JPS61167603A - Extender compositon for insecticidal and fungicidal agent to be scattered on soil - Google Patents
Extender compositon for insecticidal and fungicidal agent to be scattered on soilInfo
- Publication number
- JPS61167603A JPS61167603A JP744985A JP744985A JPS61167603A JP S61167603 A JPS61167603 A JP S61167603A JP 744985 A JP744985 A JP 744985A JP 744985 A JP744985 A JP 744985A JP S61167603 A JPS61167603 A JP S61167603A
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- Japan
- Prior art keywords
- parts
- weight
- soil
- solution
- dibenzylidene sorbitol
- 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.)
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Abstract
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。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a spreading agent composition for an insecticide and fungicide to be sprayed on 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 spreading agent composition for an insecticide and fungicide that binds the active ingredient of the insecticide and fungicide to soil particles so that the active ingredient does not run out even during watering or rain, thereby 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0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稀釈し
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 disinfectants for gardening, termite killers, etc. It is commercially available in the form of a wettable powder containing a few percent to several tens of percent of a surfactant and kerosene or xylene, and when spraying, it is diluted with water and applied in the form of an emulsion.
殺菌殺虫剤用化合物としてはDDVP(ジメチルノクロ
ルビニルホス7エート)、マラソン(ジメチルノカルベ
トキシエチルジチオホス7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、4,7.7m−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
部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。Bactericidal and insecticidal compounds include DDVP (dimethylnochlorovinylphos7ate), Marathon (dimethylnocarbethoxyethyldithiophos7ate), and chlordane (1,
2,4,5,6,7,8,8-octachlor-2,3,
There are many types such as phosphorus type and halogen type such as 3a, 4,7.7m-hexahydro-4,7-methanoindene),
1-10% of non-ionic surfactants such as sorbitan monooleate or polyoxyalkyl ethers
It is commercially available in the form of a wettable powder, usually with a composition of 5 to 6% kerosene or xylene, about 70% kerosene or xylene, and the balance active ingredient compound.
この水利剤又は濃厚乳剤は水で10〜20倍、時には5
0倍以上に希釈され攪拌して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燃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。This water conservancy or concentrated emulsion is 10 to 20 times, sometimes 5 times
The usual method of use is to dilute it to 0 times or more, stir it to make a milky lotion, and spray it on the soil with a sprayer. Termite killers and fungicidal insecticides for gardening, etc., which are commercially available in the form of wettable powders or concentrated emulsions, are excellent in that they only need to be diluted with water before application, and do not use dangerous flammable solvents. There is. However, on the other hand, if water is sprinkled or it rains after application, the active ingredient compound is easily washed away, for example, as a milky liquid, and the effect does not last. There is also a great risk of secondary pollution caused by leakage.
(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 spraying soil with sterilizing and insecticides, improves the sustainability of the sterilizing and insecticidal effects after application, and reduces the risk of secondary pollution. The purpose of this invention is to provide a composition that eliminates the above problems.
゛(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 effects for solving the problem) The present invention is a germicidal insecticide to be sprayed on soil, which contains an alginate alkali salt, dibenzylidene sorbitol or its nuclear substituted derivative, an anionic surfactant, and a polar organic solvent as essential components. This is a spreading agent composition for pharmaceuticals.
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。Preferred alginic acid alkaline salts are sodium, potassium, ammonium, and triethanolamine salts, and the most preferred is sodium salt. This is because sodium alginate is light in color and cheaper than other salts.
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、M、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。When an alkali salt of alginic acid is sprayed on soil, it causes a substitution reaction with Ca ions, M, ions, etc. in the soil, and becomes Ca alginate, Mg alginate, etc., and has the effect of producing 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F−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ろことができる0例
えばジ(pメチル)ペンシリデンソルビドール、ジ(p
−クロル)ベンツ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8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
その着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 moles of benzaldehyde and 1 mole of D-Sorbitol in the presence of an acid catalyst, and is in the form of a white powder. Nuclear-substituted derivatives of dibenzylidene sorbitol 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)pencylidene sorbitol, di(p
-chlor) benzlidene sorbitol, etc. These nuclear substituted derivatives can also be applied to the composition of the present invention in the same way as dibenzylidene sorbitol. Nuclear substituents of the 8-nuclear substituted derivatives include alkyl groups such as methyl group and ethyl group; methoxy group and ethoxy group. Alkoxy groups such as; halogen atoms such as chlorine are used. Dibenzylidene sorbitol and its nuclear-substituted derivatives, due to their inherent aggregation action, combine the active ingredient compound in the emulsified bactericidal insecticide with alginate alkali salt and Ca in the soil.
It binds to a gel generated by ions and forms a water-insoluble film around it.
7ニオン界面活性剤としては脂肪酸石けん類、アルキル
疏酸エステル、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。The types of 7-ionic surfactants that are commonly used as anionic surfactants are limited, such as fatty acid soaps, alkyl succinates, alkyl sulfonates, aromatic sulfonates, and aliphatic sulfonates. It's not a thing.
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。The anionic surfactant has the effect of emulsifying dibenzylidene sorbitol or its nuclear substituted derivative in the spreading agent composition.
極性有機溶媒としては、ツメチルホルムアミド、Nメチ
ル−2−ピロリドン、ツ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 trimethylformamide, N-methyl-2-pyrrolidone, and trimethylsulfoxide are used. Among them, dimethylformamide and N-methyl-2-pyrrolidone are preferred because they remain liquid even when the temperature drops and are easy to handle. Polar organic solvents are used as solvents for dibenzylidene sorbitol or its nuclear substituted derivatives.
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重景部;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1〜7
0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 component mentioned above is 0.5 to 10 parts by weight, preferably 0.5 to 10 parts by weight of dibenzylidene sorbitol or its nuclear substituted derivative.
5-5 parts by weight; anionic surfactant 0.5-30 parts by weight, preferably 0.5-15 parts by weight; polar organic solvent 1-7
It is contained in a ratio of 0 parts by weight, preferably 2 to 50 parts by weight, and 0.1 to 5 parts by weight, preferably 0.2 to 3 parts by weight of the alginate alkali salt. Since the alginate alkali salt is usually used in the form of an aqueous solution, the spreading agent composition of the present invention can be used in the above-mentioned 4.
It contains about 0.5 to 10 parts by weight of water per 1 part by weight of the ingredients.
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への結合効果
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。Although the content ratio of each of the above components is not particularly limited, if the content of dibenzylidene sorbitol or its nuclear substituted derivative is too large, the entire composition tends to gel and become unstable. If the amount is too small, the above-mentioned binding effect to the gel will be reduced, resulting in poor water resistance. If the content of the anionic surfactant is insufficient, the components of the composition will be difficult to emulsify, and even if it is used in excess, the emulsification will not be particularly good. It may interact with surfactants in wettable powders and impair emulsion stability.
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。If the amount of the organic solvent is too small, undissolved dibenzylidene sorbitol or its nuclear substituted derivative will remain, resulting in insufficient effects; if the amount is too large, alginate alkali salts will precipitate and the emulsified state will tend to become unstable. Also, if the alginate alkali salt content is too low, the replacement reaction with Ca ions or Mg ions in the soil will be insufficient, and if it is too high, the emulsion will become a sterilizer, and the viscosity of the insecticide will become high, causing problems in the spraying of the chemical emulsion. There is a risk that the product will become defective.
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ろ添加量は一般に
0.1〜10%、好ましくは0.2〜5%(重量%)で
ある。The spreading agent composition of the present invention is generally commercially available, and when emulsified by diluting a concentrated emulsion with water or a wettable powder of a fungicidal insecticide,
Alternatively, the amount added after emulsification is generally 0.1 to 10%, preferably 0.2 to 5% (wt%).
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7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6:)ペン
ノ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1)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開
な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せる。別にアルギン酸ナトリウム粉
末3重量部を水97重量部に加えて攪拌溶解させ粘稠な
水溶液とする。The spreading agent composition of the present invention can be obtained by mixing each of the above-mentioned components in a predetermined ratio and does not require any special manufacturing method. The alginate alkali salt powder is mixed and dissolved in a surfactant to form a solution, while the alginate alkali salt powder is mixed and dissolved in water to form an aqueous solution.The above organic solvent solution of dibenzylidene sorbitol and alginate aqueous solution are mixed to form a final composition. 6:) When mixing an organic solvent solution of pennolidene sorbitol and an alginate aqueous solution, add a small amount, for example, 1) 0.5 to 2 parts by weight of triethanol per 100 parts by weight of the total amount of both solutions. Adding an amine facilitates uniform mixing of both liquids and shortens the time required for mixing. For example, 4.5 parts by weight of dibenzylidene sorbitol, 9.5 parts by weight of anionic surfactant and 9.5 parts by weight of dimethylformamide are mixed and
℃ or less, usually about 80° C., to completely dissolve dibenzylidene sorbitol, maintain the temperature for about 10 to 15 minutes, and then cool to room temperature. Separately, 3 parts by weight of sodium alginate powder was added to 97 parts by weight of water and dissolved with stirring to form a viscous aqueous solution.
前記ジベンジリデンソルビトールの7ニオン界面活性剤
−ジメチルホルムアN?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攪拌し本発明の展着
剤を得る。The 7-ion surfactant of dibenzylidene sorbitol - dimethylforma N? 20 parts by weight of solution, 50 parts by weight of sodium alginate aqueous solution and 0 parts by weight of triethanolamine
.. 5 parts by weight were mixed and stirred until it became 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
施例において部会び%は重量部及び重量%を示す。(Example) The present invention will now be described in more detail with reference to Examples. In each example, % by weight indicates 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
(イージー化学工業(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 Easy Chemical Industry Co., Ltd.) 5 parts 36% aqueous solution of sodium lauryl sulfonate (manufactured by Koyosha Co., Ltd.) 20 parts N-methyl-2-pyrrolidone (Mitsubishi Kasei Co., Ltd.) 75 parts (manufactured by Kogyo Co., Ltd.) The above components were mixed, heated to 80°C, held for 15 minutes, and then cooled to room temperature. This is called 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℃で攪拌して溶解し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 ingredients were mixed and dissolved by stirring at a temperature of 60°C to form a 3% aqueous solution. This is called 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) Mix the solutions of (1) and (2) above in the following ratio.
溶液120部
溶液279部
トリエタノールアミン 1部製合物をゆっく
りと10〜15分間攪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
除剤りロルデン水和剤(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−2,3,3
a、4.7.7m−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ョンとなる。これを比較量
とする。この中に組成物1を2部添加してよく攪拌する
。これを試験品とする。120 parts of solution 279 parts of solution 1 part of triethanolamine When the mixture is slowly stirred for 10 to 15 minutes, the mixture is uniformly mixed to form a clear solution. This is designated as Composition 1. Commercially available termite control agent Roldane hydrating agent (Versicol Chemical 1,2
.. 4.5,6,7゜8.8-octachlor-2,3,3
When 200 parts of water (20-fold dilution) is added to 10 parts of 4.7.7m-hexahydro-4,7-methanoindene (containing 40%), a white emulsion is immediately formed. This is the comparison amount. Add 2 parts of Composition 1 to this and stir well. This is the test product.
次に200輸1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、各ビーカーに試験品
及び比較量を各20gふりかけ5分後更に100m1の
水を添加する。比較量は直ちに白く濁るが試験品は全く
濁らす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100m1の水を加えてから10分後と10時間後に
比較量の上層水(白く濁っているもの)と試験品の上層
水(澄明なもの)を2つの秤量瓶に2輪1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 200ml beakers, fill both with half the amount of soil, and smooth the surface well. Sprinkle 20g each of the test product and comparative amount into each beaker, and after 5 minutes, add another 100ml of water. . The comparison sample immediately turned white and cloudy, but the test sample did not turn cloudy at all, nor did it generate the odor characteristic of chlordane. Next, in order to concretely confirm this effect, the elution amount was measured. That is, 10 minutes and 10 hours after adding 100 ml of water, a comparison amount of upper layer water (white and cloudy) and a test sample upper layer water (clear) were taken into two weighing bottles, one at a time. was evaporated in a hot air circulating dryer at 105° C. to remove moisture, and the amount of eluate containing chlordane remaining in the weighing bottle was measured. The results are shown in Table 1 below.
上記表1に示すように試験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 elution amount of the test product is extremely small and the active ingredient does not elute into the water.
実施例 2
(1)溶液2−1
ジベンノリデンソルビトール 粉末 5部うピゾー
ルB50(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7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 Dibennolidene sorbitol powder 5 parts Upizol B50 (sodium dioctyl sulfosuccinate (manufactured by NOF Corporation) 25 parts Dimethylform 7mide (manufactured by Shin Nitto Chemical Co., Ltd.) 70 parts Mix the above components and dissolve in the same manner as in Example 1 to form a solution 2-1.
shall be.
(2)溶液2−2
アルギン酸アンモニウム 2部水
98部上記上
記各音混合し実施例1と同様に溶解し溶液2−2とする
。 ・
(3)次に上記(1)及び(2)の各溶液を次の割合で
混合する。(2) Solution 2-2 Ammonium alginate 2 parts water
98 parts The above-mentioned sounds were mixed and dissolved in the same manner as in Example 1 to obtain a solution 2-2. - (3) Next, mix each solution of (1) and (2) above in the following ratio.
溶液2−1 15部
溶液2−2 85flS
混合物を温度40℃で約30分ゆっくりと攪拌をつづけ
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 flS The mixture was kept slowly stirring 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.
市販のマラソン永和剤(ジメチルノ力ルベトキンチオホ
ス7エート50%含有)10Hに水500部(50倍希
釈)加えると直ちに白色のエマルションとなる。これを
比較量とする。When 500 parts of water (50-fold dilution) is added to commercially available Marathon Permanent Agent (containing 50% dimethylnorbetquin thiophosate) 10H, a white emulsion is immediately formed. This is the comparison amount.
比較品中に組成物2を3部入れてよく攪拌する。Add 3 parts of Composition 2 to the comparative product and stir well.
これを試験品とする。This is the test product.
比較量、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散水による影響を調べた。比較量
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 influence of watering after soil application was investigated for each of the comparison amount and test product in exactly the same manner as in Example 1. A comparative amount of the water spray 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 in exactly the same manner as in Example 1. The results are shown in Table 2 below.
上記表2に示した結果から、試験品は比較量に比べ極め
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 had extremely little elution compared to the comparative amount, and its effect was excellent.
実施例 3
(1)溶液3−1
ノ(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
タウリン酸ナトリウム)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司とする。Example 3 (1) Solution 3-1 No(P-methyl)benzylidene sorbitol powder (manufactured by Shin Nippon Chemical Co., Ltd.) 3 parts Diapon PC (
Sodium oleoyl methyl taurate) 35% manufactured by Nippon Oil & Fats Co., Ltd.
20 parts Dimethylformamide 77 parts The above components were mixed and dissolved in the same manner as in Example 1 to form a solution.
(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 were 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) Mix the solutions of (1) and (2) above 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分ゆっくりと攪拌
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水利斉す(ジメチルジクロ
ルビニル7オス7エート25%含有)10部に水200
部(20倍希釈)を加えてエマルジョンとし、これを比
較品とする。Solution 3-1: 20 parts Solution 3-2: 80 parts When the mixture is slowly stirred at a temperature of 40 DEG C. for about 25 to 30 minutes, it becomes a completely clear colorless liquid. This is designated as Composition 3. 10 parts of commercially available DDVP water solution (containing 25% dimethyldichlorovinyl 7-mole-7-ate) and 200 parts of water.
(diluted 20 times) to make an emulsion, which is used as a comparative product.
比較品の中に組成物3を5部加えてよく攪拌し、これを
試験品とする。Add 5 parts of Composition 3 to the comparison product, stir well, and use this 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
6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。The influence of watering after soil application was investigated for each of the comparison product and the test product in exactly the same manner as in Example 1. The aqueous solution of the comparison product became cloudy, but that of the test product remained transparent. 6 The elution amount was also measured in the same manner as in Example 1. The results are shown in Table 3 below.
LU
上記表3の結果が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。LU From the results in Table 3 above, it can be seen that the test product had an extremely small amount of elution and was highly effective.
(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 explanation, the spreader composition for fungicidal insecticides of the present invention can bind the active ingredients in the fungicidal insecticides well to soil particles, and can remain in the soil even during watering or rainfall. It has the excellent effect of minimizing the amount of water leakage. Therefore, it maintains its effectiveness as a bactericidal insecticide for a long time, and it also has the effect of preventing the occurrence of secondary pollution due to leakage of the active ingredient.
Claims (1)
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。 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。[Scope of Claims] 1. An insecticide and fungicide spreader for spraying on soil, characterized by containing an alginate alkali salt, dibenzylidene sorbitol or its nuclear substituted derivative, an anionic surfactant, and a polar organic solvent as essential components. agent composition. 2. Alginate alkali salt 0.1-5 parts by weight, dibenzylidene sorbitol or its nuclear substituted derivative 0.5-10
The spreading agent composition for an insecticide and fungicide according to claim 1, which contains 0.5 to 30 parts by weight of an anionic surfactant and 1 to 70 parts by weight of a polar organic solvent.
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 true JPS61167603A (en) | 1986-07-29 |
JPH0645521B2 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 (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120208700A1 (en) * | 2011-02-11 | 2012-08-16 | Dow Agrosciences Llc | Stable agrochemical oil dispersions |
CN103501613A (en) * | 2011-02-11 | 2014-01-08 | 陶氏益农公司 | 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 |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020255932A1 (en) * | 2019-06-17 | 2020-12-24 | 昭和電工株式会社 | Plant vitalizing agent containing exogenous elicitor and endogenous elicitor and use thereof |
WO2020255933A1 (en) * | 2019-06-17 | 2020-12-24 | 昭和電工株式会社 | Plant vitalizer containing cello-oligosaccharide, and use for said plant vitalizer |
-
1985
- 1985-01-21 JP JP744985A patent/JPH0645521B2/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120208700A1 (en) * | 2011-02-11 | 2012-08-16 | Dow Agrosciences Llc | Stable agrochemical oil dispersions |
CN103501613A (en) * | 2011-02-11 | 2014-01-08 | 陶氏益农公司 | Stable agrochemical oil dispersions |
JP2014505100A (en) * | 2011-02-11 | 2014-02-27 | ダウ アグロサイエンシィズ エルエルシー | Stable agricultural oil dispersion |
EP2672825A4 (en) * | 2011-02-11 | 2014-09-10 | Dow Agrosciences Llc | Stable agrochemical oil dispersions |
AU2011358608B2 (en) * | 2011-02-11 | 2016-04-14 | 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 |
Also Published As
Publication number | Publication date |
---|---|
JPH0645521B2 (en) | 1994-06-15 |
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