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JPH05155706A - Agricultural chemical composition - Google Patents

Agricultural chemical composition

Info

Publication number
JPH05155706A
JPH05155706A JP35036691A JP35036691A JPH05155706A JP H05155706 A JPH05155706 A JP H05155706A JP 35036691 A JP35036691 A JP 35036691A JP 35036691 A JP35036691 A JP 35036691A JP H05155706 A JPH05155706 A JP H05155706A
Authority
JP
Japan
Prior art keywords
agricultural chemical
composition
polyhydric alcohol
fatty acid
water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP35036691A
Other languages
Japanese (ja)
Other versions
JP3739804B2 (en
Inventor
Yuichi Maekawa
祐一 前川
Takashi Masumura
崇 増村
Toshio Mizuno
利夫 水野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Soda Co Ltd
Original Assignee
Nippon Soda Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Soda Co Ltd filed Critical Nippon Soda Co Ltd
Priority to JP35036691A priority Critical patent/JP3739804B2/en
Publication of JPH05155706A publication Critical patent/JPH05155706A/en
Application granted granted Critical
Publication of JP3739804B2 publication Critical patent/JP3739804B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To obtain an agricultural chemical composition being readily diluted with both water and an oil, having excellent suspension in the same manner as water, having large use value in an agricultural field by blending an agricultural chemical such as fungicide, insecticide or acaricide with a polyhydric alcohol fatty acid ester. CONSTITUTION:An agricultural chemical such as thiophanate, triflumizole or hexythiazox is mixed with a polyhydric alcohol fatty acid ester (e.g. sorbitan monooleate or glycerol monostearate) to give an agricultural chemical composition. The fatty acid ester of the polyhydric alcohol has preferably 3-8 HLB. The amount of the composition is preferably about 5-20wt.%. In the case the agricultural chemical composition is solid at normal temperature, the composition is used as it is and in the case of liquid, the composition is adsorbed on a carrier having high oil absorption ability and can be used in a powdery state.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、水にも油にも希釈容易
な農薬組成物に関する。
TECHNICAL FIELD The present invention relates to an agrochemical composition which is easily diluted with water or oil.

【0002】[0002]

【従来の技術】近年、特に中南米のバナナ地帯では農薬
散布の省力化及び効力の増強を目的として、農薬を鉱物
油等に希釈して航空機散布する方法がとられている。散
布用の農薬製剤品には溶剤中に農薬原体と界面活性剤等
を溶解した乳剤や、農薬原体と鉱物質担体や界面活性剤
等を混合してジェット粉砕した水和剤や、農薬原体と界
面活性剤や鉱物質担体等を混合して顆粒状に成型した顆
粒水和剤(ドライフロアブル剤)や、農薬原体を界面活
性剤と鉱物質担体や有機物ポリマ−等と共に高濃度で水
中に分散させた濃厚懸濁液剤(フロアブル剤)等があ
る。しかし、これらの剤は何れも水に希釈するための製
剤品であるため、中南米で広く行われているような鉱物
油等に希釈する方法で使用するには適さなかった。
2. Description of the Related Art In recent years, particularly in the banana areas of Central and South America, a method of diluting a pesticide in mineral oil or the like and spraying it by aircraft has been adopted for the purpose of labor saving and enhancement of efficacy. Pesticide products for spraying include emulsions in which the pesticide raw material and surfactants are dissolved in a solvent, wettable powders obtained by mixing the pesticide raw material with mineral carrier or surfactant, and jet milling, and pesticides. Granule wettable powder (dry flowable agent) formed by mixing a drug substance with a surfactant or a mineral carrier, or a pesticide drug with a high concentration of a surfactant, a mineral carrier, an organic polymer, etc. There is a thick suspension agent (flowable agent) dispersed in water at. However, since these agents are all preparations for diluting with water, they are not suitable for use in the method of diluting with mineral oil widely used in Central and South America.

【0003】[0003]

【発明が解決しようとする課題】近年、中南米のバナナ
地帯で行われているような、農薬を鉱物油等の油に高濃
度で希釈して航空機散布する方法は、農薬散布の省力化
や効力の増強あるいは環境汚染の防止等に対しては大変
有効である。しかし、希釈剤としての農薬製剤品はすべ
て水に希釈するために処方されたものであるため、鉱物
油等の油には容易に希釈されず、特に水和剤やフロアブ
ル剤は油中では激しく凝集するために使用することがで
きなかった。本発明は、水にも油にも希釈容易な農薬組
成物を提供することを目的とする。
Recently, the method of diluting pesticides into oils such as mineral oil at a high concentration in a banana area in Latin America, and spraying them by aircraft is labor-saving and effective in spraying pesticides. It is very effective for enhancing the pollution and preventing environmental pollution. However, since all pesticide preparations as diluents are formulated to be diluted in water, they are not easily diluted in oils such as mineral oils, especially wettable powders and flowable agents are violent in oil. It could not be used to agglomerate. An object of the present invention is to provide an agrochemical composition that is easily diluted with water and oil.

【0004】[0004]

【課題を解決するための手段】本発明者等は、これらの
問題を解決するため鋭意検討し、本発明を完成した。即
ち、本発明は多価アルコ−ルの脂肪酸エステルを含有す
ることを特徴とする農薬組成物である。本発明に於ける
農薬原体は殺菌剤、殺虫剤、殺ダニ剤何れも使用でき
る。例えば、殺菌剤ではベンズイミダゾ−ル系のチオフ
ァネ−トメチル,ベノミル,チアベンダゾ−ル等や、エ
チレンビス−ジチオカ−バメ−ト系のジネブ,マンネ
ブ,マンゼブ,ポリカ−バメ−ト等や、ジメチルジチオ
カ−バメ−ト系のジラム,チウラム等や、ジカルボキシ
イミド系のビンクロゾリン,イプロジオン,プロシミド
ン等や、トリアゾ−ル系のトリアジメホン,ビテルタノ
−ル,ヘキサコナゾ−ル,プロピコナゾ−ル等や、イミ
ダゾ−ル系のトリフルミゾ−ル,プロクロラズ等があげ
られる。また、殺虫剤では有機リン系のMEP,DDV
P,ダイアジノン,サリチオン等や、ピレスロイド系の
パ−メスリン,フェンバレレ−ト,エトフェンプロック
ス等や、カ−バメ−ト系のNAC,MTMC,BPM
C,メソミル,カルタップ等や、ベンゾイルフェニルウ
レア系のジフルベンズロン,テフルベンズロン等があげ
られる。また殺ダニ剤ではケルセン,フェニソブロモレ
−ト,テトラジホン,BPPS,ヘキシチアゾクス等が
あげられる。
Means for Solving the Problems The inventors of the present invention have made extensive studies to solve these problems and completed the present invention. That is, the present invention is an agrochemical composition characterized by containing a fatty acid ester of polyhydric alcohol. As the pesticide raw material in the present invention, any of a bactericide, an insecticide and an acaricide can be used. For example, as fungicides, benzimidazole-type thiophanetomethyl, benomyl, thiabendazole, etc., ethylene bis-dithiocarbamate-type Zineb, maneb, manzeb, polycarbamate, etc., and dimethyldithiocaline. -Bamate type diram, thiuram, etc., dicarboximide type vinclozolin, iprodione, procymidone, etc., triazole type triadimefone, bittertanol, hexaconazole, propiconazole, etc., imidazole type And triflumizole, prochloraz, etc. In addition, as an insecticide, organophosphorus MEP, DDV
P, diazinon, salicion, etc., pyrethroid type permethrin, fenvalerate, etofenprox, etc., carbamate type NAC, MTMC, BPM
Examples thereof include C, mesomil, cartap, and the like, and benzoylphenylurea-based diflubenzuron, teflubenzuron, and the like. Examples of the acaricide include quelsen, phenisobromolate, tetradiphone, BPPS, hexithiazox and the like.

【0005】これらの農薬原体は常温で固体の場合は何
等問題がないが、液体の場合には吸油能の大きな担体例
えば酸化珪素等に吸着して用いればよい。農薬原体の処
方中の含有量は通常の水和剤と同様に1〜90重量%
(以下%と書く)でよく、好ましくは10〜80%であ
る。水にも油にも希釈可能にするために用いる多価アル
コ−ルの脂肪酸エステルとしては、脂肪酸部がC8 〜C
18の直鎖または分岐状の飽和あるいは不飽和の脂肪酸で
あり、例えば、カプリル酸,ラウリン酸,パルミチン
酸,ミリスチン酸,ステアリン酸,イソステアリン酸,
オレイン酸,セスキオレイン酸,リノ−ル酸,リノレイ
ン酸等であり、多価アルコールは2個以上の水酸基を有
したものであり、例えばグリセリン,ペンタエリスリト
ール,ジグリセリン,ジエチレングリコ−ル,トリエチ
レングリコ−ル,ソルビタン,ソルビト−ル,糖類等が
あげられる。
These pesticide raw materials have no problem when they are solid at room temperature, but when they are liquid, they may be adsorbed on a carrier having a large oil absorption capacity, such as silicon oxide. The content of the pesticide raw material in the formulation is 1 to 90% by weight as in the case of ordinary wettable powders.
(Hereinafter referred to as “%”), and preferably 10 to 80%. The fatty acid ester of polyhydric alcohol used for diluting both water and oil has a fatty acid portion of C 8 -C.
18 straight or branched, saturated or unsaturated fatty acids such as caprylic acid, lauric acid, palmitic acid, myristic acid, stearic acid, isostearic acid,
Examples thereof include oleic acid, sesquioleic acid, linoleic acid, and linoleic acid, and the polyhydric alcohol has two or more hydroxyl groups. For example, glycerin, pentaerythritol, diglycerin, diethylene glycol, triethylene glycol. , Sorbitan, sorbitol, sugars and the like.

【0006】本発明に用いられる多価アルコ−ルの脂肪
酸エステルは、前記記載の何れも使用可能であるが、親
水性と親油性のバランスを表すHLBが2〜9の値を持
ったものがよく、好ましくは3〜8のものがよい。ま
た、処方中の添加量は2〜30%がよく、好ましくは5
〜20%がよい。また、液状の場合には吸油能の大きな
担体に吸着させ、粉状にして用いることが可能である。
As the polyhydric alcohol fatty acid ester used in the present invention, any of the above-mentioned compounds can be used, but those having HLB of 2 to 9 representing the balance between hydrophilicity and lipophilicity are preferred. Good, and preferably 3-8. Further, the addition amount in the formulation is preferably 2 to 30%, preferably 5
~ 20% is good. Further, in the case of a liquid, it can be adsorbed on a carrier having a large oil absorption ability to be used in the form of powder.

【0007】界面活性剤としては通常の水和剤に用いら
れる陰イオン系,非イオン系のすべてが使用可能であ
る。例えば、リグニンスルホン酸の金属(Na,Ca,
Mg等)塩,アルキルアリルスルホン酸の金属(Na,
Ca,Mg等)塩やアンモニウム塩,アルキルスルホン
酸の金属(Na,Ca,Mg等)塩やアンモニウム塩,
ジアルキルスルホコハク酸の金属(Na,Ca,Mg
等)塩等の陰イオン系界面活性剤や、ポリオキシエチレ
ン(以下POEと書く)アルキルエ−テル,POEアル
キルエステル,POEアルキルアリルエ−テル,POE
ヒマシ油エ−テル,POEソルビタンエ−テル等の非イ
オン系界面活性剤である。また、処方中の使用量は通常
の水和剤と同様で2〜30%がよく、好ましくは5〜2
0%がよい。
As the surfactant, all of the anionic and nonionic compounds used in ordinary wettable powders can be used. For example, metals of lignin sulfonic acid (Na, Ca,
Mg salt), metal of alkylallyl sulfonic acid (Na,
Ca, Mg, etc.) salts and ammonium salts, alkylsulfonic acid metal (Na, Ca, Mg, etc.) salts and ammonium salts,
Dialkyl sulfosuccinic acid metals (Na, Ca, Mg
Etc.) Anionic surfactants such as salts, polyoxyethylene (hereinafter referred to as POE) alkyl ether, POE alkyl ester, POE alkylallyl ether, POE
It is a nonionic surfactant such as castor oil ether and POE sorbitan ether. Further, the amount used in the formulation is similar to that of a normal wettable powder and is preferably 2 to 30%, preferably 5 to 2
0% is good.

【0008】増量剤としては通常の水和剤に用いられる
ものすべてが使用可能であるが、好ましくは焼成して付
着水分の少ないものがよい。例えば、クレー,タルク,
炭酸カルシウム,珪藻土,焼成クレ−,焼成珪藻土等で
ある。本発明の農薬組成物の製造方法としては通常の水
和剤と同様の方法で製造可能である。即ち、農薬原体と
本発明の多価アルコ−ルの脂肪酸エステルと界面活性剤
及び増量剤を混合し、粉砕することにより製造できる。
As the bulking agent, all of those used in ordinary wettable powders can be used, but preferably those which are calcined to have a small amount of attached water. For example, clay, talc,
Examples include calcium carbonate, diatomaceous earth, calcined clay, and calcined diatomaceous earth. The pesticidal composition of the present invention can be produced by the same method as that for ordinary wettable powders. That is, it can be produced by mixing the pesticide raw material, the polyhydric alcohol fatty acid ester of the present invention, the surfactant and the extender, and pulverizing.

【0009】[0009]

【実施例】以下実施例にて本発明を詳細に説明するが、
本発明はこれらの実施例に限定されるものではない。 実施例1 チオファネ−トメチル70g,二酸化珪素に50%で吸
着させたソルビタンモノオレエ−ト〔ニュ−コ−ル80
(HLB:4.6);日本乳化剤株式会社製〕10g,
二酸化珪素に50%で吸着させたPOEアルキルフェニ
ルエ−テルホルマリン縮合物7g,焼成珪藻土13gを
ビニ−ル袋で混合した後、ジェット粉砕機で粉砕し目的
の農薬組成物を得た。
The present invention will be described in detail with reference to the following examples.
The invention is not limited to these examples. Example 1 70 g of thiophanate methyl, sorbitan monooleate [Newcol 80 adsorbed on silicon dioxide at 50%]
(HLB: 4.6); Nippon Emulsifier Co., Ltd.] 10 g,
7 g of POE alkylphenyl ether formalin condensate adsorbed on silicon dioxide at 50% and 13 g of calcined diatomaceous earth were mixed in a vinyl bag and then pulverized with a jet pulverizer to obtain a target pesticide composition.

【0010】実施例2 トリフルミゾ−ル30g,二酸化珪素に50%で吸着さ
せたグリセリンモノステアレ−ト〔レオド−ルMS−6
0(HLB:3.8);花王株式会社製〕10g,二酸
化珪素に50%で吸着させたPOEアルキルエ−テル1
0g,炭酸カルシウム50gをビニ−ル袋で混合した
後、ジェット粉砕機で粉砕し目的の農薬組成物を得た。
Example 2 30 g of triflumizole, glycerin monostearate [Rheodor MS-6 adsorbed on silicon dioxide at 50%]
0 (HLB: 3.8); manufactured by Kao Corporation] 10 g, POE alkyl ether 1 adsorbed on silicon dioxide at 50%
After mixing 0 g and 50 g of calcium carbonate in a vinyl bag, the mixture was pulverized with a jet pulverizer to obtain the target agricultural chemical composition.

【0011】実施例3 ヘキシチアゾクス10g,二酸化珪素に50%で吸着さ
せたソルビタンモノステアレ−ト〔ニュ−コ−ル60
(HLB:4.6);日本乳化剤株式会社製〕10g,
二酸化珪素に50%で吸着させたPOEアルキルフェニ
ルエ−テル7g,焼成珪藻土73gをビニ−ル袋で混合
した後、ジェット粉砕機で粉砕し目的の農薬組成物を得
た。
Example 3 10 g of hexithiazox, sorbitan monostearate (Newcol 60 adsorbed on silicon dioxide at 50%)
(HLB: 4.6); Nippon Emulsifier Co., Ltd.] 10 g,
7 g of POE alkylphenyl ether adsorbed on silicon dioxide at 50% and 73 g of calcined diatomaceous earth were mixed in a vinyl bag and then pulverized with a jet pulverizer to obtain a target pesticide composition.

【0012】比較例1 実施例1の処方において、二酸化珪素に50%で吸着さ
せたソルビタンモノオレエ−ト10gの代わりに焼成珪
藻土10gを用いたものをビニ−ル袋で混合した後、ジ
ェット粉砕機で粉砕し農薬組成物を得た。
COMPARATIVE EXAMPLE 1 In the formulation of Example 1, 10 g of calcined diatomaceous earth was used in place of 10 g of sorbitan monooleate adsorbed on silicon dioxide at 50%, mixed in a vinyl bag, and then jetted. It was crushed with a crusher to obtain an agricultural chemical composition.

【0013】比較例2 実施例2の処方において、二酸化珪素に50%(w/
w)で吸着させたグリセリンモノステアレ−ト10gの
代わりに炭酸カルシウム10gを用いたものをビニ−ル
袋で混合した後、ジェット粉砕機で粉砕し農薬組成物を
得た。
Comparative Example 2 In the formulation of Example 2, 50% (w / w) was added to silicon dioxide.
A mixture containing 10 g of calcium carbonate instead of 10 g of glycerin monostearate adsorbed in w) was mixed in a vinyl bag and then pulverized with a jet pulverizer to obtain an agrochemical composition.

【0014】比較例3 実施例3の処方において、二酸化珪素に50%(w/
w)で吸着させたソルビタンモノステアレ−ト10gの
代わりに焼成珪藻土10gを用いたものをビニ−ル袋で
混合した後、ジェット粉砕機で粉砕し農薬組成物を得
た。
Comparative Example 3 In the formulation of Example 3, 50% (w / w) was added to silicon dioxide.
A mixture containing 10 g of calcined diatomaceous earth instead of 10 g of sorbitan monostearate adsorbed in w) was mixed in a vinyl bag and then ground with a jet grinder to obtain an agrochemical composition.

【0015】[0015]

【発明の効果】試験例1 懸濁安定性試験 実施例1〜3及び比較例1〜3の農薬組成物について水
(3度硬水)と油〔日石農薬オイル(日本石油化学株式
会社製)〕に対する懸濁安定性をみた。 〈水(3度硬水)に対する懸濁安定性試験〉100mlの
沈降管に3度硬水100mlを入れ、そこに試料約100
mg(1000倍)を加えて試料がすべて沈降した後、ゴ
ム栓をつけて30回/分倒立し静置する。静置後30
分,3時間,5時間,24時間後の懸濁安定性(凝集の
有無)を観察した結果を表1に示す。
EFFECT OF THE INVENTION Test Example 1 Suspension Stability Test Regarding the agrochemical compositions of Examples 1 to 3 and Comparative Examples 1 to 3, water (3 times hard water) and oil [Nisseki Agrochemical Oil (Nippon Petrochemical Co., Ltd.)] ], The suspension stability was observed. <Suspension stability test against water (3 degree hard water)> Put 100 ml of 3 degree hard water into a 100 ml settling tube and put about 100
mg (1000 times) is added and all the samples are settled, and then a rubber stopper is attached and the tube is inverted 30 times / minute and allowed to stand. 30 after standing
Table 1 shows the results of observation of suspension stability (presence or absence of aggregation) after 3 minutes, 5 hours, and 24 hours.

【0016】[0016]

【表1】 [Table 1]

【0017】〈油(日石農薬オイル)に対する懸濁安定
性試験〉10mlのビ−カ−に試料約0.7gを入れ、そ
こに日石農薬オイル約0.5mlを加えて均一になるよう
によく練る。20mlの共栓付沈降管に日石農薬オイル2
0mlを入れ、そこに先に日石農薬オイルで練った試料を
加えて、共栓をつけて30回/分倒立し静置する。静置
後30分,3時間,5時間,24時間後の懸濁安定性
(凝集の有無)を観察した結果を表2に示す。
<Suspension stability test on oil (Nisseki pesticide oil)> About 0.7 g of a sample was put in a 10 ml beaker, and about 0.5 ml of Nisseki pesticide oil was added thereto to make it uniform. Knead well. Nisseki pesticide oil 2 in a 20 ml settling tube with stopper
Add 0 ml, add the sample previously kneaded with Nisseki pesticide oil to it, attach a stopper, and invert 30 times / min. Table 2 shows the results of observation of suspension stability (presence or absence of aggregation) after 30 minutes, 3 hours, 5 hours, and 24 hours after standing.

【0018】[0018]

【表2】 [Table 2]

【0019】本発明により製造された農薬組成物は、水
に容易に懸濁し懸垂性も良好なばかりでなくマシン油の
ような油にも容易に懸濁し水の場合と同様に懸垂性も良
好であり農業分野に於ける利用価値は大きい。
The pesticide composition produced according to the present invention not only easily suspends in water and has good suspending property, but also easily suspends in oil such as machine oil and has suspending property similar to that in water. Therefore, its utility value in the agricultural field is great.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 多価アルコ−ルの脂肪酸エステルを含有
することを特徴とする農薬組成物。
1. A pesticidal composition comprising a fatty acid ester of polyhydric alcohol.
JP35036691A 1991-12-09 1991-12-09 Agrochemical composition Expired - Fee Related JP3739804B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP35036691A JP3739804B2 (en) 1991-12-09 1991-12-09 Agrochemical composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP35036691A JP3739804B2 (en) 1991-12-09 1991-12-09 Agrochemical composition

Publications (2)

Publication Number Publication Date
JPH05155706A true JPH05155706A (en) 1993-06-22
JP3739804B2 JP3739804B2 (en) 2006-01-25

Family

ID=18410002

Family Applications (1)

Application Number Title Priority Date Filing Date
JP35036691A Expired - Fee Related JP3739804B2 (en) 1991-12-09 1991-12-09 Agrochemical composition

Country Status (1)

Country Link
JP (1) JP3739804B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997037538A1 (en) * 1996-04-09 1997-10-16 Bayer Aktiengesellschaft New insecticide suspension concentrates
US5928634A (en) * 1995-01-09 1999-07-27 S. C. Johnson & Son, Inc. Liquid insect bait
US6093681A (en) * 1996-10-25 2000-07-25 Monsanto Company Composition and method for treating plants with exogenous chemicals
JP2009215185A (en) * 2008-03-07 2009-09-24 Sumika Enviro-Science Co Ltd Antibacterial composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5928634A (en) * 1995-01-09 1999-07-27 S. C. Johnson & Son, Inc. Liquid insect bait
WO1997037538A1 (en) * 1996-04-09 1997-10-16 Bayer Aktiengesellschaft New insecticide suspension concentrates
US6093681A (en) * 1996-10-25 2000-07-25 Monsanto Company Composition and method for treating plants with exogenous chemicals
US6184182B1 (en) 1996-10-25 2001-02-06 Monsanto Company Composition and method for treating plants with exogenous chemicals
US6475953B1 (en) 1996-10-25 2002-11-05 Monsanto Technology Llc Composition and method for treating plants with exogenous chemicals
JP2009215185A (en) * 2008-03-07 2009-09-24 Sumika Enviro-Science Co Ltd Antibacterial composition

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