JPS615001A - Agricultural chemical composition for application - Google Patents

Agricultural chemical composition for application

Info

Publication number
JPS615001A
JPS615001A JP12494084A JP12494084A JPS615001A JP S615001 A JPS615001 A JP S615001A JP 12494084 A JP12494084 A JP 12494084A JP 12494084 A JP12494084 A JP 12494084A JP S615001 A JPS615001 A JP S615001A
Authority
JP
Japan
Prior art keywords
group
agricultural chemical
synthetic resin
resin emulsion
plants
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
JP12494084A
Other languages
Japanese (ja)
Other versions
JPH0369321B2 (en
Inventor
Koichiro Yamada
山田 貢一郎
Sakae Shimakawa
島河 栄
Nobumasa Washiyama
鷲山 信正
Kinya Ogawa
欽也 小川
Akira Yamamoto
昭 山本
Shigehiro Nagura
茂広 名倉
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.)
Shin Etsu Chemical Co Ltd
Nissin Chemical Industry Co Ltd
Original Assignee
Shin Etsu Chemical Co Ltd
Nissin Chemical Industry 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 Shin Etsu Chemical Co Ltd, Nissin Chemical Industry Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP12494084A priority Critical patent/JPS615001A/en
Publication of JPS615001A publication Critical patent/JPS615001A/en
Publication of JPH0369321B2 publication Critical patent/JPH0369321B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:The titled composition for preventing scattering of an agricultural chemical component to other areas by the influence of wind, etc. in application, having improved adhesivity to plants, obtained by blending the agricultural chemical component with a synthetic resin emulsion of specific kinds of monomers. CONSTITUTION:An agricultural chemical is blended with a synthetic resin emulsion obtained by subjecting (A) one or more of unsaturated monocarboxylic acid ester, dicarboxylic acid diesters and fatty acid vinyl, (B) one or more of polymerizable monomers containing methylol group, hydroxyl group, amino group or amido group which may be replaced with carboxyl group, glycidyl group, or alkyl, and (C) one or more of polymerizable monomers containing vinyl group, allyl group or methallyl group and sulfonic group in the molecule, to give an agricultural chemical composition for application that is easily applicable by ordinary scattering tool, attaching surely to plants, having neither scattering nor washing away caused by rain and wind, showing long-period durability of its effect on plants in the case of a volatile agricultural chemical, etc.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は散布用組成物に関するものであり、特には農薬
成分を特定の組成からなる合成樹脂エマルジョンと混合
することにより、散布時に農薬成分が風等の影響で他地
域へ飛散するのを防ぐと供に植物体への該農薬成分の付
着固定化を目的とするものである。
Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a composition for spraying, and in particular, by mixing pesticide components with a synthetic resin emulsion having a specific composition, the pesticide components can be dispersed during spraying. The purpose is to prevent the pesticide components from being dispersed to other areas due to the influence of wind, etc., and to fix the pesticide components on the plants.

(従来の技術) 紛剤等の農薬は散布時に風の影響等により目的■場以外
の近接する田畑、家屋、畜舎池沼などへ飛散しやすく、
このような農薬の飛散は損失とういう経済的不利にとど
まらず周囲の環境に悪影響を及ぼすものであり、また十
分な病害虫防除効果が得られない原因ともなる。この解
決策として紛剤を顕粒状あるいは粒状に製剤することが
試みられているが、粉剤が粒状のものになれば当然のこ
とながら植物体への付着性が大幅に低下することになり
、風雨などにより容易に流失、飛散してしまい、この場
合にも充分な防除効果が得られない不利がある。
(Conventional technology) Pesticides such as powders tend to scatter due to the influence of wind etc. into nearby fields, houses, livestock ponds, etc. other than the intended site.
Such scattering of pesticides not only causes economic disadvantage in the form of losses, but also has a negative impact on the surrounding environment, and also causes a lack of sufficient pest control effects. As a solution to this problem, attempts have been made to formulate the powder into fine granules or granules, but if the powder is made into granules, naturally the adhesion to plants will be significantly reduced, and wind and rain It is easily washed away and scattered due to such reasons, and in this case, there is also a disadvantage that a sufficient pest control effect cannot be obtained.

一方蒸発や昇華により気化する殺虫剤、殺菌剤、忌避剤
、その他のくん蒸剤などに関しては、その効果を一時的
なものとせずに比較的長い期間にわたって平均して持続
させる目的で粒状に製剤化して使用することもすでに知
られているが、この場合には該製剤化された粒状物が植
物体の適当な高さ適当な部位に、風雨に対しても容易に
流失、飛散することのないように、安定に付着させるこ
とが重要な課題となる。
On the other hand, insecticides, fungicides, repellents, and other fumigants that vaporize through evaporation or sublimation are formulated into granules in order to maintain their effects evenly over a relatively long period of time rather than temporarily. It is also already known that the formulated granules are placed on appropriate parts of the plant at appropriate heights so that they will not be easily washed away or scattered by wind and rain. Therefore, ensuring stable adhesion is an important issue.

(発明の構成) 本発明者らは従来のかかる不利欠点にかんがみ鋭意検討
の結果、後記する特定の合成樹脂エマルジョンを混合し
たものが、一般の散布用器具による散布が容易で植物体
への付着が確実であり、風雨による飛散・流失がなく、
また気化性農薬等についてはその効果が植物体上で長期
間持続されることを確認し、本発明を完成した。
(Structure of the Invention) The present inventors have conducted intensive studies in consideration of the disadvantages of conventional methods, and have found that a mixture of a specific synthetic resin emulsion described later is easy to spray with a general spraying device, and does not adhere to plants. is reliable, and there is no scattering or washing away due to wind and rain.
Furthermore, the present invention was completed by confirming that the effects of vaporizable agricultural chemicals are sustained on plants for a long period of time.

本発明で対象とされる農薬としては、粉末状、粒状、液
状、さら(二は徐放性とするためにあらかじめ製剤化さ
れたものなど各種形態のものが包含され、またa薬の有
効成分についても特に制限はなく、一般的に殺虫剤、殺
菌剤、殺線虫剤、除草剤、殺そ剤、植物成長調整剤、忌
避剤、誘引剤、くん原剤などがあげられる。
The agricultural chemicals targeted by the present invention include those in various forms such as powder, granules, liquid, and even those formulated in advance for sustained release, and the active ingredients of drug a. There are no particular restrictions on the agents, and generally examples include insecticides, fungicides, nematicides, herbicides, rodenticides, plant growth regulators, repellents, attractants, and pesticides.

つぎに本発明に使用される合成樹脂エマルジョンは、(
イ)不飽和モノカルボン酸のエステル、不飽和ジカルボ
ン酸のジエステルおよび脂肪酸ビニルの1種または2種
以上、(ロ)カルボキシル基、グリシジル基、アルキル
置換されたもしくはされないメチロール基、ヒドロキシ
ル基、アミノ基またはアミド基を有する重合性単量体の
1種または2種以上、および(,19ビニル基、アリル
基またはメタアリル基とスルホン酸基とを分子内に有す
る重合性単量体あるいはその塩類の1種または2種以上
、を乳化共重合して得られるものであり、これを各種の
農薬と混合することにより前記諸効果を達成することが
できる。
Next, the synthetic resin emulsion used in the present invention is (
(b) One or more types of esters of unsaturated monocarboxylic acids, diesters of unsaturated dicarboxylic acids, and vinyl fatty acids, (b) Carboxyl groups, glycidyl groups, methylol groups with or without alkyl substitution, hydroxyl groups, amino groups or one or more polymerizable monomers having an amide group, and one or more polymerizable monomers having a vinyl group, an allyl group, or a metaallyl group, and a sulfonic acid group in the molecule, or a salt thereof. It is obtained by emulsion copolymerization of one species or two or more species, and the above-mentioned effects can be achieved by mixing this with various agricultural chemicals.

前記(イ)成分に相当する単量体としては、アクリル酸
やメタクリル酸のメチル、エチル、プロピル、1−プロ
ピル、n−ブチル、1−ブチル、t−ブチル、ヘキシル
、シクロヘキシル、2−エチルヘキシル、ラウリル、ス
テアリル、オレイル、エトキシエチルまなはベンジル等
のエステル類、マレイン酸、フマル酸やイタコン酸等の
不飽和ジカルボン酸類の上記のエステル形成成分のジエ
ステル類、および酢酸、プロピオン酸、ラウリン酸、ス
テアリン酸ならびにバーサチック酸等の脂肪酸類のビニ
ルエステル類が例示される。
Monomers corresponding to component (a) include methyl, ethyl, propyl, 1-propyl, n-butyl, 1-butyl, t-butyl, hexyl, cyclohexyl, 2-ethylhexyl, acrylic acid and methacrylic acid; Esters such as lauryl, stearyl, oleyl, ethoxyethyl mana or benzyl, diesters of the above-mentioned ester-forming components of unsaturated dicarboxylic acids such as maleic acid, fumaric acid and itaconic acid, and acetic acid, propionic acid, lauric acid and stearin. Examples include vinyl esters of acids and fatty acids such as versatic acid.

また(口)成分に相当する単量体としては、アクリル酸
、メタクリル酸、クロトン酸、マレイン酸、フマル酸、
イタコン酸ならびに無水マレイン酸、マレイン酸、フマ
ル酸などの不飽和ジカルボン酸のモノアルキルエステル
、グリシジルアクリレート、グリシジルアクリレート、
アリルグリシジルエーテル、2−ヒドロキシアクリレー
ト、2−ヒドロキシアクリレート、2−ヒドロキシプロ
ピルメタクリレート、ポリエチレングリコールモノアク
リレート、3−クロロ−2−ヒドロキシプロピルメタク
リレート、アクリルアミド、メタクリルアミド、+V−
エトキシメチルアクリルアミド、1マーメチロールアク
リルア5ミド、ジメチルアミノエチルメタクリレート、
ジエチルアミノエチルアクリレートなどが例示される。
In addition, monomers corresponding to (mouth) components include acrylic acid, methacrylic acid, crotonic acid, maleic acid, fumaric acid,
Itaconic acid and monoalkyl esters of unsaturated dicarboxylic acids such as maleic anhydride, maleic acid, fumaric acid, glycidyl acrylate, glycidyl acrylate,
Allyl glycidyl ether, 2-hydroxyacrylate, 2-hydroxyacrylate, 2-hydroxypropyl methacrylate, polyethylene glycol monoacrylate, 3-chloro-2-hydroxypropyl methacrylate, acrylamide, methacrylamide, +V-
Ethoxymethylacrylamide, 1-mer methylolacrylamide, dimethylaminoethyl methacrylate,
Examples include diethylaminoethyl acrylate.

さらに(ハ)成分に相当する単量体成分としては1ごニ
ルスルホン酸、3−アリロキシ−2−ヒドロキシプロパ
ンスルボン酸、スチレンスルホン酸、スルホエチルメタ
クリレート、2−アクリルアミド−2−メチルプロパン
スルホン酸、アリルスルホン酸、アリルアルギルスルホ
サクシネート、メタアリルスルホン酸、p−メタアリル
オキシベンゼンスルホン酸およびこれらのナトリウム塩
、カリウム塩またはアンモニウム塩などが例示される。
Furthermore, monomer components corresponding to component (iii) include 1-nylsulfonic acid, 3-allyloxy-2-hydroxypropanesulfonic acid, styrenesulfonic acid, sulfoethyl methacrylate, 2-acrylamido-2-methylpropanesulfonic acid, Examples include allylsulfonic acid, allylargylsulfosuccinate, methalylsulfonic acid, p-methallyloxybenzenesulfonic acid, and their sodium salts, potassium salts, or ammonium salts.

以上述べた(イ)成分、(ロ)成分および()1)成分
の各単量体はそれぞれ1種のみでも2種以上組み合せて
用いてもよい。
Each monomer of component (a), component (b) and component ()1) described above may be used alone or in combination of two or more.

乳化共重合させる際の上記成分の使用割合は、(イ)成
分99〜70重量%、(ロ)成分0.5〜15重憬%お
よび()1)成分05〜15重量%とすることが望まし
い。乳化共重合方法は一般的な方法でよく、乳化剤とし
てはアニオン系、ノニオン系、カチオン系の各種界面活
性剤が使用され、また重合開始剤としては過硫酸カリウ
ム、過硫酸アンモニウム、過酸化水素、あるいはこれら
過酸化物と還元剤とを組合せたレドックス系触媒が使用
される。なお、乳化重合系には必要に応じ連鎖移動剤、
緩衝剤、無機塩類など通常乳化重合【1使用される重合
助剤を添加してもよい。
The proportions of the above components used during emulsion copolymerization may be (a) 99 to 70% by weight of component, (b) component 0.5 to 15% by weight, and () 1) component 05 to 15% by weight. desirable. The emulsion copolymerization method may be a general method, and various anionic, nonionic, and cationic surfactants are used as emulsifiers, and potassium persulfate, ammonium persulfate, hydrogen peroxide, or A redox catalyst containing a combination of these peroxides and a reducing agent is used. In addition, a chain transfer agent or a chain transfer agent may be added to the emulsion polymerization system as necessary.
Polymerization aids commonly used in emulsion polymerization (1) such as buffers and inorganic salts may be added.

このようにして得られる乳化共重合エマルジョンは、固
形分すなわち重合体成分のTgが一10℃ないし一60
℃であることが望ましく、前記した各成分の使用割合お
よびこの’rgの範囲が外れると望まれる付着力(接着
力)が発揮されない場合がある。またこの乳化共重合エ
マルジョンを農薬と混合する場合に固形分濃度は5重量
%以上であることが好ましく、これ以下であると散布液
の粘度が充分でないために農薬の分散安定性が低下し散
布の際トラブルが生じたり、また植物体への農薬の付着
力が発揮されない場合が生じる。乳化共重合エマルジョ
ンのnHについては特に制限はないが、植物体に薬害を
及ぼさないような範囲すなわちpH5〜8のものとして
使用することが望ましい。
The emulsion copolymer emulsion thus obtained has a solid content, that is, a Tg of the polymer component ranging from 110°C to 160°C.
It is desirable that the temperature is 0.degree. C., and if the above-mentioned proportions of each component used and the range of 'rg are out of range, the desired adhesion force (adhesive force) may not be exhibited. In addition, when this emulsion copolymerization emulsion is mixed with agricultural chemicals, it is preferable that the solid content concentration is 5% by weight or more. If it is less than this, the viscosity of the spraying liquid will not be sufficient and the dispersion stability of the agricultural chemicals will decrease, resulting in the spraying. Trouble may occur during this process, or the pesticide may not be able to adhere to the plant. Although there are no particular restrictions on the nH of the emulsion copolymerization emulsion, it is desirable to use it within a range that does not cause phytotoxicity to plants, that is, within the range of pH 5 to 8.

農薬と合成樹脂エマルジョンとの混合割合については、
農薬の種類、形態ならびに合成樹脂エマルジョンの種類
、固形分濃度等によりその適切な割合が定められるので
これを画一的に論じることはできないが、通常は農薬1
重量部に対し合成樹脂エマルジョンの固形分0.2〜2
重量部、水成分1〜20重量部の範囲となるようにする
ことが望ましい。
Regarding the mixing ratio of agricultural chemicals and synthetic resin emulsion,
The appropriate ratio is determined by the type and form of the pesticide as well as the type of synthetic resin emulsion, solid content concentration, etc., so this cannot be discussed uniformly, but usually pesticide 1
Solid content of synthetic resin emulsion 0.2 to 2 parts by weight
It is desirable that the water component be in the range of 1 to 20 parts by weight.

なお、前記合成樹脂エマルジョンには付着性、接着性を
さらに向上させる目的で水溶性セルロースエーテル、ポ
リビニルアルコール、ポリアクリル酸などの増粘剤を併
用してもよい。
In addition, a thickener such as water-soluble cellulose ether, polyvinyl alcohol, polyacrylic acid, etc. may be used in combination with the synthetic resin emulsion for the purpose of further improving adhesion and adhesion.

本発明の農薬組成物を散布する方法は、適用場所、規模
等により、機械による散布、室中散布など適宜の方法に
よればよく、散布手段に特別の制限はない。なお、本発
明にかかわる該組成物は水性液であるので駆動力と吐出
ノズルを備えた背負式等の簡便な一般的散布機により容
易に散布することができ、一般の農家においてもその取
り扱いに苦労することはない。
The method of spraying the agrochemical composition of the present invention may be any suitable method such as mechanical spraying or indoor spraying depending on the application site, scale, etc., and there are no particular restrictions on the spraying means. Furthermore, since the composition according to the present invention is an aqueous liquid, it can be easily sprayed using a simple general sprayer such as a backpack type sprayer equipped with a driving force and a discharge nozzle, and is easy to handle even for ordinary farmers. It's not a struggle.

つぎi二具体的実施例をあげる。Next, two specific examples will be given.

実施例1 合成樹脂エマルジョンを下記のように製造した。Example 1 A synthetic resin emulsion was produced as follows.

合成樹脂エマルジョン(1): かくはん機、温度計、還流冷却器および窒素ガス導入管
を備えた反応容器に、 アクリル酸2−エチル      701E量部ヘキシ
ル 酢酸ビニル           2o 〃メタクリル
酸           9 〃ラウリル硫酸ナトリウ
ム     o、5〃過硫酸アンモン        
 o、2〃水                  1
oo  〃を仕込み、窒素気流中でかくはんしつつ70
’Cで6時間乳化共重合反応させた。ついで冷却しアン
モニア水でpH値6〜7になるように調整し、粗大粒子
のない安定な合成樹脂エマルジョンを得た。
Synthetic resin emulsion (1): In a reaction vessel equipped with a stirrer, a thermometer, a reflux condenser, and a nitrogen gas introduction tube, 2-ethyl acrylate 701E parts Hexyl vinyl acetate 2o Methacrylic acid 9 Sodium lauryl sulfate o, 5 Ammonium persulfate
o, 2 water 1
oo 〃 and stirred in a nitrogen stream for 70 minutes.
An emulsion copolymerization reaction was carried out at 'C for 6 hours. The mixture was then cooled and adjusted to a pH value of 6 to 7 with aqueous ammonia to obtain a stable synthetic resin emulsion free of coarse particles.

このものは固形分含有量50%、p)T6.2、粘度2
00センチポアズ(25℃、ブルックフィールド粘度計
)、TK値−38,3℃であった。
This has a solid content of 50%, p) T6.2, and a viscosity of 2.
00 centipoise (25°C, Brookfield viscometer), TK value -38.3°C.

つぎに、農薬としてダイアジノンな有効成分とする平均
粒子径0.4 amの粒剤を用意し、このもの100重
量部と上記合成樹脂エマル017100重量部および水
500重量部を混合し、散布用農薬組成物を調製した。
Next, prepare a granule with an average particle size of 0.4 am and use it as an active ingredient of diazinon as a pesticide, and mix 100 parts by weight of this with 100 parts by weight of the above synthetic resin emul 017 and 500 parts by weight of water to prepare a pesticide for spraying. A composition was prepared.

この農薬組成物を(株)共立製の背負式動力散布機(P
D−703E−13型)に仕込み、水平より45°の角
度に固定したlmX1mの大きさのポリエチレンシート
上に2mの距離から散布し、該ポリエチレンシート上に
ダイアジノン粒剤が付着した数と付着せずに落下した数
とから散布時における付着率を求めた。
This agrochemical composition was applied to a backpack-type power sprayer (P) manufactured by Kyoritsu Co., Ltd.
D-703E-13) and sprayed from a distance of 2 m onto a polyethylene sheet measuring lm x 1 m fixed at an angle of 45° from the horizontal, and the number of diazinon granules adhering to the polyethylene sheet and the adhesion rate were measured. The adhesion rate at the time of spraying was determined from the number of drops that fell without falling.

散布時の付着率−−X 100  (%)a 十b a:付着した粒剤数 b:落下した粒剤数 また、散布を行ない25℃で5時間乾燥後このダイアジ
ノン粒剤付着面に約50j/分・dの条件で1時間また
は3時間散水した際の当初の粒剤付着数に対する残存付
着数を調べ、散水後の付着率か求めた。
Adhesion rate during spraying -- When water was sprinkled for 1 hour or 3 hours under the condition of /min·d, the number of remaining particles attached to the initial number of particles attached was examined, and the adhesion rate after watering was determined.

a′ 散水後の付着率=  −x  loo  (%)b′ a′:散水後の付着粒剤数 b′:散水前の付着粒剤数 結果はそれぞれ次のとおりであった。a′ Adhesion rate after watering = −x loo (%) b′ a′: Number of adhered granules after watering b': Number of adhered granules before watering The results were as follows.

散水後付着率 : 99% 散水後付着率 散水1時間後:98% 散水3時間後:96% 実施例2〜6 合成樹脂エマルジョン(1)と同様にして下記の各組成
および性状を有する合成樹脂エマルジョン(2)〜(6
)を得た。
Adhesion rate after watering: 99% Adhesion rate after watering 1 hour after watering: 98% 3 hours after watering: 96% Examples 2 to 6 Synthetic resins having the following composition and properties in the same manner as synthetic resin emulsion (1) Emulsion (2) ~ (6
) was obtained.

合成樹脂エマルジョン(2): (単量体仕込み組成) メタクリル酸メチル    10 /lアクリル酸グリ
シジル    5  //(性 状) 固形分=52%、p)(=6.8、 粘度=100センチポアズ(25℃)、Tg=−−50
,6℃ 合成樹脂エマルジョン(3): (単量体仕込み組成) アクリル酸ブチル     64重量部メタクリル酸メ
チル    32重量部メタクリル酸        
3 〃 酸ナトリウム (性 状) 固形分−50%、p)(=5.2、 粘度=350センチポアズ(25℃)、Tg=−14,
8℃ 合成樹脂エマルジョン(4): (中11体仕込み組成) アクリル酸          6 〃(性 状) 1句形分=51%、pH=6.2、 粘度=400センチポアズ(25℃) ’1’g−−60℃ 合成樹脂エマルジョン(5): (単量体仕込み組成) 酢酸ビニル         16 〃メタクリル酸 
        7  Llビニルスルホン酸ナトリウ
ム    7ノ/(性 状) 固形分=48%、 pH=6.3、 粘度;300センチポアズ(25℃)、Tg=−40,
4℃ 合成樹脂エマルジョン(6): (単量体仕込み組成) アクリル酸ブチル      99重量部アクリル酸 
        05 〃トリウム (性 状) 固形分;49%、 pH=6.6  、粘度=50セン
チポアズ(25℃)、 Tg=−54℃ 次に実施例1で用いたと同様のダイアジノン粒剤100
重量部と上記いずれかの合成樹脂エマルジョン100重
量部および水500重量部を混合し、各組成物を調製し
た。これらについて実施例1と同様にして散布蒔付着率
(%)および散水後付着率(%) (散水1時間後およ
び散水3時間後)を測定したところ、第1表に示すとお
りの結果が得られた。
Synthetic resin emulsion (2): (Monomer composition) Methyl methacrylate 10/l Glycidyl acrylate 5 // (Properties) Solid content = 52%, p) (=6.8, Viscosity = 100 centipoise (25) ℃), Tg=--50
, 6°C Synthetic resin emulsion (3): (Monomer charge composition) Butyl acrylate 64 parts by weight Methyl methacrylate 32 parts by weight methacrylic acid
3 Sodium acid (properties) Solid content -50%, p) (=5.2, Viscosity=350 centipoise (25℃), Tg=-14,
8℃ Synthetic resin emulsion (4): (Medium 11 composition) Acrylic acid 6〃(Properties) 1 block = 51%, pH = 6.2, viscosity = 400 centipoise (25℃) '1'g --60℃ Synthetic resin emulsion (5): (Monomer charging composition) Vinyl acetate 16 Methacrylic acid
7 Ll Sodium vinyl sulfonate 7/(Properties) Solid content = 48%, pH = 6.3, Viscosity: 300 centipoise (25°C), Tg = -40,
4℃ Synthetic resin emulsion (6): (Monomer preparation composition) Butyl acrylate 99 parts by weight acrylic acid
05 Thorium (Properties) Solid content: 49%, pH = 6.6, viscosity = 50 centipoise (25°C), Tg = -54°C Next, diazinon granules 100 similar to those used in Example 1
Each part by weight was mixed with 100 parts by weight of any of the above synthetic resin emulsions and 500 parts by weight of water to prepare each composition. The adhesion rate after spraying (%) and the adhesion rate after watering (%) (1 hour after watering and 3 hours after watering) were measured for these in the same manner as in Example 1, and the results shown in Table 1 were obtained. It was done.

第   1   表 比較例1 実施例1において、合成樹脂エマルジョン(1)の代す
に酢酸ビニル樹脂エマルジョン〔コニシ(株)製、ボン
ドC!H−18)を同じ使用割合で使用したほかは同様
にして散布実験を行った。散布時の付着率は98%であ
ったが、散水1時間後の付着率は22%と低く、さらに
散水3時間後の付着率は1%でありほとんどが脱落・流
失し、充分な付着力を示さなかった。
Table 1 Comparative Example 1 In Example 1, a vinyl acetate resin emulsion [manufactured by Konishi Co., Ltd., Bond C!] was used instead of the synthetic resin emulsion (1). Spraying experiments were conducted in the same manner except that H-18) was used at the same rate. The adhesion rate at the time of spraying was 98%, but the adhesion rate after 1 hour of watering was as low as 22%, and the adhesion rate after 3 hours of watering was only 1%, meaning most of it fell off or was washed away, indicating sufficient adhesion. did not show.

実施例7 実施例1で調製した、ダイアジノン粒剤と合成樹脂エマ
ルジョン(1)とからなる組成物を、樹脂4mのリンゴ
の木に散布して1力月後の残存付着率(%) を調べた。この試験期間中降雨のあった日数は5日間で
あったが、1力月放置後の付着率は88%であり良好な
付着性能を示した。
Example 7 The composition prepared in Example 1, consisting of diazinon granules and synthetic resin emulsion (1), was sprayed on an apple tree with 4 m of resin, and the residual adhesion rate (%) after 1 month was investigated. Ta. Although there were 5 days of rain during this test period, the adhesion rate after being left for one month was 88%, indicating good adhesion performance.

比較例2 比較例1と同様の散布組成物を、実施例7の試験と並行
してリンゴの木に散布し、1力月後の残存付着率を調べ
た。最初の降雨日の後の付着率がすでに38%と低く、
1力月放置後ではほとんどが脱落しており充分な付着力
を示さなかった。
Comparative Example 2 The same spray composition as in Comparative Example 1 was sprayed on apple trees in parallel with the test in Example 7, and the residual adhesion rate after one month was examined. The adhesion rate after the first rainy day is already low at 38%.
After leaving it for one month, most of it fell off and did not show sufficient adhesion.

Claims (1)

【特許請求の範囲】[Claims] 1、農薬成分と、(イ)不飽和カルボン酸のエステル、
不飽和ジカルボン酸のジエステルおよび脂肪酸ビニルの
1種または2種以上、(ロ)カルボキシル基、グリシジ
ル基、アルキル置換されたもしくはされないメチロール
基、ヒドロキシル基、アミノ基またはアミド基を有する
重合性単量体の1種または2種以上、および(ハ)ビニ
ル基、アリル基またはメタアリル基とスルホン酸基とを
分子内に有する重合性単量体あるいはその塩類の1種ま
たは2種以上を乳化共重合して得た合成樹脂エマルジョ
ンとからなる散布用農薬組成物
1. Pesticide component and (a) unsaturated carboxylic acid ester,
Polymerizable monomer having one or more diesters of unsaturated dicarboxylic acids and vinyl fatty acids, (b) carboxyl group, glycidyl group, alkyl-substituted or non-alkyl-substituted methylol group, hydroxyl group, amino group, or amide group and (iii) emulsion copolymerization of one or more polymerizable monomers having a vinyl group, an allyl group, or a metaallyl group, and a sulfonic acid group or their salts in the molecule. A pesticide composition for spraying consisting of a synthetic resin emulsion obtained by
JP12494084A 1984-06-18 1984-06-18 Agricultural chemical composition for application Granted JPS615001A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12494084A JPS615001A (en) 1984-06-18 1984-06-18 Agricultural chemical composition for application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12494084A JPS615001A (en) 1984-06-18 1984-06-18 Agricultural chemical composition for application

Publications (2)

Publication Number Publication Date
JPS615001A true JPS615001A (en) 1986-01-10
JPH0369321B2 JPH0369321B2 (en) 1991-10-31

Family

ID=14897950

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12494084A Granted JPS615001A (en) 1984-06-18 1984-06-18 Agricultural chemical composition for application

Country Status (1)

Country Link
JP (1) JPS615001A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61291502A (en) * 1985-06-19 1986-12-22 Shinto Paint Co Ltd Method for controlling noxious life
JP2008532978A (en) * 2005-03-10 2008-08-21 ビーエーエスエフ ソシエタス・ヨーロピア Method for producing aqueous polymer dispersion containing pesticide and use thereof
WO2014010435A1 (en) * 2012-07-13 2014-01-16 日本エンバイロケミカルズ株式会社 Anti-bioactive particles and method for manufacturing same

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR071497A1 (en) * 2008-04-25 2010-06-23 Nippon Soda Co GRANULATED AGROCHEMICAL COMPOSITION AND PROCEDURE OF ITS PRODUCTION

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61291502A (en) * 1985-06-19 1986-12-22 Shinto Paint Co Ltd Method for controlling noxious life
JP2008532978A (en) * 2005-03-10 2008-08-21 ビーエーエスエフ ソシエタス・ヨーロピア Method for producing aqueous polymer dispersion containing pesticide and use thereof
WO2014010435A1 (en) * 2012-07-13 2014-01-16 日本エンバイロケミカルズ株式会社 Anti-bioactive particles and method for manufacturing same
CN104411168A (en) * 2012-07-13 2015-03-11 日本环境化学株式会社 Anti-bioactive particles and method for manufacturing same

Also Published As

Publication number Publication date
JPH0369321B2 (en) 1991-10-31

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