JPH0645521B2 - Spreading agent composition for insecticidal fungicide applied to soil - Google Patents

Spreading agent composition for insecticidal fungicide applied to soil

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Publication number
JPH0645521B2
JPH0645521B2 JP744985A JP744985A JPH0645521B2 JP H0645521 B2 JPH0645521 B2 JP H0645521B2 JP 744985 A JP744985 A JP 744985A JP 744985 A JP744985 A JP 744985A JP H0645521 B2 JPH0645521 B2 JP H0645521B2
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Japan
Prior art keywords
parts
weight
soil
solution
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.)
Expired - Lifetime
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JP744985A
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Japanese (ja)
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JPS61167603A (en
Inventor
宏 内山
Original Assignee
イーシー化学株式会社
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Priority to JP744985A priority Critical patent/JPH0645521B2/en
Publication of JPS61167603A publication Critical patent/JPS61167603A/en
Publication of JPH0645521B2 publication Critical patent/JPH0645521B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は土壌に散布する殺虫殺菌剤用展着剤組成物に関
する。
TECHNICAL FIELD The present invention relates to a spreader composition for insecticidal fungicides which is applied to soil.

更に詳しくは、殺虫殺菌剤の有効成分と土壌粒子とを結
合せしめ散水時又は降雨時においても前記有効成分の流
出がなく、持続性を向上せしめる殺虫殺菌剤用展着剤組
成物に関する。
More specifically, the present invention relates to a spreader composition for insecticidal fungicides which binds the active ingredients of insecticidal fungicides with soil particles so that the active ingredients do not flow out even during sprinkling or rain, thus improving sustainability.

(従来技術) 従来、殺菌剤又は殺虫剤は殆んど乳剤又は水和剤の形で
市販されている。例えば園芸用の殺菌消毒剤、白蟻駆除
剤等は、これらの有効成分化合物に非イオン系界面活性
剤及びケロシン又はキシレンが数%〜数十%混入された
水和剤の形態で市販され、散布時には水を加えて希釈し
乳液状にして施用される。
(Prior Art) Conventionally, most fungicides or insecticides are commercially available in the form of emulsions or wettable powders. For example, sterilizing and disinfecting agents for horticulture, termite repellents, etc. are commercially available in the form of wettable powders containing nonionic surfactants and kerosene or xylene mixed in several% to several tens% of these active ingredient compounds, and sprayed. It is sometimes applied by diluting with water to make an emulsion.

殺菌殺虫剤用化合物としてはDDVP(ジメチルジクロ
ルビニルホスフエート)、マラソン(ジメチルジカルベ
トキシエチルジチオホスフエート)、クロルデン(1,2,
4,5,6,7,8,8-オクタクロル-2,3,3a,4,7,7a-ヘキサヒド
ロ-4,7-メタノインデン)等のリン系、ハロゲン系など
多種類が存在し、例えばソルビタンモノオレエートある
いはポリオキシアルキルエーテルのような非イオン界面
活性剤1〜10%、通常5〜6%、ケロシン又はキシレ
ン約70%及び残品が有効成分化合物の組成の水和剤の
形態で市販されている。この水和剤又は濃厚乳剤は水で
10〜20倍、時には50倍以上に希釈され撹拌した乳
液とされ散布器にて土壌に散布されるのが通常の使用方
法である。このように水和剤又は濃厚乳剤の形態で市販
されている白蟻駆除剤あるいは園芸用などの殺菌殺虫剤
は、その施用にあたって水で希釈すればよく危険な可焼
性溶媒を使用しない点で優れている。しかし一方では、
施用後に散水したり降雨があると有効成分化合物は容易
に例えば乳白色状の液として流失し、その効果は持続し
ない。また流出による二次公害発生の危険も大である。
Compounds for disinfecting insecticides include DDVP (dimethyldichlorovinylphosphate), marathon (dimethyldicarbetoxyethyldithiophosphate), chlordane (1,2,
4,5,6,7,8,8-octachloro-2,3,3a, 4,7,7a-hexahydro-4,7-methanoindene) and other phosphorus-based, halogen-based, etc. Nonionic surfactant such as monooleate or polyoxyalkyl ether 1 to 10%, usually 5 to 6%, kerosene or xylene about 70% and the rest are commercially available in the form of wettable powder of the composition of the active ingredient compound. Has been done. This wettable powder or concentrated emulsion is diluted with water 10 to 20 times, sometimes 50 times or more, and is stirred to obtain a stirred emulsion, which is then sprayed on the soil by a sprayer. As described above, termite pesticides and bactericidal insecticides for horticultural use that are commercially available in the form of wettable powders or concentrated emulsions are excellent in that they do not require the use of a dangerous calcinable solvent as long as they are diluted with water for their application. ing. But on the other hand,
If water is applied or rain is applied after application, the active ingredient compound is easily washed away as, for example, a milky white liquid, and the effect does not continue. In addition, the risk of secondary pollution due to spills is great.

(発明が解決しようとする問題点) 本発明は前記した殺菌、殺虫剤の土壌散布時に発生する
問題点を解決し、施用後における殺菌殺虫効果の持続性
を向上し、二次公害発生のおそれを解消した組成物を提
供しようとするものである。
(Problems to be Solved by the Invention) The present invention solves the above-mentioned problems that occur when soil is sprayed with an insecticide, improves the sustainability of the bactericidal and insecticidal effect after application, and may cause secondary pollution. The present invention is intended to provide a composition in which

(問題点を解決する為の手段及び作用) 本発明はアルギン酸アルカリ塩、ジベンジリデンソルビ
トール又はその核置換誘導体、アニオン界面活性剤及び
極性有機溶媒を必須成分として含有する、土壌に散布す
る殺菌殺虫剤用展着剤組成物である。
(Means and Actions for Solving Problems) The present invention comprises a disinfectant insecticide sprayed on soil, which contains an alginic acid alkali salt, dibenzylidene sorbitol or a nuclear substitution derivative thereof, an anionic surfactant and a polar organic solvent as essential components. It is a spreading agent composition.

アルギン酸のアルカリ塩としてはナトリウム、カリウ
ム、アンモニウム、トリエタノールアミンの塩が好まし
く、最も好ましいのはナトリウム塩である。アルギン酸
ナトリウム塩は淡色であり、他に比して安価な為であ
る。アルギン酸のアルカリ塩は土壌に散布されたとき土
壌中のCaイオン、Mgイオン等と置換反応を生起し、アル
ギン酸Caあるいはアルギン酸Mg等となって弱いゲル状態
を生ずるという作用を有するものである。
As the alkali salt of alginic acid, sodium, potassium, ammonium and triethanolamine salts are preferable, and the most preferable is sodium salt. This is because alginic acid sodium salt is light in color and cheaper than others. The alginic acid alkali salt has a function of causing a substitution reaction with Ca ions, Mg ions and the like in the soil when sprayed on the soil to form Ca alginate or Mg alginate and the like to cause a weak gel state.

ジベンジリデンソルビトールは一般にベンズアルデヒド
2モルとD-ソルビトール1モルを酸触媒の存在下脱水
縮合して製造されるものであり、その形状は白色粉末で
ある。ジベンジリデンソルビトールのアルキル基、ハロ
ゲン基による核置換誘導体もベンズアルデヒドの核置換
誘導体を用いて上記と同様にしてうることができる。例
えばジ(pメチル)ベンジリデンソルビトール、ジ(pクロ
ル)ベンジリデンソルビトール等である。これらの核置
換誘導体も、ジベンジリデンソルビトールと全く同様に
本発明の組成物に適用できる。核置換誘導体の核置換基
としては、メチル基、エチル基のようなアルキル基;メ
トキシ基、エトキシ基のようなアルコキシ基;塩素のよ
うなハロゲン原子が用いられる。ジベンジリデンソルビ
トール及びその核置換誘導体は、本来有しているその著
しい凝集作用により、乳剤化した殺菌殺虫剤中の有効成
分化合物をアルギン酸アルカリ塩と土壌中のCaイオン等
により生じたゲルに結合させ、さらにその周囲に水不溶
性の被膜を形成する。
Dibenzylidene sorbitol is generally produced by dehydration condensation of 2 mol of benzaldehyde and 1 mol of D-sorbitol in the presence of an acid catalyst, and its shape is white powder. A nuclear-substituted derivative of dibenzylidenesorbitol with an alkyl group or a halogen group can also be obtained in the same manner as above using a nuclear-substituted derivative of benzaldehyde. For example, di (p-methyl) benzylidene sorbitol, di (p-chloro) benzylidene sorbitol and the like. These nuclear-substituted derivatives can be applied to the composition of the present invention just like dibenzylidene sorbitol. As the nuclear substituent of the nuclear substitution derivative, an alkyl group such as a methyl group and an ethyl group; an alkoxy group such as a methoxy group and an ethoxy group; and a halogen atom such as chlorine are used. Dibenzylidene sorbitol and its nuclear substitution derivative bind the active ingredient compound in the emulsified fungicidal insecticide to the gel formed by the alginic acid alkali salt and Ca ion in the soil due to its original remarkable aggregation action. , And further forms a water-insoluble film around it.

アニオン界面活性剤としては脂肪酸石けん類、アルキル
硫酸アステル、アルキルスルホン化物、芳香族スルホン
化物、脂肪族スルホン化物などアニオン界面活性剤とし
て通常使用されているものであれば特にその種類を限定
するものではない。アニオン界面活性剤は展着剤組成物
中においてジベンジリデンソルビトール又はその核置換
誘導体を乳化する作用を有する。
As the anionic surfactant, fatty acid soaps, alkyl sulfate astells, alkyl sulfonates, aromatic sulfonates, aliphatic sulfonates, and the like, which are commonly used as anionic surfactants, are not particularly limited in their types. Absent. The anionic surfactant has an action of emulsifying dibenzylidene sorbitol or its nuclear substitution derivative in the spreader composition.

極性有機溶媒としては、ジメチルホルムアミド、Nメチ
ル-2-ピロリドン、ジメチルスルホキシド等の非プロト
ン系極性溶媒が用いられる。中でもジメチルホルムアミ
ド及びNメチル-2-ピロリドンは気温の低下した時でも
液体状であり取扱い易く好ましい。極性有機溶媒はジベ
ンジリデンソルビトール又はその核置換誘導体の溶媒と
して用いられる。
As the polar organic solvent, aprotic polar solvents such as dimethylformamide, N-methyl-2-pyrrolidone and dimethylsulfoxide are used. Among them, dimethylformamide and N-methyl-2-pyrrolidone are preferable because they are liquid and easy to handle even when the temperature drops. The polar organic solvent is used as a solvent for dibenzylidene sorbitol or its nuclear substitution derivative.

以上に述べた各成分はジベンジリデンソルビトール又は
その核置換誘導体0.5〜10重量部、好ましくは0.
5〜5重量部;アニオン界面活性剤0.5〜30重量
部、好ましくは0.5〜15重量部;極性有機溶媒1〜
70重量部、好ましくは2 〜50重量部及びアルギン酸
アルカリ塩0.1〜5重量部、好ましくは0.2〜3重
量部の割合で含有される。アルギン酸アルカリ塩は通常
水溶液状で使用されるから本発明の展着剤組成物は上記
4成分の合計1重量部に対し0.5〜10重量部程度の
水を含有する。
Each of the above-mentioned components is 0.5 to 10 parts by weight of dibenzylidene sorbitol or a nucleus-substituted derivative thereof, preferably 0.
5 to 5 parts by weight; anionic surfactant 0.5 to 30 parts by weight, preferably 0.5 to 15 parts by weight; polar organic solvent 1 to
70 parts by weight, preferably 2 to 50 parts by weight, and 0.1 to 5 parts by weight, and preferably 0.2 to 3 parts by weight of alginic acid alkali salt. Since the alginic acid alkali salt is usually used in the form of an aqueous solution, the spreading agent composition of the present invention contains about 0.5 to 10 parts by weight of water per 1 part by weight of the above four components.

上記の各成分の含有割合は格別限定的なものではない
が、ジベンジリデンソルビトール又はその核置換誘導体
の含有量が多すぎると組成物全体がゲル化して不安定と
なる傾向がある。又少なすぎると前述のゲルヘの結合効
果が少なくなり耐水性に乏しくなる。アニオン界面活性
剤の含有量が不足すると組成物の成分が乳化し難く過剰
に用いても特に乳化が良好になるわけではなく、時には
展着剤を殺菌殺虫剤の水和剤に添加したとき、水和剤中
の界面活性剤と作用して乳化の安定性を損うことがあ
る。有機溶媒が少なすぎると未溶解のジベンジリデンソ
ルビトール又はその核置換誘導体が残存しその作用効果
が不充分となり、多すぎるとアルギン酸アルカリ塩が析
出し乳化状態が不安定となる傾向を生じる。又アルギン
酸アルカリ塩の含有量が少な過ぎると土壌中のCaイオン
又はMgイオン等との置換反応が不充分となり、多すぎる
と乳液化した殺菌、殺虫剤の粘度が高くなって薬剤乳液
の散布状態を不良にするおそれが生じる。
The content ratio of each of the above components is not particularly limited, but if the content of dibenzylidene sorbitol or its nuclear substitution derivative is too large, the entire composition tends to gel and become unstable. On the other hand, if the amount is too small, the effect of binding to the gel described above is reduced and the water resistance becomes poor. When the content of the anionic surfactant is insufficient, the components of the composition are difficult to emulsify and the emulsification is not particularly good even when used in excess, and sometimes when a spreading agent is added to a wettable powder of a germicidal insecticide, It may act with the surfactant in the wettable powder to impair the stability of the emulsion. If the amount of the organic solvent is too small, undissolved dibenzylidene sorbitol or a nuclear-substituted derivative thereof remains and the action and effect thereof become insufficient. If the amount is too large, the alginic acid alkali salt precipitates and the emulsified state tends to become unstable. Also, if the content of the alginic acid alkali salt is too small, the substitution reaction with Ca ions or Mg ions in the soil becomes insufficient, and if it is too large, the viscosity of the emulsified sterilization and insecticide becomes high and the dispersion state of the drug emulsion May result in a failure.

本発明の展着剤組成物は一般に市販されている殺菌殺虫
剤の水和剤又は濃厚乳剤の水希釈による乳液化時に、あ
るいは乳液化後に添加して用いられる添加量は一般に
0.1〜10%、好ましくは0.2〜5%(重量%)で
ある。
The spreader composition of the present invention is generally used at the time of emulsification by diluting a wettable powder or concentrated emulsion of a commercially available germicidal insecticide with water or after emulsification. %, Preferably 0.2 to 5% (% by weight).

本発明の展着剤組成物は以上に述べた各成分を所定の割
合で混合することによって得ることができ特別の製造方
法を必要とするわけではないが、ジベンジリデンソルビ
トールは有機溶媒とアニオン界面活性剤に混合溶解して
溶液としておき、一方アルギン酸アルカリ塩の粉末は水
と混合溶解して水溶液とし上記のジベンジリデンソルビ
トールの有機溶媒溶液とアルギン酸アルカリ水溶液を混
合して最終組成物とする方法をとるのがよい。ジベンジ
リデンソルビトールの有機溶媒溶液とアルギン酸アルカ
リ水溶液を混合する際、少量の、例えば両溶液の合計量
100重量部当り0.5〜2 重量部のトリエタノールア
ミンを加えると両液の均一混合を容易にし混合時間を短
縮することができる。例えばジベンジリデンソルビトー
ル4.5重量部、アニオン界面活性剤9.5重量部及び
ジメチルホルムアミド9.5重量部を混合し100℃以
下、通常80℃程度に加熱して完全にジベンジリデンソ
ルビトールを溶解させ約10〜15分該温度に保持した
後室温に冷却される。別にアルギン酸ナトリウム粉末3
重量部を水97重量部に加えて撹拌溶解させ粘稠な水溶
液とする。
The spreader composition of the present invention can be obtained by mixing the components described above in a predetermined ratio and does not require a special production method. However, dibenzylidene sorbitol is an organic solvent and an anion interface. A method of mixing and dissolving in an activator to form a solution, on the other hand, a powder of an alkali salt of alginic acid is mixed and dissolved in water to form an aqueous solution, and a solution of the above-mentioned organic solvent of dibenzylidene sorbitol and an alkaline aqueous solution of alginic acid is mixed to form a final composition. It is good to take. When mixing a solution of dibenzylidene sorbitol in an organic solvent and an aqueous solution of alkali alginate, adding a small amount of 0.5 to 2 parts by weight of triethanolamine per 100 parts by weight of both solutions facilitates uniform mixing of both solutions. The mixing time can be shortened. For example, 4.5 parts by weight of dibenzylidene sorbitol, 9.5 parts by weight of an anionic surfactant and 9.5 parts by weight of dimethylformamide are mixed and heated to 100 ° C. or lower, usually about 80 ° C. to completely dissolve dibenzylidene sorbitol. The temperature is maintained for about 10 to 15 minutes and then cooled to room temperature. Separately sodium alginate powder 3
Part by weight is added to 97 parts by weight of water and dissolved by stirring to form a viscous aqueous solution.

前記ジベンジリデンソルビトールのアニオン界面活性剤
-ジメチルホルムアミド溶液20重量部にアルギン酸ナ
トリウム水溶液50重量部及びトリエタノールアミン0.
5重量部を混合し澄明になるまで撹拌し本発明の展着剤
を得る。
The dibenzylidene sorbitol anionic surfactant
20 parts by weight of dimethylformamide solution, 50 parts by weight of aqueous solution of sodium alginate and 0.3 parts of triethanolamine.
5 parts by weight are mixed and stirred until clear to obtain the spreading agent of the present invention.

(実施例) 以下本発明を実施例により更に具体的に説明する。各実
施例において部含び%は重量部及び重量%を示す。
(Example) Hereinafter, the present invention will be described more specifically by way of examples. In the examples, "parts included" means "parts by weight" and "% by weight".

実施例 1 (1) 溶液1 ジベンジリデンソルビトール粉末 (イーシー化学工業(株)製造) 5部 ラウリルスルホン酸ソーダ36%水溶液 ((株)交洋社製) 20部 Nメチル-2-ピロリドン (三菱化成工業(株)製) 75部 上記の各成分を混合し80℃に加温し15分保持後室温に
冷却する。これを溶液1とする。
Example 1 (1) Solution 1 Dibenzylidene sorbitol powder (manufactured by EC Chemicals Co., Ltd.) 5 parts Sodium lauryl sulfonate 36% aqueous solution (manufactured by Kyoyo Co., Ltd.) 20 parts N-methyl-2-pyrrolidone (Mitsubishi Kasei) (Industrial Co., Ltd.) 75 parts The above components are mixed, heated to 80 ° C., kept for 15 minutes and cooled to room temperature. This is solution 1.

(2) 溶液2 アルギン酸ナトリウム(試薬) 3部 水 97部 上記の各成分を混合し温度60℃で撹拌して溶解し3%
の水溶液を作る。これを溶液2とする。
(2) Solution 2 Sodium alginate (reagent) 3 parts Water 97 parts The above components are mixed and stirred at a temperature of 60 ° C to dissolve to 3%.
Make an aqueous solution of. This is solution 2.

(3) 上記の(1)及び(2)の各溶液を次の比率で混合す
る。
(3) The above solutions (1) and (2) are mixed in the following ratio.

溶 液 1 20部 溶 液 2 79部 トリエタノールアミン 1部 混合物をゆっくりと10〜15分間撹拌すると均一に混
合されて澄明な溶液が出来る。これを組成物1とする。
市販の白アリ防除剤クロルデン水和剤(ベルシコールケ
ミカル製1,2,4,5,6,7,8,8-オクタクロル-2,3,3a,4,7,7a
-ヘキサヒドロ-4,7-メタノインデン40%含有)10部
に水200部(20倍希釈)加えると直ちに白色のエマ
ルジヨンとなる。これを比較品とする。この中に組成物
1を2部添加してよく撹拌する。これを試薬品とする。
Solution 1 20 parts Solution 2 79 parts Triethanolamine 1 part When the mixture is slowly stirred for 10 to 15 minutes, it is uniformly mixed to form a clear solution. This is designated as Composition 1.
Commercially available termite control agent chlordane wettable powder (1,2,4,5,6,7,8,8-octachloro-2,3,3a, 4,7,7a manufactured by Versicol Chemical
-Hexahydro-4,7-methanoindene (containing 40%) 10 parts (200 parts) (diluted 20 times) gives a white emulsion immediately. This is a comparative product. To this, 2 parts of Composition 1 is added and stirred well. This is a reagent product.

次に200mlのビーカーを2個用意し両方に半分量の土
を入れ表面をよくならしておく。各ビーカーに試薬品及
び比較品を各20gふりかけ5分後更に100mlの水を
添加する。比較品は直ちに白く濁るが試薬品が全く濁ら
ず又クロルデン特有の臭気も発生しなかった。次にこの
効果を具体的に確める為溶出量の測定を行った。即ち1
00mlの水を加えてから10分後と10時間後に比較品
の上層水(白く濁っているもの)と試薬品の上層水(澄
明なもの)を2つの秤量瓶に2mlづつとりそれを105
℃の熱風循環乾燥器で蒸発させ水分を除き秤量瓶中に残
存しているクロルデンを含む溶出物の量を測定した。そ
の結果は下記表1の通りである。
Next, prepare two 200 ml beakers and put half the amount of soil in both beakers to smooth the surface. Each beaker is sprinkled with 20 g of the reagent and the comparative product, and after 5 minutes, another 100 ml of water is added. The comparative product immediately became cloudy in white, but the reagent product did not become cloudy at all, and the odor characteristic of chlordane was not generated. Next, the elution amount was measured to specifically confirm this effect. Ie 1
10 minutes and 10 hours after adding 00 ml of water, take 2 ml each of the upper layer water (white and cloudy) of the comparative product and the upper layer water (clear) of the reagent product in two weighing bottles, and put them in 105
The amount of eluate containing chlordane remaining in the weighing bottle was measured by removing water by evaporating with a hot air circulation dryer at ℃. The results are shown in Table 1 below.

上記表1に示すように試薬品の溶出量が極めて少なく水
の中に有効成分が溶出しない事がわかる。
As shown in Table 1 above, it can be seen that the amount of reagent eluted is extremely small and the active ingredient does not elute in water.

実施例 2 (1) 溶液2-1 ジベンジリデンソルビトール 粉末 5部 ラピゾールB30(ジオクチルスルホ コハク酸ナトリウム(日本油脂(株)製) 25部 ジメチルホルムアミド(新日東化学(株)製) 70部 上記各成分を混合し実施例1と同様に溶解し溶液2-1と
する。
Example 2 (1) Solution 2-1 Dibenzylidene sorbitol Powder 5 parts Lapizole B30 (sodium dioctylsulfosuccinate (manufactured by NOF Corporation) 25 parts Dimethylformamide (manufactured by Shin-Nitto Kagaku Co., Ltd.) 70 parts The above components Are mixed and dissolved in the same manner as in Example 1 to obtain solution 2-1.

(2) 溶液2-2 アルギン酸アンモニウム 2部 水 98部 上記各成分を混合し実施例1と同様に溶解し溶液2-2と
する。
(2) Solution 2-2 Ammonium alginate 2 parts Water 98 parts The above components are mixed and dissolved in the same manner as in Example 1 to obtain solution 2-2.

(3) 次に上記(1)及び(2)の各溶液を次の割合で混合
する。
(3) Next, the solutions of (1) and (2) above are mixed in the following proportions.

溶 液 2-1 15部 溶 液 2-2 85部 混合物を温度40℃で約30分ゆっくりと撹拌をつづけ
完全に澄明な赤色を帯びた溶液をつくる。
Solution 2-1 15 parts Solution 2-2 85 parts The mixture is slowly stirred at a temperature of 40 ° C. for about 30 minutes to form a completely clear reddish solution.

これを組成物2とする。This is designated as Composition 2.

市販のマラソン水和剤(ジメチルジカルベトキンチオホ
スフエート50%含有)10部に水500部(50倍希
釈)加えると直ちに白色のエマルジヨンとなる。これを
比較品とする。
Addition of 500 parts of water (diluted 50 times) to 10 parts of a commercially available marathon wettable powder (containing 50% of dimethyl dicarbetquinothiophosphate) immediately gives a white emulsion. This is a comparative product.

比較品中に組成物2を3部入れてよく撹拌する。これを
試験品とする。
3 parts of the composition 2 was added to the comparative product and stirred well. This is a test product.

比較品、試験品のそれぞれについて実施例1と全く同様
の方法で土壌散布後の酸水による影響を調べた。比較品
の散水液は白濁するが試験品の方は透明なままであっ
た。
The effect of acid water after soil application was examined in the same manner as in Example 1 for each of the comparative product and the test product. The water spray of the comparative product became cloudy, but the test product remained transparent.

次に実施例1と全く同様の方法で溶出量を測定した。結
果を下記表2に示す。
Next, the elution amount was measured by the same method as in Example 1. The results are shown in Table 2 below.

上記表2に示した結果から、試験品は比較品に比べ極め
て溶出が少なく、その効果が優れていることがわかる。
From the results shown in Table 2 above, it can be seen that the test product is much less eluted than the comparative product, and its effect is excellent.

実施例 3 (1) 溶液3-1 ジ(Pメチル)ベンジリデンソルビトール 粉末(新日本理化(株)製造) 3部 ダイヤポンPC(オレオイルメチル タウリン散ナトリウム)35%日本油脂 (株)製 20部 ジメチルホルムアミド 77部 上記の各成分を混合し実施例1と同様に溶解し溶液3-1
とする。
Example 3 (1) Solution 3-1 Di (P-methyl) benzylidene sorbitol powder (manufactured by Shin Nippon Rika Co., Ltd.) 3 parts Diapon PC (oleoylmethyl taurine sodium dispersion) 35% NOF Corporation 20 parts dimethyl Formamide 77 parts The above components were mixed and dissolved in the same manner as in Example 1 to obtain solution 3-1.
And

(2) 溶液3-2 アルギン酸ナトリウム 3部 水 97部 上記各成分を混合し実施例1と同様に溶解し溶液3-2と
する。
(2) Solution 3-2 Sodium alginate 3 parts Water 97 parts The above components are mixed and dissolved in the same manner as in Example 1 to obtain solution 3-2.

(3) 上記(1)及び(2)の溶液を次の割合で混合する。(3) The above solutions (1) and (2) are mixed in the following proportions.

溶 液 3-1 20部 溶 液 3-2 80部 混合物を40℃の温度で約25〜30分ゆっくりと撹拌
をつづけると完全に澄明な無色の液になる。これを組成
物3とする。市販のDDVP水和剤(ジメチルジクロル
ビニルフオスフエート25%含有)10部に水200部
(20倍希釈)を加えてエマルジヨンとし、これを比較
品とする。
Solution 3-1 20 parts Solution 3-2 80 parts The mixture is slowly stirred at a temperature of 40 ° C. for about 25 to 30 minutes to form a completely clear colorless liquid. This is designated as Composition 3. 200 parts of water (diluted 20 times) was added to 10 parts of a commercially available DDVP wettable powder (containing 25% of dimethyldichlorovinylphosphate) to obtain emulsion, which was used as a comparative product.

比較品の中に組成物3を5部加えてよく撹拌し、これを
試験品とする。
5 parts of the composition 3 was added to the comparative product and well stirred, and this was used as a test product.

比較品、試験品のそれぞれについて実施例1と全く同じ
方法で土壌散布後の散水による影響を調べた。比較品の
散水液は白濁するが試験品のそれは透明なままであっ
た。又実施例1と同様に溶出量の測定を行った。結果を
下記表3に示す。
With respect to each of the comparative product and the test product, the effect of water sprinkling after spraying the soil was examined by the same method as in Example 1. The water spray of the comparative product became cloudy, but that of the test product remained transparent. Also, the elution amount was measured in the same manner as in Example 1. The results are shown in Table 3 below.

上記表3の結果から試験品の方は溶出量が極めて少なく
その効果の大きいことがわかる。
From the results in Table 3 above, it can be seen that the test product has an extremely small amount of elution and its effect is large.

(発明の効果) 以上の説明から明らかなように、本発明の殺菌殺虫剤用
展着剤組成物は殺菌殺虫剤中の有効成分を土壌粒子によ
く結合せしめ散水時あるいは降雨時においても土壌中へ
の流失を最小ならしめるという優れた効果を有してい
る。このため殺菌殺虫剤としての有効性を永く持続し、
さらには有効成分の流出による二次公害の発生を防止す
るという効果をも有している。
(Effects of the invention) As is clear from the above description, the spreader composition for bactericidal and insecticides of the present invention is such that the active ingredient in the bactericidal insecticide is well bound to the soil particles so that it can be sprinkled in the soil even during sprinkling or rainfall. It has the excellent effect of minimizing the loss of water. Therefore, the effectiveness as a bactericidal insecticide continues for a long time,
Furthermore, it also has the effect of preventing the occurrence of secondary pollution due to the outflow of active ingredients.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】アルギン酸アルカリ塩、ジベンジリデンソ
ルビトール又はその核置換誘導体、アニオン界面活性剤
及び極性有機溶媒を必須成分として含有することを特徴
とする土壌に散布する殺虫殺菌剤用展着剤組成物。
1. A spreader composition for insecticidal fungicides sprayed on soil, comprising an alginic acid alkali salt, dibenzylidene sorbitol or a nuclear substitution derivative thereof, an anionic surfactant and a polar organic solvent as essential components. .
【請求項2】アルギン酸アルカリ塩0.1〜5重量部、
ジベンジリデンソルビトール又はその核置換誘導体0.
5〜10重量部、アニオン界面活性剤0.5〜30重量
部及び極性有機溶媒1〜70重量部を含有する特許請求
の範囲第1項記載の殺虫殺菌剤用展着剤組成物。
2. 0.1-5 parts by weight of alginic acid alkali salt,
Dibenzylidene sorbitol or its nuclear substitution derivative 0.
The spreader composition for insecticidal fungicides according to claim 1, which contains 5 to 10 parts by weight, 0.5 to 30 parts by weight of an anionic surfactant, and 1 to 70 parts by weight of a polar organic solvent.
JP744985A 1985-01-21 1985-01-21 Spreading agent composition for insecticidal fungicide applied to soil Expired - Lifetime JPH0645521B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP744985A JPH0645521B2 (en) 1985-01-21 1985-01-21 Spreading agent composition for insecticidal fungicide applied to soil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP744985A JPH0645521B2 (en) 1985-01-21 1985-01-21 Spreading agent composition for insecticidal fungicide applied to soil

Publications (2)

Publication Number Publication Date
JPS61167603A JPS61167603A (en) 1986-07-29
JPH0645521B2 true JPH0645521B2 (en) 1994-06-15

Family

ID=11666144

Family Applications (1)

Application Number Title Priority Date Filing Date
JP744985A Expired - Lifetime JPH0645521B2 (en) 1985-01-21 1985-01-21 Spreading agent composition for insecticidal fungicide applied to soil

Country Status (1)

Country Link
JP (1) JPH0645521B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103501613A (en) * 2011-02-11 2014-01-08 陶氏益农公司 Stable agrochemical oil dispersions

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120208700A1 (en) * 2011-02-11 2012-08-16 Dow Agrosciences Llc Stable agrochemical oil dispersions
JP2016145188A (en) * 2015-12-28 2016-08-12 ダウ アグロサイエンシィズ エルエルシー Stable agrochemical oil dispersions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103501613A (en) * 2011-02-11 2014-01-08 陶氏益农公司 Stable agrochemical oil dispersions

Also Published As

Publication number Publication date
JPS61167603A (en) 1986-07-29

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