロロ−6−メチルフェニル)−4−(N,N−ジプロピルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−クロロフェニル)−4−(N−シクロペンチル−N−エチルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−クロロフェニル)−4−(N−シクロペンチル−N−プロピルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−クロロフェニル)−4−(N−シクロヘキシル−N−エチルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−クロロ−6−メチルフェニル)−4−(N−シクロペンチル−N−プロピルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−ブロモフェニル)−4−(N−シクロペンチル−N−エチルカルバモイル)−5(4H)−テトラゾリノン、
1−(2−クロロ−6−メチルフェニル)−4−(N−プロピル−N−sec−ブチルカルバモイル)−5(4H)−テトラゾリノン等を挙げることができる。
【0005】
本発明で使用される非水溶性有機溶媒は、イソパラフィン、高沸点芳香族炭化水素系溶媒、脂肪酸エステル類、芳香性エステル類及びそれらの混合物を例示することができる。
高沸点芳香族炭化水素系溶媒とは、高沸点溶剤として一般に販売されている芳香族炭化水素系溶剤を言い、農薬乳剤で広く使用されているキシレンよりも高い沸点を有する溶剤を高沸点溶剤と呼ぶことが多い。
高沸点芳香族炭化水素系溶媒の例として、ソルベッソ200(製品名 エクソン化学株式会社)、ハイゾールSAS296(製品名 日本石油化学株式会社)、カクタスソルベントP−220(製品名 日鉱石油化学株式会社)を挙げることができる。
本発明で使用される担体としては、調製された農薬溶液を担持できる多孔質の粒状担体もしくは練り込み造粒した粒状担体を挙げることができる。
練り込み造粒法で作られた粒状担体は、農薬粒剤の製造時に広く使用されている。例えば、ベントナイト、リグニンスルホン酸、キャリアー(タルク、炭酸カルシウム、クレー等)を、必要に応じ粉砕、均一に混合する。次に水を加え混練する。混練物をスクリーンで押し出し、適当な長さに解砕後、乾燥機で乾燥する。その後、粒状担体を篩別することで適当な粒径を有す粒状担体を得ることができる。
多孔質の粒状担体の例としては、軽石粉砕粒、ベントナイト粉砕粒、各種焼成粒を挙げることができる。
また、練り込み造粒時に他の農薬活性物質を添加してもよい。この場合、2種以上の農薬活性成分を含有する本発明水田用農薬粒剤を製造することができる。
【0006】
本発明の水田用農薬粒剤は、該粒剤100重量部あたり、難水溶性農薬活性成分を約0.1重量部〜約30重量部、好ましくは、約1重量部〜約20重量部、非水溶性有機溶媒を約1重量部〜約30重量部、好ましくは、約5重量部〜約20重量部、農薬粒状担体を約40重量部〜約95重量部、好ましくは、約70重量部〜約90重量部を含有することができる。
本発明の水田用農薬粒剤は、例えば、農薬活性成分を非水溶性有機溶媒に溶かし20℃における比重が0.90以上1.00未満になるよう農薬溶液を調製する。次に、粒状担体を混合機に入れ、混合しながら調製した農薬溶媒を滴下或いは噴霧する。粒状担体に完全に含浸担持され、均一になるまで混合機の運転を続け目的の水田用農薬粒剤を製造することができる。
【0007】
【実施例】
次に、本発明化合物を実施例によりさらに具体的に説明するが、本発明はこれらの実施例に限定されるものではない。
【0008】
供試化合物
化合物1 1−(2−クロロフェニル)−4−(N−シクロヘキシル−N−エチルカルバモイル)−5(4H)−テトラゾリノン、
化合物2 1−フェニル−4−(N−シクロヘプチル−N−エチルカルバモイル)−5(4H)−テトラゾリノン、
化合物3 1−(2−クロロ−6−メチルフェニル)−4−(N−プロピル−N−sec−ブチルカルバモイル)−5(4H)−テトラゾリノン、
化合物4 1−(2−クロロシクロヘキセン−1−イル)−4−(N−シクロヘキシル−N−エチルカルバモイル)−5(4H)−テトラゾリノン、
化合物5 1−(2−クロロフェニル)−4−(N−シクロペンチル−N−プロピルカルバモイル)−5(4H)−テトラゾリノン、
化合物6 1−(2−クロロ−6−メチルフェニル)−4−(N−シクロペンチル−N−プロピルカルバモイル)−5(4H)−テトラゾリノン、
化合物7 メチル 2−{(〔({〔4,6−ジメトキシ−2−ピリミジル〕アミノ}カルボニル)アミノ〕スルフォニル)メチル}ベンゾエート、
化合物8 N−(4−メチルフェニル)−N′−(1−メチル−1−フェニルエチル)ウレア、
化合物9 1−(2−クロロイミダゾ〔1,2−a〕ピリジン−3−イルスルフォニル)−3−(4,6−ジメトキシピリミジン−2−イル)ウレア。
【0009】
製剤例1
処方
化合物1 3.00%
イソパラフィン 3.60%
ソルベッソ200 11.00%
粒状担体(練り込み造粒法による) 82.40%
製造
化合物1を、イソパラフィンとソルベッソ200(製品名 エクソン化学株式会社)の混合溶媒に溶解した。この溶液の比重は0.98g/ml(20℃)であった。
粒状担体を混合機へ所定量投入した。混合機を運転しながら、上記調製した化合物1溶液を滴下して加えた。滴下終了後、溶液が完全に染み込むまで運転を続け農薬粒剤を得た。
【0010】
製剤例2
製剤例1の処方で化合物1を化合物2に替え、製剤例1と同様にして農薬粒剤を得た。
製剤例3
製剤例1の処方で化合物1を化合物3に替え、製剤例1と同様にして農薬粒剤を得た。
製剤例4
製剤例1の処方で化合物1を化合物4に替え、製剤例1と同様にして農薬粒剤を得た。
製剤例5
製剤例1の処方で化合物1を化合物5に替え、製剤例1と同様にして農薬粒剤を得た。
製剤例6
製剤例1の処方で化合物1を化合物6に替え、製剤例1と同様にして農薬粒剤を得た。
【0011】
製剤例7
処方
化合物1 3.00%
化合物7 0.75%
イソパラフィン 3.60%
ソルベッソ200 11.00%
リグニンスルホン酸ナトリウム 0.50%
ベントナイト粉末 30.00%
タルク粉末 51.15%
製造
化合物7、リグニンスルホン酸ナトリウム、ベントナイト粉末、タルク粉末をニーダーKDAJ−60(不二パウダル社製)で混合した後、水を加え混練した。押出造粒機に該混練物を移し、0.8mmのスクリーンを使って押し出した。流動床乾燥機で乾燥し農薬活性物質(化合物7)を含有した粒状担体を得た。
化合物1を、イソパラフィンとソルベッソ200の混合溶媒に溶解した。この溶液の比重は0.98g/ml(20℃)であった。
上記粒状担体を混合機へ投入した。混合機を運転しながら、調製した化合物1溶液を滴下して加えた。滴下終了後、溶液が完全に含浸被覆するまで運転を続け農薬粒剤を得た。
【0012】
製剤例8
処方
化合物1 3.00%
化合物8 15.00%
化合物9 0.75%
イソパラフィン 3.60%
ソルベッソ200 11.00%
リグニンスルホン酸ナトリウム 0.50%
ベントナイト粉末 30.00%
タルク粉末 36.15%
製造
化合物8、化合物9、リグニンスルホン酸ナトリウム、ベントナイト粉末、タルク粉末をニーダーKDAJ−60で混合した後、水を加え混練した。該混練物を押出造粒機に移し、0.8mmのスクリーンを使って押し出した。流動床乾燥機で乾燥し、農薬活性物質(化合物8、化合物9)を含有した粒状担体を得た。
化合物1を、イソパラフィンとソルベッソ200の混合溶媒に溶解した。この溶液の比重は0.98g/ml(20℃)であった。
上記粒状担体を混合機へ投入し、混合機を運転しながら、上記化合物1溶液を滴下して加えた。滴下終了後、溶液が完全にしみ込むまで運転を続け農薬粒剤を得た。
【0013】
比較例1
処方
化合物1 3.00%
リグニンスルホン酸ナトリウム 0.50%
ベントナイト粉末 30.00%
練り込み粒剤キャリアー 66.50%
製造
全成分をニーダーKDAJ−60に入れ、混合後、水を加え混練した。該混練物を押出造粒機に移し、0.8mmのスクリーンを使って押し出した。流動床乾燥機で乾燥して農薬粒剤を得た。
【0014】
比較例2
処方
化合物1 3.00%
化合物7 0.75%
ソルベッソ200 15.00%
リグニンスルホン酸ナトリウム 0.50%
ベントナイト粉末 30.00%
タルク粉末 51.15%
製造
化合物7、リグニンスルホン酸ナトリウム、ベントナイト粉末、タルク粉末をニーダーKDAJ−60で混合した後、水を加え混練した。該混練物を押出造粒機に移し、0.8mmのスクリーンを用い造粒した。流動床乾燥機で乾燥し、農薬原体を含有した粒状担体を得た。
化合物1をソルベッソ200に溶解した。この溶液の比重は1.03g/ml(20℃)であった。
上記粒状担体を混合機へ投入し運転しながら、上記化合物1溶液を滴下して加えた。滴下終了後、溶液が完全にしみ込むまで運転を続け農薬粒剤を得た。
【0015】
比較例3
処方
化合物1 3.00%
化合物8 15.00%
化合物9 0.90%
N−ドデシルピロリドン 20.00%
ポリオキシエチレンスチリル
フェニルエーテルとドデシル
ベンゼンスルホン酸カルシウ
ムの混合物 1.00%
リグニンスルホン酸ナトリウム 0.50%
ベントナイト粉末 30.00%
タルク粉末 29.60%
製造
化合物8、化合物9、リグニンスルホン酸ナトリウム、ベントナイト粉末、タルク粉末をニーダーKDAJ−60で混合した後、水を加え混練した。該混練物を押出造粒機に移し、0.8mmのスクリーンを用い造粒した。流動床乾燥機で乾燥し、農薬原体を含有した粒状担体を得た。
化合物1を、ポリオキシエチレンスチリルフェニルエーテル、ドデシルベンゼンスルホン酸カルシウム及びN−ドデシルピロリドンと混合し化合物1の乳剤を作った。この乳剤の比重は0.95g/ml(20℃)であった。
上記粒状担体を混合機へ投入した。混合機を運転しながら、該乳剤を滴下して加えた。滴下終了後、乳剤が完全にしみ込むまで運転を続け農薬粒剤を得た。
【0016】
試験例1(農薬活性成分の水中濃度の測定)
水田土壌を厚さ5cmに充填したプラスチック製(25cm×39cm×15cm)ポットに水を加え水深を4cmとした。20℃の恒温浴中に放置後、製剤例1〜8および、比較例1〜3の製剤0.1gを秤量し均一に散布した。
所定時間毎に各ポットから水を一部採取しHPLCで分析し、絶対検量線法により化合物1〜化合物6の濃度を測定した。
結果
【0017】
【表1】
【0018】
【表2】
【0019】
【発明の効果】
本発明は、試験例で示したように、難水溶性の農薬活性物質を、田面水に速やかに放出し有効な水中濃度を維持するという効果を示した。[0001]
[Industrial application fields]
The present invention relates to a pesticide granule for paddy fields. Specifically, the present invention relates to an agrochemical granule for paddy fields that has been improved so as to increase the amount of the slightly water-soluble agrochemical active ingredient to be eluted in water and to fully exert its effect.
[0002]
[Background Art and Problems to be Solved by the Invention]
So far, granules, powders, wettable powders, wettable powders, aqueous solvents, liquids, emulsions, etc. have been known as dosage forms for spraying agricultural chemicals. Recently, tablets (jumbo) Packing agents have also been developed.
Granules are widely used for reasons such as little scattering during spraying and easy application of an appropriate amount. Also, in recent years, development has been made in line with the trend of labor saving and pesticide reduction, such as the development of a small amount of granule application (from 3 kg / 10a to 1 kg / 10a).
However, when a poorly water-soluble pesticide active ingredient is processed into granules and sprayed onto paddy fields, the pesticide active ingredient is not eluted in the water, or the eluted pesticide active ingredient is adsorbed to the soil, In some cases, the concentration of the active ingredient is not sufficiently increased and the original effect of the active ingredient cannot be exhibited.
In Japanese Patent Publication Nos. 47-24731, 48-1182 and 3-76281, patents in which emulsions are impregnated into granules to improve the dissolution rate in water are published.
However, even if these methods are used, the concentration of the agricultural chemical active ingredient in the surface water may not be sufficiently increased, and the original effect of the agricultural chemical may not be exhibited.
[0003]
[Means for Solving the Problems]
In view of such circumstances, the present inventors have conducted research, and as a result, when a granule having the following composition (prescription) is applied to a paddy field, the formulation quickly dissolves the agrochemical active ingredient into the surface water. The inventors have found that the effect is sufficiently exhibited, and have completed the present invention.
That is, the present invention provides a paddy pesticide comprising a carrier having a solution having a specific gravity at 20 ° C. of 0.90 or more and less than 1.00 obtained by dissolving a poorly water-soluble pesticide active substance in a water-insoluble organic solvent. It relates to granules.
The paddy field pesticide granule of the present invention can be quickly released to the surface water after being sprayed onto the paddy field, and can be kept at an effective concentration.
Hereinafter, the agrochemical granule for paddy fields of the present invention will be described in detail.
[0004]
The poorly water-soluble agrochemical active substance used in the present invention refers to an agrochemical active substance that has low water solubility and does not exhibit its effect when applied to the water surface, and requires the addition of an auxiliary agent such as a surfactant. For example, a pesticidal active ingredient having a solubility in water at 20 ° C. of 10 ppm or less can be mentioned.
2-benzothiazol-2-yloxy-N-methylacetanilide,
1- (3-chloro-4-trifluoromethylphenyl) -4- (N, N-dimethylcarbamoyl) -5 (4H) -tetrazolinone,
1- (3-chloro-4-trifluoromethoxyphenyl) -4- (N, N-dipropylcarbamoyl) -5 (4H) -tetrazolinone,
1-phenyl-4- (N-ethyl-N-cycloheptylcarbamoyl) -5 (4H) -tetrazolinone,
1- (3-chloro-4-isopropylphenyl) -4- (N, N-dipropylcarbamoyl) -5 (4H) -tetrazolinone,
1- (2-chlorophenyl) -4- (N, N-dipropylcarbamoyl) -5 (4H) -tetrazolinone,
1- (2-chlorocyclohexen-1-yl) -4- (N-ethyl-N-cyclohexylcarbamoyl) -5 (4H) -tetrazolinone,
1- (2-chloro-6-methylphenyl) -4- (N, N-diethylcarbamoyl) -5 (4H) -tetrazolinone,
1- (2-chloro-6-methylphenyl) -4- (N, N-dipropylcarbamoyl) -5 (4H) -tetrazolinone,
1- (2-chlorophenyl) -4- (N-cyclopentyl-N-ethylcarbamoyl) -5 (4H) -tetrazolinone,
1- (2-chlorophenyl) -4- (N-cyclopentyl-N-propylcarbamoyl) -5 (4H) -tetrazolinone,
1- (2-chlorophenyl) -4- (N-cyclohexyl-N-ethylcarbamoyl) -5 (4H) -tetrazolinone,
1- (2-chloro-6-methylphenyl) -4- (N-cyclopentyl-N-propylcarbamoyl) -5 (4H) -tetrazolinone,
1- (2-bromophenyl) -4- (N-cyclopentyl-N-ethylcarbamoyl) -5 (4H) -tetrazolinone,
Examples include 1- (2-chloro-6-methylphenyl) -4- (N-propyl-N-sec-butylcarbamoyl) -5 (4H) -tetrazolinone.
[0005]
Examples of the water-insoluble organic solvent used in the present invention include isoparaffin, high-boiling aromatic hydrocarbon solvents, fatty acid esters, aromatic esters, and mixtures thereof.
The high-boiling aromatic hydrocarbon solvent refers to an aromatic hydrocarbon solvent that is generally sold as a high-boiling solvent. A solvent having a higher boiling point than xylene widely used in agricultural chemical emulsions is referred to as a high-boiling solvent. Often called.
Examples of high-boiling aromatic hydrocarbon solvents include Solvesso 200 (product name: Exxon Chemical Co., Ltd.), Hysol SAS296 (product name: Nippon Petrochemical Co., Ltd.), and Cactus Solvent P-220 (product name: Nikko Petrochemical Co., Ltd.). Can be mentioned.
Examples of the carrier used in the present invention include a porous granular carrier capable of supporting the prepared agricultural chemical solution or a granular carrier kneaded and granulated.
Granular carriers made by the kneading granulation method are widely used in the production of agricultural chemical granules. For example, bentonite, lignin sulfonic acid, and carrier (talc, calcium carbonate, clay, etc.) are pulverized and mixed uniformly as necessary. Next, water is added and kneaded. The kneaded product is extruded through a screen, pulverized to an appropriate length, and then dried in a dryer. Then, the granular carrier having an appropriate particle size can be obtained by sieving the granular carrier.
Examples of porous granular carriers include pumice crushed grains, bentonite crushed grains, and various fired grains.
Further, other agrochemical active substances may be added during kneading granulation. In this case, the agrochemical granule for paddy fields of the present invention containing two or more kinds of agrochemical active ingredients can be produced.
[0006]
The pesticide granule for paddy of the present invention has a water-insoluble pesticide active ingredient in an amount of about 0.1 to about 30 parts by weight, preferably about 1 to about 20 parts by weight per 100 parts by weight of the granules. About 1 part by weight to about 30 parts by weight of a water-insoluble organic solvent, preferably about 5 parts by weight to about 20 parts by weight, and about 40 parts by weight to about 95 parts by weight of an agrochemical granular carrier, preferably about 70 parts by weight. Up to about 90 parts by weight.
The agrochemical granule for paddy field of the present invention is prepared, for example, by dissolving an agrochemical active ingredient in a water-insoluble organic solvent so that the specific gravity at 20 ° C. is 0.90 or more and less than 1.00. Next, the granular carrier is put into a mixer, and the agrochemical solvent prepared while mixing is dropped or sprayed. The target agrochemical granule for paddy fields can be produced by completely impregnating and supporting the particulate carrier and continuing the operation of the mixer until it is uniform.
[0007]
【Example】
Next, although the compound of the present invention will be described more specifically with reference to examples, the present invention is not limited to these examples.
[0008]
Test compound Compound 1 1- (2-Chlorophenyl) -4- (N-cyclohexyl-N-ethylcarbamoyl) -5 (4H) -tetrazolinone,
Compound 2 1-phenyl-4- (N-cycloheptyl-N-ethylcarbamoyl) -5 (4H) -tetrazolinone,
Compound 3 1- (2-chloro-6-methylphenyl) -4- (N-propyl-N-sec-butylcarbamoyl) -5 (4H) -tetrazolinone,
Compound 4 1- (2-chlorocyclohexen-1-yl) -4- (N-cyclohexyl-N-ethylcarbamoyl) -5 (4H) -tetrazolinone,
Compound 5 1- (2-chlorophenyl) -4- (N-cyclopentyl-N-propylcarbamoyl) -5 (4H) -tetrazolinone,
Compound 6 1- (2-chloro-6-methylphenyl) -4- (N-cyclopentyl-N-propylcarbamoyl) -5 (4H) -tetrazolinone,
Compound 7 Methyl 2-{([({{[4,6-dimethoxy-2-pyrimidyl] amino} carbonyl) amino] sulfonyl) methyl} benzoate,
Compound 8 N- (4-methylphenyl) -N ′-(1-methyl-1-phenylethyl) urea,
Compound 9 1- (2-Chloroimidazo [1,2-a] pyridin-3-ylsulfonyl) -3- (4,6-dimethoxypyrimidin-2-yl) urea.
[0009]
Formulation Example 1
Formulated compound 1 3.00%
Isoparaffin 3.60%
Solvesso 200 11.00%
Granular carrier (by kneading granulation method) 82.40%
Production compound 1 was dissolved in a mixed solvent of isoparaffin and Solvesso 200 (product name: Exxon Chemical Co., Ltd.). The specific gravity of this solution was 0.98 g / ml (20 ° C.).
A predetermined amount of the granular carrier was charged into the mixer. While operating the mixer, the compound 1 solution prepared above was added dropwise. After completion of the dropping, the operation was continued until the solution was completely infiltrated to obtain an agrochemical granule.
[0010]
Formulation Example 2
In the formulation of Formulation Example 1, Compound 1 was changed to Compound 2, and in the same manner as Formulation Example 1, an agrochemical granule was obtained.
Formulation Example 3
In the formulation of Formulation Example 1, Compound 1 was replaced with Compound 3, and in the same manner as Formulation Example 1, agrochemical granules were obtained.
Formulation Example 4
In the formulation of Formulation Example 1, Compound 1 was replaced with Compound 4, and agrochemical granules were obtained in the same manner as Formulation Example 1.
Formulation Example 5
In the formulation of Formulation Example 1, Compound 1 was changed to Compound 5, and agrochemical granules were obtained in the same manner as Formulation Example 1.
Formulation Example 6
In the formulation of Formulation Example 1, Compound 1 was changed to Compound 6, and in the same manner as Formulation Example 1, an agrochemical granule was obtained.
[0011]
Formulation Example 7
Formulated compound 1 3.00%
Compound 7 0.75%
Isoparaffin 3.60%
Solvesso 200 11.00%
Sodium lignin sulfonate 0.50%
Bentonite powder 30.00%
Talc powder 51.15%
Production compound 7, sodium lignin sulfonate, bentonite powder and talc powder were mixed with a kneader KDAJ-60 (manufactured by Fuji Powder Co., Ltd.), and water was added and kneaded. The kneaded product was transferred to an extrusion granulator and extruded using a 0.8 mm screen. A granular carrier containing an agrochemical active substance (Compound 7) was obtained by drying in a fluid bed dryer.
Compound 1 was dissolved in a mixed solvent of isoparaffin and Solvesso 200. The specific gravity of this solution was 0.98 g / ml (20 ° C.).
The granular carrier was put into a mixer. While operating the mixer, the prepared Compound 1 solution was added dropwise. After completion of the dropping, the operation was continued until the solution was completely impregnated to obtain an agrochemical granule.
[0012]
Formulation Example 8
Formulated compound 1 3.00%
Compound 8 15.00%
Compound 9 0.75%
Isoparaffin 3.60%
Solvesso 200 11.00%
Sodium lignin sulfonate 0.50%
Bentonite powder 30.00%
Talc powder 36.15%
Production compound 8, compound 9, sodium lignin sulfonate, bentonite powder and talc powder were mixed with a kneader KDAJ-60, and water was added and kneaded. The kneaded product was transferred to an extrusion granulator and extruded using a 0.8 mm screen. It dried with the fluid bed dryer and the granular support | carrier containing an agrochemical active substance (Compound 8, Compound 9) was obtained.
Compound 1 was dissolved in a mixed solvent of isoparaffin and Solvesso 200. The specific gravity of this solution was 0.98 g / ml (20 ° C.).
The granular carrier was charged into a mixer, and the compound 1 solution was added dropwise while the mixer was operating. After completion of dropping, the operation was continued until the solution was completely soaked to obtain an agrochemical granule.
[0013]
Comparative Example 1
Formulated compound 1 3.00%
Sodium lignin sulfonate 0.50%
Bentonite powder 30.00%
Kneaded granule carrier 66.50%
All manufactured components were put into a kneader KDAJ-60, mixed and then kneaded with water. The kneaded product was transferred to an extrusion granulator and extruded using a 0.8 mm screen. It dried with the fluid bed dryer and obtained the agrochemical granule.
[0014]
Comparative Example 2
Formulated compound 1 3.00%
Compound 7 0.75%
Solvesso 200 15.00%
Sodium lignin sulfonate 0.50%
Bentonite powder 30.00%
Talc powder 51.15%
Production compound 7, sodium lignin sulfonate, bentonite powder, and talc powder were mixed with a kneader KDAJ-60, and water was added and kneaded. The kneaded product was transferred to an extrusion granulator and granulated using a 0.8 mm screen. It dried with the fluid bed dryer and obtained the granular support | carrier containing the agrochemical raw material.
Compound 1 was dissolved in Solvesso 200. The specific gravity of this solution was 1.03 g / ml (20 ° C.).
While the granular carrier was charged into the mixer and operated, the Compound 1 solution was added dropwise. After completion of dropping, the operation was continued until the solution was completely soaked to obtain an agrochemical granule.
[0015]
Comparative Example 3
Formulated compound 1 3.00%
Compound 8 15.00%
Compound 9 0.90%
N-dodecylpyrrolidone 20.00%
Mixture of polyoxyethylene styryl phenyl ether and calcium dodecylbenzenesulfonate 1.00%
Sodium lignin sulfonate 0.50%
Bentonite powder 30.00%
Talc powder 29.60%
Production compound 8, compound 9, sodium lignin sulfonate, bentonite powder and talc powder were mixed with a kneader KDAJ-60, and water was added and kneaded. The kneaded product was transferred to an extrusion granulator and granulated using a 0.8 mm screen. It dried with the fluid bed dryer and obtained the granular support | carrier containing the agrochemical raw material.
Compound 1 was mixed with polyoxyethylene styryl phenyl ether, calcium dodecylbenzenesulfonate and N-dodecylpyrrolidone to make an emulsion of Compound 1. The specific gravity of this emulsion was 0.95 g / ml (20 ° C.).
The granular carrier was put into a mixer. The emulsion was added dropwise while the mixer was running. After completion of dropping, the operation was continued until the emulsion was completely soaked to obtain an agrochemical granule.
[0016]
Test Example 1 (Measurement of concentration of agrochemical active ingredients in water)
Water was added to a plastic (25 cm × 39 cm × 15 cm) pot filled with paddy soil to a thickness of 5 cm to a depth of 4 cm. After allowed to stand in 20 ° C. in a thermostatic bath, Formulation Examples 1 to 8 and were weighed preparation 0.1g of Comparative Examples 1 to 3 were uniformly sprayed.
A part of water was collected from each pot every predetermined time and analyzed by HPLC, and the concentrations of Compound 1 to Compound 6 were measured by the absolute calibration curve method.
Results [0017]
[Table 1]
[0018]
[Table 2]
[0019]
【The invention's effect】
As shown in the test examples, the present invention showed the effect of maintaining the effective concentration in water by quickly releasing the poorly water-soluble agrochemical active substance into the surface water.
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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JP17793895A JP3772994B2 (en) | 1995-06-22 | 1995-06-22 | Pesticide granule for paddy field |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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JP17793895A JP3772994B2 (en) | 1995-06-22 | 1995-06-22 | Pesticide granule for paddy field |
Publications (2)
Publication Number | Publication Date |
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JPH0912406A JPH0912406A (en) | 1997-01-14 |
JP3772994B2 true JP3772994B2 (en) | 2006-05-10 |
Family
ID=16039700
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JP17793895A Expired - Fee Related JP3772994B2 (en) | 1995-06-22 | 1995-06-22 | Pesticide granule for paddy field |
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JP (1) | JP3772994B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
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KR100208745B1 (en) * | 1996-05-04 | 1999-07-15 | 이서봉 | Munon throwing pesticide treatment agent and its manufacturing method |
DE10142336A1 (en) | 2001-08-30 | 2003-03-20 | Bayer Cropscience Ag | Selective herbicides containing a tetrazolinone derivative |
TW200536482A (en) * | 2004-05-10 | 2005-11-16 | Earth Chemical Co | Harmful insect controlling agent, powdery insecticide preparation and behavior disturbing agent for isopods |
RU2008133618A (en) * | 2006-01-17 | 2010-02-27 | Осаму ЯМАДА (JP) | METHOD FOR STIMULING PLANT GROWTH AND IMPROVING THEIR QUALITY AND REAGENTS USED TO STIMULATE PLANT GROWTH AND IMPROVE THEIR QUALITY |
Family Cites Families (6)
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JPH085763B2 (en) * | 1986-07-09 | 1996-01-24 | 三井東圧化学株式会社 | Water-applied pesticide granules |
JP2692213B2 (en) * | 1987-12-26 | 1997-12-17 | 日産化学工業株式会社 | Controlled Release Granules for Weeding Paddy Fields |
JP2821467B2 (en) * | 1989-03-06 | 1998-11-05 | サンケイ化学株式会社 | Non-phytotoxic oil-release pesticides |
GB9016783D0 (en) * | 1989-09-01 | 1990-09-12 | Ici Plc | Agrochemical compositions |
JP2936207B2 (en) * | 1990-03-23 | 1999-08-23 | 武田薬品工業株式会社 | Granule of agrecultural chemical containing silaneofan |
JPH0517304A (en) * | 1991-07-09 | 1993-01-26 | Nissan Chem Ind Ltd | Granular herbicide |
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1995
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